Certain New Chemicals; Receipt and Status Information, 76963-76970 [2011-31645]
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Federal Register / Vol. 76, No. 237 / Friday, December 9, 2011 / Notices
Filed Date: 12/1/11.
Accession Number: 20111201–5152.
Comments Due: 5 p.m. ET 12/22/11.
The filings are accessible in the
Commission’s eLibrary system by
clicking on the links or querying the
docket number.
Any person desiring to intervene or
protest in any of the above proceedings
must file in accordance with Rules 211
and 214 of the Commission’s
Regulations (18 CFR 385.211 and
385.214) on or before 5 p.m. Eastern
time on the specified comment date.
Protests may be considered, but
intervention is necessary to become a
party to the proceeding.
eFiling is encouraged. More detailed
information relating to filing
requirements, interventions, protests,
service, and qualifying facilities filings
can be found at: https://www.ferc.gov/
docs-filing/efiling/filing-req.pdf. For
other information, call (866) 208–3676
(toll free). For TTY, call (202) 502–8659.
Dated: December 1, 2011.
Nathaniel J. Davis, Sr.,
Deputy Secretary.
[FR Doc. 2011–31611 Filed 12–8–11; 8:45 am]
BILLING CODE 6717–01–P
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPPT–2011–0832; FRL–9328–1]
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 September 26, 2011 to October 31,
2011, and provides the required notice
and status report, consists of the PMNs
and TMEs, both pending or expired, and
srobinson on DSK4SPTVN1PROD with NOTICES
SUMMARY:
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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 January 9,
2012.
ADDRESSES: Submit your comments,
identified by docket identification (ID)
number EPA–HQ–OPPT–2011–0832,
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 email comment directly
to EPA without going through
regulations.gov, your email 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
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76963
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; 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; email address: TSCAHotline@epa.gov.
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this action apply to me?
This action is directed to the public
in general. As such, the Agency has not
attempted to describe the specific
entities that this action may apply to.
Although others may be affected, this
action applies directly to the submitter
of the 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.
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Federal Register / Vol. 76, No. 237 / Friday, December 9, 2011 / Notices
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 email. Clearly mark
the part or all of the information that
you claim to be CBI. For CBI
information in a disk or CD–ROM that
you mail to EPA, mark the outside of the
disk or CD–ROM as CBI and then
identify electronically within the disk or
CD–ROM the specific information that
is claimed as CBI. In addition to one
complete version of the comment that
includes information claimed as CBI, a
copy of the comment that does not
contain the information claimed as CBI
must be submitted for inclusion in the
public docket. Information 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://ww.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 September 26,
2011 to October 31, 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—50 PMNS RECEIVED FROM SEPTEMBER 26, 2011 TO OCTOBER 31, 2011
Case No.
Received date
Projected
notice end
date
Manufacturer/importer
Use
Chemical
(G) Water and oil repellant.
(G) Epoxy catalyst .......
(G) Perfluoroalkylethyl methacrylate
copolymer.
(S) Phenol, 2-[[[3-(1h-imidazol-1yl)propyl]imino]phenylmethyl]-5(octyloxy)-.
(G) Aliphatic epoxy acrylate.
9/26/2011
12/24/2011
CBI ...............................
P–11–0654 ...........
9/26/2011
12/24/2011
CBI ...............................
P–11–0655 ...........
9/27/2011
12/25/2011
P–11–0656 ...........
srobinson on DSK4SPTVN1PROD with NOTICES
P–11–0653 ...........
9/27/2011
12/25/2011
Miwon North America,
Inc.
Omnova Solutions Inc ..
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(S) Resins for industrial
coating.
(S) Soil release coating
for textiles used for
non-consumer table
linnen.
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(S) 2-propenoic acid, 2-methyl-,
dodecyl ester, polymer with 2-hydroxyethyl 2-propenoate, .alpha.(2-methyl-1-oxo-2-propen-1-yl).omega.-methoxypoly(oxy-1,2ethanediyl)
and
3-methyl-3[(2,2,3,3,3pentafluoropropoxy)methyl]oxetane polymer with
tetrahydrofuran mono[2-[(1-oxo-2propen-1-yl)oxy]ethyl] ether.
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Federal Register / Vol. 76, No. 237 / Friday, December 9, 2011 / Notices
TABLE I—50 PMNS RECEIVED FROM SEPTEMBER 26, 2011 TO OCTOBER 31, 2011—Continued
Case No.
Received date
Projected
notice end
date
Manufacturer/importer
Use
Chemical
9/27/2011
12/25/2011
Omnova Solutions Inc ..
(S) Flow, wetting and
leveling agent for
commercial photographic film.
P–11–0658 ...........
9/27/2011
12/25/2011
BASF Corporation ........
P–11–0659 ...........
9/28/2011
12/26/2011
CBI ...............................
P–11–0660 ...........
9/28/2011
12/26/2011
CBI ...............................
(G) Catalyst ingredient
for plastics manufacture.
(G) Reactant to
produce new chemical.
(G) Oil field additive .....
P–11–0661 ...........
9/28/2011
12/26/2011
P–11–0662 ...........
9/30/2011
12/28/2011
Great Plains Oil & Exploration, LLC.
CBI ...............................
P–11–0663 ...........
9/30/2011
12/28/2011
CBI ...............................
P–12–0001 ...........
10/3/2011
12/31/2011
CBI ...............................
(G) Sealant additive .....
P–12–0002 ...........
10/6/2011
1/3/2012
CBI ...............................
P–12–0003 ...........
10/6/2011
1/3/2012
CBI ...............................
(G) Chemical intermediate.
(G) Polymeric colorant
P–12–0004 ...........
10/11/2011
1/8/2012
CBI ...............................
(G) Polymeric colorant
P–12–0005 ...........
10/11/2011
1/8/2012
Sika Corporation ..........
P–12–0006 ...........
10/13/2011
1/10/2012
CBI ...............................
(G) A dispersant for
neutralizing electrical
charges and separating particles when
grinding cement.
(G) Adhesive ................
P–12–0007 ...........
10/13/2011
1/10/2012
CBI ...............................
(G) Adhesive ................
P–12–0008 ...........
10/13/2011
1/10/2012
CBI ...............................
P–12–0009 ...........
srobinson on DSK4SPTVN1PROD with NOTICES
P–11–0657 ...........
10/12/2011
1/9/2012
CBI ...............................
(G) Open non
despersive coating.
(G) Open, non-dispersive use; ingredient
in liquid paint.
P–12–0010 ...........
10/14/2011
1/11/2012
Reichhold, Inc ..............
(S) Carrier resin for
paints and coatings.
P–12–0011 ...........
10/17/2011
1/14/2012
BASF Corporation ........
(G) Additive ..................
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(S) Feedstock for production of biofuel.
(G) Liquid moisture
cure adhesive.
(S) Curing agent for
epoxy coating systems.
E:\FR\FM\09DEN1.SGM
(S) Boron, trifluoro(tetrahydrofuran), (T-4)-, polymer with 3-methyl-3[(2,2,3,3,3pentafluoropropoxy)methyl]oxetane, ether with 2,2dimethyl-1,3-propanediol
(2:1),
polymer with .alpha.-hydroxy.omega.-hydroxypoly(oxy-1,2ethanediyl) and 5-isocyanato-1(isocyanatomethyl)-1,3,3trimethylcyclohexane.
(G) Alkoxy alkanone fluorene.
(G) Alkyl phosphonate.
(G) Copolymer containing phosphonic, sulfonic and carboxylic
acid groups.
(S) Fats and glyceridic oils,
camelina sativa.
(G)
Isocyanate-terminated
prepolymer.
(G) Amides, from C18-unsaturated
fatty acids dimers,hydrogenated
benzaldehyde
-polyethylenepolyamines reaction
products and tall-oil fatty acids.
(G) Aromatic isocyanate, alkyl phenol-blocked.
(G)
Polyalkoxylated
aromatic
amine.
(G)
Chromophore
substituted
polyoxyalkylene tint.
(G) Substituted polymeric aromatic
amine azo colorant.
(S) 2-propanol, 1,1′,1″-nitrilotris-,
acetate (1:1).
(G) Alkyldioic acid, polymer with
alkyldiol, aromatic isocyanate and
alkyloxirane polymer with oxirane
ether with alkyltrio(3:1).
(G) Alkyldioic acid, polymer with
alkyldiol, .alpha.-hydro-.omega.hydroxypoly[oxy(alkyldiyl)],
aromatic isocyanate and alkyloxirane
polymer with oxirane ether with
alkyltrio(3:1).
(G) Aliphatic polyurethane resin.
(G) Metal complex, copolymer of
substituted acrylic acid, substituted methacrylate, substituted
acrylate, and ethylene glycol substituted acrylate alkyl ether.
(G) Amine salt of vegetable oil
esters, polymer with alkanedioic
acid,
hydroxy
substituted
alkylamine, hydroxy substituted
carboxylic
acid,
alkanediol,
isocyanates, hydroxy substituted
alkane.
(G) Hydroxy, halogen substituted
diaromatic ether.
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TABLE I—50 PMNS RECEIVED FROM SEPTEMBER 26, 2011 TO OCTOBER 31, 2011—Continued
Case No.
Received date
Projected
notice end
date
Manufacturer/importer
10/17/2011
1/14/2012
Dow Chemical Company.
P–12–0013 ...........
10/17/2011
1/14/2012
CBI ...............................
P–12–0014 ...........
10/18/2011
1/15/2012
Dow Chemical Company.
P–12–0015 ...........
10/17/2011
1/14/2012
P–12–0016 ...........
10/18/2011
1/15/2012
Spectra Colors Corporation.
Innovative Science
Technology.
P–12–0017 ...........
10/19/2011
1/16/2012
Sud-Chemie Inc ...........
P–12–0018 ...........
10/20/2011
1/17/2012
CBI ...............................
P–12–0019 ...........
10/20/2011
1/17/2012
Henkel Corporation ......
P–12–0020 ...........
10/21/2011
1/18/2012
CBI ...............................
P–12–0021 ...........
10/19/2011
1/16/2012
CBI ...............................
P–12–0022 ...........
srobinson on DSK4SPTVN1PROD with NOTICES
P–12–0012 ...........
10/24/2011
1/21/2012
CBI ...............................
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Use
Chemical
(S) Reactant for polyurethane cast
elastomers.
(G) Additive in printing
inks.
(S) Reactant for polyurethane cast
elastomers.
(G) Dye for washable
ink systems.
(S) Plasticizer for polyvinyl chloride resin.
(G) Polyester polyol.
(G) Crosslinked polyalkyl methacrylate.
(G) Blocked toluene diisocyanate
prepolymer.
(G) Raw material in
manufacturing.
(S) A component of industrial epoxy adhesive formulations.
(S) Glue stick ...............
(G) A component of
leather finishing treatment.
(S) Petroleum fuel
blend and distillation/
fractionation.feedstock.
(G) The new chemical
will be used as a
photoluminescent
pigment. The pigment
will be shipped to our
customers who will
incorporate the pigment into fluids,
paints, coatings, inks,
injection molding etc.
for, but not limited to:
Emergency signs,
traffic indication
signs, switches, military applications, high
visibility signs, safety
location markings
and any other application where a long
afterglow and/or lighting is needed.
E:\FR\FM\09DEN1.SGM
(G)
Substituted
aniline,
benzenesulfonic acid salt.
(S) Waste plastics, poly(ethylene
terephthalate),
depolymerized.
with by-products from prod. of 2butoxyethanol, and isotridecanol,
ethylene glycol-free fraction.
(S) Phosphoric acid, iron(2+) lithium
salt (1:1:1).
(G) Rubberized epoxy resin.
(S)
Starch
carboxymethyl
2hydroxypropyl ether.
(G) Polyurethane aqueous dispersion.
(G) Petroleum distillate heavies.
(G) Complex strontium aluminate
rare earth doped″.
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Federal Register / Vol. 76, No. 237 / Friday, December 9, 2011 / Notices
TABLE I—50 PMNS RECEIVED FROM SEPTEMBER 26, 2011 TO OCTOBER 31, 2011—Continued
Case No.
Received date
Projected
notice end
date
Manufacturer/importer
Use
Chemical
(G) The new chemical
will be used as a
photoluminescent
pigment. The pigment
will be shipped to our
customers who will
incorporate the pigment into fluids,
paints, coatings, inks,
injection molding etc.
for, but not limited to:
Emergency signs,
traffic indication
signs, switches, military applications, high
visibility signs, safety
location markings
and any other application where a long
afterglow and/or lighting is needed.
(G) The new chemical
will be used as a
photoluminescent
pigment. The pigment
will be shipped to our
customers who will
incorporate the pigment into fluids,
paints, coatings, inks,
injection molding etc.
for, but not limited to:
Emergency signs,
traffic indication
signs, switches, military applications, high
visibility signs, safety
location markings
and any other application where a long
afterglow and/or lighting is needed.
(G) The new chemical
will be used as a
photoluminescent
pigment. The pigment
will be shipped to our
customers who will
incorporate the pigment into fluids,
paints, coatings, inks,
injection molding etc.
for, but not limited to:
Emergency signs,
traffic indication
signs, switches, military applications, high
visibility signs, safety
location markings
and any other application where a long
afterglow and/or lighting is needed.
(G) Complex strontium aluminate
rare earth doped″.
10/24/2011
1/21/2012
CBI ...............................
P–12–0024 ...........
10/24/2011
1/21/2012
CBI ...............................
P–12–0025 ...........
srobinson on DSK4SPTVN1PROD with NOTICES
P–12–0023 ...........
10/24/2011
1/21/2012
CBI ...............................
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(G) Complex strontium aluminate
rare earth doped″.
(G) Complex strontium aluminate
rare earth doped″.
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TABLE I—50 PMNS RECEIVED FROM SEPTEMBER 26, 2011 TO OCTOBER 31, 2011—Continued
Case No.
Received date
Projected
notice end
date
Manufacturer/importer
Use
Chemical
(G) The new chemical
will be used as a
photoluminescent
pigment. The pigment
will be shipped to our
customers who will
incorporate the pigment into fluids,
paints, coatings, inks,
injection molding etc.
for, but not limited to:
Emergency signs,
traffic indication
signs, switches, military applications, high
visibility signs, safety
location markings
and any other application where a long
afterglow and/or lighting is needed.
(S) Dispersant—pigment in water based
paint; hard water
cleaning.
(G) Complex strontium aluminate
rare earth doped″.
10/24/2011
1/21/2012
CBI ...............................
P–12–0027 ...........
10/26/2011
1/23/2012
Colonial Chemical, Inc
P–12–0028 ...........
10/26/2011
1/23/2012
Colonial Chemical, Inc
(S) Dispersant—pigment in water based
paint; hard water
cleaning.
P–12–0029 ...........
10/26/2011
1/23/2012
Colonial Chemical, Inc
(S) Dispersant—pigment in water based
paint; hard water
cleaning.
P–12–0030 ...........
10/27/2011
1/24/2012
CBI ...............................
P–12–0031 ...........
10/27/2011
1/24/2012
CBI ...............................
P–12–0032 ...........
10/27/2011
1/24/2012
CBI ...............................
P–12–0033 ...........
10/27/2011
1/24/2012
Aceto Corporation ........
P–12–0034 ...........
10/27/2011
1/24/2012
CBI ...............................
P–12–0035 ...........
10/29/2011
1/26/2012
CBI ...............................
P–12–0036 ...........
10/31/2011
1/28/2012
CBI ...............................
P–12–0037 ...........
srobinson on DSK4SPTVN1PROD with NOTICES
P–12–0026 ...........
10/28/2011
1/25/2012
CBI ...............................
P–12–0038 ...........
P–12–0039 ...........
10/28/2011
10/31/2011
1/25/2012
1/28/2012
CBI ...............................
CBI ...............................
(G) Open, non-dispersive textile finish.
(G) Open, non-dispersive textile finish.
(G) Open, non-dispersive textile finish.
(S) Intermediate used
in the manufacture of
an imaging/media
product.
(G) A component of
leather finishing treatment.
(G) Ferrite dispersion
ink additive to ensure
magnetic performance characteristics.
(S) Fluorescent brightener for use in cellulosic paper applications.
(G) Sizing for glass
fibre.
(G) Synthetic leather ....
(G) Open, non-dispersive use.
In Table II. of this unit, EPA provides
the following information (to the extent
that such information is not claimed as
VerDate Mar<15>2010
18:35 Dec 08, 2011
Jkt 226001
CBI) on the TMEs received by EPA
during this period: The EPA case
number assigned to the TME, the date
PO 00000
Frm 00035
Fmt 4703
Sfmt 4703
(S) D-glucopyranose, oligomeric,
C10-16-alkyl
glycosides,
2,3dihydroxypropyl ethers, hydrogen
maleates, sodium salts, polymers
with 1,3-dichloro-2-propanol.
(S) D-glucopyranose, oligomeric,
C10-16-alkyl
glycosides,
2,3dihydroxypropyl ethers, hydrogen
succinates, sodium salts, polymers with 1,3-dichloro-2-propanol.
(S) D-glucopyranose, oligomeric,
decyl octyl glycosides, 2,3dihydroxypropyl ethers, hydrogen
maleates, sodium salts, polymers
with 1,3-dichloro-2-propanol.
(G) Modified fluorinated acrylate.
(G) Modified fluorinated acrylate.
(G) Modified fluorinated acrylate.
(S)
Benzoic
acid,
dimethylethyl)-, methyl.
4-(1,1-
(G) Polyacrylate aqueous dispersion.
(G) Cobalt iron manganese oxide,
carboxylic acid-modified.
(G) Triazinylaminostilbene.
(G) Epoxy-novolac resin in nonionic water emulsion.
(G) Elastomer polyurethane.
(G) Acrylic polymer.
the TME was received by EPA, the
projected end date for EPA’s review of
the TME, the submitting manufacturer/
E:\FR\FM\09DEN1.SGM
09DEN1
76969
Federal Register / Vol. 76, No. 237 / Friday, December 9, 2011 / Notices
importer, the potential uses identified
by the manufacturer/importer in the
TME, and the chemical identity.
TABLE II—2 TMES RECEIVED FROM SEPTEMBER 26, 2011 TO OCTOBER 31, 2011
Case No.
Received date
Projected
notice end
date
Manufacturer
/importer
Use
Chemical
(S) Petroleum fuel blend and distillation/fractionation.feedstock.
(S) Plasticizer for polyvinyl chloride
resin.
(G) Petroleum distillate
heavies.
(S) Waste plastics, poly
(ethylene
terephthalate),
depolymd, with byproducts from manuf.
of 2-butoxyethanol,
and isotridecanol,
ethylene glycol-free
fraction.
T–12–0001 ............
10/19/2011
12/2/2011
CBI ...............................
T–12–0002 ............
10/25/2011
12/8/2011
Innovative Science
Technology.
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—55 NOCS RECEIVED FROM SEPTEMBER 26, 2011 TO OCTOBER 31, 2011
Case No.
P–04–0190
P–07–0143
P–07–0666
P–08–0354
Received date
Commencement
notice end
date
Chemical
...............................
...............................
...............................
...............................
10/4/2011
9/26/2011
10/8/2011
10/12/2011
9/20/2011
9/23/2011
9/26/2011
9/8/2011
P–08–0419 ...............................
10/14/2011
9/21/2011
P–09–0009 ...............................
P–09–0168 ...............................
P–09–0410 ...............................
10/7/2011
9/27/2011
10/4/2011
9/10/2011
9/9/2011
9/13/2011
...............................
...............................
...............................
...............................
...............................
...............................
...............................
...............................
...............................
...............................
...............................
...............................
...............................
...............................
...............................
...............................
...............................
...............................
...............................
10/20/2011
10/24/2011
10/20/2011
10/20/2011
10/20/2011
10/20/2011
10/20/2011
10/28/2011
9/26/2011
10/14/2011
9/27/2011
10/12/2011
10/12/2011
10/12/2011
10/12/2011
10/22/2011
9/28/2011
10/4/2011
10/7/2011
10/3/2011
10/6/2011
9/29/2011
9/28/2011
9/26/2011
9/23/2011
9/22/2011
10/17/2011
9/2/2011
10/10/2011
9/13/2011
10/10/2011
7/21/2011
7/21/2011
7/21/2011
10/11/2011
9/27/2011
8/21/2011
7/14/2011
P–11–0235 ...............................
10/11/2011
9/19/2011
P–11–0258 ...............................
P–11–0260 ...............................
P–11–0285 ...............................
10/17/2011
10/14/2011
10/25/2011
10/6/2011
9/27/2011
10/7/2011
P–11–0305 ...............................
10/31/2011
9/29/2011
srobinson on DSK4SPTVN1PROD with NOTICES
P–10–0106
P–10–0111
P–10–0150
P–10–0286
P–10–0287
P–10–0288
P–10–0289
P–10–0354
P–10–0426
P–10–0451
P–10–0529
P–11–0036
P–11–0043
P–11–0045
P–11–0046
P–11–0169
P–11–0172
P–11–0179
P–11–0233
VerDate Mar<15>2010
18:35 Dec 08, 2011
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PO 00000
Frm 00036
(G) Polyester acrylate.
(G) Alkanoldioic acid, dialkyl ester.
(G) Poly(ethylene oxide).
(G) 2-propenoic acid, 2-methyl-, methyl ester, polymer with butyl propenoate
and substituted-propyl 2-methyl-2-propenoate, 2,2′-(1,2-diazenediyl)bis[2methylbutanenitrile]-initiated.
(G) Aromatic dimethaneamine, reaction products with aromatic glycidlyl
ether.
(G) Glycolate ester.
(G) Substituted styrene acrylate copolymer.
(G) Carbonic acid di-alkyl ester polymer with polyether polyol, alkyl isocyante
and glycol ether.
(G) Hydroxyl-terminated aliphatic polycarbonate.
(G) Benzene dicarboxylic acid, polyester with glycol and polyethylene glycol.
(G) Hydroxy-terminated; aliphatic polycarbonate.
(G) Hydroxyl-terminated aliphatic polycarbonate.
(G) Hydroxyl-terminated aliphatic polycarbonate.
(G) Hydroxyl-terminated aliphatic polycarbonate.
(G) Hydroxyl-terminated aliphatic polycarbonate.
(G) Acrylonitrile-acrylate copolymer.
(G) Halo substituted sulfamidylbenzyluraciil.
(G) Acrylic silane polymer.
(G) Copolymer containing phosphonic, sulfonic and carboxylic acid groups.
(G) Alkyl alkoxy sulfate sodium salt.
(S) Disiloxane, 1-butyl-1,1,3,3-tetramethyl-*.
(S) Pentasiloxane, 1-butyl-1,1,3,3,5,5,7,7,9,9-decamethyl-*.
(S) Siloxanes and silicones, di-me, bu group- and hydrogen-terminated*.
(G) Alkyl aryl substituted pyrrolo benzotriazole dione.
(G) Methacrylated C8–18 fatty acids; methacrylate fatty acids; mc818.
(G) Water dispersed blocked isocyanate.
(G)
Phenol,
4,4′-(1-methylethylidene)bis-,
polymer
with
2(chloromethyl)oxirane,
reaction
products
with
N3-(3(dimethylamino)propyl]-N1,N1-dimethyl-alkanepolyamine, compds. with
formaldehyde-phenol polymer.
(G) Polyacrylate oligomer product from saturated dimer acid, propoxylated
glycerol and acrylic acid.
(G) Epoxy and isocyanate modified aliphatic polyamine.
(G) Isocyanate-terminated prepolymer.
(G)
Acid
anhydride,
polymer
with
aromatic
isocyanate
and
polyalkyleneglycol, alkanol and diazole alkanamine and lactone
homopolymer alkyl ester-blocked.
(G) Polyester diol.
Fmt 4703
Sfmt 4703
E:\FR\FM\09DEN1.SGM
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76970
Federal Register / Vol. 76, No. 237 / Friday, December 9, 2011 / Notices
TABLE III—55 NOCS RECEIVED FROM SEPTEMBER 26, 2011 TO OCTOBER 31, 2011—Continued
Case No.
Commencement
notice end
date
Received date
Chemical
P–11–0326
P–11–0337
P–11–0362
P–11–0369
P–11–0372
P–11–0373
...............................
...............................
...............................
...............................
...............................
...............................
10/25/2011
10/25/2011
9/28/2011
10/17/2011
10/17/2011
9/26/2011
10/20/2011
10/7/2011
9/26/2011
9/20/2011
9/19/2011
8/26/2011
P–11–0393
P–11–0398
P–11–0399
P–11–0403
P–11–0409
P–11–0410
P–11–0423
P–11–0425
P–11–0426
P–11–0427
P–11–0428
P–11–0429
P–11–0430
P–11–0434
...............................
...............................
...............................
...............................
...............................
...............................
...............................
...............................
...............................
...............................
...............................
...............................
...............................
...............................
9/28/2011
10/12/2011
10/12/2011
9/29/2011
10/11/2011
10/27/2011
10/13/2011
9/30/2011
10/5/2011
9/30/2011
9/30/2011
9/30/2011
10/5/2011
9/26/2011
9/21/2011
10/10/2011
10/10/2011
9/22/2011
9/23/2011
10/11/2011
9/27/2011
9/22/2011
9/22/2011
9/22/2011
9/22/2011
9/22/2011
9/22/2011
9/15/2011
P–11–0446 ...............................
10/21/2011
10/15/2011
P–11–0467 ...............................
P–11–0470 ...............................
10/28/2011
10/10/2011
10/26/2011
10/7/2011
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
Environmental protection, Chemicals,
Hazardous substances, Imports, Notice
of commencement, Premanufacturer,
Reporting and recordkeeping
requirements, Test marketing
exemptions.
Dated: November 16, 2011.
Chandler Sirmons,
Acting Director, Information Management
Division, Office of Pollution Prevention and
Toxics.
[FR Doc. 2011–31645 Filed 12–8–11; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
srobinson on DSK4SPTVN1PROD with NOTICES
[FRL–9504–3]
Cross-Media Electronic Reporting:
Authorized Program Revision
Approval, State of Montana
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
VerDate Mar<15>2010
18:35 Dec 08, 2011
Jkt 226001
(G) Glycerylether.
(S) 4,7-decadienal.
(G) Phosphonium-substituted heteroaromatic sulfate salt.
(G) Alkyl polyester-acrylic copolymer.
(G) Polyesterurethane.
(G) 1,1′-methylenebis[isocyanatobenzene], polymer with polyester polyols
and polypropylene glycol.
(G) Waterborne aliphatic polyurethane.
(S) Poly(oxy-1,2-ethanediyl), .alpha.-(1-oxooctyl)-.omega.-methoxy-*.
(S) Poly(oxy-1,2-ethanediyl), .alpha.-(1-oxodecyl)-.omega.-methoxy-*.
(G) Fatty acid esters.
(G) Multifunctional polycarbodiimide.
(G) Methacrylic resin containing cyclic structure unit.
(G) Acrylate copolymer.
(G) Poly (3-hydroxybutyrate-co-3-hydroxyhexanoate).
(G) Poly (3-hydroxybutyrate-co-3-hydroxyhexanoate).
(G) Poly (3-hydroxybutyrate-co-3-hydroxyhexanoate).
(G) Poly (3-hydroxybutyrate-co-3-hydroxyhexanoate).
(G) Poly (3-hydroxybutyrate-co-3-hydroxyhexanoate).
(G) Poly (3-hydroxybutyrate-co-3-hydroxyhexanoate).
(G) Cashew, nutshell liquid, polymer with arylalkylamine, bisphenol A,
epichlorohydrin and formaldehyde.
(G) Carbopolycycle-bis(diazonium), dihalo, chloride (1:2), reaction products
with metal sulfate, calcium carbonate, N-(2-alkylphenyl)-oxoalkanamide,
potassium 4-[dioxoalkylamino]substituted benzene (1:1) and sodium hydroxide.
(G) Polyether sulfate salt derivative.
(G) Polyester substituted polycyclic aromatic colorant.
This notice announces EPA’s
approval of the State of Montana’s
request to revise its EPA-authorized
program to allow electronic reporting.
DATES: EPA’s approval is effective
December 9, 2011.
FOR FURTHER INFORMATION CONTACT: Evi
Huffer, U.S. Environmental Protection
Agency, Office of Environmental
Information, Mail Stop 2823T, 1200
Pennsylvania Avenue NW., Washington,
DC 20460, (202) 566–1697,
huffer.evi@epa.gov, U.S. Environmental
Protection Agency, Office of
Environmental Information, Mail Stop
2823T, 1200 Pennsylvania Avenue NW.,
Washington, DC 20460, or Karen Seeh,
U.S. Environmental Protection Agency,
Office of Environmental Information,
Mail Stop 2823T, 1200 Pennsylvania
Avenue NW., Washington, DC 20460,
(202) 566–1175, seeh.karen@epa.gov.
SUPPLEMENTARY INFORMATION: On
October 13, 2005, the final Cross-Media
Electronic Reporting Rule (CROMERR)
was published in the Federal Register
(70 FR 59848) and codified as Part 3 of
title 40 of the CFR. CROMERR
establishes electronic reporting as an
acceptable regulatory alternative to
paper reporting and establishes
requirements to assure that electronic
documents are as legally dependable as
their paper counterparts. Under Subpart
SUMMARY:
PO 00000
Frm 00037
Fmt 4703
Sfmt 4703
D of CROMERR, state, tribe or local
government agencies that receive, or
wish to begin receiving, electronic
reports under their EPA-authorized
programs must apply to EPA for a
revision or modification of those
programs and obtain EPA approval.
Subpart D also provides standards for
such approvals based on consideration
of the electronic document receiving
systems that the state, tribe, or local
government will use to implement the
electronic reporting. Additionally, in
§ 3.1000(b) through (e) of 40 CFR part 3,
subpart D provides special procedures
for program revisions and modifications
to allow electronic reporting, to be used
at the option of the state, tribe or local
government in place of procedures
available under existing programspecific authorization regulations. An
application submitted under the
Subpart D procedures must show that
the state, tribe or local government has
sufficient legal authority to implement
the electronic reporting components of
the programs covered by the application
and will use electronic document
receiving systems that meet the
applicable Subpart D requirements.
On July 8, 2011, the Montana
Department of the Environmental
Quality (MT DEQ) submitted an
application for its Network Discharge
E:\FR\FM\09DEN1.SGM
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]]>Agencies
[Federal Register Volume 76, Number 237 (Friday, December 9, 2011)]
[Notices]
[Pages 76963-76970]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-31645]
=======================================================================
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
[EPA-HQ-OPPT-2011-0832; FRL-9328-1]
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 September 26, 2011 to October 31, 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 January 9, 2012.
ADDRESSES: Submit your comments, identified by docket identification
(ID) number EPA-HQ-OPPT-2011-0832, 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 email
comment directly to EPA without going through regulations.gov, your
email 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; 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; email 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.
[[Page 76964]]
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 email. Clearly mark the part or all of the
information that you claim to be CBI. For CBI information in a disk or
CD-ROM that you mail to EPA, mark the outside of the disk or CD-ROM as
CBI and then identify electronically within the disk or CD-ROM the
specific information that is claimed as CBI. In addition to one
complete version of the comment that includes information claimed as
CBI, a copy of the comment that does not contain the information
claimed as CBI must be submitted for inclusion in the public docket.
Information 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://ww.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 September 26, 2011 to October 31, 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--50 PMNs Received From September 26, 2011 to October 31, 2011
----------------------------------------------------------------------------------------------------------------
Projected
Case No. Received date notice end Manufacturer/ Use Chemical
date importer
----------------------------------------------------------------------------------------------------------------
P-11-0653.................... 9/26/2011 12/24/2011 CBI............ (G) Water and (G)
oil repellant. Perfluoroalkyl
ethyl
methacrylate
copolymer.
P-11-0654.................... 9/26/2011 12/24/2011 CBI............ (G) Epoxy (S) Phenol, 2-
catalyst. [[[3-(1h-
imidazol-1-
yl)propyl]imin
o]phenylmethyl
]-5-(octyloxy)-
.
P-11-0655.................... 9/27/2011 12/25/2011 Miwon North (S) Resins for (G) Aliphatic
America, Inc. industrial epoxy
coating. acrylate.
P-11-0656.................... 9/27/2011 12/25/2011 Omnova (S) Soil (S) 2-propenoic
Solutions Inc. release acid, 2-methyl-
coating for , dodecyl
textiles used ester, polymer
for non- with 2-
consumer table hydroxyethyl 2-
linnen. propenoate,
.alpha.-(2-
methyl-1-oxo-2-
propen-1-yl)-
.omega.-
methoxypoly(ox
y-1,2-
ethanediyl)
and 3-methyl-3-
[(2,2,3,3,3-
pentafluoropro
poxy)methyl]ox
etane polymer
with
tetrahydrofura
n mono[2-[(1-
oxo-2-propen-1-
yl)oxy]ethyl]
ether.
[[Page 76965]]
P-11-0657.................... 9/27/2011 12/25/2011 Omnova (S) Flow, (S) Boron,
Solutions Inc. wetting and trifluoro(tetr
leveling agent ahydrofuran)-,
for commercial (T-4)-,
photographic polymer with 3-
film. methyl-3-
[(2,2,3,3,3-
pentafluoropro
poxy)methyl]ox
etane, ether
with 2,2-
dimethyl-1,3-
propanediol
(2:1), polymer
with .alpha.-
hydroxy-
.omega.-
hydroxypoly(ox
y-1,2-
ethanediyl)
and 5-
isocyanato-1-
(isocyanatomet
hyl)-1,3,3-
trimethylcyclo
hexane.
P-11-0658.................... 9/27/2011 12/25/2011 BASF (G) Catalyst (G) Alkoxy
Corporation. ingredient for alkanone
plastics fluorene.
manufacture.
P-11-0659.................... 9/28/2011 12/26/2011 CBI............ (G) Reactant to (G) Alkyl
produce new phosphonate.
chemical.
P-11-0660.................... 9/28/2011 12/26/2011 CBI............ (G) Oil field (G) Copolymer
additive. containing
phosphonic,
sulfonic and
carboxylic
acid groups.
P-11-0661.................... 9/28/2011 12/26/2011 Great Plains (S) Feedstock (S) Fats and
Oil & for production glyceridic
Exploration, of biofuel. oils, camelina
LLC. sativa.
P-11-0662.................... 9/30/2011 12/28/2011 CBI............ (G) Liquid (G) Isocyanate-
moisture cure terminated
adhesive. prepolymer.
P-11-0663.................... 9/30/2011 12/28/2011 CBI............ (S) Curing (G) Amides,
agent for from C18-
epoxy coating unsaturated
systems. fatty acids
dimers,hydroge
nated
benzaldehyde -
polyethylenepo
lyamines
reaction
products and
tall-oil fatty
acids.
P-12-0001.................... 10/3/2011 12/31/2011 CBI............ (G) Sealant (G) Aromatic
additive. isocyanate,
alkyl phenol-
blocked.
P-12-0002.................... 10/6/2011 1/3/2012 CBI............ (G) Chemical (G)
intermediate. Polyalkoxylate
d aromatic
amine.
P-12-0003.................... 10/6/2011 1/3/2012 CBI............ (G) Polymeric (G) Chromophore
colorant. substituted
polyoxyalkylen
e tint.
P-12-0004.................... 10/11/2011 1/8/2012 CBI............ (G) Polymeric (G) Substituted
colorant. polymeric
aromatic amine
azo colorant.
P-12-0005.................... 10/11/2011 1/8/2012 Sika (G) A (S) 2-propanol,
Corporation. dispersant for 1,1',1''-
neutralizing nitrilotris-,
electrical acetate (1:1).
charges and
separating
particles when
grinding
cement.
P-12-0006.................... 10/13/2011 1/10/2012 CBI............ (G) Adhesive... (G) Alkyldioic
acid, polymer
with
alkyldiol,
aromatic
isocyanate and
alkyloxirane
polymer with
oxirane ether
with
alkyltrio(3:1)
.
P-12-0007.................... 10/13/2011 1/10/2012 CBI............ (G) Adhesive... (G) Alkyldioic
acid, polymer
with
alkyldiol,
.alpha.-hydro-
.omega.-
hydroxypoly[ox
y(alkyldiyl)],
aromatic
isocyanate and
alkyloxirane
polymer with
oxirane ether
with
alkyltrio(3:1)
.
P-12-0008.................... 10/13/2011 1/10/2012 CBI............ (G) Open non (G) Aliphatic
despersive polyurethane
coating. resin.
P-12-0009.................... 10/12/2011 1/9/2012 CBI............ (G) Open, non- (G) Metal
dispersive complex,
use; copolymer of
ingredient in substituted
liquid paint. acrylic acid,
substituted
methacrylate,
substituted
acrylate, and
ethylene
glycol
substituted
acrylate alkyl
ether.
P-12-0010.................... 10/14/2011 1/11/2012 Reichhold, Inc. (S) Carrier (G) Amine salt
resin for of vegetable
paints and oil esters,
coatings. polymer with
alkanedioic
acid, hydroxy
substituted
alkylamine,
hydroxy
substituted
carboxylic
acid,
alkanediol,
isocyanates,
hydroxy
substituted
alkane.
P-12-0011.................... 10/17/2011 1/14/2012 BASF (G) Additive... (G) Hydroxy,
Corporation. halogen
substituted
diaromatic
ether.
[[Page 76966]]
P-12-0012.................... 10/17/2011 1/14/2012 Dow Chemical (S) Reactant (G) Polyester
Company. for polyol.
polyurethane
cast
elastomers.
P-12-0013.................... 10/17/2011 1/14/2012 CBI............ (G) Additive in (G) Crosslinked
printing inks. polyalkyl
methacrylate.
P-12-0014.................... 10/18/2011 1/15/2012 Dow Chemical (S) Reactant (G) Blocked
Company. for toluene
polyurethane diisocyanate
cast prepolymer.
elastomers.
P-12-0015.................... 10/17/2011 1/14/2012 Spectra Colors (G) Dye for (G) Substituted
Corporation. washable ink aniline,
systems. benzenesulfoni
c acid salt.
P-12-0016.................... 10/18/2011 1/15/2012 Innovative (S) Plasticizer (S) Waste
Science for polyvinyl plastics,
Technology. chloride resin. poly(ethylene
terephthalate)
,
depolymerized.
with by-
products from
prod. of 2-
butoxyethanol,
and
isotridecanol,
ethylene
glycol-free
fraction.
P-12-0017.................... 10/19/2011 1/16/2012 Sud-Chemie Inc. (G) Raw (S) Phosphoric
material in acid, iron(2+)
manufacturing. lithium salt
(1:1:1).
P-12-0018.................... 10/20/2011 1/17/2012 CBI............ (S) A component (G) Rubberized
of industrial epoxy resin.
epoxy adhesive
formulations.
P-12-0019.................... 10/20/2011 1/17/2012 Henkel (S) Glue stick. (S) Starch
Corporation. carboxymethyl
2-
hydroxypropyl
ether.
P-12-0020.................... 10/21/2011 1/18/2012 CBI............ (G) A component (G)
of leather Polyurethane
finishing aqueous
treatment. dispersion.
P-12-0021.................... 10/19/2011 1/16/2012 CBI............ (S) Petroleum (G) Petroleum
fuel blend and distillate
distillation/ heavies.
fractionation.
feedstock.
P-12-0022.................... 10/24/2011 1/21/2012 CBI............ (G) The new (G) Complex
chemical will strontium
be used as a aluminate rare
photoluminesce earth doped''.
nt pigment.
The pigment
will be
shipped to our
customers who
will
incorporate
the pigment
into fluids,
paints,
coatings,
inks,
injection
molding etc.
for, but not
limited to:
Emergency
signs, traffic
indication
signs,
switches,
military
applications,
high
visibility
signs, safety
location
markings and
any other
application
where a long
afterglow and/
or lighting is
needed.
[[Page 76967]]
P-12-0023.................... 10/24/2011 1/21/2012 CBI............ (G) The new (G) Complex
chemical will strontium
be used as a aluminate rare
photoluminesce earth doped''.
nt pigment.
The pigment
will be
shipped to our
customers who
will
incorporate
the pigment
into fluids,
paints,
coatings,
inks,
injection
molding etc.
for, but not
limited to:
Emergency
signs, traffic
indication
signs,
switches,
military
applications,
high
visibility
signs, safety
location
markings and
any other
application
where a long
afterglow and/
or lighting is
needed.
P-12-0024.................... 10/24/2011 1/21/2012 CBI............ (G) The new (G) Complex
chemical will strontium
be used as a aluminate rare
photoluminesce earth doped''.
nt pigment.
The pigment
will be
shipped to our
customers who
will
incorporate
the pigment
into fluids,
paints,
coatings,
inks,
injection
molding etc.
for, but not
limited to:
Emergency
signs, traffic
indication
signs,
switches,
military
applications,
high
visibility
signs, safety
location
markings and
any other
application
where a long
afterglow and/
or lighting is
needed.
P-12-0025.................... 10/24/2011 1/21/2012 CBI............ (G) The new (G) Complex
chemical will strontium
be used as a aluminate rare
photoluminesce earth doped''.
nt pigment.
The pigment
will be
shipped to our
customers who
will
incorporate
the pigment
into fluids,
paints,
coatings,
inks,
injection
molding etc.
for, but not
limited to:
Emergency
signs, traffic
indication
signs,
switches,
military
applications,
high
visibility
signs, safety
location
markings and
any other
application
where a long
afterglow and/
or lighting is
needed.
[[Page 76968]]
P-12-0026.................... 10/24/2011 1/21/2012 CBI............ (G) The new (G) Complex
chemical will strontium
be used as a aluminate rare
photoluminesce earth doped''.
nt pigment.
The pigment
will be
shipped to our
customers who
will
incorporate
the pigment
into fluids,
paints,
coatings,
inks,
injection
molding etc.
for, but not
limited to:
Emergency
signs, traffic
indication
signs,
switches,
military
applications,
high
visibility
signs, safety
location
markings and
any other
application
where a long
afterglow and/
or lighting is
needed.
P-12-0027.................... 10/26/2011 1/23/2012 Colonial (S) Dispersant-- (S) D-
Chemical, Inc. pigment in glucopyranose,
water based oligomeric,
paint; hard C10-16-alkyl
water cleaning. glycosides,
2,3-
dihydroxypropy
l ethers,
hydrogen
maleates,
sodium salts,
polymers with
1,3-dichloro-2-
propanol.
P-12-0028.................... 10/26/2011 1/23/2012 Colonial (S) Dispersant-- (S) D-
Chemical, Inc. pigment in glucopyranose,
water based oligomeric,
paint; hard C10-16-alkyl
water cleaning. glycosides,
2,3-
dihydroxypropy
l ethers,
hydrogen
succinates,
sodium salts,
polymers with
1,3-dichloro-2-
propanol.
P-12-0029.................... 10/26/2011 1/23/2012 Colonial (S) Dispersant-- (S) D-
Chemical, Inc. pigment in glucopyranose,
water based oligomeric,
paint; hard decyl octyl
water cleaning. glycosides,
2,3-
dihydroxypropy
l ethers,
hydrogen
maleates,
sodium salts,
polymers with
1,3-dichloro-2-
propanol.
P-12-0030.................... 10/27/2011 1/24/2012 CBI............ (G) Open, non- (G) Modified
dispersive fluorinated
textile finish. acrylate.
P-12-0031.................... 10/27/2011 1/24/2012 CBI............ (G) Open, non- (G) Modified
dispersive fluorinated
textile finish. acrylate.
P-12-0032.................... 10/27/2011 1/24/2012 CBI............ (G) Open, non- (G) Modified
dispersive fluorinated
textile finish. acrylate.
P-12-0033.................... 10/27/2011 1/24/2012 Aceto (S) (S) Benzoic
Corporation. Intermediate acid, 4-(1,1-
used in the dimethylethyl)-
manufacture of , methyl.
an imaging/
media product.
P-12-0034.................... 10/27/2011 1/24/2012 CBI............ (G) A component (G)
of leather Polyacrylate
finishing aqueous
treatment. dispersion.
P-12-0035.................... 10/29/2011 1/26/2012 CBI............ (G) Ferrite (G) Cobalt iron
dispersion ink manganese
additive to oxide,
ensure carboxylic
magnetic acid-modified.
performance
characteristic
s.
P-12-0036.................... 10/31/2011 1/28/2012 CBI............ (S) Fluorescent (G)
brightener for Triazinylamino
use in stilbene.
cellulosic
paper
applications.
P-12-0037.................... 10/28/2011 1/25/2012 CBI............ (G) Sizing for (G) Epoxy-
glass fibre. novolac resin
in non-ionic
water
emulsion.
P-12-0038.................... 10/28/2011 1/25/2012 CBI............ (G) Synthetic (G) Elastomer
leather. polyurethane.
P-12-0039.................... 10/31/2011 1/28/2012 CBI............ (G) Open, non- (G) Acrylic
dispersive use. polymer.
----------------------------------------------------------------------------------------------------------------
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 EP
