Certain New Chemicals; Receipt and Status Information, 21339-21345 [2011-8574]
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Federal Register / Vol. 76, No. 73 / Friday, April 15, 2011 / Notices
process, contact Erika Mark at 978–318–
8250; by electronic mail at
Erika.L.Mark@usace.army.mil; or by
mail at 696 Virginia Road, Concord, MA
01742. Information on the EIS also is
available at DOE’s website for the
proposed action: https://
www.northernpasseis.us.
Issued in Washington, DC, on April 12,
2011.
Anthony J. Como,
Director, Permitting and Siting Office of
Electricity Delivery and Energy Reliability.
[FR Doc. 2011–9161 Filed 4–14–11; 8:45 am]
BILLING CODE 6450–01–P
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPPT–2011–0313; FRL–8869–4]
Certain New Chemicals; Receipt and
Status Information
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
Section 5 of the Toxic
Substances Control Act (TSCA) requires
any person who intends to manufacture
(defined by statute to include import) a
new chemical (i.e. a chemical not on the
TSCA Inventory) to notify EPA and
comply with the statutory provisions
pertaining to the manufacture of new
chemicals. Under 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 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
October 11, 2010 to December 3, 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 identified by the
specific PMN or TME number, must be
received on or before May 16, 2011.
ADDRESSES: Submit your comments,
identified by docket identification (ID)
number EPA–HQ–OPPT–2011–0313,
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.
srobinson on DSKHWCL6B1PROD with NOTICES
SUMMARY:
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• 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,
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
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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
Division, 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; email 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: TSCAHotline@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 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
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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.
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
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 to
October 11, 2010 to December 3, 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—75 PMNS RECEIVED FROM: 10/11/10 TO 12/03/10
Case No.
Received
date
Projected
notice end
date
Manufacturer/
Importer
Use
Chemical
(G) Adipic acid, polymer with benzenepolycarboxylic
acids,
polyakylene glycol, alkanediols,
1,1′-methylenebis
[isocyanatobenzene] and a substituted-, trialkoxysilane
(G) Aromatic diacid, polymer with
polyol, alkyl triol, alkyl alkanoate
(S) 1h-pyrrole-1-hexanoic acid, 2,5dihydro-2,5-dioxo-*
(G) Mercapto silane ester of silica
(G) Acylated alkenyl succinimide
(G) The PMN substance (polymer is
designated for use in coatings intended for us in refinishing vehicles. Through the hydroxyl group
on the polymer, the coatings is
crosslinked with polyisocyanate
(G) Methacrylic acid polymer with
isobornyl methacrylate sobornyl
acrylate 2 hydrox
10/08/10
01/05/11
CBI ..............................
(G) Coating component ....................
P–11–0017 ...
10/12/10
01/09/11
CBI ..............................
(G) Automotive coatings ..................
P–11–0018 ...
10/12/10
01/09/11
CBI ..............................
(G) Resin component .......................
P–11–0019 ...
P–11–0020 ...
P–11–0021 ...
10/13/10
10/12/10
10/12/10
01/10/11
01/09/11
01/09/11
CBI ..............................
CBI ..............................
Akzo Nobel Coatings
Inc.
P–11–0022 ...
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P–11–0016 ...
10/12/10
01/09/11
Akzo Nobel Coatings
Inc.
P–11–0023 ...
10/13/10
01/10/11
Omnova Solutions Inc.
P–11–0024 ...
10/13/10
01/10/11
Omnova Solutions Inc.
(G) Reactant .....................................
(G) Petroleum additive .....................
(S) Designated use of this polymer
is for refinishing vehicles. Through
the hydroxyl groups on the polymer, the coating is crosslinked
with a polyisocyanate material will
be atomized by spray application.
(S) Designated use of this polymer
is for refinishing vehicles. Through
the hydroxyl groups on the polymer, the coating is crosslinked
with a polyisocyanate.
(S) Intermediate in the production of (G) Methacrylic acid polymer with
functionalized polymers; surfacisobornyl methacrylate sobornyl
tant, flow, leveling, and wetting
acrylate 2 hydrox
additive for solvent borne coatings.
(S) Intermediate in the production of (G) Methacrylic acid polymer with
functionalized polymers; surfacisobornyl methacrylate sobornyl
tant, flow, leveling, and wetting
acrylate 2 hydrox
additive for solvent borne coatings.
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TABLE I—75 PMNS RECEIVED FROM: 10/11/10 TO 12/03/10—Continued
Received
date
Case No.
Projected
notice end
date
Manufacturer/
Importer
Use
Chemical
(S) Intermediate in the production of
functionalized polymers; surfactant, flow, leveling, and wetting
agent borne coatings.
(S) Intermediate in the production of
functionalized polymers; surfactant, flow, leveling, and wetting
agent borne coatings.
(G) Material for electronic parts .......
(G) Methacrylic acid polymer with
isobornyl methacrylate sobornyl
acrylate 2 hydrox
10/13/10
01/10/11
Omnova Solutions Inc.
P–11–0026 ...
10/13/10
01/10/11
Omnova Solutions Inc.
P–11–0027 ...
10/18/10
01/15/11
CBI ..............................
P–11–0028 ...
10/15/10
01/12/11
CBI ..............................
P–11–0029 ...
10/19/10
01/16/11
Zeon Chemicals L.P.
P–11–0030 ...
10/19/10
01/16/11
CBI ..............................
P–11–0031 ...
10/19/10
01/16/11
CBI ..............................
P–11–0032 ...
10/19/10
01/16/11
Cognis Corporation .....
P–11–0033 ...
10/18/10
01/15/11
CBI ..............................
(S) Hardener for epoxy resin laminating systems.
P–11–0034 ...
10/18/10
01/15/11
CBI ..............................
(S) Hardener for epoxy resin laminating systems.
P–11–0035
P–11–0036
P–11–0037
P–11–0038
...
...
...
...
10/20/10
10/20/10
10/20/10
10/21/10
01/17/11
01/17/11
01/17/11
01/18/11
Huntsman Corporation
Huntsman Corporation
Huntsman Corporation
Instrumental Polymer
Technologies, LLC.
(S)
(S)
(S)
(S)
P–11–0039 ...
P–11–0040 ...
P–11–0041 ...
10/21/10
10/22/10
10/21/10
01/18/11
01/19/11
01/18/11
CBI ..............................
CBI ..............................
Dow Chemical Company.
P–11–0042 ...
10/25/10
01/22/11
CBI ..............................
(G) Coating .......................................
(G) Component of lubricant.
(S) Production engineered lubricants
for closed system use; greases;
friction modifier for metalworking
lubricants.
(S) Hardener for epoxy resin laminating systems.
P–11–0043 ...
10/26/10
01/23/11
Gelest, Inc.
P–11–0044 ...
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P–11–0025 ...
10/26/10
01/23/11
Gelest, Inc.
P–11–0045 ...
10/26/10
01/23/11
Gelest, Inc.
P–11–0046 ...
10/26/10
01/23/11
Gelest, Inc.
P–11–0047 ...
10/22/10
01/19/11
Akzo Nobel Surface
Chemistry LLC.
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(S) Coatings for leather; water
borne industrial coatings like
wood.
(S) Dry etching agent for production
of
semiconductors;
chemical
vapor deposition (cvd) for production of semiconductors.
(S) Flame-retardant coating for textiles.
(G) The substance is used to
produce a component of polyurethane foam to insulate residential, commercial and industrial
buildings. This application is contained and non-dispersive.
(S) Defoamer for industrial and institutional cleaning applications.
Enhanced oil recovery ...............
Enhanced oil recovery ...............
Enhanced oil recovery ...............
Base polymer for coatings .........
(S)
Conversion
to
1,1,3,3tetramethyldisiloxane—see
gls138; reducing agent for organic
substrates, e.g. pharmaceutical
synthesis.
(S) End-capper for silicones; research.
(S) Oxygen permeable component
of contact lens formulation; research.
(S) Conversion to hydrophobic substrates; research.
(G) Friction modifier .........................
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(G) Methacrylic acid polymer with
isobornyl methacrylate sobornyl
acrylate 2 hydrox
(G)
(Methoxymethyl)
hydrocarbomonocycle
(G)
Hexamethylenediisocyanate
hompolymer, alkoxy-terminated
(S) Cyclopentene,
heptafluoro-*
1,3,3,4,4,5,5-
(G) Waterborne polyurethane
(G) Phenol, polymer with formaldehyde, reaction products with
diethanolamine and alkylamine
(S) Poly(oxy-1,2-ethanediyl), .alpha.(2-ethylhexyl)-.omega.-[(2hydroxydecyl)oxy]-*
(S) Formaldehyde, polymer with 4(1,1-dimethylethyl)phenol,
reactions
products
with
1piperazineethanamine*
(S) Formaldehyde, polymer with
.alpha.-(2-aminomethylethyl).omega.-(2aminomethylethoxy]poly[oxy(methyl-1,2-ethandiyl)]
and 4-(1,1-dimethylethyl)phenol.*
(G) Alkyl alkoxy sulfate sodium salt
(G) Alkyl alkoxy sulfate sodium salt
(G) Alkyl alkoxy sulfate sodium salt
(S) Carbonic acid, dimethyl ester,
polymer
with
2,2bis(hydroxymethyl)-1,3propanediol, cyclohexyl ester*
(G) Silsesquioxanes, polyacrylate
(G) Lubricant ingredient
(G) Industrial lubricants
(S) 1,2-ethanediamine, N1,N2-bis(2aminoethyl)-, reaction products
with bu glycidyl ether*
(S)
Disiloxane,
1-butyl-1,1,3,3tetramethyl-*
(S) Disiloxane, 1,3-dibutyl-1,1,3,3tetramethyl-*
(S)
Pentasiloxane,
1-butyl1,1,3,3,5,5,7,7,9,9-decamethyl-*
(S) Siloxanes and silicones, di-me,
bu group- and hydrogen-terminated *
(G) N,N-di(hydrogenated tallakyls)1,3-propanediamine
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TABLE I—75 PMNS RECEIVED FROM: 10/11/10 TO 12/03/10—Continued
Received
date
Case No.
Projected
notice end
date
Manufacturer/
Importer
Use
(G) Open, non-dispersive textile finish.
(G) Flame retardant for incorporation into polymer resins (open
non-dispersive use).
(G) Flame retardant for incorporation into polymer resins (open
non-dispersive use).
(S) Flow modifier for aqueous cleaning solutions; flow modifier for
aqueous dispersions
(S) Uv curable inks ..........................
Chemical
10/27/10
01/24/11
CBI ..............................
P–11–0049 ...
10/27/10
01/24/11
Thor Specialties, Inc.
P–11–0050 ...
10/27/10
01/24/11
Thor Specialties, Inc.
P–11–0051 ...
10/28/10
01/25/11
CBI ..............................
P–11–0052 ...
11/01/10
01/29/11
Piedmont Chemical Industries I, LLC.
P–11–0053 ...
11/03/10
01/31/11
CBI ..............................
(G) Automotive coating ....................
P–11–0054 ...
11/03/10
01/31/11
Mane, USA ..................
(G) Perfumery ingredient .................
P–11–0055 ...
P–11–0056 ...
11/02/10
11/03/10
01/30/11
01/31/11
Forbo Adhesives, LLC
CBI ..............................
P–11–0057 ...
11/03/10
01/31/11
CBI ..............................
P–11–0058 ...
P–11–0059 ...
11/02/10
11/04/10
01/30/11
02/01/11
CBI ..............................
CBI ..............................
P–11–0060 ...
11/04/10
02/01/11
CBI ..............................
(G) Hot melt polyurethane purge .....
(S) Acylic resin used in uv curable
inks and coatings.
(S) Acrylic resin used in uv curable
inks and coatings.
(G) Catalyst ingredient .....................
(G) Ingredient in paint. Degree of
containment: highly dispersive
use.
(G) Adhesive system component .....
P–11–0061 ...
11/05/10
02/02/11
Huntsman Textile Effects.
(S) Exhaust dyeing cotton fabrics ....
P–11–0062 ...
11/05/10
02/02/11
CBI ..............................
(G) Gear oil additive .........................
P–11–0063 ...
11/08/10
02/05/11
CBI ..............................
P–11–0064 ...
11/08/10
02/05/11
Isola Group .................
P–11–0065
P–11–0066
P–11–0067
P–11–0068
P–11–0069
...
...
...
...
...
11/09/10
11/09/10
11/09/10
11/12/10
11/12/10
02/06/11
02/06/11
02/06/11
02/09/11
02/09/11
CBI
CBI
CBI
CBI
CBI
(S) Coating material for use in textile and/or paper.
(G) Homide 108 is one of the monomers in the resin polymerization.
(G) Intermediate ...............................
(G) Additive in transmission fluids ...
(G) Additive in transmission fluids ...
(G) Polymeric dye carrier .................
(S) Crosslinker for polymers ............
P–11–0070 ...
11/05/10
02/02/11
Starfire Systems, Inc.
P–11–0071 ...
11/05/10
02/02/11
Starfire Systems, Inc.
P–11–0072 ...
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P–11–0048 ...
11/15/10
02/12/11
Cognis Corporation .....
P–11–0073 ...
11/12/10
02/09/11
Huntsman Corporation
P–11–0074 ...
11/19/10
02/16/11
CBI ..............................
P–11–0075 ...
11/19/10
02/16/11
CBI ..............................
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..............................
..............................
..............................
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(S) Precurser for producing silicon
oxycarbide ceramics.
(S) High temperature resistant adhesive; ceramic matrix composites; polymer matrix composits.
(G) The formulated pmn substance
will be imported for use as a lubricant oil for gear boxes.
(S) Intermediate for enhanced oil recovery surfactants.
(S) A component in ultraviolet light/
electron beam curable formulations.
(G) For use in the manufacture of
paper.
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(G) Modified fluorinated urethane
(G) Organic-N,P-compound
(G) Organic-N,P-compound
(G) Amino methacrylate copolymer
(S) Fatty acids, C18-unsaturated,
dimers, hydrogenated, esters with
pentaerythritol acrylate *
(G) Substituted alkanoic acid, polymer with alkanediol and cyclic
ether, alkanoate
(S) 2H-pyran-4-ol, 2-(1-ethylpropyl)
tetrahydro-4-methyl
(G) Polyester urethane polymer
(G) Aliphatic urethane acrylate polymer
(G) Aliphatic urethane acrylate polymer
(G) Aromatic diol, diaryl carboxylate
(G) Trialkylsilyl acrylate copolymer
(G)
Methylenebis
[isocyanatobenzene],
polymer
with alkanedioic acid, alkylene
glycols, alkoxylated alkanepolyol
and substituted trialkoxysilane
(G) Reaction product of substituted
naphthalenesulfonic
acid
diazotized and couple with substituted triazine and substituted
naphthalenesulfonic acid alkyl
amino phenyl compound
(G) Carbomonocyclic alkene polymer
with
alkyl
alkenoate,
polyalkylidene
alkenoate
and
dialkylaminoalkyl alkenamide
(G) Perfluoroalkyl acrylate copolymer
(G) N-(2,6-xylyl) maleimide
(G) Alkyl methacrylate
(G) Acrylic polymer
(G) Acrylic polymer
(G) Polyester polyamide
(G)
Dispersible
isocyanate
crosslinker
(G) Alkyl siloxane polymer
(G) Alkyl siloxane polymer
(S) Decanedioic acid, polymer with
2,2-bis(hydroxymethyl)-1,3propanediol, isooctadecanoate *
(G) Alkylxylene
(G) Glyceryl polypropylene glycol
ether polymer with isophorone
diisocyanate,
methacrylate
blocked
(G) Polyphenolic condensation polymer
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TABLE I—75 PMNS RECEIVED FROM: 10/11/10 TO 12/03/10—Continued
Case No.
Received
date
Projected
notice end
date
Manufacturer/
Importer
Use
Chemical
P–11–0076 ...
11/22/10
02/19/11
CBI ..............................
P–11–0077 ...
11/23/10
02/20/11
CBI ..............................
(S) Pigment dispersant for use in
water-based coating.
(G) Printing additive .........................
P–11–0078 ...
11/24/10
02/21/11
Shin-etsu Silicones of
America Inc.
(S) Treatment from textile; fabric
softener.
P–11–0079 ...
11/30/10
02/27/11
H.B. Fuller ...................
(G) Industrial adhesive .....................
P–11–0080 ...
P–11–0081 ...
11/30/10
11/30/10
02/27/11
02/27/11
CBI ..............................
K+S North America .....
P–11–0082 ...
11/30/10
02/27/11
CBI ..............................
P–11–0083 ...
12/02/10
03/01/11
Huntsman Textile Effects.
(G) Component of a floor coating ....
(S) Intermediate to be used in the
production of 1h-pyrazole, 3,4-dimethyl-, phosphate, a fertilizer additive.
(G) Personal care, industrial &
household hygiene, floucculants,
specialty coatings.
(S) Exhaust dyeing cotton fabrics ....
P–11–0084 ...
12/01/10
02/28/11
CBI ..............................
P–11–0085 ...
12/03/10
03/02/11
CBI ..............................
P–11–0086 ...
12/03/10
03/02/11
CBI ..............................
P–11–0087 ...
12/03/10
03/02/11
CBI ..............................
(G) Encapsulated for electronic
parts.
(G) Chemical reagent for industrial
syntheses.
(G) Chemical reagent for industrial
syntheses.
(G) Chemical processing aid ...........
P–11–0088 ...
12/03/10
03/02/11
CBI ..............................
(G) Chemical processing aid ...........
P–11–0089 ...
12/03/10
03/02/11
CBI ..............................
(G) Chemical processing aid ...........
P–11–0090 ...
12/03/10
03/02/11
CBI ..............................
(G) Chemical intermediate ...............
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
(G) Polyurethane derivative
(G) Benzenedicarboxylic acid, polymer with 1,4-butanediol, (2e)-2butenedioic acid, decanedioic
acid,
ethenylbenzene,
2ethylhexyl
2-propenoate,
hexanedioic acid, 1,6-hexane derivatives and 2-propenoic acid,
tert-bu peroxide-initiated
(S) Siloxanes and silicones, dimethyl, hydroxy terminated, reaction
products
with
N-[3(dimethoxymethylsilyl)propyl]-1,2ethanediamine *
(G) Polyester, polymer with 2-ethyl2-(hydroxymethyl)-1,3-propanediol
and
5-isocyanato-1(isocyanatomethyl)-1,3,3trimethylcyclohexane
(G) Urethane acrylate
(S) 3,4-dimethyl-1H-pyrazole *
(G) Styrene-acrylate copolymer
(G) Reaction product of substituted
naphthalenesulfonic acid and substituted
benzenesulfonic
acid
diazotized and coupled with alkyl
benzene
substituted
triazine
amino phenyl compound
(G) Epoxylated nitrile rubber
(G) Polyfluoroalkylpropionic acid
ethyl ester
(G) Polyfluoroalkyl phosphoric acid
(G) Polyfluoroalkyl phosphoric acid
salt, aqueous solution
(G) Polyfluoroalkyl phosphoric acid
salt, aqueous solution
(G) Polyfluoroalkyl phosphoric acid
salt, aqueous solution
(G) Heteroaromatic compound
the TME, the submitting manufacturer/
importer, the potential uses identified
by the manufacturer/importer in the
TME, and the chemical identity.
TABLE II—05 TMES RECEIVED FROM: 10/18/10 TO 12/03/10
srobinson on DSKHWCL6B1PROD with NOTICES
Case No.
T–11–0002 ...
VerDate Mar<15>2010
Received
date
12/13/10
16:58 Apr 14, 2011
Projected
notice end
date
Manufacturer/importer
Use
Chemical
01/26/11
Cytec Industries Inc. ...
(S) Dispersing additive for organic
and inorganic pigments and extenders.
(G) Substituted alkanoic acid, polymer with alkanoic acid alkyl
esters, with substituted polyglycolinitiated.
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TABLE II—05 TMES RECEIVED FROM: 10/18/10 TO 12/03/10—Continued
Received
date
Case No.
Projected
notice end
date
Manufacturer/importer
Use
Chemical
(G) Substituted alkyl homopolymer,
substituted
alkylacrylate
and
heteromonocyclic
homopolymer
monoester
with
substituted
alkylacrylate.
(G) Tertiary ammonium compound.
(G) Modified epoxy resin.
(G) Tertiary ammonium compound.
T–11–0003 ...
12/13/10
01/26/11
Cytec Industries Inc. ...
(G) Coatings resin ............................
T–11–0004 ...
T–11–0005 ...
T–11–0006 ...
12/13/10
12/14/10
01/11/11
01/26/11
01/27/11
02/24/11
CBI ..............................
Cytec Industries Inc. ...
CBI ..............................
(G) Inhibitor for oil field applications
(G) Binder resin ................................
(G) Inhibitor for oil field applications
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—37 NOCS RECEIVED FROM: 10/11/10 TO 12/3/10
Case No.
Commencement
notice end
date
Received
date
10/21/10
10/20/10
10/20/10
11/01/10
01/07/11
12/20/10
11/10/10
01/24/11
01/24/11
01/24/11
12/13/10
P–06–0451 ................
12/13/10 ......
11/12/10 ........
P–06–0618
P–06–0619
P–07–0353
P–07–0719
P–08–0273
P–08–0299
P–08–0376
P–08–0401
P–08–0422
P–08–0486
................
................
................
................
................
................
................
................
................
................
11/01/10
11/01/10
10/07/10
11/30/10
12/21/10
12/20/10
10/12/10
01/04/11
01/04/11
10/05/10
......
......
......
......
......
......
......
......
......
......
10/20/10
10/20/10
08/28/10
11/03/10
12/10/10
12/15/10
10/06/10
12/16/10
12/16/10
09/17/10
........
........
........
........
........
........
........
........
........
........
P–08–0502
P–08–0537
P–08–0550
P–08–0643
P–09–0083
P–09–0131
P–09–0146
................
................
................
................
................
................
................
01/12/11
11/23/10
11/29/10
12/30/10
10/04/10
11/23/10
10/01/10
......
......
......
......
......
......
......
12/16/10
11/01/10
11/20/10
12/17/10
09/03/10
11/11/10
09/28/10
........
........
........
........
........
........
........
P–09–0363
P–09–0364
P–09–0382
P–09–0416
srobinson on DSKHWCL6B1PROD with NOTICES
J–09–0004 .................
J–10–0002 .................
J–10–0003 .................
P–05–0145 ................
P–05–0297 ................
P–05–0400 ................
P–05–0526 ................
P–05–0840 ................
P–05–0842 ................
P–05–0843 ................
P–06–0450 ................
......
......
......
......
......
......
......
......
......
......
......
06/30/10
10/18/10
10/15/10
10/21/05
12/02/10
01/10/06
10/24/10
12/22/10
12/22/10
12/22/10
11/18/10
................
................
................
................
11/12/10
11/12/10
11/30/10
11/30/10
......
......
......
......
10/28/10
10/28/10
11/09/10
11/26/10
........
........
........
........
P–09–0430
P–09–0431
P–09–0432
P–09–0433
................
................
................
................
10/04/10
10/04/10
10/04/10
10/04/10
......
......
......
......
09/14/10
09/14/10
09/14/10
09/14/10
........
........
........
........
If you are interested in information
that is not included in these tables, you
VerDate Mar<15>2010
16:58 Apr 14, 2011
Jkt 223001
........
........
........
........
........
........
........
........
........
........
........
Chemical
(G) Contained use of a genetically modified microorganism trichoderma reesei.
(G) Carbohydrase.
(G) T. Reesei 3408.
(G) Polyether polyol.
(G) Aqueous polyurethane dispersion.
(S) 1-butanone, 3-(dodecylthio)-1-(2,6,6-trimethyl-3-cyclohexen-1-yl)-*.
(G) Polyurethane resin.
(G) Polycarbonate polyurethane.
(G) Polycarbonate polyurethane.
(G) Polycarbonate polyurethane.
(S) Poly(oxy-1,2-ethanediyl), .alpha.-(2-methyl-2-propenyl)-.omega.-hydroxy-, c12–15alkyl ethers*.
(S) Poly(oxy-1,2-ethanediyl), .alpha.-(2-methyl-2-propenyl)-.omega.-hydroxy-, c10–16alkyl ethers*.
(G) Salts of modified tall-oil fatty acid amidoamines.
(G) Salts of modified tall-oil fatty acids.
(G) Alkyl acid fluoride.
(S) Benzeneacetonitrile, .alpha.-butylidene-, (.alpha. z)-*.
(G) Alkyl silyl phosphonate.
(S) Propanol, 1(or 2)-(methyl-2-[(1,7,7-trimethylbicyclo[2.2.1]hept-2-yl)oxy]ethoxy]-*.
(G) Arylalkylamine, N-[4-[2-(substitutedaryl)diazenyl]aryl]-N-alkyl.
(G) Polyether modified fatty acid dimer.
(G) Potassium polystyrene maleate.
(G) Polymer with .alpha.-hydro-.omega.-hydroxypoly[oxy(methyl-1,2-ethanediyl)], 3-hydroxy-2-(hydroxymethyl)-2-methylpropanoic acid and alkyldiisocyanate, ammonium
salt.
(G) Cyclic guanidine.
(G) Comple keto-amine.
(S) 1-propene, 1,3,3,3-tetrafluoro-, (1e)-*.
(G) Fluorinated acrylic copolymer.
(G) Cationic polyamide.
(G) Aromatic carboxylic acid.
(S) Formaldehyde, polymers with acetone-phenol reaction products and phenol, sodium
salts*.
(G) Polyalkenyl derives. of aliphatic dicarboxylic anhydride, imides with melamine.
(G) Alkenoic acid, polymer with alkyl alkenoates, sodium salt.
(S) Iron, citrate phosphate potassium complexes*.
(G) 3’H-cyclopropacarbopolycycle-3’-butanoic acid, 3’-phenyl-, methyl ester; 3’Hcyclopropacarbopolycycle-3’-butanoic acid, 3’-phenyl-, methyl ester.
(G) Polymeric monoazo compound.
(G) Polymeric monoazo compound.
(G) Polymeric monoazo triphenylmethane.
(G) Polymeric triphenylmethane.
may contact the person listed under FOR
to access
FURTHER INFORMATION CONTACT
PO 00000
Frm 00027
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additional non-CBI information that
may be available.
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List of Subjects
Environmental protection, Chemicals,
Hazardous substances, Imports, Notice
of commencement, Premanufacturer,
Reporting and recordkeeping
requirements, Test marketing
exemptions.
Dated: April 4, 2011.
Darryl S. Ballard,
Acting Director, Information Management
Division, Office of Pollution Prevention and
Toxics.
[FR Doc. 2011–8574 Filed 4–14–11; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
[ER–FRL–8996–4]
Environmental Impacts Statements;
srobinson on DSKHWCL6B1PROD with NOTICES
Notice of Availability
Responsible Agency: Office of Federal
Activities, General Information (202)
564–1399 or https://www.epa.gov/
compliance/nepa/
Weekly receipt of Environmental Impact
Statements
Filed 04/04/2011 Through 04/08/2011
Pursuant to 40 CFR 1506.9.
Notice
In accordance with Section 309(a) of
the Clean Air Act, EPA is required to
make its comments on EISs issued by
other Federal agencies public.
Historically, EPA met this mandate by
publishing weekly notices of availability
of EPA comments, which includes a
brief summary of EPA’s comment
letters, in the Federal Register. Since
February 2008, EPA has included its
comment letters on EISs on its Web site
at: https://www.epa.gov/compliance/
nepa/eisdata.html. Including the entire
EIS comment letters on the Web site
satisfies the Section 309(a) requirement
to make EPA’s comments on EISs
available to the public. Accordingly, on
March 31, 2010, EPA discontinued the
publication of the notice of availability
of EPA comments in the Federal
Register.
EIS No. 20110108, Draft EIS, USFS, OR,
Kapka Butte Sno-Park Project,
Proposal to Build a New Sno-Park to
Provide more High-Elevation Parking
for Winter Recreationist, Bend-Ft.
Rock Ranger District, Deschutes
National Forest, Deschutes County,
OR, Comment Period Ends: 05/30/
2011, Contact: Beth Peer 541–383–
4769.
EIS No. 20110109, Draft EIS, USFS, OR,
Snow Basin Vegetation Management
Project, Proposal to Implementing
Commercial Harvest of Timber, Post
VerDate Mar<15>2010
16:58 Apr 14, 2011
Jkt 223001
Harvest Non-Commercial Thinning,
Whitman Ranger District, WallowaWhitman Forest, Baker County, OR,
Comment Period Ends: 05/30/2011,
Contact: Dea Nelson 541–523–1316.
EIS No. 20110110, Draft EIS, RUS, GA,
Biomass Power Plant Project,
Application for Financial Assistance
to Construction 100 Megawatt (MW)
Biomass Plant and Related Facilities,
Warren County, GA, Comment Period
Ends: 05/31/2011, Contact: Stephanie
A. Strength 970–403–3559.
EIS No. 20110111, Draft EIS, FERC, WA,
Wells Hydroelectric Project,
Application to Relicense, Public
Utility District No. 1 Columbia River
near Pateros and Brewster in Douglas,
Okanogan, and Chelan Counties, WA,
Comment Period Ends: 05/30/2011,
Contact: Mary O’Driscoll 1–866–208–
3372.
EIS No. 20110112, Draft EIS, BLM, NM,
HB In-Situ-Solution Mining Project,
Proposal to Extract the Potash
Remaining in Inactive Underground
Mine, Eddy County, NM, Comment
Period Ends: 06/13/2011, Contact:
David Alderman 575–234–6232.
EIS No. 20110113, Final EIS, FHWA, MI,
M–15 Reconstruction, I–75 to I–69,
Funding and NPDES and U.S. Army
COE Section 404 Permits Issuance,
Oakland and Genesee Counties, MI,
Review Period Ends: 05/16/2011,
Contact: David T.Williams 517–702–
1820.
EIS No. 20110114, Draft EIS, FERC, WA,
Boundary Hydroelectric Project,
Application for Hydroelectric License,
FERC Project No. 2144–038 and
Sullivan Creek Project, Application
for Surrender of Hydropower FERC
Project No. 2225–015, Pend Oreille
County, WA, Comment Period Ends:
05/30/2011, Contact: Mary O’Driscoll
1–866–208–3372.
EIS No. 20110115, Final EIS, BLM, NV,
Genesis Project, Proposes Expansion
of Existing Mine Pits and
Development of the Bluestar Ridge
Open Pit Mine, Newmont Mining
Corporation, Eureka County, NV,
Review Period Ends: 05/09/2011,
Contact: Kirk Laird 775–753–0272.
EIS No. 20110116, Draft EIS, NOAA, 00,
Amendment 10 to the Fishery
Management Plan for Spiny Lobster,
Establish Annual Catch Limits and
Accountability Measures for
Caribbean Spiny Lobster, Gulf of
Mexico and South Atlantic Regions,
Comment Period Ends: 06/01/2011,
Contact: Roy E. Crabtree, PhD 727–
824–5701.
EIS No. 20110117, Final EIS, BLM, CA,
First Solar Desert Sunlight Solar Farm
(DSSF) Project, Proposing To Develop
a 550–Megawatt Photovoltaic Solar
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21345
Project, Also Proposes to Facilitate the
Construction and Operation of the
Red Bluff Substation, California
Desert Conservation Area (CDCA)
Plan, Riverside County, CA, Review
Period Ends: 05/09/2011, Contact:
Allison Shaffer 760–833–7104.
EIS No. 20110118, Final EIS, DOI, WA,
Cle Elum Dam Fish Passage Facilities
and Fish Reintroduction Project, To
Restore Connectivity, Biodiversity,
and Natural Production of
Anadromous Salmonids, Kittitas
County, WA, Review Period Ends: 05/
08/2011, Contact: Jim Taylor 208–
378–5081.
EIS No. 20110119, Final EIS, USFS, CA,
Kings River Experimental Watershed
Forest Health and Research Project,
Implementation, Sierra National
Forest, High Sierra Ranger District,
Fresno County, CA, Review Period
Ends: 05/09/2011, Contact: Judi Tapia
559–297–0706 Ext. 4938.
Amended Notices
EIS No. 20100118, Draft EIS, USACE,
KY, Withdrawn—East Kentucky
Power Cooperative, Proposed
Baseload Power Plant, to Constructing
and Operating a 278 Megawatt
Circulating Fluidized Bed Electric
Generating Unit (CFD), and
Associated Infrastructure at the
Existing J.K. Smith Power Station,
Application for US Army COE Section
10 and 404 Permits, Clark County,
KY, Comment Period Ends: 05/24/
2010, Contact: Michael Hasty 502–
315–6676. Revision to FR Notice
Published: Officially Withdrawn by
the Preparing Agency by letter dated
04/05/2011.
Dated: April 12, 2011.
Aimee S. Hessert,
Deputy Director, NEPA Compliance Division,
Office of Federal Activities.
[FR Doc. 2011–9185 Filed 4–14–11; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
[FRL–9296–2]
Science Advisory Board Staff Office;
Notification of Two Public
Teleconferences of the Clean Air
Scientific Advisory Committee
(CASAC) Air Monitoring and Methods
Subcommittee
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
The Environmental Protection
Agency (EPA or Agency) Science
SUMMARY:
E:\FR\FM\15APN1.SGM
15APN1
]]>Agencies
[Federal Register Volume 76, Number 73 (Friday, April 15, 2011)]
[Notices]
[Pages 21339-21345]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-8574]
=======================================================================
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
[EPA-HQ-OPPT-2011-0313; FRL-8869-4]
Certain New Chemicals; Receipt and Status Information
AGENCY: Environmental Protection Agency (EPA).
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: Section 5 of the Toxic Substances Control Act (TSCA) requires
any person who intends to manufacture (defined by statute to include
import) a new chemical (i.e. a chemical not on the TSCA Inventory) to
notify EPA and comply with the statutory provisions pertaining to the
manufacture of new chemicals. Under 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 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 October 11, 2010
to December 3, 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 identified by the specific PMN or TME number, must be
received on or before May 16, 2011.
ADDRESSES: Submit your comments, identified by docket identification
(ID) number EPA-HQ-OPPT-2011-0313, 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 Division, 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
[[Page 21340]]
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.
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 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 to October 11, 2010 to December 3, 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--75 PMNs Received From: 10/11/10 to 12/03/10
----------------------------------------------------------------------------------------------------------------
Projected
Case No. Received notice end Manufacturer/ Importer Use Chemical
date date
----------------------------------------------------------------------------------------------------------------
P-11-0016......... 10/08/10 01/05/11 CBI........................... (G) Coating (G) Adipic acid,
component. polymer with
benzenepolycarbo
xylic acids,
polyakylene
glycol,
alkanediols,
1,1'-
methylenebis[iso
cyanatobenzene]
and a
substituted-,
trialkoxysilane
P-11-0017......... 10/12/10 01/09/11 CBI........................... (G) Automotive (G) Aromatic
coatings. diacid, polymer
with polyol,
alkyl triol,
alkyl alkanoate
P-11-0018......... 10/12/10 01/09/11 CBI........................... (G) Resin (S) 1h-pyrrole-1-
component. hexanoic acid,
2,5-dihydro-2,5-
dioxo-*
P-11-0019......... 10/13/10 01/10/11 CBI........................... (G) Reactant..... (G) Mercapto
silane ester of
silica
P-11-0020......... 10/12/10 01/09/11 CBI........................... (G) Petroleum (G) Acylated
additive. alkenyl
succinimide
P-11-0021......... 10/12/10 01/09/11 Akzo Nobel Coatings Inc. (S) Designated (G) The PMN
use of this substance
polymer is for (polymer is
refinishing designated for
vehicles. use in coatings
Through the intended for us
hydroxyl groups in refinishing
on the polymer, vehicles.
the coating is Through the
crosslinked with hydroxyl group
a polyisocyanate on the polymer,
material will be the coatings is
atomized by crosslinked with
spray polyisocyanate
application.
P-11-0022......... 10/12/10 01/09/11 Akzo Nobel Coatings Inc. (S) Designated (G) Methacrylic
use of this acid polymer
polymer is for with isobornyl
refinishing methacrylate
vehicles. sobornyl
Through the acrylate 2
hydroxyl groups hydrox
on the polymer,
the coating is
crosslinked with
a
polyisocyanate.
P-11-0023......... 10/13/10 01/10/11 Omnova Solutions Inc. (S) Intermediate (G) Methacrylic
in the acid polymer
production of with isobornyl
functionalized methacrylate
polymers; sobornyl
surfactant, acrylate 2
flow, leveling, hydrox
and wetting
additive for
solvent borne
coatings.
P-11-0024......... 10/13/10 01/10/11 Omnova Solutions Inc. (S) Intermediate (G) Methacrylic
in the acid polymer
production of with isobornyl
functionalized methacrylate
polymers; sobornyl
surfactant, acrylate 2
flow, leveling, hydrox
and wetting
additive for
solvent borne
coatings.
[[Page 21341]]
P-11-0025......... 10/13/10 01/10/11 Omnova Solutions Inc. (S) Intermediate (G) Methacrylic
in the acid polymer
production of with isobornyl
functionalized methacrylate
polymers; sobornyl
surfactant, acrylate 2
flow, leveling, hydrox
and wetting
agent borne
coatings.
P-11-0026......... 10/13/10 01/10/11 Omnova Solutions Inc. (S) Intermediate (G) Methacrylic
in the acid polymer
production of with isobornyl
functionalized methacrylate
polymers; sobornyl
surfactant, acrylate 2
flow, leveling, hydrox
and wetting
agent borne
coatings.
P-11-0027......... 10/18/10 01/15/11 CBI........................... (G) Material for (G)
electronic parts. (Methoxymethyl)
hydrocarbomonocy
cle
P-11-0028......... 10/15/10 01/12/11 CBI........................... (S) Coatings for (G)
leather; water Hexamethylenedii
borne industrial socyanate
coatings like hompolymer,
wood. alkoxy-
terminated
P-11-0029......... 10/19/10 01/16/11 Zeon Chemicals L.P. (S) Dry etching (S) Cyclopentene,
agent for 1,3,3,4,4,5,5-
production of heptafluoro-*
semiconductors;
chemical vapor
deposition (cvd)
for production
of
semiconductors.
P-11-0030......... 10/19/10 01/16/11 CBI........................... (S) Flame- (G) Waterborne
retardant polyurethane
coating for
textiles.
P-11-0031......... 10/19/10 01/16/11 CBI........................... (G) The substance (G) Phenol,
is used to polymer with
produce a formaldehyde,
component of reaction
polyurethane products with
foam to insulate diethanolamine
residential, and alkylamine
commercial and
industrial
buildings. This
application is
contained and
non-dispersive.
P-11-0032......... 10/19/10 01/16/11 Cognis Corporation............ (S) Defoamer for (S) Poly(oxy-1,2-
industrial and ethanediyl),
institutional .alpha.-(2-
cleaning ethylhexyl)-
applications. .omega.-[(2-
hydroxydecyl)oxy
]-*
P-11-0033......... 10/18/10 01/15/11 CBI........................... (S) Hardener for (S) Formaldehyde,
epoxy resin polymer with 4-
laminating (1,1-
systems. dimethylethyl)ph
enol, reactions
products with 1-
piperazineethana
mine*
P-11-0034......... 10/18/10 01/15/11 CBI........................... (S) Hardener for (S) Formaldehyde,
epoxy resin polymer with
laminating .alpha.-(2-
systems. aminomethylethyl
)-.omega.-(2-
aminomethylethox
y]poly[oxy(methy
l-1,2-
ethandiyl)] and
4-(1,1-
dimethylethyl)ph
enol.*
P-11-0035......... 10/20/10 01/17/11 Huntsman Corporation.......... (S) Enhanced oil (G) Alkyl alkoxy
recovery. sulfate sodium
salt
P-11-0036......... 10/20/10 01/17/11 Huntsman Corporation.......... (S) Enhanced oil (G) Alkyl alkoxy
recovery. sulfate sodium
salt
P-11-0037......... 10/20/10 01/17/11 Huntsman Corporation.......... (S) Enhanced oil (G) Alkyl alkoxy
recovery. sulfate sodium
salt
P-11-0038......... 10/21/10 01/18/11 Instrumental Polymer (S) Base polymer (S) Carbonic
Technologies, LLC. for coatings. acid, dimethyl
ester, polymer
with 2,2-
bis(hydroxymethy
l)-1,3-
propanediol,
cyclohexyl
ester*
P-11-0039......... 10/21/10 01/18/11 CBI........................... (G) Coating...... (G)
Silsesquioxanes,
polyacrylate
P-11-0040......... 10/22/10 01/19/11 CBI........................... (G) Component of (G) Lubricant
lubricant. ingredient
P-11-0041......... 10/21/10 01/18/11 Dow Chemical Company.......... (S) Production (G) Industrial
engineered lubricants
lubricants for
closed system
use; greases;
friction
modifier for
metalworking
lubricants.
P-11-0042......... 10/25/10 01/22/11 CBI........................... (S) Hardener for (S) 1,2-
epoxy resin ethanediamine,
laminating N1,N2-bis(2-
systems. aminoethyl)-,
reaction
products with bu
glycidyl ether*
P-11-0043......... 10/26/10 01/23/11 Gelest, Inc. (S) Conversion to (S) Disiloxane, 1-
1,1,3,3- butyl-1,1,3,3-
tetramethyldisil tetramethyl-*
oxane--see
gls138; reducing
agent for
organic
substrates, e.g.
pharmaceutical
synthesis.
P-11-0044......... 10/26/10 01/23/11 Gelest, Inc. (S) End-capper (S) Disiloxane,
for silicones; 1,3-dibutyl-
research. 1,1,3,3-
tetramethyl-*
P-11-0045......... 10/26/10 01/23/11 Gelest, Inc. (S) Oxygen (S)
permeable Pentasiloxane, 1-
component of butyl-
contact lens 1,1,3,3,5,5,7,7,
formulation; 9,9-decamethyl-*
research.
P-11-0046......... 10/26/10 01/23/11 Gelest, Inc. (S) Conversion to (S) Siloxanes and
hydrophobic silicones, di-
substrates; me, bu group-
research. and hydrogen-
terminated *
P-11-0047......... 10/22/10 01/19/11 Akzo Nobel Surface Chemistry (G) Friction (G) N,N-
LLC. modifier. di(hydrogenated
tallakyls)-1,3-
propanediamine
[[Page 21342]]
P-11-0048......... 10/27/10 01/24/11 CBI........................... (G) Open, non- (G) Modified
dispersive fluorinated
textile finish. urethane
P-11-0049......... 10/27/10 01/24/11 Thor Specialties, Inc. (G) Flame (G) Organic-N,P-
retardant for compound
incorporation
into polymer
resins (open non-
dispersive use).
P-11-0050......... 10/27/10 01/24/11 Thor Specialties, Inc. (G) Flame (G) Organic-N,P-
retardant for compound
incorporation
into polymer
resins (open non-
dispersive use).
P-11-0051......... 10/28/10 01/25/11 CBI........................... (S) Flow modifier (G) Amino
for aqueous methacrylate
cleaning copolymer
solutions; flow
modifier for
aqueous
dispersions
P-11-0052......... 11/01/10 01/29/11 Piedmont Chemical Industries (S) Uv curable (S) Fatty acids,
I, LLC. inks. C18-unsaturated,
dimers,
hydrogenated,
esters with
pentaerythritol
acrylate *
P-11-0053......... 11/03/10 01/31/11 CBI........................... (G) Automotive (G) Substituted
coating. alkanoic acid,
polymer with
alkanediol and
cyclic ether,
alkanoate
P-11-0054......... 11/03/10 01/31/11 Mane, USA..................... (G) Perfumery (S) 2H-pyran-4-
ingredient. ol, 2-(1-
ethylpropyl)
tetrahydro-4-
methyl
P-11-0055......... 11/02/10 01/30/11 Forbo Adhesives, LLC.......... (G) Hot melt (G) Polyester
polyurethane urethane polymer
purge.
P-11-0056......... 11/03/10 01/31/11 CBI........................... (S) Acylic resin (G) Aliphatic
used in uv urethane
curable inks and acrylate polymer
coatings.
P-11-0057......... 11/03/10 01/31/11 CBI........................... (S) Acrylic resin (G) Aliphatic
used in uv urethane
curable inks and acrylate polymer
coatings.
P-11-0058......... 11/02/10 01/30/11 CBI........................... (G) Catalyst (G) Aromatic
ingredient. diol, diaryl
carboxylate
P-11-0059......... 11/04/10 02/01/11 CBI........................... (G) Ingredient in (G) Trialkylsilyl
paint. Degree of acrylate
containment: copolymer
highly
dispersive use.
P-11-0060......... 11/04/10 02/01/11 CBI........................... (G) Adhesive (G)
system component. Methylenebis[iso
cyanatobenzene],
polymer with
alkanedioic
acid, alkylene
glycols,
alkoxylated
alkanepolyol and
substituted
trialkoxysilane
P-11-0061......... 11/05/10 02/02/11 Huntsman Textile Effects...... (S) Exhaust (G) Reaction
dyeing cotton product of
fabrics. substituted
naphthalenesulfo
nic acid
diazotized and
couple with
substituted
triazine and
substituted
naphthalenesulfo
nic acid alkyl
amino phenyl
compound
P-11-0062......... 11/05/10 02/02/11 CBI........................... (G) Gear oil (G)
additive. Carbomonocyclic
alkene polymer
with alkyl
alkenoate,
polyalkylidene
alkenoate and
dialkylaminoalky
l alkenamide
P-11-0063......... 11/08/10 02/05/11 CBI........................... (S) Coating (G)
material for use Perfluoroalkyl
in textile and/ acrylate
or paper. copolymer
P-11-0064......... 11/08/10 02/05/11 Isola Group................... (G) Homide 108 is (G) N-(2,6-xylyl)
one of the maleimide
monomers in the
resin
polymerization.
P-11-0065......... 11/09/10 02/06/11 CBI........................... (G) Intermediate. (G) Alkyl
methacrylate
P-11-0066......... 11/09/10 02/06/11 CBI........................... (G) Additive in (G) Acrylic
transmission polymer
fluids.
P-11-0067......... 11/09/10 02/06/11 CBI........................... (G) Additive in (G) Acrylic
transmission polymer
fluids.
P-11-0068......... 11/12/10 02/09/11 CBI........................... (G) Polymeric dye (G) Polyester
carrier. polyamide
P-11-0069......... 11/12/10 02/09/11 CBI........................... (S) Crosslinker (G) Dispersible
for polymers. isocyanate
crosslinker
P-11-0070......... 11/05/10 02/02/11 Starfire Systems, Inc. (S) Precurser for (G) Alkyl
producing siloxane polymer
silicon
oxycarbide
ceramics.
P-11-0071......... 11/05/10 02/02/11 Starfire Systems, Inc. (S) High (G) Alkyl
temperature siloxane polymer
resistant
adhesive;
ceramic matrix
composites;
polymer matrix
composits.
P-11-0072......... 11/15/10 02/12/11 Cognis Corporation............ (G) The (S) Decanedioic
formulated pmn acid, polymer
substance will with 2,2-
be imported for bis(hydroxymethy
use as a l)-1,3-
lubricant oil propanediol,
for gear boxes. isooctadecanoate
*
P-11-0073......... 11/12/10 02/09/11 Huntsman Corporation.......... (S) Intermediate (G) Alkylxylene
for enhanced oil
recovery
surfactants.
P-11-0074......... 11/19/10 02/16/11 CBI........................... (S) A component (G) Glyceryl
in ultraviolet polypropylene
light/electron glycol ether
beam curable polymer with
formulations. isophorone
diisocyanate,
methacrylate
blocked
P-11-0075......... 11/19/10 02/16/11 CBI........................... (G) For use in (G) Polyphenolic
the manufacture condensation
of paper. polymer
[[Page 21343]]
P-11-0076......... 11/22/10 02/19/11 CBI........................... (S) Pigment (G) Polyurethane
dispersant for derivative
use in water-
based coating.
P-11-0077......... 11/23/10 02/20/11 CBI........................... (G) Printing (G)
additive. Benzenedicarboxy
lic acid,
polymer with 1,4-
butanediol, (2e)-
2-butenedioic
acid,
decanedioic
acid,
ethenylbenzene,
2-ethylhexyl 2-
propenoate,
hexanedioic
acid, 1,6-hexane
derivatives and
2-propenoic
acid, tert-bu
peroxide-
initiated
P-11-0078......... 11/24/10 02/21/11 Shin-etsu Silicones of America (S) Treatment (S) Siloxanes and
Inc. from textile; silicones,
fabric softener. dimethyl,
hydroxy
terminated,
reaction
products with N-
[3-
(dimethoxymethyl
silyl)propyl]-
1,2-
ethanediamine *
P-11-0079......... 11/30/10 02/27/11 H.B. Fuller................... (G) Industrial (G) Polyester,
adhesive. polymer with 2-
ethyl-2-
(hydroxymethyl)-
1,3-propanediol
and 5-isocyanato-
1-
(isocyanatomethy
l)-1,3,3-
trimethylcyclohe
xane
P-11-0080......... 11/30/10 02/27/11 CBI........................... (G) Component of (G) Urethane
a floor coating. acrylate
P-11-0081......... 11/30/10 02/27/11 K+S North America............. (S) Intermediate (S) 3,4-dimethyl-
to be used in 1H-pyrazole *
the production
of 1h-pyrazole,
3,4-dimethyl-,
phosphate, a
fertilizer
additive.
P-11-0082......... 11/30/10 02/27/11 CBI........................... (G) Personal (G) Styrene-
care, industrial acrylate
& household copolymer
hygiene,
floucculants,
specialty
coatings.
P-11-0083......... 12/02/10 03/01/11 Huntsman Textile Effects...... (S) Exhaust (G) Reaction
dyeing cotton product of
fabrics. substituted
naphthalenesulfo
nic acid and
substituted
benzenesulfonic
acid diazotized
and coupled with
alkyl benzene
substituted
triazine amino
phenyl compound
P-11-0084......... 12/01/10 02/28/11 CBI........................... (G) Encapsulated (G) Epoxylated
for electronic nitrile rubber
parts.
P-11-0085......... 12/03/10 03/02/11 CBI........................... (G) Chemical (G)
reagent for Polyfluoroalkylp
industrial ropionic acid
syntheses. ethyl ester
P-11-0086......... 12/03/10 03/02/11 CBI........................... (G) Chemical (G)
reagent for Polyfluoroalkyl
industrial phosphoric acid
syntheses.
P-11-0087......... 12/03/10 03/02/11 CBI........................... (G) Chemical (G)
processing aid. Polyfluoroalkyl
phosphoric acid
salt, aqueous
solution
P-11-0088......... 12/03/10 03/02/11 CBI........................... (G) Chemical (G)
processing aid. Polyfluoroalkyl
phosphoric acid
salt, aqueous
solution
P-11-0089......... 12/03/10 03/02/11 CBI........................... (G) Chemical (G)
processing aid. Polyfluoroalkyl
phosphoric acid
salt, aqueous
solution
P-11-0090......... 12/03/10 03/02/11 CBI........................... (G) Chemical (G)
intermediate. Heteroaromatic
compound
----------------------------------------------------------------------------------------------------------------
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--05 TMEs Received From: 10/18/10 to 12/03/10
----------------------------------------------------------------------------------------------------------------
Projected
Case No. Received notice end Manufacturer/importer Use Chemical
date date
----------------------------------------------------------------------------------------------------------------
T-11-0002......... 12/13/10 01/26/11 Cytec Industries Inc.......... (S) Dispersing (G) Substituted
additive for alkanoic acid,
organic and polymer with
inorganic alkanoic acid
pigments and alkyl esters,
extenders. with substituted
polyglycol-
initiated.
[[Page 21344]]
T-11-0003......... 12/13/10 01/26/11 Cytec Industries Inc.......... (G) Coatings (G) Substituted
resin. alkyl
homopolymer,
substituted
alkylacrylate
and
heteromonocyclic
homopolymer
monoester with
substituted
