Modification of Significant New Uses of 2-Propen-1-one, 1-(4-morpholinyl)-, 68306-68312 [2010-28006]
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68306
Federal Register / Vol. 75, No. 214 / Friday, November 5, 2010 / Proposed Rules
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. For additional information
about EPA’s public docket visit the EPA
Docket Center homepage at https://
www.epa.gov/epahome/dockets.htm.
Docket: All documents in the docket
are listed in the https://
www.regulations.gov index. 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 either
electronically in https://
www.regulations.gov or in hard copy at
the USEPA Docket Center, Public
Reading Room, Room 3334, EPA West
Building, 1301 Constitution Ave., NW.,
Washington, DC. The Public Reading
Room is open from 8:30 a.m. to 4:30
p.m., Monday through Friday, excluding
legal holidays. The telephone number
for the Public Reading Room is (202)
566–1744, and the telephone number for
the EPA Docket Center is (202) 566–
2426.
FOR FURTHER INFORMATION CONTACT:
Janet Goodwin, USEPA Office of Water
by phone at (202) 566–1060 or by e-mail
at goodwin.janet@epa.gov.
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this action apply to me?
Regulated Entities
Entities potentially regulated by this
action include:
North American industry classification
system (NAICS)
code
Category
Examples of regulated entities
Industry ..................
Construction activities required to obtain 236 NPDES permit coverage and performing the following
activities: Construction of buildings, including building, developing and general contracting.
Heavy and civil engineering construction, including land subdivision.
EPA does not intend the preceding
table to be exhaustive, but provides it as
a guide for readers regarding entities
likely to be regulated by this action.
This table lists the types of entities that
EPA is now aware could potentially be
regulated by this action. Other types of
entities not listed in the table could also
be regulated. To determine whether
your facility is regulated by this action,
you should carefully examine the
applicability criteria in 40 CFR 450.10
(74 FR 62995) and the definition of
‘‘storm water discharges associated with
industrial activity’’ and ‘‘storm water
discharges associated with small
construction activity’’ in existing EPA
regulations at 40 CFR 122.26(b)(14)(x)
and 122.26(b)(15), respectively. If you
have questions regarding the
applicability of this action to a
particular site, consult the person listed
for technical information in the
preceding FOR FURTHER INFORMATION
CONTACT section.
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II. Discussion of Direct Final
Rulemaking
EPA is proposing to stay the
provisions of 40 CFR 450.22(a) and (b)
that contain the numeric limitation and
associated monitoring requirements for
the Construction and Development
Point Source category. This stay is
necessary to reconsider the record
underlying the calculation of the 280
NTU numeric limitation. After the
numeric limitation was promulgated,
and based on EPA’s examination of the
dataset underlying the 280 NTU limit,
EPA concluded that it improperly
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interpreted the data and, as a result, the
calculations in the existing
administrative record are no longer
adequate to support the 280 NTU
effluent limitation. EPA intends to
expeditiously conduct a separate
rulemaking to correct the numeric
effluent limitation. Until the new
rulemaking is effective, it is proposed
that the stay will remain in place. EPA
expects to complete a notice and
comment rulemaking to correct the data
error by May 30, 2011 so that the
revised numeric limitation will be
effective by June 29, 2011. An effective
date of June 29, 2011 for the corrected
numeric limit will enable EPA to
incorporate the revised numeric limit
and associated monitoring requirements
in EPA’s Construction General Permit.
In the ‘‘Rules and Regulations’’ section of
today’s Federal Register, we are issuing
this stay as a direct final rule without
prior proposal because we view this stay
as noncontroversial and anticipate no
adverse comment. We have described
the justification for the stay in the direct
final rule. If EPA receives no adverse
comment on either of these two actions,
the Agency will not take further action
on this proposed rule. If EPA receives
adverse comment on either of these two
actions, the Agency will publish a
timely withdrawal of the direct final
rule in the Federal Register. We would
then address all public comments in a
subsequent final rule based on this
proposed rule. We will not institute a
second comment period on this action.
Any parties interested in commenting
must do so at this time.
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For the various statutes and Executive
Orders that require findings for each
rulemaking, EPA incorporates the
findings from the direct final
rulemaking into this companion notice
for the purpose of providing public
notice and opportunity for comment.
List of Subjects in 40 CFR Part 450
Environmental protection,
Construction industry, Land
development, Erosion, Sediment,
Stormwater, Water pollution control.
Dated: November 1, 2010.
Lisa P. Jackson,
Administrator.
[FR Doc. 2010–28034 Filed 11–4–10; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 721
[EPA–HQ–OPPT–2009–0669; FRL–8849–7]
RIN 2070–AB27
Modification of Significant New Uses
of 2-Propen-1-one, 1-(4-morpholinyl)Environmental Protection
Agency (EPA).
ACTION: Proposed rule.
AGENCY:
Under the Toxic Substances
Control Act (TSCA), EPA is proposing to
amend the significant new use rule
(SNUR) for 2–Propen-1-one, 1-(4morpholinyl)- (CAS No. 5117–12–4) to
allow certain uses without requiring a
significant new use notice (SNUN). EPA
SUMMARY:
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Federal Register / Vol. 75, No. 214 / Friday, November 5, 2010 / Proposed Rules
is proposing this amendment based on
review of new toxicity test data and
receipt of a SNUN for this chemical
substance. The proposed amended
SNUR would continue to require a
SNUN for new uses that may involve
significant changes in human exposure.
DATES: Comments must be received on
or before December 6, 2010.
ADDRESSES: Submit your comments,
identified by docket identification (ID)
number EPA–HQ–OPPT–2009–0669, by
one of the following methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the on-line
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. Attention: Docket ID
Number EPA–HQ–OPPT–2009–0669.
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–
2009–0669. EPA’s policy is that all
comments received will be included in
the docket without change and may be
made available on-line 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 e-mail comment directly
to EPA without going through
regulations.gov, your e-mail 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
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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: Tracey
Klosterman, Chemical Control Division
(7405M), Office of Pollution Prevention
and Toxics, Environmental Protection
Agency, 1200 Pennsylvania Ave., NW.,
Washington, DC 20460–0001; telephone
number: (202) 564–2209; e-mail address:
klosterman.tracey@epa.gov.
For general information contact: The
TSCA-Hotline, ABVI-Goodwill, 422
South Clinton Ave., Rochester, NY
14620; telephone number: (202) 554–
1404; e-mail address: TSCAHotline@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 2-Propen-1-one, 1-(4morpholinyl)- (CAS No. 5117–12–4).
Potentially affected entities may
include, but are not limited to:
• Manufacturers, importers, or
processors of the subject chemical
substance (NAICS codes 325 and
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324110), e.g., chemical manufacturing
and petroleum refineries.
This listing is not intended to be
exhaustive, but rather provides a guide
for readers regarding entities likely to be
affected by this action. Other types of
entities not listed in this unit could also
be affected. The North American
Industrial Classification System
(NAICS) codes have been provided to
assist you and others in determining
whether this action might apply to
certain entities. To determine whether
you or your business may be affected by
this action, you should carefully
examine the applicability provisions in
§ 721.5. If you have any questions
regarding the applicability of this action
to a particular entity, consult the
technical person listed under FOR
FURTHER INFORMATION CONTACT.
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 this proposed rule
on or after December 6, 2010 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 e-mail. 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
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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
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A. What action is the agency taking?
Under section 5(a)(2) of the Toxic
Substances Control Act (TSCA), EPA is
proposing to modify the significant new
use and recordkeeping requirements at
§ 721.5185, for the chemical substance
2-Propen-1-one, 1-(4-morpholinyl)(CAS No. 5117–12–4). In this unit, EPA
provides a brief description for the
chemical substance, including the
Premanufacture Notice (PMN) number,
chemical name, CAS number, basis for
modification of the TSCA section 5(e)
consent order, and the CFR citation. The
modified SNUR would require persons
who intend to manufacture, import, or
process the chemical substance for an
activity designated as a significant new
use to notify EPA at least 90 days before
commencing that activity.
In the Federal Register of January 5,
2000 (65 FR 354) (FRL–6055–2), EPA
issued a direct final SNUR for this
chemical substance in accordance with
the procedures at § 721.160. The record
established for this proposed SNUR is
available in the docket under docket ID
number EPA–HQ–OPPT–2009–0669.
That record includes all information
considered by the Agency in developing
the direct final rule, the modified TSCA
section 5(e) consent order negotiated
with the PMN submitter, and review of
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a SNUN (S–08–07) submitted in 2008 by
a person other than the PMN submitter.
PMN Number P–95–169
Chemical name: 2-Propen-1-one, 1-(4morpholinyl)-.
CAS number: 5117–12–4.
Effective date of modified TSCA
section 5(e) consent order: May 9, 2006.
Federal Register publication date and
reference: January 5, 2000 (65 FR 354).
Basis for modified TSCA section 5(e)
consent order and SNUR: The PMN
substance will be used as a diluent for
ultraviolet (UV) and electron beam (EB)
curable resin for coatings, inks, and
curable adhesives. The consent order
was issued under sections 5(e)(1)(A)(i)
and 5(e)(l)(A)(ii)(I) of TSCA based on a
finding that the chemical substance may
present an unreasonable risk of injury to
human health and the environment. To
protect against these risks, the Agency
issued a TSCA 5(e) consent order which
became effective on November 27, 1998.
The order required the use of dermal
personal protective equipment
(including gloves demonstrated to be
impervious) and respiratory personal
protective equipment (including a
National Institute of Occupational
Safety and Health (NIOSH)-approved
respirator); required establishment of a
hazard communication program;
prohibited domestic manufacturing;
prohibited processing and use activities
in non-enclosed processes; established
maximum importation volume limits for
submission of required testing;
established waste disposal practices
(including restrictions for no release to
surface waters and requirement of
disposal only in a RCRA hazardous
waste landfill); and prohibited use of
the chemical substance involving an
application method that generates a
vapor, mist, or aerosol. The proposed
SNUR for this chemical substance is
based on and consistent with the
provisions of the modified consent
order. The proposed SNUR designates
as a ‘‘significant new use’’ the absence of
the protective measures required in the
corresponding consent order.
Toxicity concern: Under the terms of
the TSCA section 5(e) consent order, the
PMN submitter completed the following
tiered studies: An in vivo mouse
micronucleus test, a 90-day oral toxicity
study in rats, and a reproductive
toxicity screening study in rats. The
results of the micronucleus test were
negative. Based on the results of the 90day study, the Agency established a no
observed adverse effect level (NOAEL)
of 20 mg/kg/day for neurotoxicity.
Further, based on the results of the
reproductive toxicity screening study, a
NOAEL of 75 mg/kg/day (highest dose
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tested) was established for reproductive
effects. From these data, the Agency
calculated Margins of Exposure (MOEs)
for predicted workplace exposures.
Based on these new data, concerns
remain for possible effects to the liver,
testes, kidney, and blood from dermal
exposure. However, EPA no longer has
substantial human health concerns for
mutagenicity and neurotoxicity. In
addition, Agency concerns for
carcinogenicity by inhalation were
reduced, but were further mitigated by
retaining the original consent order
prohibition of industrial processing and
use in a non-enclosed process and any
use application methods that generate a
vapor, mist, or aerosol form of the PMN
substance.
In addition, to address Agency
environmental concerns, a re-review of
the environmental toxicity profile for
the PMN substance was conducted. The
results of this evaluation indicated a
low concern for chronic aquatic toxicity.
Therefore, EPA could no longer make a
‘‘may present unreasonable risk’’ finding
for releases of the PMN substance to
surface waters. As a result of the
aforementioned review, EPA issued a
modified TSCA section 5(e) consent
order which became effective on May 9,
2006. The modified order removed
requirements for respiratory protection,
waived further required trigger testing
for mutagenicity and cancer (i.e.,
required by a set production volume or
time), removed the restriction on
domestic manufacture, and removed
waste disposal restrictions (i.e., no
longer prohibiting releases to surface
waters or limiting disposal to
incineration or landfill). Pursuant to
§ 721.185(a)(5), the Agency has
examined new information and
reexamined the test data and other
information supporting its finding
under section 5(e)(1)(A)(ii)(I) of TSCA,
and has concluded that a rational basis
no longer exists to support findings that
certain activities involving the
substance may present an unreasonable
risk of injury to human health and the
environment required under section
5(e)(1)(A) of TSCA. Therefore, the
Agency is proposing to modify the
SNUR based on and consistent with the
provisions in the underlying modified
consent order. To protect against the
remaining potential risks, the modified
consent order:
• Requires the use of dermal personal
protective equipment (including gloves
demonstrated to be impervious).
• Requires establishment of a hazard
communication program.
• Prohibits processing and use
activities in non-enclosed processes.
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• Prohibits the use of the chemical
substance involving an application
method that generates a vapor, mist, or
aerosol.
The proposed modified SNUR
designates as a ‘‘significant new use’’ the
absence of these protective measures. In
addition, EPA has included, in the
proposed regulatory text, clarifying
language for those forms of the PMN
substance which are exempt from the
provisions of the proposed SNUR. These
exemptions apply to quantities of the
PMN substance after it has been
completely reacted (cured).
On June 27, 2008, the Agency
received a SNUN (S–08–07) for the
subject chemical substance. The
significant new use identified in the
notice was release to water for the
generic (non-confidential) use of
‘‘contained use in energy production’’.
The 90-day review period for the SNUN
expired on October 2, 2008 with the
Agency not taking action on the
‘‘significant new use’’ of release of the
substance to water. The proposed
modified SNUR would similarly no
longer include release to water as a
significant new use, along with the
other changes noted.
Recommended testing: EPA has
determined that the results of the
combined repeated dose toxicity with
the reproductive/developmental toxicity
screening test (OPPTS Test Guideline
870.3650 or Organisation for Economic
Co-operation and Development (OECD)
Test Guideline 422) would help further
characterize the human health effects of
the PMN substance. The modified 5(e)
consent order does not require
submission of the aforementioned
information at any specified time or
production volume. However, the
order’s restrictions on manufacturing,
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 721.5185.
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 those listed in TSCA section
5(a)(2) (see Unit III.). Once EPA
determines that a use of a chemical
substance is a significant new use,
TSCA section 5(a)(1)(B) requires persons
to submit a SNUN to EPA at least 90
days before they manufacture, import,
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or process the chemical substance for
that use. The mechanism for reporting
under this requirement is established
under § 721.5.
Section 5(a)(1) of TSCA (15 U.S.C.
2604(a)(1)) and its implementing
regulations at 40 CFR parts 720 and 721
require that any person intending to
manufacture a new chemical substance,
or to manufacture or process any
chemical substance for a significant new
use, must give EPA 90-days advance
written notice in the form of a PMN or
SNUN, respectively.
Upon reviewing those notices, if EPA
makes certain determinations regarding
potential exposures and risks that may
be presented by the activities associated
with the chemical, EPA may regulate
the chemical by issuing an order under
TSCA section 5(e) and/or a significant
new use rule (SNUR) under TSCA
section 5(a)(2) and 40 CFR part 721. The
TSCA section 5(e) order governs only
the entity who submitted the PMN
whereas the section 5(a)(2) SNUR
applies to all manufacturers and
processors of the chemical substance.
EPA may respond to SNUNs by
issuing or modifying a TSCA section
5(e) consent order and/or amending the
SNUR promulgated under TSCA section
5(a)(2). Amendment of the SNUR will
often be necessary to allow companies
other than the SNUN submitter to
engage in the newly authorized use(s),
because even after a manufacturer
submits a SNUN and the review period
expires, processors of the same
substance still must submit a SNUN
before engaging in the significant new
use. Provisions regarding EPA’s
authority to modify or revoke SNUR
requirements appear at § 721.185.
C. Applicability of General Provisions
General provisions for SNURs appear
in 40 CFR part 721, subpart A. These
provisions describe persons subject to
the proposed rule, recordkeeping
requirements, and exemptions to
reporting requirements. Provisions
relating to user fees appear at 40 CFR
part 700. According to § 721.1(c),
persons subject to this SNUR must
comply with the same notice
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 sections 5(b) and 5(d)(1), the
exemptions authorized by TSCA
sections 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
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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.
Chemical importers are subject to the
TSCA section 13 (15 U.S.C. 2612)
import certification requirements
codified at 19 CFR 12.118 through
12.127; see also 19 CFR 127.28 (the
corresponding EPA policy appears at 40
CFR part 707, subpart B). Chemical
importers must certify that the shipment
of the chemical substance complies with
all applicable rules and orders under
TSCA. Importers of chemical substances
subject to a final SNUR must certify
their compliance with the SNUR
requirements. In addition, any persons
who export or intend to export a
chemical substance identified in a
proposed 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.
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 to 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.
• 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 chemical
substance that is the subject of this
proposed rule, EPA considered relevant
information about the toxicity of the
chemical substance, likely human
exposures and environmental releases
associated with possible uses, and the
four bulleted TSCA section 5(a)(2)
factors listed in this unit.
IV. Rationale and Objectives of the
Proposed Rule
A. Rationale
During the review of test data
submitted under the TSCA section 5(e)
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consent order for 2-Propen-1-one, 1-(4morpholinyl)-, EPA determined that the
chemical substance still met one or
more of the criteria of concern
established at § 721.160. (see Unit II.)
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B. Objectives
EPA is proposing this SNUR
modification for the specific chemical
substance 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 chemical substance
that is the subject of a TSCA section 5(e)
consent order are subject to similar
requirements.
V. 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. EPA solicits comments on
whether any of the uses proposed as
significant new uses are ongoing. As
discussed in the Federal Register of
April 24, 1990 (55 FR 17376), EPA has
decided that the intent of section
5(a)(1)(B) of TSCA is best served by
designating a use as a significant new
use as of the date of publication of the
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 as of the
effective date of the final rule. Thus,
persons who begin commercial
manufacture, import, or processing
activities with the chemical substances
that would be regulated as a ‘‘significant
new use’’ through this proposed rule,
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must cease any such activity as of 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 all extensions,
expires.
EPA has promulgated provisions to
allow persons to comply with this
SNUR before the effective date. If a
person were to meet the conditions of
advance compliance under § 721.45(h),
the person would be considered to have
met the requirements of the final SNUR
for those activities.
VI. Test Data and Other Information
EPA recognizes that TSCA section 5
does not require the development of any
particular test data before submission of
a SNUN. There are two exceptions:
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
§ 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 II.
lists those tests. 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 harmonized 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 SourceOECD
at https://www.sourceoecd.org. The
American Society for Testing and
Materials (ASTM) standards are
available at https://www.astm.org/
Standard/index.shtml.
The modified TSCA section 5(e)
consent order for the chemical
substance that would be regulated under
this proposed rule does not require
submission of test data at any specified
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time or volume. However, the
restrictions on manufacture, import,
processing, distribution in commerce,
use and disposal of the PMN substance
would remain in effect until the consent
order is modified or revoked by EPA
based on submission of that or other
relevant information. These restricted
activities cannot be commenced unless
the PMN submitter first submits the
results of toxicity tests that would
permit a reasoned evaluation of the
potential risks posed by this chemical
substance. The test specified in the
modified TSCA section 5(e) consent
order is included in Unit II. The
proposed SNUR would contain the same
restrictions as the modified TSCA
section 5(e) consent order. Persons who
intend to commence non-exempt
commercial manufacture, import, or
processing for those activities proposed
as significant new uses would be
required to notify the Agency by
submitting a SNUN at least 90 days in
advance of commencement of those
activities.
The recommended tests may not be
the only means of addressing the
potential risks of the chemical
substance. However, SNUN submission
for a significant new use without any
test data may increase the likelihood
that EPA will take action under TSCA
section 5(e). 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 substance.
• Potential benefits of the chemical
substance.
• Information on risks posed by the
chemical substance compared to risks
posed by potential substitutes.
VII. SNUN Submissions
As stated in Unit II.C., according to
§ 721.1(c), persons submitting a SNUN
must comply with the same notice
requirements and EPA regulatory
procedures as persons submitting a
PMN, including submission of test data
on health and environmental effects as
described in § 720.50. SNUNs must be
submitted to EPA, on EPA Form No.
7710–25 in accordance with the
procedures set forth in § 721.25 and
§ 720.40. This form is available from
the Environmental Assistance Division
(7408M), 1200 Pennsylvania Ave., NW.,
Washington, DC 20460–0001. Forms
and information are also available
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electronically at https://www.epa.gov/
opptintr/newchems/pubs/
pmnforms.htm.
VIII. Economic Analysis
EPA evaluated the potential costs of
establishing SNUN requirements for
potential manufacturers, importers, and
processors of the chemical substances
during the development of the direct
final rule. The Agency’s complete
economic analysis is available in the
public docket under docket ID number
EPA–HQ–OPPT–2009–0669.
IX. Statutory and Executive Order
Reviews
A. Executive Order 12866
This proposed rule would modify a
SNUR for a chemical substance that is
the subject of a PMN and TSCA section
5(e) consent order. 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).
mstockstill on DSKH9S0YB1PROD with PROPOSALS
B. Paperwork Reduction Act
According to the Paperwork
Reduction Act (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 the
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 is amending the table in
40 CFR part 9 to list the OMB approval
number for the information collection
requirements contained in this proposed
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
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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
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
Pursuant to section 605(b) of the
Regulatory Flexibility Act (RFA) (5
U.S.C. 601 et seq.), the Agency hereby
certifies that promulgation of this SNUR
would not have a significant adverse
economic impact on a substantial
number of small entities. The rationale
supporting this conclusion is discussed
in this unit. The requirement to submit
a SNUN applies to any person
(including small or large entities) who
intends to engage in any activity
described in the rule as a ‘‘significant
new use.’’ Because these uses are ‘‘new,’’
based on all information currently
available to EPA, it appears that no
small or large entities presently engage
in such activities. A SNUR requires that
any person who intends to engage in
such activity in the future must first
notify EPA by submitting a SNUN.
Although some small entities may
decide to pursue a significant new use
in the future, EPA cannot presently
determine how many, if any, there may
be. However, EPA’s experience to date
is that, in response to the promulgation
of over 1,400 SNURs, the Agency
receives on average only 5 notices per
year. Of those SNUNs submitted from
2006–2008, only one appears to be from
a small entity. In addition, the estimated
reporting cost for submission of a SNUN
(see Unit VIII.) is minimal regardless of
the size of the firm. Therefore, the
potential economic impacts of
complying with this SNUR would not
be expected to be significant or
adversely impact a substantial number
of small entities. In a SNUR that
published in the Federal Register of
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68311
June 2, 1997 (62 FR 29684) (FRL–5597–
1), the Agency presented its general
determination that final SNURs are not
expected to have a significant economic
impact on a substantial number of small
entities, which was provided to the
Chief Counsel for Advocacy of the Small
Business Administration.
D. Unfunded Mandates Reform Act
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 affect on small
governments subject to the requirements
of sections 202, 203, 204, or 205 of the
Unfunded Mandates Reform Act of 1995
(UMRA) (Pub. L. 104–4).
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 or 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.
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H. Executive Order 13211
This proposed rule 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 this action is
not a significant regulatory action under
Executive Order 12866.
I. National Technology Transfer and
Advancement Act
In addition, since this action does not
involve any technical standards, section
12(d) of the National Technology
Transfer and Advancement Act of 1995
(NTTAA), Public Law 104–113, 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: November 1, 2010.
Wendy C. Hamnett,
Director, 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:
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Authority: 15 U.S.C. 2604, 2607, and
2625(c).
2. Amend § 721.5185 as follows:
a. Revise the section heading.
b. Revise paragraphs (a)(1) and
(a)(2)(i).
c. Add paragraph (a)(2)(ii).
d. Revise paragraph (a)(2)(iii).
e. Remove paragraphs (a)(2)(iv),
(a)(2)(v), and (a)(2)(vi).
f. Revise paragraph (b)(1).
The revisions and addition read as
follows:
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 after
it has been completely reacted (cured).
(2) * * *
(i) Protection in the workplace.
Requirements as specified in § 721.63
(a)(1), (a)(2)(i), (a)(2)(iv), (a)(3)(i),
(a)(3)(ii), (a)(4), (a)(6)(v), (b)
(concentration set at 1.0 percent), and
(c). Safety 4/4H EVOH/PE laminate,
Ansell Edmont Neoprene number 865,
and Solvex Nitrile Rubber number 275
gloves have been tested in accordance
with the American Society for Testing
Materials (ASTM) F739 method and
found by EPA to satisfy the consent
orders and § 721.63(a)(2)(i) requirements
for dermal protection to 100 percent
PMN substance. Gloves and other
dermal protection may not be used for
a time period longer than they are
actually tested and must be replaced at
the end of each work shift. For
additional dermal protection materials,
a company must submit all test data to
the Agency and must receive written
Agency approval for each type of
material tested prior to use of that
material as worker dermal protection.
However, for the purposes of
determining the imperviousness of
gloves, up to 1 year after the
commencement of commercial
manufacture or import, the employer
may use the method described in
§ 721.63(a)(3)(ii), thereafter, they must
use the method described in
§ 721.63(a)(3)(i).
(ii) Hazard communication program.
Requirements as specified in § 721.72
(a), (b), (c), (d), (e) (concentration set at
1.0 percent), (f), (g)(1)(iv), (g)(1)(vi),
(g)(2)(v), and (g)(5).
(iii) Industrial, commercial, and
consumer activities. Requirements as
specified in § 721.80(a), (c), and (y)(1).
(b) * * *
(1) Recordkeeping. The following
recordkeeping requirements are
applicable to manufacturers, importers,
and processors of this chemical
substance as specified in § 721.125(a)
through (i).
*
*
*
*
*
[FR Doc. 2010–28006 Filed 11–4–10; 8:45 am]
§ 721.5185 2-Propen-1-one, 1-(4morpholinyl)-.
BILLING CODE 6560–50–P
(a) * * *
(1) The chemical substance identified
as 2-Propen-1-one, 1-(4-morpholinyl)(PMN P–95–169; CAS No. 5117–12–4) is
subject to reporting under this section
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DEPARTMENT OF TRANSPORTATION
National Highway Traffic Safety
Administration
49 CFR Parts 523, 534, and 535
[Docket No. NHTSA–2010–0079]
Notice of Availability of a Draft
Environmental Impact Statement
(DEIS) for New Medium- and HeavyDuty Fuel Efficiency Improvement
Program
National Highway Traffic
Safety Administration (NHTSA),
Department of Transportation (DOT).
ACTION: Notice of availability of a Draft
Environmental Impact Statement (DEIS).
AGENCY:
NHTSA has prepared a DEIS
to disclose and analyze the potential
environmental impacts of the agency’s
newly proposed fuel consumption
standards for commercial medium- and
heavy-duty on-highway vehicles and
work trucks (‘‘HD vehicles’’), which
NHTSA recently proposed pursuant to
the Energy Independence and Security
Act of 2007. NHTSA invites Federal,
State, and local agencies, Indian tribes,
and the public to submit written
comments on the DEIS using the
instructions set forth in this notice. To
facilitate review of the DEIS, NHTSA
has posted the DEIS on its Web site
(https://www.nhtsa.gov/fuel-economy)
and placed it in the agency’s docket,
identified by the docket number at the
beginning of this notice. NHTSA will
consider all public comments received
on the DEIS in preparing final NEPA
documents to support final fuel
consumption standards, which NHTSA
plans to issue next year.
DATES: To ensure that NHTSA has the
opportunity to consider comments on
the DEIS, NHTSA must receive written
comments by January 3, 2011. NHTSA
will try to consider comments received
after that date to the extent the NEPA
and rulemaking schedules allow, but
NHTSA cannot ensure that it will be
able to do so.
FOR FURTHER INFORMATION CONTACT:
Questions concerning the DEIS should
be addressed to Ms. Angel Jackson,
Telephone: 1–202–366–0154, Fuel
Economy Division, Office of
International Vehicle, Fuel Economy
and Consumer Standards, National
Highway Traffic Safety Administration,
1200 New Jersey Avenue, SE.,
Washington, DC 20590. E-mail:
nhtsa.nepa@dot.gov. Information about
the HD vehicle rulemaking and the
NEPA process is also available at
https://www.nhtsa.gov/fuel-economy.
SUMMARY:
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Agencies
[Federal Register Volume 75, Number 214 (Friday, November 5, 2010)]
[Proposed Rules]
[Pages 68306-68312]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-28006]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 721
[EPA-HQ-OPPT-2009-0669; FRL-8849-7]
RIN 2070-AB27
Modification of Significant New Uses of 2-Propen-1-one, 1-(4-
morpholinyl)-
AGENCY: Environmental Protection Agency (EPA).
ACTION: Proposed rule.
-----------------------------------------------------------------------
SUMMARY: Under the Toxic Substances Control Act (TSCA), EPA is
proposing to amend the significant new use rule (SNUR) for 2-Propen-1-
one, 1-(4-morpholinyl)- (CAS No. 5117-12-4) to allow certain uses
without requiring a significant new use notice (SNUN). EPA
[[Page 68307]]
is proposing this amendment based on review of new toxicity test data
and receipt of a SNUN for this chemical substance. The proposed amended
SNUR would continue to require a SNUN for new uses that may involve
significant changes in human exposure.
DATES: Comments must be received on or before December 6, 2010.
ADDRESSES: Submit your comments, identified by docket identification
(ID) number EPA-HQ-OPPT-2009-0669, by one of the following methods:
Federal eRulemaking Portal: https://www.regulations.gov.
Follow the on-line 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.
Attention: Docket ID Number EPA-HQ-OPPT-2009-0669. 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-
2009-0669. EPA's policy is that all comments received will be included
in the docket without change and may be made available on-line 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 e-
mail. 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 e-
mail comment directly to EPA without going through regulations.gov,
your e-mail 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:
Tracey Klosterman, Chemical Control Division (7405M), Office of
Pollution Prevention and Toxics, Environmental Protection Agency, 1200
Pennsylvania Ave., NW., Washington, DC 20460-0001; telephone number:
(202) 564-2209; e-mail address: klosterman.tracey@epa.gov.
For general information contact: The TSCA-Hotline, ABVI-Goodwill,
422 South Clinton Ave., Rochester, NY 14620; telephone number: (202)
554-1404; e-mail 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 2-Propen-1-one, 1-(4-morpholinyl)- (CAS No.
5117-12-4). Potentially affected entities may include, but are not
limited to:
Manufacturers, importers, or processors of the subject
chemical substance (NAICS codes 325 and 324110), e.g., chemical
manufacturing and petroleum refineries.
This listing is not intended to be exhaustive, but rather provides
a guide for readers regarding entities likely to be affected by this
action. Other types of entities not listed in this unit could also be
affected. The North American Industrial Classification System (NAICS)
codes have been provided to assist you and others in determining
whether this action might apply to certain entities. To determine
whether you or your business may be affected by this action, you should
carefully examine the applicability provisions in Sec. 721.5. If you
have any questions regarding the applicability of this action to a
particular entity, consult the technical person listed under FOR
FURTHER INFORMATION CONTACT.
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 this proposed rule on or
after December 6, 2010 are subject to the export notification
provisions of TSCA section 12(b) (15 U.S.C. 2611(b)) (see Sec.
[emsp14]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 e-mail. 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
[[Page 68308]]
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?
Under section 5(a)(2) of the Toxic Substances Control Act (TSCA),
EPA is proposing to modify the significant new use and recordkeeping
requirements at Sec. 721.5185, for the chemical substance 2-Propen-1-
one, 1-(4-morpholinyl)- (CAS No. 5117-12-4). In this unit, EPA provides
a brief description for the chemical substance, including the
Premanufacture Notice (PMN) number, chemical name, CAS number, basis
for modification of the TSCA section 5(e) consent order, and the CFR
citation. The modified SNUR would require persons who intend to
manufacture, import, or process the chemical substance for an activity
designated as a significant new use to notify EPA at least 90 days
before commencing that activity.
In the Federal Register of January 5, 2000 (65 FR 354) (FRL-6055-
2), EPA issued a direct final SNUR for this chemical substance in
accordance with the procedures at Sec. 721.160. The record established
for this proposed SNUR is available in the docket under docket ID
number EPA-HQ-OPPT-2009-0669. That record includes all information
considered by the Agency in developing the direct final rule, the
modified TSCA section 5(e) consent order negotiated with the PMN
submitter, and review of a SNUN (S-08-07) submitted in 2008 by a person
other than the PMN submitter.
PMN Number P-95-169
Chemical name: 2-Propen-1-one, 1-(4-morpholinyl)-.
CAS number: 5117-12-4.
Effective date of modified TSCA section 5(e) consent order: May 9,
2006. Federal Register publication date and reference: January 5, 2000
(65 FR 354).
Basis for modified TSCA section 5(e) consent order and SNUR: The
PMN substance will be used as a diluent for ultraviolet (UV) and
electron beam (EB) curable resin for coatings, inks, and curable
adhesives. The consent order was issued under sections 5(e)(1)(A)(i)
and 5(e)(l)(A)(ii)(I) of TSCA based on a finding that the chemical
substance may present an unreasonable risk of injury to human health
and the environment. To protect against these risks, the Agency issued
a TSCA 5(e) consent order which became effective on November 27, 1998.
The order required the use of dermal personal protective equipment
(including gloves demonstrated to be impervious) and respiratory
personal protective equipment (including a National Institute of
Occupational Safety and Health (NIOSH)-approved respirator); required
establishment of a hazard communication program; prohibited domestic
manufacturing; prohibited processing and use activities in non-enclosed
processes; established maximum importation volume limits for submission
of required testing; established waste disposal practices (including
restrictions for no release to surface waters and requirement of
disposal only in a RCRA hazardous waste landfill); and prohibited use
of the chemical substance involving an application method that
generates a vapor, mist, or aerosol. The proposed SNUR for this
chemical substance is based on and consistent with the provisions of
the modified consent order. The proposed SNUR designates as a
``significant new use'' the absence of the protective measures required
in the corresponding consent order.
Toxicity concern: Under the terms of the TSCA section 5(e) consent
order, the PMN submitter completed the following tiered studies: An in
vivo mouse micronucleus test, a 90-day oral toxicity study in rats, and
a reproductive toxicity screening study in rats. The results of the
micronucleus test were negative. Based on the results of the 90-day
study, the Agency established a no observed adverse effect level
(NOAEL) of 20 mg/kg/day for neurotoxicity. Further, based on the
results of the reproductive toxicity screening study, a NOAEL of 75 mg/
kg/day (highest dose tested) was established for reproductive effects.
From these data, the Agency calculated Margins of Exposure (MOEs) for
predicted workplace exposures. Based on these new data, concerns remain
for possible effects to the liver, testes, kidney, and blood from
dermal exposure. However, EPA no longer has substantial human health
concerns for mutagenicity and neurotoxicity. In addition, Agency
concerns for carcinogenicity by inhalation were reduced, but were
further mitigated by retaining the original consent order prohibition
of industrial processing and use in a non-enclosed process and any use
application methods that generate a vapor, mist, or aerosol form of the
PMN substance.
In addition, to address Agency environmental concerns, a re-review
of the environmental toxicity profile for the PMN substance was
conducted. The results of this evaluation indicated a low concern for
chronic aquatic toxicity. Therefore, EPA could no longer make a ``may
present unreasonable risk'' finding for releases of the PMN substance
to surface waters. As a result of the aforementioned review, EPA issued
a modified TSCA section 5(e) consent order which became effective on
May 9, 2006. The modified order removed requirements for respiratory
protection, waived further required trigger testing for mutagenicity
and cancer (i.e., required by a set production volume or time), removed
the restriction on domestic manufacture, and removed waste disposal
restrictions (i.e., no longer prohibiting releases to surface waters or
limiting disposal to incineration or landfill). Pursuant to Sec.
721.185(a)(5), the Agency has examined new information and reexamined
the test data and other information supporting its finding under
section 5(e)(1)(A)(ii)(I) of TSCA, and has concluded that a rational
basis no longer exists to support findings that certain activities
involving the substance may present an unreasonable risk of injury to
human health and the environment required under section 5(e)(1)(A) of
TSCA. Therefore, the Agency is proposing to modify the SNUR based on
and consistent with the provisions in the underlying modified consent
order. To protect against the remaining potential risks, the modified
consent order:
Requires the use of dermal personal protective equipment
(including gloves demonstrated to be impervious).
Requires establishment of a hazard communication program.
Prohibits processing and use activities in non-enclosed
processes.
[[Page 68309]]
Prohibits the use of the chemical substance involving an
application method that generates a vapor, mist, or aerosol.
The proposed modified SNUR designates as a ``significant new use''
the absence of these protective measures. In addition, EPA has
included, in the proposed regulatory text, clarifying language for
those forms of the PMN substance which are exempt from the provisions
of the proposed SNUR. These exemptions apply to quantities of the PMN
substance after it has been completely reacted (cured).
On June 27, 2008, the Agency received a SNUN (S-08-07) for the
subject chemical substance. The significant new use identified in the
notice was release to water for the generic (non-confidential) use of
``contained use in energy production''. The 90-day review period for
the SNUN expired on October 2, 2008 with the Agency not taking action
on the ``significant new use'' of release of the substance to water.
The proposed modified SNUR would similarly no longer include release to
water as a significant new use, along with the other changes noted.
Recommended testing: EPA has determined that the results of the
combined repeated dose toxicity with the reproductive/developmental
toxicity screening test (OPPTS Test Guideline 870.3650 or Organisation
for Economic Co-operation and Development (OECD) Test Guideline 422)
would help further characterize the human health effects of the PMN
substance. The modified 5(e) consent order does not require submission
of the aforementioned information at any specified time or production
volume. However, the order's restrictions on manufacturing, 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 721.5185.
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 those listed in TSCA section 5(a)(2) (see
Unit III.). Once EPA determines that a use of a chemical substance is a
significant new use, TSCA section 5(a)(1)(B) requires persons to submit
a SNUN to EPA at least 90 days before they manufacture, import, or
process the chemical substance for that use. The mechanism for
reporting under this requirement is established under Sec. 721.5.
Section 5(a)(1) of TSCA (15 U.S.C. 2604(a)(1)) and its implementing
regulations at 40 CFR parts 720 and 721 require that any person
intending to manufacture a new chemical substance, or to manufacture or
process any chemical substance for a significant new use, must give EPA
90-days advance written notice in the form of a PMN or SNUN,
respectively.
Upon reviewing those notices, if EPA makes certain determinations
regarding potential exposures and risks that may be presented by the
activities associated with the chemical, EPA may regulate the chemical
by issuing an order under TSCA section 5(e) and/or a significant new
use rule (SNUR) under TSCA section 5(a)(2) and 40 CFR part 721. The
TSCA section 5(e) order governs only the entity who submitted the PMN
whereas the section 5(a)(2) SNUR applies to all manufacturers and
processors of the chemical substance.
EPA may respond to SNUNs by issuing or modifying a TSCA section
5(e) consent order and/or amending the SNUR promulgated under TSCA
section 5(a)(2). Amendment of the SNUR will often be necessary to allow
companies other than the SNUN submitter to engage in the newly
authorized use(s), because even after a manufacturer submits a SNUN and
the review period expires, processors of the same substance still must
submit a SNUN before engaging in the significant new use. Provisions
regarding EPA's authority to modify or revoke SNUR requirements appear
at Sec. 721.185.
C. Applicability of General Provisions
General provisions for SNURs appear in 40 CFR part 721, subpart A.
These provisions describe persons subject to the proposed rule,
recordkeeping requirements, and exemptions to reporting requirements.
Provisions relating to user fees appear at 40 CFR part 700. According
to Sec. 721.1(c), persons subject to this SNUR must comply with the
same notice 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 sections 5(b)
and 5(d)(1), the exemptions authorized by TSCA sections 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.
Chemical importers are subject to the TSCA section 13 (15 U.S.C.
2612) import certification requirements codified at 19 CFR 12.118
through 12.127; see also 19 CFR 127.28 (the corresponding EPA policy
appears at 40 CFR part 707, subpart B). Chemical importers must certify
that the shipment of the chemical substance complies with all
applicable rules and orders under TSCA. Importers of chemical
substances subject to a final SNUR must certify their compliance with
the SNUR requirements. In addition, any persons who export or intend to
export a chemical substance identified in a proposed 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.
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 to 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.
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
chemical substance that is the subject of this proposed rule, EPA
considered relevant information about the toxicity of the chemical
substance, likely human exposures and environmental releases associated
with possible uses, and the four bulleted TSCA section 5(a)(2) factors
listed in this unit.
IV. Rationale and Objectives of the Proposed Rule
A. Rationale
During the review of test data submitted under the TSCA section
5(e)
[[Page 68310]]
consent order for 2-Propen-1-one, 1-(4-morpholinyl)-, EPA determined
that the chemical substance still met one or more of the criteria of
concern established at Sec. 721.160. (see Unit II.)
B. Objectives
EPA is proposing this SNUR modification for the specific chemical
substance 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 chemical substance that is the subject of a TSCA
section 5(e) consent order are subject to similar requirements.
V. 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. EPA solicits comments on whether any of the uses
proposed as significant new uses are ongoing. As discussed in the
Federal Register of April 24, 1990 (55 FR 17376), EPA has decided that
the intent of section 5(a)(1)(B) of TSCA is best served by designating
a use as a significant new use as of the date of publication of the
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 as of the effective date of the
final rule. Thus, persons who begin commercial manufacture, import, or
processing activities with the chemical substances that would be
regulated as a ``significant new use'' through this proposed rule, must
cease any such activity as of 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 all extensions, expires.
EPA has promulgated provisions to allow persons to comply with this
SNUR before the effective date. If a person were to meet the conditions
of advance compliance under Sec. 721.45(h), the person would be
considered to have met the requirements of the final SNUR for those
activities.
VI. Test Data and Other Information
EPA recognizes that TSCA section 5 does not require the development
of any particular test data before submission of a SNUN. There are two
exceptions:
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 Sec.
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 II. lists those tests. 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 harmonized 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
SourceOECD at https://www.sourceoecd.org. The American Society for
Testing and Materials (ASTM) standards are available at https://www.astm.org/Standard/index.shtml.
The modified TSCA section 5(e) consent order for the chemical
substance that would be regulated under this proposed rule does not
require submission of test data at any specified time or volume.
However, the restrictions on manufacture, import, processing,
distribution in commerce, use and disposal of the PMN substance would
remain in effect until the consent order is modified or revoked by EPA
based on submission of that or other relevant information. These
restricted activities cannot be commenced unless the PMN submitter
first submits the results of toxicity tests that would permit a
reasoned evaluation of the potential risks posed by this chemical
substance. The test specified in the modified TSCA section 5(e) consent
order is included in Unit II. The proposed SNUR would contain the same
restrictions as the modified TSCA section 5(e) consent order. Persons
who intend to commence non-exempt commercial manufacture, import, or
processing for those activities proposed as significant new uses would
be required to notify the Agency by submitting a SNUN at least 90 days
in advance of commencement of those activities.
The recommended tests may not be the only means of addressing the
potential risks of the chemical substance. However, SNUN submission for
a significant new use without any test data may increase the likelihood
that EPA will take action under TSCA section 5(e). 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 substance.
Potential benefits of the chemical substance.
Information on risks posed by the chemical substance
compared to risks posed by potential substitutes.
VII. SNUN Submissions
As stated in Unit II.C., according to Sec. [emsp14]721.1(c),
persons submitting a SNUN must comply with the same notice requirements
and EPA regulatory procedures as persons submitting a PMN, including
submission of test data on health and environmental effects as
described in Sec. [emsp14]720.50. SNUNs must be submitted to EPA, on
EPA Form No. 7710-25 in accordance with the procedures set forth in
Sec. [emsp14]721.25 and Sec. [emsp14]720.40. This form is available
from the Environmental Assistance Division (7408M), 1200 Pennsylvania
Ave., NW., Washington, DC 20460-0001. Forms and information are also
available
[[Page 68311]]
electronically at https://www.epa.gov/opptintr/newchems/pubs/pmnforms.htm.
VIII. Economic Analysis
EPA evaluated the potential costs of establishing SNUN requirements
for potential manufacturers, importers, and processors of the chemical
substances during the development of the direct final rule. The
Agency's complete economic analysis is available in the public docket
under docket ID number EPA-HQ-OPPT-2009-0669.
IX. Statutory and Executive Order Reviews
A. Executive Order 12866
This proposed rule would modify a SNUR for a chemical substance
that is the subject of a PMN and TSCA section 5(e) consent order. 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
According to the Paperwork Reduction Act (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 the 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 is amending the table
in 40 CFR part 9 to list the OMB approval number for the information
collection requirements contained in this proposed 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 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
Pursuant to section 605(b) of the Regulatory Flexibility Act (RFA)
(5 U.S.C. 601 et seq.), the Agency hereby certifies that promulgation
of this SNUR would not have a significant adverse economic impact on a
substantial number of small entities. The rationale supporting this
conclusion is discussed in this unit. The requirement to submit a SNUN
applies to any person (including small or large entities) who intends
to engage in any activity described in the rule as a ``significant new
use.'' Because these uses are ``new,'' based on all information
currently available to EPA, it appears that no small or large entities
presently engage in such activities. A SNUR requires that any person
who intends to engage in such activity in the future must first notify
EPA by submitting a SNUN. Although some small entities may decide to
pursue a significant new use in the future, EPA cannot presently
determine how many, if any, there may be. However, EPA's experience to
date is that, in response to the promulgation of over 1,400 SNURs, the
Agency receives on average only 5 notices per year. Of those SNUNs
submitted from 2006-2008, only one appears to be from a small entity.
In addition, the estimated reporting cost for submission of a SNUN (see
Unit VIII.) is minimal regardless of the size of the firm. Therefore,
the potential economic impacts of complying with this SNUR would not be
expected to be significant or adversely impact a substantial number of
small entities. In a SNUR that published in the Federal Register of
June 2, 1997 (62 FR 29684) (FRL-5597-1), the Agency presented its
general determination that final SNURs are not expected to have a
significant economic impact on a substantial number of small entities,
which was provided to the Chief Counsel for Advocacy of the Small
Business Administration.
D. Unfunded Mandates Reform Act
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 affect on small governments subject to the requirements of
sections 202, 203, 204, or 205 of the Unfunded Mandates Reform Act of
1995 (UMRA) (Pub. L. 104-4).
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 or 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.
[[Page 68312]]
H. Executive Order 13211
This proposed rule 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 this action is not a significant regulatory action under
Executive Order 12866.
I. National Technology Transfer and Advancement Act
In addition, since this action does not involve any technical
standards, section 12(d) of the National Technology Transfer and
Advancement Act of 1995 (NTTAA), Public Law 104-113, 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: November 1, 2010.
Wendy C. Hamnett,
Director, 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. Amend Sec. [emsp14]721.5185 as follows:
a. Revise the section heading.
b. Revise paragraphs (a)(1) and (a)(2)(i).
c. Add paragraph (a)(2)(ii).
d. Revise paragraph (a)(2)(iii).
e. Remove paragraphs (a)(2)(iv), (a)(2)(v), and (a)(2)(vi).
f. Revise paragraph (b)(1).
The revisions and addition read as follows:
Sec. 721.5185 2-Propen-1-one, 1-(4-morpholinyl)-.
(a) * * *
(1) The chemical substance identified as 2-Propen-1-one, 1-(4-
morpholinyl)- (PMN P-95-169; CAS No. 5117-12-4) 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 after it has been completely reacted
(cured).
(2) * * *
(i) Protection in the workplace. Requirements as specified in Sec.
721.63 (a)(1), (a)(2)(i), (a)(2)(iv), (a)(3)(i), (a)(3)(ii), (a)(4),
(a)(6)(v), (b) (concentration set at 1.0 percent), and (c). Safety 4/4H
EVOH/PE laminate, Ansell Edmont Neoprene number 865, and Solvex Nitrile
Rubber number 275 gloves have been tested in accordance with the
American Society for Testing Materials (ASTM) F739 method and found by
EPA to satisfy the consent orders and Sec. 721.63(a)(2)(i)
requirements for dermal protection to 100 percent PMN substance. Gloves
and other dermal protection may not be used for a time period longer
than they are actually tested and must be replaced at the end of each
work shift. For additional dermal protection materials, a company must
submit all test data to the Agency and must receive written Agency
approval for each type of material tested prior to use of that material
as worker dermal protection. However, for the purposes of determining
the imperviousness of gloves, up to 1 year after the commencement of
commercial manufacture or import, the employer may use the method
described in Sec. 721.63(a)(3)(ii), thereafter, they must use the
method described in Sec. 721.63(a)(3)(i).
(ii) Hazard communication program. Requirements as specified in
Sec. 721.72 (a), (b), (c), (d), (e) (concentration set at 1.0
percent), (f), (g)(1)(iv), (g)(1)(vi), (g)(2)(v), and (g)(5).
(iii) Industrial, commercial, and consumer activities. Requirements
as specified in Sec. 721.80(a), (c), and (y)(1).
(b) * * *
(1) Recordkeeping. The following recordkeeping requirements are
applicable to manufacturers, importers, and processors of this chemical
substance as specified in Sec. 721.125(a) through (i).
* * * * *
[FR Doc. 2010-28006 Filed 11-4-10; 8:45 am]
BILLING CODE 6560-50-P