Certain New Chemicals; Receipt and Status Information, 58498-58506 [2011-23973]
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58498
Federal Register / Vol. 76, No. 183 / Wednesday, September 21, 2011 / Notices
that MSWLFs and non-municipal, nonhazardous waste disposal units that
receive household hazardous waste or
CESQG hazardous waste are in
compliance with the revised criteria for
the design and operation of nonmunicipal, non-hazardous waste
disposal units under 40 CFR part 257,
Subpart B and MSWLFs under 40 CFR
Part 258. (40 CFR part 257, subpart B
and 40 CFR part 258 are henceforth
referred to as the ‘‘revised federal
criteria’’.) Section 4005(c) of RCRA
further mandates the EPA Administrator
to determine the adequacy of state
permit programs to ensure owner and/
or operator compliance with the revised
federal criteria. A state program that is
deemed adequate to ensure compliance
may afford flexibility to owners or
operators in the approaches they use to
meet federal requirements, significantly
reducing the burden associated with
compliance.
In response to the statutory
requirement in § 4005(c), EPA
developed 40 CFR Part 239, commonly
referred to as the State Implementation
Rule (SIR). The SIR describes the state
application and EPA review procedures
and defines the elements of an adequate
state permit program.
The collection of information from the
state during the permit program
adequacy determination process allows
EPA to evaluate whether a program for
which approval is requested is
appropriate in structure and authority to
ensure owner or operator compliance
with the revised federal criteria. The SIR
does not require the use of a particular
application form. Section 239.3 of the
SIR, however, requires that all state
applications contain the following five
components:
(1) A transmittal letter requesting
permit program approval.
(2) A narrative description of the state
permit program, including a
demonstration that the state’s standards
for non-municipal, non-hazardous waste
disposal units that receive CESQG
hazardous waste are technically
comparable to the part 257, subpart B
criteria and/or that its MSWLF
standards are technically comparable to
the Part 258 criteria.
(3) A legal certification demonstrating
that the state has the authority to carry
out the program.
(4) Copies of state laws, regulations,
and guidance that the state believes
demonstrate program adequacy.
(5) Copies of relevant state-tribal
agreements if the state has negotiated
with a tribe for the implementation of a
permit program for non-municipal, nonhazardous waste disposal units that
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receive CESQG hazardous waste and/or
MSWLFs on tribal lands.
The EPA Administrator has delegated
the authority to make determinations of
adequacy, as contained in the statute, to
the EPA Regional Administrator. The
appropriate EPA Regional Office,
therefore, will use the information
provided by each state to determine
whether the state’s permit program
satisfies the statutory test reflected in
the requirements of 40 CFR part 239. In
all cases, the information will be
analyzed to determine the adequacy of
the state’s permit program for ensuring
compliance with the federal revised
criteria.
Burden Statement: The annual public
reporting burden for this collection of
information is estimated to average 242
hours per response. There is no
recordkeeping burden associated with
this ICR. Burden means the total time,
effort, or financial resources expended
by persons to generate, maintain, retain,
or disclose or provide information to or
for a Federal agency. This includes the
time needed to review instructions;
develop, acquire, install, and utilize
technology and systems for the purposes
of collecting, validating, and verifying
information, processing and
maintaining information, and disclosing
and providing information; adjust the
existing ways to comply with any
previously applicable instructions and
requirements; train personnel to be able
to respond to a collection of
information; search data sources;
complete and review the collection of
information; and transmit or otherwise
disclose the information.
The ICR provides a detailed
explanation of the Agency’s estimate,
which is only briefly summarized here:
Estimated total number of potential
respondents: 12.
Frequency of response: On occasion.
Estimated total average number of
responses for each respondent: 1.
Estimated total annual burden hours:
2,405.
Estimated total annual costs:
$128,268. All costs are labor costs, there
are no capital/start-up or O&M costs
associated with this ICR.
What is the next step in the process for
this ICR?
EPA will consider the comments
received and amend the ICR as
appropriate. The final ICR package will
then be submitted to OMB for review
and approval pursuant to 5 CFR
1320.12. At that time, EPA will issue
another Federal Register notice
pursuant to 5 CFR 1320.5(a)(1)(iv) to
announce the submission of the ICR to
OMB and the opportunity to submit
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additional comments to OMB. If you
have any questions about this ICR or the
approval process, please contact the
technical person listed under FOR
FURTHER INFORMATION CONTACT.
Dated: September 14, 2011.
Suzanne Rudzinski,
Director, Office of Resource Conservation and
Recovery.
[FR Doc. 2011–24273 Filed 9–20–11; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPPT–2011–0768; FRL–8889–6]
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.
This document, which covers the period
from July 1, 2011 to August 26, 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 October
21, 2011.
ADDRESSES: Submit your comments,
identified by docket identification (ID)
number EPA–HQ–OPPT–2011–0768,
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
SUMMARY:
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Federal Register / Vol. 76, No. 183 / Wednesday, September 21, 2011 / Notices
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
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
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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: TSCA–
Hotline@epa.gov.
SUPPLEMENTARY INFORMATION:
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.
I. General Information
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
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 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
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Federal Register / Vol. 76, No. 183 / Wednesday, September 21, 2011 / Notices
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 July 1, 2011 to
August 26, 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—131 PMNS RECEIVED FROM JULY 1, 2011 TO AUGUST 26, 2011
Manufacturer/importer
Received date
Projected notice end date
P–11–0478 ..
7/1/2011
9/28/2011
CBI .............
P–11–0479 ..
7/1/2011
9/28/2011
CBI .............
P–11–0480 ..
7/1/2011
9/28/2011
CBI .............
P–11–0481 ..
7/6/2011
10/3/2011
P–11–0482 ..
P–11–0483 ..
7/8/2011
7/8/2011
10/5/2011
10/5/2011
Ferro Corporation.
CBI .............
CBI .............
P–11–0484 ..
P–11–0485 ..
7/8/2011
7/8/2011
10/5/2011
10/5/2011
CBI .............
CBI .............
P–11–0486 ..
7/8/2011
10/5/2011
P–11–0487 ..
P–11–0488 ..
7/8/2011
7/8/2011
10/5/2011
10/5/2011
Asahi Kasei
America,
Inc.
CBI .............
CBI .............
P–11–0489 ..
7/8/2011
10/5/2011
CBI .............
P–11–0490 ..
7/8/2011
10/5/2011
Sasol North
America.
(G) Surfactant .................
(G) Hardener for industrial coatings.
(G) Hardener for industrial coatings.
(S) Anti-graying agent in
fabric washes.
P–11–0491 ..
7/8/2011
10/5/2011
Sasol North
America.
(S) Anti-graying agent in
fabric washes.
P–11–0492 ..
P–11–0493 ..
7/8/2011
7/5/2011
10/5/2011
10/2/2011
CBI .............
CBI .............
P–11–0494 ..
7/5/2011
10/2/2011
CBI .............
P–11–0495 ..
7/5/2011
10/2/2011
CBI .............
P–11–0496 ..
7/5/2011
10/2/2011
CBI .............
P–11–0497 ..
7/5/2011
10/2/2011
CBI .............
P–11–0498 ..
7/12/2011
10/9/2011
GE Water &
Process
Technologies.
(G) Raw material ............
(G) Chelating agent for
hydrogen sulfide removal.
(G) Chelating agent for
hydrogen sulfide removal.
(G) Chelating agent for
hydrogen sulfide removal.
(G) Chelating agent for
hydrogen sulfide removal.
(G) Chelating agent for
hydrogen sulfide removal.
(S) Heavy metal precipitant for wastewater.
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Use
Chemical
(S) Textile wet processing enhancer.
(S) Intermediate for rubber processing additives.
(G) Processing additive
intermediate.
(G) Additive for polymers
(G) Amino-modified polyalkyleneoxide silicone copolymer.
(G) Vinylalkoxysilane.
(G) Specialty additive .....
(G) Chemical intermediate.
(G) Surfactant .................
(G) Hardener for industrial coatings.
(G) Hardener for industrial coatings.
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(G) Mercaptoalkoxysilane.
(S) 1,2-cyclohexanedicarboxylic acid, 1-butyl 2(phenylmethyl) ester.
(G) Carbon nanotubes.
(G) Alkyl thiol.
(G) Alkyl sulfate salt.
(G) Polyoxyalkylene ether, polymer with aliphatic
diisocyanate, homopolymer, alkanol-blocked.
(G) Alkyl substituted alkanediol polymer with aliphatic and alicyclic diisocyanates.
(G) Alkyl polyamide.
(G) Aliphatic diisocyanate, homopolymer, alkanolblocked.
(G) Aliphatic diisocyanate polymer with alkanediol
and alkylglycol.
(S) 1,4-benzenedicarboxylic acid, 1,4-dimethyl
ester, polymer with 1,2-ethanediol and 1,2,3propanetriol, ester with .alpha.-methyl-.omega.hydroxypoly(oxy-1,2-ethanediyl).
(S) 1,4-benzenedicarboxylic acid, 1,4-dimethyl
ester, polymer with 1,2-propanediol, ester with
.alpha.-methyl-.omega.-hydroxypoly(oxy-1,2ethanediyl).
(G) Glycine derivative.
(G) Aminocarboxylic acid iron chelate complex.
(G) Aminocarboxylic acid iron chelate complex.
(G) Aminocarboxylic acid iron chelate complex.
(G) Aminocarboxylic acid iron chelate complex.
(G) Aminocarboxylic acid iron chelate complex.
(G) Sodium polyethylenimine dithiocarbamate, polymeric dithiocarbamate.
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58501
TABLE I—131 PMNS RECEIVED FROM JULY 1, 2011 TO AUGUST 26, 2011—Continued
Received date
Projected notice end date
Manufacturer/importer
P–11–0499 ..
7/12/2011
10/9/2011
P–11–0500 ..
P–11–0501 ..
7/12/2011
7/1/2011
P–11–0502 ..
Use
Chemical
Sika Corporation.
(G) Water soluable
polyamine curing agent
for epoxy coatings.
10/9/2011
9/28/2011
CBI .............
CBI .............
(G) Processing additive ..
(G) Adhesive ...................
7/14/2011
10/11/2011
CBI .............
7/15/2011
10/12/2011
CBI .............
P–11–0504 ..
7/13/2011
10/10/2011
CBI .............
P–11–0505 ..
7/14/2011
10/11/2011
CBI .............
P–11–0506 ..
7/14/2011
10/11/2011
CBI .............
P–11–0507 ..
7/14/2011
10/11/2011
CBI .............
P–11–0508 ..
7/18/2011
10/15/2011
P–11–0509 ..
7/18/2011
10/15/2011
Dow Chemical Company.
CBI .............
(G) Acrylic pressure sensitive adhesive.
(G) Pigment formulation
additive.
(S) Binder for ultra violet
curable coatings.
(S) Polymer for can coatings.
(G) Polymer backbone
for further processing.
(S) Wastewater heavy
metals removal.
(G) Inert ingredient .........
(S) Phenol, 4,4’-(1-methylethylidene)bis-, polymer
with
5-amino-1,3,3trimethylcyclohexanemethanamine, n1,n2-bis(2aminoethyl)-1,2-ethanediamine, 2-(chloromethyl)
oxirane,
.alpha.-hydro-.omega.hydroxypoly[oxy(methyl-1,2-ethanediyl)], 2,2’-[(1methylethylidene)bis(4,1phenyleneoxymethylene)]bis[oxirane]
and
.alpha.-(2-oxiranylmethyl)-.omega.-(2oxiranylmethoxy)poly[oxy(methyl-1,2-ethanediyl)],
reaction
products
with
2-[[4-(1,1dimethylethyl)phenoxy]methyl]oxirane, acetates
(salts).
(G) Polysulfide silane.
(G) Alkyldioic acid, polymer with alkyl acrylate,
alkenearomatic, alkyldiol, hydroxyalkyl methacrylate, aromatic isocyanate, alkyl methacrylate and
acrylic acid.
(G) Acrylic solution polymer.
P–11–0503 ..
P–11–0510 ..
7/18/2011
10/15/2011
IGM Resins
Inc.
P–11–0511 ..
7/18/2011
10/15/2011
CBI .............
P–11–0512 ..
P–11–0513 ..
7/18/2011
7/18/2011
10/15/2011
10/15/2011
CBI .............
CBI .............
P–11–0514 ..
7/18/2011
10/15/2011
CBI .............
P–11–0515 ..
7/18/2011
10/15/2011
CBI .............
P–11–0516 ..
7/18/2011
10/15/2011
CBI .............
P–11–0517 ..
7/18/2011
10/15/2011
CBI .............
P–11–0518 ..
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Case No.
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10/15/2011
CBI .............
P–11–0519
P–11–0520
P–11–0521
P–11–0522
P–11–0523
P–11–0524
P–11–0525
..
..
..
..
..
..
..
7/18/2011
7/18/2011
7/18/2011
7/18/2011
7/18/2011
7/18/2011
7/19/2011
10/15/2011
10/15/2011
10/15/2011
10/15/2011
10/15/2011
10/15/2011
10/16/2011
CBI
CBI
CBI
CBI
CBI
CBI
CBI
P–11–0526 ..
P–11–0527 ..
7/19/2011
7/20/2011
10/16/2011
10/17/2011
CBI .............
CBI .............
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.............
.............
.............
.............
.............
.............
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(S) Wire & cable insulation; film; injection
molding.
(G) Ultra violet initiator ....
(G) Petroleum substitute
base.
(G) Petroleum substitutes
(G) Intermediate petroleum substitutes.
(G) Intermediate petroleum substitutes.
(G) Intermediate petroleum substitutes.
(G) Intermediate petroleum substitutes.
(G) Intermediate petroleum substitutes.
(G) Intermediate petroleum substitutes.
(G) Petroleum substitutes
(G) Petroleum substitutes
(G) Petroleum substitutes
(G) Petroleum substitute
(G) Petroleum substitute
(G) Petroleum substitute
(G) Material for semi-conductor.
(G) Surface active agent
(G) Chemical intermediate.
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(G) Siloxanes and silicones, 3-aminoalkyl, hydroxy
terminated.
(G) Ultra violet curable polyurethane acrylate.
(G) Polyester polymer.
(G) Polyaminoamide.
(G) Polymeric sulfide.
(G) Acrylic polymer.
(G) Etfe, ethylene-tetrafluoroethylene copolymer.
(S)
Poly(oxy-1,2-ethanediyl),
.alpha.-[4(dimethylamino)benzoyl]-,
.omega.-[[4(dimethylamino)benzoyl]oxy]- (ca index name).
(G) C15 olefins.
(G) C15 paraffinic hydrocarbon.
(G) Highly branched isoolefinic hydrocarbons.
(G) Highly branched isoolefinic hydrocarbons.
(G) Highly branched isoolefinic hydrocarbons.
(G) Highly branched isoparaffinic hydrocarbons.
(G) Highly branched isoparaffinic hydrocarbons.
(G) Highly branched isoparaffinic hydrocarbons.
(G) Highly branched isoparaffinic hydrocarbons.
(G) Highly branched isoparaffinic hydrocarbons.
(G) Highly branched isoparaffinic hydrocarbons.
(G) Highly branched isoparaffinic hydrocarbons.
(G) Highly branched isoparaffinic hydrocarbons.
(G) Highly branched isoparaffinic hydrocarbons.
(G) Oxibiscarbomonocyclic acid, polymer wth
oxibis[heteropolycyclic
ketone],
(alkyl(c-15)substituted)
bis
[alkane(c-2-6)amine],[halo
(haloalkyl(c-1-5))alkylidene]bis[aminocarbomono
cyclic
alcohol]
and
[[halo(haloalkyl(c-1-5))
alkylidene]]bis(hydroxycarbomonocycle)]
bis[aminobenzamide].
(G) Amphoteric fluorinated surfactant.
(G) Substituted fluoroalkane.
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58502
Federal Register / Vol. 76, No. 183 / Wednesday, September 21, 2011 / Notices
TABLE I—131 PMNS RECEIVED FROM JULY 1, 2011 TO AUGUST 26, 2011—Continued
Manufacturer/importer
Received date
Projected notice end date
P–11–0528 ..
7/20/2011
10/17/2011
CBI .............
P–11–0529 ..
7/20/2011
10/17/2011
CBI .............
P–11–0530 ..
P–11–0531 ..
P–11–0532 ..
7/20/2011
7/20/2011
7/20/2011
10/17/2011
10/17/2011
10/17/2011
CBI .............
CBI .............
CBI .............
P–11–0533 ..
P–11–0534 ..
P–11–0535 ..
7/20/2011
7/20/2011
7/21/2011
10/17/2011
10/17/2011
10/18/2011
CBI .............
CBI .............
CBI .............
P–11–0536 ..
7/21/2011
10/18/2011
CBI .............
P–11–0537 ..
P–11–0538 ..
7/22/2011
7/22/2011
10/19/2011
10/19/2011
CBI .............
H.B. Fuller
Company.
P–11–0539 ..
7/22/2011
10/19/2011
H.B. Fuller
Company.
(G) Industrial adhesive ...
P–11–0540 ..
7/22/2011
10/19/2011
H.B. Fuller
Company.
(G) Industrial adhesive ...
P–11–0541 ..
7/22/2011
10/19/2011
H.B. Fuller
Company.
(G) Industrial adhesive ...
P–11–0542 ..
7/22/2011
10/19/2011
H.B. Fuller
Company.
(G) Industrial adhesive ...
P–11–0543 ..
P–11–0544 ..
P–11–0545 ..
7/26/2011
7/27/2011
7/28/2011
10/23/2011
10/24/2011
10/25/2011
CBI .............
CBI .............
CBI .............
P–11–0546 ..
7/27/2011
10/24/2011
P–11–0547 ..
7/27/2011
10/24/2011
Chemetall
Foote
Corporation.
ICL–IP
America
Inc.
(G) Surfactant .................
(G) Colourant ..................
(G) Chemical intermediate.
(S) Brazing (metal joining) agent.
P–11–0548 ..
7/28/2011
10/25/2011
P–11–0549 ..
P–11–0550 ..
8/1/2011
8/2/2011
10/29/2011
10/30/2011
P–11–0551 ..
8/2/2011
10/30/2011
Sika Corporation.
P–11–0552 ..
8/1/2011
10/29/2011
CBI .............
P–11–0553 ..
P–11–0554 ..
8/2/2011
8/2/2011
10/30/2011
10/30/2011
CBI .............
CBI .............
P–11–0555 ..
8/2/2011
10/30/2011
CBI .............
wreier-aviles on DSK7SPTVN1PROD with NOTICES
Case No.
VerDate Mar<15>2010
15:20 Sep 20, 2011
Jkt 223001
Advanced
polymer
technology.
CBI .............
Sika Corporation.
PO 00000
Frm 00043
Use
Chemical
(G) Chemical intermediate.
(G) Chemical intermediate.
(G) Surfactant .................
(S) Dye intermediate ......
(G) Chemical intermediate.
(G) Surfactant .................
(G) Surfactant .................
(S) Leather processing
waterproofing agent.
(S) Leather processing
waterproofing agent.
(G) Colourant ..................
(G) Industrial adhesive ...
(G) Fluorinated thiol.
(G) Fluorinated monomer.
(G) Fluoropolyacrylamide.
(G) Diazo substituted copper salt.
(G) Polyfluoroalkyl amine.
(G) Non-ionic fluorosurfactant.
(G) Anioinic fluorosurfactant.
(G) Carboxy functional polydimethylsiloxane.
(G) Modified aminosiloxane.
(G) Pyrazole azo thiadiazole derivative.
(G) Mixture of: acrylic polymer with polymerized organic acid, potassium salt and organic acid, potassium salt.
(G) Mixture of: acrylic polymer with polymerized organic acid, compd. with 2-aminoethanol and organic acid, 2-aminoethanol salt.
(G) Mixture of: acrylic polymer with polymerized organic acid, ammonium salt and organic acid,
ammonium salt.
(G) Mixture of: acrylic polymer with polymerized organic acid, sodium salt and organic acid, sodium
salt.
(G) Mixture of: acrylic polymer with polymerized organic acid, potassium salt and organic acid, potassium salt.
(G) Polyfluorinated alkyl quaternary amine chloride.
(G) Diazopyridine derivative.
(G) Substituted hydrogen phosphite.
(S) Silicate (2-) hexafluoro-cesium.
(G) The final formulation
is a halogen-free flame
retardant pmn that will
be coated on the surface of composite or
textile surface.
(G) Polymer crosslinking
agent.
(G) Phosphoric acid, inorganic salt.
(G) Heat transfer fluid .....
(G) Used as an emulsifier
in a hardener of a waterborne 2 part epoxy
system.
(G) Used as an emulsifier
in a hardener of a waterborne 2 part epoxy
system.
(G) Productivity aid in the
paper industry.
(G) Coatings ...................
(G) Fuel blending component.
(G) Coating agent ...........
(S) 2-butene, 1,1,1,4,4,4-hexafluoro-, (2z)-.
(G) N-coco alkyltrimethylene0-, polymers with
bisphenol a, epichlorohydrin and amodified aliphatic amine.
Fmt 4703
Sfmt 4703
(S) Imidodicarbonic diamide, n,n-dibutyl-n′,2-bis[4[(4-isocyanatophenyl)methyl]phenyl]-.
(G) N-coco alkyltrimethylenedi-, polymer with
bisphenol a, epichlorohydrin and modified aliphatic amine.
(G) Polyaminoamide, sulfate salt.
(G) Urethane acrylate.
(G) Petroleum distillate lights.
(G) 2-propenoic acid, 2-methyl-1,1-dimethylethyl
ester, polymer with 2,2-dimethyl-1,3-propanediol,
ethenylbenzene, 2-ethyl-2-(hydroxymethyl)-1,3propanediol, cycloaliphatic dicarboxylic anhydride
and
1,2-propanediol
mono(2-methyl-2propenoate), bis(1,1-dimethylpropyl)peroxide-initiated.
E:\FR\FM\21SEN1.SGM
21SEN1
Federal Register / Vol. 76, No. 183 / Wednesday, September 21, 2011 / Notices
58503
TABLE I—131 PMNS RECEIVED FROM JULY 1, 2011 TO AUGUST 26, 2011—Continued
Manufacturer/importer
Use
Chemical
10/30/2011
CBI .............
(G) Coating agent ...........
8/3/2011
10/31/2011
CBI .............
(G) Water and oil repellant.
P–11–0558 ..
8/3/2011
10/31/2011
CBI .............
P–11–0559 ..
P–11–0560 ..
8/4/2011
8/4/2011
11/1/2011
11/1/2011
P–11–0561 ..
8/4/2011
11/1/2011
CBI .............
Moresco
USA Inc.
CBI .............
P–11–0562 ..
8/8/2011
11/5/2011
(G) Component of cleaning agent used in electronic applications..
(G) Releasing agent .......
(S) Additive-grease for
bearings.
(S) Automotive fuel hose;
semi conductor/chemical tubing.
(G) Import only ................
(G) 2-propenoic acid, 2-methyl-, polymer with 2,2dimethyl-1,3-propanediol, ethenylbenzene, 2ethyl-2-(hydroxymethyl)-1,3-propanediol,
cycloaliphatic dicarboxylic anhydride, 2-hydroxyethyl 2-methyl-2-propenoate, methyl 2-methyl-2propenoate and 2-methylpropyl 2-methyl-2propenoate,
2-hydroxy-3-[(1-oxoneodecy]oxy]propyl ester.
(G) 2-propenoic acid, 2-methyl-, 2-hydroxyethyl
ester, telomers with c18–26 alkyl acrylate, 1dodecanthiol,
n-(hydroxymethyl)-2-methyl-2propenamide, polyfluorooctyl methacrylate and
vinylidene chloride, 2,2′-[1,2-diazenediylbis(1methylethylidene)]-bis[4,5-dihydro-1h-imidazole]hydrochloride (1:2)-initiated.
(S) D-glucitol, 1,2,3,4,5,6-hexakis-o-[3-(hydroxyamino)-3-iminopropyl]-.
(G) Vegetable oil, modified.
P–11–0563 ..
8/8/2011
11/5/2011
(G) Import only ................
(G) Vegetable oil, modified.
P–11–0564 ..
8/8/2011
11/5/2011
(S) Hard surface cleaner
P–11–0565 ..
8/8/2011
11/5/2011
Colonial
Chemical,
Inc.
(S) Hard surface cleaner
P–11–0566 ..
8/8/2011
11/5/2011
CBI .............
P–11–0567 ..
8/8/2011
11/5/2011
CBI .............
P–11–0568 ..
P–11–0569 ..
8/8/2011
8/8/2011
11/5/2011
11/5/2011
CBI .............
CBI .............
P–11–0570 ..
8/8/2011
11/5/2011
CBI .............
(G) Component of an industrial coating.
(G) Manufacturing of
elastomer containing
items.
(G) Film, wire and cable
(G) Manufacturing of
elastomer containing
items.
(G) Industrial lubricant ....
(S) D-glucopyranose, oligomeric, c10-16-alkyl decyl
octyl glycosides, 3-[(carboxymethyl)bis(2-hydroxyethyl)ammonio]-2-hydroxypropyl
ethers,
inner salts, polymers with 1,3-dichloro-2-propanol.
(S) D-glucopyranose, oligomeric, c10-16-alkyl
glycosides,
3-[(carboxymethyl)bis(2-hydroxyethyl)ammonio]-2-hydroxypropyl ethers, inner
salts, polymers with 1,3-dichloro-2-propanol.
(G) Cycloaliphatic polyacid functional polyester.
P–11–0571 ..
8/10/2011
11/7/2011
(G) Intermediate .............
P–11–0572 ..
8/11/2011
11/8/2011
3M Company.
Henkel Corporation.
P–11–0573 ..
8/11/2011
11/8/2011
CBI .............
P–11–0574 ..
8/11/2011
11/8/2011
CBI .............
P–11–0575 ..
8/11/2011
11/8/2011
CBI .............
P–11–0576 ..
8/11/2011
11/8/2011
CBI .............
P–11–0577 ..
8/12/2011
11/9/2011
(S) Butanoic acid, 3-mercapto-, ethyl ester.
P–11–0578 ..
8/12/2011
11/9/2011
International
flavors &
Fragrances,
Inc.
Eastman
Kodak
Company.
(G) For use as an exterior can coating.
(G) For use as an exterior can coating.
(G) For use as an exterior paper coating.
(G) For use as an exterior paper coating.
(S) Fragrance ingredient
(S) Intermediate ..............
(S) Benzoic acid, 4-(1,1-dimethylethyl)-, hydrazide.
Received date
Projected notice end date
P–11–0556 ..
8/2/2011
P–11–0557 ..
wreier-aviles on DSK7SPTVN1PROD with NOTICES
Case No.
VerDate Mar<15>2010
15:20 Sep 20, 2011
Jkt 223001
Ask chemicals L.P.
Ask chemicals L.P.
Colonial
Chemical,
Inc.
PO 00000
Frm 00044
(S) An adhesive used for
panel lamination and
other assemblies.
Fmt 4703
Sfmt 4703
(G) Polyglycerol fatty acid ester.
(G) Alkylated diphenyl ethers.
(G) Tetrafluoroethylene chlorotrifluoroethylene copolymer.
(G) Fluoropolymer.
(G) Fluoropolymer.
(G) Fluoropolymer.
(G) Polypentaerythritol, mixed esters with mono
carboxylic acids.
(G) Aryloxy dialkanol.
(S) 1,4-cyclohexanedimethanol, polymer with 2hydroxymethylethyl-terminated
polybutadiene
and
1,1′-methylenebis[4-isocyanatobenzene],
c14 alcs.-blocked.
(G) Acrylic latex resin.
(G) Acrylic latex resin.
(G) Fatty acid modified pet.
(G) Fatty acid modified pet.
E:\FR\FM\21SEN1.SGM
21SEN1
58504
Federal Register / Vol. 76, No. 183 / Wednesday, September 21, 2011 / Notices
TABLE I—131 PMNS RECEIVED FROM JULY 1, 2011 TO AUGUST 26, 2011—Continued
Received date
P–11–0579 ..
8/12/2011
11/9/2011
P–11–0580 ..
8/12/2011
11/9/2011
P–11–0581 ..
8/12/2011
11/9/2011
P–11–0582 ..
8/12/2011
11/9/2011
P–11–0583 ..
8/12/2011
11/9/2011
P–11–0584 ..
8/12/2011
P–11–0585 ..
P–11–0586
P–11–0587
P–11–0588
P–11–0589
Manufacturer/importer
Projected notice end date
Case No.
Use
Chemical
(S) Intermediate ..............
(S) 1h-1,2,4-triazole-3-acetic
dimethylethyl)phenyl]-.
(S) Intermediate ..............
(S)
Cyclohexanol,
methyl-.
(S) Intermediate in the
manufacture of an imaging chemical.
(S) Intermediate in manufacture of imaging
chemical.
(S) Coupler for imaging
products; for export.
11/9/2011
CBI .............
8/15/2011
11/12/2011
AOC L.L.C.
..
..
..
..
8/16/2011
8/16/2011
8/17/2011
8/19/2011
11/13/2011
11/13/2011
11/14/2011
11/16/2011
CBI .............
CBI .............
CBI .............
Wacker
Chemical
Corporation.
8/19/2011
11/16/2011
CBI .............
(S) Crosslinker for waterborne polymers/coatings.
(S) Polymer component
for laminating of fiber
reinforced plastic composites.
(G) Dyestuff ....................
(G) Dyestuff ....................
(G) Plastic additive .........
(G) For both uses the
production ‘‘is 100%
because after industrial
production formulations
they are 100% consumed during final application’’.
(G) Dispersant ................
(S) 1h-1,2,4-triazole-5-acetic acid, 1-acetyl-3-[4(1,1,-dimethylethyl)phenyl]-,
2,6-bis(1,1dimethylethyl)-4-methylcyclohexyl ester.
(S) 1h-1,2,4-triazole-5-acetic acid, 1-acetyl-.alpha.bromo-3-[4-(1,1-dimethylethyl)phenyl]-,
2,6bis(1,1-dimethylethyl)-4-methylcyclohexyl ester.
(S)
3h-pyrrolo[1,2-b][1,2,4]triazole-7-carboxylic
acid,
5-[[[bis(2-ethoxy-2oxoethyl)amino]carbonyl]oxy]-6-cyano-2-[4-(1,1dimethylethyl)phenyl]-, 2,6-bis(1,1-dimethylethyl)4-methylcyclohexyl ester.
(G) Isocyanate crosslinker.
P–11–0590 ..
P–11–0591 ..
P–11–0592 ..
8/19/2011
8/19/2011
11/16/2011
11/16/2011
CBI .............
CBI .............
P–11–0593 ..
8/22/2011
11/19/2011
CBI .............
P–11–0594 ..
P–11–0595 ..
8/22/2011
8/23/2011
11/19/2011
11/20/2011
8/23/2011
11/20/2011
CBI .............
Dow Chemical Company.
CBI .............
(G) Rubber component ...
(G) Water reducer in concrete intermediate.
P–11–0596 ..
P–11–0597
P–11–0598
P–11–0599
P–11–0600
P–11–0601
P–11–0602
P–11–0603
..
..
..
..
..
..
..
8/24/2011
8/24/2011
8/24/2011
8/24/2011
8/24/2011
8/24/2011
8/25/2011
11/21/2011
11/21/2011
11/21/2011
11/21/2011
11/21/2011
11/21/2011
11/22/2011
CBI
CBI
CBI
CBI
CBI
CBI
CBI
P–11–0604 ..
wreier-aviles on DSK7SPTVN1PROD with NOTICES
Eastman
Kodak
Company.
Eastman
Kodak
Company.
Eastman
Kodak
Company.
Eastman
Kodak
Company.
Eastman
Kodak
Company.
8/26/2011
11/23/2011
CBI .............
P–11–0605 ..
8/26/2011
11/23/2011
CBI .............
P–11–0606 ..
8/26/2011
11/23/2011
CBI .............
P–11–0607 ..
8/26/2011
11/23/2011
CBI .............
P–11–0608 ..
8/26/2011
11/23/2011
CBI .............
(G) Packaging material ...
(G) Packaging material ...
(G) Packaging material ...
(G) Packaging material ...
(G) Packaging material ...
(G) Packaging material ...
(G) Additive for manufacture of articles.
(S) Polymer for flame-retardant coatings.
(G) Resin for protective
industrial coatings.
(G) Contained use in energy production.
(G) Additve flame retardant (open, non-dispersive use).
(G) Epoxy catalyst ..........
VerDate Mar<15>2010
15:20 Sep 20, 2011
Jkt 223001
PO 00000
.............
.............
.............
.............
.............
.............
.............
Frm 00045
(G) Lamination adhesive
(G) Site limited intermediate.
(G) Component of polyurethane foam.
(S) Polyurethane catalyst
Fmt 4703
Sfmt 4703
acid,
5-[4-(1,1-
2,6-bis(1,1-dimethylethyl)-4-
(S) 1,4-benzenedicarboxylic acid, polymer with 1,2ethanediol, 2,5-furandione and 1,2-propanediol,
reaction products with dicyclopentadiene.
(G) Substituted phthalocyanine derivative.
(G) Substituted benzimidazol sulfonic acid.
(G) Alkyl amine ester.
(G) Copolymer of vinyl alkanoates and alkene sulfonic acid sodium salt.
(G) Alkyl acrylate, (alkylamino)alkyl ester, telomer
with alkyl acrylate and dialkyl- trialkylalkoxyaromatic- heterocycloaliphaticketone.
(G) Ipdi modified polyester resin.
(G) 2-substituted phtalic acid ester.
(G) Formaldehydem reaction products with
alkylphenol
and
diethanolamine,
alkoxy
alkylated.
(G) Mercaptoalkoxysilane.
(G) Sodium salt initiated acrylic polymer.
(G)
Hexanedioic
acid,
compound
polyalkylenepolyamine.
(G) Poly(3-hydroxybutyrate).
(G) Poly(3-hydroxybutyrate).
(G) Poly(3-hydroxybutyrate).
(G) Poly(3-hydroxybutyrate).
(G) Poly(3-hydroxybutyrate).
(G) Poly(3-hydroxybutyrate).
(G) Modified starch acrylate polymer.
with
(G) Flame retardant polymer for coatings.
(G) Water based acrylic dispersion.
(G) Cationic polyacrylate.
(G) Polyaromatic organophosphorus compound.
(S)
1,3-benzenediol,
yl)propyl]imino)ethyl]-.
E:\FR\FM\21SEN1.SGM
21SEN1
4-[1-[[3-(1h-imidazol-1-
Federal Register / Vol. 76, No. 183 / Wednesday, September 21, 2011 / Notices
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
58505
the TME, the submitting manufacturer/
importer, the potential uses identified
by the manufacturer/importer in the
TME, and the chemical identity.
TABLE II—4 TMES RECEIVED FROM JULY 1, 2011 TO AUGUST 26, 2011
Manufacturer/Importer
Received date
Projected notice end date
T–11–0011 ..
7/14/2011
8/27/2011
CBI .............
T–11–0012 ..
7/29/2011
9/11/2011
Shell Chemical LP.
T–11–0013 ..
8/1/2011
9/14/2011
CBI .............
T–11–0014 ..
8/2/2011
9/15/2011
CBI .............
Case no.
In Table III. of this unit, EPA provides
the following information (to the extent
that such information is not claimed as
Use
Chemical
(S) Wastewater heavy
metals removal.
(S) This product is a gas
to liquids (gtl)’’ base oil
used for drilling fluids
and a guar polymer
and/or proppant carrier
for hydraulic fracturing’’.
(G) Productivity aid in the
paper industry.
(G) Fuel blending component.
CBI) on the NOCs received by EPA
during this period: The EPA case
number assigned to the NOC, the date
(G) Polymeric sulfide.
(S) Distillates(fischer-tropsch), c10-20 branched
and linear.
(G) Polyaminoamide, sulfate salt.
(G) Petroleum distillate lights.
the NOC was received by EPA, the
projected end date for EPA’s review of
the NOC, and chemical identity.
TABLE III— 63 NOCS RECEIVED FROM JULY 1, 2011 TO AUGUST 26, 2011
Case no.
Commencement notice
end date
......
......
......
......
......
......
......
......
......
7/25/2011
7/27/2011
8/25/2011
7/22/2011
7/26/2011
7/13/2011
7/25/2011
8/24/2011
7/6/2011
7/14/2011
6/30/2011
8/16/2011
6/27/2011
7/3/2011
7/4/2011
6/7/2011
3/16/2011
6/13/2011
P–09–0639 ......
P–10–0047 ......
7/14/2011
8/2/2011
6/21/2011
7/12/2011
P–10–0064 ......
P–10–0081 ......
7/29/2011
8/25/2011
7/6/2011
7/12/2011
P–10–0083
P–10–0084
P–10–0152
P–10–0175
P–10–0275
P–10–0278
P–10–0370
P–10–0438
P–10–0471
P–10–0472
P–10–0500
wreier-aviles on DSK7SPTVN1PROD with NOTICES
P–06–0370
P–07–0298
P–08–0052
P–08–0359
P–08–0620
P–09–0129
P–09–0434
P–09–0515
P–09–0628
Received date
......
......
......
......
......
......
......
......
......
......
......
8/2/2011
7/14/2011
7/26/2011
7/15/2011
7/28/2011
7/28/2011
7/8/2011
7/26/2011
7/25/2011
7/25/2011
7/28/2011
7/12/2011
6/21/2011
7/19/2011
6/21/2011
7/12/2011
7/12/2011
6/8/2011
7/19/2011
7/21/2011
7/21/2011
7/12/2011
P–10–0509
P–10–0543
P–10–0579
P–10–0588
P–11–0027
P–11–0035
P–11–0058
P–11–0076
P–11–0106
P–11–0107
......
......
......
......
......
......
......
......
......
......
7/22/2011
7/28/2011
7/21/2011
8/24/2011
7/28/2011
8/3/2011
8/26/2011
7/1/2011
7/18/2011
7/18/2011
6/24/2011
7/12/2011
6/28/2011
7/30/2011
7/12/2011
8/2/2011
8/23/2011
6/28/2011
6/21/2011
6/22/2011
VerDate Mar<15>2010
15:20 Sep 20, 2011
Jkt 223001
PO 00000
Chemical
(S) Benzoic acid nonyl ester, branched and linear.
(G) Ethyl methacrylate based polymer.
(S) Nitrotriazolone 3-nitro-1,2,4-triazol-5-one.
(G) Alkyl alcohol reaction product with alkyl diisocyanate.
(G) Lauryllactam, polymer with alkanedicarboxylic acid and alkanediamine.
(G) Aqueous polyurethane resin dispersion.
(S) 7-octen-4-one, 2,6-dimethyl-.
(S) 2,5-furandione, polymer with 2-methyl-1-propene, amide, ammonium salt.
(G) 1-substituted propane, 3-(triethoxysilyl)-, reaction products with polyethylene glycol
mono-branched tridecyl) ether.
(G) Alkyl substituted azo metal salt.
(G) Alkenoic acid, 2-methyl-, 2-oxiranylmethyl ester, reaction products with 4,4′methylenebis (cyclohexanamine).
(G) Amidosilane.
(G) Phenol, polymer with formaldehyde, glycidyl ether, reaction products with 5-amino1,3,3-trialkylcycloalkanemethanamine.
(G) Hydroxy-aryl, polymer with substituted benzene, cyanate.
(G) Carbazole violet sulfonamide derivs.
(G) Phosphated polyalkoxylate.
(G) Aliphatic hydroxyfunctional polyester-polyurethane dispersion.
(G) Substituted polyhydro-oxo-naphthalene sulfonate with alkylidene polycarbomonocycle.
(G) Polycarbomono cyclic sulphonium camphosulphonate.
(G) Alkylol methacrylate.
(G) Polyacrylic polyether graft.
(G) Fluoro modified polyether modified polyacrylate.
(G) Fluoro modified polyether modified polyacrylate.
(G) Oxybiscarbomonocyclic acid, polymer with oxybis[heteropolycyclic ketone],(alkyl(c=1-4)substituted
bis
[alkyl(c=2-5)amine],[halo(haloalkyl(c=1-4)alkylidene]bis[aminocarbo
monocyclic )alcohol] and [halo(haloalkyl(c=1-4)alkyidene]bis(hydroxycarbomonocycle)]bis
[aminobenzamide], alkyl(c=1-4)ester.
(G) Ester polyol, fatty acid ester.
(G) Substituted polyhydro-oxo-naphthalene sulfonate with alkylidyne polycarbomonocycle.
(G) Aromatic isocyanate, polymer with alkoxides and diol.
(S) Benzenamine, 4,4′-[1,3-phenylenebis(1-methylethylidene)]bis-.
(G) (methoxymethyl) hydrocarbomonocycle.
(G) Alkyl alkoxy sulfate sodium salt.
(G) Aromatic diol, diaryl carboxylate.
(G) Polyurethane derivative.
(G) Unsaturated fatty acids, amides with polyethylenepolyamine.
(G) Fatty acids, amides with triethylenetetramine.
Frm 00046
Fmt 4703
Sfmt 4703
E:\FR\FM\21SEN1.SGM
21SEN1
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Federal Register / Vol. 76, No. 183 / Wednesday, September 21, 2011 / Notices
TABLE III— 63 NOCS RECEIVED FROM JULY 1, 2011 TO AUGUST 26, 2011—Continued
Case no.
Received date
Commencement notice
end date
P–11–0108 ......
7/11/2011
6/17/2011
P–11–0151 ......
8/1/2011
7/28/2011
......
......
......
......
......
......
......
7/6/2011
7/15/2011
8/17/2011
7/22/2011
7/21/2011
8/23/2011
8/10/2011
6/15/2011
6/25/2011
7/27/2011
7/4/2011
7/12/2011
8/17/2011
7/21/2011
P–11–0216 ......
8/10/2011
7/21/2011
P–11–0218 ......
7/26/2011
7/25/2011
P–11–0223 ......
P–11–0229 ......
8/23/2011
7/26/2011
8/11/2011
7/13/2011
P–11–0255 ......
8/4/2011
8/3/2011
P–11–0167
P–11–0175
P–11–0185
P–11–0194
P–11–0199
P–11–0200
P–11–0215
P–11–0261
P–11–0262
P–11–0280
P–11–0281
P–11–0282
P–11–0286
P–11–0289
P–11–0293
......
......
......
......
......
......
......
......
7/12/2011
7/19/2011
7/25/2011
7/14/2011
7/14/2011
7/21/2011
8/8/2011
8/4/2011
7/5/2011
7/18/2011
7/23/2011
6/27/2011
6/27/2011
7/20/2011
7/27/2011
7/29/2011
P–11–0298
P–11–0299
P–11–0306
P–11–0308
P–11–0334
P–11–0350
P–11–0367
......
......
......
......
......
......
......
8/11/2011
8/11/2011
8/19/2011
8/11/2011
8/23/2011
8/16/2011
8/19/2011
7/18/2011
7/18/2011
7/28/2011
7/26/2011
8/20/2011
8/11/2011
8/11/2011
If you are interested in information
that is not included in these tables, you
may contact EPA as described in Unit II.
to access additional non-CBI
information that may be available.
List of Subjects
wreier-aviles on DSK7SPTVN1PROD with NOTICES
Environmental Protection, Chemicals,
Hazardous substances, Imports, Notice
of Commencement, Premanufacturer,
Reporting and recordkeeping
requirements, Test marketing
exemptions.
Dated: September 9, 2011.
Darryl S. Ballard,
Acting Director, Information Management
Division, Office of Pollution Prevention and
Toxics.
[FR Doc. 2011–23973 Filed 9–20–11; 8:45 am]
BILLING CODE 6560–50–P
VerDate Mar<15>2010
15:20 Sep 20, 2011
Jkt 223001
Chemical
(G) Substituted alkanoic acid, polymer with alkanoic acid alkyl esters, with substituted
polyglycol-initiated.
(G)
N-sulfoalkyl-aminocarbonylalkenyl,
polymer
modified
with
n,n-dialkylaminocarbonylalkenyl, sodium salt.
(G) Aromatic isocyanate polymer with alkyldioic acid, polyol, and unsaturated alkyl acid.
(G) Polyglycerol fatty acid ester.
(G) Oil derived from the pyrolysis of rubber tire shreds.
(S) 1,2,3-propanetricarboxylic acid, 2-(acetyloxy)-, 1,2,3-tris(2-ethylhexyl) ester.
(G) Acrylic polymer.
(G) Aluminum alkoxide complex, alkoxylated aluminum chelate.
(S) 2-propenoic 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.
(S) 2-propenoic acid, 2-methyl-, dodecyl ester, telomer with butyl 2-propenoate, methyl 2methyl-2-propenoate, tridecyl 2-methyl-2-propenoate, 3-(trimethoxysilyl)-1-propanethiol
and 3-(trimethoxysilyl) propyl 2-methyl-2-propenoate.
(G) Benzenedioic acid, polymer with alkanediol and carboxyaminoalkyl carbamic acid
alkoxyalkylester.
(G) Substituted tris-phenyl thiophenyl-sulfonium halogenide.
(G) Polyester, polymer with 1,4-butanediol, dodecanedioic, 1,6-heaxanediol, .alpha.-hydro.omega.-hydroxypoly (oxy-1,4-butanediyl) and isocyanate.
(S) D-glucopyranose, oligomeric, decyl octyl glycosides, 2,3-dihydroxypropyl ethers,
phosphates, sodium salts, polymers with 1,3-dichloro-2-propanol.
(S) Aluminum barium europium magnesium oxide.
(S) Europium strontium borate metaphosphate oxide.
(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) Blocked polyester polyurethane, neutralized.
(S) Heptanoic acid, 1,2,3-propanetriyl ester (9ci).
(S) D-glucopyronase, oligomeric, c10-16-alkyl glycosides, 2-hydroxy-3-sulfopropyl ethers,
sodium salts, polymers with 1,3-dichloro-2-propanol.
(G) Ethoxylated epoxy amine polymer.
(G) Polypropylene glycol, epoxy amine polymer.
(G) Tertiary amine acrylate.
(G) Acrylic polymer.
(G) Aliphatic and alicyclic alcohol type polyester.
(S) Phenol, 4,4′-sulfonylbis-, bis(mixed acetates and propionates).
(G) Elastomer polyurethane.
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPP–2011–0711; FRL–8889–9]
Pesticide Program Dialogue
Committee; Notice of Public Meeting
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
Pursuant to the Federal
Advisory Committee Act, EPA gives
notice that a public meeting of the
Pesticide Program Dialogue Committee
(PPDC) is scheduled for October 12–13,
2011. A draft agenda is under
development and will be posted by
September 26, 2011. Four PPDC
workgroup meetings are also scheduled
for October 11, 2011: Integrated Pest
Management, Comparative Safety
Statements, Pollinator Protection, and
the 21st Century Toxicology/Integrated
Testing Strategies Workgroup’s
SUMMARY:
PO 00000
Frm 00047
Fmt 4703
Sfmt 4703
Workshop on Diagnostic Tools and
Biomarkers in Pesticide Medical
Management, Exposure Surveillance,
and Epidemiologic Research. The PPDC
Public Health Work Group is planning
to meet on October 13, 2011, following
the PPDC meeting. All meetings are free,
open to the public, and no advance
registration is required.
The PPDC meeting will be held
on Wednesday, October 12, 2011, from
9 a.m. to 5 p.m., and Thursday, October
13, 2011, from 9 a.m. to noon. On
Tuesday, October 11, 2011, Workgroup
meeting schedules are as follows:
Integrated Pest Management from 8 a.m.
to noon; Comparative Safety Statements
from 1 p.m. to 4 p.m.; Pollinator
Protection from 1 p.m. to 5 p.m.; and
21st Century Toxicology/Integrated
Testing Strategies Workshop from 8:30
a.m. to 5 p.m. On Thursday, October 13,
the PPDC Public Health Work Group
will meet from 1 p.m. to 4 p.m.
Information regarding PPDC
DATES:
E:\FR\FM\21SEN1.SGM
21SEN1
]]>Agencies
[Federal Register Volume 76, Number 183 (Wednesday, September 21, 2011)]
[Notices]
[Pages 58498-58506]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-23973]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
[EPA-HQ-OPPT-2011-0768; FRL-8889-6]
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 July 1, 2011 to August 26, 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 October 21, 2011.
ADDRESSES: Submit your comments, identified by docket identification
(ID) number EPA-HQ-OPPT-2011-0768, 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
[[Page 58499]]
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. 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
[[Page 58500]]
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 July 1, 2011 to August 26, 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--131 PMNs Received From July 1, 2011 to August 26, 2011
--------------------------------------------------------------------------------------------------------------------------------------------------------
Projected
Case No. Received date notice end Manufacturer/importer Use Chemical
date
--------------------------------------------------------------------------------------------------------------------------------------------------------
P-11-0478............................ 7/1/2011 9/28/2011 CBI..................... (S) Textile wet (G) Amino-modified
processing enhancer. polyalkyleneoxide silicone
copolymer.
P-11-0479............................ 7/1/2011 9/28/2011 CBI..................... (S) Intermediate for (G) Vinylalkoxysilane.
rubber processing
additives.
P-11-0480............................ 7/1/2011 9/28/2011 CBI..................... (G) Processing additive (G) Mercaptoalkoxysilane.
intermediate.
P-11-0481............................ 7/6/2011 10/3/2011 Ferro Corporation....... (G) Additive for (S) 1,2-
polymers. cyclohexanedicarboxylic
acid, 1-butyl 2-
(phenylmethyl) ester.
P-11-0482............................ 7/8/2011 10/5/2011 CBI..................... (G) Specialty additive.. (G) Carbon nanotubes.
P-11-0483............................ 7/8/2011 10/5/2011 CBI..................... (G) Chemical (G) Alkyl thiol.
intermediate.
P-11-0484............................ 7/8/2011 10/5/2011 CBI..................... (G) Surfactant.......... (G) Alkyl sulfate salt.
P-11-0485............................ 7/8/2011 10/5/2011 CBI..................... (G) Hardener for (G) Polyoxyalkylene ether,
industrial coatings. polymer with aliphatic
diisocyanate, homopolymer,
alkanol-blocked.
P-11-0486............................ 7/8/2011 10/5/2011 Asahi Kasei America, Inc (G) Hardener for (G) Alkyl substituted
industrial coatings. alkanediol polymer with
aliphatic and alicyclic
diisocyanates.
P-11-0487............................ 7/8/2011 10/5/2011 CBI..................... (G) Surfactant.......... (G) Alkyl polyamide.
P-11-0488............................ 7/8/2011 10/5/2011 CBI..................... (G) Hardener for (G) Aliphatic diisocyanate,
industrial coatings. homopolymer, alkanol-
blocked.
P-11-0489............................ 7/8/2011 10/5/2011 CBI..................... (G) Hardener for (G) Aliphatic diisocyanate
industrial coatings. polymer with alkanediol and
alkylglycol.
P-11-0490............................ 7/8/2011 10/5/2011 Sasol North America..... (S) Anti-graying agent (S) 1,4-benzenedicarboxylic
in fabric washes. acid, 1,4-dimethyl ester,
polymer with 1,2-ethanediol
and 1,2,3-propanetriol,
ester with .alpha.-methyl-
.omega.-hydroxypoly(oxy-1,2-
ethanediyl).
P-11-0491............................ 7/8/2011 10/5/2011 Sasol North America..... (S) Anti-graying agent (S) 1,4-benzenedicarboxylic
in fabric washes. acid, 1,4-dimethyl ester,
polymer with 1,2-
propanediol, ester with
.alpha.-methyl-.omega.-
hydroxypoly(oxy-1,2-
ethanediyl).
P-11-0492............................ 7/8/2011 10/5/2011 CBI..................... (G) Raw material........ (G) Glycine derivative.
P-11-0493............................ 7/5/2011 10/2/2011 CBI..................... (G) Chelating agent for (G) Aminocarboxylic acid iron
hydrogen sulfide chelate complex.
removal.
P-11-0494............................ 7/5/2011 10/2/2011 CBI..................... (G) Chelating agent for (G) Aminocarboxylic acid iron
hydrogen sulfide chelate complex.
removal.
P-11-0495............................ 7/5/2011 10/2/2011 CBI..................... (G) Chelating agent for (G) Aminocarboxylic acid iron
hydrogen sulfide chelate complex.
removal.
P-11-0496............................ 7/5/2011 10/2/2011 CBI..................... (G) Chelating agent for (G) Aminocarboxylic acid iron
hydrogen sulfide chelate complex.
removal.
P-11-0497............................ 7/5/2011 10/2/2011 CBI..................... (G) Chelating agent for (G) Aminocarboxylic acid iron
hydrogen sulfide chelate complex.
removal.
P-11-0498............................ 7/12/2011 10/9/2011 GE Water & Process (S) Heavy metal (G) Sodium polyethylenimine
Technologies. precipitant for dithiocarbamate, polymeric
wastewater. dithiocarbamate.
[[Page 58501]]
P-11-0499............................ 7/12/2011 10/9/2011 Sika Corporation........ (G) Water soluable (S) Phenol, 4,4'-(1-
polyamine curing agent methylethylidene)bis-,
for epoxy coatings. polymer with 5-amino-1,3,3-
trimethylcyclohexanemethanam
ine, n1,n2-bis(2-aminoethyl)-
1,2-ethanediamine, 2-
(chloromethyl) oxirane,
.alpha.-hydro-.omega.-
hydroxypoly[oxy(methyl-1,2-
ethanediyl)], 2,2'-[(1-
methylethylidene)bis(4,1-
phenyleneoxymethylene)]bis[o
xirane] and .alpha.-(2-
oxiranylmethyl)-.omega.-(2-
oxiranylmethoxy)poly[oxy(met
hyl-1,2-ethanediyl)],
reaction products with 2-[[4-
(1,1-
dimethylethyl)phenoxy]methyl
]oxirane, acetates (salts).
P-11-0500............................ 7/12/2011 10/9/2011 CBI..................... (G) Processing additive. (G) Polysulfide silane.
P-11-0501............................ 7/1/2011 9/28/2011 CBI..................... (G) Adhesive............ (G) Alkyldioic acid, polymer
with alkyl acrylate,
alkenearomatic, alkyldiol,
hydroxyalkyl methacrylate,
aromatic isocyanate, alkyl
methacrylate and acrylic
acid.
P-11-0502............................ 7/14/2011 10/11/2011 CBI..................... (G) Acrylic pressure (G) Acrylic solution polymer.
sensitive adhesive.
P-11-0503............................ 7/15/2011 10/12/2011 CBI..................... (G) Pigment formulation (G) Siloxanes and silicones,
additive. 3-aminoalkyl, hydroxy
terminated.
P-11-0504............................ 7/13/2011 10/10/2011 CBI..................... (S) Binder for ultra (G) Ultra violet curable
violet curable coatings. polyurethane acrylate.
P-11-0505............................ 7/14/2011 10/11/2011 CBI..................... (S) Polymer for can (G) Polyester polymer.
coatings.
P-11-0506............................ 7/14/2011 10/11/2011 CBI..................... (G) Polymer backbone for (G) Polyaminoamide.
further processing.
P-11-0507............................ 7/14/2011 10/11/2011 CBI..................... (S) Wastewater heavy (G) Polymeric sulfide.
metals removal.
P-11-0508............................ 7/18/2011 10/15/2011 Dow Chemical Company.... (G) Inert ingredient.... (G) Acrylic polymer.
P-11-0509............................ 7/18/2011 10/15/2011 CBI..................... (S) Wire & cable (G) Etfe, ethylene-
insulation; film; tetrafluoroethylene
injection molding. copolymer.
P-11-0510............................ 7/18/2011 10/15/2011 IGM Resins Inc.......... (G) Ultra violet (S) Poly(oxy-1,2-ethanediyl),
initiator. .alpha.-[4-
(dimethylamino)benzoyl]-,
.omega.-[[4-
(dimethylamino)benzoyl]oxy]-
(ca index name).
P-11-0511............................ 7/18/2011 10/15/2011 CBI..................... (G) Petroleum substitute (G) C15 olefins.
base.
P-11-0512............................ 7/18/2011 10/15/2011 CBI..................... (G) Petroleum (G) C15 paraffinic
substitutes. hydrocarbon.
P-11-0513............................ 7/18/2011 10/15/2011 CBI..................... (G) Intermediate (G) Highly branched
petroleum substitutes. isoolefinic hydrocarbons.
P-11-0514............................ 7/18/2011 10/15/2011 CBI..................... (G) Intermediate (G) Highly branched
petroleum substitutes. isoolefinic hydrocarbons.
P-11-0515............................ 7/18/2011 10/15/2011 CBI..................... (G) Intermediate (G) Highly branched
petroleum substitutes. isoolefinic hydrocarbons.
P-11-0516............................ 7/18/2011 10/15/2011 CBI..................... (G) Intermediate (G) Highly branched
petroleum substitutes. isoparaffinic hydrocarbons.
P-11-0517............................ 7/18/2011 10/15/2011 CBI..................... (G) Intermediate (G) Highly branched
petroleum substitutes. isoparaffinic hydrocarbons.
P-11-0518............................ 7/18/2011 10/15/2011 CBI..................... (G) Intermediate (G) Highly branched
petroleum substitutes. isoparaffinic hydrocarbons.
P-11-0519............................ 7/18/2011 10/15/2011 CBI..................... (G) Petroleum (G) Highly branched
substitutes. isoparaffinic hydrocarbons.
P-11-0520............................ 7/18/2011 10/15/2011 CBI..................... (G) Petroleum (G) Highly branched
substitutes. isoparaffinic hydrocarbons.
P-11-0521............................ 7/18/2011 10/15/2011 CBI..................... (G) Petroleum (G) Highly branched
substitutes. isoparaffinic hydrocarbons.
P-11-0522............................ 7/18/2011 10/15/2011 CBI..................... (G) Petroleum substitute (G) Highly branched
isoparaffinic hydrocarbons.
P-11-0523............................ 7/18/2011 10/15/2011 CBI..................... (G) Petroleum substitute (G) Highly branched
isoparaffinic hydrocarbons.
P-11-0524............................ 7/18/2011 10/15/2011 CBI..................... (G) Petroleum substitute (G) Highly branched
isoparaffinic hydrocarbons.
P-11-0525............................ 7/19/2011 10/16/2011 CBI..................... (G) Material for semi- (G) Oxibiscarbomonocyclic
conductor. acid, polymer wth
oxibis[heteropolycyclic
ketone], (alkyl(c-1-
5)substituted) bis [alkane(c-
2-6)amine],[halo(haloalkyl(c-
1-
5))alkylidene]bis[aminocarbo
monocyclic alcohol] and
[[halo(haloalkyl(c-1-
5))alkylidene]]bis(hydroxyca
rbomonocycle)]bis[aminobenza
mide].
P-11-0526............................ 7/19/2011 10/16/2011 CBI..................... (G) Surface active agent (G) Amphoteric fluorinated
surfactant.
P-11-0527............................ 7/20/2011 10/17/2011 CBI..................... (G) Chemical (G) Substituted fluoroalkane.
intermediate.
[[Page 58502]]
P-11-0528............................ 7/20/2011 10/17/2011 CBI..................... (G) Chemical (G) Fluorinated thiol.
intermediate.
P-11-0529............................ 7/20/2011 10/17/2011 CBI..................... (G) Chemical (G) Fluorinated monomer.
intermediate.
P-11-0530............................ 7/20/2011 10/17/2011 CBI..................... (G) Surfactant.......... (G) Fluoropolyacrylamide.
P-11-0531............................ 7/20/2011 10/17/2011 CBI..................... (S) Dye intermediate.... (G) Diazo substituted copper
salt.
P-11-0532............................ 7/20/2011 10/17/2011 CBI..................... (G) Chemical (G) Polyfluoroalkyl amine.
intermediate.
P-11-0533............................ 7/20/2011 10/17/2011 CBI..................... (G) Surfactant.......... (G) Non-ionic
fluorosurfactant.
P-11-0534............................ 7/20/2011 10/17/2011 CBI..................... (G) Surfactant.......... (G) Anioinic
fluorosurfactant.
P-11-0535............................ 7/21/2011 10/18/2011 CBI..................... (S) Leather processing (G) Carboxy functional
waterproofing agent. polydimethylsiloxane.
P-11-0536............................ 7/21/2011 10/18/2011 CBI..................... (S) Leather processing (G) Modified aminosiloxane.
waterproofing agent.
P-11-0537............................ 7/22/2011 10/19/2011 CBI..................... (G) Colourant........... (G) Pyrazole azo thiadiazole
derivative.
P-11-0538............................ 7/22/2011 10/19/2011 H.B. Fuller Company..... (G) Industrial adhesive. (G) Mixture of: acrylic
polymer with polymerized
organic acid, potassium salt
and organic acid, potassium
salt.
P-11-0539............................ 7/22/2011 10/19/2011 H.B. Fuller Company..... (G) Industrial adhesive. (G) Mixture of: acrylic
polymer with polymerized
organic acid, compd. with 2-
aminoethanol and organic
acid, 2-aminoethanol salt.
P-11-0540............................ 7/22/2011 10/19/2011 H.B. Fuller Company..... (G) Industrial adhesive. (G) Mixture of: acrylic
polymer with polymerized
organic acid, ammonium salt
and organic acid, ammonium
salt.
P-11-0541............................ 7/22/2011 10/19/2011 H.B. Fuller Company..... (G) Industrial adhesive. (G) Mixture of: acrylic
polymer with polymerized
organic acid, sodium salt
and organic acid, sodium
salt.
P-11-0542............................ 7/22/2011 10/19/2011 H.B. Fuller Company..... (G) Industrial adhesive. (G) Mixture of: acrylic
polymer with polymerized
organic acid, potassium salt
and organic acid, potassium
salt.
P-11-0543............................ 7/26/2011 10/23/2011 CBI..................... (G) Surfactant.......... (G) Polyfluorinated alkyl
quaternary amine chloride.
P-11-0544............................ 7/27/2011 10/24/2011 CBI..................... (G) Colourant........... (G) Diazopyridine derivative.
P-11-0545............................ 7/28/2011 10/25/2011 CBI..................... (G) Chemical (G) Substituted hydrogen
intermediate. phosphite.
P-11-0546............................ 7/27/2011 10/24/2011 Chemetall Foote (S) Brazing (metal (S) Silicate (2-) hexafluoro-
Corporation. joining) agent. cesium.
P-11-0547............................ 7/27/2011 10/24/2011 ICL-IP America Inc...... (G) The final (G) Phosphoric acid,
formulation is a inorganic salt.
halogen-free flame
retardant pmn that will
be coated on the
surface of composite or
textile surface.
P-11-0548............................ 7/28/2011 10/25/2011 Advanced polymer (G) Polymer crosslinking (S) Imidodicarbonic diamide,
technology. agent. n,n-dibutyl-n',2-bis[4-[(4-
isocyanatophenyl)methyl]phen
yl]-.
P-11-0549............................ 8/1/2011 10/29/2011 CBI..................... (G) Heat transfer fluid. (S) 2-butene, 1,1,1,4,4,4-
hexafluoro-, (2z)-.
P-11-0550............................ 8/2/2011 10/30/2011 Sika Corporation........ (G) Used as an (G) N-coco alkyltrimethylene0-
emulsifier in a , polymers with bisphenol a,
hardener of a epichlorohydrin and
waterborne 2 part epoxy amodified aliphatic amine.
system.
P-11-0551............................ 8/2/2011 10/30/2011 Sika Corporation........ (G) Used as an (G) N-coco
emulsifier in a alkyltrimethylenedi-,
hardener of a polymer with bisphenol a,
waterborne 2 part epoxy epichlorohydrin and modified
system. aliphatic amine.
P-11-0552............................ 8/1/2011 10/29/2011 CBI..................... (G) Productivity aid in (G) Polyaminoamide, sulfate
the paper industry. salt.
P-11-0553............................ 8/2/2011 10/30/2011 CBI..................... (G) Coatings............ (G) Urethane acrylate.
P-11-0554............................ 8/2/2011 10/30/2011 CBI..................... (G) Fuel blending (G) Petroleum distillate
component. lights.
P-11-0555............................ 8/2/2011 10/30/2011 CBI..................... (G) Coating agent....... (G) 2-propenoic acid, 2-
methyl-1,1-dimethylethyl
ester, polymer with 2,2-
dimethyl-1,3-propanediol,
ethenylbenzene, 2-ethyl-2-
(hydroxymethyl)-1,3-
propanediol, cycloaliphatic
dicarboxylic anhydride and
1,2-propanediol mono(2-
methyl-2-propenoate),
bis(1,1-
dimethylpropyl)peroxide-
initiated.
[[Page 58503]]
P-11-0556............................ 8/2/2011 10/30/2011 CBI..................... (G) Coating agent....... (G) 2-propenoic acid, 2-
methyl-, polymer with 2,2-
dimethyl-1,3-propanediol,
ethenylbenzene, 2-ethyl-2-
(hydroxymethyl)-1,3-
propanediol, cycloaliphatic
dicarboxylic anhydride, 2-
hydroxyethyl 2-methyl-2-
propenoate, methyl 2-methyl-
2-propenoate and 2-
methylpropyl 2-methyl-2-
propenoate, 2-hydroxy-3-[(1-
oxoneodecy]- oxy]propyl
ester.
P-11-0557............................ 8/3/2011 10/31/2011 CBI..................... (G) Water and oil (G) 2-propenoic acid, 2-
repellant. methyl-, 2-hydroxyethyl
ester, telomers with c18-26
alkyl acrylate, 1-
dodecanthiol, n-
(hydroxymethyl)-2-methyl-2-
propenamide, polyfluorooctyl
methacrylate and vinylidene
chloride, 2,2'-[1,2-
diazenediylbis(1-
methylethylidene)]-bis[4,5-
dihydro-1h-
imidazole]hydrochloride
(1:2)-initiated.
P-11-0558............................ 8/3/2011 10/31/2011 CBI..................... (G) Component of (S) D-glucitol, 1,2,3,4,5,6-
cleaning agent used in hexakis-o-[3-(hydroxyamino)-
electronic 3-iminopropyl]-.
applications..
P-11-0559............................ 8/4/2011 11/1/2011 CBI..................... (G) Releasing agent..... (G) Polyglycerol fatty acid
ester.
P-11-0560............................ 8/4/2011 11/1/2011 Moresco USA Inc......... (S) Additive-grease for (G) Alkylated diphenyl
bearings. ethers.
P-11-0561............................ 8/4/2011 11/1/2011 CBI..................... (S) Automotive fuel (G) Tetrafluoroethylene
hose; semi conductor/ chlorotrifluoroethylene
chemical tubing. copolymer.
P-11-0562............................ 8/8/2011 11/5/2011 Ask chemicals L.P....... (G) Import only......... (G) Vegetable oil, modified.
P-11-0563............................ 8/8/2011 11/5/2011 Ask chemicals L.P....... (G) Import only......... (G) Vegetable oil, modified.
P-11-0564............................ 8/8/2011 11/5/2011 Colonial Chemical, Inc.. (S) Hard surface cleaner (S) D-glucopyranose,
oligomeric, c10-16-alkyl
decyl octyl glycosides, 3-
[(carboxymethyl)bis(2-
hydroxyethyl)ammonio]-2-
hydroxypropyl ethers, inner
salts, polymers with 1,3-
dichloro-2-propanol.
P-11-0565............................ 8/8/2011 11/5/2011 Colonial Chemical, Inc.. (S) Hard surface cleaner (S) D-glucopyranose,
oligomeric, c10-16-alkyl
glycosides, 3-
[(carboxymethyl)bis(2-
hydroxyethyl)ammonio]-2-
hydroxypropyl ethers, inner
salts, polymers with 1,3-
dichloro-2-propanol.
P-11-0566............................ 8/8/2011 11/5/2011 CBI..................... (G) Component of an (G) Cycloaliphatic polyacid
industrial coating. functional polyester.
P-11-0567............................ 8/8/2011 11/5/2011 CBI..................... (G) Manufacturing of (G) Fluoropolymer.
elastomer containing
items.
P-11-0568............................ 8/8/2011 11/5/2011 CBI..................... (G) Film, wire and cable (G) Fluoropolymer.
P-11-0569............................ 8/8/2011 11/5/2011 CBI..................... (G) Manufacturing of (G) Fluoropolymer.
elastomer containing
items.
P-11-0570............................ 8/8/2011 11/5/2011 CBI..................... (G) Industrial lubricant (G) Polypentaerythritol,
mixed esters with mono
carboxylic acids.
P-11-0571............................ 8/10/2011 11/7/2011 3M Company.............. (G) Intermediate........ (G) Aryloxy dialkanol.
P-11-0572............................ 8/11/2011 11/8/2011 Henkel Corporation...... (S) An adhesive used for (S) 1,4-
panel lamination and cyclohexanedimethanol,
other assemblies. polymer with 2-
hydroxymethylethyl-
terminated polybutadiene and
1,1'-methylenebis[4-
isocyanatobenzene], c14
alcs.-blocked.
P-11-0573............................ 8/11/2011 11/8/2011 CBI..................... (G) For use as an (G) Acrylic latex resin.
exterior can coating.
P-11-0574............................ 8/11/2011 11/8/2011 CBI..................... (G) For use as an (G) Acrylic latex resin.
exterior can coating.
P-11-0575............................ 8/11/2011 11/8/2011 CBI..................... (G) For use as an (G) Fatty acid modified pet.
exterior paper coating.
P-11-0576............................ 8/11/2011 11/8/2011 CBI..................... (G) For use as an (G) Fatty acid modified pet.
exterior paper coating.
P-11-0577............................ 8/12/2011 11/9/2011 International flavors & (S) Fragrance ingredient (S) Butanoic acid, 3-mercapto-
Fragrances, Inc. , ethyl ester.
P-11-0578............................ 8/12/2011 11/9/2011 Eastman Kodak Company... (S) Intermediate........ (S) Benzoic acid, 4-(1,1-
dimethylethyl)-, hydrazide.
[[Page 58504]]
P-11-0579............................ 8/12/2011 11/9/2011 Eastman Kodak Company... (S) Intermediate........ (S) 1h-1,2,4-triazole-3-
acetic acid, 5-[4-(1,1-
dimethylethyl)phenyl]-.
P-11-0580............................ 8/12/2011 11/9/2011 Eastman Kodak Company... (S) Intermediate........ (S) Cyclohexanol, 2,6-bis(1,1-
dimethylethyl)-4-methyl-.
P-11-0581............................ 8/12/2011 11/9/2011 Eastman Kodak Company... (S) Intermediate in the (S) 1h-1,2,4-triazole-5-
manufacture of an acetic acid, 1-acetyl-3-[4-
imaging chemical. (1,1,-dimethylethyl)phenyl]-
, 2,6-bis(1,1-dimethylethyl)-
4-methylcyclohexyl ester.
P-11-0582............................ 8/12/2011 11/9/2011 Eastman Kodak Company... (S) Intermediate in (S) 1h-1,2,4-triazole-5-
manufacture of imaging acetic acid, 1-acetyl-
chemical. .alpha.-bromo-3-[4-(1,1-
dimethylethyl)phenyl]-, 2,6-
bis(1,1-dimethylethyl)-4-
methylcyclohexyl ester.
P-11-0583............................ 8/12/2011 11/9/2011 Eastman Kodak Company... (S) Coupler for imaging (S) 3h-pyrrolo[1,2-
products; for export. b][1,2,4]triazole-7-
carboxylic acid, 5-[[[bis(2-
ethoxy-2-
oxoethyl)amino]carbonyl]oxy]-
6-cyano-2-[4-(1,1-
dimethylethyl)phenyl]-, 2,6-
bis(1,1-dimethylethyl)-4-
methylcyclohexyl ester.
P-11-0584............................ 8/12/2011 11/9/2011 CBI..................... (S) Crosslinker for (G) Isocyanate crosslinker.
waterborne polymers/
coatings.
P-11-0585............................ 8/15/2011 11/12/2011 AOC L.L.C............... (S) Polymer component (S) 1,4-benzenedicarboxylic
for laminating of fiber acid, polymer with 1,2-
reinforced plastic ethanediol, 2,5-furandione
composites. and 1,2-propanediol,
