Certain New Chemicals; Receipt and Status Information for December 2015, 7337-7341 [2016-02830]
Download as PDF
Federal Register / Vol. 81, No. 28 / Thursday, February 11, 2016 / Notices
Commission, 888 First Street NE., Room
1A, Washington, DC 20426.
Any person seeking to become a party
to the proceeding must file a motion to
intervene pursuant to Rule 214 of the
Commission’s Rules of Practice and
Procedures (18 CFR 385.214).1 Only
intervenors have the right to seek
rehearing of the Commission’s decision.
The Commission grants affected
landowners and others with
environmental concerns intervenor
status upon showing good cause by
stating that they have a clear and direct
interest in this proceeding that no other
party can adequately represent. Simply
filing environmental comments will not
give you intervenor status, but you do
not need intervenor status to have your
comments considered.
Additional information about the
Project is available from the
Commission’s Office of External Affairs,
at (866) 208–FERC, or on the FERC Web
site (www.ferc.gov) using the eLibrary
link. Click on the eLibrary link, click on
‘‘General Search,’’ and enter the docket
number excluding the last three digits in
the Docket Number field (i.e., CP14–103
and/or CP14–115). Be sure you have
selected an appropriate date range. For
assistance, please contact FERC Online
Support at FercOnlineSupport@ferc.gov
or toll free at (866) 208–3676, or for
TTY, contact (202) 502–8659. The
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texts of formal documents issued by the
Commission, such as orders, notices,
and rulemakings.
In addition, the Commission offers a
free service called eSubscription, which
allows you to keep track of all formal
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by automatically providing you with
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summaries, and direct links to the
documents. Go to www.ferc.gov/docsfiling/esubscription.asp.
DEPARTMENT OF ENERGY
I. General Information
Federal Energy Regulatory
Commission
A. Does this action apply to me?
Dated: February 5, 2016.
Nathaniel J. Davis, Sr.,
Deputy Secretary.
SUMMARY:
The Agency included in the October
15, 2015 notice a list of those who may
be potentially affected by this action.
[Docket No. EL16–32–000]
Talen Energy Marketing, LLC; Notice of
Institution of Section 206 Proceeding
and Refund Effective Date
On February 5, 2016, the Commission
issued an order in Docket No. EL16–32–
000, pursuant to section 206 of the
Federal Power Act (FPA), 16 U.S.C.
824e (2012), instituting an investigation
into the justness and reasonableness of
Talen Energy Marketing, LLC’s
informational filing pursuant to
Schedule 2 to the PJM Interconnection,
LLC’s Open Access Transmission Tariff
supporting the revenue requirement for
reactive supply and voltage control
service (Reactive Service) of Talen
Ironwood, LLC. Talen Energy
Marketing, LLC, 154 FERC ¶ 61,087
(2016).
The refund effective date in Docket
No. EL16–32–000, established pursuant
to section 206(b) of the FPA, will be the
date of publication of this notice in the
Federal Register.
Dated: February 5, 2016.
Nathaniel J. Davis, Sr.,
Deputy Secretary.
[FR Doc. 2016–02759 Filed 2–10–16; 8:45 am]
BILLING CODE 6717–01–P
BILLING CODE 6717–01–P
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPP–2015–0393; FRL–9941–55]
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16:52 Feb 10, 2016
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The docket for this action, identified
by docket identification (ID) number
EPA–HQ–OPP–2015–0393, is available
at https://www.regulations.gov or at the
Office of Pesticide Programs Regulatory
Public Docket (OPP Docket) in the
Environmental Protection Agency
Docket Center (EPA/DC), West William
Jefferson Clinton Bldg., Rm. 3334, 1301
Constitution Ave. NW., Washington, DC
20460–0001. The Public Reading Room
is open from 8:30 a.m. to 4:30 p.m.,
Monday through Friday, excluding legal
holidays. The telephone number for the
Public Reading Room is (202) 566–1744,
and the telephone number for the OPP
Docket is (703) 305–5805. Please review
the visitor instructions and additional
information about the docket available
at https://www.epa.gov/dockets.
II. What does this correction do?
FR Doc. 2015–26299 published in the
Federal Register of October 15, 2015 (80
FR 62069) (FRL–9934–06) is corrected
as follows:
1. On page 62071, in the second
column, at the end of the document, the
signature is corrected to read Richard P.
Keigwin, Jr.
Dated: January 27, 2016.
Michael Goodis,
Acting Director, Pesticide Re-Evaluation
Division, Office of Pesticide Programs.
[FR Doc. 2016–02820 Filed 2–10–16; 8:45 am]
Registration Review Interim Decisions;
Notice of Availability; Correction
BILLING CODE 6560–50–P
Environmental Protection
Agency (EPA).
ENVIRONMENTAL PROTECTION
AGENCY
AGENCY:
ACTION:
[EPA–HQ–OPPT–2015–0507; FRL–9942–09]
Notice; correction.
FOR FURTHER INFORMATION CONTACT:
1 See the previous discussion on the methods for
filing comments.
B. How can I get copies of this document
and other related information?
Authority: 7 U.S.C. 136 et seq.
EPA issued a notice in the
Federal Register of October 15, 2015,
concerning Registration Review Interim
Decisions, Notice of Availability. This
document corrects a typographical error.
[FR Doc. 2016–02756 Filed 2–10–16; 8:45 am]
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7337
Richard Dumas, Pesticide Re-Evaluation
Division, (7508P), Office of Pesticide
Programs, Environmental Protection
Agency, 1200 Pennsylvania Ave. NW.,
Washington, DC 20460–0001; telephone
number: (703) 308–8015; email address:
dumas.richard@epa.gov.
SUPPLEMENTARY INFORMATION:
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Certain New Chemicals; Receipt and
Status Information for December 2015
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
EPA is required under the
Toxic Substances Control Act (TSCA) to
publish in the Federal Register a notice
of receipt of a premanufacture notice
(PMN); an application for a test
marketing exemption (TME), both
pending and/or expired; and a periodic
status report on any new chemicals
under EPA review and the receipt of
SUMMARY:
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Federal Register / Vol. 81, No. 28 / Thursday, February 11, 2016 / Notices
notices of commencement (NOC) to
manufacture those chemicals. This
document covers the period from
December 1, 2015 to December 31, 2015.
Comments identified by the
specific case number provided in this
document, must be received on or
before March 14, 2016.
DATES:
Submit your comments,
identified by docket identification (ID)
number EPA–HQ–OPPT–2015–0507,
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 online
instructions for submitting comments.
Do not submit electronically any
information you consider to be
Confidential Business Information (CBI)
or other information whose disclosure is
restricted by statute.
• 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: To make special
arrangements for hand delivery or
delivery of boxed information, please
follow the instructions at https://
www.epa.gov/dockets/contacts.html.
Additional instructions on
commenting or visiting the docket,
along with more information about
dockets generally, is available at
https://www.epa.gov/dockets.
ADDRESSES:
FOR FURTHER INFORMATION CONTACT:
For technical information contact: Jim
Rahai, IMD 7407M, Office of Pollution
Prevention and Toxics, Environmental
Protection Agency, 1200 Pennsylvania
Ave. NW., Washington, DC 20460–0001;
telephone number: (202) 564–8593;
email address: rahai.jim@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 submitters
of the actions addressed in this
document.
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 preparing and submitting your
comments, see the commenting tips at
https://www.epa.gov/dockets/
comments.html.
II. What action is the Agency taking?
This document provides receipt and
status reports, which cover the period
from December 1, 2015 to December 31,
2015, and consists of the PMNs and
TMEs both pending and/or expired, and
the NOCs to manufacture a new
chemical that the Agency has received
under TSCA section 5 during this time
period.
III. What is the Agency’s authority for
taking this action?
Under TSCA, 15 U.S.C. 2601 et seq.,
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/oppt/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 reports on the status of new
chemicals under review and the receipt
of NOCs to manufacture those
chemicals.
IV. Receipt and Status Reports
As used in each of the tables in this
unit, (S) indicates that the information
in the table is the specific information
provided by the submitter, and (G)
indicates that the information in the
table is generic information because the
specific information provided by the
submitter was claimed as CBI.
For the 46 PMNs received by EPA
during this period, Table 1 provides the
following information (to the extent that
such information is not claimed as CBI):
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.
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TABLE 1—PMNS RECEIVED FROM DECEMBER 1, 2015 TO DECEMBER 31, 2015
Case No.
P–16–0015 ......
VerDate Sep<11>2014
Date
received
Projected
end date for
EPA review
Manufacturer/importer
Use(s)
3/14/2016
CBI .............................
(S) New substance is a polymer used as a
hydropholbic coating for metal oxide particular in industrial formulations used a
functional surface treatment on metal
oxide which is used in cosmetic and sunscreen formulations.
12/15/2015
16:52 Feb 10, 2016
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Chemical identity
(G) Dimethicone crosspolymer and Silica.
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7339
TABLE 1—PMNS RECEIVED FROM DECEMBER 1, 2015 TO DECEMBER 31, 2015—Continued
Case No.
Date
received
Projected
end date for
EPA review
Manufacturer/importer
Use(s)
Chemical identity
(S) Phosphoric acid, mixed 2-hexlydecyl and
2-hexyldodecyl and 2-octyldecyl and 2octyldodecyl mono- and diesters.
(G) Dimethyl ester, polymer with 1,6hexanediol,
5-iscocyanato-1(isocyanatomethyl)-1,3,3trimethylcyclohexane and 2-oxepanone, 2hydroxyethyl acrylate-blocked.
(G) Heteropolycycle hydrogen carbonate,
polycondensate with alkyl hydrogen carbonate.
(G) Heteropolycycle hydrogen carbonate,
polycondensate with alkyl hydrogen carbonate.
(G) Fatty acids, reaction products with
alkylamine, polymers with substituted
carbomonocycle, substituted alkylamines,
heteromonocycle
and
substituted
alkanoate, acetates (salts).
(G) Substituted heteromonocycle, polymer
with substituted carbomonocycle and alkyl
(hydroxyalkyl)alkanediol,
alkoxyalkanolblocked.
(G)
2-Propanediol,
polymer
with
2ethyloxirane, oxirane and cycloaliphatic anhydride,
polymer
with
2,2′-[(1methylethylidene)bis(4,1phenyleneoxymethylene)]bis[oxirane].
(S) Magnesium hydroxide hypochlorite oxide.
12/10/2015
3/9/2016
Blaser Swisslube, Inc
(S) Metal working fluid component ................
P–16–0108 ......
12/2/2015
3/1/2016
CBI .............................
(G) Use in uv/eb adhesives and coatings ......
P–16–0109 ......
12/2/2015
3/1/2016
CBI .............................
(G) Raw material of polyurethane ..................
P–16–0110 ......
12/2/2015
3/1/2016
CBI .............................
(G) Raw material of polyurethane ..................
P–16–0111 ......
12/3/2015
3/2/2016
Allnex USA, Inc .........
(S) Electro-deposition primer .........................
P–16–0112 ......
12/3/2015
3/2/2016
Allnex USA, Inc .........
(S) Isolated intermediate for electro deposition primer.
P–16–0115 ......
12/4/2015
3/3/2016
CBI .............................
(S) Component of flexible foam .....................
P–16–0117 ......
12/5/2015
3/4/2016
CBI .............................
P–16–0118 ......
P–16–0119 ......
P–16–0120 ......
12/8/2015
12/14/2015
12/8/2015
3/7/2016
3/13/2016
3/7/2016
12/8/2015
3/7/2016
CBI .............................
CBI .............................
The Shepherd Color
Company.
CBI .............................
(S) Bleach for whitening, deodorizing and/or
cleaning.
(G) Additives for lubricating oil .......................
(G) Intermediate .............................................
(G) Pigment for anti-corrosive paints .............
P–16–0121 ......
(S) Water reducing agent for use in concrete
P–16–0122 ......
P–16–0123 ......
12/8/2015
12/8/2015
3/7/2016
3/7/2016
CBI .............................
Infineum USA, L.P .....
(G) Intermediate .............................................
(G) Oil additive ...............................................
P–16–0124 ......
12/9/2015
3/8/2016
CBI .............................
(G) Resin for coatings ....................................
P–16–0125 ......
12/9/2015
3/8/2016
CBI .............................
(G) Resin for coatings ....................................
P–16–0126 ......
12/9/2015
3/8/2016
CBI .............................
(G) Resin for coatings ....................................
P–16–0127 ......
12/10/2015
3/9/2016
CBI .............................
P–16–0128 ......
12/10/2015
3/9/2016
Cardolite Corporation
(S) Flotation of silica from iron ore and selected nonferrous minerals.
(S) Epoxy curing agent for light colored coatings.
P–16–0129 ......
P–16–0131 ......
P–16–0132 ......
12/10/2015
12/14/2015
12/14/2015
3/9/2016
3/13/2016
3/13/2016
Zeon Chemicals, L.P
CBI .............................
CBI .............................
P–16–0133 ......
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P–16–0054 ......
12/14/2015
3/13/2016
CBI .............................
P–16–0134
P–16–0135
P–16–0136
P–16–0139
P–16–0140
P–16–0141
P–16–0142
P–16–0143
12/15/2015
12/16/2015
12/15/2015
12/15/2015
12/15/2015
12/22/2015
12/16/2015
12/16/2015
3/14/2016
3/15/2016
3/14/2016
3/14/2016
3/14/2016
3/21/2016
3/15/2016
3/15/2016
CBI
CBI
CBI
CBI
CBI
CBI
CBI
CBI
......
......
......
......
......
......
......
......
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.............................
.............................
.............................
.............................
.............................
.............................
.............................
.............................
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(S) Resin for hot melt adhesives ...................
(G) Dye ...........................................................
(S) Emulsifier and lubricant for use in metal
working fluids.
(S) Raw material used to impart high heat
resistance to heat resistant plastics used
in the manufacture of LED reflectors used
in reflective plates.
(G) Cured coatings and inks ..........................
(G) Pigment wetting and dispersing additive
(G) Oil production ...........................................
(G) Oil production ...........................................
(G) Oil production ...........................................
(G) Lubricant additive .....................................
(G) Polymer for coatings ................................
(G) Chemical intermediate .............................
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(G) Akyl methacrylates copolymer.
(G) Chlorofluorocarbon.
(S) Aluminum vanadium zinc hydroxide
oxide.
(G) Acrylic acid polymer with polyethylene
glycol.
(G) Chlorofluorocarbon.
(G) Formaldehyde polymers with substitutedcarbomonocycle, (tetraalkenyl) derivs.
(G) Substituted alkanoic acid-, salts with substituted
alkanol-blocked
haloalkyl
heteromonocycle
substituted
carbomonocycle polymer alkyl alkanoatesubstituted
carbomonocycletrialkylcarbomonocycle-alkyl imine reaction
products.
(G) Alkoxy alkyl substituted alkanoic acid,
ion(1-),
salts
with
substituted
carbomonocycle
substituted
heteromonocyclic polymer ester with substituted carbomonocycle alkyl ester-alkyl
substituted alkanol reaction products.
(G) Substituted carbomonocycle, polymer
with substituted heteromonocycle, reaction
products with substituted amine, substituted amine and substituted alkanol,
alkylalkanoates
substituted
carbomonocycle.
(G) dialkyl ether ammonium salts.
(G) Fatty acids, c18-unsatd.,dimers,polymers
with cashew nutshell liq., glycidyl ethers
and polyethylenepolyamines.
(G) Hydrocarbon Resin, Hydrogenated.
(G) Polyethoxylated monoazo.
(G) Alkyoxylated fatty alcohol phosphate
ester.
(S) 1,4-Benzenedicarboxylic acid, polymer
with 2-methyl-1,8-octanediamine and 1,9nonanediamine, reaction products with
benzoic acid.
(G) Acrylic oligomer.
(G) Polyesters, fatty alkyl amides terminated.
(G) Dialkylamino alkylamide inner salt.
(G) Dialkylamino alkylamide inner salt, salts.
(G) Dialkylamino alkylamide inner salt, salts.
(G) Polyalkyl methacrylate copolymer.
(G) Amine salted polyacrylate.
(G) Haloalkylfurancarboxaldehyde.
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TABLE 1—PMNS RECEIVED FROM DECEMBER 1, 2015 TO DECEMBER 31, 2015—Continued
Date
received
Case No.
Projected
end date for
EPA review
Manufacturer/importer
Use(s)
Chemical identity
(G) Urethane acrylate.
(G) Urethane acrylate.
(G) Urethane acrylate.
(G) Urethane acrylate.
(G) Dialkylamino alkylamide inner salt.
(G) 2-alkenoic acid, alkyl ester, polymer with
ethenyl benzene, alkyl 2-alky alkenoate
and alkene carboxylic acid.
(G) Chlorofluorocarbon.
(G) Perfluoropolyether halide.
(G) Perfluoropolyether aryl.
(G) Substituted aryl perfluoropolyether.
(G) Sulfonated perfluoropolyether aromatic
transition metal salt.
(G) Sulfonated perfluoropolyether aryl alkali
metal salt.
(G) Sulfonated perfluoropolyether aryl alkali
metal salt.
(G) Polyethylenepolyamines.
P–16–0144
P–16–0145
P–16–0146
P–16–0147
P–16–0148
P–16–0149
......
......
......
......
......
......
12/16/2015
12/16/2015
12/16/2015
12/16/2015
12/16/2015
12/17/2015
3/15/2016
3/15/2016
3/15/2016
3/15/2016
3/15/2016
3/16/2016
H. B. Fuller Company
H. B. Fuller Company
H. B. Fuller Company
H. B. Fuller Company
CBI .............................
Cadence Chemical
Corporation.
(G) Industrial adhesive ...................................
(G) Urethane acrylate .....................................
(G) Industrial adhesive ...................................
(G) Industrial adhesive ...................................
(G) Oil production ...........................................
(S) Paints for wood, metal and plastic ...........
P–16–0150
P–16–0151
P–16–0152
P–16–0153
P–16–0154
......
......
......
......
......
12/18/2015
12/18/2015
12/18/2015
12/18/2015
12/18/2015
3/17/2016
3/17/2016
3/17/2016
3/17/2016
3/17/2016
CBI
CBI
CBI
CBI
CBI
(G)
(G)
(G)
(G)
(G)
P–16–0155 ......
12/18/2015
3/17/2016
CBI .............................
(G) Lubricant additive .....................................
P–16–0156 ......
12/18/2015
3/17/2016
CBI .............................
(G) Lubricant additive .....................................
P–16–0160 ......
12/30/2015
3/29/2016
CBI .............................
(G) Curing agent and curing agent precursor,
adhesion promoter and adhesion promoter
precursor.
.............................
.............................
.............................
.............................
.............................
For the 4 TMEs received by EPA
during this period, Table 2 provides the
following information (to the extent that
such information is not claimed as CBI):
Intermediate .............................................
Intermediate .............................................
Intermediate .............................................
Lubricant additive .....................................
Lubricant additive .....................................
The EPA case number assigned to the
TME, the date the TME was received by
EPA, the projected end date for EPA’s
review of the TME, the submitting
manufacturer/importer, the potential
uses identified by the manufacturer/
importer in the TME, and the chemical
identity.
TABLE 2—TMES RECEIVED FROM DECEMBER 1, 2015 TO DECEMBER 31, 2015
Date received
Case No.
T–16–0013
T–16–0014
T–16–0015
T–16–0016
........
........
........
........
Projected end
date for EPA
review
12/15/2015
12/15/2015
12/15/2015
12/16/2015
1/29/2016
1/29/2016
1/29/2016
1/30/2016
For the 38 NOCs received by EPA
during this period, Table 3 provides the
following information (to the extent that
such information is not claimed as CBI):
Manufacturer/
Importer
CBI
CBI
CBI
CBI
Use(s)
(G)
(G)
(G)
(G)
Oil
Oil
Oil
Oil
production
production
production
production
Chemical identity
......
......
......
......
The EPA case number assigned to the
NOC; the date the NOC was received by
EPA; the projected date of
commencement provided by the
(G)
(G)
(G)
(G)
Dialkylamino
Dialkylamino
Dialkylamino
Dialkylamino
alkylamide
alkylamide
alkylamide
alkylamide
inner
inner
inner
inner
salt.
salt, salts.
salt, salts.
salt.
submitter in the NOC; and the chemical
identity.
TABLE 3—NOCS RECEIVED FROM DECEMBER 1, 2015 TO DECEMBER 31, 2015
Case No.
Date received
Projected
date of
commencement
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J–15–0034 ........
P–11–0543 .......
P–12–0118 .......
P–12–0549 .......
P–13–0558 .......
P–13–0853 .......
P–14–0492 .......
12/21/2015
12/1/2015
12/16/2015
12/10/2015
12/3/2015
12/15/2015
12/1/2015
12/18/2015
11/3/2015
12/2/2015
11/11/2015
11/28/2015
10/28/2015
10/18/2015
P–14–0643
P–14–0838
P–15–0065
P–15–0177
P–15–0326
P–15–0341
.......
.......
.......
.......
.......
.......
12/16/2015
12/10/2015
12/9/2015
12/16/2015
12/21/2015
12/22/2015
11/16/2015
12/7/2015
12/5/2015
12/4/2015
10/19/2015
12/15/2015
P–15–0349 .......
12/3/2015
11/23/2015
P–15–0355 .......
12/8/2015
11/21/2015
VerDate Sep<11>2014
16:52 Feb 10, 2016
Jkt 238001
PO 00000
Chemical identity
(G) Saccharomyces cerevisiae modified.
(G) Polyfluorinated alkyl quanternary ammonium chloride.
(G) Substituted pyridinium salt.
(G) Modified polyester.
(G) Alkylene imine homopolymer, alkyl derivatives.
(G) Inorganic acid, triphenyl ester, polymer with mixed diols and alcohols.
(S) Ethanol, 2,2′,2″-nitrilotris-, compd. with alpha, alpha′—[[[4-[2-(4-sulfo-1-naphthalenyl)
diazenyl] phenyl] imino] di-2,1-ethanediyl]bis[omega-hydroxypoly(oxy-1,2-ethanediyl)]
(1:1).
(G) Titanium oxide derivative.
(G) Modified copolymer of buta-1,3-diene and styrene.
(G) Mixture of aminopropyl-terminated N-methylated polyalkylenepolyamines.
(G) Phenol, 2,2′-[1,2-disubstituted-1,2-ethanediyl]bis(iminomethylene)bis[substituted.
(G) Polyfluorohydrocarbon.
(G) Propenoic acid alkyl ester(s), telomer with alkanethiol, 2-methyl-2-propenoic acid and
2-hydroxyethyl 2-propenoate.
(G) Carbonic acid, diethyl ester, polymer with 1,6-hexanediol, 5-isocyanato-1(isocyanatomethyl)-1,3,3- trimethylcyclohexane 2-hydroxyethyl acrylate-blocked.
(S) Hexane, 1,6-diisocyanato-, homopolymer, di-et malonate-blocked.
Frm 00057
Fmt 4703
Sfmt 4703
E:\FR\FM\11FEN1.SGM
11FEN1
Federal Register / Vol. 81, No. 28 / Thursday, February 11, 2016 / Notices
7341
TABLE 3—NOCS RECEIVED FROM DECEMBER 1, 2015 TO DECEMBER 31, 2015—Continued
Case No.
Date received
Projected
date of
commencement
P–15–0455 .......
12/15/2015
12/4/2015
P–15–0468
P–15–0544
P–15–0581
P–15–0587
.......
.......
.......
.......
12/16/2015
12/1/2015
12/10/2015
12/14/2015
12/15/2015
11/25/2015
11/23/2015
12/2/2015
P–15–0596 .......
P–15–0602 .......
P–15–0606 .......
12/3/2015
12/9/2015
12/2/2015
11/16/2015
11/12/2015
11/24/2015
.......
.......
.......
.......
.......
.......
.......
.......
.......
.......
.......
.......
12/2/2015
12/23/2015
12/23/2015
12/23/2015
12/23/2015
12/23/2015
12/23/2015
12/2/2015
12/29/2015
12/11/2015
12/9/2015
12/7/2015
11/26/2015
12/22/2015
12/22/2015
12/22/2015
12/22/2015
12/22/2015
12/22/2015
11/22/2015
12/13/2015
12/10/2015
11/22/2015
12/3/2015
P–15–0687 .......
P–15–0696 .......
P–15–0712 .......
12/10/2015
12/14/2015
12/14/2015
12/8/2015
12/7/2015
12/11/2015
P–15–0608
P–15–0612
P–15–0613
P–15–0614
P–15–0615
P–15–0616
P–15–0618
P–15–0624
P–15–0635
P–15–0648
P–15–0657
P–15–0684
Authority: 15 U.S.C. 2601 et seq.
Dated: February 5, 2016.
Pamela Myrick,
Acting, Information Management Division,
Office of Pollution Prevention and Toxics.
[FR Doc. 2016–02830 Filed 2–10–16; 8:45 am]
BILLING CODE 6560–50–P
FEDERAL RESERVE SYSTEM
mstockstill on DSK4VPTVN1PROD with NOTICES
Notice of Proposals To Engage in or
To Acquire Companies Engaged in
Permissible Nonbanking Activities
The companies listed in this notice
have given notice under section 4 of the
Bank Holding Company Act (12 U.S.C.
1843) (BHC Act) and Regulation Y, (12
CFR part 225) to engage de novo, or to
acquire or control voting securities or
assets of a company, including the
companies listed below, that engages
either directly or through a subsidiary or
other company, in a nonbanking activity
that is listed in § 225.28 of Regulation Y
(12 CFR 225.28) or that the Board has
determined by Order to be closely
related to banking and permissible for
bank holding companies. Unless
otherwise noted, these activities will be
conducted throughout the United States.
Each notice is available for inspection
at the Federal Reserve Bank indicated.
The notice also will be available for
VerDate Sep<11>2014
16:52 Feb 10, 2016
Jkt 238001
Chemical identity
(S) 1,4-Cyclohexanedicarboxylic acid, 1,4-dimethyl ester, polymer with 1,4cyclohexanedimethanol.
(G) Polycyclecarboxylic acid, hydroxy-(substituted phenyl)diazenyl, metal salt.
(G) Trialkyl cycloalkylammonium hydroxide.
(G) L-amino acid, homopolymer, carboxylate.
(G) vegetable oil polymer with 1,1′-methylenebis[isocyantobenzene], oxepanone and
trimethylolpropane.
(G) Methyl alkaryl methyl hydrogen cyclosiloxanes.
(G) Copolymer of tetrafluoroethene and perfluorosulfonylvinylether.
(S) Alkenes, C18–22, mixed with polyethylene, oxidized, hydrolyzed, distn. residues, from
C20–22 alcs. manufacturer.
(G) Modified rosin polyol ester.
(S) Sulfur thulium ytterbium yttrium oxide.
(S) Gadolinium sulfur ytterbium yttrium oxide, erbium- and thulium-doped.
(S) Neodymium sulfur yttrium oxide.
(S) Erbium gadolinium neodymium sulfur ytterbium yttrium oxide.
(S) Erbium gadolinium sulfur ytterbium yttrium oxide.
(S) Erbium gadolinium sulfur ytterbium oxide.
(G) Modified urethane polymer.
(G) Polymer of an aromatic olefin and one or more substituted aromatic olefins.
(G) Alkylamino alcohol.
(G) Allyl triazine oligomer.
(G) Substituted alkenoic acid, alkyl ester, telomer with alkanethiol and oxiranylalkyl alkylalkenoatenoate.
(G) Polyester adduct.
(G) Urethane acrylate.
(S) Cyclopropanemethanol, 2-(1,4-dimethyl-3-penten-1-yl)-1-methyl-.
inspection at the offices of the Board of
Governors. Interested persons may
express their views in writing on the
question whether the proposal complies
with the standards of section 4 of the
BHC Act.
Unless otherwise noted, comments
regarding the notices must be received
at the Reserve Bank indicated or the
offices of the Board of Governors not
later than February 26, 2016.
A. Federal Reserve Bank of New York
(Ivan Hurwitz, Vice President) 33
Liberty Street, New York, New York
10045–0001. Comments can also be sent
electronically to
Comments.applications@ny.frb.org:
1. Sumitomo Mitsui Trust Holdings,
Inc., and Sumitomo Mitsui Trust Bank,
Limited, both in Tokyo, Japan; to
acquire 50 percent of the voting shares
of Marubeni Rail Transport, Inc.,
Wilmington, Delaware, and indirectly
acquire voting shares of Midwest Railcar
Corporation, Maryville, Illinois, and
thereby engage in personal property
leasing, incidental fleet management,
and consulting activities, pursuant to
sections 225.28(b)(3) and 225.28(b)(9).
Board of Governors of the Federal Reserve
System, February 8, 2016.
Michael J. Lewandowski,
Associate Secretary of the Board.
[FR Doc. 2016–02781 Filed 2–10–16; 8:45 am]
BILLING CODE 6210–01–P
PO 00000
Frm 00058
Fmt 4703
Sfmt 4703
FEDERAL RESERVE SYSTEM
Formations of, Acquisitions by, and
Mergers of Bank Holding Companies
The companies listed in this notice
have applied to the Board for approval,
pursuant to the Bank Holding Company
Act of 1956 (12 U.S.C. 1841 et seq.)
(BHC Act), Regulation Y (12 CFR part
225), and all other applicable statutes
and regulations to become a bank
holding company and/or to acquire the
assets or the ownership of, control of, or
the power to vote shares of a bank or
bank holding company and all of the
banks and nonbanking companies
owned by the bank holding company,
including the companies listed below.
The applications listed below, as well
as other related filings required by the
Board, are available for immediate
inspection at the Federal Reserve Bank
indicated. The applications will also be
available for inspection at the offices of
the Board of Governors. Interested
persons may express their views in
writing on the standards enumerated in
the BHC Act (12 U.S.C. 1842(c)). If the
proposal also involves the acquisition of
a nonbanking company, the review also
includes whether the acquisition of the
nonbanking company complies with the
standards in section 4 of the BHC Act
(12 U.S.C. 1843). Unless otherwise
E:\FR\FM\11FEN1.SGM
11FEN1
Agencies
[Federal Register Volume 81, Number 28 (Thursday, February 11, 2016)]
[Notices]
[Pages 7337-7341]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-02830]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
[EPA-HQ-OPPT-2015-0507; FRL-9942-09]
Certain New Chemicals; Receipt and Status Information for
December 2015
AGENCY: Environmental Protection Agency (EPA).
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: EPA is required under the Toxic Substances Control Act (TSCA)
to publish in the Federal Register a notice of receipt of a
premanufacture notice (PMN); an application for a test marketing
exemption (TME), both pending and/or expired; and a periodic status
report on any new chemicals under EPA review and the receipt of
[[Page 7338]]
notices of commencement (NOC) to manufacture those chemicals. This
document covers the period from December 1, 2015 to December 31, 2015.
DATES: Comments identified by the specific case number provided in this
document, must be received on or before March 14, 2016.
ADDRESSES: Submit your comments, identified by docket identification
(ID) number EPA-HQ-OPPT-2015-0507, 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 online instructions for submitting comments. Do not submit
electronically any information you consider to be Confidential Business
Information (CBI) or other information whose disclosure is restricted
by statute.
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: To make special arrangements for hand
delivery or delivery of boxed information, please follow the
instructions at https://www.epa.gov/dockets/contacts.html.
Additional instructions on commenting or visiting the docket, along
with more information about dockets generally, is available at https://www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT:
For technical information contact: Jim Rahai, IMD 7407M, Office of
Pollution Prevention and Toxics, Environmental Protection Agency, 1200
Pennsylvania Ave. NW., Washington, DC 20460-0001; telephone number:
(202) 564-8593; email address: rahai.jim@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 submitters of the actions addressed in this
document.
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 preparing and submitting
your comments, see the commenting tips at https://www.epa.gov/dockets/comments.html.
II. What action is the Agency taking?
This document provides receipt and status reports, which cover the
period from December 1, 2015 to December 31, 2015, and consists of the
PMNs and TMEs both pending and/or expired, and the NOCs to manufacture
a new chemical that the Agency has received under TSCA section 5 during
this time period.
III. What is the Agency's authority for taking this action?
Under TSCA, 15 U.S.C. 2601 et seq., 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/oppt/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 reports on
the status of new chemicals under review and the receipt of NOCs to
manufacture those chemicals.
IV. Receipt and Status Reports
As used in each of the tables in this unit, (S) indicates that the
information in the table is the specific information provided by the
submitter, and (G) indicates that the information in the table is
generic information because the specific information provided by the
submitter was claimed as CBI.
For the 46 PMNs received by EPA during this period, Table 1
provides the following information (to the extent that such information
is not claimed as CBI): 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 1--PMNs Received From December 1, 2015 to December 31, 2015
----------------------------------------------------------------------------------------------------------------
Projected
Date end date
Case No. received for EPA Manufacturer/importer Use(s) Chemical identity
review
----------------------------------------------------------------------------------------------------------------
P-16-0015.......... 12/15/2015 3/14/2016 CBI....................... (S) New substance (G) Dimethicone
is a polymer used crosspolymer and
as a hydropholbic Silica.
coating for metal
oxide particular
in industrial
formulations used
a functional
surface treatment
on metal oxide
which is used in
cosmetic and
sunscreen
formulations.
[[Page 7339]]
P-16-0054.......... 12/10/2015 3/9/2016 Blaser Swisslube, Inc..... (S) Metal working (S) Phosphoric
fluid component. acid, mixed 2-
hexlydecyl and 2-
hexyldodecyl and
2-octyldecyl and
2-octyldodecyl
mono- and
diesters.
P-16-0108.......... 12/2/2015 3/1/2016 CBI....................... (G) Use in uv/eb (G) Dimethyl
adhesives and ester, polymer
coatings. with 1,6-
hexanediol, 5-
iscocyanato-1-
(isocyanatomethy
l)-1,3,3-
trimethylcyclohe
xane and 2-
oxepanone, 2-
hydroxyethyl
acrylate-
blocked.
P-16-0109.......... 12/2/2015 3/1/2016 CBI....................... (G) Raw material (G)
of polyurethane. Heteropolycycle
hydrogen
carbonate,
polycondensate
with alkyl
hydrogen
carbonate.
P-16-0110.......... 12/2/2015 3/1/2016 CBI....................... (G) Raw material (G)
of polyurethane. Heteropolycycle
hydrogen
carbonate,
polycondensate
with alkyl
hydrogen
carbonate.
P-16-0111.......... 12/3/2015 3/2/2016 Allnex USA, Inc........... (S) Electro- (G) Fatty acids,
deposition primer. reaction
products with
alkylamine,
polymers with
substituted
carbomonocycle,
substituted
alkylamines,
heteromonocycle
and substituted
alkanoate,
acetates
(salts).
P-16-0112.......... 12/3/2015 3/2/2016 Allnex USA, Inc........... (S) Isolated (G) Substituted
intermediate for heteromonocycle,
electro polymer with
deposition primer. substituted
carbomonocycle
and alkyl
(hydroxyalkyl)al
kanediol,
alkoxyalkanol-
blocked.
P-16-0115.......... 12/4/2015 3/3/2016 CBI....................... (S) Component of (G) 2-
flexible foam. Propanediol,
polymer with 2-
ethyloxirane,
oxirane and
cycloaliphatic
anhydride,
polymer with
2,2'-[(1-
methylethylidene
)bis(4,1-
phenyleneoxymeth
ylene)]bis[oxira
ne].
P-16-0117.......... 12/5/2015 3/4/2016 CBI....................... (S) Bleach for (S) Magnesium
whitening, hydroxide
deodorizing and/ hypochlorite
or cleaning. oxide.
P-16-0118.......... 12/8/2015 3/7/2016 CBI....................... (G) Additives for (G) Akyl
lubricating oil. methacrylates
copolymer.
P-16-0119.......... 12/14/2015 3/13/2016 CBI....................... (G) Intermediate.. (G)
Chlorofluorocarb
on.
P-16-0120.......... 12/8/2015 3/7/2016 The Shepherd Color Company (G) Pigment for (S) Aluminum
anti-corrosive vanadium zinc
paints. hydroxide oxide.
P-16-0121.......... 12/8/2015 3/7/2016 CBI....................... (S) Water reducing (G) Acrylic acid
agent for use in polymer with
concrete. polyethylene
glycol.
P-16-0122.......... 12/8/2015 3/7/2016 CBI....................... (G) Intermediate.. (G)
Chlorofluorocarb
on.
P-16-0123.......... 12/8/2015 3/7/2016 Infineum USA, L.P......... (G) Oil additive.. (G) Formaldehyde
polymers with
substituted-
carbomonocycle,
(tetraalkenyl)
derivs.
P-16-0124.......... 12/9/2015 3/8/2016 CBI....................... (G) Resin for (G) Substituted
coatings. alkanoic acid-,
salts with
substituted
alkanol-blocked
haloalkyl
heteromonocycle
substituted
carbomonocycle
polymer alkyl
alkanoate-
substituted
carbomonocycle-
trialkylcarbomon
ocycle-alkyl
imine reaction
products.
P-16-0125.......... 12/9/2015 3/8/2016 CBI....................... (G) Resin for (G) Alkoxy alkyl
coatings. substituted
alkanoic acid,
ion(1-), salts
with substituted
carbomonocycle
substituted
heteromonocyclic
polymer ester
with substituted
carbomonocycle
alkyl ester-
alkyl
substituted
alkanol reaction
products.
P-16-0126.......... 12/9/2015 3/8/2016 CBI....................... (G) Resin for (G) Substituted
coatings. carbomonocycle,
polymer with
substituted
heteromonocycle,
reaction
products with
substituted
amine,
substituted
amine and
substituted
alkanol,
alkylalkanoates
substituted
carbomonocycle.
P-16-0127.......... 12/10/2015 3/9/2016 CBI....................... (S) Flotation of (G) dialkyl ether
silica from iron ammonium salts.
ore and selected
nonferrous
minerals.
P-16-0128.......... 12/10/2015 3/9/2016 Cardolite Corporation..... (S) Epoxy curing (G) Fatty acids,
agent for light c18-
colored coatings. unsatd.,dimers,p
olymers with
cashew nutshell
liq., glycidyl
ethers and
polyethylenepoly
amines.
P-16-0129.......... 12/10/2015 3/9/2016 Zeon Chemicals, L.P....... (S) Resin for hot (G) Hydrocarbon
melt adhesives. Resin,
Hydrogenated.
P-16-0131.......... 12/14/2015 3/13/2016 CBI....................... (G) Dye........... (G)
Polyethoxylated
monoazo.
P-16-0132.......... 12/14/2015 3/13/2016 CBI....................... (S) Emulsifier and (G) Alkyoxylated
lubricant for use fatty alcohol
in metal working phosphate ester.
fluids.
P-16-0133.......... 12/14/2015 3/13/2016 CBI....................... (S) Raw material (S) 1,4-
used to impart Benzenedicarboxy
high heat lic acid,
resistance to polymer with 2-
heat resistant methyl-1,8-
plastics used in octanediamine
the manufacture and 1,9-
of LED reflectors nonanediamine,
used in reaction
reflective plates. products with
benzoic acid.
P-16-0134.......... 12/15/2015 3/14/2016 CBI....................... (G) Cured coatings (G) Acrylic
and inks. oligomer.
P-16-0135.......... 12/16/2015 3/15/2016 CBI....................... (G) Pigment (G) Polyesters,
wetting and fatty alkyl
dispersing amides
additive. terminated.
P-16-0136.......... 12/15/2015 3/14/2016 CBI....................... (G) Oil production (G) Dialkylamino
alkylamide inner
salt.
P-16-0139.......... 12/15/2015 3/14/2016 CBI....................... (G) Oil production (G) Dialkylamino
alkylamide inner
salt, salts.
P-16-0140.......... 12/15/2015 3/14/2016 CBI....................... (G) Oil production (G) Dialkylamino
alkylamide inner
salt, salts.
P-16-0141.......... 12/22/2015 3/21/2016 CBI....................... (G) Lubricant (G) Polyalkyl
additive. methacrylate
copolymer.
P-16-0142.......... 12/16/2015 3/15/2016 CBI....................... (G) Polymer for (G) Amine salted
coatings. polyacrylate.
P-16-0143.......... 12/16/2015 3/15/2016 CBI....................... (G) Chemical (G)
intermediate. Haloalkylfuranca
rboxaldehyde.
[[Page 7340]]
P-16-0144.......... 12/16/2015 3/15/2016 H. B. Fuller Company...... (G) Industrial (G) Urethane
adhesive. acrylate.
P-16-0145.......... 12/16/2015 3/15/2016 H. B. Fuller Company...... (G) Urethane (G) Urethane
acrylate. acrylate.
P-16-0146.......... 12/16/2015 3/15/2016 H. B. Fuller Company...... (G) Industrial (G) Urethane
adhesive. acrylate.
P-16-0147.......... 12/16/2015 3/15/2016 H. B. Fuller Company...... (G) Industrial (G) Urethane
adhesive. acrylate.
P-16-0148.......... 12/16/2015 3/15/2016 CBI....................... (G) Oil production (G) Dialkylamino
alkylamide inner
salt.
P-16-0149.......... 12/17/2015 3/16/2016 Cadence Chemical (S) Paints for (G) 2-alkenoic
Corporation. wood, metal and acid, alkyl
plastic. ester, polymer
with ethenyl
benzene, alkyl 2-
alky alkenoate
and alkene
carboxylic acid.
P-16-0150.......... 12/18/2015 3/17/2016 CBI....................... (G) Intermediate.. (G)
Chlorofluorocarb
on.
P-16-0151.......... 12/18/2015 3/17/2016 CBI....................... (G) Intermediate.. (G)
Perfluoropolyeth
er halide.
P-16-0152.......... 12/18/2015 3/17/2016 CBI....................... (G) Intermediate.. (G)
Perfluoropolyeth
er aryl.
P-16-0153.......... 12/18/2015 3/17/2016 CBI....................... (G) Lubricant (G) Substituted
additive. aryl
perfluoropolyeth
er.
P-16-0154.......... 12/18/2015 3/17/2016 CBI....................... (G) Lubricant (G) Sulfonated
additive. perfluoropolyeth
er aromatic
transition metal
salt.
P-16-0155.......... 12/18/2015 3/17/2016 CBI....................... (G) Lubricant (G) Sulfonated
additive. perfluoropolyeth
er aryl alkali
metal salt.
P-16-0156.......... 12/18/2015 3/17/2016 CBI....................... (G) Lubricant (G) Sulfonated
additive. perfluoropolyeth
er aryl alkali
metal salt.
P-16-0160.......... 12/30/2015 3/29/2016 CBI....................... (G) Curing agent (G)
and curing agent Polyethylenepoly
precursor, amines.
adhesion promoter
and adhesion
promoter
precursor.
----------------------------------------------------------------------------------------------------------------
For the 4 TMEs received by EPA during this period, Table 2 provides
the following information (to the extent that such information is not
claimed as CBI): The EPA case number assigned to the TME, the date the
TME was received by EPA, the projected end date for EPA's review of the
TME, the submitting manufacturer/importer, the potential uses
identified by the manufacturer/importer in the TME, and the chemical
identity.
Table 2--TMEs Received From December 1, 2015 to December 31, 2015
--------------------------------------------------------------------------------------------------------------------------------------------------------
Projected end
Case No. Date received date for EPA Manufacturer/Importer Use(s) Chemical identity
review
--------------------------------------------------------------------------------------------------------------------------------------------------------
T-16-0013.................... 12/15/2015 1/29/2016 CBI (G) Oil production................ (G) Dialkylamino
alkylamide inner salt.
T-16-0014.................... 12/15/2015 1/29/2016 CBI (G) Oil production................ (G) Dialkylamino
alkylamide inner salt,
salts.
T-16-0015.................... 12/15/2015 1/29/2016 CBI (G) Oil production................ (G) Dialkylamino
alkylamide inner salt,
salts.
T-16-0016.................... 12/16/2015 1/30/2016 CBI (G) Oil production................ (G) Dialkylamino
alkylamide inner salt.
--------------------------------------------------------------------------------------------------------------------------------------------------------
For the 38 NOCs received by EPA during this period, Table 3
provides the following information (to the extent that such information
is not claimed as CBI): The EPA case number assigned to the NOC; the
date the NOC was received by EPA; the projected date of commencement
provided by the submitter in the NOC; and the chemical identity.
Table 3--NOCs Received From December 1, 2015 to December 31, 2015
------------------------------------------------------------------------
Projected date
Case No. Date received of Chemical
commencement identity
------------------------------------------------------------------------
J-15-0034............. 12/21/2015 12/18/2015 (G)
Saccharomyces
cerevisiae
modified.
P-11-0543............. 12/1/2015 11/3/2015 (G)
Polyfluorinated
alkyl
quanternary
ammonium
chloride.
P-12-0118............. 12/16/2015 12/2/2015 (G) Substituted
pyridinium
salt.
P-12-0549............. 12/10/2015 11/11/2015 (G) Modified
polyester.
P-13-0558............. 12/3/2015 11/28/2015 (G) Alkylene
imine
homopolymer,
alkyl
derivatives.
P-13-0853............. 12/15/2015 10/28/2015 (G) Inorganic
acid, triphenyl
ester, polymer
with mixed
diols and
alcohols.
P-14-0492............. 12/1/2015 10/18/2015 (S) Ethanol,
2,2',2''-
nitrilotris-,
compd. with
alpha, alpha'--
[[[4-[2-(4-
sulfo-1-
naphthalenyl)
diazenyl]
phenyl] imino]
di-2,1-
ethanediyl]bis[
omega-
hydroxypoly(oxy-
1,2-
ethanediyl)]
(1:1).
P-14-0643............. 12/16/2015 11/16/2015 (G) Titanium
oxide
derivative.
P-14-0838............. 12/10/2015 12/7/2015 (G) Modified
copolymer of
buta-1,3-diene
and styrene.
P-15-0065............. 12/9/2015 12/5/2015 (G) Mixture of
aminopropyl-
terminated N-
methylated
polyalkylenepol
yamines.
P-15-0177............. 12/16/2015 12/4/2015 (G) Phenol, 2,2'-
[1,2-
disubstituted-
1,2-
ethanediyl]bis(
iminomethylene)
bis[substituted
.
P-15-0326............. 12/21/2015 10/19/2015 (G)
Polyfluorohydro
carbon.
P-15-0341............. 12/22/2015 12/15/2015 (G) Propenoic
acid alkyl
ester(s),
telomer with
alkanethiol, 2-
methyl-2-
propenoic acid
and 2-
hydroxyethyl 2-
propenoate.
P-15-0349............. 12/3/2015 11/23/2015 (G) Carbonic
acid, diethyl
ester, polymer
with 1,6-
hexanediol, 5-
isocyanato-1-
(isocyanatometh
yl)-1,3,3-
trimethylcycloh
exane 2-
hydroxyethyl
acrylate-
blocked.
P-15-0355............. 12/8/2015 11/21/2015 (S) Hexane, 1,6-
diisocyanato-,
homopolymer, di-
et malonate-
blocked.
[[Page 7341]]
P-15-0455............. 12/15/2015 12/4/2015 (S) 1,4-
Cyclohexanedica
rboxylic acid,
1,4-dimethyl
ester, polymer
with 1,4-
cyclohexanedime
thanol.
P-15-0468............. 12/16/2015 12/15/2015 (G)
Polycyclecarbox
ylic acid,
hydroxy-
(substituted
phenyl)diazenyl
, metal salt.
P-15-0544............. 12/1/2015 11/25/2015 (G) Trialkyl
cycloalkylammon
ium hydroxide.
P-15-0581............. 12/10/2015 11/23/2015 (G) L-amino
acid,
homopolymer,
carboxylate.
P-15-0587............. 12/14/2015 12/2/2015 (G) vegetable
oil polymer
with 1,1'-
methylenebis[is
ocyantobenzene]
, oxepanone and
trimethylolprop
ane.
P-15-0596............. 12/3/2015 11/16/2015 (G) Methyl
alkaryl methyl
hydrogen
cyclosiloxanes.
P-15-0602............. 12/9/2015 11/12/2015 (G) Copolymer of
tetrafluoroethe
ne and
perfluorosulfon
ylvinylether.
P-15-0606............. 12/2/2015 11/24/2015 (S) Alkenes, C18-
22, mixed with
polyethylene,
oxidized,
hydrolyzed,
distn.
residues, from
C20-22 alcs.
manufacturer.
P-15-0608............. 12/2/2015 11/26/2015 (G) Modified
rosin polyol
ester.
P-15-0612............. 12/23/2015 12/22/2015 (S) Sulfur
thulium
ytterbium
yttrium oxide.
P-15-0613............. 12/23/2015 12/22/2015 (S) Gadolinium
sulfur
ytterbium
yttrium oxide,
erbium- and
thulium-doped.
P-15-0614............. 12/23/2015 12/22/2015 (S) Neodymium
sulfur yttrium
oxide.
P-15-0615............. 12/23/2015 12/22/2015 (S) Erbium
gadolinium
neodymium
sulfur
ytterbium
yttrium oxide.
P-15-0616............. 12/23/2015 12/22/2015 (S) Erbium
gadolinium
sulfur
ytterbium
yttrium oxide.
P-15-0618............. 12/23/2015 12/22/2015 (S) Erbium
gadolinium
sulfur
ytterbium
oxide.
P-15-0624............. 12/2/2015 11/22/2015 (G) Modified
urethane
polymer.
P-15-0635............. 12/29/2015 12/13/2015 (G) Polymer of
an aromatic
olefin and one
or more
substituted
aromatic
olefins.
P-15-0648............. 12/11/2015 12/10/2015 (G) Alkylamino
alcohol.
P-15-0657............. 12/9/2015 11/22/2015 (G) Allyl
triazine
oligomer.
P-15-0684............. 12/7/2015 12/3/2015 (G) Substituted
alkenoic acid,
alkyl ester,
telomer with
alkanethiol and
oxiranylalkyl
alkyl-
alkenoatenoate.
P-15-0687............. 12/10/2015 12/8/2015 (G) Polyester
adduct.
P-15-0696............. 12/14/2015 12/7/2015 (G) Urethane
acrylate.
P-15-0712............. 12/14/2015 12/11/2015 (S)
Cyclopropanemet
hanol, 2-(1,4-
dimethyl-3-
penten-1-yl)-1-
methyl-.
------------------------------------------------------------------------
Authority: 15 U.S.C. 2601 et seq.
Dated: February 5, 2016.
Pamela Myrick,
Acting, Information Management Division, Office of Pollution Prevention
and Toxics.
[FR Doc. 2016-02830 Filed 2-10-16; 8:45 am]
BILLING CODE 6560-50-P