Proposed Significant New Use Rules on Certain Chemical Substances, 12684-12701 [2013-04298]
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If your GAP is submitted . . .
Your GAP will be handled as follows:
(a) Before lease or grant issuance ..........
You will furnish a copy of your GAP, consistency certification, and necessary data and information
pursuant to 15 CFR part 930, subpart D, to the State’s CZM agency and BOEM at the same time.
You will submit a copy of your GAP, consistency certification, and necessary data and information
pursuant to 15 CFR 93, subpart E to BOEM. BOEM will forward to the State CZMA agency one
paper copy and one electronic copy of your GAP, consistency certification, and necessary data and
information required under 15 CFR part 930, subpart E, after BOEM has determined that all information requirements for the GAP are met.
(b) After lease or grant issuance .............
25. Revise § 585.902 paragraph (f) to
read as follows:
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§ 585.902 What are the general
requirements for decommissioning facilities
authorized under my SAP, COP, or GAP?
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(f) Provide BOEM with
documentation of any coordination
efforts you have made with the State
CZMA agencies, and any affected States,
local, and Tribal governments.
PART 590—APPEAL PROCEDURES
26. The authority citation for part 590
is revised to read as follows:
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Authority: 5 U.S.C. 301 et seq.; 31 U.S.C.
9701; 43 U.S.C. 1334.
27. Revise § 590.4 paragraph (b)(1) to
read as follows:
■
§ 590.4
How do I file an appeal?
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(b) * * *
(1) You must pay electronically
through the Fees for Services page on
the BOEM Web site at https://
www.boem.gov, and you must include a
copy of the Pay.gov confirmation receipt
page with your Notice of Appeal.
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[FR Doc. 2013–03992 Filed 2–22–13; 8:45 am]
BILLING CODE 4310–MR–P
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 721
[EPA–HQ–OPPT–2012–0727; FRL–9376–7]
RIN 2070–AB27
Proposed Significant New Use Rules
on Certain Chemical Substances
Environmental Protection
Agency (EPA).
ACTION: Proposed rule.
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AGENCY:
EPA is proposing significant
new use rules (SNURs) under the Toxic
Substances Control Act (TSCA) for 37
chemical substances which were the
subject of premanufacture notices
(PMNs). Seventeen of these chemical
substances are subject to TSCA section
5(e) consent orders issued by EPA. This
SUMMARY:
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action would require persons who
intend to manufacture, import, or
process any of these 37 chemical
substances for an activity that is
designated as a significant new use by
this proposed rule to notify EPA at least
90 days before commencing that
activity. The required notification
would provide EPA with the
opportunity to evaluate the intended
use and, if necessary, to prohibit or limit
that activity before it occurs.
DATES: Comments must be received on
or before April 26, 2013.
ADDRESSES: Submit your comments,
identified by docket identification (ID)
number EPA–HQ–OPPT–2012–0727, by
one of the following methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the online
instructions for submitting comments.
• Mail: Document Control Office
(7407M), Office of Pollution Prevention
and Toxics (OPPT), Environmental
Protection Agency, 1200 Pennsylvania
Ave. NW., Washington, DC 20460–0001.
• Hand Delivery: OPPT Document
Control Office (DCO), EPA East Bldg.,
Rm. 6428, 1201 Constitution Ave., NW.,
Washington, DC. ATTN: Docket ID
Number EPA–HQ–OPPT–2012–0727.
The DCO is open from 8 a.m. to 4 p.m.,
Monday through Friday, excluding legal
holidays. The telephone number for the
DCO is (202) 564–8930. Such deliveries
are only accepted during the DCO’s
normal hours of operation, and special
arrangements should be made for
deliveries of boxed information.
Instructions: Direct your comments to
docket ID number EPA–HQ–OPPT–
2012–0727. EPA’s policy is that all
comments received will be included in
the docket without change and may be
made available online at https://
www.regulations.gov, including any
personal information provided, unless
the comment includes information
claimed to be Confidential Business
Information (CBI) or other information
whose disclosure is restricted by statute.
Do not submit information that you
consider to be CBI or otherwise
protected through regulations.gov or
email. The regulations.gov Web site is
an ‘‘anonymous access’’ system, which
means EPA will not know your identity
or contact information unless you
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provide it in the body of your comment.
If you send an email comment directly
to EPA without going through
regulations.gov, your email address will
be automatically captured and included
as part of the comment that is placed in
the docket and made available on the
Internet. If you submit an electronic
comment, EPA recommends that you
include your name and other contact
information in the body of your
comment and with any disk or CD–ROM
you submit. If EPA cannot read your
comment due to technical difficulties
and cannot contact you for clarification,
EPA may not be able to consider your
comment. Electronic files should avoid
the use of special characters, any form
of encryption, and be free of any defects
or viruses.
Docket: All documents in the docket
are listed in the docket index available
at https://www.regulations.gov. Although
listed in the index, some information is
not publicly available, e.g., CBI or other
information whose disclosure is
restricted by statute. Certain other
material, such as copyrighted material,
will be publicly available only in hard
copy. Publicly available docket
materials are available electronically at
https://www.regulations.gov, or, if only
available in hard copy, at the OPPT
Docket. The OPPT Docket is located in
the EPA Docket Center (EPA/DC) at Rm.
3334, EPA West Bldg., 1301
Constitution Ave. NW., Washington,
DC. The EPA/DC Public Reading Room
hours of operation are 8:30 a.m. to 4:30
p.m., Monday through Friday, excluding
legal holidays. The telephone number of
the EPA/DC Public Reading Room is
(202) 566–1744, and the telephone
number for the OPPT Docket is (202)
566–0280. Docket visitors are required
to show photographic identification,
pass through a metal detector, and sign
the EPA visitor log. All visitor bags are
processed through an X-ray machine
and subject to search. Visitors will be
provided an EPA/DC badge that must be
visible at all times in the building and
returned upon departure.
FOR FURTHER INFORMATION CONTACT: For
technical information contact: Kenneth
Moss, Chemical Control Division
(7405M), Office of Pollution Prevention
and Toxics, Environmental Protection
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Agency, 1200 Pennsylvania Ave. NW.,
Washington, DC 20460–0001; telephone
number: (202) 564–9232; email address:
moss.kenneth@epa.gov.
For general information contact: The
TSCA-Hotline, ABVI-Goodwill, 422
South Clinton Ave., Rochester, NY
14620; telephone number: (202) 554–
1404; email address: TSCAHotline@epa.gov.
SUPPLEMENTARY INFORMATION:
I. General Information
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A. Does this action apply to me?
You may be potentially affected by
this action if you manufacture, import,
process, or use the chemical substances
in this proposed rule. The following list
of North American Classification
System (NAICS) codes is not intended
to be exhaustive, but rather provides a
guide to help readers determine whether
this document applies to them.
Potentially affected entities may
include:
• Manufacturers, importers, or
processors of one or more subject
chemical substances (NAICS codes 325
and 324110), e.g., chemical
manufacturing and petroleum refineries.
This action may also affect certain
entities through pre-existing import
certification and export notification
rules under TSCA. Chemical importers
are subject to the TSCA section 13 (15
U.S.C. 2612) import certification
requirements promulgated at 19 CFR
12.118 through 12.127; see also 19 CFR
127.28. Chemical importers must certify
that the shipment of the chemical
substance complies with all applicable
rules and orders under TSCA. Importers
of chemicals subject to a final SNUR
must certify their compliance with the
SNUR requirements. The EPA policy in
support of import certification appears
at 40 CFR part 707, subpart B. In
addition, any persons who export or
intend to export a chemical substance
that is the subject of a proposed or final
SNUR are subject to the export
notification provisions of TSCA section
12(b) (15 U.S.C. 2611(b)) (see § 721.20)
and must comply with the export
notification requirements in 40 CFR part
707, subpart D.
B. What should I consider as I prepare
my comments for EPA?
1. Submitting CBI. Do not submit this
information to EPA through
regulations.gov or email. Clearly mark
the part or all of the information that
you claim to be CBI. For CBI
information in a disk or CD–ROM that
you mail to EPA, mark the outside of the
disk or CD–ROM as CBI and then
identify electronically within the disk or
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CD–ROM the specific information that
is claimed as CBI. In addition to one
complete version of the comment that
includes information claimed as CBI, a
copy of the comment that does not
contain the information claimed as CBI
must be submitted for inclusion in the
public docket. Information so marked
will not be disclosed except in
accordance with procedures set forth in
40 CFR part 2.
2. Tips for preparing your comments.
When submitting comments, remember
to:
i. Identify the document by docket ID
number and other identifying
information (subject heading, Federal
Register date and page number).
ii. Follow directions. The Agency may
ask you to respond to specific questions
or organize comments by referencing a
Code of Federal Regulations (CFR) part
or section number.
iii. Explain why you agree or disagree;
suggest alternatives and substitute
language for your requested changes.
iv. Describe any assumptions and
provide any technical information and/
or data that you used.
v. If you estimate potential costs or
burdens, explain how you arrived at
your estimate in sufficient detail to
allow for it to be reproduced.
vi. Provide specific examples to
illustrate your concerns and suggest
alternatives.
vii. Explain your views as clearly as
possible, avoiding the use of profanity
or personal threats.
viii. Make sure to submit your
comments by the comment period
deadline identified.
II. Background
A. What action is the agency taking?
These proposed SNURs would, when
finalized, require persons to notify EPA
at least 90 days before commencing the
manufacture, import, or processing of
the specific chemical substances
identified in the PMNs for any activity
designated by these SNURs as a
significant new use. Receipt of such
notices allows EPA to assess risks that
may be presented by the intended uses
and, if appropriate, to regulate the
proposed use before it occurs.
Additional rationale and background to
these rules are more fully set out in the
preamble to EPA’s first direct final
SNUR published in the Federal Register
of April 24, 1990 (55 FR 17376). Consult
that preamble for further information on
the objectives, rationale, and procedures
for SNURs and on the basis for
significant new use designations,
including provisions for developing test
data.
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B. What is the Agency’s authority for
taking this action?
Section 5(a)(2) of TSCA (15 U.S.C.
2604(a)(2)) authorizes EPA to determine
that a use of a chemical substance is a
‘‘significant new use.’’ EPA must make
this determination by rule after
considering all relevant factors,
including the four bulleted TSCA
section 5(a)(2) factors listed in Unit III.
Once EPA determines that a use of a
chemical substance is a significant new
use, TSCA section 5(a)(1)(B) and 40 CFR
part 721 require persons to submit a
significant new use notice (SNUN) to
EPA at least 90 days before they
manufacture, import, or process the
chemical substance for that use. Persons
who must report are described in
§ 721.5.
C. Applicability of General Provisions
General provisions for SNURs appear
in 40 CFR part 721, subpart A. These
provisions describe persons subject to
the rule, recordkeeping requirements,
exemptions to reporting requirements,
and applicability of the rule to uses
occurring before the effective date of the
final rule. Provisions relating to user
fees appear at 40 CFR part 700.
According to § 721.1(c), persons
subject to these SNURs must comply
with the same SNUN requirements and
EPA regulatory procedures as submitters
of PMNs under TSCA section 5(a)(1)(A).
In particular, these requirements
include the information submission
requirements of TSCA section 5(b) and
5(d)(1), the exemptions authorized by
TSCA section 5(h)(1), (h)(2), (h)(3), and
(h)(5), and the regulations at 40 CFR
part 720. Once EPA receives a SNUN,
EPA may take regulatory action under
TSCA section 5(e), 5(f), 6, or 7 to control
the activities for which it has received
the SNUN. If EPA does not take action,
EPA is required under TSCA section
5(g) to explain in the Federal Register
its reasons for not taking action.
III. Significant New Use Determination
Section 5(a)(2) of TSCA states that
EPA’s determination that a use of a
chemical substance is a significant new
use must be made after consideration of
all relevant factors, including:
• The projected volume of
manufacturing and processing of a
chemical substance.
• The extent to which a use changes
the type or form of exposure of human
beings or the environment to a chemical
substance.
• The extent to which a use increases
the magnitude and duration of exposure
of human beings or the environment to
a chemical substance.
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• The reasonably anticipated manner
and methods of manufacturing,
processing, distribution in commerce,
and disposal of a chemical substance.
In addition to these factors
enumerated in TSCA section 5(a)(2), the
statute authorized EPA to consider any
other relevant factors.
To determine what would constitute a
significant new use for the 37 chemical
substances that are the subject of these
proposed SNURs, EPA considered
relevant information about the toxicity
of the chemical substances, likely
human exposures and environmental
releases associated with possible uses,
taking into consideration the four
bulleted TSCA section 5(a)(2) factors
listed in this unit.
IV. Substances Subject to This Proposed
Rule
EPA is proposing to establish
significant new use and recordkeeping
requirements for 37 chemical substances
in 40 CFR part 721, subpart E. In this
unit, EPA provides the following
information for each chemical
substance:
• PMN number.
• Chemical name (generic name, if
the specific name is claimed as CBI).
• Chemical Abstracts Service (CAS)
number (if assigned for non-confidential
chemical identities).
• Basis for the TSCA section 5(e)
consent order or, for TSCA non-section
5(e) SNURs, the basis for the SNUR (i.e.,
SNURs without TSCA section 5(e)
consent orders).
• Tests recommended by EPA to
provide sufficient information to
evaluate the chemical substance (see
Unit VIII. for more information).
• CFR citation assigned in the
regulatory text section of this proposed
rule.
This proposed rule includes 14 PMN
substances whose reported chemical
names include the term ‘‘carbon
nanotube’’ or ‘‘carbon nanofibers.’’
Because of a lack of established
nomenclature for carbon nanotubes, the
TSCA Inventory names for carbon
nanotubes are currently in generic form,
e.g., carbon nanotube (CNT), multiwalled carbon nanotube (MWCNT),
double-walled carbon nanotube
(DWCNT), or single-walled carbon
nanotube (SWCNT). EPA uses the
specific structural characteristics
provided by the PMN submitter to more
specifically characterize the TSCA
Inventory listing for an individual CNT.
All submitters of new chemical notices
for CNTs have claimed those specific
structural characteristics as CBI. EPA is
publishing the generic chemical name
along with the PMN number to identify
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that a distinct chemical substance was
the subject of the PMN without
revealing the confidential chemical
identity of the PMN substance.
Confidentiality claims preclude a more
detailed description of the identity of
these CNTs. If an intended
manufacturer, importer, or processor of
CNTs is unsure of whether its CNTs are
subject to this proposed SNUR or any
other SNUR, the company can either
contact EPA or obtain a written
determination from EPA pursuant to the
bona fide procedures at § 721.11. EPA is
using the specific structural
characteristics for all CNTs submitted as
new chemical substances under TSCA
to help develop standard nomenclature
for placing these chemical substances
on the TSCA Inventory. EPA has
compiled a generic list of those
structural characteristics entitled
‘‘Material Characterization of Carbon
Nanotubes for Molecular Identity (MI)
Determination & Nomenclature.’’ A
copy of this list is available in the
docket for these proposed SNURs under
docket ID number EPA–HQ–OPPT–
2012–0727. If EPA develops a more
specific generic chemical name for these
materials, that name will be made
publicly available.
The regulatory text section of this
proposed rule specifies the activities
designated as significant new uses.
Certain new uses, including exceeding
production volume limits (i.e., limits on
manufacture and importation volume)
and other uses designated in this
proposed rule, may be claimed as CBI.
This proposed rule includes 17 PMN
substances for which EPA determined,
pursuant to TSCA section 5(e), that
uncontrolled manufacture, import,
processing, distribution in commerce,
use, and disposal may present an
unreasonable risk of injury to human
health or the environment. Accordingly,
these substances are subject to ‘‘riskbased’’ consent orders under TSCA
section 5(e)(1)(A)(ii)(I). Those consent
orders require protective measures to
limit exposures or otherwise mitigate
the potential unreasonable risk. The socalled ‘‘section 5(e) SNURs’’ on these
PMN substances are proposed pursuant
to § 721.160, and are based on and
consistent with the provisions in the
underlying consent orders. The section
5(e) SNURs designate as a ‘‘significant
new use’’ the absence of the protective
measures required in the corresponding
consent orders.
Where EPA determined that the PMN
substance may present an unreasonable
risk of injury to human health via
inhalation exposure, the underlying
TSCA section 5(e) consent order usually
requires, among other things, that
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potentially exposed employees wear
specified respirators unless actual
measurements of the workplace air
show that air-borne concentrations of
the PMN substance are below a New
Chemical Exposure Limit (NCEL) that is
established by EPA to provide adequate
protection to human health. In addition
to the actual NCEL concentration, the
comprehensive NCELs provisions in
TSCA section 5(e) consent orders,
which are modeled after Occupational
Safety and Health Administration
(OSHA) Permissible Exposure Limits
(PELs) provisions, include requirements
addressing performance criteria for
sampling and analytical methods,
periodic monitoring, respiratory
protection, and recordkeeping.
However, no comparable NCEL
provisions currently exist in 40 CFR
part 721, subpart B, for SNURs.
Therefore, for these cases, the
individual SNURs in 40 CFR part 721,
subpart E, will normally state that
persons subject to the SNUR who wish
to pursue NCELs as an alternative to the
§ 721.63 respirator requirements may
request to do so under § 721.30. EPA
expects that persons whose § 721.30
requests to use the NCELs approach for
SNURs are approved by EPA will be
required to comply with NCELs
provisions that are comparable to those
contained in the corresponding TSCA
section 5(e) consent order for the same
chemical substance.
This proposed rule also includes
SNURs on 20 PMN substances that are
not subject to consent orders under
TSCA section 5(e). In these cases, for a
variety of reasons, EPA did not find that
the use scenario described in the PMN
triggered the determinations set forth
under TSCA section 5(e). However, EPA
does believe that certain changes from
the use scenario described in the PMN
could result in increased exposures,
thereby constituting a ‘‘significant new
use.’’ These so-called ‘‘non-section 5(e)
SNURs’’ are promulgated pursuant to
§ 721.170. EPA has determined that
every activity designated as a
‘‘significant new use’’ in all non-section
5(e) SNURs issued under § 721.170
satisfies the two requirements stipulated
in § 721.170(c)(2), i.e., these significant
new use activities, ‘‘(i) are different from
those described in the premanufacture
notice for the substance, including any
amendments, deletions, and additions
of activities to the premanufacture
notice, and (ii) may be accompanied by
changes in exposure or release levels
that are significant in relation to the
health or environmental concerns
identified’’ for the PMN substance.
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PMN Number P–00–835
Chemical name: Substituted
picolinate (generic).
CAS number: Claimed as confidential.
Basis for action: The PMN states that
the substance will be used as an
intermediate in the manufacture of
agricultural chemicals. Based on
ecological structure activity relationship
(EcoSAR) analysis of test data on
analogous esters, EPA predicts toxicity
to aquatic organisms may occur at
concentrations that exceed 90 parts per
billion (ppb) of the PMN substance in
surface waters. As described in the
PMN, releases to surface water are not
expected. Therefore, EPA has not
determined that the proposed
manufacturing, processing, or use of the
substance may present an unreasonable
risk. EPA has determined, however, that
any use of the substance resulting in
surface water concentrations exceeding
90 ppb may cause significant adverse
environmental effects. Based on this
information, the PMN substance meets
the concern criteria at
§ 721.170(b)(4)(ii).
Recommended testing: EPA has
determined that the results of a fish
acute toxicity test, freshwater and
marine (OPPTS Test Guideline
850.1075); an aquatic invertebrate acute
toxicity test, freshwater daphnids
(OPPTS Test Guideline 850.1010); and
an algal toxicity test (Office of Chemical
Safety and Pollution Prevention
(OCSPP) Test Guideline 850.4500)
would help characterize the
environmental effects of the PMN
substance.
CFR citation: 40 CFR 721.10637.
PMN Number P–02–167
Chemical name: Lithium metal
phosphate (generic).
CAS number: Claimed as confidential.
Basis for action: The PMN states that
the generic (non-confidential) use of the
substance will be as an electrode
material. Based on EcoSAR analysis of
test data on analogous inorganic
phosphates, EPA predicts toxicity to
aquatic organisms may occur at
concentrations that exceed 1 ppb of the
PMN substance in surface waters. As
described in the PMN, releases to water
are not expected to exceed 1 ppb.
Therefore, EPA has not determined that
the proposed manufacturing,
processing, or use of the substance
presents an unreasonable risk. EPA has
determined, however, that any use of
the substance resulting in surface water
concentrations exceeding 1 ppb may
cause significant adverse environmental
effects. Based on this information, the
PMN substance meets the concern
criteria at § 721.170(b)(4)(ii).
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Recommended testing: EPA has
determined that the results of a fish
acute toxicity test, freshwater and
marine (OPPTS Test Guideline
850.1075); an aquatic invertebrate acute
toxicity test, freshwater daphnids
(OPPTS Test Guideline 850.1010); and
an algal toxicity test (OCSPP Test
Guideline 850.4500) would help
characterize the environmental effects of
the PMN substance.
CFR citation: 40 CFR 721.10638.
PMN Number P–02–668
Chemical name: Siloxanes and
Silicones, di-Me, polymers with Ph
silsesquioxanes, hydrolyzed, reaction
products with 2-[[3-(trimethoxysilyl)
propoxy]methyl]oxirane.
CAS number: 478823–10–8.
Basis for action: The PMN substance
will be used as a binder for silicone
coatings. Based on structure activity
relationship (SAR) analysis of test data
on analogous epoxides and
alkoxysilanes, EPA identified concerns
for mutagenicity, oncogenicity,
reproductive toxicity, developmental
toxicity, lung toxicity, and sensitization
from dermal and inhalation exposures
to the PMN substance. For the use
described in the PMN, significant
occupational dermal and inhalation
exposures are not expected due to the
use of impervious gloves and a National
Institute for Occupational Safety and
Health (NIOSH)-certified respirator with
an assigned protection factor (APF) of at
least 10, and consumer exposures are
not expected as the substance is not
used in consumer products. Therefore,
EPA has not determined that
manufacturing, processing, and use of
the substance may present an
unreasonable risk. EPA has determined,
however, that use of the substance
without impervious gloves where there
is a potential for dermal exposure; any
use of the substance without a NIOSHcertified respirator with an APF of at
least 10; or any use of the substance in
consumer products may result in
serious health effects. Based on this
information, the PMN substance meets
the concern criteria at § 721.170
(b)(1)(i)(C) and (b)(3)(ii).
Recommended testing: EPA has
determined that the results of a 90-day
inhalation toxicity test (OPPTS Test
Guideline 870.3465), with attention to
the pathology of the reproductive
organs, and a carcinogenicity test
(OPPTS Test Guideline 870.4200) would
help to characterize the human health
effects of the PMN substance.
CFR citation: 40 CFR 721.10639.
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PMN Number P–03–135
Chemical name: 1,2Cyclohexanedicarboxylic acid, 1-(2ethylhexyl) 2-(2-methylpropyl) ester.
CAS number: 252958–29–5.
Basis for action: The PMN states that
the generic (non-confidential) use of the
substance will be as a compressor
lubricant. Based on EcoSAR analysis of
test data on analogous esters, EPA
predicts toxicity to aquatic organisms
may occur at concentrations that exceed
1 ppb of the PMN substance in surface
waters. As described in the PMN, the
substance is not released to surface
waters. Therefore, EPA has not
determined that the proposed
manufacturing, processing, or use of the
substance may present an unreasonable
risk. EPA has determined, however, that
any use of the substance resulting in
surface water concentrations exceeding
1 ppb may cause significant adverse
environmental effects. There are two
other chemical substances identified in
the PMN that are already on the TSCA
Inventory. The SNUR does not apply to
those chemical substances. Based on
this information, the PMN substance
meets the concern criteria at
§ 721.170(b)(4)(ii).
Recommended testing: EPA has
determined that the results of a fish
early-life stage toxicity test (OPPTS Test
Guideline 850.1400); a daphnid chronic
toxicity test (OPPTS Test Guideline
850.1300); and an algal toxicity test
(OCSPP Test Guideline 850.4500) would
help to characterize the environmental
effects of the PMN substance.
CFR citation: 40 CFR 721.10640.
PMN Number P–03–255
Chemical name: Phenol and
vinyltoluene based hydrocarbon resin
(generic).
CAS number: Claimed as confidential.
Basis for action: The PMN states that
the generic (non-confidential) use of the
substance will be as a diluent for
coatings. Based on EcoSAR analysis of
test data on analogous neutral organics,
EPA predicts toxicity to aquatic
organisms may occur at concentrations
that exceed 1 ppb of the PMN substance
in surface waters. As described in the
PMN, releases to water are not expected.
Therefore, EPA has not determined that
the proposed manufacturing,
processing, or use of the substance may
present an unreasonable risk. EPA has
determined, however, that any use of
the substance resulting in surface water
concentrations exceeding 1 ppb may
cause significant adverse environmental
effects. Based on this information, the
PMN substance meets the concern
criteria at § 721.170(b)(4)(ii).
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Recommended testing: EPA has
determined that the results of a fish
early-life stage toxicity test (OPPTS Test
Guideline 850.1400); a daphnid chronic
toxicity test (OPPTS Test Guideline
850.1300); and an algal toxicity test
(OCSPP Test Guideline 850.4500) would
help to characterize the environmental
effects of the PMN substance.
CFR citation: 40 CFR 721.10641.
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PMN Numbers P–03–762 and P–03–763
Chemical name: Modified
polyisocyanates (generic).
CAS number: Claimed as confidential.
Basis for action: The consolidated
PMN states that the generic (nonconfidential) use of the substances will
be as hardeners. Based on SAR analysis
of test data on analogous isocyanates,
EPA has identified concerns for
sensitization and irritation from dermal
and inhalation exposure to the PMN
substances. For the use described in the
PMN, significant occupational
inhalation and dermal exposures are not
expected due to no domestic
manufacture, use of impervious gloves,
and no use of the substances involving
an application method that generates a
vapor, mist, or aerosol. Further,
consumer exposures are not expected as
the substance is not used in consumer
products. Therefore, EPA has not
determined that the proposed
processing or use of the substances may
present an unreasonable risk. EPA has
determined, however, that any domestic
manufacture of the substances; any use
of the substances without impervious
gloves where there is a potential for
dermal exposures; any use of the
substance in consumer products; or any
use of the substances involving an
application method that generates a
vapor, mist, or aerosol may result in
serious health effects. Based on this
information, the PMN substances meet
the concern criteria at
§ 721.170(b)(3)(ii).
Recommended testing: EPA has
determined that the results of a skin
sensitization test (OPPTS Test Guideline
870.2600) and a 90-day inhalation
toxicity test (OPPTS Test Guideline
870.3465) would help characterize the
human health effects of the PMN
substances.
CFR citation: 40 CFR 721.10642.
PMN Number P–04–640
Chemical name: Diisocyanate
terminated polycarbodiimide (generic).
CAS number: Claimed as confidential.
Effective date of TSCA section 5(e)
consent order: February 1, 2006.
Basis for TSCA section 5(e) consent
order: The PMN states that the generic
(non-confidential) use of the substance
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will be as a crosslinking agent for
solvent-based inks; a monomer for
polymerization; and a water scavenger
for producing anhydrous polymers. The
PMN did not identify consumer uses for
the PMN substance. Based on SAR
analysis of test data on structurally
similar diisocyanates, EPA identified
concerns for dermal sensitization,
respiratory sensitization, and
pulmonary toxicity from exposure to the
PMN substance by the inhalation and
dermal routes. The order was issued
under sections 5(e)(1)(A)(i) and
5(e)(1)(A)(ii)(I) of TSCA based on a
finding that this substance may present
an unreasonable risk of injury to human
health. To protect against these risks,
the order requires:
1. Use of personal protective
equipment including impervious gloves
(when there is potential dermal
exposure) and either a NIOSH-certified
respirator with an APF of at least 2,000,
or compliance with a NCEL of 0.05 mg/
m3 as an 8-hour time-weighted average
(when there is potential inhalation
exposure).
2. Establishment and use of a hazard
communication program. The SNUR
would designate as a ‘‘significant new
use’’ the absence of these protective
measures and consumer use of the PMN
substance.
Recommended testing: EPA has
determined that data from worker
exposure to the PMN substance (such as
inhalation monitoring data generated
according to the NCELs section of the
consent order) or a 90-day inhalation
toxicity test (OPPTS Test Guideline
870.3465) would help characterize the
human health effects of the PMN
substance. The order does not require
submission of the testing at any
specified time or production volume.
However, the order’s restrictions on
manufacture, import, processing,
distribution in commerce, use, and
disposal of the PMN substance will
remain in effect until the order is
modified or revoked by EPA based on
submission of that or other relevant
information.
CFR citation: 40 CFR 721.10643.
PMN Number P–07–553
Chemical name: Reaction product of
aluminum hydroxide and modified
alkoxysilane (generic).
CAS number: Claimed as confidential.
Basis for action: The PMN states that
the substance will be used as a flame
retardant. Based on SAR analysis of test
data on analogous respirable, poorly
soluble particulates, EPA identified
concerns for lung toxicity from
inhalation exposures to the PMN
substance. At an annual production
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volume of 100,000 kilograms (kgs),
significant occupational inhalation
exposures are not expected due to the
use of a NIOSH-certified respirator with
an APF of at least 10. Therefore, EPA
has not determined that the proposed
manufacturing, processing, or use of the
substance may present an unreasonable
risk. EPA has determined, however, that
any use of the substance without a
NIOSH-certified respirator with an APF
of at least 10, where there is a potential
for inhalation exposure; or any increase
of the annual 100,000 kg production
volume may result in increased
exposure to the PMN substance, which
may cause serious human health effects.
Based on this information, the PMN
substance meets the concern criteria at
§ 721.170(b)(3)(ii).
Recommended testing: EPA has
determined that the results of a 90-day
inhalation toxicity test (OPPTS Test
Guideline 870.3465) with a 60-day
holding period would help characterize
the health effects of the PMN substance.
CFR citation: 40 CFR 721.10644.
PMN Number P–08–392
Chemical name: Multi-walled carbon
nanotube (generic) (P–08–392).
CAS number: Claimed as confidential.
Effective date of TSCA section 5(e)
consent order: November 14, 2008.
Basis for TSCA section 5(e) consent
order: The PMN states that the generic
(non-confidential) use of the substance
will be as an antistatic, reinforcement
additive. Based on test data on the PMN
substance, and SAR analysis of test data
on structurally similar respirable, poorly
soluble particulates, EPA identified
concerns for pulmonary toxicity,
fibrosis, carcinogenicity, mutagenicity,
and immunotoxicity. The order was
issued under sections 5(e)(1)(A)(i) and
5(e)(1)(A)(ii)(I) of TSCA, based on a
finding that the PMN substance may
present an unreasonable risk of injury to
human health. To protect against these
risks, the order:
1. Requires use of personal protective
equipment including impervious gloves
and protective clothing (when there is a
potential dermal exposure) and a
NIOSH-certified air-purifying, tightfitting full-face respirator equipped with
N100 filters with an APF of at least 50
(when there is potential inhalation
exposure).
2. Prohibits manufacture of the PMN
substance in the United States.
3. Restricts processing and use of the
PMN substance to those uses specified
in the consent order.
The SNUR would designate as a
‘‘significant new use’’ the absence of
these protective measures.
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Recommended testing: EPA has
determined that the results of a 90-day
inhalation toxicity test (OPPTS Test
Guideline 870.3465 or Organisation for
Economic Co-operation and
Development (OECD) Test Guideline
413) in rats with a post exposure
observation period of up to 3 months,
including bronchoalveolar lavage fluid
(BALF) analysis and certain material
characterization data, would help
characterize possible effects of the
substance. In the consent order, the
PMN submitter has agreed to perform
these tests within 18 months of
commencing non-exempt commercial
manufacture.
CFR citation: 40 CFR 721.10645.
PMN Number P–09–257
Chemical name: Multi-walled carbon
nanotube (generic) (P–09–257).
CAS number: Claimed as confidential.
Effective date of TSCA section 5(e)
consent order: August 11, 2009.
Basis for TSCA section 5(e) consent
order: The PMN states that the generic
(non-confidential) uses of the substance
will be as an electric conductive filler to
replace conventional material such as
carbon black or carbon fiber in matrixes
such as polymer resin for conductive
applications, and an additive for
elastomers, polymers, and resins to
enhance mechanical properties. Based
on SAR analysis of test data on
analogous respirable, poorly soluble
particulates and other CNTs, EPA
identified concerns for pulmonary
toxicity, fibrosis, carcinogenicity,
mutagenicity, and immunotoxicity.
Further, available data suggests that
pulmonary deposition of some
nanoparticles, including CNTs, may
induce cardiovascular toxicity if
inhaled. Although there are no
environmental toxicity studies on CNTs
available, EPA expects that some
fraction of the CNTs, if released into the
environment, will eventually be
suspended in water. There have been
sublethal effects observed for single
walled CNTs in rainbow trout at levels
as low as 100 ppb. The order was issued
under section 5(e)(1)(A)(i) and
(e)(1)(A)(ii)(I) of TSCA based on a
finding that this substance may present
an unreasonable risk of injury to human
health and the environment. To protect
against these risks, the order:
1. Requires use of personal protective
equipment including impervious gloves
and protective clothing (when there is a
potential dermal exposure) and a
NIOSH-certified air-purifying, tightfitting full-face respirator equipped with
N100 filters with an APF of at least 50
(when there is potential inhalation
exposure).
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2. Prohibits manufacture of the PMN
substance in the United States.
3. Restricts processing and use of the
PMN substance to those uses specified
in the consent order.
4. Prohibits release to water during
processing and use.
The SNUR would designate as a
‘‘significant new use’’ the absence of
these protective measures.
Recommended testing: EPA has
determined that the results of a 90-day
inhalation toxicity test (OPPTS Test
Guideline 870.3465 or OECD Test
Guideline 413) in rats with a post
exposure observation period of up to 3
months (including BALF analysis, a
determination of cardiovascular toxicity
(clinically-based blood/plasma protein
analyses), and histopathology of the
heart) and development of data on
certain physical/chemical properties
would help characterize possible effects
of the substance. In the consent order,
the PMN submitter has agreed not to
exceed a specified production volume/
time limit (whichever comes first)
without performing the 90-day test on
the PMN substance. In addition, in the
consent order, the PMN submitter
agreed to provide the physical/chemical
properties data within a specified time
limit.
CFR citation: 40 CFR 721.10646.
PMN Numbers P–10–115, P–10–116, P–
10–117, P–10–118, P–10–119, P–10–120,
P–10–121, P–10–122, P–10–123, P–10–
124, P–10–125, and P–10–126
Chemical name: Multi-walled carbon
nanofibers (generic).
CAS number: Claimed as confidential.
Effective date of TSCA section 5(e)
consent order: May 9, 2011.
Basis for TSCA section 5(e) consent
order: The PMNs state that the uses of
the substances will be as electrical and
thermal conductivity additives,
mechanical reinforcement additives,
energy storage additives, and chemical
intermediates. Based on SAR analysis of
test data on analogous respirable, poorly
soluble particulates and other CNTs,
EPA identified concerns for pulmonary
toxicity, fibrosis, carcinogenicity,
mutagenicity, and immunotoxicity.
Further, available data suggests that
pulmonary deposition of some
nanoparticles, including CNTs may
induce cardiovascular toxicity if
inhaled. Although there are no
environmental toxicity studies on CNTs
available, EPA expects that some
fraction of the CNTs, if released into the
environment, will eventually be
suspended in water. There have been
sub-lethal effects observed for single
walled CNTs in rainbow trout at levels
as low as 100 ppb. The order was issued
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under sections 5(e)(1)(A)(i) and
5(e)(1)(A)(ii)(I) of TSCA based on a
finding that these substances may
present an unreasonable risk of injury to
human health and the environment. To
protect against this risk, the order:
1. Requires use of personal protective
equipment including impervious gloves
and protective clothing (when there is a
potential dermal exposure) and a
NIOSH-certified air-purifying, tightfitting full-face respirator equipped with
N100 filters with an APF of at least 50
(when there is potential inhalation
exposure).
2. Restricts use of the PMN substances
to use only as electrical and thermal
conductivity additives, mechanical
reinforcement additives, energy storage
additives, and chemical intermediates
as specified in the consent order.
3. Restricts processing and use of the
PMN substances to industrial settings.
4. Prohibits release of the PMN
substances into the waters of the United
States during processing and use
activities.
The SNUR would designate as a
‘‘significant new use’’ the absence of
these protective measures.
Recommended testing: EPA has
determined that the results of certain
physical/chemical properties data,
workplace exposure monitoring and
characterization testing, and a 90-day
inhalation toxicity test (OPPTS Test
Guideline 870.3465 or OECD Test
Guideline 413) in rats would help
characterize the human health effects of
the PMN substances. The PMN
submitter agreed to provide the
physical/chemical properties data for
the PMN substances within one year
after submitting the notice of
commencement. The consent order
contains two additional production
volume limits. The PMN submitter
agreed not to exceed the first production
volume limit without submitting
workplace exposure monitoring and
characterization testing (including
byproducts) as well as quantification
and characterization of substances that
may be released during exposures
typical during the use phase, such as
handling, tearing and cutting the PMN
substances. The PMN submitter has also
agreed not to exceed the second
production volume limit without
performing two 90-day inhalation
toxicity tests, with a post-exposure
observation period of up to 3 months,
BALF analysis, aggregation/
agglomeration state, shape, size/size
particle distribution and surface
properties of materials as administered,
aggregation/agglomeration state, shape,
size/size particle distribution and
surface properties of materials of the
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delivered materials after administration,
determination of cardiovascular
toxicity, heart histopathology, and data
on pulmonary deposition. One 90-day
inhalation toxicity test will be
conducted from a representative PMN
substance in the group P–10–115, P–10–
116, P–10–117, P–10–118, P–10–119,
and the other 90-day inhalation toxicity
test will be conducted from a
representative PMN substance in the
group P–10–120, P–10–121, P–10–122,
P–10–123, P–10–124, P–10–125, and P–
10–126.
CFR citation: 40 CFR 721.10647.
PMN Numbers P–10–545 and P–10–546
Chemical name: Modified lithium
iron phosphates (generic).
CAS number: Claimed as confidential.
Effective date of TSCA section 5(e)
consent order: December 10, 2010.
Basis for TSCA section 5(e) consent
order: The consolidated PMN states that
the generic (non-confidential) use of the
substances will be as battery electrode
components, contained use. Based on
test data on analogous respirable, poorly
soluble particulates, there is potential
risk for adverse lung effects including
cancer, lung fibrosis, lung inflammation
and systemic effects, including
immunotoxicity. EPA has identified
concerns for these health effects from
exposures to the PMN substances. Based
on EcoSAR analysis of test data on
analogous phosphates, EPA predicts
toxicity to aquatic organisms may occur
at concentrations that exceed 2 ppb of
the PMN substance in surface waters.
The order was issued under sections
5(e)(1)(A)(i) and 5(e)(1)(A)(ii)(I) of TSCA
based on a finding that these substances
may present an unreasonable risk of
injury to human health or the
environment. To protect against these
risks, the consent order:
1. Restricts manufacturing,
processing, and use of the substances to
a fully-enclosed and automated process,
including all loading and unloading
activities.
2. Restricts use of the PMN substances
to use only as specified in the consent
order.
3. Prohibits release of the PMN
substances into the waters of the United
States during processing and use
activities.
The SNUR would designate as a
‘‘significant new use’’ the absence of
these protective measures.
Recommended testing: EPA has
determined that the results of a 90-day
inhalation toxicity test (OPPTS Test
Guideline 870.3465) in rats with a postexposure observation period of up to 3
months, including BALF analysis; an
algal toxicity test (OCSPP Test
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Guideline 850.5400); and physical/
chemical properties testing for: Water
solubility (OECD Test Guideline 105);
surface chemistry, particle size
distribution of the PMN substances,
dustiness test (European Standard
15051); and particle size distribution,
aggregation state, and porosity would
help characterize the human health and
environmental effects of the PMN
substances. The PMN submitter has
agreed not to exceed the confidential
production volume in the consent order
without performing the 90-day
inhalation toxicity test and the physical/
chemical properties tests.
CFR citation: 40 CFR 721.10648.
PMN Number P–11–115
Chemical name: MDI modified
polyalkylene glycol adipate polyester
(generic).
CAS number: Claimed as confidential.
Basis for action: The PMN states that
the generic (non-confidential) use of the
substance will be as an adhesive. Based
on SAR analysis of test data on
analogous diisocyanates, EPA identified
concerns for respiratory and dermal
sensitization. For the use described in
the PMN, significant occupational
dermal and inhalation exposures are not
expected due to the use of a NIOSHcertified respirator with an APF of at
least 10, and consumer exposures are
not expected as the substance is not
used in consumer products. Therefore,
EPA has not determined that the
proposed manufacturing, processing, or
use of the substance may present an
unreasonable risk. EPA has determined,
however, that any use of the substance
without a NIOSH-certified respirator
with an APF of at least 10, where there
is a potential for inhalation exposures,
or any use of the substance in consumer
products may cause serious health
effects. Based on this information, the
PMN substance meets the concern
criteria at § 721.170(b)(3)(ii).
Recommended testing: EPA has
determined that the results of a skin
sensitization test (OPPTS Test Guideline
870.2600) and a 90-day inhalation
toxicity test (OPPTS Test Guideline
870.3465) would help characterize the
human health effects of the PMN
substance.
CFR citation: 40 CFR 721.10649.
PMN Number P–11–155
Chemical name: Polyether substituted
anthraquinone derivative (generic).
CAS number: Claimed as confidential.
Basis for action: The PMN states that
the generic (non-confidential) use of the
substance will be used as a colorant for
cleaners and detergents. Based on
EcoSAR analysis of test data on
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analogous aromatic amines and
nonionic dyes, EPA predicts toxicity to
aquatic organisms may occur at
concentrations that exceed 2 ppb of the
PMN substance in surface waters for
greater than 20 days per year. This 20day criterion is derived from partial life
cycle tests (daphnid chronic and fish
early life stage tests) that typically range
from 21 to 28 days in duration. EPA
predicts toxicity to aquatic organisms
may occur if releases of the PMN
substance to surface water, from uses
other than as described in the PMN,
exceed releases from the use described
in the PMN. For the use described in the
PMN, environmental releases did not
exceed 1 ppb for more than 20 days per
year.
Therefore, EPA has not determined
that the proposed manufacturing,
processing, or use of the substance may
present an unreasonable risk. EPA has
determined, however, that any use of
the substance other than as a colorant
for cleaners and detergents may cause
significant adverse environmental
effects. Based on this information, the
PMN substance meets the concern
criteria at § 721.170(b)(4)(ii).
Recommended testing: EPA has
determined that the results of a fish
acute toxicity test, freshwater and
marine (OPPTS Test Guideline
850.1075) and an aquatic invertebrate
acute toxicity test, freshwater daphnids
(OPPTS Test Guideline 850.1010) would
help characterize the environmental
effects of the PMN substance.
CFR citation: 40 CFR 721.10650.
PMN Number P–11–290
Chemical name: Carbide derived
nanocarbon (generic).
CAS number: Claimed as confidential.
Basis for action: The PMN states that
the generic (non-confidential) use of the
substance will be as a sensor element in
an electrochemical sensor. Based on
SAR analysis of test data on respirable,
poorly soluble particulates, EPA
identified concerns for pulmonary
toxicity, fibrosis, carcinogenicity,
mutagenicity, and immunotoxicity if the
substances were manufactured by a
method other than described in the
PMN. Further, available data suggests
that pulmonary deposition of some
carbon-based nanoparticles, may induce
cardiovascular toxicity if inhaled. EPA
identified concerns for lung toxicity to
workers from inhalation exposures to
the PMN substance. For the
manufacture method described in the
PMN, significant dermal and inhalation
exposures are not expected. Therefore,
EPA has not determined that the
proposed manufacturing, processing, or
use of the substance may present an
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unreasonable risk. EPA has determined,
however, that manufacture of the
substance by a method other than as
described in the PMN may cause serious
health effects. Based on this
information, the PMN substance meets
the concern criteria at
§ 721.170(b)(3)(ii).
Recommended testing: EPA has
determined that inhalation monitoring
data collected during the manufacturing
process according to the EPA draft
Inhalation Monitoring Data Collection
Guidelines (located in the docket under
docket ID number EPA–HQ–OPPT–
2012–0727) would help characterize the
human health effects of the PMN
substance.
CFR citation: 40 CFR 721.10651.
PMN Numbers P–11–309, P–11–311, P–
11–312, P–11–313, and P–11–314
Chemical names: (P–11–309)
Hexanedioic acid, polymer with
polyether polyol, 1,1′-methylenebis[4isocyanatobenzene] and
dihydroxydialkyl ether (generic); (P–11–
311) Hexanedioic acid, polymer with
.alpha.-hydro-.omega.hydroxypoly[oxy(methyl-1,2ethanediyl)],1,1′-methylenebis[4isocyanatobenzene], dihydroxydialkyl
ether and dialkanol ether (generic); (P–
11–312) Hexanedioic acid, polymer
with .alpha.-hydro-.omega.hydroxypoly[oxy(methyl-1,2ethanediyl)],1,1′methylenebis[isocyanatobenzene],
dihydroxydialkyl ether and dialkanol
ether (generic); (P–11–313) Hexanedioic
acid, polymer with .alpha.-hydro.omega.-hydroxypoly[oxy(methyl-1,2ethanediyl)],1,1′-methylenebis[4isocyanatobenzene], dihydroxydialkyl
ether, reaction products with
dialkylcarbinol (generic); and (P–11–
314) Hexanedioic acid, polymer with
.alpha.-hydro-.omega.hydroxypoly[oxy(methyl-1,2ethanediyl)],1,1′-methylenebis[4isocyanatobenzene], dihydroxydialkyl
ether reaction products with
dialkylcarbinol (generic).
CAS numbers: Claimed as
confidential.
Basis for action: The PMNs state that
the generic (non-confidential) use of the
substances will be as industrial
adhesives. Based on SAR analysis of test
data on analogous isocyanates, EPA
identified concerns for sensitization
from dermal and inhalation exposure to
the PMN substances. For the use
described in the PMNs, significant
occupational dermal and inhalation
exposures are not expected due to the
use of a NIOSH-certified respirator with
an APF of at least 10, and consumer
exposures are not expected. Therefore,
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EPA has not determined that the
proposed manufacturing, processing, or
use of the substances may present an
unreasonable risk. EPA has determined,
however, that any use of the substances
without a NIOSH-certified respirator
with an APF of at least 10, where there
is a potential for inhalation exposures,
or any use of the substances in
consumer products may cause serious
health effects. Based on this
information, the PMN substances meet
the concern criteria at
§ 721.170(b)(3)(ii).
Recommended testing: EPA has
determined that the results of a skin
sensitization test (OPPTS Test Guideline
870.2600) and a 90-day inhalation
toxicity test (OPPTS Test Guideline
870.3465) would help characterize the
human health effects of the PMN
substances.
CFR citations: 40 CFR 721.10652 (P–
11–309); 40 CFR 721.10653 (P–11–311);
40 CFR 721.10654 (P–11–312); 40 CFR
721.10655 (P–11–313); and 40 CFR
721.10656 (P–11–314).
PMN Number P–12–73
Chemical name: Castor oil, polymer
with hydrogenated vegetable oil, 1,1′methylenebis[isocyanatobenzene] and
isocyanate (generic).
CAS number: Claimed as confidential.
Basis for action: The PMN states that
the generic (non-confidential) use of the
substance is as an industrial adhesive.
Based on SAR analysis of test data on
analogous diisocyanates, EPA identified
concerns for sensitization. For the use
described in the PMN, significant
occupational dermal and inhalation
exposures are not expected due to the
use of a NIOSH-certified respirator with
an APF of at least 10, and consumer
exposures are not expected as the
substance is not used in consumer
products. Therefore, EPA has not
determined that the proposed
manufacturing, processing, or use of the
substance may present an unreasonable
risk. EPA has determined, however, that
any use of the substance without a
NIOSH-certified respirator with an APF
of at least 10, where there is a potential
for inhalation exposures, or any use of
the substances in consumer products
may cause serious health effects. Based
on this information, the PMN substance
meets the concern criteria at
§ 721.170(b)(3)(ii).
Recommended testing: EPA has
determined that the results of a skin
sensitization (OPPTS Test Guideline
870.2600) and a 90-day subchronic
inhalation toxicity test (OPPTS Test
Guideline 870.3465) in rodents would
help characterize the human health
effects of the PMN substance.
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CFR citation: 40 CFR 721.10657.
PMN Number P–12–133
Chemical name: 2-Oxepanone,
polymer with 1,6-diisocyanatohexane,
2,2″dimethyl-1;3-propanediol and 2,2′oxybis[ethanol].
CAS number: 1313708–90–5.
Basis for action: The PMN states that
the substance will be used as a coating
for wind craft wings. Based on SAR
analysis of test data on structurally
similar chemicals submitted under
TSCA section 8(e), EPA identified
concerns for oncogenicity and
mutagenicity. Additionally, based on
the isocyanate moiety, the Agency
identified concerns for sensitization. For
the use described in the PMN,
significant occupational inhalation
exposures are not expected due to the
use of a NIOSH-certified respirator with
an APF of at least 10, and consumer
exposures are not expected as the
substance is not used in consumer
products. Therefore, EPA has not
determined that the proposed
manufacturing, processing, or use of the
substance may present an unreasonable
risk. EPA has determined, however, that
any use of the substance without a
NIOSH-certified respirator with an APF
of at least 10, where there is a potential
for inhalation exposures, or any use of
the substance in consumer products
may cause serious health effects. Based
on this information, the PMN substance
meets the concern criteria at
§ 721.170(b)(3)(ii).
Recommended testing: EPA has
determined that the results of a skin
sensitization test (OPPTS Test Guideline
870.2600) and a 90-day inhalation
toxicity study (OPPTS Test Guideline
870.3465) would help characterize the
human health effects of the PMN
substance.
CFR citation: 40 CFR 721.10658.
PMN Number P–12–143
Chemical name: Poly(oxy-1,4butanediyl), -hydro—hydroxy-, polymer
with alkyldiisocyanates (generic).
CAS number: Claimed as confidential.
Basis for action: The PMN states that
the generic (non-confidential) use of the
substance will be as a crosslinking resin.
Based on SAR analysis of test data on
analogous isocyanates, EPA identified
concerns for sensitization from dermal
and respiratory exposures to the PMN
substance. For the use described in the
PMN, significant occupational dermal
and inhalation exposures are not
expected due to the use of a NIOSHcertified respirator with an APF of at
least 10, and consumer exposures are
not expected as the substance is not
used in consumer products. Therefore,
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EPA has not determined that the
proposed manufacturing, processing, or
use of the substance may present an
unreasonable risk. EPA has determined,
however, that any use of the substance
without a NIOSH-certified respirator
with an APF of at least 10, where there
is a potential for inhalation exposures,
or any use of the substance in consumer
products may cause serious health
effects. Based on this information, the
PMN substance meets the concern
criteria at § 721.170(b)(3)(ii).
Recommended testing: EPA has
determined that the results of a skin
sensitization test (OPPTS Test Guideline
870.2600) and a 90-day inhalation
toxicity test (OPPTS Test Guideline
870.3465) would help characterize the
human health effects of the PMN
substance.
CFR citation: 40 CFR 721.10659.
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PMN Number P–12–274
Chemical name: Aliphatic
diisocyanate adduct with substituted
amino alkyl silane (generic).
CAS number: Claimed as confidential.
Basis for action: The PMN states that
the generic (non-confidential) use of the
substance will be as an adhesive. Based
on SAR analysis of test data on
analogous isocyanates, EPA identified
concern for sensitization from dermal
and inhalation exposure to the PMN
substance. Additionally, liquid and
vapor contact with the eye can cause
moderate to severe irritation. For the use
described in the PMN, significant
occupational dermal and inhalation
exposures are not expected due to the
use of a NIOSH-certified respirator with
an APF of at least 10, and consumer
exposures are not expected as the
substance is not used in consumer
products. Therefore, EPA has not
determined that the proposed
manufacturing, processing, or use of the
substance may present an unreasonable
risk. EPA has determined, however, that
any use of the substance without a
NIOSH-certified respirator with an APF
of at least 10, where there is a potential
for inhalation exposures; or any use of
the substance in consumer products
may cause serious health effects. Based
on this information, the PMN substance
meets the concern criteria at
§ 721.170(b)(3)(ii).
Recommended testing: EPA has
determined that the results of a skin
sensitization test (OPPTS Test Guideline
870.2600) and a 90-day inhalation
toxicity test (OPPTS Test Guideline
870.3465) would help characterize the
human health effects of the PMN
substance.
CFR citation: 40 CFR 721.10660.
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V. Rationale and Objectives of the
Proposed Rule
A. Rationale
During review of the PMNs submitted
for the chemical substances that are
subject to these proposed SNURs, EPA
concluded that for 17 of the 37 chemical
substances regulation was warranted
under TSCA section 5(e) pending the
development of information sufficient to
make reasoned evaluations of the health
or environmental effects of the chemical
substances. The basis for such findings
is outlined in Unit IV. Based on these
findings, TSCA section 5(e) consent
orders requiring the use of appropriate
exposure controls were negotiated with
the PMN submitters. The proposed
SNUR provisions for these chemical
substances are consistent with the
provisions of the TSCA section 5(e)
consent orders. These SNURs are being
proposed pursuant to § 721.160.
In the other 20 cases, where the uses
are not regulated under a TSCA section
5(e) consent order, EPA determined that
one or more of the criteria of concern
established at § 721.170 were met, as
discussed in Unit IV.
B. Objectives
EPA is proposing these SNURs for
specific chemical substances which
have undergone premanufacture review
because the Agency wants to achieve
the following objectives with regard to
the significant new uses designated in
this proposed rule:
• EPA would receive notice of any
person’s intent to manufacture, import,
or process a listed chemical substance
for the described significant new use
before that activity begins.
• EPA would have an opportunity to
review and evaluate data submitted in a
SNUN before the notice submitter
begins manufacturing, importing, or
processing a listed chemical substance
for the described significant new use.
• EPA would be able to regulate
prospective manufacturers, importers,
or processors of a listed chemical
substance before the described
significant new use of that chemical
substance occurs, provided that
regulation is warranted pursuant to
TSCA sections 5(e), 5(f), 6, or 7.
• EPA would ensure that all
manufacturers, importers, and
processors of the same chemical
substance that is subject to a TSCA
section 5(e) consent order are subject to
similar requirements.
Issuance of a SNUR for a chemical
substance does not signify that the
chemical substance is listed on the
TSCA Chemical Substance Inventory
(TSCA Inventory). Guidance on how to
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determine if a chemical substance is on
the TSCA Inventory is available on the
Internet at https://www.epa.gov/opptintr/
existingchemicals/pubs/tscainventory/
index.html.
VI. Notice and Comment Procedures
EPA is issuing these SNURs by notice
and comment procedure, as described in
§ 721.170(d)(4). In accordance with
§ 721.170(d)(4)(ii)(A), persons are being
given the opportunity to submit
comments on or before April 26, 2013
on whether EPA should establish
notification requirements.
VII. Applicability of Proposed Rule to
Uses Occurring Before Effective Date of
the Final Rule
To establish a significant ‘‘new’’ use,
EPA must determine that the use is not
ongoing. The chemical substances
subject to this proposed rule have
undergone premanufacture review.
TSCA section 5(e) consent orders have
been issued for 17 chemical substances
and the PMN submitters are prohibited
by the TSCA section 5(e) consent orders
from undertaking activities which EPA
is designating as significant new uses.
EPA is soliciting comments on whether
any of the uses proposed as significant
new uses are ongoing.
As discussed in the Federal Register
of April 24, 1990 SNUR, EPA has
decided that the intent of TSCA section
5(a)(1)(B) is best served by designating
a use as a significant new use as of the
date of publication of this proposed rule
rather than as of the effective date of the
final rule. If uses begun after publication
of the proposed rule were considered
ongoing rather than new, it would be
difficult for EPA to establish SNUR
notice requirements because a person
could defeat the SNUR by initiating the
significant new use before the rule
became final, and then argue that the
use was ongoing before the effective
date of the final rule. Thus, persons who
begin commercial manufacture, import,
or processing of the chemical substances
that would be regulated through these
proposed SNURs will have to cease any
such activity before the effective date of
the rule if and when finalized. To
resume their activities, these persons
would have to comply with all
applicable SNUR notice requirements
and wait until the notice review period,
including any extensions, expires.
EPA has promulgated provisions to
allow persons to comply with these
proposed SNURs before the effective
date. If a person meets the conditions of
advance compliance under § 721.45(h),
the person would be considered exempt
from the requirements of the SNUR.
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VIII. Test Data and Other Information
EPA recognizes that TSCA section 5
does not require developing any
particular test data before submission of
a SNUN. The two exceptions are:
1. Development of test data is
required where the chemical substance
subject to the SNUR is also subject to a
test rule under TSCA section 4 (see
TSCA section 5(b)(1)).
2. Development of test data may be
necessary where the chemical substance
has been listed under TSCA section
5(b)(4) (see TSCA section 5(b)(2)).
In the absence of a TSCA section 4
test rule or a TSCA section 5(b)(4)
listing covering the chemical substance,
persons are required only to submit test
data in their possession or control and
to describe any other data known to or
reasonably ascertainable by them (see 40
CFR 720.50). However, upon review of
PMNs and SNUNs, the Agency has the
authority to require appropriate testing.
In cases where EPA issued a TSCA
section 5(e) consent order that requires
or recommends certain testing, Unit IV.
lists those tests. Unit IV. also lists
recommended testing for non-5(e)
SNURs. Descriptions of tests are
provided for informational purposes.
EPA strongly encourages persons, before
performing any testing, to consult with
the Agency pertaining to protocol
selection. To access the OCSPP test
guidelines referenced in this document
electronically, please go to https://
www.epa.gov/ocspp and select ‘‘Test
Methods and Guidelines.’’ The
Organisation for Economic Co-operation
and Development (OECD) test
guidelines are available from the OECD
Bookshop at https://
www.oecdbookshop.org or Source OECD
at https://www.sourceoecd.org. To access
the European Standard, EN 15051
method, issued by The European
Committee for Standardization (CEN),
please go to https://www.cen.eu/cen/
products.
In the TSCA section 5(e) consent
orders for several of the chemical
substances regulated under this
proposed rule, EPA has established
production volume limits in view of the
lack of data on the potential health and
environmental risks that may be posed
by the significant new uses or increased
exposure to the chemical substances.
These limits cannot be exceeded unless
the PMN submitter first submits the
results of toxicity tests that would
permit a reasoned evaluation of the
potential risks posed by these chemical
substances. Listings of the tests
specified in the TSCA section 5(e)
consent orders are included in Unit IV.
The SNURs contain the same
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production volume limits as the TSCA
section 5(e) consent orders. Exceeding
these production limits is defined as a
significant new use. Persons who intend
to exceed the production limit must
notify the Agency by submitting a
SNUN at least 90 days in advance of
commencement of non-exempt
commercial manufacture, import, or
processing.
When physical/chemical properties of
test material and/or material
characterization tests are recommended
for nanoscale substances that are the
subject of this proposed rule, you
should take into consideration the
characterizations identified in the
Guidance Manual for the Testing of
Manufactured Nanomaterials: OECD’s
Sponsorship Programme, which is
available at https://www.oecd.org/
officialdocuments/displaydocumentpdf/
?cote=env/jm/mono(2009)20/
rev&doclanguage=en.
The recommended tests specified in
Unit IV. may not be the only means of
addressing the potential risks of the
chemical substance. However,
submitting a SNUN without any test
data may increase the likelihood that
EPA will take action under TSCA
section 5(e), particularly if satisfactory
test results have not been obtained from
a prior PMN or SNUN submitter. EPA
recommends that potential SNUN
submitters contact EPA early enough so
that they will be able to conduct the
appropriate tests.
SNUN submitters should be aware
that EPA will be better able to evaluate
SNUNs which provide detailed
information on the following:
• Human exposure and
environmental release that may result
from the significant new use of the
chemical substances.
• Potential benefits of the chemical
substances.
• Information on risks posed by the
chemical substances compared to risks
posed by potential substitutes.
IX. SNUN Submissions
According to § 721.1(c), persons
submitting a SNUN must comply with
the same notification requirements and
EPA regulatory procedures as persons
submitting a PMN, including
submission of test data on health and
environmental effects as described in 40
CFR 720.50. SNUNs must be submitted
on EPA Form No. 7710–25, generated
using e-PMN software, and submitted to
the Agency in accordance with the
procedures set forth in 40 CFR 720.40
and § 721.25. E–PMN software is
available electronically at https://
www.epa.gov/opptintr/newchems.
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X. Economic Analysis
EPA has evaluated the potential costs
of establishing SNUN requirements for
potential manufacturers, importers, and
processors of the chemical substances
subject to this proposed rule. EPA’s
complete economic analysis is available
in the docket under docket ID number
EPA–HQ–OPPT–2012–0727.
XI. Statutory and Executive Order
Reviews
A. Executive Order 12866
This proposed rule would establish
SNURs for several new chemical
substances that were the subject of
PMNs, and, in some cases, TSCA
section 5(e) consent orders. The Office
of Management and Budget (OMB) has
exempted these types of actions from
review under Executive Order 12866,
entitled ‘‘Regulatory Planning and
Review’’ (58 FR 51735, October 4, 1993).
B. Paperwork Reduction Act (PRA)
According to PRA (44 U.S.C. 3501 et
seq.), an agency may not conduct or
sponsor, and a person is not required to
respond to a collection of information
that requires OMB approval under PRA,
unless it has been approved by OMB
and displays a currently valid OMB
control number. The OMB control
numbers for EPA’s regulations in title 40
of the CFR, after appearing in the
Federal Register, are listed in 40 CFR
part 9, and included on the related
collection instrument or form, if
applicable. EPA would amend the table
in 40 CFR part 9 to list the OMB
approval number for the information
collection requirements contained in
this proposed rule, if the SNUR is
subsequently issued as a final rule. This
listing of the OMB control numbers and
their subsequent codification in the CFR
satisfies the display requirements of
PRA and OMB’s implementing
regulations at 5 CFR part 1320. This
Information Collection Request (ICR)
was previously subject to public notice
and comment prior to OMB approval,
and given the technical nature of the
table, EPA finds that further notice and
comment to amend it is unnecessary. As
a result, EPA finds that there is ‘‘good
cause’’ under section 553(b)(3)(B) of the
Administrative Procedure Act (5 U.S.C.
553(b)(3)(B)) to amend this table
without further notice and comment.
The information collection
requirements related to this action have
already been approved by OMB
pursuant to PRA under OMB control
number 2070–0012 (EPA ICR No. 574).
This action would not impose any
burden requiring additional OMB
approval. If an entity were to submit a
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SNUN to the Agency, the annual burden
is estimated to average between 30 and
170 hours per response. This burden
estimate includes the time needed to
review instructions, search existing data
sources, gather and maintain the data
needed, and complete, review, and
submit the required SNUN.
Send any comments about the
accuracy of the burden estimate, and
any suggested methods for minimizing
respondent burden, including through
the use of automated collection
techniques, to the Director, Collection
Strategies Division, Office of
Environmental Information (2822T),
Environmental Protection Agency, 1200
Pennsylvania Ave. NW., Washington,
DC 20460–0001. Please remember to
include the OMB control number in any
correspondence, but do not submit any
completed forms to this address.
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C. Regulatory Flexibility Act (RFA)
On February 18, 2012, EPA certified
pursuant to RFA section 605(b) (5 U.S.C.
601 et seq.), that promulgation of these
SNURS would not have a significant
economic impact on a substantial
number of small entities where the
following are true:
1. A significant number of SNUNs
would not be submitted by small
entities in response to the SNUR.
2. The SNUR submitted by any small
entity would not cost significantly more
than $8,300.
A copy of that certification is
available in the docket for this proposed
rule.
This proposed rule is within the
scope of the February 18, 2012
certification. Based on the Economic
Analysis discussed in Unit X. and EPA’s
experience promulgating SNURs
(discussed in the certification), EPA
believes that the following are true:
• A significant number of SNUNs
would not be submitted by small
entities in response to the SNUR.
• Submission of the SNUN would not
cost any small entity significantly more
than $8,300.
Therefore, the promulgation of the
SNUR would not have a significant
economic impact on a substantial
number of small entities.
D. Unfunded Mandates Reform Act
(UMRA)
Based on EPA’s experience with
proposing and finalizing SNURs, State,
local, and Tribal governments have not
been impacted by these rulemakings,
and EPA does not have any reasons to
believe that any State, local, or Tribal
government would be impacted by this
proposed rule. As such, EPA has
determined that this proposed rule
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would not impose any enforceable duty,
contain any unfunded mandate, or
otherwise have any effect on small
governments subject to the requirements
of UMRA sections 202, 203, 204, or 205
(2 U.S.C. 1501 et seq.).
E. Executive Order 13132
This action would not have a
substantial direct effect on States, on the
relationship between the national
government and the States, or on the
distribution of power and
responsibilities among the various
levels of government, as specified in
Executive Order 13132, entitled
‘‘Federalism’’ (64 FR 43255, August 10,
1999).
F. Executive Order 13175
This proposed rule would not have
Tribal implications because it is not
expected to have substantial direct
effects on Indian Tribes. This proposed
rule would not significantly nor
uniquely affect the communities of
Indian Tribal governments, nor would it
involve or impose any requirements that
affect Indian Tribes. Accordingly, the
requirements of Executive Order 13175,
entitled ‘‘Consultation and Coordination
with Indian Tribal Governments’’ (65 FR
67249, November 9, 2000), do not apply
to this proposed rule.
related issues as delineated by
Executive Order 12898, entitled
‘‘Federal Actions to Address
Environmental Justice in Minority
Populations and Low-Income
Populations’’ (59 FR 7629, February 16,
1994).
List of Subjects in 40 CFR Part 721
Environmental protection, Chemicals,
Hazardous substances, Reporting and
recordkeeping requirements.
Dated: February 15, 2013.
Maria J. Doa,
Director, Chemical Control Division, Office
of Pollution Prevention and Toxics.
Therefore, it is proposed that 40 CFR
part 721 be amended as follows:
PART 721—[AMENDED]
1. The authority citation for part 721
continues to read as follows:
■
Authority: 15 U.S.C. 2604, 2607, and
2625(c).
2. Add § 721.10637 to subpart E to
read as follows:
■
§ 721.10637
(generic).
Substituted picolinate
This action is not subject to Executive
Order 13211, entitled ‘‘Actions
Concerning Regulations That
Significantly Affect Energy Supply,
Distribution, or Use’’ (66 FR 28355, May
22, 2001), because this action is not
expected to affect energy supply,
distribution, or use and because this
action is not a significant regulatory
action under Executive Order 12866.
(a) Chemical substance and
significant new uses subject to reporting.
(1) The chemical substance identified
generically as substituted picolinate
(PMN P–00–835) is subject to reporting
under this section for the significant
new uses described in paragraph (a)(2)
of this section.
(2) The significant new uses are:
(i) Release to water. Requirements as
specified in § 721.90 (a)(4), (b)(4), and
(c)(4) (N=90).
(ii) [Reserved]
(b) Specific requirements. The
provisions of subpart A of this part
apply to this section except as modified
by this paragraph.
(1) Recordkeeping. Recordkeeping
requirements as specified in § 721.125
(a), (b), (c), and (k) are applicable to
manufacturers, importers, and
processors of this substance.
(2) Limitations or revocation of
certain notification requirements. The
provisions of § 721.185 apply to this
section.
■ 3. Add § 721.10638 to subpart E to
read as follows:
I. National Technology Transfer and
Advancement Act (NTTAA)
§ 721.10638
(generic).
In addition, since this action does not
involve any technical standards,
NTTAA section 12(d) (15 U.S.C. 272
note), does not apply to this action.
(a) Chemical substance and
significant new uses subject to reporting.
(1) The chemical substance identified
generically as lithium metal phosphate
(PMN P–02–167) is subject to reporting
under this section for the significant
new uses described in paragraph (a)(2)
of this section.
G. Executive Order 13045
This action is not subject to Executive
Order 13045, entitled ‘‘Protection of
Children from Environmental Health
Risks and Safety Risks’’ (62 FR 19885,
April 23, 1997), because this is not an
economically significant regulatory
action as defined by Executive Order
12866, and this action does not address
environmental health or safety risks
disproportionately affecting children.
H. Executive Order 13211
J. Executive Order 12898
This action does not entail special
considerations of environmental justice
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(2) The significant new uses are:
(i) Release to water. Requirements as
specified in § 721.90 (a)(4), (b)(4), and
(c)(4) (N=1).
(ii) [Reserved]
(b) Specific requirements. The
provisions of subpart A of this part
apply to this section except as modified
by this paragraph.
(1) Recordkeeping. Recordkeeping
requirements as specified in § 721.125
(a), (b), (c), and (k) are applicable to
manufacturers, importers, and
processors of this substance.
(2) Limitations or revocation of
certain notification requirements. The
provisions of § 721.185 apply to this
section.
■ 4. Add § 721.10639 to subpart E to
read as follows:
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§ 721.10639 Siloxanes and Silicones, diMe, polymers with Ph silsesquioxanes,
hydrolyzed, reaction products with 2-[[3-(
trimethoxysilyl)propoxy]methyl]oxirane.
(a) Chemical substance and
significant new uses subject to reporting.
(1) The chemical substance identified as
siloxanes and silicones, di-Me,
polymers with Ph silsesquioxanes,
hydrolyzed, reaction products with 2[[3-(trimethoxysilyl)propoxy]methyl
]oxirane (PMN P–02–668; CAS No.
478823–10–8) is subject to reporting
under this section for the significant
new uses described in paragraph (a)(2)
of this section.
(2) The significant new uses are:
(i) Protection in the workplace.
Requirements as specified in § 721.63
(a)(1), (a)(2)(i), (a)(3), (a)(4), (a)(6)(v), (b)
(concentration set at 0.1 percent), and
(c). When determining which persons
are reasonably likely to be exposed as
required for § 721.63 (a)(1) and (a)(4),
engineering control measures (e.g.,
enclosure or confinement of the
operation, general and local ventilation)
or administrative control measures (e.g.,
workplace policies and procedures)
shall be considered and implemented to
prevent exposure, where feasible. The
following National Institute for
Occupational Safety and Health
(NIOSH)-certified respirators with an
assigned protection factor (APF) of at
least 10 meet the requirements of
§ 721.63(a)(4):
(A) NIOSH-certified air-purifying,
tight-fitting half-face respirator
equipped with N100 (if oil aerosols
absent), R100, or P100 filters;
(B) NIOSH-certified air-purifying,
tight-fitting full-face respirator equipped
with N100 (if oil aerosols absent), R100,
or P100 filters;
(C) NIOSH-certified powered airpurifying respirator equipped with a
loose-fitting hood or helmet and high
efficiency particulate air (HEPA) filters;
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(D) NIOSH-certified powered airpurifying respirator equipped with a
tight-fitting facepiece (either half-face or
full-face) and HEPA filters; and
(E) NIOSH-certified supplied-air
respirator operated in pressure demand
or continuous flow mode and equipped
with a hood or helmet, or tight-fitting
facepiece (either half-face or full-face).
(ii) Industrial, commercial, and
consumer activities. Requirements as
specified in § 721.80(o).
(b) Specific requirements. The
provisions of subpart A of this part
apply to this section except as modified
by this paragraph.
(1) Recordkeeping. Recordkeeping
requirements as specified in § 721.125
(a), (b), (c), (d), (e), and (i) are applicable
to manufacturers, importers, and
processors of this substance.
(2) Limitations or revocation of
certain notification requirements. The
provisions of § 721.185 apply to this
section.
■ 5. Add § 721.10640 to subpart E to
read as follows:
§ 721.10640 11,2-Cyclohexanedicarboxylic
acid, 1-(2-ethylhexyl) 2-(2-methylpropyl)
ester.
(a) Chemical substance and
significant new uses subject to reporting.
(1) The chemical substance identified as
1,2-cyclohexanedicarboxylic acid, 1-(2ethylhexyl) 2-(2-methylpropyl) ester
(PMN P–03–135; CAS Nos. 252958–29–
5) is subject to reporting under this
section for the significant new uses
described in paragraph (a)(2) of this
section.
(2) The significant new uses are:
(i) Release to water. Requirements as
specified in § 721.90 (a)(4), (b)(4), and
(c)(4) (N=1).
(ii) [Reserved]
(b) Specific requirements. The
provisions of subpart A of this part
apply to this section except as modified
by this paragraph.
(1) Recordkeeping. Recordkeeping
requirements as specified in § 721.125
(a), (b), (c), and (k) are applicable to
manufacturers, importers, and
processors of this substance.
(2) Limitations or revocation of
certain notification requirements. The
provisions of § 721.185 apply to this
section.
■ 6. Add § 721.10641 to subpart E to
read as follows:
§ 721.10641 Phenol and vinyltoluene
based hydrocarbon resin (generic).
(a) Chemical substance and
significant new uses subject to reporting.
(1) The chemical substance identified
generically as phenol and vinyltoluene
based hydrocarbon resin (PMN P–03–
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255) is subject to reporting under this
section for the significant new uses
described in paragraph (a)(2) of this
section.
(2) The significant new uses are:
(i) Release to water. Requirements as
specified in § 721.90 (a)(4), (b)(4), and
(c)(4) (N=1).
(ii) [Reserved]
(b) Specific requirements. The
provisions of subpart A of this part
apply to this section except as modified
by this paragraph.
(1) Recordkeeping. Recordkeeping
requirements as specified in § 721.125
(a), (b), (c), and (k) are applicable to
manufacturers, importers, and
processors of this substance.
(2) Limitations or revocation of
certain notification requirements. The
provisions of § 721.185 apply to this
section.
■ 7. Add § 721.10642 to subpart E to
read as follows:
§ 721.10642
(generic).
Modified polyisocyanates
(a) Chemical substance and
significant new uses subject to reporting.
(1) The chemical substances identified
generically as modified polyisocyanates
(PMNs P–03–762 and P–03–763) are
subject to reporting under this section
for the significant new uses described in
paragraph (a)(2) of this section.
(2) The significant new uses are:
(i) Protection in the workplace.
Requirements as specified in § 721.63
(a)(1), (a)(2)(i), (a)(3), (b) (concentration
set at 0.1 percent), and (c).
(ii) Industrial, commercial, and
consumer activities. Requirements as
specified in § 721.80 (f), (o), and (y)(l).
(b) Specific requirements. The
provisions of subpart A of this part
apply to this section except as modified
by this paragraph.
(1) Recordkeeping. Recordkeeping
requirements as specified in § 721.125
(a), (b), (c), (d), (e), and (i) are applicable
to manufacturers, importers, and
processors of these substances.
(2) Limitations or revocation of
certain notification requirements. The
provisions of § 721.185 apply to this
section.
■ 8. Add § 721.10643 to subpart E to
read as follows:
§ 721.10643 Diisocyanate terminated
polycarbodiimide (generic).
(a) Chemical substance and
significant new uses subject to reporting.
(1) The chemical substance identified
generically as diisocyanate terminated
polycarbodiimide (PMN P–04–640) is
subject to reporting under this section
for the significant new uses described in
paragraph (a)(2) of this section. The
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requirements of this rule do not apply
to quantities of the PMN substance that
have been completely reacted (cured).
(2) The significant new uses are:
(i) Protection in the workplace.
Requirements as specified in § 721.63
(a)(1), (a)(3), (a)(4), and (a)(6)(ii). When
determining which persons are
reasonably likely to be exposed as
required for § 721.63 (a)(1) and (a)(4),
engineering control measures (e.g.,
enclosure or confinement of the
operation, general and local ventilation)
or administrative control measures (e.g.,
workplace policies and procedures)
shall be considered and implemented to
prevent exposure, where feasible. A
National Institute for Occupational
Safety and Health (NIOSH)-certified
supplied-air respirator operated in
pressure demand or other positive
pressure mode and equipped with a
tight-fitting full facepiece with an
assigned protection factor (APF) of at
least 2,000 meets the minimum
requirements § 721.63(a)(4). As an
alternative to the respiratory
requirements listed here, a
manufacturer, importer, or processor
may choose to follow the new chemical
exposure limit (NCEL) provisions listed
in the TSCA section 5(e) consent order
for this substance. The NCEL is 0.05 mg/
m3. Persons whose § 721.30 requests to
use the NCELs approach are approved
by EPA will receive NCELs provisions
comparable to those contained in the
corresponding section 5(e) consent
order.
(ii) Hazard communication program.
Requirements as specified in § 721.72
(a), (b), (c), (d), (f), (g)(1)(i), (g)(1)(ii),
(g)(2)(i), (g)(2)(ii), (g)(2)(iii), (g)(2)(iv)
(use respiratory protection or maintain
airborne concentrations at or below an
8-hour time-weighted average of 0.05
mg/m3), (g)(2)(v), and (g)(5).
(iii) Industrial, commercial, and
consumer activities. Requirements as
specified in § 721.80(o).
(b) Specific requirements. The
provisions of subpart A of this part
apply to this section except as modified
by this paragraph.
(1) Recordkeeping. Recordkeeping
requirements as specified in § 721.125
(a) through (i) are applicable to
manufacturers, importers, and
processors of this substance.
(2) Limitations or revocation of
certain notification requirements. The
provisions of § 721.185 apply to this
section.
■ 9. Add § 721.10644 to subpart E to
read as follows:
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§ 721.10644 Reaction product of aluminum
hydroxide and modified alkoxysilane
(generic).
(a) Chemical substance and
significant new uses subject to reporting.
(1) The chemical substance identified
generically as reaction product of
aluminum hydroxide and modified
alkoxysilane (PMN P–07–553) is subject
to reporting under this section for the
significant new uses described in
paragraph (a)(2) of this section.
(2) The significant new uses are:
(i) Protection in the workplace.
Requirements as specified in § 721.63
(a)(4), (a)(6)(i), (b) (concentrations set at
0.1 percent), and (c). When determining
which persons are reasonably likely to
be exposed as required for
§ 721.63(a)(4), engineering control
measures (e.g., enclosure or
confinement of the operation, general
and local ventilation) or administrative
control measures (e.g., workplace
policies and procedures) shall be
considered and implemented to prevent
exposure, where feasible. The following
National Institute for Occupational
Safety and Health (NIOSH)-certified
respirators with an assigned protection
factor (APF) of at least 10 meet the
requirements of § 721.63(a)(4):
(A) NIOSH-certified air-purifying,
tight-fitting half-face respirator
equipped with N100 (if oil aerosols
absent), R100, or P100 filters;
(B) NIOSH-certified air-purifying,
tight-fitting full-face respirator equipped
with N100 (if oil aerosols absent), R100,
or P100 filters;
(C) NIOSH-certified powered airpurifying respirator equipped with a
loose-fitting hood or helmet and high
efficiency particulate air (HEPA) filters;
(D) NIOSH-certified powered airpurifying respirator equipped with a
tight-fitting facepiece (either half-face or
full-face) and HEPA filters; and
(E) NIOSH-certified supplied-air
respirator operated in pressure demand
or continuous flow mode and equipped
with a hood or helmet, or tight-fitting
facepiece (either half-face or full-face).
(ii) Industrial, commercial, and
consumer activities. Requirements as
specified in § 721.80(s) (100,000
kilograms).
(b) Specific requirements. The
provisions of subpart A of this part
apply to this section except as modified
by this paragraph.
(1) Recordkeeping. Recordkeeping
requirements as specified in § 721.125
(a), (b), (c), (d), and (i) are applicable to
manufacturers, importers, and
processors of this substance.
(2) Limitations or revocation of
certain notification requirements. The
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provisions of § 721.185 apply to this
section.
■ 10. Add § 721.10645 to subpart E to
read as follows:
§ 721.10645 Multi-walled carbon nanotube
(generic) (P–08–392).
(a) Chemical substance and
significant new uses subject to reporting.
(1) The chemical substance identified
generically as multi-walled carbon
nanotube (PMN P–08–392) is subject to
reporting under this section for the
significant new uses described in
paragraph (a)(2) of this section. The
requirements of this rule do not apply
to quantities of the PMN substance that
have been completely reacted (cured);
incorporated or embedded into a
polymer matrix that itself has been
completely reacted (cured); or
embedded in a permanent solid polymer
form that is not intended to undergo
further processing except for
mechanical processing.
(2) The significant new uses are:
(i) Protection in the workplace.
Requirements as specified in § 721.63
(a)(1), (a)(2)(i), (a)(2)(ii), (a)(3), (a)(4),
and (a)(6) (particulate, including solids
or liquid droplets). When determining
which persons are reasonably likely to
be exposed as required for § 721.63
(a)(1) and (a)(4), engineering control
measures (e.g., enclosure or
confinement of the operation, general
and local ventilation) or administrative
control measures (e.g., workplace
policies and procedures) shall be
considered and implemented to prevent
exposure, where feasible. A National
Institute for Occupational Safety and
Health (NIOSH)-certified air-purifying,
tight-fitting full-face respirator equipped
with N100 filters with an assigned
protection factor (APF) of at least 50
meet the minimum requirements of
§ 721.63(a)(4).
(ii) Industrial, commercial, and
consumer activities. Requirements as
specified in § 721.80 (f), (k), and (q)
(within 18 months of commencing nonexempt commercial manufacture).
(b) Specific requirements. The
provisions of subpart A of this part
apply to this section except as modified
by this paragraph.
(1) Recordkeeping. Recordkeeping
requirements as specified in § 721.125
(a), (b), (c), (d), (e), and (i) are applicable
to manufacturers, importers, and
processors of this substance.
(2) Limitations or revocation of
certain notification requirements. The
provisions of § 721.185 apply to this
section.
(3) Determining whether a specific use
is subject to this section. The provisions
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of § 721.1725(b)(1) apply to paragraph
(a)(2)(ii) of this section.
■ 12. Add § 721.10647 to subpart E to
read as follows:
§ 721.10646 Multi-walled carbon nanotube
(generic) (P–09–257).
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of § 721.1725(b)(1) apply to paragraph
(a)(2)(ii) of this section.
■ 11. Add § 721.10646 to subpart E to
read as follows:
§ 721.10647 Multi-walled carbon
nanofibers (generic).
(a) Chemical substance and
significant new uses subject to reporting.
(1) The chemical substance identified
generically as multi-walled carbon
nanotube (PMN P–09–257) is subject to
reporting under this section for the
significant new uses described in
paragraph (a)(2) of this section. The
requirements of this rule do not apply
to quantities of the PMN substance that
have been completely reacted (cured);
incorporated or embedded into a
polymer matrix that itself has been
completely reacted (cured); embedded
in a permanent solid polymer form that
is not intended to undergo further
processing except for mechanical
processing; or incorporated into an
article as defined at 40 CFR 720.3(c).
(2) The significant new uses are:
(i) Protection in the workplace.
Requirements as specified in § 721.63
(a)(1), (a)(2)(i), (a)(2)(ii), (a)(3), (a)(4),
and (a)(6) (particulate, including solids
or liquid droplets). When determining
which persons are reasonably likely to
be exposed as required for § 721.63
(a)(1) and (a)(4), engineering control
measures (e.g., enclosure or
confinement of the operation, general
and local ventilation) or administrative
control measures (e.g., workplace
policies and procedures) shall be
considered and implemented to prevent
exposure, where feasible. A National
Institute for Occupational Safety and
Health (NIOSH)-certified air-purifying,
tight-fitting full-face respirator equipped
with N100 filters with an assigned
protection factor (APF) of at least 50
meets the minimum requirements of
§ 721.63(a)(4).
(ii) Industrial, commercial, and
consumer activities. Requirements as
specified in § 721.80 (f), (k), and (q).
(iii) Release to water. Requirements as
specified in § 721.90 (b)(1) and (c)(1).
(b) Specific requirements. The
provisions of subpart A of this part
apply to this section except as modified
by this paragraph.
(1) Recordkeeping. Recordkeeping
requirements as specified in § 721.125
(a), (b), (c), (d), (e), (i), and (k) are
applicable to manufacturers, importers,
and processors of this substance.
(2) Limitations or revocation of
certain notification requirements. The
provisions of § 721.185 apply to this
section.
(3) Determining whether a specific use
is subject to this section. The provisions
(a) Chemical substance and
significant new uses subject to reporting.
(1) The chemical substance identified
generically as multi-walled carbon
nanofibers (PMNs P–10–115, P–10–116,
P–10–117, P–10–118, P–10–119, P–10–
120, P–10–121, P–10–122, P–10–123, P–
10–124, P–10–125, and P–10–126) are
subject to reporting under this section
for the significant new uses described in
paragraph (a)(2) of this section. The
requirements of this rule do not apply
to quantities of the PMN substances
after they have been completely reacted
(cured); incorporated or embedded into
a polymer matrix that itself has been
reacted (cured); embedded into a
permanent solid polymer form that is
not intended to undergo further
processing except for mechanical
processing; or incorporated into an
article as defined at 40 CFR 720.3(c).
(2) The significant new uses are:
(i) Protection in the workplace.
Requirements as specified in § 721.63
(a)(1), (a)(2)(i), (a)(2)(ii), (a)(3), (a)(4),
and (a)(6)(i). When determining which
persons are reasonably likely to be
exposed as required for § 721.63 (a)(1)
and (a)(4), engineering control measures
(e.g., enclosure or confinement of the
operation, general and local ventilation)
or administrative control measures (e.g.,
workplace policies and procedures)
shall be considered and implemented to
prevent exposure, where feasible. A
National Institute for Occupational
Safety and Health (NIOSH)-certified airpurifying, tight-fitting full-face
respirator equipped with N100 filters
with an assigned protection factor (APF)
of at least 50 meets the minimum
requirements of § 721.63(a)(4).
(ii) Industrial, commercial, and
consumer activities. Requirements as
specified in § 721.80 (k) (electrical and
thermal conductivity additive in
encapsulated thermoplastics,
thermosets, elastomers, glass, metals,
and ceramics; mechanical reinforcement
additive in encapsulated thermoplastics,
thermosets, elastomers, glass, metals,
and ceramics; energy storage additive;
or chemical intermediate), (l) and (q).
(iii) Release to water. Requirements as
specified in § 721.90 (b)(1) and (c)(1).
(b) Specific requirements. The
provisions of subpart A of this part
apply to this section except as modified
by this paragraph.
(1) Recordkeeping. Recordkeeping
requirements as specified in § 721.125
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(a), (b), (c), (d), (e), (i), and (k) are
applicable to manufacturers, importers,
and processors of these substances.
(2) Limitations or revocation of
certain notification requirements. The
provisions of § 721.185 apply to this
section.
(3) Determining whether a specific use
is subject to this section. The provisions
of § 721.1725(b)(1) apply to paragraph
(a)(2)(ii) of this section.
■ 13. Add § 721.10648 to subpart E to
read as follows:
§ 721.10648 Modified lithium iron
phosphates (generic).
(a) Chemical substance and
significant new uses subject to reporting.
(1) The chemical substances identified
generically as modified lithium iron
phosphates (PMNs P–10–545 and P–10–
546) are subject to reporting under this
section for the significant new uses
described in paragraph (a)(2) of this
section. The requirements of this rule do
not apply to quantities of the PMN
substances after they have been
completely reacted (cured), embedded
or incorporated into a polymer matrix
that has been reacted (cured), or
embedded in a permanent solid polymer
form that is not intended to undergo
further processing, except mechanical.
(2) The significant new uses are:
(i) Industrial, commercial, and
consumer activities. Requirements as
specified in § 721.80 (a), (b), (c), (k), and
(q).
(ii) Release to water. Requirements as
specified in § 721.90 (b)(1) and (c)(1).
(b) Specific requirements. The
provisions of subpart A of this part
apply to this section except as modified
by this paragraph.
(1) Recordkeeping. Recordkeeping
requirements as specified in § 721.125
(a), (b), (c), (i), and (k) are applicable to
manufacturers, importers, and
processors of these substances.
(2) Limitations or revocation of
certain notification requirements. The
provisions of § 721.185 apply to this
section.
(3) Determining whether a specific use
is subject to this section. The provisions
of § 721.1725(b)(1) apply to paragraph
(a)(2)(i) of this section.
■ 14. Add § 721.10649 to subpart E to
read as follows:
§ 721.10649 MDI modified polyalkylene
glycol adipate polyester (generic).
(a) Chemical substance and
significant new uses subject to reporting.
(1) The chemical substance identified
generically as MDI modified
polyalkylene glycol adipate polyester
(PMN P–11–115) is subject to reporting
under this section for the significant
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new uses described in paragraph (a)(2)
of this section.
(2) The significant new uses are:
(i) Protection in the workplace.
Requirements as specified in § 721.63
(a)(4), (a)(6)(i), (a)(6)(ii), (a)(6)(v), (b)
(concentration set at 0.1 percent), and
(c). When determining which persons
are reasonably likely to be exposed as
required for § 721.63 (a)(4), engineering
control measures (e.g., enclosure or
confinement of the operation, general
and local ventilation) or administrative
control measures (e.g., workplace
policies and procedures) shall be
considered and implemented to prevent
exposure, where feasible. The following
National Institute for Occupational
Safety and Health (NIOSH)-certified
respirators with an assigned protection
factor (APF) of at least 10 meet the
requirements of § 721.63(a)(4):
(A) NIOSH-certified air-purifying,
tight-fitting half-face respirator
equipped with N100 (if oil aerosols
absent), R100, or P100 filters;
(B) NIOSH-certified air-purifying,
tight-fitting full-face respirator equipped
with N100 (if oil aerosols absent), R100,
or P100 filters;
(C) NIOSH-certified powered airpurifying respirator equipped with a
loose-fitting hood or helmet and high
efficiency particulate air (HEPA) filters;
(D) NIOSH-certified powered airpurifying respirator equipped with a
tight-fitting facepiece (either half-face or
full-face) and HEPA filters; and
(E) NIOSH-certified supplied-air
respirator operated in pressure demand
or continuous flow mode and equipped
with a hood or helmet, or tight-fitting
facepiece (either half-face or full-face).
(ii) Industrial, commercial, and
consumer activities. Requirements as
specified in § 721.80(o).
(b) Specific requirements. The
provisions of subpart A of this part
apply to this section except as modified
by this paragraph.
(1) Recordkeeping. Recordkeeping
requirements as specified in § 721.125
(a), (b), (c), (d), and (i) are applicable to
manufacturers, importers, and
processors of this substance.
(2) Limitations or revocation of
certain notification requirements. The
provisions of § 721.185 apply to this
section.
■ 15. Add § 721.10650 to subpart E to
read as follows:
§ 721.10650 Polyether substituted
anthraquinone derivative (generic).
(a) Chemical substance and
significant new uses subject to reporting.
(1) The chemical substance identified
generically as polyether substituted
anthraquinone derivative (PMN P–11–
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155) is subject to reporting under this
section for the significant new uses
described in paragraph (a)(2) of this
section.
(2) The significant new uses are:
(i) Industrial, commercial, and
consumer activities. Requirements as
specified in § 721.80(j) (colorant for
cleaners and detergents).
(ii) [Reserved]
(b) Specific requirements. The
provisions of subpart A of this part
apply to this section except as modified
by this paragraph.
(1) Recordkeeping. Recordkeeping
requirements as specified in § 721.125
(a), (b), (c), and (i) are applicable to
manufacturers, importers, and
processors of this substance.
(2) Limitations or revocation of
certain notification requirements. The
provisions of § 721.185 apply to this
section.
■ 16. Add § 721.10651 to subpart E to
read as follows:
§ 721.10651
(generic).
Carbide derived nanocarbon
(a) Chemical substance and
significant new uses subject to reporting.
(1) The chemical substance identified
generically as carbide derived
nanocarbon (PMN P–11–290) is subject
to reporting under this section for the
significant new uses described in
paragraph (a)(2) of this section.
(2) The significant new uses are:
(i) Industrial, commercial, and
consumer activities. Requirements as
specified in § 721.80(j) (manufacture of
the substance by the method described
in the premanufacture notice).
(ii) [Reserved]
(b) Specific requirements. The
provisions of subpart A of this part
apply to this section except as modified
by this paragraph.
(1) Recordkeeping. Recordkeeping
requirements as specified in § 721.125
(a), (b), (c), and (i) are applicable to
manufacturers, importers, and
processors of this substance.
(2) Limitations or revocation of
certain notification requirements. The
provisions of § 721.185 apply to this
section.
(3) Determining whether a specific use
is subject to this section. The provisions
of § 721.1725(b)(1) apply to paragraph
(a)(2)(i) of this section.
■ 17. Add § 721.10652 to subpart E to
read as follows:
§ 721.10652 Hexanedioic acid, polymer
with polyether polyol, 1,1′-methylenebis[4isocyanatobenzene] and dihydroxydialkyl
ether (generic).
(a) Chemical substance and
significant new uses subject to reporting.
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(1) The chemical substance identified
generically as hexanedioic acid,
polymer with polyether polyol, 1,1′methylenebis[4-isocyanatobenzene] and
dihydroxydialkyl ether (PMN P–11–309)
is subject to reporting under this section
for the significant new uses described in
paragraph (a)(2) of this section.
(2) The significant new uses are:
(i) Protection in the workplace.
Requirements as specified in § 721.63
(a)(4), (a)(6)(i), (a)(6)(ii), (a)(6)(v), (b)
(concentration set at 0.1 percent), and
(c). When determining which persons
are reasonably likely to be exposed as
required for § 721.63(a)(4), engineering
control measures (e.g., enclosure or
confinement of the operation, general
and local ventilation) or administrative
control measures (e.g., workplace
policies and procedures) shall be
considered and implemented to prevent
exposure, where feasible. The following
National Institute for Occupational
Safety and Health (NIOSH)-certified
respirators with an assigned protection
factor (APF) of at least 10 meet the
requirements of § 721.63(a)(4):
(A) NIOSH-certified air-purifying,
tight-fitting half-face respirator
equipped with N100 (if oil aerosols
absent), R100, or P100 filters;
(B) NIOSH-certified air-purifying,
tight-fitting full-face respirator equipped
with N100 (if oil aerosols absent), R100,
or P100 filters;
(C) NIOSH-certified powered airpurifying respirator equipped with a
loose-fitting hood or helmet and high
efficiency particulate air (HEPA) filters;
(D) NIOSH-certified powered airpurifying respirator equipped with a
tight-fitting facepiece (either half-face or
full-face) and HEPA filters; and
(E) NIOSH-certified supplied-air
respirator operated in pressure demand
or continuous flow mode and equipped
with a hood or helmet, or tight-fitting
facepiece (either half-face or full-face).
(ii) Industrial, commercial, and
consumer activities. Requirements as
specified in § 721.80(o).
(b) Specific requirements. The
provisions of subpart A of this part
apply to this section except as modified
by this paragraph.
(1) Recordkeeping. Recordkeeping
requirements as specified in § 721.125
(a), (b), (c), (d), and (i) are applicable to
manufacturers, importers, and
processors of this substance.
(2) Limitations or revocation of
certain notification requirements. The
provisions of § 721.185 apply to this
section.
■ 18. Add § 721.10653 to subpart E to
read as follows:
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§ 721.10653 Hexanedioic acid, polymer
with .alpha.-hydro-.omega.hydroxypoly[oxy(methyl-1,2ethanediyl)],1,1′-methylenebis[4isocyanatobenzene], dihydroxydialkyl ether
and dialkanol ether (generic).
(a) Chemical substance and
significant new uses subject to reporting.
(1) The chemical substance identified
generically as hexanedioic acid,
polymer with .alpha.-hydro-.omega.hydroxypoly[oxy(methyl-1,2ethanediyl)],1,1′-methylenebis[4isocyanatobenzene], dihydroxydialkyl
ether and dialkanol ether (PMN P–11–
311) is subject to reporting under this
section for the significant new uses
described in paragraph (a)(2) of this
section.
(2) The significant new uses are:
(i) Protection in the workplace.
Requirements as specified in § 721.63
(a)(4), (a)(6)(i), (a)(6)(ii), (a)(6)(v), (b)
(concentration set at 0.1 percent), and
(c). When determining which persons
are reasonably likely to be exposed as
required for § 721.63(a)(4), engineering
control measures (e.g., enclosure or
confinement of the operation, general
and local ventilation) or administrative
control measures (e.g., workplace
policies and procedures) shall be
considered and implemented to prevent
exposure, where feasible. The following
National Institute for Occupational
Safety and Health (NIOSH)-certified
respirators with an assigned protection
factor (APF) of at least 10 meet the
requirements of § 721.63(a)(4):
(A) NIOSH-certified air-purifying,
tight-fitting half-face respirator
equipped with N100 (if oil aerosols
absent), R100, or P100 filters;
(B) NIOSH-certified air-purifying,
tight-fitting full-face respirator equipped
with N100 (if oil aerosols absent), R100,
or P100 filters;
(C) NIOSH-certified powered airpurifying respirator equipped with a
loose-fitting hood or helmet and high
efficiency particulate air (HEPA) filters;
(D) NIOSH-certified powered airpurifying respirator equipped with a
tight-fitting facepiece (either half-face or
full-face) and HEPA filters; and
(E) NIOSH-certified supplied-air
respirator operated in pressure demand
or continuous flow mode and equipped
with a hood or helmet, or tight-fitting
facepiece (either half-face or full-face).
(ii) Industrial, commercial, and
consumer activities. Requirements as
specified in § 721.80(o).
(b) Specific requirements. The
provisions of subpart A of this part
apply to this section except as modified
by this paragraph.
(1) Recordkeeping. Recordkeeping
requirements as specified in § 721.125
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(a), (b), (c), (d), and (i) are applicable to
manufacturers, importers, and
processors of this substance.
(2) Limitations or revocation of
certain notification requirements. The
provisions of § 721.185 apply to this
section.
■ 19. Add § 721.10654 to subpart E to
read as follows:
§ 721.10654 Hexanedioic acid, polymer
with .alpha.-hydro-.omega.hydroxypoly[oxy(methyl-1,2ethanediyl)],1,1’methylenebis[isocyanatobenzene],
dihydroxydialkyl ether and dialkanol ether
(generic).
(a) Chemical substance and
significant new uses subject to reporting.
(1) The chemical substance identified
generically as hexanedioic acid,
polymer with .alpha.-hydro-.omega.hydroxypoly[oxy(methyl-1,2ethanediyl)],1,1’methylenebis[isocyanatobenzene],
dihydroxydialkyl ether and dialkanol
ether (PMN P–11–312) is subject to
reporting under this section for the
significant new uses described in
paragraph (a)(2) of this section.
(2) The significant new uses are:
(i) Protection in the workplace.
Requirements as specified in § 721.63
(a)(4), (a)(6)(i), (a)(6)(ii), (a)(6)(v), (b)
(concentration set at 0.1 percent), and
(c). When determining which persons
are reasonably likely to be exposed as
required for § 721.63 (a)(4), engineering
control measures (e.g., enclosure or
confinement of the operation, general
and local ventilation) or administrative
control measures (e.g., workplace
policies and procedures) shall be
considered and implemented to prevent
exposure, where feasible. The following
National Institute for Occupational
Safety and Health (NIOSH)-certified
respirators with an assigned protection
factor (APF) of at least 10 meet the
requirements of § 721.63(a)(4):
(A) NIOSH-certified air-purifying,
tight-fitting half-face respirator
equipped with N100 (if oil aerosols
absent), R100, or P100 filters;
(B) NIOSH-certified air-purifying,
tight-fitting full-face respirator equipped
with N100 (if oil aerosols absent), R100,
or P100 filters;
(C) NIOSH-certified powered airpurifying respirator equipped with a
loose-fitting hood or helmet and high
efficiency particulate air (HEPA) filters;
(D) NIOSH-certified powered airpurifying respirator equipped with a
tight-fitting facepiece (either half-face or
full-face) and HEPA filters; and
(E) NIOSH-certified supplied-air
respirator operated in pressure demand
or continuous flow mode and equipped
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12699
with a hood or helmet, or tight-fitting
facepiece (either half-face or full-face).
(ii) Industrial, commercial, and
consumer activities. Requirements as
specified in § 721.80(o).
(b) Specific requirements. The
provisions of subpart A of this part
apply to this section except as modified
by this paragraph.
(1) Recordkeeping. Recordkeeping
requirements as specified in § 721.125
(a), (b), (c), (d), and (i) are applicable to
manufacturers, importers, and
processors of this substance.
(2) Limitations or revocation of
certain notification requirements. The
provisions of § 721.185 apply to this
section.
■ 20. Add § 721.10655 to subpart E to
read as follows:
§ 721.10655 Hexanedioic acid, polymer
with .alpha.-hydro-.omega.-hydroxypoly
[oxy(methyl-1,2-ethanediyl)],1,1’methylenebis[4-isocyanatobenzene],
dihydroxydialkyl ether, reaction products
with dialkylcarbinol (generic).
(a) Chemical substance and
significant new uses subject to reporting.
(1) The chemical substance identified
generically as hexanedioic acid,
polymer with .alpha.-hydro-.omega.hydroxypoly[oxy(methyl-1,2ethanediyl)],1,1’-methylenebis[4isocyanatobenzene], dihydroxydialkyl
ether, reaction products with
dialkylcarbinol (PMN P–11–313) is
subject to reporting under this section
for the significant new uses described in
paragraph (a)(2) of this section.
(2) The significant new uses are:
(i) Protection in the workplace.
Requirements as specified in § 721.63
(a)(4), (a)(6)(i), (a)(6)(ii), (a)(6)(v), (b)
(concentration set at 0.1 percent), and
(c). When determining which persons
are reasonably likely to be exposed as
required for § 721.63(a)(4), engineering
control measures (e.g., enclosure or
confinement of the operation, general
and local ventilation) or administrative
control measures (e.g., workplace
policies and procedures) shall be
considered and implemented to prevent
exposure, where feasible. The following
National Institute for Occupational
Safety and Health (NIOSH)-certified
respirators with an assigned protection
factor (APF) of at least 10 meet the
requirements of § 721.63(a)(4):
(A) NIOSH-certified air-purifying,
tight-fitting half-face respirator
equipped with N100 (if oil aerosols
absent), R100, or P100 filters;
(B) NIOSH-certified air-purifying,
tight-fitting full-face respirator equipped
with N100 (if oil aerosols absent), R100,
or P100 filters;
(C) NIOSH-certified powered airpurifying respirator equipped with a
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loose-fitting hood or helmet and high
efficiency particulate air (HEPA) filters;
(D) NIOSH-certified powered airpurifying respirator equipped with a
tight-fitting facepiece (either half-face or
full-face) and HEPA filters; and
(E) NIOSH-certified supplied-air
respirator operated in pressure demand
or continuous flow mode and equipped
with a hood or helmet, or tight-fitting
facepiece (either half-face or full-face).
(ii) Industrial, commercial, and
consumer activities. Requirements as
specified in § 721.80(o).
(b) Specific requirements. The
provisions of subpart A of this part
apply to this section except as modified
by this paragraph.
(1) Recordkeeping. Recordkeeping
requirements as specified in § 721.125
(a), (b), (c), (d), and (i) are applicable to
manufacturers, importers, and
processors of this substance.
(2) Limitations or revocation of
certain notification requirements. The
provisions of § 721.185 apply to this
section.
■ 21. Add § 721.10656 to subpart E to
read as follows:
erowe on DSK2VPTVN1PROD with PROPOSALS-1
§ 721.10656 Hexanedioic acid, polymer
with .alpha.-hydro-.omega.hydroxypoly[oxy(methyl-1,2ethanediyl)],1,1’-methylenebis[4isocyanatobenzene], dihydroxydialkyl ether
reaction products with dialkylcarbinol
(generic).
(a) Chemical substance and
significant new uses subject to reporting.
(1) The chemical substance identified
generically as hexanedioic acid,
polymer with .alpha.-hydro-.omega.hydroxypoly[oxy(methyl-1,2ethanediyl)],1,1’-methylenebis[4isocyanatobenzene], dihydroxydialkyl
ether reaction products with
dialkylcarbinol (PMN P–11–314) is
subject to reporting under this section
for the significant new uses described in
paragraph (a)(2) of this section.
(2) The significant new uses are:
(i) Protection in the workplace.
Requirements as specified in § 721.63
(a)(4), (a)(6)(i), (a)(6)(ii), (a)(6)(v), (b)
(concentration set at 0.1 percent), and
(c). When determining which persons
are reasonably likely to be exposed as
required for § 721.63(a)(4), engineering
control measures (e.g., enclosure or
confinement of the operation, general
and local ventilation) or administrative
control measures (e.g., workplace
policies and procedures) shall be
considered and implemented to prevent
exposure, where feasible. The following
National Institute for Occupational
Safety and Health (NIOSH)-certified
respirators with an assigned protection
factor (APF) of at least 10 meet the
requirements of § 721.63(a)(4):
VerDate Mar<15>2010
14:27 Feb 22, 2013
Jkt 229001
(A) NIOSH-certified air-purifying,
tight-fitting half-face respirator
equipped with N100 (if oil aerosols
absent), R100, or P100 filters;
(B) NIOSH-certified air-purifying,
tight-fitting full-face respirator equipped
with N100 (if oil aerosols absent), R100,
or P100 filters;
(C) NIOSH-certified powered airpurifying respirator equipped with a
loose-fitting hood or helmet and high
efficiency particulate air (HEPA) filters;
(D) NIOSH-certified powered airpurifying respirator equipped with a
tight-fitting facepiece (either half-face or
full-face) and HEPA filters; and
(E) NIOSH-certified supplied-air
respirator operated in pressure demand
or continuous flow mode and equipped
with a hood or helmet, or tight-fitting
facepiece (either half-face or full-face).
(ii) Industrial, commercial, and
consumer activities. Requirements as
specified in § 721.80(o).
(b) Specific requirements. The
provisions of subpart A of this part
apply to this section except as modified
by this paragraph.
(1) Recordkeeping. Recordkeeping
requirements as specified in § 721.125
(a), (b), (c), (d), and (i) are applicable to
manufacturers, importers, and
processors of this substance.
(2) Limitations or revocation of
certain notification requirements. The
provisions of § 721.185 apply to this
section.
■ 22. Add § 721.10657 to subpart E to
read as follows:
§ 721.10657 Castor oil, polymer with
hydrogenated vegetable oil, 1,1’methylenebis[isocyanatobenzene] and
isocyanate (generic).
(a) Chemical substance and
significant new uses subject to reporting.
(1) The chemical substance identified
generically as castor oil, polymer with
hydrogenated vegetable oil, 1,1’methylenebis[isocyanatobenzene] and
isocyanate (PMN P–12–73) is subject to
reporting under this section for the
significant new uses described in
paragraph (a)(2) of this section.
(2) The significant new uses are:
(i) Protection in the workplace.
Requirements as specified in § 721.63
(a)(4), (a)(6)(i), (a)(6)(ii), (a)(6)(v), (b)
(concentration set at 0.1 percent), and
(c). When determining which persons
are reasonably likely to be exposed as
required for § 721.63(a)(4), engineering
control measures (e.g., enclosure or
confinement of the operation, general
and local ventilation) or administrative
control measures (e.g., workplace
policies and procedures) shall be
considered and implemented to prevent
exposure, where feasible. The following
PO 00000
Frm 00068
Fmt 4702
Sfmt 4702
National Institute for Occupational
Safety and Health (NIOSH)-certified
respirators with an assigned protection
factor (APF) of at least 10 meet the
requirements of § 721.63(a)(4):
(A) NIOSH-certified air-purifying,
tight-fitting half-face respirator
equipped with N100 (if oil aerosols
absent), R100, or P100 filters;
(B) NIOSH-certified air-purifying,
tight-fitting full-face respirator equipped
with N100 (if oil aerosols absent), R100,
or P100 filters;
(C) NIOSH-certified powered airpurifying respirator equipped with a
loose-fitting hood or helmet and high
efficiency particulate air (HEPA) filters;
(D) NIOSH-certified powered airpurifying respirator equipped with a
tight-fitting facepiece (either half-face or
full-face) and HEPA filters; and
(E) NIOSH-certified supplied-air
respirator operated in pressure demand
or continuous flow mode and equipped
with a hood or helmet, or tight-fitting
facepiece (either half-face or full-face).
(ii) Industrial, commercial, and
consumer activities. Requirements as
specified in § 721.80(o).
(b) Specific requirements. The
provisions of subpart A of this part
apply to this section except as modified
by this paragraph.
(1) Recordkeeping. Recordkeeping
requirements as specified in § 721.125
(a), (b), (c), (d), and (i) are applicable to
manufacturers, importers, and
processors of this substance.
(2) Limitations or revocation of
certain notification requirements. The
provisions of § 721.185 apply to this
section.
■ 23. Add § 721.10658 to subpart E to
read as follows:
§ 721.10658 2-Oxepanone, polymer with
1,6-diisocyanatohexane, 2,2-dimethyl-1,3propanediol and 2,2’-oxybis[ethanol].
(a) Chemical substance and
significant new uses subject to reporting.
(1) The chemical substance identified as
2-oxepanone, polymer with 1,6diisocyimatohexane, 2,2-dimethyl-1,3propanediol and 2,2’-oxybis[ethanol]
(PMN P–12–133; CAS No. 1313708–90–
5) is subject to reporting under this
section for the significant new uses
described in paragraph (a)(2) of this
section.
(2) The significant new uses are:
(i) Protection in the workplace.
Requirements as specified in § 721.63
(a)(4), (a)(6)(i), (a)(6)(ii), (a)(6)(v), (b)
(concentration set at 0.1 percent), and
(c). When determining which persons
are reasonably likely to be exposed as
required for § 721.63(a)(4), engineering
control measures (e.g., enclosure or
confinement of the operation, general
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and local ventilation) or administrative
control measures (e.g., workplace
policies and procedures) shall be
considered and implemented to prevent
exposure, where feasible. The following
National Institute for Occupational
Safety and Health (NIOSH)-certified
respirators with an assigned protection
factor (APF) of at least 10 meet the
requirements of § 721.63(a)(4):
(A) NIOSH-certified air-purifying,
tight-fitting half-face respirator
equipped with N100 (if oil aerosols
absent), R100, or P100 filters;
(B) NIOSH-certified air-purifying,
tight-fitting full-face respirator equipped
with N100 (if oil aerosols absent), R100,
or P100 filters;
(C) NIOSH-certified powered airpurifying respirator equipped with a
loose-fitting hood or helmet and high
efficiency particulate air (HEPA) filters;
(D) NIOSH-certified powered airpurifying respirator equipped with a
tight-fitting facepiece (either half-face or
full-face) and HEPA filters; and
(E) NIOSH-certified supplied-air
respirator operated in pressure demand
or continuous flow mode and equipped
with a hood or helmet, or tight-fitting
facepiece (either half-face or full-face).
(ii) Industrial, commercial, and
consumer activities. Requirements as
specified in § 721.80(o).
(b) Specific requirements. The
provisions of subpart A of this part
apply to this section except as modified
by this paragraph.
(1) Recordkeeping. Recordkeeping
requirements as specified in § 721.125
(a), (b), (c), (d), and (i) are applicable to
manufacturers, importers, and
processors of this substance.
(2) Limitations or revocation of
certain notification requirements. The
provisions of § 721.185 apply to this
section.
■ 24. Add § 721.10659 to subpart E to
read as follows:
erowe on DSK2VPTVN1PROD with PROPOSALS-1
§ 721.10659 Poly(oxy-1,4-butanediyl),
-hydro—hydroxy-, polymer with
alkyldiisocyanates (generic).
(a) Chemical substance and
significant new uses subject to reporting.
(1) The chemical substance identified
generically as poly(oxy-1,4-butanediyl),
-hydro—hydroxy-, polymer with
alkyldiisocyanates (PMN P–12–143) is
subject to reporting under this section
for the significant new uses described in
paragraph (a)(2) of this section.
(2) The significant new uses are:
(i) Protection in the workplace.
Requirements as specified in § 721.63
(a)(4), (a)(6)(i), (a)(6)(ii), (a)(6)(v), (b)
(concentration set at 0.1 percent), and
(c). When determining which persons
are reasonably likely to be exposed as
VerDate Mar<15>2010
14:27 Feb 22, 2013
Jkt 229001
required for § 721.63(a)(4), engineering
control measures (e.g., enclosure or
confinement of the operation, general
and local ventilation) or administrative
control measures (e.g., workplace
policies and procedures) shall be
considered and implemented to prevent
exposure, where feasible. The following
National Institute for Occupational
Safety and Health (NIOSH)-certified
respirators with an assigned protection
factor (APF) of at least 10 meet the
requirements of § 721.63(a)(4):
(A) NIOSH-certified air-purifying,
tight-fitting half-face respirator
equipped with N100 (if oil aerosols
absent), R100, or P100 filters;
(B) NIOSH-certified air-purifying,
tight-fitting full-face respirator equipped
with N100 (if oil aerosols absent), R100,
or P100 filters;
(C) NIOSH-certified powered airpurifying respirator equipped with a
loose-fitting hood or helmet and high
efficiency particulate air (HEPA) filters;
(D) NIOSH-certified powered airpurifying respirator equipped with a
tight-fitting facepiece (either half-face or
full-face) and HEPA filters; and
(E) NIOSH-certified supplied-air
respirator operated in pressure demand
or continuous flow mode and equipped
with a hood or helmet, or tight-fitting
facepiece (either half-face or full-face).
(ii) Industrial, commercial, and
consumer activities. Requirements as
specified in § 721.80(o).
(b) Specific requirements. The
provisions of subpart A of this part
apply to this section except as modified
by this paragraph.
(1) Recordkeeping. Recordkeeping
requirements as specified in § 721.125
(a), (b), (c), (d), and (i) are applicable to
manufacturers, importers, and
processors of this substance.
(2) Limitations or revocation of
certain notification requirements. The
provisions of § 721.185 apply to this
section.
■ 25. Add § 721.10660 to subpart E to
read as follows:
§ 721.10660 Aliphatic diisocyanate adduct
with substituted amino alkyl silane
(generic).
(a) Chemical substance and
significant new uses subject to reporting.
(1) The chemical substance identified
generically as aliphatic diisocyanate
adduct with substituted amino alkyl
silane (PMN P–12–274) is subject to
reporting under this section for the
significant new uses described in
paragraph (a)(2) of this section.
(2) The significant new uses are:
(i) Protection in the workplace.
Requirements as specified in
§ 721.63(a)(4), (a)(6)(i), (a)(6)(ii),
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Sfmt 9990
12701
(a)(6)(v), (b) (concentration set at 0.1
percent), and (c). When determining
which persons are reasonably likely to
be exposed as required for
§ 721.63(a)(4), engineering control
measures (e.g., enclosure or
confinement of the operation, general
and local ventilation) or administrative
control measures (e.g., workplace
policies and procedures) shall be
considered and implemented to prevent
exposure, where feasible. The following
National Institute for Occupational
Safety and Health (NIOSH)-certified
respirators with an assigned protection
factor (APF) of at least 10 meet the
requirements of § 721.63(a)(4):
(A) NIOSH-certified air-purifying,
tight-fitting half-face respirator
equipped with N100 (if oil aerosols
absent), R100, or P100 filters;
(B) NIOSH-certified air-purifying,
tight-fitting full-face respirator equipped
with N100 (if oil aerosols absent), R100,
or P100 filters;
(C) NIOSH-certified powered airpurifying respirator equipped with a
loose-fitting hood or helmet and high
efficiency particulate air (HEPA) filters;
(D) NIOSH-certified powered airpurifying respirator equipped with a
tight-fitting facepiece (either half-face or
full-face) and HEPA filters; and
(E) NIOSH-certified supplied-air
respirator operated in pressure demand
or continuous flow mode and equipped
with a hood or helmet, or tight-fitting
facepiece (either half-face or full-face).
(ii) Industrial, commercial, and
consumer activities. Requirements as
specified in § 721.80(o).
(b) Specific requirements. The
provisions of subpart A of this part
apply to this section except as modified
by this paragraph.
(1) Recordkeeping. Recordkeeping
requirements as specified in § 721.125
(a), (b), (c), (d), and (i) are applicable to
manufacturers, importers, and
processors of this substance.
(2) Limitations or revocation of
certain notification requirements. The
provisions of § 721.185 apply to this
section.
[FR Doc. 2013–04298 Filed 2–22–13; 8:45 am]
BILLING CODE 6560–50–P
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Agencies
[Federal Register Volume 78, Number 37 (Monday, February 25, 2013)]
[Proposed Rules]
[Pages 12684-12701]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-04298]
=======================================================================
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ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 721
[EPA-HQ-OPPT-2012-0727; FRL-9376-7]
RIN 2070-AB27
Proposed Significant New Use Rules on Certain Chemical Substances
AGENCY: Environmental Protection Agency (EPA).
ACTION: Proposed rule.
-----------------------------------------------------------------------
SUMMARY: EPA is proposing significant new use rules (SNURs) under the
Toxic Substances Control Act (TSCA) for 37 chemical substances which
were the subject of premanufacture notices (PMNs). Seventeen of these
chemical substances are subject to TSCA section 5(e) consent orders
issued by EPA. This action would require persons who intend to
manufacture, import, or process any of these 37 chemical substances for
an activity that is designated as a significant new use by this
proposed rule to notify EPA at least 90 days before commencing that
activity. The required notification would provide EPA with the
opportunity to evaluate the intended use and, if necessary, to prohibit
or limit that activity before it occurs.
DATES: Comments must be received on or before April 26, 2013.
ADDRESSES: Submit your comments, identified by docket identification
(ID) number EPA-HQ-OPPT-2012-0727, by one of the following methods:
Federal eRulemaking Portal: https://www.regulations.gov.
Follow the online instructions for submitting comments.
Mail: Document Control Office (7407M), Office of Pollution
Prevention and Toxics (OPPT), Environmental Protection Agency, 1200
Pennsylvania Ave. NW., Washington, DC 20460-0001.
Hand Delivery: OPPT Document Control Office (DCO), EPA
East Bldg., Rm. 6428, 1201 Constitution Ave., NW., Washington, DC.
ATTN: Docket ID Number EPA-HQ-OPPT-2012-0727. The DCO is open from 8
a.m. to 4 p.m., Monday through Friday, excluding legal holidays. The
telephone number for the DCO is (202) 564-8930. Such deliveries are
only accepted during the DCO's normal hours of operation, and special
arrangements should be made for deliveries of boxed information.
Instructions: Direct your comments to docket ID number EPA-HQ-OPPT-
2012-0727. EPA's policy is that all comments received will be included
in the docket without change and may be made available online at https://www.regulations.gov, including any personal information provided,
unless the comment includes information claimed to be Confidential
Business Information (CBI) or other information whose disclosure is
restricted by statute. Do not submit information that you consider to
be CBI or otherwise protected through regulations.gov or email. The
regulations.gov Web site is an ``anonymous access'' system, which means
EPA will not know your identity or contact information unless you
provide it in the body of your comment. If you send an email comment
directly to EPA without going through regulations.gov, your email
address will be automatically captured and included as part of the
comment that is placed in the docket and made available on the
Internet. If you submit an electronic comment, EPA recommends that you
include your name and other contact information in the body of your
comment and with any disk or CD-ROM you submit. If EPA cannot read your
comment due to technical difficulties and cannot contact you for
clarification, EPA may not be able to consider your comment. Electronic
files should avoid the use of special characters, any form of
encryption, and be free of any defects or viruses.
Docket: All documents in the docket are listed in the docket index
available at https://www.regulations.gov. Although listed in the index,
some information is not publicly available, e.g., CBI or other
information whose disclosure is restricted by statute. Certain other
material, such as copyrighted material, will be publicly available only
in hard copy. Publicly available docket materials are available
electronically at https://www.regulations.gov, or, if only available in
hard copy, at the OPPT Docket. The OPPT Docket is located in the EPA
Docket Center (EPA/DC) at Rm. 3334, EPA West Bldg., 1301 Constitution
Ave. NW., Washington, DC. The EPA/DC Public Reading Room hours of
operation are 8:30 a.m. to 4:30 p.m., Monday through Friday, excluding
legal holidays. The telephone number of the EPA/DC Public Reading Room
is (202) 566-1744, and the telephone number for the OPPT Docket is
(202) 566-0280. Docket visitors are required to show photographic
identification, pass through a metal detector, and sign the EPA visitor
log. All visitor bags are processed through an X-ray machine and
subject to search. Visitors will be provided an EPA/DC badge that must
be visible at all times in the building and returned upon departure.
FOR FURTHER INFORMATION CONTACT: For technical information contact:
Kenneth Moss, Chemical Control Division (7405M), Office of Pollution
Prevention and Toxics, Environmental Protection
[[Page 12685]]
Agency, 1200 Pennsylvania Ave. NW., Washington, DC 20460-0001;
telephone number: (202) 564-9232; email address: moss.kenneth@epa.gov.
For general information contact: The TSCA-Hotline, ABVI-Goodwill,
422 South Clinton Ave., Rochester, NY 14620; telephone number: (202)
554-1404; email address: TSCA-Hotline@epa.gov.
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this action apply to me?
You may be potentially affected by this action if you manufacture,
import, process, or use the chemical substances in this proposed rule.
The following list of North American Classification System (NAICS)
codes is not intended to be exhaustive, but rather provides a guide to
help readers determine whether this document applies to them.
Potentially affected entities may include:
Manufacturers, importers, or processors of one or more
subject chemical substances (NAICS codes 325 and 324110), e.g.,
chemical manufacturing and petroleum refineries.
This action may also affect certain entities through pre-existing
import certification and export notification rules under TSCA. Chemical
importers are subject to the TSCA section 13 (15 U.S.C. 2612) import
certification requirements promulgated at 19 CFR 12.118 through 12.127;
see also 19 CFR 127.28. Chemical importers must certify that the
shipment of the chemical substance complies with all applicable rules
and orders under TSCA. Importers of chemicals subject to a final SNUR
must certify their compliance with the SNUR requirements. The EPA
policy in support of import certification appears at 40 CFR part 707,
subpart B. In addition, any persons who export or intend to export a
chemical substance that is the subject of a proposed or final SNUR are
subject to the export notification provisions of TSCA section 12(b) (15
U.S.C. 2611(b)) (see Sec. 721.20) and must comply with the export
notification requirements in 40 CFR part 707, subpart D.
B. What should I consider as I prepare my comments for EPA?
1. Submitting CBI. Do not submit this information to EPA through
regulations.gov or email. Clearly mark the part or all of the
information that you claim to be CBI. For CBI information in a disk or
CD-ROM that you mail to EPA, mark the outside of the disk or CD-ROM as
CBI and then identify electronically within the disk or CD-ROM the
specific information that is claimed as CBI. In addition to one
complete version of the comment that includes information claimed as
CBI, a copy of the comment that does not contain the information
claimed as CBI must be submitted for inclusion in the public docket.
Information so marked will not be disclosed except in accordance with
procedures set forth in 40 CFR part 2.
2. Tips for preparing your comments. When submitting comments,
remember to:
i. Identify the document by docket ID number and other identifying
information (subject heading, Federal Register date and page number).
ii. Follow directions. The Agency may ask you to respond to
specific questions or organize comments by referencing a Code of
Federal Regulations (CFR) part or section number.
iii. Explain why you agree or disagree; suggest alternatives and
substitute language for your requested changes.
iv. Describe any assumptions and provide any technical information
and/or data that you used.
v. If you estimate potential costs or burdens, explain how you
arrived at your estimate in sufficient detail to allow for it to be
reproduced.
vi. Provide specific examples to illustrate your concerns and
suggest alternatives.
vii. Explain your views as clearly as possible, avoiding the use of
profanity or personal threats.
viii. Make sure to submit your comments by the comment period
deadline identified.
II. Background
A. What action is the agency taking?
These proposed SNURs would, when finalized, require persons to
notify EPA at least 90 days before commencing the manufacture, import,
or processing of the specific chemical substances identified in the
PMNs for any activity designated by these SNURs as a significant new
use. Receipt of such notices allows EPA to assess risks that may be
presented by the intended uses and, if appropriate, to regulate the
proposed use before it occurs. Additional rationale and background to
these rules are more fully set out in the preamble to EPA's first
direct final SNUR published in the Federal Register of April 24, 1990
(55 FR 17376). Consult that preamble for further information on the
objectives, rationale, and procedures for SNURs and on the basis for
significant new use designations, including provisions for developing
test data.
B. What is the Agency's authority for taking this action?
Section 5(a)(2) of TSCA (15 U.S.C. 2604(a)(2)) authorizes EPA to
determine that a use of a chemical substance is a ``significant new
use.'' EPA must make this determination by rule after considering all
relevant factors, including the four bulleted TSCA section 5(a)(2)
factors listed in Unit III. Once EPA determines that a use of a
chemical substance is a significant new use, TSCA section 5(a)(1)(B)
and 40 CFR part 721 require persons to submit a significant new use
notice (SNUN) to EPA at least 90 days before they manufacture, import,
or process the chemical substance for that use. Persons who must report
are described in Sec. [emsp14]721.5.
C. Applicability of General Provisions
General provisions for SNURs appear in 40 CFR part 721, subpart A.
These provisions describe persons subject to the rule, recordkeeping
requirements, exemptions to reporting requirements, and applicability
of the rule to uses occurring before the effective date of the final
rule. Provisions relating to user fees appear at 40 CFR part 700.
According to Sec. [emsp14]721.1(c), persons subject to these SNURs
must comply with the same SNUN requirements and EPA regulatory
procedures as submitters of PMNs under TSCA section 5(a)(1)(A). In
particular, these requirements include the information submission
requirements of TSCA section 5(b) and 5(d)(1), the exemptions
authorized by TSCA section 5(h)(1), (h)(2), (h)(3), and (h)(5), and the
regulations at 40 CFR part 720. Once EPA receives a SNUN, EPA may take
regulatory action under TSCA section 5(e), 5(f), 6, or 7 to control the
activities for which it has received the SNUN. If EPA does not take
action, EPA is required under TSCA section 5(g) to explain in the
Federal Register its reasons for not taking action.
III. Significant New Use Determination
Section 5(a)(2) of TSCA states that EPA's determination that a use
of a chemical substance is a significant new use must be made after
consideration of all relevant factors, including:
The projected volume of manufacturing and processing of a
chemical substance.
The extent to which a use changes the type or form of
exposure of human beings or the environment to a chemical substance.
The extent to which a use increases the magnitude and
duration of exposure of human beings or the environment to a chemical
substance.
[[Page 12686]]
The reasonably anticipated manner and methods of
manufacturing, processing, distribution in commerce, and disposal of a
chemical substance.
In addition to these factors enumerated in TSCA section 5(a)(2),
the statute authorized EPA to consider any other relevant factors.
To determine what would constitute a significant new use for the 37
chemical substances that are the subject of these proposed SNURs, EPA
considered relevant information about the toxicity of the chemical
substances, likely human exposures and environmental releases
associated with possible uses, taking into consideration the four
bulleted TSCA section 5(a)(2) factors listed in this unit.
IV. Substances Subject to This Proposed Rule
EPA is proposing to establish significant new use and recordkeeping
requirements for 37 chemical substances in 40 CFR part 721, subpart E.
In this unit, EPA provides the following information for each chemical
substance:
PMN number.
Chemical name (generic name, if the specific name is
claimed as CBI).
Chemical Abstracts Service (CAS) number (if assigned for
non-confidential chemical identities).
Basis for the TSCA section 5(e) consent order or, for TSCA
non-section 5(e) SNURs, the basis for the SNUR (i.e., SNURs without
TSCA section 5(e) consent orders).
Tests recommended by EPA to provide sufficient information
to evaluate the chemical substance (see Unit VIII. for more
information).
CFR citation assigned in the regulatory text section of
this proposed rule.
This proposed rule includes 14 PMN substances whose reported
chemical names include the term ``carbon nanotube'' or ``carbon
nanofibers.'' Because of a lack of established nomenclature for carbon
nanotubes, the TSCA Inventory names for carbon nanotubes are currently
in generic form, e.g., carbon nanotube (CNT), multi-walled carbon
nanotube (MWCNT), double-walled carbon nanotube (DWCNT), or single-
walled carbon nanotube (SWCNT). EPA uses the specific structural
characteristics provided by the PMN submitter to more specifically
characterize the TSCA Inventory listing for an individual CNT. All
submitters of new chemical notices for CNTs have claimed those specific
structural characteristics as CBI. EPA is publishing the generic
chemical name along with the PMN number to identify that a distinct
chemical substance was the subject of the PMN without revealing the
confidential chemical identity of the PMN substance. Confidentiality
claims preclude a more detailed description of the identity of these
CNTs. If an intended manufacturer, importer, or processor of CNTs is
unsure of whether its CNTs are subject to this proposed SNUR or any
other SNUR, the company can either contact EPA or obtain a written
determination from EPA pursuant to the bona fide procedures at Sec.
721.11. EPA is using the specific structural characteristics for all
CNTs submitted as new chemical substances under TSCA to help develop
standard nomenclature for placing these chemical substances on the TSCA
Inventory. EPA has compiled a generic list of those structural
characteristics entitled ``Material Characterization of Carbon
Nanotubes for Molecular Identity (MI) Determination & Nomenclature.'' A
copy of this list is available in the docket for these proposed SNURs
under docket ID number EPA-HQ-OPPT-2012-0727. If EPA develops a more
specific generic chemical name for these materials, that name will be
made publicly available.
The regulatory text section of this proposed rule specifies the
activities designated as significant new uses. Certain new uses,
including exceeding production volume limits (i.e., limits on
manufacture and importation volume) and other uses designated in this
proposed rule, may be claimed as CBI.
This proposed rule includes 17 PMN substances for which EPA
determined, pursuant to TSCA section 5(e), that uncontrolled
manufacture, import, processing, distribution in commerce, use, and
disposal may present an unreasonable risk of injury to human health or
the environment. Accordingly, these substances are subject to ``risk-
based'' consent orders under TSCA section 5(e)(1)(A)(ii)(I). Those
consent orders require protective measures to limit exposures or
otherwise mitigate the potential unreasonable risk. The so-called
``section 5(e) SNURs'' on these PMN substances are proposed pursuant to
Sec. 721.160, and are based on and consistent with the provisions in
the underlying consent orders. The section 5(e) SNURs designate as a
``significant new use'' the absence of the protective measures required
in the corresponding consent orders.
Where EPA determined that the PMN substance may present an
unreasonable risk of injury to human health via inhalation exposure,
the underlying TSCA section 5(e) consent order usually requires, among
other things, that potentially exposed employees wear specified
respirators unless actual measurements of the workplace air show that
air-borne concentrations of the PMN substance are below a New Chemical
Exposure Limit (NCEL) that is established by EPA to provide adequate
protection to human health. In addition to the actual NCEL
concentration, the comprehensive NCELs provisions in TSCA section 5(e)
consent orders, which are modeled after Occupational Safety and Health
Administration (OSHA) Permissible Exposure Limits (PELs) provisions,
include requirements addressing performance criteria for sampling and
analytical methods, periodic monitoring, respiratory protection, and
recordkeeping. However, no comparable NCEL provisions currently exist
in 40 CFR part 721, subpart B, for SNURs. Therefore, for these cases,
the individual SNURs in 40 CFR part 721, subpart E, will normally state
that persons subject to the SNUR who wish to pursue NCELs as an
alternative to the Sec. 721.63 respirator requirements may request to
do so under Sec. [emsp14]721.30. EPA expects that persons whose Sec.
721.30 requests to use the NCELs approach for SNURs are approved by EPA
will be required to comply with NCELs provisions that are comparable to
those contained in the corresponding TSCA section 5(e) consent order
for the same chemical substance.
This proposed rule also includes SNURs on 20 PMN substances that
are not subject to consent orders under TSCA section 5(e). In these
cases, for a variety of reasons, EPA did not find that the use scenario
described in the PMN triggered the determinations set forth under TSCA
section 5(e). However, EPA does believe that certain changes from the
use scenario described in the PMN could result in increased exposures,
thereby constituting a ``significant new use.'' These so-called ``non-
section 5(e) SNURs'' are promulgated pursuant to Sec. [emsp14]721.170.
EPA has determined that every activity designated as a ``significant
new use'' in all non-section 5(e) SNURs issued under Sec.
[emsp14]721.170 satisfies the two requirements stipulated in Sec.
721.170(c)(2), i.e., these significant new use activities, ``(i) are
different from those described in the premanufacture notice for the
substance, including any amendments, deletions, and additions of
activities to the premanufacture notice, and (ii) may be accompanied by
changes in exposure or release levels that are significant in relation
to the health or environmental concerns identified'' for the PMN
substance.
[[Page 12687]]
PMN Number P-00-835
Chemical name: Substituted picolinate (generic).
CAS number: Claimed as confidential.
Basis for action: The PMN states that the substance will be used as
an intermediate in the manufacture of agricultural chemicals. Based on
ecological structure activity relationship (EcoSAR) analysis of test
data on analogous esters, EPA predicts toxicity to aquatic organisms
may occur at concentrations that exceed 90 parts per billion (ppb) of
the PMN substance in surface waters. As described in the PMN, releases
to surface water are not expected. Therefore, EPA has not determined
that the proposed manufacturing, processing, or use of the substance
may present an unreasonable risk. EPA has determined, however, that any
use of the substance resulting in surface water concentrations
exceeding 90 ppb may cause significant adverse environmental effects.
Based on this information, the PMN substance meets the concern criteria
at Sec. 721.170(b)(4)(ii).
Recommended testing: EPA has determined that the results of a fish
acute toxicity test, freshwater and marine (OPPTS Test Guideline
850.1075); an aquatic invertebrate acute toxicity test, freshwater
daphnids (OPPTS Test Guideline 850.1010); and an algal toxicity test
(Office of Chemical Safety and Pollution Prevention (OCSPP) Test
Guideline 850.4500) would help characterize the environmental effects
of the PMN substance.
CFR citation: 40 CFR 721.10637.
PMN Number P-02-167
Chemical name: Lithium metal phosphate (generic).
CAS number: Claimed as confidential.
Basis for action: The PMN states that the generic (non-
confidential) use of the substance will be as an electrode material.
Based on EcoSAR analysis of test data on analogous inorganic
phosphates, EPA predicts toxicity to aquatic organisms may occur at
concentrations that exceed 1 ppb of the PMN substance in surface
waters. As described in the PMN, releases to water are not expected to
exceed 1 ppb. Therefore, EPA has not determined that the proposed
manufacturing, processing, or use of the substance presents an
unreasonable risk. EPA has determined, however, that any use of the
substance resulting in surface water concentrations exceeding 1 ppb may
cause significant adverse environmental effects. Based on this
information, the PMN substance meets the concern criteria at Sec.
721.170(b)(4)(ii).
Recommended testing: EPA has determined that the results of a fish
acute toxicity test, freshwater and marine (OPPTS Test Guideline
850.1075); an aquatic invertebrate acute toxicity test, freshwater
daphnids (OPPTS Test Guideline 850.1010); and an algal toxicity test
(OCSPP Test Guideline 850.4500) would help characterize the
environmental effects of the PMN substance.
CFR citation: 40 CFR 721.10638.
PMN Number P-02-668
Chemical name: Siloxanes and Silicones, di-Me, polymers with Ph
silsesquioxanes, hydrolyzed, reaction products with 2-[[3-
(trimethoxysilyl)propoxy]methyl]oxirane.
CAS number: 478823-10-8.
Basis for action: The PMN substance will be used as a binder for
silicone coatings. Based on structure activity relationship (SAR)
analysis of test data on analogous epoxides and alkoxysilanes, EPA
identified concerns for mutagenicity, oncogenicity, reproductive
toxicity, developmental toxicity, lung toxicity, and sensitization from
dermal and inhalation exposures to the PMN substance. For the use
described in the PMN, significant occupational dermal and inhalation
exposures are not expected due to the use of impervious gloves and a
National Institute for Occupational Safety and Health (NIOSH)-certified
respirator with an assigned protection factor (APF) of at least 10, and
consumer exposures are not expected as the substance is not used in
consumer products. Therefore, EPA has not determined that
manufacturing, processing, and use of the substance may present an
unreasonable risk. EPA has determined, however, that use of the
substance without impervious gloves where there is a potential for
dermal exposure; any use of the substance without a NIOSH-certified
respirator with an APF of at least 10; or any use of the substance in
consumer products may result in serious health effects. Based on this
information, the PMN substance meets the concern criteria at Sec.
721.170 (b)(1)(i)(C) and (b)(3)(ii).
Recommended testing: EPA has determined that the results of a 90-
day inhalation toxicity test (OPPTS Test Guideline 870.3465), with
attention to the pathology of the reproductive organs, and a
carcinogenicity test (OPPTS Test Guideline 870.4200) would help to
characterize the human health effects of the PMN substance.
CFR citation: 40 CFR 721.10639.
PMN Number P-03-135
Chemical name: 1,2-Cyclohexanedicarboxylic acid, 1-(2-ethylhexyl)
2-(2-methylpropyl) ester.
CAS number: 252958-29-5.
Basis for action: The PMN states that the generic (non-
confidential) use of the substance will be as a compressor lubricant.
Based on EcoSAR analysis of test data on analogous esters, EPA predicts
toxicity to aquatic organisms may occur at concentrations that exceed 1
ppb of the PMN substance in surface waters. As described in the PMN,
the substance is not released to surface waters. Therefore, EPA has not
determined that the proposed manufacturing, processing, or use of the
substance may present an unreasonable risk. EPA has determined,
however, that any use of the substance resulting in surface water
concentrations exceeding 1 ppb may cause significant adverse
environmental effects. There are two other chemical substances
identified in the PMN that are already on the TSCA Inventory. The SNUR
does not apply to those chemical substances. Based on this information,
the PMN substance meets the concern criteria at Sec.
721.170(b)(4)(ii).
Recommended testing: EPA has determined that the results of a fish
early-life stage toxicity test (OPPTS Test Guideline 850.1400); a
daphnid chronic toxicity test (OPPTS Test Guideline 850.1300); and an
algal toxicity test (OCSPP Test Guideline 850.4500) would help to
characterize the environmental effects of the PMN substance.
CFR citation: 40 CFR 721.10640.
PMN Number P-03-255
Chemical name: Phenol and vinyltoluene based hydrocarbon resin
(generic).
CAS number: Claimed as confidential.
Basis for action: The PMN states that the generic (non-
confidential) use of the substance will be as a diluent for coatings.
Based on EcoSAR analysis of test data on analogous neutral organics,
EPA predicts toxicity to aquatic organisms may occur at concentrations
that exceed 1 ppb of the PMN substance in surface waters. As described
in the PMN, releases to water are not expected. Therefore, EPA has not
determined that the proposed manufacturing, processing, or use of the
substance may present an unreasonable risk. EPA has determined,
however, that any use of the substance resulting in surface water
concentrations exceeding 1 ppb may cause significant adverse
environmental effects. Based on this information, the PMN substance
meets the concern criteria at Sec. 721.170(b)(4)(ii).
[[Page 12688]]
Recommended testing: EPA has determined that the results of a fish
early-life stage toxicity test (OPPTS Test Guideline 850.1400); a
daphnid chronic toxicity test (OPPTS Test Guideline 850.1300); and an
algal toxicity test (OCSPP Test Guideline 850.4500) would help to
characterize the environmental effects of the PMN substance.
CFR citation: 40 CFR 721.10641.
PMN Numbers P-03-762 and P-03-763
Chemical name: Modified polyisocyanates (generic).
CAS number: Claimed as confidential.
Basis for action: The consolidated PMN states that the generic
(non-confidential) use of the substances will be as hardeners. Based on
SAR analysis of test data on analogous isocyanates, EPA has identified
concerns for sensitization and irritation from dermal and inhalation
exposure to the PMN substances. For the use described in the PMN,
significant occupational inhalation and dermal exposures are not
expected due to no domestic manufacture, use of impervious gloves, and
no use of the substances involving an application method that generates
a vapor, mist, or aerosol. Further, consumer exposures are not expected
as the substance is not used in consumer products. Therefore, EPA has
not determined that the proposed processing or use of the substances
may present an unreasonable risk. EPA has determined, however, that any
domestic manufacture of the substances; any use of the substances
without impervious gloves where there is a potential for dermal
exposures; any use of the substance in consumer products; or any use of
the substances involving an application method that generates a vapor,
mist, or aerosol may result in serious health effects. Based on this
information, the PMN substances meet the concern criteria at Sec.
721.170(b)(3)(ii).
Recommended testing: EPA has determined that the results of a skin
sensitization test (OPPTS Test Guideline 870.2600) and a 90-day
inhalation toxicity test (OPPTS Test Guideline 870.3465) would help
characterize the human health effects of the PMN substances.
CFR citation: 40 CFR 721.10642.
PMN Number P-04-640
Chemical name: Diisocyanate terminated polycarbodiimide (generic).
CAS number: Claimed as confidential.
Effective date of TSCA section 5(e) consent order: February 1,
2006.
Basis for TSCA section 5(e) consent order: The PMN states that the
generic (non-confidential) use of the substance will be as a
crosslinking agent for solvent-based inks; a monomer for
polymerization; and a water scavenger for producing anhydrous polymers.
The PMN did not identify consumer uses for the PMN substance. Based on
SAR analysis of test data on structurally similar diisocyanates, EPA
identified concerns for dermal sensitization, respiratory
sensitization, and pulmonary toxicity from exposure to the PMN
substance by the inhalation and dermal routes. The order was issued
under sections 5(e)(1)(A)(i) and 5(e)(1)(A)(ii)(I) of TSCA based on a
finding that this substance may present an unreasonable risk of injury
to human health. To protect against these risks, the order requires:
1. Use of personal protective equipment including impervious gloves
(when there is potential dermal exposure) and either a NIOSH-certified
respirator with an APF of at least 2,000, or compliance with a NCEL of
0.05 mg/m\3\ as an 8-hour time-weighted average (when there is
potential inhalation exposure).
2. Establishment and use of a hazard communication program. The
SNUR would designate as a ``significant new use'' the absence of these
protective measures and consumer use of the PMN substance.
Recommended testing: EPA has determined that data from worker
exposure to the PMN substance (such as inhalation monitoring data
generated according to the NCELs section of the consent order) or a 90-
day inhalation toxicity test (OPPTS Test Guideline 870.3465) would help
characterize the human health effects of the PMN substance. The order
does not require submission of the testing at any specified time or
production volume. However, the order's restrictions on manufacture,
import, processing, distribution in commerce, use, and disposal of the
PMN substance will remain in effect until the order is modified or
revoked by EPA based on submission of that or other relevant
information.
CFR citation: 40 CFR 721.10643.
PMN Number P-07-553
Chemical name: Reaction product of aluminum hydroxide and modified
alkoxysilane (generic).
CAS number: Claimed as confidential.
Basis for action: The PMN states that the substance will be used as
a flame retardant. Based on SAR analysis of test data on analogous
respirable, poorly soluble particulates, EPA identified concerns for
lung toxicity from inhalation exposures to the PMN substance. At an
annual production volume of 100,000 kilograms (kgs), significant
occupational inhalation exposures are not expected due to the use of a
NIOSH-certified respirator with an APF of at least 10. Therefore, EPA
has not determined that the proposed manufacturing, processing, or use
of the substance may present an unreasonable risk. EPA has determined,
however, that any use of the substance without a NIOSH-certified
respirator with an APF of at least 10, where there is a potential for
inhalation exposure; or any increase of the annual 100,000 kg
production volume may result in increased exposure to the PMN
substance, which may cause serious human health effects. Based on this
information, the PMN substance meets the concern criteria at Sec.
721.170(b)(3)(ii).
Recommended testing: EPA has determined that the results of a 90-
day inhalation toxicity test (OPPTS Test Guideline 870.3465) with a 60-
day holding period would help characterize the health effects of the
PMN substance.
CFR citation: 40 CFR 721.10644.
PMN Number P-08-392
Chemical name: Multi-walled carbon nanotube (generic) (P-08-392).
CAS number: Claimed as confidential.
Effective date of TSCA section 5(e) consent order: November 14,
2008.
Basis for TSCA section 5(e) consent order: The PMN states that the
generic (non-confidential) use of the substance will be as an
antistatic, reinforcement additive. Based on test data on the PMN
substance, and SAR analysis of test data on structurally similar
respirable, poorly soluble particulates, EPA identified concerns for
pulmonary toxicity, fibrosis, carcinogenicity, mutagenicity, and
immunotoxicity. The order was issued under sections 5(e)(1)(A)(i) and
5(e)(1)(A)(ii)(I) of TSCA, based on a finding that the PMN substance
may present an unreasonable risk of injury to human health. To protect
against these risks, the order:
1. Requires use of personal protective equipment including
impervious gloves and protective clothing (when there is a potential
dermal exposure) and a NIOSH-certified air-purifying, tight-fitting
full-face respirator equipped with N100 filters with an APF of at least
50 (when there is potential inhalation exposure).
2. Prohibits manufacture of the PMN substance in the United States.
3. Restricts processing and use of the PMN substance to those uses
specified in the consent order.
The SNUR would designate as a ``significant new use'' the absence
of these protective measures.
[[Page 12689]]
Recommended testing: EPA has determined that the results of a 90-
day inhalation toxicity test (OPPTS Test Guideline 870.3465 or
Organisation for Economic Co-operation and Development (OECD) Test
Guideline 413) in rats with a post exposure observation period of up to
3 months, including bronchoalveolar lavage fluid (BALF) analysis and
certain material characterization data, would help characterize
possible effects of the substance. In the consent order, the PMN
submitter has agreed to perform these tests within 18 months of
commencing non-exempt commercial manufacture.
CFR citation: 40 CFR 721.10645.
PMN Number P-09-257
Chemical name: Multi-walled carbon nanotube (generic) (P-09-257).
CAS number: Claimed as confidential.
Effective date of TSCA section 5(e) consent order: August 11, 2009.
Basis for TSCA section 5(e) consent order: The PMN states that the
generic (non-confidential) uses of the substance will be as an electric
conductive filler to replace conventional material such as carbon black
or carbon fiber in matrixes such as polymer resin for conductive
applications, and an additive for elastomers, polymers, and resins to
enhance mechanical properties. Based on SAR analysis of test data on
analogous respirable, poorly soluble particulates and other CNTs, EPA
identified concerns for pulmonary toxicity, fibrosis, carcinogenicity,
mutagenicity, and immunotoxicity. Further, available data suggests that
pulmonary deposition of some nanoparticles, including CNTs, may induce
cardiovascular toxicity if inhaled. Although there are no environmental
toxicity studies on CNTs available, EPA expects that some fraction of
the CNTs, if released into the environment, will eventually be
suspended in water. There have been sublethal effects observed for
single walled CNTs in rainbow trout at levels as low as 100 ppb. The
order was issued under section 5(e)(1)(A)(i) and (e)(1)(A)(ii)(I) of
TSCA based on a finding that this substance may present an unreasonable
risk of injury to human health and the environment. To protect against
these risks, the order:
1. Requires use of personal protective equipment including
impervious gloves and protective clothing (when there is a potential
dermal exposure) and a NIOSH-certified air-purifying, tight-fitting
full-face respirator equipped with N100 filters with an APF of at least
50 (when there is potential inhalation exposure).
2. Prohibits manufacture of the PMN substance in the United States.
3. Restricts processing and use of the PMN substance to those uses
specified in the consent order.
4. Prohibits release to water during processing and use.
The SNUR would designate as a ``significant new use'' the absence
of these protective measures.
Recommended testing: EPA has determined that the results of a 90-
day inhalation toxicity test (OPPTS Test Guideline 870.3465 or OECD
Test Guideline 413) in rats with a post exposure observation period of
up to 3 months (including BALF analysis, a determination of
cardiovascular toxicity (clinically-based blood/plasma protein
analyses), and histopathology of the heart) and development of data on
certain physical/chemical properties would help characterize possible
effects of the substance. In the consent order, the PMN submitter has
agreed not to exceed a specified production volume/time limit
(whichever comes first) without performing the 90-day test on the PMN
substance. In addition, in the consent order, the PMN submitter agreed
to provide the physical/chemical properties data within a specified
time limit.
CFR citation: 40 CFR 721.10646.
PMN Numbers P-10-115, P-10-116, P-10-117, P-10-118, P-10-119, P-10-120,
P-10-121, P-10-122, P-10-123, P-10-124, P-10-125, and P-10-126
Chemical name: Multi-walled carbon nanofibers (generic).
CAS number: Claimed as confidential.
Effective date of TSCA section 5(e) consent order: May 9, 2011.
Basis for TSCA section 5(e) consent order: The PMNs state that the
uses of the substances will be as electrical and thermal conductivity
additives, mechanical reinforcement additives, energy storage
additives, and chemical intermediates. Based on SAR analysis of test
data on analogous respirable, poorly soluble particulates and other
CNTs, EPA identified concerns for pulmonary toxicity, fibrosis,
carcinogenicity, mutagenicity, and immunotoxicity. Further, available
data suggests that pulmonary deposition of some nanoparticles,
including CNTs may induce cardiovascular toxicity if inhaled. Although
there are no environmental toxicity studies on CNTs available, EPA
expects that some fraction of the CNTs, if released into the
environment, will eventually be suspended in water. There have been
sub-lethal effects observed for single walled CNTs in rainbow trout at
levels as low as 100 ppb. The order was issued under sections
5(e)(1)(A)(i) and 5(e)(1)(A)(ii)(I) of TSCA based on a finding that
these substances may present an unreasonable risk of injury to human
health and the environment. To protect against this risk, the order:
1. Requires use of personal protective equipment including
impervious gloves and protective clothing (when there is a potential
dermal exposure) and a NIOSH-certified air-purifying, tight-fitting
full-face respirator equipped with N100 filters with an APF of at least
50 (when there is potential inhalation exposure).
2. Restricts use of the PMN substances to use only as electrical
and thermal conductivity additives, mechanical reinforcement additives,
energy storage additives, and chemical intermediates as specified in
the consent order.
3. Restricts processing and use of the PMN substances to industrial
settings.
4. Prohibits release of the PMN substances into the waters of the
United States during processing and use activities.
The SNUR would designate as a ``significant new use'' the absence
of these protective measures.
Recommended testing: EPA has determined that the results of certain
physical/chemical properties data, workplace exposure monitoring and
characterization testing, and a 90-day inhalation toxicity test (OPPTS
Test Guideline 870.3465 or OECD Test Guideline 413) in rats would help
characterize the human health effects of the PMN substances. The PMN
submitter agreed to provide the physical/chemical properties data for
the PMN substances within one year after submitting the notice of
commencement. The consent order contains two additional production
volume limits. The PMN submitter agreed not to exceed the first
production volume limit without submitting workplace exposure
monitoring and characterization testing (including byproducts) as well
as quantification and characterization of substances that may be
released during exposures typical during the use phase, such as
handling, tearing and cutting the PMN substances. The PMN submitter has
also agreed not to exceed the second production volume limit without
performing two 90-day inhalation toxicity tests, with a post-exposure
observation period of up to 3 months, BALF analysis, aggregation/
agglomeration state, shape, size/size particle distribution and surface
properties of materials as administered, aggregation/agglomeration
state, shape, size/size particle distribution and surface properties of
materials of the
[[Page 12690]]
delivered materials after administration, determination of
cardiovascular toxicity, heart histopathology, and data on pulmonary
deposition. One 90-day inhalation toxicity test will be conducted from
a representative PMN substance in the group P-10-115, P-10-116, P-10-
117, P-10-118, P-10-119, and the other 90-day inhalation toxicity test
will be conducted from a representative PMN substance in the group P-
10-120, P-10-121, P-10-122, P-10-123, P-10-124, P-10-125, and P-10-126.
CFR citation: 40 CFR 721.10647.
PMN Numbers P-10-545 and P-10-546
Chemical name: Modified lithium iron phosphates (generic).
CAS number: Claimed as confidential.
Effective date of TSCA section 5(e) consent order: December 10,
2010.
Basis for TSCA section 5(e) consent order: The consolidated PMN
states that the generic (non-confidential) use of the substances will
be as battery electrode components, contained use. Based on test data
on analogous respirable, poorly soluble particulates, there is
potential risk for adverse lung effects including cancer, lung
fibrosis, lung inflammation and systemic effects, including
immunotoxicity. EPA has identified concerns for these health effects
from exposures to the PMN substances. Based on EcoSAR analysis of test
data on analogous phosphates, EPA predicts toxicity to aquatic
organisms may occur at concentrations that exceed 2 ppb of the PMN
substance in surface waters. The order was issued under sections
5(e)(1)(A)(i) and 5(e)(1)(A)(ii)(I) of TSCA based on a finding that
these substances may present an unreasonable risk of injury to human
health or the environment. To protect against these risks, the consent
order:
1. Restricts manufacturing, processing, and use of the substances
to a fully-enclosed and automated process, including all loading and
unloading activities.
2. Restricts use of the PMN substances to use only as specified in
the consent order.
3. Prohibits release of the PMN substances into the waters of the
United States during processing and use activities.
The SNUR would designate as a ``significant new use'' the absence
of these protective measures.
Recommended testing: EPA has determined that the results of a 90-
day inhalation toxicity test (OPPTS Test Guideline 870.3465) in rats
with a post-exposure observation period of up to 3 months, including
BALF analysis; an algal toxicity test (OCSPP Test Guideline 850.5400);
and physical/chemical properties testing for: Water solubility (OECD
Test Guideline 105); surface chemistry, particle size distribution of
the PMN substances, dustiness test (European Standard 15051); and
particle size distribution, aggregation state, and porosity would help
characterize the human health and environmental effects of the PMN
substances. The PMN submitter has agreed not to exceed the confidential
production volume in the consent order without performing the 90-day
inhalation toxicity test and the physical/chemical properties tests.
CFR citation: 40 CFR 721.10648.
PMN Number P-11-115
Chemical name: MDI modified polyalkylene glycol adipate polyester
(generic).
CAS number: Claimed as confidential.
Basis for action: The PMN states that the generic (non-
confidential) use of the substance will be as an adhesive. Based on SAR
analysis of test data on analogous diisocyanates, EPA identified
concerns for respiratory and dermal sensitization. For the use
described in the PMN, significant occupational dermal and inhalation
exposures are not expected due to the use of a NIOSH-certified
respirator with an APF of at least 10, and consumer exposures are not
expected as the substance is not used in consumer products. Therefore,
EPA has not determined that the proposed manufacturing, processing, or
use of the substance may present an unreasonable risk. EPA has
determined, however, that any use of the substance without a NIOSH-
certified respirator with an APF of at least 10, where there is a
potential for inhalation exposures, or any use of the substance in
consumer products may cause serious health effects. Based on this
information, the PMN substance meets the concern criteria at Sec.
721.170(b)(3)(ii).
Recommended testing: EPA has determined that the results of a skin
sensitization test (OPPTS Test Guideline 870.2600) and a 90-day
inhalation toxicity test (OPPTS Test Guideline 870.3465) would help
characterize the human health effects of the PMN substance.
CFR citation: 40 CFR 721.10649.
PMN Number P-11-155
Chemical name: Polyether substituted anthraquinone derivative
(generic).
CAS number: Claimed as confidential.
Basis for action: The PMN states that the generic (non-
confidential) use of the substance will be used as a colorant for
cleaners and detergents. Based on EcoSAR analysis of test data on
analogous aromatic amines and nonionic dyes, EPA predicts toxicity to
aquatic organisms may occur at concentrations that exceed 2 ppb of the
PMN substance in surface waters for greater than 20 days per year. This
20-day criterion is derived from partial life cycle tests (daphnid
chronic and fish early life stage tests) that typically range from 21
to 28 days in duration. EPA predicts toxicity to aquatic organisms may
occur if releases of the PMN substance to surface water, from uses
other than as described in the PMN, exceed releases from the use
described in the PMN. For the use described in the PMN, environmental
releases did not exceed 1 ppb for more than 20 days per year.
Therefore, EPA has not determined that the proposed manufacturing,
processing, or use of the substance may present an unreasonable risk.
EPA has determined, however, that any use of the substance other than
as a colorant for cleaners and detergents may cause significant adverse
environmental effects. Based on this information, the PMN substance
meets the concern criteria at Sec. 721.170(b)(4)(ii).
Recommended testing: EPA has determined that the results of a fish
acute toxicity test, freshwater and marine (OPPTS Test Guideline
850.1075) and an aquatic invertebrate acute toxicity test, freshwater
daphnids (OPPTS Test Guideline 850.1010) would help characterize the
environmental effects of the PMN substance.
CFR citation: 40 CFR 721.10650.
PMN Number P-11-290
Chemical name: Carbide derived nanocarbon (generic).
CAS number: Claimed as confidential.
Basis for action: The PMN states that the generic (non-
confidential) use of the substance will be as a sensor element in an
electrochemical sensor. Based on SAR analysis of test data on
respirable, poorly soluble particulates, EPA identified concerns for
pulmonary toxicity, fibrosis, carcinogenicity, mutagenicity, and
immunotoxicity if the substances were manufactured by a method other
than described in the PMN. Further, available data suggests that
pulmonary deposition of some carbon-based nanoparticles, may induce
cardiovascular toxicity if inhaled. EPA identified concerns for lung
toxicity to workers from inhalation exposures to the PMN substance. For
the manufacture method described in the PMN, significant dermal and
inhalation exposures are not expected. Therefore, EPA has not
determined that the proposed manufacturing, processing, or use of the
substance may present an
[[Page 12691]]
unreasonable risk. EPA has determined, however, that manufacture of the
substance by a method other than as described in the PMN may cause
serious health effects. Based on this information, the PMN substance
meets the concern criteria at Sec. 721.170(b)(3)(ii).
Recommended testing: EPA has determined that inhalation monitoring
data collected during the manufacturing process according to the EPA
draft Inhalation Monitoring Data Collection Guidelines (located in the
docket under docket ID number EPA-HQ-OPPT-2012-0727) would help
characterize the human health effects of the PMN substance.
CFR citation: 40 CFR 721.10651.
PMN Numbers P-11-309, P-11-311, P-11-312, P-11-313, and P-11-314
Chemical names: (P-11-309) Hexanedioic acid, polymer with polyether
polyol, 1,1'-methylenebis[4-isocyanatobenzene] and dihydroxydialkyl
ether (generic); (P-11-311) Hexanedioic acid, polymer with .alpha.-
hydro-.omega.-hydroxypoly[oxy(methyl-1,2-ethanediyl)],1,1'-
methylenebis[4-isocyanatobenzene], dihydroxydialkyl ether and dialkanol
ether (generic); (P-11-312) Hexanedioic acid, polymer with .alpha.-
hydro-.omega.-hydroxypoly[oxy(methyl-1,2-ethanediyl)],1,1'-
methylenebis[isocyanatobenzene], dihydroxydialkyl ether and dialkanol
ether (generic); (P-11-313) Hexanedioic acid, polymer with .alpha.-
hydro-.omega.-hydroxypoly[oxy(methyl-1,2-ethanediyl)],1,1'-
methylenebis[4-isocyanatobenzene], dihydroxydialkyl ether, reaction
products with dialkylcarbinol (generic); and (P-11-314) Hexanedioic
acid, polymer with .alpha.-hydro-.omega.-hydroxypoly[oxy(methyl-1,2-
ethanediyl)],1,1'-methylenebis[4-isocyanatobenzene], dihydroxydialkyl
ether reaction products with dialkylcarbinol (generic).
CAS numbers: Claimed as confidential.
Basis for action: The PMNs state that the generic (non-
confidential) use of the substances will be as industrial adhesives.
Based on SAR analysis of test data on analogous isocyanates, EPA
identified concerns for sensitization from dermal and inhalation
exposure to the PMN substances. For the use described in the PMNs,
significant occupational dermal and inhalation exposures are not
expected due to the use of a NIOSH-certified respirator with an APF of
at least 10, and consumer exposures are not expected. Therefore, EPA
has not determined that the proposed manufacturing, processing, or use
of the substances may present an unreasonable risk. EPA has determined,
however, that any use of the substances without a NIOSH-certified
respirator with an APF of at least 10, where there is a potential for
inhalation exposures, or any use of the substances in consumer products
may cause serious health effects. Based on this information, the PMN
substances meet the concern criteria at Sec. 721.170(b)(3)(ii).
Recommended testing: EPA has determined that the results of a skin
sensitization test (OPPTS Test Guideline 870.2600) and a 90-day
inhalation toxicity test (OPPTS Test Guideline 870.3465) would help
characterize the human health effects of the PMN substances.
CFR citations: 40 CFR 721.10652 (P-11-309); 40 CFR 721.10653 (P-11-
311); 40 CFR 721.10654 (P-11-312); 40 CFR 721.10655 (P-11-313); and 40
CFR 721.10656 (P-11-314).
PMN Number P-12-73
Chemical name: Castor oil, polymer with hydrogenated vegetable oil,
1,1'-methylenebis[isocyanatobenzene] and isocyanate (generic).
CAS number: Claimed as confidential.
Basis for action: The PMN states that the generic (non-
confidential) use of the substance is as an industrial adhesive. Based
on SAR analysis of test data on analogous diisocyanates, EPA identified
concerns for sensitization. For the use described in the PMN,
significant occupational dermal and inhalation exposures are not
expected due to the use of a NIOSH-certified respirator with an APF of
at least 10, and consumer exposures are not expected as the substance
is not used in consumer products. Therefore, EPA has not determined
that the proposed manufacturing, processing, or use of the substance
may present an unreasonable risk. EPA has determined, however, that any
use of the substance without a NIOSH-certified respirator with an APF
of at least 10, where there is a potential for inhalation exposures, or
any use of the substances in consumer products may cause serious health
effects. Based on this information, the PMN substance meets the concern
criteria at Sec. 721.170(b)(3)(ii).
Recommended testing: EPA has determined that the results of a skin
sensitization (OPPTS Test Guideline 870.2600) and a 90-day subchronic
inhalation toxicity test (OPPTS Test Guideline 870.3465) in rodents
would help characterize the human health effects of the PMN substance.
CFR citation: 40 CFR 721.10657.
PMN Number P-12-133
Chemical name: 2-Oxepanone, polymer with 1,6-diisocyanatohexane,
2,2''dimethyl-1;3-propanediol and 2,2'-oxybis[ethanol].
CAS number: 1313708-90-5.
Basis for action: The PMN states that the substance will be used as
a coating for wind craft wings. Based on SAR analysis of test data on
structurally similar chemicals submitted under TSCA section 8(e), EPA
identified concerns for oncogenicity and mutagenicity. Additionally,
based on the isocyanate moiety, the Agency identified concerns for
sensitization. For the use described in the PMN, significant
occupational inhalation exposures are not expected due to the use of a
NIOSH-certified respirator with an APF of at least 10, and consumer
exposures are not expected as the substance is not used in consumer
products. Therefore, EPA has not determined that the proposed
manufacturing, processing, or use of the substance may present an
unreasonable risk. EPA has determined, however, that any use of the
substance without a NIOSH-certified respirator with an APF of at least
10, where there is a potential for inhalation exposures, or any use of
the substance in consumer products may cause serious health effects.
Based on this information, the PMN substance meets the concern criteria
at Sec. 721.170(b)(3)(ii).
Recommended testing: EPA has determined that the results of a skin
sensitization test (OPPTS Test Guideline 870.2600) and a 90-day
inhalation toxicity study (OPPTS Test Guideline 870.3465) would help
characterize the human health effects of the PMN substance.
CFR citation: 40 CFR 721.10658.
PMN Number P-12-143
Chemical name: Poly(oxy-1,4-butanediyl), -hydro--hydroxy-, polymer
with alkyldiisocyanates (generic).
CAS number: Claimed as confidential.
Basis for action: The PMN states that the generic (non-
confidential) use of the substance will be as a crosslinking resin.
Based on SAR analysis of test data on analogous isocyanates, EPA
identified concerns for sensitization from dermal and respiratory
exposures to the PMN substance. For the use described in the PMN,
significant occupational dermal and inhalation exposures are not
expected due to the use of a NIOSH-certified respirator with an APF of
at least 10, and consumer exposures are not expected as the substance
is not used in consumer products. Therefore,
[[Page 12692]]
EPA has not determined that the proposed manufacturing, processing, or
use of the substance may present an unreasonable risk. EPA has
determined, however, that any use of the substance without a NIOSH-
certified respirator with an APF of at least 10, where there is a
potential for inhalation exposures, or any use of the substance in
consumer products may cause serious health effects. Based on this
information, the PMN substance meets the concern criteria at Sec.
721.170(b)(3)(ii).
Recommended testing: EPA has determined that the results of a skin
sensitization test (OPPTS Test Guideline 870.2600) and a 90-day
inhalation toxicity test (OPPTS Test Guideline 870.3465) would help
characterize the human health effects of the PMN substance.
CFR citation: 40 CFR 721.10659.
PMN Number P-12-274
Chemical name: Aliphatic diisocyanate adduct with substituted amino
alkyl silane (generic).
CAS number: Claimed as confidential.
Basis for action: The PMN states that the generic (non-
confidential) use of the substance will be as an adhesive. Based on SAR
analysis of test data on analogous isocyanates, EPA identified concern
for sensitization from dermal and inhalation exposure to the PMN
substance. Additionally, liquid and vapor contact with the eye can
cause moderate to severe irritation. For the use described in the PMN,
significant occupational dermal and inhalation exposures are not
expected due to the use of a NIOSH-certified respirator with an APF of
at least 10, and consumer exposures are not expected as the substance
is not used in consumer products. Therefore, EPA has not determined
that the proposed manufacturing, processing, or use of the substance
may present an unreasonable risk. EPA has determined, however, that any
use of the substance without a NIOSH-certified respirator with an APF
of at least 10, where there is a potential for inhalation exposures; or
any use of the substance in consumer products may cause serious health
effects. Based on this information, the PMN substance meets the concern
criteria at Sec. [emsp14]721.170(b)(3)(ii).
Recommended testing: EPA has determined that the results of a skin
sensitization test (OPPTS Test Guideline 870.2600) and a 90-day
inhalation toxicity test (OPPTS Test Guideline 870.3465) would help
characterize the human health effects of the PMN substance.
CFR citation: 40 CFR 721.10660.
V. Rationale and Objectives of the Proposed Rule
A. Rationale
During review of the PMNs submitted for the chemical substances
that are subject to these proposed SNURs, EPA concluded that for 17 of
the 37 chemical substances regulation was warranted under TSCA section
5(e) pending the development of information sufficient to make reasoned
evaluations of the health or environmental effects of the chemical
substances. The basis for such findings is outlined in Unit IV. Based
on these findings, TSCA section 5(e) consent orders requiring the use
of appropriate exposure controls were negotiated with the PMN
submitters. The proposed SNUR provisions for these chemical substances
are consistent with the provisions of the TSCA section 5(e) consent
orders. These SNURs are being proposed pursuant to Sec.
[emsp14]721.160.
In the other 20 cases, where the uses are not regulated under a
TSCA section 5(e) consent order, EPA determined that one or more of the
criteria of concern established at Sec. [emsp14]721.170 were met, as
discussed in Unit IV.
B. Objectives
EPA is proposing these SNURs for specific chemical substances which
have undergone premanufacture review because the Agency wants to
achieve the following objectives with regard to the significant new
uses designated in this proposed rule:
EPA would receive notice of any person's intent to
manufacture, import, or process a listed chemical substance for the
described significant new use before that activity begins.
EPA would have an opportunity to review and evaluate data
submitted in a SNUN before the notice submitter begins manufacturing,
importing, or processing a listed chemical substance for the described
significant new use.
EPA would be able to regulate prospective manufacturers,
importers, or processors of a listed chemical substance before the
described significant new use of that chemical substance occurs,
provided that regulation is warranted pursuant to TSCA sections 5(e),
5(f), 6, or 7.
EPA would ensure that all manufacturers, importers, and
processors of the same chemical substance that is subject to a TSCA
section 5(e) consent order are subject to similar requirements.
Issuance of a SNUR for a chemical substance does not signify that
the chemical substance is listed on the TSCA Chemical Substance
Inventory (TSCA Inventory). Guidance on how to determine if a chemical
substance is on the TSCA Inventory is available on the Internet at
https://www.epa.gov/opptintr/existingchemicals/pubs/tscainventory/.
VI. Notice and Comment Procedures
EPA is issuing these SNURs by notice and comment procedure, as
described in Sec. [emsp14]721.170(d)(4). In accordance with Sec.
[emsp14]721.170(d)(4)(ii)(A), persons are being given the opportunity
to submit comments on or before April 26, 2013 on whether EPA should
establish notification requirements.
VII. Applicability of Proposed Rule to Uses Occurring Before Effective
Date of the Final Rule
To establish a significant ``new'' use, EPA must determine that the
use is not ongoing. The chemical substances subject to this proposed
rule have undergone premanufacture review. TSCA section 5(e) consent
orders have been issued for 17 chemical substances and the PMN
submitters are prohibited by the TSCA section 5(e) consent orders from
undertaking activities which EPA is designating as significant new
uses. EPA is soliciting comments on whether any of the uses proposed as
significant new uses are ongoing.
As discussed in the Federal Register of April 24, 1990 SNUR, EPA
has decided that the intent of TSCA section 5(a)(1)(B) is best served
by designating a use as a significant new use as of the date of
publication of this proposed rule rather than as of the effective date
of the final rule. If uses begun after publication of the proposed rule
were considered ongoing rather than new, it would be difficult for EPA
to establish SNUR notice requirements because a person could defeat the
SNUR by initiating the significant new use before the rule became
final, and then argue that the use was ongoing before the effective
date of the final rule. Thus, persons who begin commercial manufacture,
import, or processing of the chemical substances that would be
regulated through these proposed SNURs will have to cease any such
activity before the effective date of the rule if and when finalized.
To resume their activities, these persons would have to comply with all
applicable SNUR notice requirements and wait until the notice review
period, including any extensions, expires.
EPA has promulgated provisions to allow persons to comply with
these proposed SNURs before the effective date. If a person meets the
conditions of advance compliance under Sec. [emsp14]721.45(h), the
person would be considered exempt from the requirements of the SNUR.
[[Page 12693]]
VIII. Test Data and Other Information
EPA recognizes that TSCA section 5 does not require developing any
particular test data before submission of a SNUN. The two exceptions
are:
1. Development of test data is required where the chemical
substance subject to the SNUR is also subject to a test rule under TSCA
section 4 (see TSCA section 5(b)(1)).
2. Development of test data may be necessary where the chemical
substance has been listed under TSCA section 5(b)(4) (see TSCA section
5(b)(2)).
In the absence of a TSCA section 4 test rule or a TSCA section
5(b)(4) listing covering the chemical substance, persons are required
only to submit test data in their possession or control and to describe
any other data known to or reasonably ascertainable by them (see 40 CFR
720.50). However, upon review of PMNs and SNUNs, the Agency has the
authority to require appropriate testing. In cases where EPA issued a
TSCA section 5(e) consent order that requires or recommends certain
testing, Unit IV. lists those tests. Unit IV. also lists recommended
testing for non-5(e) SNURs. Descriptions of tests are provided for
informational purposes. EPA strongly encourages persons, before
performing any testing, to consult with the Agency pertaining to
protocol selection. To access the OCSPP test guidelines referenced in
this document electronically, please go to https://www.epa.gov/ocspp and
select ``Test Methods and Guidelines.'' The Organisation for Economic
Co-operation and Development (OECD) test guidelines are available from
the OECD Bookshop at https://www.oecdbookshop.org or Source OECD at
https://www.sourceoecd.org. To access the European Standard, EN 15051
method, issued by The European Committee for Standardization (CEN),
please go to https://www.cen.eu/cen/products.
In the TSCA section 5(e) consent orders for several of the chemical
substances regulated under this proposed rule, EPA has established
production volume limits in view of the lack of data on the potential
health and environmental risks that may be posed by the significant new
uses or increased exposure to the chemical substances. These limits
cannot be exceeded unless the PMN submitter first submits the results
of toxicity tests that would permit a reasoned evaluation of the
potential risks posed by these chemical substances. Listings of the
tests specified in the TSCA section 5(e) consent orders are included in
Unit IV. The SNURs contain the same production volume limits as the
TSCA section 5(e) consent orders. Exceeding these production limits is
defined as a significant new use. Persons who intend to exceed the
production limit must notify the Agency by submitting a SNUN at least
90 days in advance of commencement of non-exempt commercial
manufacture, import, or processing.
When physical/chemical properties of test material and/or material
characterization tests are recommended for nanoscale substances that
are the subject of this proposed rule, you should take into
consideration the characterizations identified in the Guidance Manual
for the Testing of Manufactured Nanomaterials: OECD's Sponsorship
Programme, which is available at https://www.oecd.org/officialdocuments/displaydocumentpdf/?cote=env/jm/mono(2009)20/rev&doclanguage=en.
The recommended tests specified in Unit IV. may not be the only
means of addressing the potential risks of the chemical substance.
However, submitting a SNUN without any test data may increase the
likelihood that EPA will take action under TSCA section 5(e),
particularly if satisfactory test results have not been obtained from a
prior PMN or SNUN submitter. EPA recommends that potential SNUN
submitters contact EPA early enough so that they will be able to
conduct the appropriate tests.
SNUN submitters should be aware that EPA will be better able to
evaluate SNUNs which provide detailed information on the following:
Human exposure and environmental release that may result
from the significant new use of the chemical substances.
Potential benefits of the chemical substances.
Information on risks posed by the chemical substances
compared to risks posed by potential substitutes.
IX. SNUN Submissions
According to Sec. [emsp14]721.1(c), persons submitting a SNUN must
comply with the same notification requirements and EPA regulatory
procedures as persons submitting a PMN, including submission of test
data on health and environmental effects as described in 40 CFR 720.50.
SNUNs must be submitted on EPA Form No. 7710-25, generated using e-PMN
software, and submitted to the Agency in accordance with the procedures
set forth in 40 CFR 720.40 and Sec. 721.25. E-PMN software is
available electronically at https://www.epa.gov/opptintr/newchems.
X. Economic Analysis
EPA has evaluated the potential costs of establishing SNUN
requirements for potential manufacturers, importers, and processors of
the chemical substances subject to this proposed rule. EPA's complete
economic analysis is available in the docket under docket ID number
EPA-HQ-OPPT-2012-0727.
XI. Statutory and Executive Order Reviews
A. Executive Order 12866
This proposed rule would establish SNURs for several new chemical
substances that were the subject of PMNs, and, in some cases, TSCA
section 5(e) consent orders. The Office of Management and Budget (OMB)
has exempted these types of actions from review under Executive Order
12866, entitled ``Regulatory Planning and Review'' (58 FR 51735,
October 4, 1993).
B. Paperwork Reduction Act (PRA)
According to PRA (44 U.S.C. 3501 et seq.), an agency may not
conduct or sponsor, and a person is not required to respond to a
collection of information that requires OMB approval under PRA, unless
it has been approved by OMB and displays a currently valid OMB control
number. The OMB control numbers for EPA's regulations in title 40 of
the CFR, after appearing in the Federal Register, are listed in 40 CFR
part 9, and included on the related collection instrument or form, if
applicable. EPA would amend the table in 40 CFR part 9 to list the OMB
approval number for the information collection requirements contained
in this proposed rule, if the SNUR is subsequently issued as a final
rule. This listing of the OMB control numbers and their subsequent
codification in the CFR satisfies the display requirements of PRA and
OMB's implementing regulations at 5 CFR part 1320. This Information
Collection Request (ICR) was previously subject to public notice and
comment prior to OMB approval, and given the technical nature of the
table, EPA finds that further notice and comment to amend it is
unnecessary. As a result, EPA finds that there is ``good cause'' under
section 553(b)(3)(B) of the Administrative Procedure Act (5 U.S.C.
553(b)(3)(B)) to amend this table without further notice and comment.
The information collection requirements related to this action have
already been approved by OMB pursuant to PRA under OMB control number
2070-0012 (EPA ICR No. 574). This action would not impose any burden
requiring additional OMB approval. If an entity were to submit a
[[Page 12694]]
SNUN to the Agency, the annual burden is estimated to average between
30 and 170 hours per response. This burden estimate includes the time
needed to review instructions, search existing data sources, gather and
maintain the data needed, and complete, review, and submit the required
SNUN.
Send any comments about the accuracy of the burden estimate, and
any suggested methods for minimizing respondent burden, including
through the use of automated collection techniques, to the Director,
Collection Strategies Division, Office of Environmental Information
(2822T), Environmental Protection Agency, 1200 Pennsylvania Ave. NW.,
Washington, DC 20460-0001. Please remember to include the OMB control
number in any correspondence, but do not submit any completed forms to
this address.
C. Regulatory Flexibility Act (RFA)
On February 18, 2012, EPA certified pursuant to RFA section 605(b)
(5 U.S.C. 601 et seq.), that promulgation of these SNURS would not have
a significant economic impact on a substantial number of small entities
where the following are true:
1. A significant number of SNUNs would not be submitted by small
entities in response to the SNUR.
2. The SNUR submitted by any small entity would not cost
significantly more than $8,300.
A copy of that certification is available in the docket for this
proposed rule.
This proposed rule is within the scope of the February 18, 2012
certification. Based on the Economic Analysis discussed in Unit X. and
EPA's experience promulgating SNURs (discussed in the certification),
EPA believes that the following are true:
A significant number of SNUNs would not be submitted by
small entities in response to the SNUR.
Submission of the SNUN would not cost any small entity
significantly more than $8,300.
Therefore, the promulgation of the SNUR would not have a
significant economic impact on a substantial number of small entities.
D. Unfunded Mandates Reform Act (UMRA)
Based on EPA's experience with proposing and finalizing SNURs,
State, local, and Tribal governments have not been impacted by these
rulemakings, and EPA does not have any reasons to believe that any
State, local, or Tribal government would be impacted by this proposed
rule. As such, EPA has determined that this proposed rule would not
impose any enforceable duty, contain any unfunded mandate, or otherwise
have any effect on small governments subject to the requirements of
UMRA sections 202, 203, 204, or 205 (2 U.S.C. 1501 et seq.).
E. Executive Order 13132
This action would not have a substantial direct effect on States,
on the relationship between the national government and the States, or
on the distribution of power and responsibilities among the various
levels of government, as specified in Executive Order 13132, entitled
``Federalism'' (64 FR 43255, August 10, 1999).
F. Executive Order 13175
This proposed rule would not have Tribal implications because it is
not expected to have substantial direct effects on Indian Tribes. This
proposed rule would not significantly nor uniquely affect the
communities of Indian Tribal governments, nor would it involve or
impose any requirements that affect Indian Tribes. Accordingly, the
requirements of Executive Order 13175, entitled ``Consultation and
Coordination with Indian Tribal Governments'' (65 FR 67249, November 9,
2000), do not apply to this proposed rule.
G. Executive Order 13045
This action is not subject to Executive Order 13045, entitled
``Protection of Children from Environmental Health Risks and Safety
Risks'' (62 FR 19885, April 23, 1997), because this is not an
economically significant regulatory action as defined by Executive
Order 12866, and this action does not address environmental health or
safety risks disproportionately affecting children.
H. Executive Order 13211
This action is not subject to Executive Order 13211, entitled
``Actions Concerning Regulations That Significantly Affect Energy
Supply, Distribution, or Use'' (66 FR 28355, May 22, 2001), because
this action is not expected to affect energy supply, distribution, or
use and because this action is not a significant regulatory action
under Executive Order 12866.
I. National Technology Transfer and Advancement Act (NTTAA)
In addition, since this action does not involve any technical
standards, NTTAA section 12(d) (15 U.S.C. 272 note), does not apply to
this action.
J. Executive Order 12898
This action does not entail special considerations of environmental
justice related issues as delineated by Executive Order 12898, entitled
``Federal Actions to Address Environmental Justice in Minority
Populations and Low-Income Populations'' (59 FR 7629, February 16,
1994).
List of Subjects in 40 CFR Part 721
Environmental protection, Chemicals, Hazardous substances,
Reporting and recordkeeping requirements.
Dated: February 15, 2013.
Maria J. Doa,
Director, Chemical Control Division, Office of Pollution Prevention and
Toxics.
Therefore, it is proposed that 40 CFR part 721 be amended as
follows:
PART 721--[AMENDED]
0
1. The authority citation for part 721 continues to read as follows:
Authority: 15 U.S.C. 2604, 2607, and 2625(c).
0
2. Add Sec. 721.10637 to subpart E to read as follows:
Sec. 721.10637 Substituted picolinate (generic).
(a) Chemical substance and significant new uses subject to
reporting. (1) The chemical substance identified generically as
substituted picolinate (PMN P-00-835) is subject to reporting under
this section for the significant new uses described in paragraph (a)(2)
of this section.
(2) The significant new uses are:
(i) Release to water. Requirements as specified in Sec. 721.90
(a)(4), (b)(4), and (c)(4) (N=90).
(ii) [Reserved]
(b) Specific requirements. The provisions of subpart A of this part
apply to this section except as modified by this paragraph.
(1) Recordkeeping. Recordkeeping requirements as specified in Sec.
721.125 (a), (b), (c), and (k) are applicable to manufacturers,
importers, and processors of this substance.
(2) Limitations or revocation of certain notification requirements.
The provisions of Sec. 721.185 apply to this section.
0
3. Add Sec. 721.10638 to subpart E to read as follows:
Sec. 721.10638 Lithium metal phosphate (generic).
(a) Chemical substance and significant new uses subject to
reporting. (1) The chemical substance identified generically as lithium
metal phosphate (PMN P-02-167) is subject to reporting under this
section for the significant new uses described in paragraph (a)(2) of
this section.
[[Page 12695]]
(2) The significant new uses are:
(i) Release to water. Requirements as specified in Sec. 721.90
(a)(4), (b)(4), and (c)(4) (N=1).
(ii) [Reserved]
(b) Specific requirements. The provisions of subpart A of this part
apply to this section except as modified by this paragraph.
(1) Recordkeeping. Recordkeeping requirements as specified in Sec.
721.125 (a), (b), (c), and (k) are applicable to manufacturers,
importers, and processors of this substance.
(2) Limitations or revocation of certain notification requirements.
The provisions of Sec. 721.185 apply to this section.
0
4. Add Sec. 721.10639 to subpart E to read as follows:
Sec. 721.10639 Siloxanes and Silicones, di-Me, polymers with Ph
silsesquioxanes, hydrolyzed, reaction products with 2-[[3-
(trimethoxysilyl)propoxy]methyl]oxirane.
(a) Chemical substance and significant new uses subject to
reporting. (1) The chemical substance identified as siloxanes and
silicones, di-Me, polymers with Ph silsesquioxanes, hydrolyzed,
reaction products with 2-[[3-(trimethoxysilyl)propoxy]methyl]oxirane
(PMN P-02-668; CAS No. 478823-10-8) is subject to reporting under this
section for the significant new uses described in paragraph (a)(2) of
this section.
(2) The significant new uses are:
(i) Protection in the workplace. Requirements as specified in Sec.
721.63 (a)(1), (a)(2)(i), (a)(3), (a)(4), (a)(6)(v), (b) (concentration
set at 0.1 percent), and (c). When determining which persons are
reasonably likely to be exposed as required for Sec. 721.63 (a)(1) and
(a)(4), engineering control measures (e.g., enclosure or confinement of
the operation, general and local ventilation) or administrative control
measures (e.g., workplace policies and procedures) shall be considered
and implemented to prevent exposure, where feasible. The following
National Institute for Occupational Safety and Health (NIOSH)-certified
respirators with an assigned protection factor (APF) of at least 10
meet the requirements of Sec. 721.63(a)(4):
(A) NIOSH-certified air-purifying, tight-fitting half-face
respirator equipped with N100 (if oil aerosols absent), R100, or P100
filters;
(B) NIOSH-certified air-purifying, tight-fitting full-face
respirator equipped with N100 (if oil aerosols absent), R100, or P100
filters;
(C) NIOSH-certified powered air-purifying respirator equipped with
a loose-fitting hood or helmet and high efficiency particulate air
(HEPA) filters;
(D) NIOSH-certified powered air-purifying respirator equipped with
a tight-fitting facepiece (either half-face or full-face) and HEPA
filters; and
(E) NIOSH-certified supplied-air respirator operated in pressure
demand or continuous flow mode and equipped with a hood or helmet, or
tight-fitting facepiece (either half-face or full-face).
(ii) Industrial, commercial, and consumer activities. Requirements
as specified in Sec. 721.80(o).
(b) Specific requirements. The provisions of subpart A of this part
apply to this section except as modified by this paragraph.
(1) Recordkeeping. Recordkeeping requirements as specified in Sec.
721.125 (a), (b), (c), (d), (e), and (i) are applicable to
manufacturers, importers, and processors of this substance.
(2) Limitations or revocation of certain notification requirements.
The provisions of Sec. 721.185 apply to this section.
0
5. Add Sec. 721.10640 to subpart E to read as follows:
Sec. 721.10640 11,2-Cyclohexanedicarboxylic acid, 1-(2-ethylhexyl) 2-
(2-methylpropyl) ester.
(a) Chemical substance and significant new uses subject to
reporting. (1) The chemical substance identified as 1,2-
cyclohexanedicarboxylic acid, 1-(2-ethylhexyl) 2-(2-methylpropyl) ester
(PMN P-03-135; CAS Nos. 252958-29-5) is subject to reporting under this
section for the significant new uses described in paragraph (a)(2) of
this section.
(2) The significant new uses are:
(i) Release to water. Requirements as specified in Sec. 721.90
(a)(4), (b)(4), and (c)(4) (N=1).
(ii) [Reserved]
(b) Specific requirements. The provisions of subpart A of this part
apply to this section except as modified by this paragraph.
(1) Recordkeeping. Recordkeeping requirements as specified in Sec.
721.125 (a), (b), (c), and (k) are applicable to manufacturers,
importers, and processors of this substance.
(2) Limitations or revocation of certain notification requirements.
The provisions of Sec. 721.185 apply to this section.
0
6. Add Sec. 721.10641 to subpart E to read as follows:
Sec. 721.10641 Phenol and vinyltoluene based hydrocarbon resin
(generic).
(a) Chemical substance and significant new uses subject to
reporting. (1) The chemical substance identified generically as phenol
and vinyltoluene based hydrocarbon resin (PMN P-03-255) is subject to
reporting under this section for the significant new uses described in
paragraph (a)(2) of this section.
(2) The significant new uses are:
(i) Release to water. Requirements as specified in Sec. 721.90
(a)(4), (b)(4), and (c)(4) (N=1).
(ii) [Reserved]
(b) Specific requirements. The provisions of subpart A of this part
apply to this section except as modified by this paragraph.
(1) Recordkeeping. Recordkeeping requirements as specified in Sec.
721.125 (a), (b), (c), and (k) are applicable to manufacturers,
importers, and processors of this substance.
(2) Limitations or revocation of certain notification requirements.
The provisions of Sec. 721.185 apply to this section.
0
7. Add Sec. 721.10642 to subpart E to read as follows:
Sec. 721.10642 Modified polyisocyanates (generic).
(a) Chemical substance and significant new uses subject to
reporting. (1) The chemical substances identified generically as
modified polyisocyanates (PMNs P-03-762 and P-03-763) are subject to
reporting under this section for the significant new uses described in
paragraph (a)(2) of this section.
(2) The significant new uses are:
(i) Protection in the workplace. Requirements as specified in Sec.
721.63 (a)(1), (a)(2)(i), (a)(3), (b) (concentration set at 0.1
percent), and (c).
(ii) Industrial, commercial, and consumer activities. Requirements
as specified in Sec. 721.80 (f), (o), and (y)(l).
(b) Specific requirements. The provisions of subpart A of this part
apply to this section except as modified by this paragraph.
(1) Recordkeeping. Recordkeeping requirements as specified in Sec.
721.125 (a), (b), (c), (d), (e), and (i) are applicable to
manufacturers, importers, and processors of these substances.
(2) Limitations or revocation of certain notification requirements.
The provisions of Sec. 721.185 apply to this section.
0
8. Add Sec. 721.10643 to subpart E to read as follows:
Sec. 721.10643 Diisocyanate terminated polycarbodiimide (generic).
(a) Chemical substance and significant new uses subject to
reporting. (1) The chemical substance identified generically as
diisocyanate terminated polycarbodiimide (PMN P-04-640) is subject to
reporting under this section for the significant new uses described in
paragraph (a)(2) of this section. The
[[Page 12696]]
requirements of this rule do not apply to quantities of the PMN
substance that have been completely reacted (cured).
(2) The significant new uses are:
(i) Protection in the workplace. Requirements as specified in Sec.
721.63 (a)(1), (a)(3), (a)(4), and (a)(6)(ii). When determining which
persons are reasonably likely to be exposed as required for Sec.
721.63 (a)(1) and (a)(4), engineering control measures (e.g., enclosure
or confinement of the operation, general and local ventilation) or
administrative control measures (e.g., workplace policies and
procedures) shall be considered and implemented to prevent exposure,
where feasible. A National Institute for Occupational Safety and Health
(NIOSH)-certified supplied-air respirator operated in pressure demand
or other positive pressure mode and equipped with a tight-fitting full
facepiece with an assigned protection factor (APF) of at least 2,000
meets the minimum requirements Sec. 721.63(a)(4). As an alternative to
the respiratory requirements listed here, a manufacturer, importer, or
processor may choose to follow the new chemical exposure limit (NCEL)
provisions listed in the TSCA section 5(e) consent order for this
substance. The NCEL is 0.05 mg/m\3\. Persons whose Sec. 721.30
requests to use the NCELs approach are approved by EPA will receive
NCELs provisions comparable to those contained in the corresponding
section 5(e) consent order.
(ii) Hazard communication program. Requirements as specified in
Sec. 721.72 (a), (b), (c), (d), (f), (g)(1)(i), (g)(1)(ii), (g)(2)(i),
(g)(2)(ii), (g)(2)(iii), (g)(2)(iv) (use respiratory protection or
maintain airborne concentrations at or below an 8-hour time-weighted
average of 0.05 mg/m\3\), (g)(2)(v), and (g)(5).
(iii) Industrial, commercial, and consumer activities. Requirements
as specified in Sec. 721.80(o).
(b) Specific requirements. The provisions of subpart A of this part
apply to this section except as modified by this paragraph.
(1) Recordkeeping. Recordkeeping requirements as specified in Sec.
721.125 (a) through (i) are applicable to manufacturers, importers, and
processors of this substance.
(2) Limitations or revocation of certain notification requirements.
The provisions of Sec. 721.185 apply to this section.
0
9. Add Sec. 721.10644 to subpart E to read as follows:
Sec. 721.10644 Reaction product of aluminum hydroxide and modified
alkoxysilane (generic).
(a) Chemical substance and significant new uses subject to
reporting. (1) The chemical substance identified generically as
reaction product of aluminum hydroxide and modified alkoxysilane (PMN
P-07-553) is subject to reporting under this section for the
significant new uses described in paragraph (a)(2) of this section.
(2) The significant new uses are:
(i) Protection in the workplace. Requirements as specified in Sec.
721.63 (a)(4), (a)(6)(i), (b) (concentrations set at 0.1 percent), and
(c). When determining which persons are reasonably likely to be exposed
as required for Sec. 721.63(a)(4), engineering control measures (e.g.,
enclosure or confinement of the operation, general and local
ventilation) or administrative control measures (e.g., workplace
policies and procedures) shall be considered and implemented to prevent
exposure, where feasible. The following National Institute for
Occupational Safety and Health (NIOSH)-certified respirators with an
assigned protection factor (APF) of at least 10 meet the requirements
of Sec. 721.63(a)(4):
(A) NIOSH-certified air-purifying, tight-fitting half-face
respirator equipped with N100 (if oil aerosols absent), R100, or P100
filters;
(B) NIOSH-certified air-purifying, tight-fitting full-face
respirator equipped with N100 (if oil aerosols absent), R100, or P100
filters;
(C) NIOSH-certified powered air-purifying respirator equipped with
a loose-fitting hood or helmet and high efficiency particulate air
(HEPA) filters;
(D) NIOSH-certified powered air-purifying respirator equipped with
a tight-fitting facepiece (either half-face or full-face) and HEPA
filters; and
(E) NIOSH-certified supplied-air respirator operated in pressure
demand or continuous flow mode and equipped with a hood or helmet, or
tight-fitting facepiece (either half-face or full-face).
(ii) Industrial, commercial, and consumer activities. Requirements
as specified in Sec. 721.80(s) (100,000 kilograms).
(b) Specific requirements. The provisions of subpart A of this part
apply to this section except as modified by this paragraph.
(1) Recordkeeping. Recordkeeping requirements as specified in Sec.
721.125 (a), (b), (c), (d), and (i) are applicable to manufacturers,
importers, and processors of this substance.
(2) Limitations or revocation of certain notification requirements.
The provisions of Sec. 721.185 apply to this section.
0
10. Add Sec. [emsp14]721.10645 to subpart E to read as follows:
Sec. [emsp14]721.10645 Multi-walled carbon nanotube (generic) (P-08-
392).
(a) Chemical substance and significant new uses subject to
reporting. (1) The chemical substance identified generically as multi-
walled carbon nanotube (PMN P-08-392) is subject to reporting under
this section for the significant new uses described in paragraph (a)(2)
of this section. The requirements of this rule do not apply to
quantities of the PMN substance that have been completely reacted
(cured); incorporated or embedded into a polymer matrix that itself has
been completely reacted (cured); or embedded in a permanent solid
polymer form that is not intended to undergo further processing except
for mechanical processing.
(2) The significant new uses are:
(i) Protection in the workplace. Requirements as specified in Sec.
721.63 (a)(1), (a)(2)(i), (a)(2)(ii), (a)(3), (a)(4), and (a)(6)
(particulate, including solids or liquid droplets). When determining
which persons are reasonably likely to be exposed as required for Sec.
721.63 (a)(1) and (a)(4), engineering control measures (e.g., enclosure
or confinement of the operation, general and local ventilation) or
administrative control measures (e.g., workplace policies and
procedures) shall be considered and implemented to prevent exposure,
where feasible. A National Institute for Occupational Safety and Health
(NIOSH)-certified air-purifying, tight-fitting full-face respirator
equipped with N100 filters with an assigned protection factor (APF) of
at least 50 meet the minimum requirements of Sec. 721.63(a)(4).
(ii) Industrial, commercial, and consumer activities. Requirements
as specified in Sec. 721.80 (f), (k), and (q) (within 18 months of
commencing non-exempt commercial manufacture).
(b) Specific requirements. The provisions of subpart A of this part
apply to this section except as modified by this paragraph.
(1) Recordkeeping. Recordkeeping requirements as specified in Sec.
721.125 (a), (b), (c), (d), (e), and (i) are applicable to
manufacturers, importers, and processors of this substance.
(2) Limitations or revocation of certain notification requirements.
The provisions of Sec. 721.185 apply to this section.
(3) Determining whether a specific use is subject to this section.
The provisions
[[Page 12697]]
of Sec. 721.1725(b)(1) apply to paragraph (a)(2)(ii) of this section.
0
11. Add Sec. [emsp14]721.10646 to subpart E to read as follows:
Sec. [emsp14]721.10646 Multi-walled carbon nanotube (generic) (P-09-
257).
(a) Chemical substance and significant new uses subject to
reporting. (1) The chemical substance identified generically as multi-
walled carbon nanotube (PMN P-09-257) is subject to reporting under
this section for the significant new uses described in paragraph (a)(2)
of this section. The requirements of this rule do not apply to
quantities of the PMN substance that have been completely reacted
(cured); incorporated or embedded into a polymer matrix that itself has
been completely reacted (cured); embedded in a permanent solid polymer
form that is not intended to undergo further processing except for
mechanical processing; or incorporated into an article as defined at 40
CFR 720.3(c).
(2) The significant new uses are:
(i) Protection in the workplace. Requirements as specified in Sec.
721.63 (a)(1), (a)(2)(i), (a)(2)(ii), (a)(3), (a)(4), and (a)(6)
(particulate, including solids or liquid droplets). When determining
which persons are reasonably likely to be exposed as required for Sec.
721.63 (a)(1) and (a)(4), engineering control measures (e.g., enclosure
or confinement of the operation, general and local ventilation) or
administrative control measures (e.g., workplace policies and
procedures) shall be considered and implemented to prevent exposure,
where feasible. A National Institute for Occupational Safety and Health
(NIOSH)-certified air-purifying, tight-fitting full-face respirator
equipped with N100 filters with an assigned protection factor (APF) of
at least 50 meets the minimum requirements of Sec. 721.63(a)(4).
(ii) Industrial, commercial, and consumer activities. Requirements
as specified in Sec. 721.80 (f), (k), and (q).
(iii) Release to water. Requirements as specified in Sec. 721.90
(b)(1) and (c)(1).
(b) Specific requirements. The provisions of subpart A of this part
apply to this section except as modified by this paragraph.
(1) Recordkeeping. Recordkeeping requirements as specified in Sec.
721.125 (a), (b), (c), (d), (e), (i), and (k) are applicable to
manufacturers, importers, and processors of this substance.
(2) Limitations or revocation of certain notification requirements.
The provisions of Sec. 721.185 apply to this section.
(3) Determining whether a specific use is subject to this section.
The provisions of Sec. 721.1725(b)(1) apply to paragraph (a)(2)(ii) of
this section.
0
12. Add Sec. [emsp14]721.10647 to subpart E to read as follows:
Sec. [emsp14]721.10647 Multi-walled carbon nanofibers (generic).
(a) Chemical substance and significant new uses subject to
reporting. (1) The chemical substance identified generically as multi-
walled carbon nanofibers (PMNs P-10-115, P-10-116, P-10-117, P-10-118,
P-10-119, P-10-120, P-10-121, P-10-122, P-10-123, P-10-124, P-10-125,
and P-10-126) are subject to reporting under this section for the
significant new uses described in paragraph (a)(2) of this section. The
requirements of this rule do not apply to quantities of the PMN
substances after they have been completely reacted (cured);
incorporated or embedded into a polymer matrix that itself has been
reacted (cured); embedded into a permanent solid polymer form that is
not intended to undergo further processing except for mechanical
processing; or incorporated into an article as defined at 40 CFR
720.3(c).
(2) The significant new uses are:
(i) Protection in the workplace. Requirements as specified in Sec.
721.63 (a)(1), (a)(2)(i), (a)(2)(ii), (a)(3), (a)(4), and (a)(6)(i).
When determining which persons are reasonably likely to be exposed as
required for Sec. 721.63 (a)(1) and (a)(4), engineering control
measures (e.g., enclosure or confinement of the operation, general and
local ventilation) or administrative control measures (e.g., workplace
policies and procedures) shall be considered and implemented to prevent
exposure, where feasible. A National Institute for Occupational Safety
and Health (NIOSH)-certified air-purifying, tight-fitting full-face
respirator equipped with N100 filters with an assigned protection
factor (APF) of at least 50 meets the minimum requirements of Sec.
721.63(a)(4).
(ii) Industrial, commercial, and consumer activities. Requirements
as specified in Sec. 721.80 (k) (electrical and thermal conductivity
additive in encapsulated thermoplastics, thermosets, elastomers, glass,
metals, and ceramics; mechanical reinforcement additive in encapsulated
thermoplastics, thermosets, elastomers, glass, metals, and ceramics;
energy storage additive; or chemical intermediate), (l) and (q).
(iii) Release to water. Requirements as specified in Sec. 721.90
(b)(1) and (c)(1).
(b) Specific requirements. The provisions of subpart A of this part
apply to this section except as modified by this paragraph.
(1) Recordkeeping. Recordkeeping requirements as specified in Sec.
721.125 (a), (b), (c), (d), (e), (i), and (k) are applicable to
manufacturers, importers, and processors of these substances.
(2) Limitations or revocation of certain notification requirements.
The provisions of Sec. 721.185 apply to this section.
(3) Determining whether a specific use is subject to this section.
The provisions of Sec. 721.1725(b)(1) apply to paragraph (a)(2)(ii) of
this section.
0
13. Add Sec. [emsp14]721.10648 to subpart E to read as follows:
Sec. [emsp14]721.10648 Modified lithium iron phosphates (generic).
(a) Chemical substance and significant new uses subject to
reporting. (1) The chemical substances identified generically as
modified lithium iron phosphates (PMNs P-10-545 and P-10-546) are
subject to reporting under this section for the significant new uses
described in paragraph (a)(2) of this section. The requirements of this
rule do not apply to quantities of the PMN substances after they have
been completely reacted (cured), embedded or incorporated into a
polymer matrix that has been reacted (cured), or embedded in a
permanent solid polymer form that is not intended to undergo further
processing, except mechanical.
(2) The significant new uses are:
(i) Industrial, commercial, and consumer activities. Requirements
as specified in Sec. 721.80 (a), (b), (c), (k), and (q).
(ii) Release to water. Requirements as specified in Sec. 721.90
(b)(1) and (c)(1).
(b) Specific requirements. The provisions of subpart A of this part
apply to this section except as modified by this paragraph.
(1) Recordkeeping. Recordkeeping requirements as specified in Sec.
721.125 (a), (b), (c), (i), and (k) are applicable to manufacturers,
importers, and processors of these substances.
(2) Limitations or revocation of certain notification requirements.
The provisions of Sec. 721.185 apply to this section.
(3) Determining whether a specific use is subject to this section.
The provisions of Sec. 721.1725(b)(1) apply to paragraph (a)(2)(i) of
this section.
0
14. Add Sec. [emsp14]721.10649 to subpart E to read as follows:
Sec. [emsp14]721.10649 MDI modified polyalkylene glycol adipate
polyester (generic).
(a) Chemical substance and significant new uses subject to
reporting. (1) The chemical substance identified generically as MDI
modified polyalkylene glycol adipate polyester (PMN P-11-115) is
subject to reporting under this section for the significant
[[Page 12698]]
new uses described in paragraph (a)(2) of this section.
(2) The significant new uses are:
(i) Protection in the workplace. Requirements as specified in Sec.
721.63 (a)(4), (a)(6)(i), (a)(6)(ii), (a)(6)(v), (b) (concentration set
at 0.1 percent), and (c). When determining which persons are reasonably
likely to be exposed as required for Sec. 721.63 (a)(4), engineering
control measures (e.g., enclosure or confinement of the operation,
general and local ventilation) or administrative control measures
(e.g., workplace policies and procedures) shall be considered and
implemented to prevent exposure, where feasible. The following National
Institute for Occupational Safety and Health (NIOSH)-certified
respirators with an assigned protection factor (APF) of at least 10
meet the requirements of Sec. 721.63(a)(4):
(A) NIOSH-certified air-purifying, tight-fitting half-face
respirator equipped with N100 (if oil aerosols absent), R100, or P100
filters;
(B) NIOSH-certified air-purifying, tight-fitting full-face
respirator equipped with N100 (if oil aerosols absent), R100, or P100
filters;
(C) NIOSH-certified powered air-purifying respirator equipped with
a loose-fitting hood or helmet and high efficiency particulate air
(HEPA) filters;
(D) NIOSH-certified powered air-purifying respirator equipped with
a tight-fitting facepiece (either half-face or full-face) and HEPA
filters; and
(E) NIOSH-certified supplied-air respirator operated in pressure
demand or continuous flow mode and equipped with a hood or helmet, or
tight-fitting facepiece (either half-face or full-face).
(ii) Industrial, commercial, and consumer activities. Requirements
as specified in Sec. 721.80(o).
(b) Specific requirements. The provisions of subpart A of this part
apply to this section except as modified by this paragraph.
(1) Recordkeeping. Recordkeeping requirements as specified in Sec.
721.125 (a), (b), (c), (d), and (i) are applicable to manufacturers,
importers, and processors of this substance.
(2) Limitations or revocation of certain notification requirements.
The provisions of Sec. 721.185 apply to this section.
0
15. Add Sec. [emsp14]721.10650 to subpart E to read as follows:
Sec. [emsp14]721.10650 Polyether substituted anthraquinone derivative
(generic).
(a) Chemical substance and significant new uses subject to
reporting. (1) The chemical substance identified generically as
polyether substituted anthraquinone derivative (PMN P-11-155) is
subject to reporting under this section for the significant new uses
described in paragraph (a)(2) of this section.
(2) The significant new uses are:
(i) Industrial, commercial, and consumer activities. Requirements
as specified in Sec. 721.80(j) (colorant for cleaners and detergents).
(ii) [Reserved]
(b) Specific requirements. The provisions of subpart A of this part
apply to this section except as modified by this paragraph.
(1) Recordkeeping. Recordkeeping requirements as specified in Sec.
721.125 (a), (b), (c), and (i) are applicable to manufacturers,
importers, and processors of this substance.
(2) Limitations or revocation of certain notification requirements.
The provisions of Sec. 721.185 apply to this section.
0
16. Add Sec. [emsp14]721.10651 to subpart E to read as follows:
Sec. [emsp14]721.10651 Carbide derived nanocarbon (generic).
(a) Chemical substance and significant new uses subject to
reporting. (1) The chemical substance identified generically as carbide
derived nanocarbon (PMN P-11-290) is subject to reporting under this
section for the significant new uses described in paragraph (a)(2) of
this section.
(2) The significant new uses are:
(i) Industrial, commercial, and consumer activities. Requirements
as specified in Sec. 721.80(j) (manufacture of the substance by the
method described in the premanufacture notice).
(ii) [Reserved]
(b) Specific requirements. The provisions of subpart A of this part
apply to this section except as modified by this paragraph.
(1) Recordkeeping. Recordkeeping requirements as specified in Sec.
721.125 (a), (b), (c), and (i) are applicable to manufacturers,
importers, and processors of this substance.
(2) Limitations or revocation of certain notification requirements.
The provisions of Sec. 721.185 apply to this section.
(3) Determining whether a specific use is subject to this section.
The provisions of Sec. 721.1725(b)(1) apply to paragraph (a)(2)(i) of
this section.
0
17. Add Sec. [emsp14]721.10652 to subpart E to read as follows:
Sec. [emsp14]721.10652 Hexanedioic acid, polymer with polyether
polyol, 1,1'-methylenebis[4-isocyanatobenzene] and dihydroxydialkyl
ether (generic).
(a) Chemical substance and significant new uses subject to
reporting. (1) The chemical substance identified generically as
hexanedioic acid, polymer with polyether polyol, 1,1'-methylenebis[4-
isocyanatobenzene] and dihydroxydialkyl ether (PMN P-11-309) is subject
to reporting under this section for the significant new uses described
in paragraph (a)(2) of this section.
(2) The significant new uses are:
(i) Protection in the workplace. Requirements as specified in Sec.
721.63 (a)(4), (a)(6)(i), (a)(6)(ii), (a)(6)(v), (b) (concentration set
at 0.1 percent), and (c). When determining which persons are reasonably
likely to be exposed as required for Sec. 721.63(a)(4), engineering
control measures (e.g., enclosure or confinement of the operation,
general and local ventilation) or administrative control measures
(e.g., workplace policies and procedures) shall be considered and
implemented to prevent exposure, where feasible. The following National
Institute for Occupational Safety and Health (NIOSH)-certified
respirators with an assigned protection factor (APF) of at least 10
meet the requirements of Sec. 721.63(a)(4):
(A) NIOSH-certified air-purifying, tight-fitting half-face
respirator equipped with N100 (if oil aerosols absent), R100, or P100
filters;
(B) NIOSH-certified air-purifying, tight-fitting full-face
respirator equipped with N100 (if oil aerosols absent), R100, or P100
filters;
(C) NIOSH-certified powered air-purifying respirator equipped with
a loose-fitting hood or helmet and high efficiency particulate air
(HEPA) filters;
(D) NIOSH-certified powered air-purifying respirator equipped with
a tight-fitting facepiece (either half-face or full-face) and HEPA
filters; and
(E) NIOSH-certified supplied-air respirator operated in pressure
demand or continuous flow mode and equipped with a hood or helmet, or
tight-fitting facepiece (either half-face or full-face).
(ii) Industrial, commercial, and consumer activities. Requirements
as specified in Sec. 721.80(o).
(b) Specific requirements. The provisions of subpart A of this part
apply to this section except as modified by this paragraph.
(1) Recordkeeping. Recordkeeping requirements as specified in Sec.
721.125 (a), (b), (c), (d), and (i) are applicable to manufacturers,
importers, and processors of this substance.
(2) Limitations or revocation of certain notification requirements.
The provisions of Sec. 721.185 apply to this section.
0
18. Add Sec. [emsp14]721.10653 to subpart E to read as follows:
[[Page 12699]]
Sec. [emsp14]721.10653 Hexanedioic acid, polymer with .alpha.-
hydro-.omega.-hydroxypoly[oxy(methyl-1,2-ethanediyl)],1,1'-
methylenebis[4-isocyanatobenzene], dihydroxydialkyl ether and dialkanol
ether (generic).
(a) Chemical substance and significant new uses subject to
reporting. (1) The chemical substance identified generically as
hexanedioic acid, polymer with .alpha.-hydro-.omega.-
hydroxypoly[oxy(methyl-1,2-ethanediyl)],1,1'-methylenebis[4-
isocyanatobenzene], dihydroxydialkyl ether and dialkanol ether (PMN P-
11-311) is subject to reporting under this section for the significant
new uses described in paragraph (a)(2) of this section.
(2) The significant new uses are:
(i) Protection in the workplace. Requirements as specified in Sec.
721.63 (a)(4), (a)(6)(i), (a)(6)(ii), (a)(6)(v), (b) (concentration set
at 0.1 percent), and (c). When determining which persons are reasonably
likely to be exposed as required for Sec. 721.63(a)(4), engineering
control measures (e.g., enclosure or confinement of the operation,
general and local ventilation) or administrative control measures
(e.g., workplace policies and procedures) shall be considered and
implemented to prevent exposure, where feasible. The following National
Institute for Occupational Safety and Health (NIOSH)-certified
respirators with an assigned protection factor (APF) of at least 10
meet the requirements of Sec. 721.63(a)(4):
(A) NIOSH-certified air-purifying, tight-fitting half-face
respirator equipped with N100 (if oil aerosols absent), R100, or P100
filters;
(B) NIOSH-certified air-purifying, tight-fitting full-face
respirator equipped with N100 (if oil aerosols absent), R100, or P100
filters;
(C) NIOSH-certified powered air-purifying respirator equipped with
a loose-fitting hood or helmet and high efficiency particulate air
(HEPA) filters;
(D) NIOSH-certified powered air-purifying respirator equipped with
a tight-fitting facepiece (either half-face or full-face) and HEPA
filters; and
(E) NIOSH-certified supplied-air respirator operated in pressure
demand or continuous flow mode and equipped with a hood or helmet, or
tight-fitting facepiece (either half-face or full-face).
(ii) Industrial, commercial, and consumer activities. Requirements
as specified in Sec. 721.80(o).
(b) Specific requirements. The provisions of subpart A of this part
apply to this section except as modified by this paragraph.
(1) Recordkeeping. Recordkeeping requirements as specified in Sec.
721.125 (a), (b), (c), (d), and (i) are applicable to manufacturers,
importers, and processors of this substance.
(2) Limitations or revocation of certain notification requirements.
The provisions of Sec. 721.185 apply to this section.
0
19. Add Sec. [emsp14]721.10654 to subpart E to read as follows:
Sec. [emsp14]721.10654 Hexanedioic acid, polymer with .alpha.-
hydro-.omega.-hydroxypoly[oxy(methyl-1,2-ethanediyl)],1,1'-
methylenebis[isocyanatobenzene], dihydroxydialkyl ether and dialkanol
ether (generic).
(a) Chemical substance and significant new uses subject to
reporting. (1) The chemical substance identified generically as
hexanedioic acid, polymer with .alpha.-hydro-.omega.-
hydroxypoly[oxy(methyl-1,2-ethanediyl)],1,1'-
methylenebis[isocyanatobenzene], dihydroxydialkyl ether and dialkanol
ether (PMN P-11-312) is subject to reporting under this section for the
significant new uses described in paragraph (a)(2) of this section.
(2) The significant new uses are:
(i) Protection in the workplace. Requirements as specified in Sec.
721.63 (a)(4), (a)(6)(i), (a)(6)(ii), (a)(6)(v), (b) (concentration set
at 0.1 percent), and (c). When determining which persons are reasonably
likely to be exposed as required for Sec. 721.63 (a)(4), engineering
control measures (e.g., enclosure or confinement of the operation,
general and local ventilation) or administrative control measures
(e.g., workplace policies and procedures) shall be considered and
implemented to prevent exposure, where feasible. The following National
Institute for Occupational Safety and Health (NIOSH)-certified
respirators with an assigned protection factor (APF) of at least 10
meet the requirements of Sec. 721.63(a)(4):
(A) NIOSH-certified air-purifying, tight-fitting half-face
respirator equipped with N100 (if oil aerosols absent), R100, or P100
filters;
(B) NIOSH-certified air-purifying, tight-fitting full-face
respirator equipped with N100 (if oil aerosols absent), R100, or P100
filters;
(C) NIOSH-certified powered air-purifying respirator equipped with
a loose-fitting hood or helmet and high efficiency particulate air
(HEPA) filters;
(D) NIOSH-certified powered air-purifying respirator equipped with
a tight-fitting facepiece (either half-face or full-face) and HEPA
filters; and
(E) NIOSH-certified supplied-air respirator operated in pressure
demand or continuous flow mode and equipped with a hood or helmet, or
tight-fitting facepiece (either half-face or full-face).
(ii) Industrial, commercial, and consumer activities. Requirements
as specified in Sec. 721.80(o).
(b) Specific requirements. The provisions of subpart A of this part
apply to this section except as modified by this paragraph.
(1) Recordkeeping. Recordkeeping requirements as specified in Sec.
721.125 (a), (b), (c), (d), and (i) are applicable to manufacturers,
importers, and processors of this substance.
(2) Limitations or revocation of certain notification requirements.
The provisions of Sec. 721.185 apply to this section.
0
20. Add Sec. [emsp14]721.10655 to subpart E to read as follows:
Sec. [emsp14]721.10655 Hexanedioic acid, polymer with .alpha.-
hydro-.omega.-hydroxypoly[oxy(methyl-1,2-ethanediyl)],1,1'-
methylenebis[4-isocyanatobenzene], dihydroxydialkyl ether, reaction
products with dialkylcarbinol (generic).
(a) Chemical substance and significant new uses subject to
reporting. (1) The chemical substance identified generically as
hexanedioic acid, polymer with .alpha.-hydro-.omega.-
hydroxypoly[oxy(methyl-1,2-ethanediyl)],1,1'-methylenebis[4-
isocyanatobenzene], dihydroxydialkyl ether, reaction products with
dialkylcarbinol (PMN P-11-313) is subject to reporting under this
section for the significant new uses described in paragraph (a)(2) of
this section.
(2) The significant new uses are:
(i) Protection in the workplace. Requirements as specified in Sec.
721.63 (a)(4), (a)(6)(i), (a)(6)(ii), (a)(6)(v), (b) (concentration set
at 0.1 percent), and (c). When determining which persons are reasonably
likely to be exposed as required for Sec. 721.63(a)(4), engineering
control measures (e.g., enclosure or confinement of the operation,
general and local ventilation) or administrative control measures
(e.g., workplace policies and procedures) shall be considered and
implemented to prevent exposure, where feasible. The following National
Institute for Occupational Safety and Health (NIOSH)-certified
respirators with an assigned protection factor (APF) of at least 10
meet the requirements of Sec. 721.63(a)(4):
(A) NIOSH-certified air-purifying, tight-fitting half-face
respirator equipped with N100 (if oil aerosols absent), R100, or P100
filters;
(B) NIOSH-certified air-purifying, tight-fitting full-face
respirator equipped with N100 (if oil aerosols absent), R100, or P100
filters;
(C) NIOSH-certified powered air-purifying respirator equipped with
a
[[Page 12700]]
loose-fitting hood or helmet and high efficiency particulate air (HEPA)
filters;
(D) NIOSH-certified powered air-purifying respirator equipped with
a tight-fitting facepiece (either half-face or full-face) and HEPA
filters; and
(E) NIOSH-certified supplied-air respirator operated in pressure
demand or continuous flow mode and equipped with a hood or helmet, or
tight-fitting facepiece (either half-face or full-face).
(ii) Industrial, commercial, and consumer activities. Requirements
as specified in Sec. 721.80(o).
(b) Specific requirements. The provisions of subpart A of this part
apply to this section except as modified by this paragraph.
(1) Recordkeeping. Recordkeeping requirements as specified in Sec.
721.125 (a), (b), (c), (d), and (i) are applicable to manufacturers,
importers, and processors of this substance.
(2) Limitations or revocation of certain notification requirements.
The provisions of Sec. 721.185 apply to this section.
0
21. Add Sec. [emsp14]721.10656 to subpart E to read as follows:
Sec. [emsp14]721.10656 Hexanedioic acid, polymer with .alpha.-
hydro-.omega.-hydroxypoly[oxy(methyl-1,2-ethanediyl)],1,1'-
methylenebis[4-isocyanatobenzene], dihydroxydialkyl ether reaction
products with dialkylcarbinol (generic).
(a) Chemical substance and significant new uses subject to
reporting. (1) The chemical substance identified generically as
hexanedioic acid, polymer with .alpha.-hydro-.omega.-
hydroxypoly[oxy(methyl-1,2-ethanediyl)],1,1'-methylenebis[4-
isocyanatobenzene], dihydroxydialkyl ether reaction products with
dialkylcarbinol (PMN P-11-314) is subject to reporting under this
section for the significant new uses described in paragraph (a)(2) of
this section.
(2) The significant new uses are:
(i) Protection in the workplace. Requirements as specified in Sec.
721.63 (a)(4), (a)(6)(i), (a)(6)(ii), (a)(6)(v), (b) (concentration set
at 0.1 percent), and (c). When determining which persons are reasonably
likely to be exposed as required for Sec. 721.63(a)(4), engineering
control measures (e.g., enclosure or confinement of the operation,
general and local ventilation) or administrative control measures
(e.g., workplace policies and procedures) shall be considered and
implemented to prevent exposure, where feasible. The following National
Institute for Occupational Safety and Health (NIOSH)-certified
respirators with an assigned protection factor (APF) of at least 10
meet the requirements of Sec. 721.63(a)(4):
(A) NIOSH-certified air-purifying, tight-fitting half-face
respirator equipped with N100 (if oil aerosols absent), R100, or P100
filters;
(B) NIOSH-certified air-purifying, tight-fitting full-face
respirator equipped with N100 (if oil aerosols absent), R100, or P100
filters;
(C) NIOSH-certified powered air-purifying respirator equipped with
a loose-fitting hood or helmet and high efficiency particulate air
(HEPA) filters;
(D) NIOSH-certified powered air-purifying respirator equipped with
a tight-fitting facepiece (either half-face or full-face) and HEPA
filters; and
(E) NIOSH-certified supplied-air respirator operated in pressure
demand or continuous flow mode and equipped with a hood or helmet, or
tight-fitting facepiece (either half-face or full-face).
(ii) Industrial, commercial, and consumer activities. Requirements
as specified in Sec. 721.80(o).
(b) Specific requirements. The provisions of subpart A of this part
apply to this section except as modified by this paragraph.
(1) Recordkeeping. Recordkeeping requirements as specified in Sec.
721.125 (a), (b), (c), (d), and (i) are applicable to manufacturers,
importers, and processors of this substance.
(2) Limitations or revocation of certain notification requirements.
The provisions of Sec. 721.185 apply to this section.
0
22. Add Sec. [emsp14]721.10657 to subpart E to read as follows:
Sec. [emsp14]721.10657 Castor oil, polymer with hydrogenated
vegetable oil, 1,1'-methylenebis[isocyanatobenzene] and isocyanate
(generic).
(a) Chemical substance and significant new uses subject to
reporting. (1) The chemical substance identified generically as castor
oil, polymer with hydrogenated vegetable oil, 1,1'-
methylenebis[isocyanatobenzene] and isocyanate (PMN P-12-73) is subject
to reporting under this section for the significant new uses described
in paragraph (a)(2) of this section.
(2) The significant new uses are:
(i) Protection in the workplace. Requirements as specified in Sec.
721.63 (a)(4), (a)(6)(i), (a)(6)(ii), (a)(6)(v), (b) (concentration set
at 0.1 percent), and (c). When determining which persons are reasonably
likely to be exposed as required for Sec. 721.63(a)(4), engineering
control measures (e.g., enclosure or confinement of the operation,
general and local ventilation) or administrative control measures
(e.g., workplace policies and procedures) shall be considered and
implemented to prevent exposure, where feasible. The following National
Institute for Occupational Safety and Health (NIOSH)-certified
respirators with an assigned protection factor (APF) of at least 10
meet the requirements of Sec. 721.63(a)(4):
(A) NIOSH-certified air-purifying, tight-fitting half-face
respirator equipped with N100 (if oil aerosols absent), R100, or P100
filters;
(B) NIOSH-certified air-purifying, tight-fitting full-face
respirator equipped with N100 (if oil aerosols absent), R100, or P100
filters;
(C) NIOSH-certified powered air-purifying respirator equipped with
a loose-fitting hood or helmet and high efficiency particulate air
(HEPA) filters;
(D) NIOSH-certified powered air-purifying respirator equipped with
a tight-fitting facepiece (either half-face or full-face) and HEPA
filters; and
(E) NIOSH-certified supplied-air respirator operated in pressure
demand or continuous flow mode and equipped with a hood or helmet, or
tight-fitting facepiece (either half-face or full-face).
(ii) Industrial, commercial, and consumer activities. Requirements
as specified in Sec. 721.80(o).
(b) Specific requirements. The provisions of subpart A of this part
apply to this section except as modified by this paragraph.
(1) Recordkeeping. Recordkeeping requirements as specified in Sec.
721.125 (a), (b), (c), (d), and (i) are applicable to manufacturers,
importers, and processors of this substance.
(2) Limitations or revocation of certain notification requirements.
The provisions of Sec. 721.185 apply to this section.
0
23. Add Sec. [emsp14]721.10658 to subpart E to read as follows:
Sec. [emsp14]721.10658 2-Oxepanone, polymer with 1,6-
diisocyanatohexane, 2,2-dimethyl-1,3-propanediol and 2,2'-
oxybis[ethanol].
(a) Chemical substance and significant new uses subject to
reporting. (1) The chemical substance identified as 2-oxepanone,
polymer with 1,6-diisocyimatohexane, 2,2-dimethyl-1,3-propanediol and
2,2'-oxybis[ethanol] (PMN P-12-133; CAS No. 1313708-90-5) is subject to
reporting under this section for the significant new uses described in
paragraph (a)(2) of this section.
(2) The significant new uses are:
(i) Protection in the workplace. Requirements as specified in Sec.
721.63 (a)(4), (a)(6)(i), (a)(6)(ii), (a)(6)(v), (b) (concentration set
at 0.1 percent), and (c). When determining which persons are reasonably
likely to be exposed as required for Sec. 721.63(a)(4), engineering
control measures (e.g., enclosure or confinement of the operation,
general
[[Page 12701]]
and local ventilation) or administrative control measures (e.g.,
workplace policies and procedures) shall be considered and implemented
to prevent exposure, where feasible. The following National Institute
for Occupational Safety and Health (NIOSH)-certified respirators with
an assigned protection factor (APF) of at least 10 meet the
requirements of Sec. 721.63(a)(4):
(A) NIOSH-certified air-purifying, tight-fitting half-face
respirator equipped with N100 (if oil aerosols absent), R100, or P100
filters;
(B) NIOSH-certified air-purifying, tight-fitting full-face
respirator equipped with N100 (if oil aerosols absent), R100, or P100
filters;
(C) NIOSH-certified powered air-purifying respirator equipped with
a loose-fitting hood or helmet and high efficiency particulate air
(HEPA) filters;
(D) NIOSH-certified powered air-purifying respirator equipped with
a tight-fitting facepiece (either half-face or full-face) and HEPA
filters; and
(E) NIOSH-certified supplied-air respirator operated in pressure
demand or continuous flow mode and equipped with a hood or helmet, or
tight-fitting facepiece (either half-face or full-face).
(ii) Industrial, commercial, and consumer activities. Requirements
as specified in Sec. 721.80(o).
(b) Specific requirements. The provisions of subpart A of this part
apply to this section except as modified by this paragraph.
(1) Recordkeeping. Recordkeeping requirements as specified in Sec.
721.125 (a), (b), (c), (d), and (i) are applicable to manufacturers,
importers, and processors of this substance.
(2) Limitations or revocation of certain notification requirements.
The provisions of Sec. 721.185 apply to this section.
0
24. Add Sec. [emsp14]721.10659 to subpart E to read as follows:
Sec. [emsp14]721.10659 Poly(oxy-1,4-butanediyl), -hydro--hydroxy-,
polymer with alkyldiisocyanates (generic).
(a) Chemical substance and significant new uses subject to
reporting. (1) The chemical substance identified generically as
poly(oxy-1,4-butanediyl), -hydro--hydroxy-, polymer with
alkyldiisocyanates (PMN P-12-143) is subject to reporting under this
section for the significant new uses described in paragraph (a)(2) of
this section.
(2) The significant new uses are:
(i) Protection in the workplace. Requirements as specified in Sec.
721.63 (a)(4), (a)(6)(i), (a)(6)(ii), (a)(6)(v), (b) (concentration set
at 0.1 percent), and (c). When determining which persons are reasonably
likely to be exposed as required for Sec. 721.63(a)(4), engineering
control measures (e.g., enclosure or confinement of the operation,
general and local ventilation) or administrative control measures
(e.g., workplace policies and procedures) shall be considered and
implemented to prevent exposure, where feasible. The following National
Institute for Occupational Safety and Health (NIOSH)-certified
respirators with an assigned protection factor (APF) of at least 10
meet the requirements of Sec. 721.63(a)(4):
(A) NIOSH-certified air-purifying, tight-fitting half-face
respirator equipped with N100 (if oil aerosols absent), R100, or P100
filters;
(B) NIOSH-certified air-purifying, tight-fitting full-face
respirator equipped with N100 (if oil aerosols absent), R100, or P100
filters;
(C) NIOSH-certified powered air-purifying respirator equipped with
a loose-fitting hood or helmet and high efficiency particulate air
(HEPA) filters;
(D) NIOSH-certified powered air-purifying respirator equipped with
a tight-fitting facepiece (either half-face or full-face) and HEPA
filters; and
(E) NIOSH-certified supplied-air respirator operated in pressure
demand or continuous flow mode and equipped with a hood or helmet, or
tight-fitting facepiece (either half-face or full-face).
(ii) Industrial, commercial, and consumer activities. Requirements
as specified in Sec. 721.80(o).
(b) Specific requirements. The provisions of subpart A of this part
apply to this section except as modified by this paragraph.
(1) Recordkeeping. Recordkeeping requirements as specified in Sec.
721.125 (a), (b), (c), (d), and (i) are applicable to manufacturers,
importers, and processors of this substance.
(2) Limitations or revocation of certain notification requirements.
The provisions of Sec. 721.185 apply to this section.
0
25. Add Sec. [emsp14]721.10660 to subpart E to read as follows:
Sec. [emsp14]721.10660 Aliphatic diisocyanate adduct with substituted
amino alkyl silane (generic).
(a) Chemical substance and significant new uses subject to
reporting. (1) The chemical substance identified generically as
aliphatic diisocyanate adduct with substituted amino alkyl silane (PMN
P-12-274) is subject to reporting under this section for the
significant new uses described in paragraph (a)(2) of this section.
(2) The significant new uses are:
(i) Protection in the workplace. Requirements as specified in Sec.
721.63(a)(4), (a)(6)(i), (a)(6)(ii), (a)(6)(v), (b) (concentration set
at 0.1 percent), and (c). When determining which persons are reasonably
likely to be exposed as required for Sec. 721.63(a)(4), engineering
control measures (e.g., enclosure or confinement of the operation,
general and local ventilation) or administrative control measures
(e.g., workplace policies and procedures) shall be considered and
implemented to prevent exposure, where feasible. The following National
Institute for Occupational Safety and Health (NIOSH)-certified
respirators with an assigned protection factor (APF) of at least 10
meet the requirements of Sec. 721.63(a)(4):
(A) NIOSH-certified air-purifying, tight-fitting half-face
respirator equipped with N100 (if oil aerosols absent), R100, or P100
filters;
(B) NIOSH-certified air-purifying, tight-fitting full-face
respirator equipped with N100 (if oil aerosols absent), R100, or P100
filters;
(C) NIOSH-certified powered air-purifying respirator equipped with
a loose-fitting hood or helmet and high efficiency particulate air
(HEPA) filters;
(D) NIOSH-certified powered air-purifying respirator equipped with
a tight-fitting facepiece (either half-face or full-face) and HEPA
filters; and
(E) NIOSH-certified supplied-air respirator operated in pressure
demand or continuous flow mode and equipped with a hood or helmet, or
tight-fitting facepiece (either half-face or full-face).
(ii) Industrial, commercial, and consumer activities. Requirements
as specified in Sec. 721.80(o).
(b) Specific requirements. The provisions of subpart A of this part
apply to this section except as modified by this paragraph.
(1) Recordkeeping. Recordkeeping requirements as specified in Sec.
721.125 (a), (b), (c), (d), and (i) are applicable to manufacturers,
importers, and processors of this substance.
(2) Limitations or revocation of certain notification requirements.
The provisions of Sec. 721.185 apply to this section.
[FR Doc. 2013-04298 Filed 2-22-13; 8:45 am]
BILLING CODE 6560-50-P