Certain New Chemicals; Receipt and Status Information, 36109-36120 [2011-15246]
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Federal Register / Vol. 76, No. 119 / Tuesday, June 21, 2011 / Notices
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protestants parties to the proceeding.
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comment date. Anyone filing a protest
must serve a copy of that document on
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file electronically should submit an
original and 14 copies of the protest to
the Federal Energy Regulatory
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Washington, DC 20426.
This filing is accessible on-line at
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Dated: June 9, 2011.
Nathaniel J. Davis, Sr.,
Deputy Secretary.
[FR Doc. 2011–15421 Filed 6–20–11; 8:45 am]
BILLING CODE 6717–01–P
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPPT–2011–0496; FRL–8876–3]
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 Chemical Substances
Inventory (TSCA Inventory)) to notify
EPA and comply with the statutory
provisions pertaining to the
manufacture of new chemicals. Under
TSCA sections 5(d)(2) and 5(d)(3), 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 manufacture those chemicals.
wwoods2 on DSK1DXX6B1PROD with NOTICES_PART 1
SUMMARY:
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This document, which covers the period
from February 1, 2011 to April 22, 2011,
and provides the required notice and
status report, consists of the PMNs and
TMEs, both pending or expired, and the
NOC 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 number or TME number,
must be received on or before July 21,
2011.
ADDRESSES: Submit your comments,
identified by docket identification (ID)
number EPA–HQ–OPPT–2011–0496,
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 comment directly
to EPA without going through
regulations.gov, your e-mail address
will be automatically captured and
included as part of the comment that is
placed in the docket and made available
on the Internet. If you submit an
electronic comment, EPA recommends
that you include your name and other
contact information in the body of your
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36109
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: 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.
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Federal Register / Vol. 76, No. 119 / Tuesday, June 21, 2011 / Notices
Although others may be affected, this
action applies directly to the submitter
of the PMNs addressed in this action. 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 this
information to EPA through
regulations.gov or e-mail. Clearly mark
the part or all of the information that
you claim to be CBI. For CBI
information in a disk or CD–ROM that
you mail to EPA, mark the outside of the
disk or CD–ROM as CBI and then
identify electronically within the disk or
CD–ROM the specific information that
is claimed as CBI. In addition to one
complete version of the comment that
includes information claimed as CBI, a
copy of the comment that does not
contain the information claimed as CBI
must be submitted for inclusion in the
public docket. Information so marked
will not be disclosed except in
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 a chemical substance as
either an ‘‘existing’’ chemical or a
‘‘new’’ chemical. Any chemical
substance that is not on EPA’s 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 TSCA section 5 to provide EPA with
a PMN, before initiating the activity.
Section 5(h)(1) of TSCA 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/opt/
newchems.
Under TSCA sections 5(d)(2) and
5(d)(3), 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 NOCs to manufacture those
chemicals. This status report, which
covers the period from February 1, 2011
to April 22, 2011, consists of 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/
importer, the potential uses identified
by the manufacturer/importer in the
PMN, and the chemical identity.
TABLE I—149 PMNS RECEIVED FROM FEBRUARY 1, 2011 TO APRIL 22, 2011
Received
date
Case No.
Projected
notice
end date
Manufacturer/
importer
Use
Chemical
(G) Dialdehyde, reaction products
with
hydrolyzed
n-vinylamide
homopolymer hydrohalides.
(G) Ultra violet curable polyester
polyurethane acrylate.
02/02/11
05/02/11
CBI ...................
(G) Paper additive .............................
P–11–0191 .......
02/01/11
05/01/11
CBI ...................
P–11–0192 .......
P–11–0193 .......
P–11–0194 .......
02/02/11
02/02/11
02/02/11
05/02/11
05/02/11
05/02/11
CBI ...................
CBI ...................
CBI ...................
(S) Ultra violet curable polymer for
kitchen cabinets and office furniture finishes.
(G) Additive for paper ........................
(G) Deposit control additive for fuels
(G) Plasticizer ....................................
P–11–0195 .......
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P–11–0190 .......
02/03/11
05/03/11
3M ....................
P–11–0196 .......
02/08/11
05/08/11
Croda Inc. .........
(S) Prepolymer for sprayable adhesive/sealant; prepolymer for high
viscosity adhesive/sealant.
(G) Hard surface cleaner ...................
P–11–0197
P–11–0198
P–11–0199
P–11–0200
02/08/11
02/08/11
02/08/11
02/07/11
05/08/11
05/08/11
05/08/11
05/07/11
CBI
CBI
CBI
CBI
(G)
(G)
(G)
(G)
.......
.......
.......
.......
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...................
...................
...................
...................
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Colourant dispersant ...................
Colourant dispersant ...................
Colourant dispersant ...................
Resin solution additive ................
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(G) Amphoteric polyacrylamide.
(G) Poly alkyl amido hydrazide.
(S) 1,2,3-propanetricarboxylic acid,
2-(acetyloxy)-,
1,2,3-tris(2ethylhexyl) ester.
(G) Alkoxysilyl polyether prepolymer.
(G) Quaternized ethylene oxide propylene oxide polymer.
(G) Acrylic polymer.
(G) Acrylic polymer.
(G) Acrylic polymer.
(G) Aluminum alkoxide complex,
alkoxylated aluminum chelate.
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TABLE I—149 PMNS RECEIVED FROM FEBRUARY 1, 2011 TO APRIL 22, 2011—Continued
Received
date
Case No.
Projected
notice
end date
Manufacturer/
importer
Use
Chemical
02/09/11
05/09/11
Lubrigreen ........
(G) Bio-based lubricant base oil ........
P–11–0202 .......
02/09/11
05/09/11
Lubrigreen ........
(G) Bio-based lubricant base oil ........
P–11–0203 .......
02/09/11
05/09/11
CBI ...................
(G) Paper treatment ..........................
P–11–0204 .......
02/11/11
05/11/11
CBI ...................
(S) Brightener for nickel electroplating.
P–11–0205 .......
02/15/11
05/15/11
CBI ...................
(G) Non-dispersive ink additive .........
P–11–0206 .......
02/15/11
05/15/11
(G) Intermediate ................................
02/15/11
05/15/11
(G) Contained use in an article .........
(G) Substituted aromatic borate salt.
P–11–0208 .......
02/16/11
05/16/11
Eastman Kodak
Company.
Eastman Kodak
Company.
Lubrigreen ........
(S) Fatty acids, C8–18 and C18-unsaturated, reaction products with
isomerized
oleic
acid
homopolymer.
(S) Fatty acids, coco, reaction products with isomerized oleic acid
homopolymer.
(G) Perfluoroalkylethyl methacrylate
copolymer, salt.
(G) Acetaldehyde, substituted-, reaction products with 2-butyne-1,4diol.
(G) Polyalkene, maleated potassium
salts.
(G) Bisaryl iodonium salt.
P–11–0207 .......
(G) Lubricant base oil ........................
P–11–0209 .......
02/16/11
05/16/11
Lubrigreen ........
(G) Lubricant base oil ........................
P–11–0210 .......
02/16/11
05/16/11
Lubrigreen ........
(G) Lubricant base oil ........................
P–11–0211 .......
02/16/11
05/16/11
Lubrigreen ........
(G) Lubricant base oil ........................
P–11–0212 .......
02/16/11
05/16/11
Lubrigreen ........
(G) Lubricant base oil ........................
P–11–0213 .......
02/16/11
05/16/11
Lubrigreen ........
(G) Lubricant base oil ........................
P–11–0214 .......
02/16/11
05/16/11
Lubrigreen ........
(G) Lubricant base oil ........................
P–11–0215 .......
02/16/11
05/16/11
CBI ...................
(G) Base polymer for adhesive .........
P–11–0216 .......
02/16/11
05/16/11
CBI ...................
(G) Base polymer for adhesive .........
P–11–0217 .......
P–11–0218 .......
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P–11–0201 .......
02/17/11
02/17/11
05/17/11
05/17/11
CBI ...................
CBI ...................
(G) Additive, open, non-dispersive ....
(G) Radiation curing agent ................
P–11–0219 .......
02/18/11
05/18/11
CBI ...................
(G) Paint ............................................
P–11–0220 .......
02/18/11
05/18/11
CBI ...................
(G) Paint ............................................
P–11–0221 .......
02/18/11
05/18/11
CBI ...................
(G) Paint ............................................
(S) Fatty acids, C8–18 and C18-unsaturated, reaction products with
isomerized oleic acid homopolymer
2-ethylhexyl ester.
(S) Fatty acids, coco, reaction products with isomerized oleic acid
homopolymer 2-ethylhexyl ester.
(S) Fatty acids, C8–18 and C18-unsaturated, reaction products with
isomerized oleic acid dimer 2ethylhexyl ester.
(S) Fatty acids, coco, reaction products with isomerized oleic acid
dimer 2-ethylhexyl ester.
(S)
9-octadecenoic
acid
(9z)-,
homopolymer, isomerized.
(S) Fatty acids, C8–18 and C18-unsaturated, reaction products with
isomerized
oleic
acid
homopolymer.
(S) Fatty acids, coco, reaction products with isomerized oleic acid
homopolymer.
(S) 2-propenoic acid, 2-methyl-,
dodecyl ester, telomer with methyl
2-methyl-2-propenoate, tridecyl 2methyl-2-propenoate,
3(trimethoxysilyl)-1-propanethiol and
3-(trimethoxysilyl) propyl 2-methyl2-propenoate.
(S) 2-propenoic acid, 2-methyl-,
dodecyl ester, telomer with butyl 2propenoate, methyl 2-methyl-2propenoate, tridecyl 2-methyl-2propenoate, 3-(trimethoxysilyl)-1propanethiol and 3-(trimethoxysilyl)
propyl 2-methyl-2-propenoate.
(G) Polyetherfluoro urethane.
(G) Benzenedioic acid, polymer with
alkanediol and carboxyaminoalkyl
carbamic acid alkoxyalkylester.
(G) Alkyl acrylate, polymer with alkyl
acrylate, alkyl methacrylates, and
styrene, peroxide-initiated.
(G) Alkyl acrylate, polymer with alkyl
acrylate, alkyl methacrylates, and
styrene, peroxide-initiated.
(G) Alkyl acrylate, polymer with alkyl
acrylate, alkyl methacrylates, and
styrene, peroxide-initiated.
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TABLE I—149 PMNS RECEIVED FROM FEBRUARY 1, 2011 TO APRIL 22, 2011—Continued
Received
date
Case No.
Projected
notice
end date
Manufacturer/
importer
Use
Chemical
(G) Alkyl acrylate, polymer with alkyl
acrylate, alkyl methacrylates, and
styrene, peroxide-initiated.
(G)
Substituted
tris-phenyl
thiophenyl-sulfonium halogenide.
(G) Fluoro ether.
(S) Amines, C36-alkylenedi-, polymers with 6-aminohexanoic acid,
1,6-diisocyanato-2,2,4trimethylhexane, 1,6-diisocyanato2,4,4-trimethylhexane,
5,5’-[(1methylethylidene)bis(4,1phenyleneoxy)]bis[1,3isobenzofurandione]
and
pyromellitic
dianhydride,
2,5dihydro-2,5-dioxo-1h-pyrrole-1hexanoic acid-blocked.
(G) N-(2-hydroxyethyl) alkenamide.
02/18/11
05/18/11
CBI ...................
(G) Paint ............................................
P–11–0223 .......
02/18/11
05/18/11
CBI ...................
(G) Use as photoinitiator ...................
P–11–0224 .......
P–11–0225 .......
02/22/11
02/23/11
05/22/11
05/23/11
CBI ...................
CBI ...................
(S) Electrolyte for battery ..................
(G) Adhesive component ...................
P–11–0226 .......
02/23/11
05/23/11
CBI ...................
P–11–0227 .......
P–11–0228 .......
02/23/11
02/22/11
05/23/11
05/22/11
CBI ...................
CBI ...................
(G) As a component of adhesives
and Cosmetics.
(G) Coatings ......................................
(S) Used internally as raw material
for polyamide manufacture.
P–11–0229 .......
02/24/11
05/24/11
H.B. Fuller ........
(G) Industrial adhesive ......................
P–11–0230 .......
02/24/11
05/24/11
02/25/11
05/25/11
P–11–0232 .......
P–11–0233 .......
02/28/11
02/25/11
05/28/11
05/25/11
Goulston technologies, Inc.
Cardolite Corporation.
CBI ...................
CBI ...................
(G) Antistatic agent for acrylic yam ...
P–11–0231 .......
P–11–0234 .......
P–11–0235 .......
03/01/11
03/01/11
05/29/11
05/29/11
CBI ...................
CBI ...................
(G) Chemical intermediate ................
(G) Ink, coating, adhesive .................
P–11–0236 .......
03/01/11
05/29/11
CBI ...................
(G) Ink, coating, adhesive .................
P–11–0237 .......
03/02/11
05/30/11
Colonial Chemical, Inc.
(S) Oil dispersant ...............................
P–11–0238 .......
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P–11–0222 .......
03/01/11
05/29/11
IGM Resins Inc.
(G) Ultra violet initiator ......................
P–11–0239 .......
03/02/11
05/30/11
CBI ...................
(G) Emulsifier .....................................
P–11–0240 .......
03/02/11
05/30/11
CBI ...................
P–11–0241 .......
03/04/11
06/01/11
CBI ...................
(G) Component of an industrial adhesive.
(G) Used to adjust (retard) set times
in calcium sulfate based binders
such as gypsum boards, plaster
boards or wall boards.
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(S) Amine based epoxy curing agent
for 2 part epoxy surface coating.
(G) Sealant and adhesive .................
(S) Curing agent for epoxy resin .......
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(G) Urethane acrylate.
(G) Benzaldehyde, reaction products
with polyalkylenepolyamines, hydrogenated.
(G) Polyester, polymer with 1,4butanediol, dodecanedioic, 1,6heaxanediol,
.alpha.-hydro.omega.-hydroxypoly
(oxy-1,4butanediyl) and isocyanate.
(G) Alkyl amine salt.
(G) Cashew nutshell liquid amine
polymer.
(G) Acryloxy functional siloxane.
(G)
Phenol,
4,4’-(1methylethylidene)bis-, polymer with
2-(chloromethyl)oxirane, reaction
products
with
n3-(3(dimethylamino)propyl]-n1,n1-dimethyl-alkanepolyamine,
compounds with formaldehyde-phenol
polymer.
(G) Oligmeric phenolic ether.
(G) Polyacrylate oligomer product
from
saturated
dimer
acid,
propoxylated glycerol and acrylic
acid.
(G) Polyacrylate oligomer product
from
saturated
dimer
acid,
propoxylated glycerol and acrylic
acid.
(S) D-glucopyranose, oligomeric,
decyl octyl glycosides, polymer
with 1,3-dichloro-2-propanol and
sorbitan
mono-(9z)-9octadecenoate.
(S) Poly(oxy-1,2-ethanediyl), .alpha.[2-(4-benzoylphenoxy)acetyl].omega.-[[2-(4benzoylphenoxy)acetyl]oxy]-.
(G)
Butanedioic
acid,
monopolyisobutylene
derivates,
(alkylimino)di-2,1-ethanediyl esters,
compounds with akylamino alcohol(1:2).
(G) Modified epoxy resin.
(S) L-lysine, n2, n6-bis (3-carboxy-1oxopropyl)-, sodium salt (1:3).
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TABLE I—149 PMNS RECEIVED FROM FEBRUARY 1, 2011 TO APRIL 22, 2011—Continued
Received
date
Case No.
Manufacturer/
importer
Use
Chemical
.......
.......
.......
.......
03/04/11
03/07/11
03/07/11
03/07/11
06/01/11
06/04/11
06/04/11
06/04/11
Materia Inc. ......
CBI ...................
CBI ...................
CBI ...................
(G)
(G)
(G)
(G)
P–11–0246 .......
03/08/11
06/05/11
P–11–0247 .......
03/04/11
06/01/11
Oleon Americas
Inc.
CBI ...................
(S) Emulsifier for commercial (I&I)
and household floor cleaners.
(G) Treatment for textiles ..................
P–11–0248 .......
03/08/11
06/05/11
CBI ...................
(G) Printing additive ...........................
P–11–0249 .......
P–11–0250 .......
03/08/11
03/09/11
06/05/11
06/06/11
P–11–0251 .......
03/10/11
06/07/11
CBI ...................
Henkel Corporation.
CBI ...................
(G) Resin for use in coatings ............
(S) Cure initiator in adhesive formulations.
(G) Printing inks .................................
P–11–0252 .......
03/10/11
06/07/11
CBI ...................
(G) Photografic chemical ...................
P–11–0253 .......
03/10/11
06/07/11
03/09/11
06/06/11
Dow Chemical
Company.
H.B. Fuller ........
(G) Detergents and cleaner additive
P–11–0254 .......
P–11–0255 .......
03/10/11
06/07/11
Colonial Chemical, Inc.
(S) Hard surface cleaner in high
caustic solutions.
P–11–0256 .......
03/10/11
06/07/11
Colonial Chemical, Inc.
(S) Hard surface cleaner in high
caustic solutions.
P–11–0257 .......
03/10/11
06/07/11
Nanotech Industries, Inc.
(S) Flooring; paints; top coating ........
P–11–0258 .......
03/10/11
06/07/11
CBI ...................
(G) Curing agent for epoxy resin ......
P–11–0259 .......
03/04/11
06/01/11
CBI ...................
(G) Flexible packaging adhesive .......
P–11–0260 .......
03/11/11
06/08/11
CBI ...................
(G) Urethane adhesive ......................
P–11–0261 .......
03/16/11
06/13/11
(S) Luminescent phosphor for use in
fluorescent lamp manufacturing.
03/16/11
06/13/11
(S) Luminescent phosphor for use in
fluorescent lamp manufacture.
(S) Europium strontium
metaphosphate oxide.
P–11–0263 .......
P–11–0264 .......
P–11–0265 .......
03/15/11
03/17/11
03/17/11
06/12/11
06/14/11
06/14/11
Global Tungsten
and Powders
Corp.
Global Tungsten
and Powders
Corp.
CBI ...................
CBI ...................
CBI ...................
(G) Alkanedioic acid, polymer with
ethenyl
acetate,
alkyl
2propenoate, and 2-propenoic acid.
(S) D-glucopyranose, oligomeric,
decyl
octyl
glycosides,
2,3dihydroxypropyl
ethers,
phosphates, sodium salts, polymers with 1,3-dichloro-2-propanol.
(S) D-glucopyranose, oligomeric,
c10–16-alkyl
glycosides,
2,3dihydroxypropyl
ethers,
phosphates, sodium salts, polymers with 1,3-dichloro-2-propanol.
(S) Carbamic acid, N,N’-(trimethyl1,6-hexanediyl)bis-, ester with 1,2propanediol (1:2).
(G) Epoxy and isocyanate modified
aliphatic polyamine.
(G) Polyether polyester polyurethane
adhesive.
(G)
Isocyanate-terminated
prepolymer.
(S) Aluminum barium europium magnesium oxide.
P–11–0262 .......
03/17/11
06/14/11
CBI ...................
(G) Curing agent for epoxy resin ......
(G) Flame retardant ...........................
(G) Antistatic additive in polymers,
antistatic additive in liquid resins.
(G) Industrial lubricant .......................
(G) Modified aliphatic polyamine.
(G) Brominated aromatic oligomer.
(G) Dialkyl imidazolium salt.
P–11–0266 .......
wwoods2 on DSK1DXX6B1PROD with NOTICES_PART 1
P–11–0242
P–11–0243
P–11–0244
P–11–0245
Projected
notice
end date
P–11–0267 .......
03/18/11
06/15/11
Hybrid Plastics,
Inc.
(G) Thermoplastics and coatings additive; elastomer additive.
P–11–0268 .......
03/21/11
06/18/11
CBI ...................
(G) Flame retardant ...........................
P–11–0269 .......
03/21/11
06/18/11
CBI ...................
(G) Optical material component ........
P–11–0270 .......
03/21/11
06/18/11
Lockheed Martin
(S) Piezoelectric ceramics used for
active and passive underwater
acoustic systems.
VerDate Mar<15>2010
15:25 Jun 20, 2011
Jkt 223001
PO 00000
Frm 00036
Resin formulation additive ...........
Thermoplastic urethane ..............
Thermoplastic urethane ..............
Concrete additive ........................
(G) Industrial adhesive ......................
Fmt 4703
Sfmt 4703
E:\FR\FM\21JNN1.SGM
(G) Hydroxy-olefin.
(G) Aliphatic thermoplastic urethane.
(G) Aliphatic thermoplastic urethane.
(G)
Alkoxylate
polymer,
mono(alkenyl) ether.
(S)
D-xylopyranose,
oligomeric,
C16–18-alkyl glycosides.
(G) Perfluoroalkylethyl methacrylate
copolymer.
(G) Roin, polymer with ethylene glycol,
propanediol,
alkanedicarboxylic acid, terephthalic acid and trimellitic anhydride.
(G) Acrylic latex.
(S)
Benzamide,
n(aminothioxomethyl)-.
(G) Cycloaliphatic anhydride polymer
with alkyldiol.
(G)
Benzeneacetonitrile,
alkoxy[[(alkylsulfonyl)oxy]imino]-.
(G) Acrylic copolymer.
borate
(G) Polypentaerythritol, mixed esters
with
straight
and
branched
monoacids.
(S)
Tricyclo[7.3.3.15,11]heptasiloxane3,7,14-triol-1,3,5,7,9,11,14heptakis(2,4,4-trimethylpentyl)-.
(G) Phosphoric acid, diaryl alkyl
ester.
(G) Perfluorinated cyclo oxyaliphatic
polymer.
(S) Lead strontium titanium zirconium
oxide.
21JNN1
36114
Federal Register / Vol. 76, No. 119 / Tuesday, June 21, 2011 / Notices
TABLE I—149 PMNS RECEIVED FROM FEBRUARY 1, 2011 TO APRIL 22, 2011—Continued
Received
date
Case No.
Projected
notice
end date
Manufacturer/
importer
Use
Chemical
(S) Calcium cobalt lead titanium
tungsten oxide.
03/21/11
06/18/11
Lockheed Martin
P–11–0272 .......
03/21/11
06/18/11
Lockheed Martin
P–11–0273 .......
03/21/11
06/18/11
Lockheed Martin
P–11–0274 .......
03/21/11
06/18/11
Lockheed Martin
P–11–0275 .......
03/23/11
06/20/11
CBI ...................
(S) Piezoelectric ceramics used for
active and passive underwater
acoustic systems..
(S) Piezoelectric ceramics used for
active and passive underwater
acoustic systems.
(S) Piezoelectric ceramics used for
active and passive underwater
acoustic systems.
(S) Piezoelectric ceramics used for
active and passive underwater
acoustic systems.
(G) Coating applications ....................
P–11–0276 .......
03/24/11
06/21/11
Mane, USA .......
(G) Perfumery ingredient ...................
P–11–0277 .......
03/24/11
06/21/11
03/24/11
06/21/11
Zeon Chemicals
L.P.
Cytec Industries
Inc.
(S) Automotive seals and gaskets ....
P–11–0278 .......
P–11–0279 .......
P–11–0280 .......
03/24/11
03/25/11
06/21/11
06/22/11
03/25/11
06/22/11
CBI ...................
Cytec Industries
Inc.
CBI ...................
(S) Automotive coatings ....................
(G) Coating resin ...............................
P–11–0281 .......
P–11–0282 .......
03/25/11
06/22/11
CBI ...................
P–11–0283 .......
P–11–0284 .......
P–11–0285 .......
03/25/11
03/25/11
03/28/11
06/22/11
06/22/11
06/25/11
3M Company ....
3M Company ....
CBI ...................
(S) Lubricant additive for the purposes of anti corrosion, viscosity
control and dispersant improver.
(S) Lubricant additive for the purposes of anti corrosion, viscosity
control and dispersant improver.
(G) Surfactant ....................................
(G) Surfactant ....................................
(G) Coating additive ..........................
P–11–0286 .......
03/28/11
06/25/11
CBI ...................
(G) Open, non-dispersive ..................
P–11–0287 .......
P–11–0288 .......
03/28/11
03/25/11
06/25/11
06/22/11
CBI ...................
CBI ...................
(G) Open, non-dispersive use ...........
(S) Photoinitiator ................................
P–11–0289 .......
03/28/11
....................
P–11–0290 .......
wwoods2 on DSK1DXX6B1PROD with NOTICES_PART 1
P–11–0271 .......
03/29/11
06/26/11
Oleon Americas
Inc.
Scnte LLC ........
P–11–0291 .......
03/28/11
06/25/11
CBI ...................
P–11–0292 .......
03/29/11
06/26/11
Colonial Chemical, Inc.
(S) Additive (tracer) for natural fats
and oils.
(G) The material will be used as the
sensor element in an electrochemical sensor. one carbon
nanotube-sic device will be use
per one sensor. the maximum estimated annual quantity of sensors
will be 10,000. this completed sensor will be able to detect metals
and nutrients in water.
(G) For use as an exterior coating for
food containers.
(S) Hard surface cleaner in high
caustic solutions.
VerDate Mar<15>2010
15:25 Jun 20, 2011
Jkt 223001
PO 00000
Frm 00037
(G) Coatings resin .............................
Fmt 4703
Sfmt 4703
E:\FR\FM\21JNN1.SGM
(S) Calcium cobalt lead strontium titanium tungsten oxide.
(S) Lanthanum lead titanium zirconium oxide.
(S) Lead niobium titanium zirconium
oxide.
(G) Hydroxy alkyl alkyl acrylate, polymer with alkyl acrylate, aromatic
vinyl monomer, dialkyl acrylate and
alkyl alkyl acrylate.
(S)
1,5-cyclododecadiene,
10methoxy-1,5,9-trimethyl1,5-cyclododecadiene,
9-methoxy1,5,10-trimethyl1,5-cyclododecadiene,
9-methoxy1,6,10-trimethyl1,5-cylcododecadiene,
9-methoxy2,5,10-trimethyl-.
(G) Modified acrylonitrile, butadiene
polymer, hydrogenated.
(G) Heteromonocycle, polymer with
disubstituted carbomonocyle and
alkylene glycol, alkyl acrylate
blocked.
(G) Polyester resin.
(G) Epoxy modified alkyd resin, partially neutralized.
(S) Fatty acids, lanolin, esters with
cholesterol-low lanolin alcs.
(S) Fatty acids, C10–30, esters with
cholesterol-low lanolin alcs.
(G) Oleate.
(G) Oleyl acrylate.
(G) Acid anhydride, polymer with aromatic
isocyanate
and
polyalkyleneglycol, alkanol and diazole alkanamine and lactone
homopolymer alkyl ester-blocked.
(G) Blocked polyester polyurethane,
neutralized.
(G) Acrylic silane polymer.
(G) Biphenyl alkyl morpholino ketone.
(S) Heptanoic acid, 1,2,3-propanetriyl
ester (9ci).
(G) Carbon nanotubes.
(G) Polyester resin.
(S) D-glucopyronase, oligomeric,
decyl octyl glycosides, 2-hydroxy3-sulfopropyl ethers, sodium salts,
polymers with 1,3-dichloro-2-propanol.
21JNN1
36115
Federal Register / Vol. 76, No. 119 / Tuesday, June 21, 2011 / Notices
TABLE I—149 PMNS RECEIVED FROM FEBRUARY 1, 2011 TO APRIL 22, 2011—Continued
Received
date
Case No.
Projected
notice
end date
Manufacturer/
importer
Use
Chemical
(S) D-glucopyronase, oligomeric,
C10–16-alkyl glycosides, 2-hydroxy3-sulfopropyl ethers, sodium salts,
polymers with 1,3-dichloro-2-propanol.
(G) Polycarbonate.
03/29/11
06/26/11
Colonial Chemical, Inc.
(S) Hard surface cleaner in high
caustic solutions.
P–11–0294 .......
03/30/11
06/27/11
CBI ...................
P–11–0295 .......
03/30/11
06/27/11
CBI ...................
P–11–0296 .......
03/30/11
06/27/11
CBI ...................
P–11–0297 .......
P–11–0298 .......
04/04/11
04/04/11
07/02/11
07/02/11
P–11–0299 .......
04/04/11
07/02/11
P–11–0300 .......
04/04/11
07/02/11
CBI ...................
Dow Chemical
Company.
Dow Chemical
Company.
CBI ...................
P–11–0301 .......
04/04/11
07/02/11
CBI ...................
P–11–0302 .......
04/04/11
07/02/11
CBI ...................
P–11–0303 .......
04/04/11
07/02/11
CBI ...................
P–11–0304 .......
04/04/11
07/02/11
CBI ...................
P–11–0305 .......
04/04/11
07/02/11
P–11–0306 .......
04/04/11
07/02/11
King Industries,
Inc.
CBI ...................
P–11–0307 .......
04/04/11
07/02/11
(G)
Open,
non-dispersive
use
(polycarbonate).
(G) The PMN substance will be used
as a component in detergents, a
corrosion inhibitor in multiple applications, and a concrete additive.
(G) The PMN substance will be used
as a component in detergents, a
corrosion inhibitor in multiple applications, and a concrete additive.
(G) Open, non-dispersive use ...........
(S) Hardener for epoxy thermosetting
coatings.
(S) Hardener for epoxy thermosetting
coatings.
(S) Reactant in the manufacture of
polyurethane and polyisocyanurate
rigid foams; polyol resin blend with
additives for polyurethane b-side
reactant.
(S) Reactant in the manufacture of
polyurethane and polyisocyanurate
rigid foams; polyol resin blend with
additives for polyurethane b-side
reactant.
(S) Reactant in the manufacture of
polyurethane and polyisocyanurate
rigid foams; polyol resin blend with
additives for polyurethane b-side
reactant.
(S) Reactant in the manufacture of
polyurethane and polyisocyanurate
rigid foams; polyol resin blend with
additives for polyurethane b-side
reactant.
(S) Reactant in the manufacture of
polyurethane and polyisocyanurate
rigid foams; polyol resin blend with
additives for polyurethane b-side
reactant.
(G) Resin modifier for thermoplastic
polyurethane elastomers.
(S) Acrylic resin used in ultra violet
curable inks and coatings.
(S) Epoxy curing agent ......................
P–11–0308 .......
04/05/11
07/03/11
P–11–0309 .......
wwoods2 on DSK1DXX6B1PROD with NOTICES_PART 1
P–11–0293 .......
04/06/11
07/04/11
P–11–0310 .......
04/06/11
07/04/11
H.B. Fuller Company.
(G) Industrial adhesive ......................
P–11–0311 .......
04/06/11
07/04/11
H.B. Fuller Company.
(G) Industrial adhesive ......................
VerDate Mar<15>2010
15:25 Jun 20, 2011
Jkt 223001
Cardolite Corporation.
Dow Chemical
Company.
H.B. Fuller Company.
PO 00000
Frm 00038
(G) Dispersant ...................................
(G) Industrial adhesive ......................
Fmt 4703
Sfmt 4703
E:\FR\FM\21JNN1.SGM
(G) Reaction product from the oxidation of D-glucose, neutralized with
naoh.
(G) Reaction products from the oxidation of d-glucose, neutralized
with sodium hydroxide and potassium hydroxide.
(G) Azo dyestuff.
(G) Ethoxylated epoxy amine polymer.
(G) Polypropylene glycol, epoxy
amine polymer.
(G) Aromatic polyester polyol.
(G) Aromatic polyester polyol
(G) Aromatic polyester polyol.
(G) Aromatic polyester polyol.
(G) Aromatic polyester polyol.
(G) Polyester diol.
(G) Tertiary amine acrylate.
(G) Cashew nutshell liquid amine
polymer.
(G) Acrylic polymer.
(G) Hexanedioic acid, polymer with
polyether
polyol,
1,1’methylenebis[4isocyanatobenzene]
and
dihydroxydialkyl ether.
(G) Hexanedioic acid, polymer with
polyether
polyol,
1,1’methylenebis[isocyanatobenzene]
and dihydroxydialkyl ether.
(G) Hexanedioic acid, polymer with
A-hydro-W-hydroxypoly
[oxy
(methyl-1,2-ethanediyl)],
1,1’methylenebis[4isocyanatobenzene],
dihydroxydialkyl
ether
and
dialkanol ether.
21JNN1
36116
Federal Register / Vol. 76, No. 119 / Tuesday, June 21, 2011 / Notices
TABLE I—149 PMNS RECEIVED FROM FEBRUARY 1, 2011 TO APRIL 22, 2011—Continued
Received
date
Case No.
Projected
notice
end date
Manufacturer/
importer
Use
Chemical
(G) Hexanedioic acid, polymer with
A-hydro-W-hydroxypoly
[oxy
(methyl-1,2-ethanediyl)],
1,1’methylenebis[isocyanatobenzene],
dihydroxydialkyl
ether
and
dialkanol ether.
(G) Hexanedioic acid, polymer with
A-hydro-W-hydroxypoly
[oxy
(methyl-1,2-ethanediyl)],
1,1’methylenebis[4isocyanatobenzene],
and
dihydroxydialkyl ether, reaction
products with dialkylcarbinol.
(G) Hexanedioic acid, polymer with
A-hydro-W-hydroxypoly
[oxy
(methyl-1,2-ethanediyl)],
1,1’methylenebis[isocyanatobenzene] ,
and dihydroxydialkyl ether, reaction products with dialkylcarbinol.
(S) 1H-pyrazole, 3,4-dimethyl-, phosphate(1:1).
(S) Cyclohexane, oxidized, by-products from, distillation residues.
04/06/11
07/04/11
H.B. Fuller Company.
(G) Industrial adhesive ......................
P–11–0313 .......
04/06/11
07/04/11
H.B. Fuller Company.
(G) Industrial adhesive ......................
P–11–0314 .......
04/06/11
07/04/11
H.B. Fuller Company.
(G) Industrial adhesive ......................
P–11–0315 .......
04/07/11
07/05/11
04/07/11
07/05/11
P–11–0317 .......
04/08/11
07/06/11
K+A North
America.
Ascend Performance Materials, LLC.
Lubrizol Corporation.
(S) Fertilizer additive .........................
P–11–0316 .......
P–11–0318 .......
P–11–0319 .......
04/11/11
04/11/11
07/09/11
07/09/11
CBI ...................
CBI ...................
(G) Additive ........................................
(G) Additive, open, non-dispersive ....
P–11–0320 .......
04/11/11
07/09/11
CBI ...................
(G) Additive, open, non-dispersive ....
P–11–0321 .......
04/11/11
07/09/11
CBI ...................
(G) Additive, open, non-dispersive ....
P–11–0322 .......
04/11/11
07/09/11
CBI ...................
(G) Additive, open, non-dispersive ....
P–11–0323 .......
04/11/11
07/09/11
CBI ...................
(G) Additive, open, non-dispersive ....
P–11–0324 .......
04/11/11
07/09/11
CBI ...................
(G) Additive, open, non-dispersive ....
P–11–0325 .......
04/13/11
07/11/11
CBI ...................
P–11–0326 .......
04/13/11
07/11/11
CBI ...................
P–11–0327 .......
04/14/11
....................
Kior ...................
P–11–0328 .......
04/14/11
....................
Kior ...................
(G) Battery component manufacturing.
(G) Cleaning additive for cpu manufacturing.
(G)
Distillation
feedstock
after
hydrotreatment.
(G) Feedstock ....................................
P–11–0329 .......
04/14/11
....................
Kior ...................
P–11–0330 .......
04/14/11
....................
Kior ...................
P–11–0331 .......
wwoods2 on DSK1DXX6B1PROD with NOTICES_PART 1
P–11–0312 .......
04/14/11
....................
Kior ...................
P–11–0332 .......
04/14/11
....................
Kior ...................
P–11–0333 .......
P–11–0334 .......
04/14/11
04/15/11
....................
....................
CBI ...................
CBI ...................
P–11–0335 .......
04/15/11
....................
CBI ...................
(S)
Hydrotreated
lignocellulosic
naphtha will be used as blendstock
for conventional fossil fuels.
(S) Hydrotreated lignocellulosic kerosene will be used as blendstock
for conventional fossil fuels.
(S) Hydrotreated lignocellulosic distillate will be used as blendstock
for conventional fossil fuels.
(S) Intended for use in a manner
comparable to gas oil as it is currently used in industry.
(G) Component of industrial coating
(G) An open non-dispersive use in
ink.
(G) Cross-linker .................................
P–11–0337 .......
04/19/11
....................
CBI ...................
(S) Ingredient in fragance compound
VerDate Mar<15>2010
15:25 Jun 20, 2011
Jkt 223001
PO 00000
Frm 00039
(G) Industrial solvent, in (closed and
open systems. accelerant in permitted industrial explosives.
(G) Lubricant additive ........................
Fmt 4703
Sfmt 4703
E:\FR\FM\21JNN1.SGM
(G) Formaldehyde, reaction products
with ethylene-maleic anhydridepropene polymer, aryl amine and
succinic
anhydride
monopolyisobutylene derivates.
(G) Perfluoro multiphenylbenzene.
(G) Polyester polyether urethane
block copolymer.
(G) Polyester polyether urethane
block copolymer.
(G) Polyester polyether urethane
block copolymer.
(G) Siloxanes and silicones, methyl
alkyl, polyether modified.
(G) Siloxanes and silicones, methyl
alkyl, polyether modified.
(G) Siloxanes and silicones, methyl
alkyl, polyester modified.
(G) Beta alumina powder.
(G) Glycerylether.
(S) Distillates (lignocellulosic), C5–40.
(S) Parraffin waxes (lignocellulosic),
hydrotreated, C5–40-branched, cyclic and linear.
(S)
Naphtha
(lignocellulosic),
hydrotreated, C5–12-branched, cyclic and linear.
(S)
Kerosine
(lignocellulosic),
hydrotreated, C8–16-branched,cyclic
and linear.
(S)
Distillates
(lignocellulosic),
hydrotreated, C8–26-branched, cyclic, and linear.
(S) Residual oils (lignocellulosic),
hydrotreated, C20–40-branched, cyclic and linear.
(G) Phosphated polyester.
(G) Aliphatic and alicyclic alcohol
type polyester.
(G) Methyl, phenyl, amino-functional
siloxanes and silsesquioxane.
(S) 4,7-decadienal.
21JNN1
36117
Federal Register / Vol. 76, No. 119 / Tuesday, June 21, 2011 / Notices
TABLE I—149 PMNS RECEIVED FROM FEBRUARY 1, 2011 TO APRIL 22, 2011—Continued
Projected
notice
end date
Received
date
Case No.
Manufacturer/
importer
Use
Chemical
CBI ...................
(S) Photoinitiator ................................
(S) Additives for resins, thermoplastics, and elastomers for mechanical reinforcement and enhanced electrical properties; coatings on metallic foils for battery applications; manufacture of fabric
composites using mwnt.
(G) Reactant ......................................
(G) Biphenyl alkyl morpholino ketone.
(S) Multi-wall carbon nanotube also
know as—mwnt (multi-wall carbon
nanotube),
smwcnt
(specialty
multi-wall carbon nanotube), and
smwxxx and where xxx represents
our identifier for a new generation
of the same products.
(G) Formaldehyde polymer with reaction products of alkylated phenol
and polyalkyltriamine.
P–11–0338 .......
04/21/11
....................
P–11–0339 .......
04/22/11
07/20/11
Southwest
Nanotechnologies Inc.
P–11–0340 .......
04/22/11
07/20/11
CBI ...................
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—2 TMES RECEIVED FROM FEBRUARY 1, 2011 TO APRIL 22, 2011
Projected
review end
date
Received
date
Case No.
Manufacturer/importer
Use
Chemical
(G) Heteromonocycle, polymer with
substituted carbomonocycle and
alkylene glycol, alkyl acrylate
blocked.
(G) Epoxy modified alkyd resin,
partially neutralized.
T–11–0007 .......
03/24/11
05/07/11
Cytec Industries Inc ...........
(G) Coating resin ................
T–11–0008 .......
03/25/11
05/08/11
Cytec Industries Inc ...........
(G) Coating resin ................
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 chemical identity.
TABLE III—122 NOCS RECEIVED FROM FEBRUARY 1, 2011 TO APRIL 22, 2011
Case No.
wwoods2 on DSK1DXX6B1PROD with NOTICES_PART 1
P–00–0141
P–00–0142
P–00–0145
P–01–0932
P–02–0249
P–04–0479
P–04–0575
P–04–0670
P–05–0267
P–06–0255
Received date
Commencement notice
end date
.......
.......
.......
.......
.......
.......
.......
.......
.......
.......
02/03/11
02/03/11
02/03/11
03/08/11
04/04/11
04/19/11
04/01/11
04/01/11
02/14/11
04/06/11
01/23/11
01/23/11
01/23/11
03/04/11
03/23/11
04/04/11
02/23/11
03/15/11
01/31/11
03/14/11
P–06–0394 .......
P–06–0702 .......
P–07–0010 .......
03/31/11
02/01/11
04/04/11
03/03/11
01/28/11
03/25/11
P–07–0090
P–07–0257
P–07–0407
P–07–0601
P–08–0080
.......
.......
.......
.......
.......
03/31/11
02/15/11
02/10/11
02/17/11
03/14/11
03/03/11
02/07/11
01/29/11
01/27/11
11/18/10
P–08–0524 .......
P–08–0545 .......
P–08–0558 .......
03/31/11
03/11/11
03/31/11
03/03/11
03/02/11
03/03/11
VerDate Mar<15>2010
15:25 Jun 20, 2011
Jkt 223001
PO 00000
Chemical
(S) L-aspartic acid, N,N′-1,2-ethanediylbis-, magnesium salt.
(S) L-aspartic acid, N,N′-1,2-ethanediylbis-, magnesium sodium salt.
(S) L-aspartic acid, N,N′-1,2-ethanediylbis-, magnesium sodium salt (1:1:1).
(G) Aliphatic epoxide.
(S) Fatty acids, C16–18 and C18-unsatd., me esters, epoxidized.
(G) Mixture containing alcohols, aminoalcohols and their sodium salts.
(G) Alkoxyated dihalogenated aromatic heterocycle.
(G) Poly(alkoxy aromatic heterocycle).
(G) Polydimethyl fluoroalkyl hydrogen siloxane.
(S)
Fatty
acids,
C18-unsatd.,
dimers,
hydrogenated,
polymers
with
1,4cyclohexanedicarboxylic acid, polyethylene-polypropylene glycol bis(2-aminopropyl)
ether, polypropylene glycol diamine and propionic acid.
(G) Epoxy acrylate oligomer.
(G) Substituted aliphatic amine.
(G) Styrene-maleic anhydride copolymer, reaction products with polyether, salt with
alkanolamin.
(G) Aliphatic urethane acrylate oligomer.
(G) Aqueous, aliphatic polyether polyurethane dispersion polymer.
(G) Fatty acid polymer with aliphatic diol and aromatic diacid.
(G) Hydrofluoroolefin.
(G) Amine salt of polyester polyol, cycloaliphatic glycol, hydroxy substituted carboxylic acid,
alkyldiamine and aliphatic diisocyanate.
(G) Unsaturated polyester.
(G) Surface-active, blocked isocyanate polymer.
(G) Polyurethane acrylate.
Frm 00040
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E:\FR\FM\21JNN1.SGM
21JNN1
36118
Federal Register / Vol. 76, No. 119 / Tuesday, June 21, 2011 / Notices
TABLE III—122 NOCS RECEIVED FROM FEBRUARY 1, 2011 TO APRIL 22, 2011—Continued
Case No.
Commencement notice
end date
.......
.......
.......
.......
.......
02/14/11
03/31/11
03/08/11
03/04/11
03/01/11
02/04/11
03/03/11
02/24/11
02/27/11
02/14/11
P–09–0258 .......
P–09–0359 .......
03/31/11
03/31/11
03/03/11
03/03/11
P–09–0360 .......
03/31/11
03/03/11
P–09–0391
P–09–0403
P–09–0505
P–09–0533
.......
.......
.......
.......
02/01/11
03/31/11
02/18/11
03/08/11
01/10/11
03/03/11
02/16/11
02/28/11
P–09–0568
P–10–0079
P–10–0179
P–10–0232
P–10–0269
P–10–0282
P–10–0326
P–10–0327
P–10–0338
P–10–0339
P–10–0342
P–10–0343
P–10–0358
P–10–0374
.......
.......
.......
.......
.......
.......
.......
.......
.......
.......
.......
.......
.......
.......
03/22/11
04/19/11
04/19/11
02/22/11
03/01/11
01/31/11
02/22/11
03/04/11
02/22/11
02/22/11
04/07/11
02/09/11
02/18/11
02/08/11
03/14/11
04/14/11
04/13/11
02/09/11
02/07/11
01/12/11
01/26/11
02/08/11
02/10/11
01/31/11
03/07/11
01/15/11
02/14/11
02/01/11
P–10–0399 .......
P–10–0406 .......
P–10–0423 .......
02/24/11
03/10/11
02/01/11
02/21/11
03/08/11
01/24/11
P–10–0435
P–10–0454
P–10–0455
P–10–0456
P–10–0457
P–10–0460
P–10–0489
P–10–0496
P–10–0501
P–10–0517
P–10–0536
P–10–0546
P–10–0547
P–10–0548
P–10–0549
P–10–0557
P–10–0562
.......
.......
.......
.......
.......
.......
.......
.......
.......
.......
.......
.......
.......
.......
.......
.......
.......
04/07/11
02/22/11
02/15/11
03/28/11
02/15/11
03/18/11
02/15/11
03/21/11
02/09/11
02/17/11
04/01/11
02/15/11
03/30/11
03/30/11
03/30/11
04/01/11
03/23/11
03/24/11
01/26/11
02/10/11
03/14/11
01/26/11
03/02/11
02/14/11
02/27/11
01/17/11
02/15/11
03/26/11
01/15/11
01/29/11
02/15/11
02/14/11
03/26/11
03/16/11
P–10–0570
P–10–0576
P–10–0577
P–10–0578
wwoods2 on DSK1DXX6B1PROD with NOTICES_PART 1
P–08–0664
P–09–0029
P–09–0162
P–09–0175
P–09–0209
Received date
.......
.......
.......
.......
04/01/11
04/19/11
03/18/11
03/23/11
03/26/11
04/09/11
02/24/11
03/16/11
P–10–0580 .......
03/11/11
02/28/11
P–10–0582
P–10–0583
P–10–0584
P–10–0585
P–10–0586
P–10–0587
P–10–0589
03/08/11
03/08/11
03/08/11
03/08/11
01/31/11
01/31/11
02/22/11
02/03/11
02/24/11
02/02/11
02/17/11
01/05/11
01/06/11
01/31/11
.......
.......
.......
.......
.......
.......
.......
VerDate Mar<15>2010
15:25 Jun 20, 2011
Jkt 223001
PO 00000
Chemical
(G) Fluorinated acrylic copolymer.
(G) Polyester acrylate.
(G) Styrenic polymers.
(G) Aqueous polyurethane resin dispersion.
(S) Poly(oxy-1,2-ethanediyl), .alpha.-undecyl-.omega.-hydroxy-, branched and linear, ethers
with 1,2-decanediol (1:1).
(G) Bis-phenoxyethanol fluorene diacrylate.
(G) Methylene bis-(4-cyclohexylisocyanate), oligomeric reaction products with polyester
polyol and hydroxyethyl acrylate and 2,2-bis(hydroxymethyl) propionic acid, compound
with amine.
(G) Methylene bis-(4-cyclohexylisocyanate), oligomeric reaction products with polyester
polyol and hydroxyethyl acrylate and 2,2-bis(hydroxymethyl) propionic acid.
(G) Polyamide epichlorohydrin resin salt (PMN substances A–F).
(G) Alkyd resin.
(G) Aliphatic urethane acrylate.
(S) Siloxanes and silicones, me hydrogen, me 3-(2-oxiranylmethoxy)propyl, ethoxy- and
methoxy-terminated.
(G) Formaldehyde, polymer with 2-(chloromethyl)oxirane, polyoxyalkane, and phenols.
(G) Substituted naphthalene mixed salt.
(G) Polymer of tall oil fatty acid, aliphatic diols, aliphatic polyols, and aromatic acids.
(G) Polycarboxylic acid/polysulfonate derivative.
(G) Polymer of aromatic dicarboxylic acid and alkane diamine.
(G) Maleated nylon graft copolymer.
(S) Propane, 1,1,1,2,3,3-hexafluoro-.
(S) 1-propene, 1,2,3,3,3-pentafluoro-.
(G) Acrylate copolymer.
(G) Acrylate copolymer.
(G) Poly 2-ethylhexyl methacrylate.
(G) Substituted cyclomethacrylate.
(G) Polycyclic polyamine diester organometallic compound.
(G) Modified polyalkylene polyamine reacted with bisphenol a diglycidyl ether 1 and modified epoxy resin.
(G) Styrene-maleinate copolymer.
(G) Alkene acrylate copolymer.
(S)
Benzenesulfonic
acid
3,3′-[(9,10-dihydro-5,8-dihydroxy-9,10-dioxo-1,4anthracenediyl)dimino]bis[6-butyl-], disodium salt.
(G) Substituted anthraquionone derivative.
(S) 1,3-divinyl imidazolidin-2-one.
(G) Hexahalosubstituted alkane.
(G) Alkenes, polymer with anhydride esters.
(G) Pentahalosubstituted alkane.
(G) Fatty acids, reaction product with adipic and trifunctional alcohol.
(G) Pentahalosubstituted alkene.
(G) Poly acrylate.
(G) Substituted pyridone.
(S) Oxirane, 2-ethyl-, polymer with oxirane, mono-C12–14-sec-alkyl ethers.
(G) Styrene-maleic anhydride copolymer, reaction product with amino compounds.
(G) Modified lithium iron phosphate.
(G) Vegetable oil, modified products.
(G) Vegetable oil, modified products.
(G) Vegetable oil, modified products.
(G) Aromatic polyester.
(G) Alkyl methacrylates, polymer with alkyl acrylates, styrene, hydroxyalkyl methacrylates,
epoxypropyl acrylates and polyalkene glycol hydrogen sulfate, alkyloxyalkyl alkenyloxy
alkyl, ammonium salt.
(G) Polyester.
(G) Alkyloxypropyliminodipropionic acid, monosodium salt.
(G) Polyamideimide.
(G) Alkylenealkanedioic acid, polymer with alkenylbenzene and alkenenitrile, ammonium
salt, alkylhydroperoxide-initiated.
(G)
Hetromonocyclic[3,4-b]thiophene,
homopolymer,
2-[1-[difluoro[(1,2,2trifluoroethenyl)oxy]methyl]-1,2,2,2-tetrafluoroethoxy]-1,1,2,2-tetrafluoroethyoxy]-1,1,2,2tetrafluoroethanesulfonic acid-tetrafluoroethylene polymer-doped.
(G) Isocyanate terminated urethane polymer.
(G) Isocyanate terminated urethane polymer.
(G) Isocyanate terminated urethane polymer.
(G) Isocyanate terminated urethane polymer.
(G) Isocyanate terminated urethane polymer.
(G) Isocyanate terminated urethane polymer.
(G) Dibasic acid ester.
Frm 00041
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Federal Register / Vol. 76, No. 119 / Tuesday, June 21, 2011 / Notices
36119
TABLE III—122 NOCS RECEIVED FROM FEBRUARY 1, 2011 TO APRIL 22, 2011—Continued
Case No.
Commencement notice
end date
.......
.......
.......
.......
.......
02/04/11
02/17/11
02/04/11
02/09/11
02/11/11
01/10/11
02/09/11
01/05/11
02/04/11
02/09/11
P–11–0017 .......
P–11–0019 .......
P–11–0023 .......
03/07/11
04/07/11
04/07/11
02/18/11
03/28/11
03/29/11
P–11–0024 .......
04/11/11
03/18/11
P–11–0029
P–11–0030
P–11–0041
P–11–0051
P–11–0054
P–11–0056
P–11–0057
P–11–0061
.......
.......
.......
.......
.......
.......
.......
.......
03/28/11
02/23/11
02/22/11
04/05/11
03/23/11
03/31/11
03/31/11
03/04/11
03/25/11
02/11/11
02/11/11
03/09/11
02/28/11
03/03/11
03/03/11
02/23/11
P–11–0062 .......
04/19/11
04/07/11
P–11–0065
P–11–0068
P–11–0070
P–11–0071
P–11–0073
P–11–0083
.......
.......
.......
.......
.......
.......
02/24/11
03/28/11
03/10/11
03/10/11
02/15/11
04/01/11
02/16/11
03/09/11
03/09/11
02/23/11
02/10/11
03/28/11
P–11–0094 .......
P–11–0095 .......
P–11–0096 .......
04/05/11
03/23/11
03/22/11
03/13/11
03/21/11
03/15/11
P–11–0099 .......
04/01/11
03/24/11
P–11–0110
P–11–0112
P–11–0113
P–11–0115
P–11–0126
.......
.......
.......
.......
.......
04/19/11
04/20/11
04/12/11
03/28/11
04/16/11
03/25/11
04/13/11
03/28/11
03/17/11
04/13/11
P–11–0127 .......
P–11–0134 .......
04/12/11
04/19/11
03/16/11
04/08/11
P–11–0143
P–11–0155
P–98–0317
P–11–0127
P–11–0134
wwoods2 on DSK1DXX6B1PROD with NOTICES_PART 1
P–10–0593
P–11–0001
P–11–0010
P–11–0011
P–11–0013
Received date
.......
.......
.......
.......
.......
04/08/11
03/21/11
04/08/11
04/12/11
04/19/11
04/04/11
03/18/11
03/01/11
03/16/11
04/08/11
P–11–0143 .......
P–11–0155 .......
P–98–0317 .......
04/08/11
03/21/11
04/08/11
04/04/11
03/18/11
03/01/11
If you are interested in information
that is not included in these tables, you
may contact EPA as described in Unit II.
VerDate Mar<15>2010
15:25 Jun 20, 2011
Jkt 223001
Chemical
(G) Modified starch.
(G) Aromatic polyisocyanate, aliphatic polyol blocked.
(G) Fatty acid modified polyester aliphatic polyurethane dispersion.
(G) Polyol blocked cycloaliphatic amine polymer.
(G) Alkyl dioic acid, polymer with substituted alkanoate, alkyl diisocyanate, alkyldiol, and
substituted alkanoic acid.
(G) Aromatic diacid, polymer with polyol, alkyl triol, alkyl alkanoate.
(G) Mercapto silane ester of silica.
(S)
Boron,
trifluoro(tetrahydrofuran)-,
(t-4)-,
polymer
with
3-methyl-3-[(2,2,2trifluoroethoxy)methyl]oxetane, ether with 2,2-dimethyl-1,3-propanediol (2:1).
(S) Boron, trifluoro(tetrahydrofuran)-, (t-4)-, polymer with 3-methyl-3-[(2,2,3,3,3pentafluoropropoxy)methyl]oxtane, ether with 2,2-dimethyl-1,3-propanediol (2:1).
(S) Cyclopentene, 1,3,3,4,4,5,5-heptafluoro-.
(G) Waterborne polyurethane.
(S) Oxirane, 2-ethyl-, polymer with 2-methyloxirane, monododecyl ether.
(G) Amino methacrylate copolymer.
(S) 2H-pyran-4-ol, 2-(1-ethylpropyl) tetrahydro-4-methyl.
(G) Aliphatic urethane acrylate polymer.
(G) Aliphatic urethane acrylate polymer.
(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, alkyl alkenoate, alkyl alkenoate,
alkyl alkenoate, polyalkylidene alkenoate and dialkylaminoalkyl alkenamide.
(G) Alkyl methacrylate.
(G) Polyester polyamide.
(S) Siloxanes and silicones, me hydrogen, me vinyl.
(S) Siloxanes and silicones, di-ph, me hydrogen, me vinyl.
(G) Alkylxylene.
(G) Reaction product of substituted naphthalenesulfonic acid and substituted
benzenesulfonic acid diazotized and coupled with alkyl benzene substituted triazine
amino phenyl compound.
(G) 2-naphthalenecarboxylic acid, substituted diazenyl calcium salt.
(S) Tricyclo[7.3.3.15,11]heptasiloxane-3,7,14-triol, 1,3,5,7,9,11,14-heptaphenyl.
(S)
1,4-benzenedicarboxylic
acid,
1,4-dimethyl
ester,
polymer
with
1,4cyclohexanedimethanol and 2,2,4,4-tetramethyl-1,3-cyclobutanediol, manufacture of, byproducts from, reaction products with ethylene glycol, polymers with 1,4cyclohexanedimethanol, diethylene glycol, ethylene glycol, maleic anhydride and phthalic
anhydride, 3a,4,5,6,7,7a-hexahydro-4,7-methano-1h-inden-5(or 6)-yl esters.
(G) Condensation sodium/potassium salt reaction product of substituted naphthalene sulfonic acid azo substituted phenyl amino substituted triazine and alkylsulfonyl
benzenesulfonic acid azo substituted phenylamino substituted triazine.
(G) Tertiary ammonium compound.
(G) Modified epoxy resin.
(G) Heteromonocyclo, 4-methyl-, oxide, methanesulfonate salt.
(G) Mdi modified polyester resin.
(S) 1,3-benzenedicarboxylic acid, polymers with by-products from manuf. of 1,4cyclohexanedimethanol-di-me terephthalate-2,2,4,4-tetramethyl-1,3-cyclobutanediol polymer-ethylene glycol reaction products, 1,4-cyclohexanedimethanol, diethylene glycol,
ethylene glycol, maleic anhyride and triethylene glycol.
(G) Epoxidized fatty acids, unsaturated, me esters, polymers with trimethylolpropane.
(G) Carbomonocyclic alkene polymer with alkyl alkenoate, alkyl alkenoate, alkyl alkenoate,
alkyl alkenoate, polyalkylidiene alkenoate and heteromonocyclic alkene.
(G) Acrylic polymer.
(G) Polymer substituted anthraquinone derivative.
(G) Substituted cyclic olefin.
(G) Epoxidized fatty acids, unsaturated, me esters, polymers with trimethylolpropane.
(G) Carbomonocyclic alkene polymer with alkyl alkenoate, alkyl alkenoate, alkyl alkenoate,
alkyl alkenoate, polyalkylidiene alkenoate and heteromonocyclic alkene.
(G) Acrylic polymer.
(G) Polymer substituted anthraquinone derivative.
(G) Substituted cyclic olefin.
to access additional non-CBI
information that may be available.
PO 00000
Frm 00042
Fmt 4703
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List of Subjects
Environmental protection, Chemicals,
Hazardous substances, Imports, Notice
of commencement, Premanufacturer,
E:\FR\FM\21JNN1.SGM
21JNN1
36120
Federal Register / Vol. 76, No. 119 / Tuesday, June 21, 2011 / Notices
Reporting and recordkeeping
requirements, Test marketing
exemptions.
Dated: June 8, 2011.
Chandler Sirmons,
Acting Director, Information Management
Division, Office of Pollution Prevention and
Toxics.
[FR Doc. 2011–15246 Filed 6–17–11; 11:15 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
[FRL–9321–9]
Science Advisory Board Staff Office
Notification of a Public Meeting of the
Clean Air Scientific Advisory
Committee (CASAC) Lead Review
Panel
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
The EPA Science Advisory
Board (SAB) Staff Office announces a
public meeting of the CASAC Lead
Review Panel to conduct a peer review
of EPA’s Integrated Science Assessment
for Lead (First External Review Draft)
and a consultation on EPA’s Review of
the National Ambient Air Quality
Standards for Lead: Risk and Exposure
Assessment Planning Document.
DATES: The CASAC Lead Review Panel
meeting will be held on Wednesday,
July 20, 2011, from 9 a.m. to 5:30 p.m.
(Eastern Time) and on Thursday, July
21, 2011, from 8:30 a.m. to 12:30 p.m.
(Eastern Time).
ADDRESSES: The public meeting will be
held at the Marriott at Research Triangle
Park hotel, 4700 Guardian Drive,
Durham, North Carolina 27703 (919)
941–6200.
FOR FURTHER INFORMATION CONTACT: Any
member of the public wishing to obtain
general information concerning the
public meeting may contact Mr. Aaron
Yeow, Designated Federal Officer
(DFO), via telephone at (202) 564–2050
or e-mail at yeow.aaron@epa.gov.
General information concerning the EPA
CASAC can be found on the EPA Web
site at https://www.epa.gov/casac.
SUPPLEMENTARY INFORMATION: The
CASAC was established pursuant to the
Clean Air Act (CAA) Amendments of
1977, codified at 42 U.S.C. 7409D(d)(2),
to provide advice, information, and
recommendations to the Administrator
on the scientific and technical aspects of
issues related to the criteria for air
quality standards, research related to air
quality, sources of air pollution, and the
strategies to attain and maintain air
wwoods2 on DSK1DXX6B1PROD with NOTICES_PART 1
SUMMARY:
VerDate Mar<15>2010
15:25 Jun 20, 2011
Jkt 223001
quality standards and to prevent
significant deterioration of air quality.
The CASAC is a Federal Advisory
Committee chartered under the Federal
Advisory Committee Act (FACA), 5
U.S.C., App. 2. Pursuant to FACA and
EPA policy, notice is hereby given that
the CASAC Lead Review Panel will
hold a public meeting to peer review
EPA’s Integrated Science Assessment for
Lead (First External Review Draft). The
Panel will also provide consultative
advice on EPA’s Review of the National
Ambient Air Quality Standards for
Lead: Risk and Exposure Assessment
Planning Document. These are being
prepared as part of the review of the
National Ambient Air Quality Standards
for Lead. The CASAC Lead Review
Panel and the CASAC will comply with
the provisions of FACA and all
appropriate SAB Staff Office procedural
policies.
Section 109(d)(1) of the CAA requires
that the Agency periodically review and
revise, as appropriate, the air quality
criteria and the NAAQS for the six
‘‘criteria’’ air pollutants, including lead.
EPA is currently reviewing the primary
(health-based) and secondary (welfarebased) NAAQS for lead. The CASAC
Lead Review Panel previously provided
consultative advice on EPA’s Integrated
Review Plan for the National Ambient
Air Quality Standards for Lead
(External Review Draft) in a
teleconference on May 5, 2011 (76 FR
21346–21347) as reported in a letter to
the EPA Administrator, dated May 25,
2011 (EPA–CASAC–11–007).
The Integrated Science Assessment
(ISA) provides a concise review,
synthesis and evaluation of the most
policy-relevant science, including key
science judgments that are important to
the design and scope of exposure and
risk assessments, as well as other
aspects of the NAAQS review. The risk/
exposure assessment planning
document considers the extent to which
information and conclusions presented
in the ISA provide support for the
development of quantitative
assessments of risk and exposure for
health and/or welfare effects.
Availability of Meeting Materials:
Agendas and materials in support of the
meeting will be placed on the CASAC
Web site at https://www.epa.gov/casac in
advance of the meeting. For technical
questions and information concerning
EPA’s Integrated Science Assessment for
Lead (First External Review Draft),
please contact Dr. Ellen Kirrane of
EPA’s Office of Research and
Development at (919) 541–1340, or
kirrane.ellen@epa.gov. For technical
questions and information concerning
EPA’s Review of the National Ambient
PO 00000
Frm 00043
Fmt 4703
Sfmt 4703
Air Quality Standards for Lead: Risk
and Exposure Assessment Planning
Document, please contact Dr. Deirdre
Murphy of EPA’s Office of Air and
Radiation at (919) 541–0729, or
murphy.deirdre@epa.gov.
Procedures for Providing Public Input:
Public comment for consideration by
EPA’s federal advisory committees and
panels has a different purpose from
public comment provided to EPA
program offices. Therefore, the process
for submitting comments to a federal
advisory committee is different from the
process used to submit comments to an
EPA program office.
Federal advisory committees and
panels, including scientific advisory
committees, provide independent
advice to EPA. Members of the public
can submit comments for a federal
advisory committee to consider as it
develops advice for EPA. Input from the
public to the CASAC will have the most
impact if it provides specific scientific
or technical information or analysis for
CASAC panels to consider or if it relates
to the clarity or accuracy of the
technical information. Members of the
public wishing to provide comment
should contact the Designated Federal
Officer directly.
Oral Statements: In general,
individuals or groups requesting an oral
presentation at a public meeting will be
limited to five minutes. Interested
parties should contact Mr. Aaron Yeow,
DFO, in writing (preferably via e-mail)
at the contact information noted above
by July 13, 2011, to be placed on the list
of public speakers for the meeting.
Written Statements: Written
statements should be supplied to the
DFO via e-mail at the contact
information noted above by July 13,
2011 for the meeting so that the
information may be made available to
the Panel members for their
consideration. Written statements
should be supplied in one of the
following electronic formats: Adobe
Acrobat PDF, MS Word, MS
PowerPoint, or Rich Text files in IBM–
PC/Windows 98/2000/XP format. It is
the SAB Staff Office general policy to
post written comments on the Web page
for the advisory meeting or
teleconference. Submitters are requested
to provide an unsigned version of each
document because the SAB Staff Office
does not publish documents with
signatures on its Web sites. Members of
the public should be aware that their
personal contact information, if
included in any written comments, may
be posted to the CASAC Web site.
Copyrighted material will not be posted
without explicit permission of the
copyright holder.
E:\FR\FM\21JNN1.SGM
21JNN1
]]>Agencies
[Federal Register Volume 76, Number 119 (Tuesday, June 21, 2011)]
[Notices]
[Pages 36109-36120]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-15246]
=======================================================================
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
[EPA-HQ-OPPT-2011-0496; FRL-8876-3]
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 Chemical
Substances Inventory (TSCA Inventory)) to notify EPA and comply with
the statutory provisions pertaining to the manufacture of new
chemicals. Under TSCA sections 5(d)(2) and 5(d)(3), 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 manufacture those chemicals. This document, which covers the
period from February 1, 2011 to April 22, 2011, and provides the
required notice and status report, consists of the PMNs and TMEs, both
pending or expired, and the NOC 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 number or TME number,
must be received on or before July 21, 2011.
ADDRESSES: Submit your comments, identified by docket identification
(ID) number EPA-HQ-OPPT-2011-0496, 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 comment directly to EPA without going through regulations.gov,
your e-mail address will be automatically captured and included as part
of the comment that is placed in the docket and made available on the
Internet. If you submit an electronic comment, EPA recommends that you
include your name and other contact information in the body of your
comment and with any disk or CD-ROM you submit. If EPA cannot read your
comment due to technical difficulties and cannot contact you for
clarification, EPA may not be able to consider your comment. Electronic
files should avoid the use of special characters, any form of
encryption, and be free of any defects or viruses.
Docket: All documents in the docket are listed in the docket index
available at https://www.regulations.gov. Although listed in the index,
some information is not publicly available, e.g., CBI or other
information whose disclosure is restricted by statute. Certain other
material, such as copyrighted material, will be publicly available only
in hard copy. Publicly available docket materials are available
electronically at https://www.regulations.gov, or, if only available in
hard copy, at the OPPT Docket. The OPPT Docket is located in the EPA
Docket Center (EPA/DC) at Rm. 3334, EPA West Bldg., 1301 Constitution
Ave., NW., Washington, DC. The EPA/DC Public Reading Room hours of
operation are 8:30 a.m. to 4:30 p.m., Monday through Friday, excluding
legal holidays. The telephone number of the EPA/DC Public Reading Room
is (202) 566-1744, and the telephone number for the OPPT Docket is
(202) 566-0280. Docket visitors are required to show photographic
identification, pass through a metal detector, and sign the EPA visitor
log. All visitor bags are processed through an X-ray machine and
subject to search. Visitors will be provided an EPA/DC badge that must
be visible at all times in the building and returned upon departure.
FOR FURTHER INFORMATION CONTACT:
For technical information contact: 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.
[[Page 36110]]
Although others may be affected, this action applies directly to the
submitter of the PMNs addressed in this action. 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 this information to EPA through
regulations.gov or e-mail. Clearly mark the part or all of the
information that you claim to be CBI. For CBI information in a disk or
CD-ROM that you mail to EPA, mark the outside of the disk or CD-ROM as
CBI and then identify electronically within the disk or CD-ROM the
specific information that is claimed as CBI. In addition to one
complete version of the comment that includes information claimed as
CBI, a copy of the comment that does not contain the information
claimed as CBI must be submitted for inclusion in the public docket.
Information so marked will not be disclosed except in 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 a chemical substance as either an ``existing''
chemical or a ``new'' chemical. Any chemical substance that is not on
EPA's 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 TSCA section 5 to provide EPA with a
PMN, before initiating the activity. Section 5(h)(1) of TSCA 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/opt/newchems.
Under TSCA sections 5(d)(2) and 5(d)(3), 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 NOCs to
manufacture those chemicals. This status report, which covers the
period from February 1, 2011 to April 22, 2011, consists of 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/importer, the
potential uses identified by the manufacturer/importer in the PMN, and
the chemical identity.
Table I--149 PMNs Received From February 1, 2011 to April 22, 2011
----------------------------------------------------------------------------------------------------------------
Projected
Case No. Received notice end Manufacturer/ importer Use Chemical
date date
----------------------------------------------------------------------------------------------------------------
P-11-0190.............. 02/02/11 05/02/11 CBI.................... (G) Paper (G) Dialdehyde,
additive. reaction
products with
hydrolyzed n-
vinylamide
homopolymer
hydrohalides.
P-11-0191.............. 02/01/11 05/01/11 CBI.................... (S) Ultra violet (G) Ultra violet
curable polymer curable
for kitchen polyester
cabinets and polyurethane
office furniture acrylate.
finishes.
P-11-0192.............. 02/02/11 05/02/11 CBI.................... (G) Additive for (G) Amphoteric
paper. polyacrylamide.
P-11-0193.............. 02/02/11 05/02/11 CBI.................... (G) Deposit (G) Poly alkyl
control additive amido hydrazide.
for fuels.
P-11-0194.............. 02/02/11 05/02/11 CBI.................... (G) Plasticizer.. (S) 1,2,3-
propanetricarbox
ylic acid, 2-
(acetyloxy)-,
1,2,3-tris(2-
ethylhexyl)
ester.
P-11-0195.............. 02/03/11 05/03/11 3M..................... (S) Prepolymer (G) Alkoxysilyl
for sprayable polyether
adhesive/ prepolymer.
sealant;
prepolymer for
high viscosity
adhesive/sealant.
P-11-0196.............. 02/08/11 05/08/11 Croda Inc.............. (G) Hard surface (G) Quaternized
cleaner. ethylene oxide
propylene oxide
polymer.
P-11-0197.............. 02/08/11 05/08/11 CBI.................... (G) Colourant (G) Acrylic
dispersant. polymer.
P-11-0198.............. 02/08/11 05/08/11 CBI.................... (G) Colourant (G) Acrylic
dispersant. polymer.
P-11-0199.............. 02/08/11 05/08/11 CBI.................... (G) Colourant (G) Acrylic
dispersant. polymer.
P-11-0200.............. 02/07/11 05/07/11 CBI.................... (G) Resin (G) Aluminum
solution alkoxide
additive. complex,
alkoxylated
aluminum
chelate.
[[Page 36111]]
P-11-0201.............. 02/09/11 05/09/11 Lubrigreen............. (G) Bio-based (S) Fatty acids,
lubricant base C8 18 and C18-
oil. unsaturated,
reaction
products with
isomerized oleic
acid
homopolymer.
P-11-0202.............. 02/09/11 05/09/11 Lubrigreen............. (G) Bio-based (S) Fatty acids,
lubricant base coco, reaction
oil. products with
isomerized oleic
acid
homopolymer.
P-11-0203.............. 02/09/11 05/09/11 CBI.................... (G) Paper (G)
treatment. Perfluoroalkylet
hyl methacrylate
copolymer, salt.
P-11-0204.............. 02/11/11 05/11/11 CBI.................... (S) Brightener (G) Acetaldehyde,
for nickel substituted-,
electroplating. reaction
products with 2-
butyne-1,4-diol.
P-11-0205.............. 02/15/11 05/15/11 CBI.................... (G) Non- (G) Polyalkene,
dispersive ink maleated
additive. potassium salts.
P-11-0206.............. 02/15/11 05/15/11 Eastman Kodak Company.. (G) Intermediate. (G) Bisaryl
iodonium salt.
P-11-0207.............. 02/15/11 05/15/11 Eastman Kodak Company.. (G) Contained use (G) Substituted
in an article. aromatic borate
salt.
P-11-0208.............. 02/16/11 05/16/11 Lubrigreen............. (G) Lubricant (S) Fatty acids,
base oil. C8 18 and C18-
unsaturated,
reaction
products with
isomerized oleic
acid homopolymer
2-ethylhexyl
ester.
P-11-0209.............. 02/16/11 05/16/11 Lubrigreen............. (G) Lubricant (S) Fatty acids,
base oil. coco, reaction
products with
isomerized oleic
acid homopolymer
2-ethylhexyl
ester.
P-11-0210.............. 02/16/11 05/16/11 Lubrigreen............. (G) Lubricant (S) Fatty acids,
base oil. C8 18 and C18-
unsaturated,
reaction
products with
isomerized oleic
acid dimer 2-
ethylhexyl
ester.
P-11-0211.............. 02/16/11 05/16/11 Lubrigreen............. (G) Lubricant (S) Fatty acids,
base oil. coco, reaction
products with
isomerized oleic
acid dimer 2-
ethylhexyl
ester.
P-11-0212.............. 02/16/11 05/16/11 Lubrigreen............. (G) Lubricant (S) 9-
base oil. octadecenoic
acid (9z)-,
homopolymer,
isomerized.
P-11-0213.............. 02/16/11 05/16/11 Lubrigreen............. (G) Lubricant (S) Fatty acids,
base oil. C8 18 and C18-
unsaturated,
reaction
products with
isomerized oleic
acid
homopolymer.
P-11-0214.............. 02/16/11 05/16/11 Lubrigreen............. (G) Lubricant (S) Fatty acids,
base oil. coco, reaction
products with
isomerized oleic
acid
homopolymer.
P-11-0215.............. 02/16/11 05/16/11 CBI.................... (G) Base polymer (S) 2-propenoic
for adhesive. acid, 2-methyl-,
dodecyl ester,
telomer with
methyl 2-methyl-
2-propenoate,
tridecyl 2-
methyl-2-
propenoate, 3-
(trimethoxysilyl
)-1-propanethiol
and 3-
(trimethoxysilyl
) propyl 2-
methyl-2-
propenoate.
P-11-0216.............. 02/16/11 05/16/11 CBI.................... (G) Base polymer (S) 2-propenoic
for adhesive. acid, 2-methyl-,
dodecyl ester,
telomer with
butyl 2-
propenoate,
methyl 2-methyl-
2-propenoate,
tridecyl 2-
methyl-2-
propenoate, 3-
(trimethoxysilyl
)-1-propanethiol
and 3-
(trimethoxysilyl
) propyl 2-
methyl-2-
propenoate.
P-11-0217.............. 02/17/11 05/17/11 CBI.................... (G) Additive, (G)
open, non- Polyetherfluoro
dispersive. urethane.
P-11-0218.............. 02/17/11 05/17/11 CBI.................... (G) Radiation (G) Benzenedioic
curing agent. acid, polymer
with alkanediol
and
carboxyaminoalky
l carbamic acid
alkoxyalkylester
.
P-11-0219.............. 02/18/11 05/18/11 CBI.................... (G) Paint........ (G) Alkyl
acrylate,
polymer with
alkyl acrylate,
alkyl
methacrylates,
and styrene,
peroxide-
initiated.
P-11-0220.............. 02/18/11 05/18/11 CBI.................... (G) Paint........ (G) Alkyl
acrylate,
polymer with
alkyl acrylate,
alkyl
methacrylates,
and styrene,
peroxide-
initiated.
P-11-0221.............. 02/18/11 05/18/11 CBI.................... (G) Paint........ (G) Alkyl
acrylate,
polymer with
alkyl acrylate,
alkyl
methacrylates,
and styrene,
peroxide-
initiated.
[[Page 36112]]
P-11-0222.............. 02/18/11 05/18/11 CBI.................... (G) Paint........ (G) Alkyl
acrylate,
polymer with
alkyl acrylate,
alkyl
methacrylates,
and styrene,
peroxide-
initiated.
P-11-0223.............. 02/18/11 05/18/11 CBI.................... (G) Use as (G) Substituted
photoinitiator. tris-phenyl
thiophenyl-
sulfonium
halogenide.
P-11-0224.............. 02/22/11 05/22/11 CBI.................... (S) Electrolyte (G) Fluoro ether.
for battery.
P-11-0225.............. 02/23/11 05/23/11 CBI.................... (G) Adhesive (S) Amines, C36-
component. alkylenedi-,
polymers with 6-
aminohexanoic
acid, 1,6-
diisocyanato-
2,2,4-
trimethylhexane,
1,6-diisocyanato-
2,4,4-
trimethylhexane,
5,5'-[(1-
methylethylidene
)bis(4,1-
phenyleneoxy)]bi
s[1,3-
isobenzofurandio
ne] and
pyromellitic
dianhydride, 2,5-
dihydro-2,5-
dioxo-1h-pyrrole-
1-hexanoic acid-
blocked.
P-11-0226.............. 02/23/11 05/23/11 CBI.................... (G) As a (G) N-(2-
component of hydroxyethyl)
adhesives and alkenamide.
Cosmetics.
P-11-0227.............. 02/23/11 05/23/11 CBI.................... (G) Coatings..... (G) Urethane
acrylate.
P-11-0228.............. 02/22/11 05/22/11 CBI.................... (S) Used (G) Benzaldehyde,
internally as reaction
raw material for products with
polyamide polyalkylenepoly
manufacture. amines,
hydrogenated.
P-11-0229.............. 02/24/11 05/24/11 H.B. Fuller............ (G) Industrial (G) Polyester,
adhesive. polymer with 1,4-
butanediol,
dodecanedioic,
1,6-heaxanediol,
.alpha.-hydro-
.omega.-
hydroxypoly (oxy-
1,4-butanediyl)
and isocyanate.
P-11-0230.............. 02/24/11 05/24/11 Goulston technologies, (G) Antistatic (G) Alkyl amine
Inc. agent for salt.
acrylic yam.
P-11-0231.............. 02/25/11 05/25/11 Cardolite Corporation.. (S) Amine based (G) Cashew
epoxy curing nutshell liquid
agent for 2 part amine polymer.
epoxy surface
coating.
P-11-0232.............. 02/28/11 05/28/11 CBI.................... (G) Sealant and (G) Acryloxy
adhesive. functional
siloxane.
P-11-0233.............. 02/25/11 05/25/11 CBI.................... (S) Curing agent (G) Phenol, 4,4'-
for epoxy resin. (1-
methylethylidene
)bis-, polymer
with 2-
(chloromethyl)ox
irane, reaction
products with n3-
(3-
(dimethylamino)p
ropyl]-n1,n1-
dimethyl-
alkanepolyamine,
compounds with
formaldehyde-
phenol polymer.
P-11-0234.............. 03/01/11 05/29/11 CBI.................... (G) Chemical (G) Oligmeric
intermediate. phenolic ether.
P-11-0235.............. 03/01/11 05/29/11 CBI.................... (G) Ink, coating, (G) Polyacrylate
adhesive. oligomer product
from saturated
dimer acid,
propoxylated
glycerol and
acrylic acid.
P-11-0236.............. 03/01/11 05/29/11 CBI.................... (G) Ink, coating, (G) Polyacrylate
adhesive. oligomer product
from saturated
dimer acid,
propoxylated
glycerol and
acrylic acid.
P-11-0237.............. 03/02/11 05/30/11 Colonial Chemical, Inc. (S) Oil (S) D-
dispersant. glucopyranose,
oligomeric,
decyl octyl
glycosides,
polymer with 1,3-
dichloro-2-
propanol and
sorbitan mono-
(9z)-9-
octadecenoate.
P-11-0238.............. 03/01/11 05/29/11 IGM Resins Inc. (G) Ultra violet (S) Poly(oxy-1,2-
initiator. ethanediyl),
.alpha.-[2-(4-
benzoylphenoxy)a
cetyl]-.omega.-
[[2-(4-
benzoylphenoxy)a
cetyl]oxy]-.
P-11-0239.............. 03/02/11 05/30/11 CBI.................... (G) Emulsifier... (G) Butanedioic
acid,
monopolyisobutyl
ene derivates,
(alkylimino)di-
2,1-ethanediyl
esters,
compounds with
akylamino
alcohol(1:2).
P-11-0240.............. 03/02/11 05/30/11 CBI.................... (G) Component of (G) Modified
an industrial epoxy resin.
adhesive.
P-11-0241.............. 03/04/11 06/01/11 CBI.................... (G) Used to (S) L-lysine, n2,
adjust (retard) n6-bis (3-
set times in carboxy-1-
calcium sulfate oxopropyl)-,
based binders sodium salt
such as gypsum (1:3).
boards, plaster
boards or wall
boards.
[[Page 36113]]
P-11-0242.............. 03/04/11 06/01/11 Materia Inc............ (G) Resin (G) Hydroxy-
formulation olefin.
additive.
P-11-0243.............. 03/07/11 06/04/11 CBI.................... (G) Thermoplastic (G) Aliphatic
urethane. thermoplastic
urethane.
P-11-0244.............. 03/07/11 06/04/11 CBI.................... (G) Thermoplastic (G) Aliphatic
urethane. thermoplastic
urethane.
P-11-0245.............. 03/07/11 06/04/11 CBI.................... (G) Concrete (G) Alkoxylate
additive. polymer,
mono(alkenyl)
ether.
P-11-0246.............. 03/08/11 06/05/11 Oleon Americas Inc. (S) Emulsifier (S) D-
for commercial xylopyranose,
(I&I) and oligomeric,
household floor C16 18-alkyl
cleaners. glycosides.
P-11-0247.............. 03/04/11 06/01/11 CBI.................... (G) Treatment for (G)
textiles. Perfluoroalkylet
hyl methacrylate
copolymer.
P-11-0248.............. 03/08/11 06/05/11 CBI.................... (G) Printing (G) Roin, polymer
additive. with ethylene
glycol,
propanediol,
alkanedicarboxyl
ic acid,
terephthalic
acid and
trimellitic
anhydride.
P-11-0249.............. 03/08/11 06/05/11 CBI.................... (G) Resin for use (G) Acrylic
in coatings. latex.
P-11-0250.............. 03/09/11 06/06/11 Henkel Corporation..... (S) Cure (S) Benzamide, n-
initiator in (aminothioxometh
adhesive yl)-.
formulations.
P-11-0251.............. 03/10/11 06/07/11 CBI.................... (G) Printing inks (G)
Cycloaliphatic
anhydride
polymer with
alkyldiol.
P-11-0252.............. 03/10/11 06/07/11 CBI.................... (G) Photografic (G)
chemical. Benzeneacetonitr
ile, alkoxy-
[[(alkylsulfonyl
)oxy]imino]-.
P-11-0253.............. 03/10/11 06/07/11 Dow Chemical Company... (G) Detergents (G) Acrylic
and cleaner copolymer.
additive.
P-11-0254.............. 03/09/11 06/06/11 H.B. Fuller............ (G) Industrial (G) Alkanedioic
adhesive. acid, polymer
with ethenyl
acetate, alkyl 2-
propenoate, and
2-propenoic
acid.
P-11-0255.............. 03/10/11 06/07/11 Colonial Chemical, Inc. (S) Hard surface (S) D-
cleaner in high glucopyranose,
caustic oligomeric,
solutions. decyl octyl
glycosides, 2,3-
dihydroxypropyl
ethers,
phosphates,
sodium salts,
polymers with
1,3-dichloro-2-
propanol.
P-11-0256.............. 03/10/11 06/07/11 Colonial Chemical, Inc. (S) Hard surface (S) D-
cleaner in high glucopyranose,
caustic oligomeric, c10-
solutions. 16-alkyl
glycosides, 2,3-
dihydroxypropyl
ethers,
phosphates,
sodium salts,
polymers with
1,3-dichloro-2-
propanol.
P-11-0257.............. 03/10/11 06/07/11 Nanotech Industries, (S) Flooring; (S) Carbamic
Inc. paints; top acid, N,N'-
coating. (trimethyl-1,6-
hexanediyl)bis-,
ester with 1,2-
propanediol
(1:2).
P-11-0258.............. 03/10/11 06/07/11 CBI.................... (G) Curing agent (G) Epoxy and
for epoxy resin. isocyanate
modified
aliphatic
polyamine.
P-11-0259.............. 03/04/11 06/01/11 CBI.................... (G) Flexible (G) Polyether
packaging polyester
adhesive. polyurethane
adhesive.
P-11-0260.............. 03/11/11 06/08/11 CBI.................... (G) Urethane (G) Isocyanate-
adhesive. terminated
prepolymer.
P-11-0261.............. 03/16/11 06/13/11 Global Tungsten and (S) Luminescent (S) Aluminum
Powders Corp. phosphor for use barium europium
in fluorescent magnesium oxide.
lamp
manufacturing.
P-11-0262.............. 03/16/11 06/13/11 Global Tungsten and (S) Luminescent (S) Europium
Powders Corp. phosphor for use strontium borate
in fluorescent metaphosphate
lamp manufacture. oxide.
P-11-0263.............. 03/15/11 06/12/11 CBI.................... (G) Curing agent (G) Modified
for epoxy resin. aliphatic
polyamine.
P-11-0264.............. 03/17/11 06/14/11 CBI.................... (G) Flame (G) Brominated
retardant. aromatic
oligomer.
P-11-0265.............. 03/17/11 06/14/11 CBI.................... (G) Antistatic (G) Dialkyl
additive in imidazolium
polymers, salt.
antistatic
additive in
liquid resins.
P-11-0266.............. 03/17/11 06/14/11 CBI.................... (G) Industrial (G)
lubricant. Polypentaerythri
tol, mixed
esters with
straight and
branched
monoacids.
P-11-0267.............. 03/18/11 06/15/11 Hybrid Plastics, Inc. (G) (S)
Thermoplastics Tricyclo[7.3.3.1
and coatings 5,11]heptasiloxa
additive; ne-3,7,14-triol-
elastomer 1,3,5,7,9,11,14-
additive. heptakis(2,4,4-
trimethylpentyl)-
.
P-11-0268.............. 03/21/11 06/18/11 CBI.................... (G) Flame (G) Phosphoric
retardant. acid, diaryl
alkyl ester.
P-11-0269.............. 03/21/11 06/18/11 CBI.................... (G) Optical (G)
material Perfluorinated
component. cyclo
oxyaliphatic
polymer.
P-11-0270.............. 03/21/11 06/18/11 Lockheed Martin........ (S) Piezoelectric (S) Lead
ceramics used strontium
for active and titanium
passive zirconium oxide.
underwater
acoustic systems.
[[Page 36114]]
P-11-0271.............. 03/21/11 06/18/11 Lockheed Martin........ (S) Piezoelectric (S) Calci
