Proposed Significant New Use Rules on Certain Chemical Substances, 32508-32514 [E8-12862]
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examiner. Assuming that the IRS mails to D
a Letter 3569 with regard to this transfer, and
that D complies with the administrative
procedures set forth in this section, including
the exhaustion of all administrative remedies
available within the IRS, then D may file a
petition for declaratory judgment with the
Tax Court pursuant to section 7477.
Example 5. Transfers in controversy. On
April 16, 2007, D timely files a Form 709 on
which D reports gifts made in 2006 of
fractional interests in certain real property
and of interests in a family limited
partnership (FLP). However, although the
gifts are disclosed on the return, the return
does not contain information sufficient to
constitute adequate disclosure under
§ 301.6501(c)–1(e) or (f) for purposes of the
application of the statute of limitations on
assessment of gift tax with respect to the
reported gifts. The IRS conducts an
examination and concludes that the value of
both the interests in the real property and the
FLP interests on the date(s) of the transfers
are greater than the values reported on the
return. No gift tax deficiency will result from
the adjustments because D has a sufficient
amount of remaining applicable credit
amount under section 2505. However, D does
not agree with the adjustments. The IRS
sends a Preliminary Determination Letter to
D informing D of the proposed adjustments
in the value of the reported gifts. D, within
30 calendar days after the mailing date of the
letter, submits a written request for Appeals
consideration. The Appeals office and D are
unable to reach an agreement regarding the
value of any of the gifts. In the exercise of
its discretion, the IRS decides to resolve
currently only the value of the real property
interests, and to defer the resolution of the
value of the FLP interests. On May 28, 2009,
the Appeals office sends D a Letter 3569
addressing only the value of the gifts of
interests in the real property. Because none
of the gifts reported on the return filed on
April 16, 2007, were adequately disclosed for
purposes of § 301.6501(c)–1(e) or (f), the
period of limitations during which the IRS
may adjust the value of those gifts has not
begun to run. Accordingly, the Letter 3569 is
timely mailed. If D timely files a petition in
Tax Court pursuant to section 7477 with
regard to the value of the interests in the real
property, then, assuming the other
requirements of section 7477 are satisfied
with regard to those interests, the Tax Court’s
declaratory judgment, once it becomes final,
will determine the value of the gifts of the
interests in the real property. Because the IRS
has not yet put the gift tax value of the
interests in the FLP into controversy, the
procedure under section 7477 is not available
with regard to those gifts.
Par. 3. Section 301.7477–2 is added to
read as follows:
§ 301.7477–2
Effective date.
Section 301.7477–1 applies to civil
proceedings described in section 7477
filed in the United States Tax Court on
or after the date these regulations are
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published as final regulations in the
Federal Register.
Linda E. Stiff,
Deputy Commissioner for Services and
Enforcement.
[FR Doc. E8–12894 Filed 6–6–08; 8:45 am]
BILLING CODE 4830–01–P
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 721
[EPA–HQ–OPPT–2006–0898; FRL–8351–4]
RIN 2070–AB27
Proposed Significant New Use Rules
on Certain Chemical Substances
Environmental Protection
Agency (EPA).
ACTION: Proposed rule.
AGENCY:
SUMMARY: EPA is proposing significant
new use rules (SNURs) under section
5(a)(2) of the Toxic Substances Control
Act (TSCA) for two chemical substances
which were the subject of
premanufacture notices (PMNs). The
two substances are dodecandioic acid,
1, 12-dihydrazide (CAS No. 4080–98–2;
PMNs P–01–759 and P–05–555) and
thiophene, 2,5-dibromo-3-hexyl- (CAS
No. 116971–11–0; PMN P–07–283). This
action would require persons who
intend to manufacture, import, or
process either of these two 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 July 9, 2008.
ADDRESSES: Submit your comments,
identified by docket identification (ID)
number EPA–HQ–OPPT–2006–0898, 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–2006–0898.
The DCO is open from 8 a.m. to 4 p.m.,
Monday through Friday, excluding legal
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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–
2006–0898. 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 website 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. 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 docket index available
in regulations.gov. To access the
electronic docket, go to https://
www.regulations.gov, select ‘‘Advanced
Search,’’ then ‘‘Docket Search.’’ Insert
the docket ID number where indicated
and select the ‘‘Submit’’ button. Follow
the instructions on the regulations.gov
website to view the docket index or
access available documents. 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
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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
Federal 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
general information contact: Colby
Lintner, Regulatory Coordinator,
Environmental Assistance Division
(7408M), Office of Pollution Prevention
and Toxics, Environmental Protection
Agency, 1200 Pennsylvania Ave., NW.,
Washington, DC 20460–0001; telephone
number: (202) 554–1404; e-mail address:
TSCA-Hotline@epa.gov.
For technical information contact:
Tracey Pennington, 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:
pennington.tracey@epa.gov.
SUPPLEMENTARY INFORMATION:
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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
contained in this proposed rule.
Potentially affected entities may
include, but are not limited to:
Manufacturers, importers, or
processors of one or both subject
chemical substances (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
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40 CFR 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. Persons who import
any chemical substance governed by a
final SNUR are subject to the TSCA
section 13 (15 U.S.C. 2612) import
certification requirements and the
corresponding regulations at 19 CFR
12.118 through 12.127 and 19 CFR
127.28. Those persons must certify that
the shipment of the chemical substance
complies with all applicable rules and
orders under TSCA, including any
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 July 9, 2008 are subject to the
export notification provisions of TSCA
section 12(b) (15 U.S.C. 2611(b)) (see 40
CFR 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 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.
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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?
EPA is proposing significant new use
rules (SNURs) under section 5(a)(2) of
TSCA for two chemical substances
which were the subject of
premanufacture notices (PMNs). The
two substances are dodecandioic acid,
1, 12-dihydrazide (CAS No. 4080–98–2;
PMNs P–01–759 and P–05–555) and
thiophene, 2,5-dibromo-3-hexyl- (CAS
No. 116971–11–0; PMN P–07–283).
These SNURs would require persons
who intend to manufacture, import, or
process either of these two substances
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 September
19, 2007 (72 FR 53470) (FRL–8135–8),
EPA issued direct final SNURs on these
two substances in accordance with the
procedures at 40 CFR
721.170(d)(4)(i)(A). EPA received
notices of intent to submit adverse
comments on these SNURs. Therefore,
as required by 40 CFR
721.170(d)(4)(i)(B), on November 19,
2007 (72 FR 64951) (FRL–8340–8), EPA
withdrew the direct final SNURs on
these two substances and is now
proposing these SNURs. The record for
the direct final SNURs for these
substances was established as docket
EPA–HQ–OPPT–2006–0898. That
record includes information considered
by the Agency in developing the direct
final rules and the notices of intent to
submit adverse comments.
The rationale for this proposed rule as
well as requests for public comment on
specific issues is included in Unit IV.
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
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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). 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 significant
new use notice (SNUN) to EPA at least
90 days before they manufacture,
import, or process the chemical
substance for that use (15 U.S.C.
2604(a)(1)(B)). As described in unit II.C.,
the general SNUR provisions are found
at 40 CFR part 721, subpart A.
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C. Applicability of General Provisions
General provisions for SNURs appear
under 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 40 CFR
721.1(c), persons subject to these SNURs
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 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
significant new use activities described
in 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.
Persons who export or intend to
export a chemical substance identified
in a proposed or final SNUR are subject
to the export notification provisions of
TSCA section 12(b). The regulations that
interpret TSCA section 12(b) appear at
40 CFR part 707, subpart D. Persons
who import a chemical substance
identified in a final SNUR are subject to
the TSCA section 13 import certification
requirements, codified at 19 CFR 12.118
through 12.127 and 19 CFR 127.28.
Such persons must certify that the
shipment of the chemical substance
complies with all applicable rules and
orders under TSCA, including any
SNUR requirements. The EPA policy
statement in support of the import
certification appears at 40 CFR part 707,
subpart B.
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III. Substances Subject to this Rule
EPA is proposing to establish
significant new use and recordkeeping
requirements for two chemical
substances under 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).
• CAS number (if assigned for nonconfidential chemical identities).
• Basis for the SNUR.
• Toxicity concerns.
• Tests recommended by EPA to
provide sufficient information to
evaluate the chemical substance (see
Unit VI. for more information).
• CFR citation assigned in the
regulatory text section of this proposed
rule.
The specific activities designated as
significant new uses are listed in 40 CFR
part 721, subpart E.
PMN Numbers P–01–759 and P–05–555
Chemical name: Dodecandioic acid, 1,
12-dihydrazide.
CAS number: 4080–98–2.
Basis for action: The PMNs (submitted
by two different chemical
manufacturing companies) state that the
generic (non–confidential) uses of the
substance will be as a raw material for
coating and sealants and as a curing
agent, respectively. Based on the
molecular structure of the PMN
substance and test data on analogous
substances, EPA believes the PMN
substance may cause carcinogenicity,
developmental toxicity, and irritation to
mucous membranes. Also, based on test
data on the PMN substance, it may
cause dermal sensitization. As described
in the companies’ PMNs and
accompanying Material Safety Data
Sheets, workers will be warned that the
substance may cause dermal
sensitization and will wear gloves and
National Institute for Occupational
Safety and Health (NIOSH) approved
respirators with an assigned protection
factor (APF) of 50 or greater. Based on
this expectation that adequate hazard
communication and personal protective
equipment will be used, EPA believes
significant worker exposure is unlikely.
Further, consumer use is not expected.
EPA has determined, however, that
potential use of the substance without
workers wearing gloves and a respirator,
and without an appropriate hazard
communication program, may cause
serious human health effects.
Respirators must provide a NIOSH APF
of at least 50. The following NIOSHapproved respirators meet the minimum
requirement for § 721.63(a)(4): Air-
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purifying, tight-fitting full-face
respirator equipped with N100 (if oil
aerosols absent), R100, or P100 filters;
powered air-purifying respirator
equipped with a tight-fitting full
facepiece and High Efficiency
Particulate Air (HEPA) filters; supplied
air respirator operated in pressure
demand or continuous flow mode and
equipped with a tight-fitting full
facepiece. Because the substance is a
dermal sensitizer and irritates mucous
membranes, half–face respirators do not
provide adequate protection. Based on
this information, the PMN substance
meets the concern criteria at § 721.170
(b)(1)(i)(C), (b)(3)(i), and (b)(3)(ii).
Recommended testing: EPA has
determined that the results of a 90-day
oral toxicity test in rats (OPPTS
870.3100 test guideline) and a
mammalian erythrocyte micronucleus
test (OPPTS 870.5395 test guideline)
would help characterize the human
health effects of the PMN substance.
CFR citation: 40 CFR 721.10057.
PMN Number P–07–283
Chemical name: Thiophene, 2,5dibromo-3-hexyl-.
CAS number: 116971–11–0.
Basis for action: The PMN states that the
substance will be used as a reactive
intermediate monomer for use in
manufacturing a p-type organic
semiconductor polymer. The polymer
will be used in printed organic
electronics applications. Based on
structure activity relationship analyses
for thiophenes, EPA is concerned that
toxicity to aquatic organisms may occur
at concentrations above 1 part per
billion (ppb) of the PMN substance in
surface waters. At the production
volume stated for the company in the
PMN, releases of the PMN substance are
not expected to result in surface water
concentrations above 1 ppb. Therefore,
EPA has not determined that the
proposed manufacturing, processing, or
use of the substance, as described in the
PMN, may present an unreasonable risk.
EPA has determined, however, that
potential increased production or
importation volumes or other uses of the
substance resulting in surface water
concentrations above 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).
Recommended testing: EPA has
determined that the results of a fish
early-life stage toxicity test (OPPTS
850.1400 test guideline (public draft)); a
daphnid chronic toxicity test (OPPTS
850.1300 test guideline (public draft));
and an algal toxicity test, tiers I and II
(OPPTS 850.5400 test guideline (public
draft)) would help characterize the
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environmental effects of the PMN
substance. The fish and daphnid tests
should use flow-through conditions and
measured concentrations.
CFR citation: 40 CFR 721.10088.
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IV. Objectives and Rationale of the Rule
A. Rationale
During review of the PMNs submitted
for these two chemical substances, EPA
determined that one or more of the
criteria of concern established at 40 CFR
721.170 were met, as discussed in Unit
III.
1. Rationale for the proposed SNUR
for dodecandioic acid, 1, 12dihydrazide (CAS No. 4080–98–2). The
hazard communication terms of the
SNUR being proposed today for
dodecandioic acid, 1, 12-dihydrazide
(CAS No. 4080–98–2) differ from the
terms in the direct final SNUR, based on
submitted comments that clarified
existing uses of the substance. The
notice of intent to submit adverse
comment states that hazard
communication materials currently in
use for this substance in the
marketplace do not contain two of the
health hazard statements included in
the direct final SNUR. The two
statements are, ‘‘this substance may
cause cancer’’ and ‘‘this substance may
cause developmental toxicity.’’ As EPA
interprets its SNUR authority under
section 5(a)(2) of TSCA, if an activity is
already ongoing before EPA first
publishes a Federal Register notice of
intent to designate that activity as a
significant new use, then EPA may not
issue a SNUR designating that activity
as a significant ‘‘new’’ use. Therefore,
EPA is proposing a SNUR that would
not designate as a ‘‘significant new use’’
the failure to identify cancer and
developmental toxicity in workplace
hazard communication materials
accompanying this chemical substance
(under 40 CFR 721.72). However, for the
reasons described in this paragraph and
in the direct final rule preamble, the
Agency’s concerns for these toxic
endpoints remain. Therefore, the
Agency encourages companies to
voluntarily include these potential
health concerns in their hazard
communication materials for the
substance. The workplace personal
protective equipment requirements
(under 40 CFR 721.63) and other
requirements listed in the direct final
rule would remain unchanged in today’s
proposed SNUR. The Agency requests
comments on the approach being taken
in the proposed SNUR for this
substance.
2. Rationale for the proposed SNUR
for thiophene, 2,5-dibromo-3-hexyl-
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(CAS No. 116971–11–0). The Agency is
requesting comments on the proposed
SNUR for this substance as well as two
alternative approaches. A discussion of
the rationale behind each option and
specific issues on which the Agency is
requesting comment follows. EPA
requests that commenters making
specific recommendations include
supporting documentation where
appropriate.
i. Proposed SNUR - maximum surface
water concentration of 1 ppb from
manufacturing, processing, or use
activities and annual company
production limit of 500 kg. The terms of
the SNUR being proposed today for
thiophene, 2,5-dibromo-3-hexyl- (CAS
No. 116971–11–0) remain the same as in
the direct final SNUR. See proposed
§ 721.10088 (a)(2)(i) and (a)(2)(ii). EPA
is proposing to designate the surface
water release and production volume
limits as significant new uses for the
reasons stated in Unit V., including
concerns associated with potential
changes in the extent to which these
activities could increase the magnitude
and duration of exposure of human
beings or the environment to the
chemical substance. Inclusion of a
production volume limit gives the
Agency an opportunity to review the
substance again at a higher production
volume.
ii. Alternative A -maximum surface
water concentration of 1 ppb from
manufacture, processing, or use
activities up to an annual production
volume of 500 kg, and no release to
surface water at annual company
production volumes higher than 500 kg.
This option was suggested in the notice
of intent to submit adverse comment on
the direct final SNUR for this substance.
The commenter also stated that they
recognize the Agency’s concern for
water releases of the substance. While
this option would be protective of the
aquatic environment, the Agency
requests comment on whether industry
compliance would be impractical or
confusing.
iii. Alternative B - SNUR for no
release to surface water. If the substance
is not currently being released to water
during manufacturing, processing, or
use activities, the Agency could
consider finalizing a SNUR designating
any release to water during those
activities as a significant new use. This
option would be sufficiently protective
of the aquatic environment and is less
complicated than Alternative A. To
implement this option, EPA would need
to be satisfied that there are no ongoing
releases to water, taking into account 40
CFR 721.90 (a)(1), (b)(1), and (c)(1). EPA
solicits comment on whether there are
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ongoing releases to water during
manufacturing, processing, or use
activities.
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.
V. 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.
• 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 authorizes EPA to consider any
other relevant factors.
To determine what would constitute a
significant new use of the two chemical
substances that are the subject of this
proposed rule, EPA considered relevant
information about the toxicity of the
substances, likely human exposures and
environmental releases associated with
possible uses, and the four factors listed
in section 5(a)(2) of TSCA. In these
cases, EPA did not find that the use
scenarios described in the three PMNs
triggered the determinations set forth
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under section 5(e) of TSCA. EPA did,
however, believe that certain changes
from the use scenarios described in the
PMNs could result in increased
exposures, and constitute ‘‘significant
new uses.’’ These so-called ‘‘Non-5(e)
SNURs’’ (i.e., SNURs for chemicals that
are not regulated by a section 5(e)
Consent Order under § 721.160) are
promulgated pursuant to 40 CFR
721.170. EPA has determined that every
activity designated as a ‘‘significant new
use’’ in all the non-5(e) SNURs issued
under 40 CFR 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.
VI. Applicability of 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
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advance compliance under § 721.45(h),
the person would be considered to have
met the requirements of the final SNUR
for those activities.
VII. Test Data and Other Information
EPA recognizes that TSCA section 5
does not require developing any
particular test data before submission of
a SNUN. 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 (15 U.S.C. 2604(d); 40 CFR 721.25
and 720.50). However, upon review of
PMNs and SNUNs, the Agency has the
authority to require appropriate testing.
Unit III. lists recommended testing for
the two chemical substances that are the
subject of these proposed 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. Many
test guidelines are now available on the
Internet at https://www.epa.gov/opptsfrs/
home/guidelin.htm.
The recommended tests may not be
the only means of assessing the
potential toxicity, exposure, and risks of
the chemical substances regulated under
this rule. However, submitting SNUNs
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 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.
VIII. SNUN Submissions
EPA recommends that submitters
consult with the Agency prior to
submitting a SNUN to discuss what data
may be useful in evaluating a significant
new use. Discussions with the Agency
prior to notice submission can afford
ample time to conduct any tests that
might be helpful in evaluating risks
posed by the substance. According to 40
CFR 721.1(c), persons submitting a
SNUN must comply with the same
notice requirements and EPA regulatory
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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 mailed to the
Environmental Protection Agency,
OPPT Document Control Office
(7407M), 1200 Pennsylvania Ave., NW.,
Washington, DC 20460–0001.
Information must be submitted in the
form and manner set forth in EPA Form
No. 7710–25. This form is available
from the Environmental Assistance
Division (7408M), 1200 Pennsylvania
Ave., NW., Washington, DC 20460–0001
(see 40 CFR 721.25 and 720.40). Forms
and information are also available
electronically at https://www.epa.gov/
opptintr/newchems/pubs/
pmnforms.htm.
IX. Economic Analysis
EPA has evaluated the potential costs
of establishing SNUN requirements for
potential manufacturers, importers, and
processors of the chemical substances at
the time of the direct final rule. The
Agency’s complete economic analysis is
available in the public docket for the
direct final rule (EPA–HQ–OPPT–2006–
0898). The difference in hazard
communication requirements in the
direct final SNUR and this proposed
rule (i.e., removal of the requirement for
specific identification of cancer and
developmental toxicity endpoints in
workplace hazard communication
materials) could slightly reduce
estimated costs to regulated entities.
The difference in a production volume
trigger and type of release to water
restriction in the direct final SNUR and
this proposed rule will not impact the
estimated costs to regulated entities.
X. Statutory and Executive Order
Reviews
A. Executive Order 12866
Under Executive Order 12866,
entitled Regulatory Planning and
Review (58 FR 51735, October 4, 1993),
the Office of Management and Budget
(OMB) has determined that this
proposed rule is not a ‘‘significant
regulatory action’’ because it does not
meet the criteria in section 3(f) of the
Executive order.
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
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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.
The information collection
requirements related to this action have
already been approved by OMB
pursuant to the PRA under OMB control
number 2070–0012 (EPA ICR No. 574).
This action does 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 submission. 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 these
SNURs would not have a significant
adverse economic impact on a
substantial number of small entities.
The rationale supporting this
conclusion is as follows. A SNUR
applies to any person (including small
or large entities) who intends to engage
in any activity described in the
proposed rule as a ‘‘significant new
use.’’ By definition of the word ‘‘new,’’
and based on all information currently
available to EPA, it appears that no
small or large entities presently engage
in such activity. Since a SNUR only
requires that any person who intends to
engage in such activity in the future
must first notify EPA by submitting a
SNUN, no economic impact would even
occur until someone decides to engage
in those activities. Although some small
entities may decide to conduct such
activities 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 1,000 SNURs,
the Agency receives on average only 10
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32513
notices per year. Of those SNUNs
submitted, none appear to be from small
entities in response to any SNUR. In
addition, the estimated reporting cost
for submission of a SNUN (see Unit IX.)
are minimal regardless of the size of the
firm. Therefore, EPA believes that the
potential economic impacts of
complying with these SNURs are not
expected to be significant or adversely
impact a substantial number of small
entities. In a SNUR that published on
June 2, 1997 (62 FR 29684) (FRL–5597–
1), the Agency presented its general
determination that 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.
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.
D. Unfunded Mandates Reform Act
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.
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
rulemaking. As such, EPA has
determined that this regulatory action
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) (Public Law 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 6, 2000), do not apply
to this proposed rule.
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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.
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).
K. Executive Order 12988
In issuing this proposed rule, EPA has
taken the necessary steps to eliminate
drafting errors and ambiguity, minimize
potential litigation, and provide a clear
legal standard for affected conduct, as
required by section 3 of Executive Order
12988, entitled Civil Justice Reform (61
FR 4729, February 7, 1996).
List of Subjects in 40 CFR Part 721
Environmental protection, Chemicals,
Hazardous substances, Reporting and
recordkeeping requirements.
Dated: May 30, 2008.
Charles M. Auer,
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
would continue to read as follows:
Authority: 15 U.S.C. 2604, 2607, and
2625(c).
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2. By adding new § 721.10057 to
subpart E to read as follows:
§ 721.10057 Dodecanedioic acid, 1, 12dihydrazide.
(a) Chemical substance and
significant new uses subject to reporting.
(1) The chemical substance identified as
dodecanedioic acid, 1, 12-dihydrazide
(PMNs P–01–759 and P–05–555; CAS
No. 4080–98–2) 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)(5),
(a)(6)(i), (a)(6)(ii), (b), and (c).
Respirators must provide a National
Institute for Occupational Safety and
Health (NIOSH) assigned protection
factor (APF) of at least 50. The following
NIOSH-approved respirators meet the
minimum requirement for
§ 721.63(a)(4): Air-purifying, tight-fitting
full-face respirator equipped with N100
(if oil aerosols absent), R100, or P100
filters; powered air-purifying respirator
equipped with a tight-fitting full
facepiece and High Efficiency
Particulate Air (HEPA) filters; supplied
air respirator operated in pressure
demand or continuous flow mode and
equipped with a tight-fitting full
facepiece. Because the substance is a
dermal sensitizer and irritates mucous
membranes, half-face respirators do not
provide adequate protection.
(ii) Hazard communication program.
Requirements as specified in § 721.72
(a), (b), (c), (d), (e) (concentration set at
0.1 percent), (f), (g)(1)(i), and (g)(2)(i).
(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), (f), (g), and (h) 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. By adding new § 721.10088 to
subpart E to read as follows:
jlentini on PROD1PC65 with PROPOSALS
§ 721.10088
hexyl-.
Thiophene, 2,5-dibromo-3-
(a) Chemical substance and
significant new uses subject to reporting.
(1) The chemical substance identified as
thiophene, 2,5-dibromo-3-hexyl- (PMN
P–07–283; CAS No. 116971–11–0) is
subject to reporting under this section
for the significant new uses described in
paragraph (a)(2) of this section.
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[GSAR Case 2007–G501; Docket 2008–0007;
Sequence 1]
G501. Follow the instructions provided
to complete the ‘‘Public Comment and
Submission Form’’. Please include your
name, company name (if any), and
‘‘GSAR Case 2007–G501’’ on your
attached document.
• Fax: 202–501–4067.
• Mail: General Services
Administration, Regulatory Secretariat
(VPR), 1800 F Street, NW, Room 4041,
ATTN: Laurieann Duarte, Washington,
DC 20405.
Instructions: Please submit comments
only and cite GSAR Case 2007–G501 in
all correspondence related to this case.
All comments received will be posted
without change to https://
www.regulations.gov, including any
personal and/or business confidential
information provided.
FOR FURTHER INFORMATION CONTACT: For
clarification of content, contact Ms.
Meredith Murphy at (202) 208–6925, or
by e-mail at meredith.murphy@gsa.gov.
For information pertaining to the status
or publication schedules, contact the
Regulatory Secretariat (VPR), Room
4041, GS Building, Washington, DC
20405, (202) 501–4755. Please cite
GSAR Case 2007–G501.
SUPPLEMENTARY INFORMATION:
RIN 3090–AI49
A. Background
General Services Acquisition
Regulation; GSAR Case 2007–
G501;Protests, Disputes, and Appeals
The General Services Administration
(GSA) proposes to amend the General
Services Administration Acquisition
Regulation (GSAR) to update the text
addressing protests, disputes, and
appeals. This rule is a result of the
General Services Administration
Acquisition Manual (GSAM) Rewrite
initiative undertaken by GSA to revise
the GSAM to maintain consistency with
the FAR and implement streamlined
and innovative acquisition procedures
that contractors, offerors, and GSA
contracting personnel can utilize when
entering into and administering
contractual relationships. The GSAM
incorporates the General Services
Administration Acquisition Regulation
(GSAR) as well as internal agency
acquisition policy.
GSA will rewrite each part of the
GSAR and GSAM, and as each GSAR
part is rewritten, will publish it in the
Federal Register.
This rule covers the rewrite of GSAR
Part 533, Protests, Disputes, and
Appeals. GSAR Part 533 includes two
subparts. GSAR Subpart 533.1, Protests,
included only the prescription for a
GSA-unique clause, 552.233–70,
Protests Filed Directly with the General
Services Administration. However, GSA
proposes to delete this clause in its
entirety because it repeated much of the
FAR clause, and the remaining
(2) The significant new uses are:
(i) Industrial, commercial, and
consumer activities. Requirements as
specified in § 721.80(s) (500 kilograms).
(ii) Release to water. Requirements as
specified in § 721.90 (a)(4), (b)(4), and
(c)(4) (N=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 this substance.
(2) Limitations or revocation of
certain notification requirements. The
provisions of § 721.185 apply to this
section.
[FR Doc. E8–12862 Filed 6–6–08; 8:45 am]
BILLING CODE 6560–50–S
GENERAL SERVICES
ADMINISTRATION
48 CFR Parts 533 and 552
Office of the Chief Acquisition
Officer, General Services
Administration (GSA).
ACTION: Proposed rule.
AGENCY:
SUMMARY: The General Services
Administration (GSA) is proposing to
amend the General Services Acquisition
Regulation (GSAR) to update language
pertaining to protests, disputes, and
appeals. This project is part of the
GSAM Rewrite Project, in which all
parts of the regulation are being
reviewed and updated to include new
statutes, legislation, and policies.
DATES: Interested parties should submit
written comments to the Regulatory
Secretariat on or before August 8, 2008
to be considered in the formulation of
a final rule.
ADDRESSES: Submit comments
identified by GSAR Case 2007–G501 by
any of the following methods:
• Regulations.gov: https://
www.regulations.gov.
Submit comments via the Federal
eRulemaking portal by inputting ‘‘GSAR
Case 2007–G501’’ under the heading
‘‘Comment or Submission’’. Select the
link ‘‘Send a Comment or Submission’’
that corresponds with GSAR Case 2007–
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Agencies
[Federal Register Volume 73, Number 111 (Monday, June 9, 2008)]
[Proposed Rules]
[Pages 32508-32514]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-12862]
=======================================================================
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 721
[EPA-HQ-OPPT-2006-0898; FRL-8351-4]
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
section 5(a)(2) of the Toxic Substances Control Act (TSCA) for two
chemical substances which were the subject of premanufacture notices
(PMNs). The two substances are dodecandioic acid, 1, 12-dihydrazide
(CAS No. 4080-98-2; PMNs P-01-759 and P-05-555) and thiophene, 2,5-
dibromo-3-hexyl- (CAS No. 116971-11-0; PMN P-07-283). This action would
require persons who intend to manufacture, import, or process either of
these two 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 July 9, 2008.
ADDRESSES: Submit your comments, identified by docket identification
(ID) number EPA-HQ-OPPT-2006-0898, 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-2006-0898. 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-
2006-0898. 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 website 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. 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 docket index
available in regulations.gov. To access the electronic docket, go to
https://www.regulations.gov, select ``Advanced Search,'' then ``Docket
Search.'' Insert the docket ID number where indicated and select the
``Submit'' button. Follow the instructions on the regulations.gov
website to view the docket index or access available documents.
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
[[Page 32509]]
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 Federal 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 general information contact: Colby
Lintner, Regulatory Coordinator, Environmental Assistance Division
(7408M), Office of Pollution Prevention and Toxics, Environmental
Protection Agency, 1200 Pennsylvania Ave., NW., Washington, DC 20460-
0001; telephone number: (202) 554-1404; e-mail address: TSCA-
Hotline@epa.gov.
For technical information contact: Tracey Pennington, 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: pennington.tracey@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 contained in this
proposed rule. Potentially affected entities may include, but are not
limited to:
Manufacturers, importers, or processors of one or both subject
chemical substances (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 40 CFR 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. Persons
who import any chemical substance governed by a final SNUR are subject
to the TSCA section 13 (15 U.S.C. 2612) import certification
requirements and the corresponding regulations at 19 CFR 12.118 through
12.127 and 19 CFR 127.28. Those persons must certify that the shipment
of the chemical substance complies with all applicable rules and orders
under TSCA, including any 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 July 9,
2008 are subject to the export notification provisions of TSCA section
12(b) (15 U.S.C. 2611(b)) (see 40 CFR 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
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?
EPA is proposing significant new use rules (SNURs) under section
5(a)(2) of TSCA for two chemical substances which were the subject of
premanufacture notices (PMNs). The two substances are dodecandioic
acid, 1, 12-dihydrazide (CAS No. 4080-98-2; PMNs P-01-759 and P-05-555)
and thiophene, 2,5-dibromo-3-hexyl- (CAS No. 116971-11-0; PMN P-07-
283). These SNURs would require persons who intend to manufacture,
import, or process either of these two substances 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 September 19, 2007 (72 FR 53470) (FRL-
8135-8), EPA issued direct final SNURs on these two substances in
accordance with the procedures at 40 CFR 721.170(d)(4)(i)(A). EPA
received notices of intent to submit adverse comments on these SNURs.
Therefore, as required by 40 CFR 721.170(d)(4)(i)(B), on November 19,
2007 (72 FR 64951) (FRL-8340-8), EPA withdrew the direct final SNURs on
these two substances and is now proposing these SNURs. The record for
the direct final SNURs for these substances was established as docket
EPA-HQ-OPPT-2006-0898. That record includes information considered by
the Agency in developing the direct final rules and the notices of
intent to submit adverse comments.
The rationale for this proposed rule as well as requests for public
comment on specific issues is included in Unit IV.
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
[[Page 32510]]
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). 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 significant new
use notice (SNUN) to EPA at least 90 days before they manufacture,
import, or process the chemical substance for that use (15 U.S.C.
2604(a)(1)(B)). As described in unit II.C., the general SNUR provisions
are found at 40 CFR part 721, subpart A.
C. Applicability of General Provisions
General provisions for SNURs appear under 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 40 CFR 721.1(c), persons subject to these SNURs 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 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 significant new
use activities described in 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.
Persons who export or intend to export a chemical substance
identified in a proposed or final SNUR are subject to the export
notification provisions of TSCA section 12(b). The regulations that
interpret TSCA section 12(b) appear at 40 CFR part 707, subpart D.
Persons who import a chemical substance identified in a final SNUR are
subject to the TSCA section 13 import certification requirements,
codified at 19 CFR 12.118 through 12.127 and 19 CFR 127.28. Such
persons must certify that the shipment of the chemical substance
complies with all applicable rules and orders under TSCA, including any
SNUR requirements. The EPA policy statement in support of the import
certification appears at 40 CFR part 707, subpart B.
III. Substances Subject to this Rule
EPA is proposing to establish significant new use and recordkeeping
requirements for two chemical substances under 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).
CAS number (if assigned for non-confidential chemical
identities).
Basis for the SNUR.
Toxicity concerns.
Tests recommended by EPA to provide sufficient information
to evaluate the chemical substance (see Unit VI. for more information).
CFR citation assigned in the regulatory text section of
this proposed rule.
The specific activities designated as significant new uses are
listed in 40 CFR part 721, subpart E.
PMN Numbers P-01-759 and P-05-555
Chemical name: Dodecandioic acid, 1, 12-dihydrazide.
CAS number: 4080-98-2.
Basis for action: The PMNs (submitted by two different chemical
manufacturing companies) state that the generic (non-confidential) uses
of the substance will be as a raw material for coating and sealants and
as a curing agent, respectively. Based on the molecular structure of
the PMN substance and test data on analogous substances, EPA believes
the PMN substance may cause carcinogenicity, developmental toxicity,
and irritation to mucous membranes. Also, based on test data on the PMN
substance, it may cause dermal sensitization. As described in the
companies' PMNs and accompanying Material Safety Data Sheets, workers
will be warned that the substance may cause dermal sensitization and
will wear gloves and National Institute for Occupational Safety and
Health (NIOSH) approved respirators with an assigned protection factor
(APF) of 50 or greater. Based on this expectation that adequate hazard
communication and personal protective equipment will be used, EPA
believes significant worker exposure is unlikely. Further, consumer use
is not expected. EPA has determined, however, that potential use of the
substance without workers wearing gloves and a respirator, and without
an appropriate hazard communication program, may cause serious human
health effects. Respirators must provide a NIOSH APF of at least 50.
The following NIOSH-approved respirators meet the minimum requirement
for Sec. 721.63(a)(4): Air-purifying, tight-fitting full-face
respirator equipped with N100 (if oil aerosols absent), R100, or P100
filters; powered air-purifying respirator equipped with a tight-fitting
full facepiece and High Efficiency Particulate Air (HEPA) filters;
supplied air respirator operated in pressure demand or continuous flow
mode and equipped with a tight-fitting full facepiece. Because the
substance is a dermal sensitizer and irritates mucous membranes, half-
face respirators do not provide adequate protection. Based on this
information, the PMN substance meets the concern criteria at Sec.
721.170 (b)(1)(i)(C), (b)(3)(i), and (b)(3)(ii).
Recommended testing: EPA has determined that the results of a 90-day
oral toxicity test in rats (OPPTS 870.3100 test guideline) and a
mammalian erythrocyte micronucleus test (OPPTS 870.5395 test guideline)
would help characterize the human health effects of the PMN substance.
CFR citation: 40 CFR 721.10057.
PMN Number P-07-283
Chemical name: Thiophene, 2,5-dibromo-3-hexyl-.
CAS number: 116971-11-0.
Basis for action: The PMN states that the substance will be used as a
reactive intermediate monomer for use in manufacturing a p-type organic
semiconductor polymer. The polymer will be used in printed organic
electronics applications. Based on structure activity relationship
analyses for thiophenes, EPA is concerned that toxicity to aquatic
organisms may occur at concentrations above 1 part per billion (ppb) of
the PMN substance in surface waters. At the production volume stated
for the company in the PMN, releases of the PMN substance are not
expected to result in surface water concentrations above 1 ppb.
Therefore, EPA has not determined that the proposed manufacturing,
processing, or use of the substance, as described in the PMN, may
present an unreasonable risk. EPA has determined, however, that
potential increased production or importation volumes or other uses of
the substance resulting in surface water concentrations above 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
early-life stage toxicity test (OPPTS 850.1400 test guideline (public
draft)); a daphnid chronic toxicity test (OPPTS 850.1300 test guideline
(public draft)); and an algal toxicity test, tiers I and II (OPPTS
850.5400 test guideline (public draft)) would help characterize the
[[Page 32511]]
environmental effects of the PMN substance. The fish and daphnid tests
should use flow-through conditions and measured concentrations.
CFR citation: 40 CFR 721.10088.
IV. Objectives and Rationale of the Rule
A. Rationale
During review of the PMNs submitted for these two chemical
substances, EPA determined that one or more of the criteria of concern
established at 40 CFR 721.170 were met, as discussed in Unit III.
1. Rationale for the proposed SNUR for dodecandioic acid, 1, 12-
dihydrazide (CAS No. 4080-98-2). The hazard communication terms of the
SNUR being proposed today for dodecandioic acid, 1, 12-dihydrazide (CAS
No. 4080-98-2) differ from the terms in the direct final SNUR, based on
submitted comments that clarified existing uses of the substance. The
notice of intent to submit adverse comment states that hazard
communication materials currently in use for this substance in the
marketplace do not contain two of the health hazard statements included
in the direct final SNUR. The two statements are, ``this substance may
cause cancer'' and ``this substance may cause developmental toxicity.''
As EPA interprets its SNUR authority under section 5(a)(2) of TSCA, if
an activity is already ongoing before EPA first publishes a Federal
Register notice of intent to designate that activity as a significant
new use, then EPA may not issue a SNUR designating that activity as a
significant ``new'' use. Therefore, EPA is proposing a SNUR that would
not designate as a ``significant new use'' the failure to identify
cancer and developmental toxicity in workplace hazard communication
materials accompanying this chemical substance (under 40 CFR 721.72).
However, for the reasons described in this paragraph and in the direct
final rule preamble, the Agency's concerns for these toxic endpoints
remain. Therefore, the Agency encourages companies to voluntarily
include these potential health concerns in their hazard communication
materials for the substance. The workplace personal protective
equipment requirements (under 40 CFR 721.63) and other requirements
listed in the direct final rule would remain unchanged in today's
proposed SNUR. The Agency requests comments on the approach being taken
in the proposed SNUR for this substance.
2. Rationale for the proposed SNUR for thiophene, 2,5-dibromo-3-
hexyl- (CAS No. 116971-11-0). The Agency is requesting comments on the
proposed SNUR for this substance as well as two alternative approaches.
A discussion of the rationale behind each option and specific issues on
which the Agency is requesting comment follows. EPA requests that
commenters making specific recommendations include supporting
documentation where appropriate.
i. Proposed SNUR - maximum surface water concentration of 1 ppb
from manufacturing, processing, or use activities and annual company
production limit of 500 kg. The terms of the SNUR being proposed today
for thiophene, 2,5-dibromo-3-hexyl- (CAS No. 116971-11-0) remain the
same as in the direct final SNUR. See proposed Sec. 721.10088
(a)(2)(i) and (a)(2)(ii). EPA is proposing to designate the surface
water release and production volume limits as significant new uses for
the reasons stated in Unit V., including concerns associated with
potential changes in the extent to which these activities could
increase the magnitude and duration of exposure of human beings or the
environment to the chemical substance. Inclusion of a production volume
limit gives the Agency an opportunity to review the substance again at
a higher production volume.
ii. Alternative A -maximum surface water concentration of 1 ppb
from manufacture, processing, or use activities up to an annual
production volume of 500 kg, and no release to surface water at annual
company production volumes higher than 500 kg. This option was
suggested in the notice of intent to submit adverse comment on the
direct final SNUR for this substance. The commenter also stated that
they recognize the Agency's concern for water releases of the
substance. While this option would be protective of the aquatic
environment, the Agency requests comment on whether industry compliance
would be impractical or confusing.
iii. Alternative B - SNUR for no release to surface water. If the
substance is not currently being released to water during
manufacturing, processing, or use activities, the Agency could consider
finalizing a SNUR designating any release to water during those
activities as a significant new use. This option would be sufficiently
protective of the aquatic environment and is less complicated than
Alternative A. To implement this option, EPA would need to be satisfied
that there are no ongoing releases to water, taking into account 40 CFR
721.90 (a)(1), (b)(1), and (c)(1). EPA solicits comment on whether
there are ongoing releases to water during manufacturing, processing,
or use activities.
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.
V. 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.
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 authorizes EPA to consider any other relevant factors.
To determine what would constitute a significant new use of the two
chemical substances that are the subject of this proposed rule, EPA
considered relevant information about the toxicity of the substances,
likely human exposures and environmental releases associated with
possible uses, and the four factors listed in section 5(a)(2) of TSCA.
In these cases, EPA did not find that the use scenarios described in
the three PMNs triggered the determinations set forth
[[Page 32512]]
under section 5(e) of TSCA. EPA did, however, believe that certain
changes from the use scenarios described in the PMNs could result in
increased exposures, and constitute ``significant new uses.'' These so-
called ``Non-5(e) SNURs'' (i.e., SNURs for chemicals that are not
regulated by a section 5(e) Consent Order under Sec. 721.160) are
promulgated pursuant to 40 CFR 721.170. EPA has determined that every
activity designated as a ``significant new use'' in all the non-5(e)
SNURs issued under 40 CFR 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.
VI. Applicability of 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.
VII. Test Data and Other Information
EPA recognizes that TSCA section 5 does not require developing any
particular test data before submission of a SNUN. 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 (15 U.S.C.
2604(d); 40 CFR 721.25 and 720.50). However, upon review of PMNs and
SNUNs, the Agency has the authority to require appropriate testing.
Unit III. lists recommended testing for the two chemical substances
that are the subject of these proposed 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. Many test guidelines are now available on the
Internet at https://www.epa.gov/opptsfrs/home/guidelin.htm.
The recommended tests may not be the only means of assessing the
potential toxicity, exposure, and risks of the chemical substances
regulated under this rule. However, submitting SNUNs 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 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.
VIII. SNUN Submissions
EPA recommends that submitters consult with the Agency prior to
submitting a SNUN to discuss what data may be useful in evaluating a
significant new use. Discussions with the Agency prior to notice
submission can afford ample time to conduct any tests that might be
helpful in evaluating risks posed by the substance. According to 40 CFR
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 40 CFR 720.50.
SNUNs must be mailed to the Environmental Protection Agency, OPPT
Document Control Office (7407M), 1200 Pennsylvania Ave., NW.,
Washington, DC 20460-0001. Information must be submitted in the form
and manner set forth in EPA Form No. 7710-25. This form is available
from the Environmental Assistance Division (7408M), 1200 Pennsylvania
Ave., NW., Washington, DC 20460-0001 (see 40 CFR 721.25 and 720.40).
Forms and information are also available electronically at https://
www.epa.gov/opptintr/newchems/pubs/pmnforms.htm.
IX. Economic Analysis
EPA has evaluated the potential costs of establishing SNUN
requirements for potential manufacturers, importers, and processors of
the chemical substances at the time of the direct final rule. The
Agency's complete economic analysis is available in the public docket
for the direct final rule (EPA-HQ-OPPT-2006-0898). The difference in
hazard communication requirements in the direct final SNUR and this
proposed rule (i.e., removal of the requirement for specific
identification of cancer and developmental toxicity endpoints in
workplace hazard communication materials) could slightly reduce
estimated costs to regulated entities. The difference in a production
volume trigger and type of release to water restriction in the direct
final SNUR and this proposed rule will not impact the estimated costs
to regulated entities.
X. Statutory and Executive Order Reviews
A. Executive Order 12866
Under Executive Order 12866, entitled Regulatory Planning and
Review (58 FR 51735, October 4, 1993), the Office of Management and
Budget (OMB) has determined that this proposed rule is not a
``significant regulatory action'' because it does not meet the criteria
in section 3(f) of the Executive order.
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
[[Page 32513]]
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.
The information collection requirements related to this action have
already been approved by OMB pursuant to the PRA under OMB control
number 2070-0012 (EPA ICR No. 574). This action does 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 submission. 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 these SNURs would not have a significant adverse economic impact on
a substantial number of small entities. The rationale supporting this
conclusion is as follows. A SNUR applies to any person (including small
or large entities) who intends to engage in any activity described in
the proposed rule as a ``significant new use.'' By definition of the
word ``new,'' and based on all information currently available to EPA,
it appears that no small or large entities presently engage in such
activity. Since a SNUR only requires that any person who intends to
engage in such activity in the future must first notify EPA by
submitting a SNUN, no economic impact would even occur until someone
decides to engage in those activities. Although some small entities may
decide to conduct such activities 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 1,000 SNURs, the
Agency receives on average only 10 notices per year. Of those SNUNs
submitted, none appear to be from small entities in response to any
SNUR. In addition, the estimated reporting cost for submission of a
SNUN (see Unit IX.) are minimal regardless of the size of the firm.
Therefore, EPA believes that the potential economic impacts of
complying with these SNURs are not expected to be significant or
adversely impact a substantial number of small entities. In a SNUR that
published on June 2, 1997 (62 FR 29684) (FRL-5597-1), the Agency
presented its general determination that 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
rulemaking. As such, EPA has determined that this regulatory action
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) (Public Law 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 6,
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 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.
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).
K. Executive Order 12988
In issuing this proposed rule, EPA has taken the necessary steps to
eliminate drafting errors and ambiguity, minimize potential litigation,
and provide a clear legal standard for affected conduct, as required by
section 3 of Executive Order 12988, entitled Civil Justice Reform (61
FR 4729, February 7, 1996).
List of Subjects in 40 CFR Part 721
Environmental protection, Chemicals, Hazardous substances,
Reporting and recordkeeping requirements.
Dated: May 30, 2008.
Charles M. Auer,
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 would continue to read as
follows:
Authority: 15 U.S.C. 2604, 2607, and 2625(c).
[[Page 32514]]
2. By adding new Sec. 721.10057 to subpart E to read as follows:
Sec. 721.10057 Dodecanedioic acid, 1, 12-dihydrazide.
(a) Chemical substance and significant new uses subject to
reporting. (1) The chemical substance identified as dodecanedioic acid,
1, 12-dihydrazide (PMNs P-01-759 and P-05-555; CAS No. 4080-98-2) 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)(5), (a)(6)(i),
(a)(6)(ii), (b), and (c). Respirators must provide a National Institute
for Occupational Safety and Health (NIOSH) assigned protection factor
(APF) of at least 50. The following NIOSH-approved respirators meet the
minimum requirement for Sec. 721.63(a)(4): Air-purifying, tight-
fitting full-face respirator equipped with N100 (if oil aerosols
absent), R100, or P100 filters; powered air-purifying respirator
equipped with a tight-fitting full facepiece and High Efficiency
Particulate Air (HEPA) filters; supplied air respirator operated in
pressure demand or continuous flow mode and equipped with a tight-
fitting full facepiece. Because the substance is a dermal sensitizer
and irritates mucous membranes, half-face respirators do not provide
adequate protection.
(ii) Hazard communication program. Requirements as specified in
Sec. 721.72 (a), (b), (c), (d), (e) (concentration set at 0.1
percent), (f), (g)(1)(i), and (g)(2)(i).
(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), (f), (g), and (h) 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. By adding new Sec. 721.10088 to subpart E to read as follows:
Sec. 721.10088 Thiophene, 2,5-dibromo-3-hexyl-.
(a) Chemical substance and significant new uses subject to
reporting. (1) The chemical substance identified as thiophene, 2,5-
dibromo-3-hexyl- (PMN P-07-283; CAS No. 116971-11-0) 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(s) (500 kilograms).
(ii) Release to water. Requirements as specified in Sec. 721.90
(a)(4), (b)(4), and (c)(4) (N=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 this substance.
(2) Limitations or revocation of certain notification requirements.
The provisions of Sec. 721.185 apply to this section.
[FR Doc. E8-12862 Filed 6-6-08; 8:45 am]
BILLING CODE 6560-50-S