Certain New Chemicals; Receipt and Status Information, 71688-71693 [2010-29674]
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Federal Register / Vol. 75, No. 226 / Wednesday, November 24, 2010 / Notices
below, describes the nature of the
information collection and its estimated
burden and cost.
DATES: Additional comments may be
submitted on or before December 27,
2010.
ADDRESSES: Submit your comments,
referencing Docket ID No. EPA–HQ–
OAR–2010–0410, to (1) EPA online
using https://www.regulations.gov (our
preferred method), or by mail to: EPA
Docket Center, Environmental
Protection Agency, Air and Radiation
Docket, Mail Code 28221T, 1200
Pennsylvania Ave., NW., Washington,
DC 20460, and (2) OMB by mail to:
Office of Information and Regulatory
Affairs, Office of Management and
Budget (OMB), Attention: Desk Officer
for EPA, 725 17th Street, NW.,
Washington, DC 20503.
FOR FURTHER INFORMATION CONTACT:
Jeremy Arling, Office of Air and
Radiation, Stratospheric Protection
Division (6205J), Environmental
Protection Agency, 1200 Pennsylvania
Ave., NW., Washington, DC 20460;
telephone number: 202–343–9055; fax
number: 202–343–2362; e-mail address:
arling.jeremy@epa.gov.
SUPPLEMENTARY INFORMATION: EPA has
submitted the following ICR to OMB for
review and approval according to the
procedures prescribed in 5 CFR 1320.12.
On July 7, 2010 (75 FR 39012), EPA
sought comments on this ICR pursuant
to 5 CFR 1320.8(d). EPA received no
comments. Any additional comments on
this ICR should be submitted to EPA
and OMB within 30 days of this notice.
EPA has established a public docket
for this ICR under Docket ID No. EPA–
OAR–HQ–2010–0410, which is
available for online viewing at https://
www.regulations.gov, or in person
viewing at the Air and Radiation Docket
in the EPA Docket Center (EPA/DC),
EPA West, Room 3334, 1301
Constitution Ave., NW., Washington,
DC. The EPA/DC Public Reading Room
is open from 8 a.m. to 4:30 p.m.,
Monday through Friday, excluding legal
holidays. The telephone number for the
Reading Room is 202–566–1744, and the
telephone number for the Air and
Radiation Docket is 202–566–1742.
Use EPA’s electronic docket and
comment system at https://
www.regulations.gov, to submit or view
public comments, access the index
listing of the contents of the docket, and
to access those documents in the docket
that are available electronically. Once in
the system, select ‘‘docket search,’’ then
key in the docket ID number identified
above. Please note that EPA’s policy is
that public comments, whether
submitted electronically or in paper,
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15:30 Nov 23, 2010
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will be made available for public
viewing at https://www.regulations.gov
as EPA receives them and without
change, unless the comment contains
copyrighted material, confidential
business information (CBI), or other
information whose public disclosure is
restricted by statute. For further
information about the electronic docket,
go to https://www.regulations.gov.
Title: Nomination Application for the
U.S. EPA Montreal Protocol Awards
ICR numbers: EPA ICR No. 2389.01,
OMB Control No. 2060–NEW.
ICR Status: This ICR is for a new
information collection activity. An
Agency may not conduct or sponsor,
and a person is not required to respond
to, a collection of information, unless it
displays a currently valid OMB control
number. The OMB control numbers for
EPA’s regulations in title 40 of the CFR,
after appearing in the Federal Register
when approved, are listed in 40 CFR
part 9, are displayed either by
publication in the Federal Register or
by other appropriate means, such as on
the related collection instrument or
form, if applicable. The display of OMB
control numbers in certain EPA
regulations is consolidated in 40 CFR
part 9.
Abstract: The U.S. Environmental
Protection Agency (EPA) Stratospheric
Protection Division established the U.S.
EPA Montreal Protocol Award (USMPA)
program in 1990 to recognize
outstanding contributions to the
protection of the Earth’s stratospheric
ozone layer. It is named after the
international treaty that aims to reverse
erosion of the ozone layer by replacing
and/or phasing out the production of
ozone-depleting substances (ODS).
Since 1990, EPA has presented more
than 500 awards to outstanding
individuals, teams, companies,
organizations, and government
institutions in 54 countries. Awards are
particularly prestigious because
nominees compete globally against the
accomplishments of many other
potential awardees, and recipients are
selected by previous awardees and EPA.
Participation in the program requires
applicants (called nominees or
nominators) to complete a nomination
form that details the project or activity
they believe is worthy of the USMPA
award. EPA seeks nominations for the
following accomplishments: Originality
and public purpose; leadership and
corporate responsibility; global
perspective and implication; actual
elimination of ozone-depleting
substance emissions; success in
eliminating substances that deplete the
ozone layer and contribute to climate
change or in transitioning to alternatives
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with reduced environmental impact; or
leadership in improving awareness of
the harmful health effects of
overexposure to ultraviolet radiation.
Burden Statement: The annual public
reporting and recordkeeping burden for
this collection of information is
estimated to average less than three
hours per response. Burden means the
total time, effort, or financial resources
expended by persons to generate,
maintain, retain, or disclose or provide
information to or for a Federal agency.
This includes the time needed to review
instructions; develop, acquire, install,
and utilize technology and systems for
the purposes of collecting, validating,
and verifying information, processing
and maintaining information, and
disclosing and providing information;
adjust the existing ways to comply with
any previously applicable instructions
and requirements which have
subsequently changed; train personnel
to be able to respond to a collection of
information; search data sources;
complete and review the collection of
information; and transmit or otherwise
disclose the information.
Respondents/Affected Entities:
Entities potentially affected by this
action include those working in public
administration; chemical
manufacturing; professional, scientific
and technical services; voluntary health
organizations; environment,
conservation and wildlife organizations;
business associations; and professional
organizations
Estimated Number of Respondents:
25.
Frequency of Response: Annually,
occasionally.
Estimated Total Annual Hour Burden:
63.
Estimated Total Annual Cost: $2,080,
which includes no annualized capital or
O&M costs.
Dated: November 18, 2010.
John Moses,
Director, Collection Strategies Division.
[FR Doc. 2010–29631 Filed 11–23–10; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPPT–2010–0880; FRL–8852–1]
Certain New Chemicals; Receipt and
Status Information
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
Under sections 5(d)(2) and
5(d)(3) of the Toxic Substances Control
SUMMARY:
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WReier-Aviles on DSKGBLS3C1PROD with NOTICES
Federal Register / Vol. 75, No. 226 / Wednesday, November 24, 2010 / Notices
Act (TSCA), EPA is required to publish
in the Federal Register a notice of
receipt of a premanufacture notice
(PMN) or an application for a test
marketing exemption (TME), and to
publish in the Federal Register periodic
status reports on the new chemicals
under review and the receipt of notices
of commencement (NOC) to begin the
manufacture of those chemicals. This
document covers the period from
September 20, 2010, to October 8, 2010,
and provides the required notice and
status report for the PMNs and TMEs,
both pending or expired, and the NOCs
to manufacture a new chemical that the
Agency has received under TSCA
section 5 during this time period.
DATES: Comments must be received on
or before December 27, 2010.
ADDRESSES: Submit your comments,
identified by docket identification (ID)
number EPA–HQ–OPPT–2010–0880,
and the specific PMN number or TME
number for the chemical related to your
comment, 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. 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: EPA’s policy is that all
comments received will be included in
the docket without change and may be
made available on-line at https://
www.regulations.gov, including any
personal information provided, unless
the comment includes information
claimed to be Confidential Business
Information (CBI) or other information
whose disclosure is restricted by statute.
Do not submit information that you
consider to be CBI or otherwise
protected through regulations.gov or email. The regulations.gov Web site is an
‘‘anonymous access’’ system, which
means EPA will not know your identity
or contact information unless you
provide it in the body of your comment.
If you send an e-mail directly to EPA
without going through regulations.gov,
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15:30 Nov 23, 2010
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your e-mail address will be
automatically captured and included as
part of the comment that is placed in the
docket and made available on the
Internet. If you submit an electronic
comment, EPA recommends that you
include your name and other contact
information in the body of your
comment and with any disk or CD–ROM
you submit. If EPA cannot read your
comment due to technical difficulties
and cannot contact you for clarification,
EPA may not be able to consider your
comment. Electronic files should avoid
the use of special characters, any form
of encryption, and be free of any defects
or viruses.
Docket: All documents in the docket
are listed in the docket index available
at https://www.regulations.gov. Although
listed in the index, some information is
not publicly available, e.g., CBI or other
information whose disclosure is
restricted by statute. Certain other
material, such as copyrighted material,
will be publicly available only in hard
copy. Publicly available docket
materials are available electronically at
https://www.regulations.gov, or, if only
available in hard copy, at the OPPT
Docket. The OPPT Docket is located in
the EPA Docket Center (EPA/DC) at Rm.
3334, EPA West Bldg., 1301
Constitution Ave., NW., Washington,
DC. The EPA/DC Public Reading Room
hours of operation are 8:30 a.m. to 4:30
p.m., Monday through Friday, excluding
legal holidays. The telephone number of
the EPA/DC Public Reading Room is
(202) 566–1744, and the telephone
number for the OPPT Docket is (202)
566–0280. Docket visitors are required
to show photographic identification,
pass through a metal detector, and sign
the EPA visitor log. All visitor bags are
processed through an X-ray machine
and subject to search. Visitors will be
provided an EPA/DC badge that must be
visible at all times in the building and
returned upon departure.
For
technical information contact: Bernice
Mudd, Information Management 7407M,
Office of Pollution Prevention and
Toxics, Environmental Protection
Agency, 1200 Pennsylvania Ave., NW.,
Washington, DC 20460–0001; telephone
number: (202) 564–8951; fax number:
(202) 564–8955; e-mail address:
mudd.bernice@epa.gov.
For general information contact: The
TSCA–Hotline, ABVI–Goodwill, 422
South Clinton Ave., Rochester, NY
14620; telephone number: (202) 554–
1404; e-mail address: TSCA–
Hotline@epa.gov.
FOR FURTHER INFORMATION CONTACT:
SUPPLEMENTARY INFORMATION:
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I. General Information
A. Does this action apply to me?
This action is directed to the public
in general. As such, the Agency has not
attempted to describe the specific
entities that this action may apply to.
Although others may be affected, this
action applies directly to the submitter
of the particular PMN or TME addressed
in this document. If you have any
questions regarding the applicability of
this action to a particular entity, consult
the person listed under FOR FURTHER
INFORMATION CONTACT.
B. What should I consider as I prepare
my comments for EPA?
1. Submitting CBI. Do not submit CBI
to EPA through regulations.gov or email. Clearly mark the part or all of the
information that you claim to be CBI.
For CBI information in a disk or CD–
ROM that you mail to EPA, mark the
outside of the disk or CD–ROM as CBI
and then identify electronically within
the disk or CD–ROM the specific
information that is claimed as CBI. In
addition to one complete version of the
comment that includes information
claimed as CBI, a copy of the comment
that does not contain the information
claimed as CBI must be submitted for
inclusion in the public docket.
Information marked as CBI 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.
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Federal Register / Vol. 75, No. 226 / Wednesday, November 24, 2010 / Notices
II. Why is EPA taking this action?
EPA classifies chemical substances as
either ‘‘existing’’ chemicals or ‘‘new’’
chemicals. Any substance that is not on
EPA’s TSCA Chemical Substances
Inventory, commonly referred to as the
the TSCA Inventory, is classified as a
‘‘new chemical,’’ while those that are on
the TSCA Inventory are classified as an
‘‘existing chemical.’’ For more
information about the TSCA Inventory
go to: https://www.epa.gov/opptintr/
newchems/pubs/inventory.htm. Anyone
who plans to manufacture or import a
new chemical substance for a nonexempt commercial purpose is required
by section 5 of TSCA to provide EPA
with a premanufacture notice, or PMN,
before initiating the activity. Section
5(h)(1) authorizes EPA to allow persons,
upon application, to manufacture
(includes import) or process a new
chemical substance, or a chemical
substance subject to a significant new
use rule (SNUR) issued under TSCA
section 5(a), for ‘‘test marketing’’
purposes, which is referred to as a test
marketing exemption, or TME. For more
information about the requirements
applicable to a new chemical go to:
https://www.epa.gov/oppt/newchems/.
Under TSCA sections 5(d)(2) and
5(d)(3) of TSCA, EPA is required to
publish in the Federal Register a notice
of receipt of a PMN or an application for
a TME and to publish in the Federal
Register periodic status reports on the
new chemicals under review and the
receipt of the NOCs to begin the
manufacture of those chemicals. This
document, covers the period from
September 20, 2010 to October 8, 2010,
and provides the required notice and
status report for the PMNs and TMEs,
both pending or expired, and the NOCs
to manufacture a new chemical that the
Agency has received under TSCA
section 5 during this time period.
III. Receipt and Status Reports
In Table I. of this Unit, EPA provides
the following information (to the extent
that such information is not claimed as
CBI) on the PMNs received by EPA
during this period: The EPA case
number assigned to the PMN, the date
the PMN was received by EPA, the
projected end date for EPA’s review of
the PMN, the submitting manufacturer;
the potential uses identified by the
manufacturer/importer in the PMN, and
the chemical identity.
TABLE I—PREMANUFACTURE NOTICES RECEIVED FROM: 9/21/10 TO 10/08/10
Case No.
Received
date
Projected
review
end date
Manufacturer/
importer
Use
Chemical
(G) Quaternary ammonium compound.
(G)
Hexamethylenediisocyanate
homopolymer, alkoxy-terminated.
09/21/10
12/19/10
CBI .................................
(G) Inhibitor for oil applications ......
P–10–0572
09/22/10
12/20/10
CBI .................................
P–10–0573
09/23/10
12/21/10
CBI .................................
P–10–0574
09/23/10
12/21/10
CBI .................................
P–10–0575
09/27/10
12/25/10
Eastman Kodak Company.
(S) Coatings for leather; water
borne industiral coatings like
wood.
(G) Polyurethane (open, nondispersive).
(G) Additive, open, non-dispersive
use.
(S) Polymer used in manufacture
of imaging media/products; for
export.
P–10–0576
09/27/10
12/25/10
CBI .................................
P–10–0577
P–10–0578
09/27/10
09/27/10
12/25/10
12/25/10
CBI .................................
CBI .................................
P–10–0579
09/27/10
12/25/10
CBI .................................
P–10–0580
09/27/10
12/25/10
CBI .................................
(S) An isocyanate for adhesives
formulations.
(G) Hole injection layer in a
polylmeric photovoltaic module.
P–10–0581
09/29/10
12/27/10
CBI .................................
(G) Anti-caking agent .....................
P–10–0582
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P–10–0571
09/28/10
12/26/10
CBI .................................
P–10–0583
09/28/10
12/26/10
CBI .................................
(G) Moisture curing polyurethane
adhesive. The predicted volume
for every application is same for
all 6 chemical substances. The
production is same for all 6 substances.
(G) Moisture curing polyurethane
adhesive. The predicted volume
for every application is same for
all 6 chemical substances. The
production is same for all 6 substances.
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(S) A surfactant in hard surface
cleaning detergent; laundry detergent.
(G) Anti-friction coating ..................
(G) Used in industrial coatings .......
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(G) Thermoplastic polyurethane.
(G) Polyisocyanate, reaction product with polyalkylene oxide.
(G) Methacrylic acid polymer with
isoalkylmethacrylamide,
arylmethacrylate,
and
alkenylmethacrylate.
(G) Alkyloxypropyliminodipropionic
acid, monosodium salt.
(G) Polyamideimide.
(G) Alkylenealkanedioic acid, polymer with alkenylbenzene and
alkenenitrile, ammonium salt,
alkylhydroperoxide-initiated.
(G) Aromatic isocyanate, polymer
with alkoxides and diol.
(G)
Hetromonocyclic[3,4b]thiophene, homopolymer, 2-[1[difluoro[(1,2,2-trifluoroethenyl)
oxy]methyl]-1,2,2,2tetrafluoroethoxy]-1,1,2,2tetrafluoroethyoxy]-1,1,2,2-tetra
fluoroethanesulfonic
acid-tetra
fluoroethylene polyer-doped.
(S) Iron, isomerized tartarate sodium complexes.
(G) Isocyanate terminated urethane polymer.
(G) Isocyanate terminated
thane polymer.
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Federal Register / Vol. 75, No. 226 / Wednesday, November 24, 2010 / Notices
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TABLE I—PREMANUFACTURE NOTICES RECEIVED FROM: 9/21/10 TO 10/08/10—Continued
Case No.
Received
date
Projected
review
end date
Manufacturer/
importer
Use
Chemical
09/28/10
12/26/10
CBI .................................
P–10–0585
09/28/10
12/26/10
CBI .................................
P–10–0586
09/28/10
12/26/10
CBI .................................
P–10–0587
09/28/10
12/26/10
CBI .................................
P–10–0588
09/29/10
12/27/10
CBI .................................
P–10–0589
P–10–0590
09/30/10
09/28/10
12/28/10
12/26/10
CBI .................................
CBI .................................
P–10–0591
09/30/10
12/28/10
CBI .................................
(G) Moisture curing polyurethane
adhesive. The predicted volume
for every application is same for
all 6 chemical substances. The
production is same for all 6 substances.
(G) Moisture curing polyurethane
adhesive. The predicted volume
for every application is same for
all 6 chemical substances. The
production is same for all 6 substances.
(G) Moisture curing polyurethane
adhesive. The predicted volume
for every application is same for
all 6 chemical substances. The
production is same for all 6 substances.
(G) Moisture curing polyurethane
adhesive. The predicted volume
for every application is same for
all 6 chemical substances. The
production is same for all 6 substances.
(S) Precursor to polyimide resin
used in aircraft material; precursor to polyimide resin used in
electronic and it material.
(G) Plasticizer for resin ..................
(G) Component/additive in polymer
resins.
(G) Adhesive system component ...
P–10–0592
09/28/10
12/26/10
Cytec Industries Inc .......
(G) Coating resin ............................
P–10–0593
P–11–0001
09/29/10
10/01/10
12/27/10
12/29/10
CBI .................................
CBI .................................
(G) Adhesive ingredient .................
(G) Crosslinking agent for coatings
P–11–0002
10/01/10
12/29/10
CBI .................................
(G) Crosslinking agent for coatings
P–11–0003
10/01/10
12/29/10
CBI .................................
(G) Crosslinking agent for coatings
P–11–0004
10/01/10
12/29/10
CBI .................................
(G) Crosslinking agent for coatings
P–11–0005
10/01/10
12/29/10
CBI .................................
(G) Crosslinking agent for coatings
P–11–0006
10/01/10
12/29/10
CBI .................................
(G) Crosslinking agent for coatings
P–11–0007
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P–10–0584
10/01/10
12/29/10
Organic Dyestuffs Corporation.
(S) Leather dye for distribution;
other dyeing applications as
needed.
P–11–0008
P–11–0009
10/01/10
10/04/10
12/29/10
01/01/11
CBI .................................
Interchem, Inc. ...............
P–11–0010
10/04/10
01/01/11
CBI .................................
(G) Component in resins ................
(S) Water soluble corrosion inhibitor.
(S) Resin for coatings, stains,
primes and lacquers.
P–11–0011
10/05/10
01/02/11
Dic International (USA)
LLC.
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(G) Adhesive ..................................
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(G) Isocyanate terminated
thane polymer.
ure-
(G) Isocyanate terminated
thane polymer.
ure-
(G) Isocyanate terminated
thane polymer.
ure-
(G) Isocyanate terminated
thane polymer.
ure-
(S)
Benzenamine,
4,4’-[1,3phenylenebis(1methylethylidene)]bis-.
(G) Dibasic acid ester.
(G) Modified ketal ester.
(G)
Methylenebis[isocyanatobenzene], polymer with alkanedioic
acid,
alkylene
glycols,
alkoxylated alkanepolyol and
substituted trialkoxysilane.
(G) Fatty acids, polymer with substituted
carbopolycycle,
substuted
alkylamines,
substituted
alkyleneoxide
and
glycidyl alkanoate, substituted
alkanoic acid (salts).
(G) Modified starch.
(G) Aromatic polyisocyanate, aliphatic polyol blocked.
(G) Aromatic polyisocyanate, aliphatic polyol blocked.
(G) Aromatic polyisocyanate, aliphatic polyol blocked.
(G) Aromatic polyisocyanate, aliphatic polyol blocked.
(G) Aromatic polyisocyanate, aliphatic polyol blocked.
(G) Aromatic polyisocyanate, aliphatic polyol blocked.
(S) 2,7-naphthalenedisulfonic acid,
4-amino-6-[[4-[[[4-[(2,4diaminophenyl)azo]phenyl]amino]
sulfonyl]phenyl]azo]-5-hydroxy-3[(4-nitrophenyl)azo]-, dipotassium
salt.
(G) Modified ketal ester.
(G) Alkoxylated imidazoline.
(G) Fatty acid modified polyester
aliphatic polyurethane dispersion.
(G) Polyol blocked cycloaliphatic
amine polymer.
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TABLE I—PREMANUFACTURE NOTICES RECEIVED FROM: 9/21/10 TO 10/08/10—Continued
Projected
review
end date
Received
date
Case No.
Manufacturer/
importer
Use
Chemical
(G) 2-propenoic acid, 2-methyl-,
telomer with 2-propenoic acid
and sodium phosphinate (1:1),
ester with polyethylene glycol,
peroxydisulfuric acid ([ho)s(o)2]
2o2)sodium salt (1:2)-initiated.
(G) Alkyl dioic acid, polymer with
substituted
alkanoate,
alkyl
diisocyanate, alkyldiol, and substituted alkanoic acid.
(G) Alkyl amine salt.
P–11–0012
10/07/10
01/04/11
CBI .................................
(G) A polymer used in a concrete
admixture which retains workability by retaining slump in concrete precast applications.
P–11–0013
10/05/10
01/02/11
Cytec Industries Inc .......
(G) Coatings resin ..........................
P–11–0014
10/05/10
01/02/11
P–11–0015
10/06/10
01/03/11
Goulston Technologies,
Inc.
CBI .................................
(G) Component of lubricant for finish product for fiber and yarn.
(S) Ingredient for fragrance production.
In Table II. of this Unit, EPA provides
the following information (to the extent
that such information is not claimed as
CBI) on the TMEs received by EPA
during this period: The EPA case
number assigned to the TME, the date
the TME was received by EPA, the
projected end date for EPA’s review of
(S) Cyclohexanepentanol, -methyl-.
the TME, the submitting manufacturer/
importer, the potential uses identified
by the manufacturer/importer in the
TME, and the chemical identity.
TABLE II—TEST MARKETING EXEMPTION NOTICES RECEIVED FROM: 09/21/10 TO 10/08/10
Received date
Projected review end date
Manufacturer/importer
Use
Chemical
T–10–0009 ...
09/28/10
11/11/10
Cytec Industries Inc. ..
(G) Coating resin .......
T–11–0001 ...
10/05/10
11/18/10
Cytec Industries Inc. ..
(G) Coating resin .......
(G) Fatty acids, polymer with substituted
carbopolycycle, substituted akylamines,
substituted akylneoxide and glycidyl
alkenoate, substituted alkanoic acid
(salts).
(G) Alkyl dioic acid, polymer with substituted
alkanoate, alkyl diisocyanate, alkyldiol,
and substituted alkanoic acid.
Case No.
In Table III. of this Unit, EPA provides
the following information (to the extent
that such information is not claimed as
CBI) on the NOCs received by EPA
during this period: The EPA case
number assigned to the NOC, the date
the NOC was received by EPA, the
projected end date for EPA’s review of
the NOC, and the chemical identity.
TABLE III—NOTICES OF COMMENCEMENT FROM: 9/21/10 TO 10/08/10
Case No.
WReier-Aviles on DSKGBLS3C1PROD with NOTICES
P–00–0129
P–00–0130
P–00–0131
P–00–0135
P–00–0136
P–00–0139
P–00–0140
P–00–0144
P–00–0146
P–00–0153
P–00–0154
Received date
Commencement notice
review end
date
...
...
...
...
...
...
...
...
...
...
...
10/01/10
10/01/10
10/01/10
10/01/10
10/01/10
10/01/10
10/01/10
10/01/10
10/01/10
10/01/10
10/01/10
09/07/10
09/07/10
09/07/10
09/07/10
09/07/10
09/07/10
09/07/10
09/07/10
09/07/10
09/07/10
09/07/10
P–00–0155 ...
10/01/10
09/07/10
P–00–0156 ...
10/01/10
09/07/10
P–07–0353 ...
P–08–0486 ...
10/07/10
10/05/10
08/28/10
09/17/10
P–09–0083 ...
P–09–0084 ...
10/04/10
09/22/10
09/03/10
09/02/10
VerDate Mar<15>2010
15:30 Nov 23, 2010
Jkt 223001
Chemical
(S) L-aspartic acid, N,N’-1,2-ethanediylbis-, compound with 2-aminoethanol (1:3).
(S) L-aspartic acid, N,N’-1,2-ethanediylbis-, compound with 2-aminoethanol (1:4).
(S) L-aspartic acid, N,N’-1,2-ethanediylbis-, sodium salt.
(S) L-aspartic acid, N,N’-1,2-ethanediylbis-, tetrasodium salt.
(S) L-aspartic acid, N,N’-1,2-ethanediylbis-, potassium salt.
(S) L-aspartic acid, N,N’-1,2-ethanediylbis-, tripotassium salt.
(S) L-aspartic acid, N,N’-1,2-ethanediylbis-, tetrapotassium salt.
(S) L-aspartic acid, N,N’-1,2-ethanediylbis-, magnesium salt (1:2).
(S) L-aspartic acid, N,N’-1,2-ethanediylbis-, magnesium sodium salt (1:1:2).
(S) L-aspartic acid, N,N’-1,2-ethanediylbis- sodium salt, compound with 2-aminoethanol.
(S) L-aspartic acid, N,N’-1,2-ethanediylbis- monosodium salt, compound with 2-aminoethanol
(1:3).
(S) L-aspartic acid, N,N’-1,2-ethanediylbis- disodium salt, compound with 2-aminoethanol
(1:2).
(S) L-aspartic acid, N,N’-1,2-ethanediylbis- trisodium salt, compound with 2-aminoethanol
(1:1).
(G) Alkyl acid fluoride.
(G) Polymer with .alpha.-hydro-.omega.-hydroxypoly[oxy(methyl-1,2-ethanediyl)], 3-hydroxy-2(hydroxymethyl)-2-methylpropanoic acid and alkyldiisocyanate, ammonium salt.
(G) Cationic polyamide.
(G) Benzenesulfonic acid salt.
PO 00000
Frm 00027
Fmt 4703
Sfmt 4703
E:\FR\FM\24NON1.SGM
24NON1
Federal Register / Vol. 75, No. 226 / Wednesday, November 24, 2010 / Notices
71693
TABLE III—NOTICES OF COMMENCEMENT FROM: 9/21/10 TO 10/08/10—Continued
Case No.
Received date
Commencement notice
review end
date
P–09–0146
P–09–0288
P–09–0430
P–09–0431
P–09–0432
P–09–0433
P–09–0558
P–09–0610
P–10–0050
P–10–0128
...
...
...
...
...
...
...
...
...
...
10/01/10
09/22/10
10/04/10
10/04/10
10/04/10
10/04/10
09/27/10
09/22/10
09/29/10
09/23/10
09/28/10
08/21/10
09/14/10
09/14/10
09/14/10
09/14/10
09/10/10
09/01/10
08/30/10
08/02/10
P–10–0133
P–10–0186
P–10–0293
P–10–0306
P–10–0325
P–10–0388
...
...
...
...
...
...
09/29/10
09/27/10
09/21/10
09/30/10
10/07/10
10/06/10
09/21/10
09/08/10
08/23/10
08/31/10
09/20/10
08/23/10
P–10–0389 ...
10/04/10
09/08/10
P–10–0394 ...
P–10–0395 ...
P–10–0417 ...
10/07/10
10/07/10
09/22/10
09/28/10
10/01/10
09/21/10
P–10–0430 ...
10/06/10
09/28/10
If you are interested in information
that is not included in these tables, you
may contact the person listed under FOR
FURTHER INFORMATION CONTACT to access
additional non-CBI information that
may be available.
List of Subjects
Environmental protection, Chemicals,
Hazardous substances, Imports, Notice
of commencement, Premanufacturer,
Reporting and recordkeeping
requirements, Test marketing
exemptions.
Dated: November 17, 2010.
Darryl S. Ballaard,
Acting Director, Information Management
Division, Office of Pollution Prevention and
Toxics.
[FR Doc. 2010–29674 Filed 11–23–10; 8:45 am]
WReier-Aviles on DSKGBLS3C1PROD with NOTICES
BILLING CODE 6560–50–P
VerDate Mar<15>2010
15:30 Nov 23, 2010
Jkt 223001
Chemical
(S) Formaldehyde, polymers with acetone-phenol reaction products and phenol, sodium salts.
(G) Alkyl silsesquioxanes.
(G) Polymeric monoazo compound.
(G) Polymeric monoazo compound.
(G) Polymeric monoazo triphenylmethane.
(G) Polymeric triphenylmethane.
(G) Modified ketal.
(G) Alkylbenzene sulfonic acid.
(G) Amine salt.s of fatty acids.
(S) Siloxanes and silicones, di-me, 3-hydroxypropyl group-terminated, ethoxylated, polymers
with 1,6-diisocyanato-2,2,4-trimethylhexane, 1,6-diisocyanato-2,4,4-trimethylhexane, polypropylene glycol ether with glycerol (3:1) and polypropylene glycol ether with pentaerythritol
(4:1), polypropylene glycol mono-bu ether-blocked.
(G) Alkyl sulfide, manuf. of, by-products from, distn. lights.
(G) Alkyl phosphate salt.
(G) Methacrylate copolymer.
(G) Unsaturated polyester resin.
(G) Neodymium ziegler-natta catalyst.
(G) 2-propenoic acid, 2-methyl-, polymer with alkyl 2-propenoates, ethenyl acetate and methyl-2-methyl-2-propenoate.
(G) Amino acid, N-(2-aminoalkyl)-, salt. (1:1), polymers with cycloaliphatic diamine,
alkyldiisocyanate, alpha-hydro-omega-hydroxy(alkyldiyl) and polyalkyl glycol mono alkyl
ether blocked, alkyldiisocyanate-aromatic diisocyanate, polyalkyl glycol mono alkyl ether
blocked.
(G) Aromatic carboxylic acid.
(G) Organic carboxylic acid.
(S)
Amines,
C36-alkylenedi-,
polymers
with
5,5’-[(1-methylethylidene)bis(4,1phenyleneoxy)]bis[1,3-isobenzofurandione], maleated.
(G) Urethane acrylate.
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPP–2010–0966; FRL–8854–9]
Pesticide Program Dialogue
Committee; Announcement of New
Membership and Notice of Public
Meetings
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
Pursuant to the Federal
Advisory Committee Act, EPA gives
notice that a public meeting of the new
membership to the Pesticide Program
Dialogue Committee (PPDC) is
scheduled for December 14 and 15,
2010. A draft agenda is under
development that will include reports
from and discussions about current
issues from the following PPDC work
groups: 21st Century Toxicology/New
Integrated Testing Strategies; Pesticide
Registration Improvement Act (PRIA)
Process Improvements; Comparative
Safety Statements for Pesticide Product
Labeling; and Public Health Work
Group. Discussion topics will also cover
spray drift, current Endangered Species
Act issues, and brief program updates
on current regulatory topics. PPDC work
group meetings are also being scheduled
SUMMARY:
PO 00000
Frm 00028
Fmt 4703
Sfmt 4703
and are open to the public. The 21st
Century Toxicology/New Integrated
Testing Strategies Work Group is
holding a workshop on 21st Century
Science and Integrated Testing and
Assessment Strategies: Transitioning
Research to Regulatory Practice on
December 13, 2010, from 9 a.m. to 5
p.m. The meeting will also be available
via webinar. A brochure and agenda
regarding this Workshop and
information and instructions for
participating in the webinar is found at:
https://www.epa.gov/oppfead1/cb/ppdc/
testing/. The PPDC PRIA
Process Improvements Work Group will
meet on December 13, 2010, from 1 p.m.
to 4 p.m. Information about this work
group meeting can be found on EPA’s
Web site at: https://www.epa.gov/
pesticides/ppdc.
The PPDC meeting will be held
on Tuesday, December 14, 2010, from 9
a.m. to 5 p.m., and Wednesday,
December 15, 2010, from 9 a.m. to noon.
To request accommodation of a
disability, please contact the person
listed under FOR FURTHER INFORMATON
CONTACT, preferably at least 10 days
prior to the meeting, to give EPA as
much time as possible to process your
request.
DATES:
E:\FR\FM\24NON1.SGM
24NON1
Agencies
[Federal Register Volume 75, Number 226 (Wednesday, November 24, 2010)]
[Notices]
[Pages 71688-71693]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-29674]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
[EPA-HQ-OPPT-2010-0880; FRL-8852-1]
Certain New Chemicals; Receipt and Status Information
AGENCY: Environmental Protection Agency (EPA).
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: Under sections 5(d)(2) and 5(d)(3) of the Toxic Substances
Control
[[Page 71689]]
Act (TSCA), EPA is required to publish in the Federal Register a notice
of receipt of a premanufacture notice (PMN) or an application for a
test marketing exemption (TME), and to publish in the Federal Register
periodic status reports on the new chemicals under review and the
receipt of notices of commencement (NOC) to begin the manufacture of
those chemicals. This document covers the period from September 20,
2010, to October 8, 2010, and provides the required notice and status
report for the PMNs and TMEs, both pending or expired, and the NOCs to
manufacture a new chemical that the Agency has received under TSCA
section 5 during this time period.
DATES: Comments must be received on or before December 27, 2010.
ADDRESSES: Submit your comments, identified by docket identification
(ID) number EPA-HQ-OPPT-2010-0880, and the specific PMN number or TME
number for the chemical related to your comment, 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. 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: EPA's policy is that all comments received will be
included in the docket without change and may be made available on-line
at https://www.regulations.gov, including any personal information
provided, unless the comment includes information claimed to be
Confidential Business Information (CBI) or other information whose
disclosure is restricted by statute. Do not submit information that you
consider to be CBI or otherwise protected through regulations.gov or e-
mail. The regulations.gov Web site is an ``anonymous access'' system,
which means EPA will not know your identity or contact information
unless you provide it in the body of your comment. If you send an e-
mail directly to EPA without going through regulations.gov, your e-mail
address will be automatically captured and included as part of the
comment that is placed in the docket and made available on the
Internet. If you submit an electronic comment, EPA recommends that you
include your name and other contact information in the body of your
comment and with any disk or CD-ROM you submit. If EPA cannot read your
comment due to technical difficulties and cannot contact you for
clarification, EPA may not be able to consider your comment. Electronic
files should avoid the use of special characters, any form of
encryption, and be free of any defects or viruses.
Docket: All documents in the docket are listed in the docket index
available at https://www.regulations.gov. Although listed in the index,
some information is not publicly available, e.g., CBI or other
information whose disclosure is restricted by statute. Certain other
material, such as copyrighted material, will be publicly available only
in hard copy. Publicly available docket materials are available
electronically at https://www.regulations.gov, or, if only available in
hard copy, at the OPPT Docket. The OPPT Docket is located in the EPA
Docket Center (EPA/DC) at Rm. 3334, EPA West Bldg., 1301 Constitution
Ave., NW., Washington, DC. The EPA/DC Public Reading Room hours of
operation are 8:30 a.m. to 4:30 p.m., Monday through Friday, excluding
legal holidays. The telephone number of the EPA/DC Public Reading Room
is (202) 566-1744, and the telephone number for the OPPT Docket is
(202) 566-0280. Docket visitors are required to show photographic
identification, pass through a metal detector, and sign the EPA visitor
log. All visitor bags are processed through an X-ray machine and
subject to search. Visitors will be provided an EPA/DC badge that must
be visible at all times in the building and returned upon departure.
FOR FURTHER INFORMATION CONTACT: For technical information contact:
Bernice Mudd, Information Management 7407M, Office of Pollution
Prevention and Toxics, Environmental Protection Agency, 1200
Pennsylvania Ave., NW., Washington, DC 20460-0001; telephone number:
(202) 564-8951; fax number: (202) 564-8955; e-mail address:
mudd.bernice@epa.gov.
For general information contact: The TSCA-Hotline, ABVI-Goodwill,
422 South Clinton Ave., Rochester, NY 14620; telephone number: (202)
554-1404; e-mail address: TSCA-Hotline@epa.gov.
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this action apply to me?
This action is directed to the public in general. As such, the
Agency has not attempted to describe the specific entities that this
action may apply to. Although others may be affected, this action
applies directly to the submitter of the particular PMN or TME
addressed in this document. If you have any questions regarding the
applicability of this action to a particular entity, consult the person
listed under FOR FURTHER INFORMATION CONTACT.
B. What should I consider as I prepare my comments for EPA?
1. Submitting CBI. Do not submit CBI to EPA through regulations.gov
or e-mail. Clearly mark the part or all of the information that you
claim to be CBI. For CBI information in a disk or CD-ROM that you mail
to EPA, mark the outside of the disk or CD-ROM as CBI and then identify
electronically within the disk or CD-ROM the specific information that
is claimed as CBI. In addition to one complete version of the comment
that includes information claimed as CBI, a copy of the comment that
does not contain the information claimed as CBI must be submitted for
inclusion in the public docket. Information marked as CBI 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.
[[Page 71690]]
II. Why is EPA taking this action?
EPA classifies chemical substances as either ``existing'' chemicals
or ``new'' chemicals. Any substance that is not on EPA's TSCA Chemical
Substances Inventory, commonly referred to as the the TSCA Inventory,
is classified as a ``new chemical,'' while those that are on the TSCA
Inventory are classified as an ``existing chemical.'' For more
information about the TSCA Inventory go to: https://www.epa.gov/opptintr/newchems/pubs/inventory.htm. Anyone who plans to manufacture
or import a new chemical substance for a non-exempt commercial purpose
is required by section 5 of TSCA to provide EPA with a premanufacture
notice, or PMN, before initiating the activity. Section 5(h)(1)
authorizes EPA to allow persons, upon application, to manufacture
(includes import) or process a new chemical substance, or a chemical
substance subject to a significant new use rule (SNUR) issued under
TSCA section 5(a), for ``test marketing'' purposes, which is referred
to as a test marketing exemption, or TME. For more information about
the requirements applicable to a new chemical go to: https://www.epa.gov/oppt/newchems/.
Under TSCA sections 5(d)(2) and 5(d)(3) of TSCA, EPA is required to
publish in the Federal Register a notice of receipt of a PMN or an
application for a TME and to publish in the Federal Register periodic
status reports on the new chemicals under review and the receipt of the
NOCs to begin the manufacture of those chemicals. This document, covers
the period from September 20, 2010 to October 8, 2010, and provides the
required notice and status report for the PMNs and TMEs, both pending
or expired, and the NOCs to manufacture a new chemical that the Agency
has received under TSCA section 5 during this time period.
III. Receipt and Status Reports
In Table I. of this Unit, EPA provides the following information
(to the extent that such information is not claimed as CBI) on the PMNs
received by EPA during this period: The EPA case number assigned to the
PMN, the date the PMN was received by EPA, the projected end date for
EPA's review of the PMN, the submitting manufacturer; the potential
uses identified by the manufacturer/importer in the PMN, and the
chemical identity.
Table I--Premanufacture Notices Received From: 9/21/10 to 10/08/10
----------------------------------------------------------------------------------------------------------------
Projected
Case No. Received review end Manufacturer/ Use Chemical
date date importer
----------------------------------------------------------------------------------------------------------------
P-10-0571........... 09/21/10 12/19/10 CBI................. (G) Inhibitor for (G) Quaternary
oil applications. ammonium compound.
P-10-0572........... 09/22/10 12/20/10 CBI................. (S) Coatings for (G)
leather; water Hexamethylenediisoc
borne industiral yanate homopolymer,
coatings like wood. alkoxy-terminated.
P-10-0573........... 09/23/10 12/21/10 CBI................. (G) Polyurethane (G) Thermoplastic
(open, polyurethane.
nondispersive).
P-10-0574........... 09/23/10 12/21/10 CBI................. (G) Additive, open, (G) Polyisocyanate,
non-dispersive use. reaction product
with polyalkylene
oxide.
P-10-0575........... 09/27/10 12/25/10 Eastman Kodak (S) Polymer used in (G) Methacrylic acid
Company. manufacture of polymer with
imaging media/ isoalkylmethacrylam
products; for ide,
export. arylmethacrylate,
and
alkenylmethacrylate
.
P-10-0576........... 09/27/10 12/25/10 CBI................. (S) A surfactant in (G)
hard surface Alkyloxypropylimino
cleaning detergent; dipropionic acid,
laundry detergent. monosodium salt.
P-10-0577........... 09/27/10 12/25/10 CBI................. (G) Anti-friction (G) Polyamideimide.
coating.
P-10-0578........... 09/27/10 12/25/10 CBI................. (G) Used in (G)
industrial coatings. Alkylenealkanedioic
acid, polymer with
alkenylbenzene and
alkenenitrile,
ammonium salt,
alkylhydroperoxide-
initiated.
P-10-0579........... 09/27/10 12/25/10 CBI................. (S) An isocyanate (G) Aromatic
for adhesives isocyanate, polymer
formulations. with alkoxides and
diol.
P-10-0580........... 09/27/10 12/25/10 CBI................. (G) Hole injection (G)
layer in a Hetromonocyclic[3,4-
polylmeric b]thiophene,
photovoltaic module. homopolymer, 2-[1-
[difluoro[(1,2,2-
trifluoroethenyl)ox
y]methyl]-1,2,2,2-
tetrafluoroethoxy]-
1,1,2,2-
tetrafluoroethyoxy]-
1,1,2,2-
tetrafluoroethanesu
lfonic acid-
tetrafluoroethylene
polyer-doped.
P-10-0581........... 09/29/10 12/27/10 CBI................. (G) Anti-caking (S) Iron, isomerized
agent. tartarate sodium
complexes.
P-10-0582........... 09/28/10 12/26/10 CBI................. (G) Moisture curing (G) Isocyanate
polyurethane terminated urethane
adhesive. The polymer.
predicted volume
for every
application is same
for all 6 chemical
substances. The
production is same
for all 6
substances.
P-10-0583........... 09/28/10 12/26/10 CBI................. (G) Moisture curing (G) Isocyanate
polyurethane terminated urethane
adhesive. The polymer.
predicted volume
for every
application is same
for all 6 chemical
substances. The
production is same
for all 6
substances.
[[Page 71691]]
P-10-0584........... 09/28/10 12/26/10 CBI................. (G) Moisture curing (G) Isocyanate
polyurethane terminated urethane
adhesive. The polymer.
predicted volume
for every
application is same
for all 6 chemical
substances. The
production is same
for all 6
substances.
P-10-0585........... 09/28/10 12/26/10 CBI................. (G) Moisture curing (G) Isocyanate
polyurethane terminated urethane
adhesive. The polymer.
predicted volume
for every
application is same
for all 6 chemical
substances. The
production is same
for all 6
substances.
P-10-0586........... 09/28/10 12/26/10 CBI................. (G) Moisture curing (G) Isocyanate
polyurethane terminated urethane
adhesive. The polymer.
predicted volume
for every
application is same
for all 6 chemical
substances. The
production is same
for all 6
substances.
P-10-0587........... 09/28/10 12/26/10 CBI................. (G) Moisture curing (G) Isocyanate
polyurethane terminated urethane
adhesive. The polymer.
predicted volume
for every
application is same
for all 6 chemical
substances. The
production is same
for all 6
substances.
P-10-0588........... 09/29/10 12/27/10 CBI................. (S) Precursor to (S) Benzenamine,
polyimide resin 4,4'-[1,3-
used in aircraft phenylenebis(1-
material; precursor methylethylidene)]b
to polyimide resin is-.
used in electronic
and it material.
P-10-0589........... 09/30/10 12/28/10 CBI................. (G) Plasticizer for (G) Dibasic acid
resin. ester.
P-10-0590........... 09/28/10 12/26/10 CBI................. (G) Component/ (G) Modified ketal
additive in polymer ester.
resins.
P-10-0591........... 09/30/10 12/28/10 CBI................. (G) Adhesive system (G)
component. Methylenebis[isocya
natobenzene],
polymer with
alkanedioic acid,
alkylene glycols,
alkoxylated
alkanepolyol and
substituted
trialkoxysilane.
P-10-0592........... 09/28/10 12/26/10 Cytec Industries Inc (G) Coating resin... (G) Fatty acids,
polymer with
substituted
carbopolycycle,
substuted
alkylamines,
substituted
alkyleneoxide and
glycidyl alkanoate,
substituted
alkanoic acid
(salts).
P-10-0593........... 09/29/10 12/27/10 CBI................. (G) Adhesive (G) Modified starch.
ingredient.
P-11-0001........... 10/01/10 12/29/10 CBI................. (G) Crosslinking (G) Aromatic
agent for coatings. polyisocyanate,
aliphatic polyol
blocked.
P-11-0002........... 10/01/10 12/29/10 CBI................. (G) Crosslinking (G) Aromatic
agent for coatings. polyisocyanate,
aliphatic polyol
blocked.
P-11-0003........... 10/01/10 12/29/10 CBI................. (G) Crosslinking (G) Aromatic
agent for coatings. polyisocyanate,
aliphatic polyol
blocked.
P-11-0004........... 10/01/10 12/29/10 CBI................. (G) Crosslinking (G) Aromatic
agent for coatings. polyisocyanate,
aliphatic polyol
blocked.
P-11-0005........... 10/01/10 12/29/10 CBI................. (G) Crosslinking (G) Aromatic
agent for coatings. polyisocyanate,
aliphatic polyol
blocked.
P-11-0006........... 10/01/10 12/29/10 CBI................. (G) Crosslinking (G) Aromatic
agent for coatings. polyisocyanate,
aliphatic polyol
blocked.
P-11-0007........... 10/01/10 12/29/10 Organic Dyestuffs (S) Leather dye for (S) 2,7-
Corporation. distribution; other naphthalenedisulfon
dyeing applications ic acid, 4-amino-6-
as needed. [[4-[[[4-[(2,4-
diaminophenyl)azo]p
henyl]amino]sulfony
l]phenyl]azo]-5-
hydroxy-3-[(4-
nitrophenyl)azo]-,
dipotassium salt.
P-11-0008........... 10/01/10 12/29/10 CBI................. (G) Component in (G) Modified ketal
resins. ester.
P-11-0009........... 10/04/10 01/01/11 Interchem, Inc...... (S) Water soluble (G) Alkoxylated
corrosion inhibitor. imidazoline.
P-11-0010........... 10/04/10 01/01/11 CBI................. (S) Resin for (G) Fatty acid
coatings, stains, modified polyester
primes and lacquers. aliphatic
polyurethane
dispersion.
P-11-0011........... 10/05/10 01/02/11 Dic International (G) Adhesive........ (G) Polyol blocked
(USA) LLC. cycloaliphatic
amine polymer.
[[Page 71692]]
P-11-0012........... 10/07/10 01/04/11 CBI................. (G) A polymer used (G) 2-propenoic
in a concrete acid, 2-methyl-,
admixture which telomer with 2-
retains workability propenoic acid and
by retaining slump sodium phosphinate
in concrete precast (1:1), ester with
applications. polyethylene
glycol,
peroxydisulfuric
acid
([ho)s(o)2]2o2)sodi
um salt (1:2)-
initiated.
P-11-0013........... 10/05/10 01/02/11 Cytec Industries Inc (G) Coatings resin.. (G) Alkyl dioic
acid, polymer with
substituted
alkanoate, alkyl
diisocyanate,
alkyldiol, and
substituted
alkanoic acid.
P-11-0014........... 10/05/10 01/02/11 Goulston (G) Component of (G) Alkyl amine
Technologies, Inc. lubricant for salt.
finish product for
fiber and yarn.
P-11-0015........... 10/06/10 01/03/11 CBI................. (S) Ingredient for (S)
fragrance Cyclohexanepentanol
production. , -methyl-.
----------------------------------------------------------------------------------------------------------------
In Table II. of this Unit, EPA provides the following information
(to the extent that such information is not claimed as CBI) on the TMEs
received by EPA during this period: The EPA case number assigned to the
TME, the date the TME was received by EPA, the projected end date for
EPA's review of the TME, the submitting manufacturer/importer, the
potential uses identified by the manufacturer/importer in the TME, and
the chemical identity.
Table II--Test Marketing Exemption Notices Received From: 09/21/10 to 10/08/10
----------------------------------------------------------------------------------------------------------------
Projected
Case No. Received date review end Manufacturer/ Use Chemical
date importer
----------------------------------------------------------------------------------------------------------------
T-10-0009........... 09/28/10 11/11/10 Cytec Industries (G) Coating resin. (G) Fatty acids,
Inc.. polymer with
substituted
carbopolycycle,
substituted
akylamines,
substituted
akylneoxide and
glycidyl
alkenoate,
substituted
alkanoic acid
(salts).
T-11-0001........... 10/05/10 11/18/10 Cytec Industries (G) Coating resin. (G) Alkyl dioic
Inc.. acid, polymer
with substituted
alkanoate, alkyl
diisocyanate,
alkyldiol, and
substituted
alkanoic acid.
----------------------------------------------------------------------------------------------------------------
In Table III. of this Unit, EPA provides the following information
(to the extent that such information is not claimed as CBI) on the NOCs
received by EPA during this period: The EPA case number assigned to the
NOC, the date the NOC was received by EPA, the projected end date for
EPA's review of the NOC, and the chemical identity.
Table III--Notices of Commencement From: 9/21/10 to 10/08/10
------------------------------------------------------------------------
Commencement
Case No. Received date notice review Chemical
end date
------------------------------------------------------------------------
P-00-0129........ 10/01/10 09/07/10 (S) L-aspartic acid,
N,N'-1,2-
ethanediylbis-,
compound with 2-
aminoethanol (1:3).
P-00-0130........ 10/01/10 09/07/10 (S) L-aspartic acid,
N,N'-1,2-
ethanediylbis-,
compound with 2-
aminoethanol (1:4).
P-00-0131........ 10/01/10 09/07/10 (S) L-aspartic acid,
N,N'-1,2-
ethanediylbis-,
sodium salt.
P-00-0135........ 10/01/10 09/07/10 (S) L-aspartic acid,
N,N'-1,2-
ethanediylbis-,
tetrasodium salt.
P-00-0136........ 10/01/10 09/07/10 (S) L-aspartic acid,
N,N'-1,2-
ethanediylbis-,
potassium salt.
P-00-0139........ 10/01/10 09/07/10 (S) L-aspartic acid,
N,N'-1,2-
ethanediylbis-,
tripotassium salt.
P-00-0140........ 10/01/10 09/07/10 (S) L-aspartic acid,
N,N'-1,2-
ethanediylbis-,
tetrapotassium salt.
P-00-0144........ 10/01/10 09/07/10 (S) L-aspartic acid,
N,N'-1,2-
ethanediylbis-,
magnesium salt
(1:2).
P-00-0146........ 10/01/10 09/07/10 (S) L-aspartic acid,
N,N'-1,2-
ethanediylbis-,
magnesium sodium
salt (1:1:2).
P-00-0153........ 10/01/10 09/07/10 (S) L-aspartic acid,
N,N'-1,2-
ethanediylbis-
sodium salt,
compound with 2-
aminoethanol.
P-00-0154........ 10/01/10 09/07/10 (S) L-aspartic acid,
N,N'-1,2-
ethanediylbis-
monosodium salt,
compound with 2-
aminoethanol (1:3).
P-00-0155........ 10/01/10 09/07/10 (S) L-aspartic acid,
N,N'-1,2-
ethanediylbis-
disodium salt,
compound with 2-
aminoethanol (1:2).
P-00-0156........ 10/01/10 09/07/10 (S) L-aspartic acid,
N,N'-1,2-
ethanediylbis-
trisodium salt,
compound with 2-
aminoethanol (1:1).
P-07-0353........ 10/07/10 08/28/10 (G) Alkyl acid
fluoride.
P-08-0486........ 10/05/10 09/17/10 (G) Polymer with
.alpha.-hydro-
.omega.-
hydroxypoly[oxy(meth
yl-1,2-ethanediyl)],
3-hydroxy-2-
(hydroxymethyl)-2-
methylpropanoic acid
and
alkyldiisocyanate,
ammonium salt.
P-09-0083........ 10/04/10 09/03/10 (G) Cationic
polyamide.
P-09-0084........ 09/22/10 09/02/10 (G) Benzenesulfonic
acid salt.
[[Page 71693]]
P-09-0146........ 10/01/10 09/28/10 (S) Formaldehyde,
polymers with
acetone-phenol
reaction products
and phenol, sodium
salts.
P-09-0288........ 09/22/10 08/21/10 (G) Alkyl
silsesquioxanes.
P-09-0430........ 10/04/10 09/14/10 (G) Polymeric monoazo
compound.
P-09-0431........ 10/04/10 09/14/10 (G) Polymeric monoazo
compound.
P-09-0432........ 10/04/10 09/14/10 (G) Polymeric monoazo
triphenylmethane.
P-09-0433........ 10/04/10 09/14/10 (G) Polymeric
triphenylmethane.
P-09-0558........ 09/27/10 09/10/10 (G) Modified ketal.
P-09-0610........ 09/22/10 09/01/10 (G) Alkylbenzene
sulfonic acid.
P-10-0050........ 09/29/10 08/30/10 (G) Amine salt.s of
fatty acids.
P-10-0128........ 09/23/10 08/02/10 (S) Siloxanes and
silicones, di-me, 3-
hydroxypropyl group-
terminated,
ethoxylated,
polymers with 1,6-
diisocyanato-2,2,4-
trimethylhexane, 1,6-
diisocyanato-2,4,4-
trimethylhexane,
polypropylene glycol
ether with glycerol
(3:1) and
polypropylene glycol
ether with
pentaerythritol
(4:1), polypropylene
glycol mono-bu ether-
blocked.
P-10-0133........ 09/29/10 09/21/10 (G) Alkyl sulfide,
manuf. of, by-
products from,
distn. lights.
P-10-0186........ 09/27/10 09/08/10 (G) Alkyl phosphate
salt.
P-10-0293........ 09/21/10 08/23/10 (G) Methacrylate
copolymer.
P-10-0306........ 09/30/10 08/31/10 (G) Unsaturated
polyester resin.
P-10-0325........ 10/07/10 09/20/10 (G) Neodymium ziegler-
natta catalyst.
P-10-0388........ 10/06/10 08/23/10 (G) 2-propenoic acid,
2-methyl-, polymer
with alkyl 2-
propenoates, ethenyl
acetate and methyl-2-
methyl-2-propenoate.
P-10-0389........ 10/04/10 09/08/10 (G) Amino acid, N-(2-
aminoalkyl)-, salt.
(1:1), polymers with
cycloaliphatic
diamine,
alkyldiisocyanate,
alpha-hydro-omega-
hydroxy(alkyldiyl)
and polyalkyl glycol
mono alkyl ether
blocked,
alkyldiisocyanate-
aromatic
diisocyanate,
polyalkyl glycol
mono alkyl ether
blocked.
P-10-0394........ 10/07/10 09/28/10 (G) Aromatic
carboxylic acid.
P-10-0395........ 10/07/10 10/01/10 (G) Organic
carboxylic acid.
P-10-0417........ 09/22/10 09/21/10 (S) Amines, C36-
alkylenedi-,
polymers with 5,5'-
[(1-
methylethylidene)bis
(4,1-
phenyleneoxy)]bis[1,
3-
isobenzofurandione],
maleated.
P-10-0430........ 10/06/10 09/28/10 (G) Urethane
acrylate.
------------------------------------------------------------------------
If you are interested in information that is not included in these
tables, you may contact the person listed under FOR FURTHER INFORMATION
CONTACT to access additional non-CBI information that may be available.
List of Subjects
Environmental protection, Chemicals, Hazardous substances, Imports,
Notice of commencement, Premanufacturer, Reporting and recordkeeping
requirements, Test marketing exemptions.
Dated: November 17, 2010.
Darryl S. Ballaard,
Acting Director, Information Management Division, Office of Pollution
Prevention and Toxics.
[FR Doc. 2010-29674 Filed 11-23-10; 8:45 am]
BILLING CODE 6560-50-P