Certain New Chemicals; Receipt and Status Information for September 2016, 79020-79027 [2016-27195]
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79020
Federal Register / Vol. 81, No. 218 / Thursday, November 10, 2016 / Notices
analysis support and planning for OPPT
programs such as Lead Programs and
other technology and exposure related
studies.
In accordance with 40 CFR 2.306(j),
EPA has determined that under EPA
contract number EP–W–16–017, BMI
and Avanti Corporation required access
to CBI submitted to EPA under sections
4, 5, 6, 8(a), 11 and 21 of TSCA to
perform successfully the duties
specified under the contract. BMI and
Avanti Corporation personnel were
given access to information submitted to
EPA under sections 4, 5, 6, 8(a), 11 and
21 of TSCA. Some of the information
may be claimed or determined to be
CBI.
EPA is issuing this notice to inform
all submitters of information under
sections 4, 5, 6, 8(a), 11 and 21 of TSCA
that EPA has provided BMI and Avanti
Corporation access to these CBI
materials on a need-to-know basis only.
All access to TSCA CBI under this
contract is taking place at EPA
Headquarters and BMI’s site located in
Columbus, OH, in accordance with
EPA’s TSCA CBI Protection Manual.
Access to TSCA data, including CBI,
will continue until June 12, 2021. If the
contract is extended, this access will
also continue for the duration of the
extended contract without further
notice.
BMI and Avanti Corporation
personnel have signed nondisclosure
agreements and were briefed on
appropriate security procedures before
they are permitted access to TSCA CBI.
Authority: 15 U.S.C. 2601 et seq.
Dated: November 2, 2016.
Pamela S. Myrick,
Director, Information Management Division,
Office of Pollution Prevention and Toxics.
[FR Doc. 2016–27188 Filed 11–9–16; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPPT–2003–0004; FRL–9954–70]
Access to Confidential Business
Information by Eastern Research
Group, Inc.
Environmental Protection
Agency (EPA).
ACTION: Notice.
asabaliauskas on DSK3SPTVN1PROD with NOTICES
AGENCY:
EPA has authorized its
contractor, Eastern Research Group, Inc.
(ERG) of Lexington, MA, access to
information which has been submitted
to EPA under all sections of the Toxic
Substances Control Act (TSCA). Some of
the information may be claimed or
SUMMARY:
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(CDR) data; and reviewing CBI data for
Existing Chemical engineering reports.
In accordance with 40 CFR 2.306(j),
EPA has determined that under EPA
contract number EP–W–12–006, work
assignment number 4–28, ERG required
access to CBI submitted to EPA under
all sections of TSCA to perform
successfully the duties specified under
the contract. ERG’s personnel were
given access to information submitted to
EPA under all sections of TSCA. Some
of the information may be claimed or
determined to be CBI.
EPA is issuing this notice to inform
all submitters of information under all
sections of TSCA that EPA has provided
ERG access to these CBI materials on a
need-to-know basis only. All access to
TSCA CBI under this contract is taking
place at EPA Headquarters and ERG’s
site located at 14555 Avion Parkway,
Suite 200, Chantilly, Va. in accordance
I. General Information
with EPA’s TSCA CBI Protection
Manual.
A. Does this action apply to me?
Access to TSCA data, including CBI,
This action is directed to the public
will continue until December 31, 2016.
in general. This action may, however, be If the contract is extended, this access
of interest to all who manufacture,
will also continue for the duration of the
process, or distribute industrial
extended contract without further
chemicals. Since other entities may also notice.
be interested, the Agency has not
ERG personnel were required to sign
attempted to describe all the specific
nondisclosure agreements and were
entities that may be affected by this
briefed on appropriate security
action.
procedures before they are permitted
B. How can I get copies of this document access to TSCA CBI.
and other related information?
Authority: 15 U.S.C. 2601 et seq.
The docket for this action, identified
Dated: November 2, 2016.
by docket identification (ID) number
Pamela S. Myrick,
EPA–HQ–OPPT–2003–0004 is available Director, Information Management Division,
at https://www.regulations.gov or at the
Office of Pollution Prevention and Toxics.
Office of Pollution Prevention and
[FR Doc. 2016–27189 Filed 11–9–16; 8:45 am]
Toxics Docket (OPPT Docket),
BILLING CODE 6560–50–P
Environmental Protection Agency
Docket Center (EPA/DC), West William
Jefferson Clinton Bldg., Rm. 3334, 1301
ENVIRONMENTAL PROTECTION
Constitution Ave. NW., Washington,
AGENCY
DC. The Public Reading Room is open
[EPA–HQ–OPPT–2016–0484; FRL–9954–52]
from 8:30 a.m. to 4:30 p.m., Monday
through Friday, excluding legal
Certain New Chemicals; Receipt and
holidays. The telephone number for the Status Information for September 2016
Public Reading Room is (202) 566–1744,
and the telephone number for the OPPT AGENCY: Environmental Protection
Docket is (202) 566–0280. Please review Agency (EPA).
the visitor instructions and additional
ACTION: Notice.
information about the docket available
SUMMARY: EPA is required under the
at https://www.epa.gov/dockets.
Toxic Substances Control Act (TSCA) to
II. What action is the Agency taking?
publish in the Federal Register a notice
Under EPA contract number EP–W–
of receipt of a premanufacture notice
12–006, work assignment number 4–28, (PMN); an application for a test
contractor ERG of 110 Hartwell Ave,
marketing exemption (TME), both
Suite 1, Lexington, MA is assisting the
pending and/or expired; and a periodic
Office of Pollution Prevention and
status report on any new chemicals
Toxics (OPPT) in preparing engineering under EPA review and the receipt of
reports for the Premanufacture Notice
notices of commencement (NOC) to
(PMN) review program; performing
manufacture those chemicals. This
analyses of Chemical Data Reporting
document covers the period from
determined to be Confidential Business
Information (CBI).
DATES: Access to the confidential data
occurred on or about October 5, 2016.
FOR FURTHER INFORMATION CONTACT:
For technical information contact:
Scott Sherlock, Environmental
Assistance Division (7408M), Office of
Pollution Prevention and Toxics,
Environmental Protection Agency, 1200
Pennsylvania Ave. NW., Washington,
DC 20460–0001; telephone number:
(202) 564–8257; fax number: (202) 564–
8251; email address: sherlock.scott@
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:
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Federal Register / Vol. 81, No. 218 / Thursday, November 10, 2016 / Notices
September 1, 2016 to September 30,
2016.
DATES: Comments identified by the
specific case number provided in this
document, must be received on or
before December 12, 2016.
ADDRESSES: Submit your comments,
identified by docket identification (ID)
number EPA–HQ–OPPT–2016–0484,
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 September 1, 2016 to September
30, 2016, 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,
please 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 71 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.
asabaliauskas on DSK3SPTVN1PROD with NOTICES
TABLE 1—PMNS RECEIVED FROM SEPTEMBER 1, 2016 TO SEPTEMBER 30, 2016
Case No.
Received date
Projected
notice end
date
Manufacturer
importer
Use
(G) Intermediate for polymer synthesis.
(S) Compound to be used in preparation of advanced seed coatings.
P–16–0379 .......
9/26/2016
12/25/2016
CBI ...................
P–16–0399 .......
9/16/2016
12/15/2016
Tryeco LLC .......
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Chemical
(G) Vinyl functional
polymethylalkylpolymer.
(S) Starch, polymer with 2-propenoic acid, potassium salt.
oxidized.
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TABLE 1—PMNS RECEIVED FROM SEPTEMBER 1, 2016 TO SEPTEMBER 30, 2016—Continued
Case No.
Received date
Projected
notice end
date
Manufacturer
importer
Use
(S) Agricultural soil amendment for
turf applications and direct soil
injection with fertilizers.
(S) Agricultural soil amendment for
filed crops as ‘‘agrisorb plus’’
granular soil amendment.
(G) Universal tint paste resin having high solids.
(G) Process aid .............................
(G) Process aid .............................
(G) Process aid .............................
(G) Process aid .............................
(G) Process aid .............................
(S) Mass coloration of paper .........
Chemical
9/16/2016
12/15/2016
Tryeco LLC .......
P–16–0399 .......
9/16/2016
12/15/2016
Tryeco LLC .......
P–16–0429 .......
9/20/2016
12/19/2016
CBI ...................
P–16–0460
P–16–0461
P–16–0462
P–16–0463
P–16–0464
P–16–0487
.......
.......
.......
.......
.......
.......
9/28/2016
9/28/2016
9/28/2016
9/28/2016
9/28/2016
9/22/2016
12/27/2016
12/27/2016
12/27/2016
12/27/2016
12/27/2016
12/21/2016
CBI ...................
CBI ...................
CBI ...................
CBI ...................
CBI ...................
Jaychem LLC ...
P–16–0520 .......
9/26/2016
12/25/2016
CBI ...................
(G) As described above, the notified polymer will be use as a
pigment dispersant.
P–16–0520 .......
9/26/2016
12/25/2016
CBI ...................
(G) The anticipated use is as a
deposit control agent and pigment dispersant.
P–16–0520 .......
9/26/2016
12/25/2016
CBI ...................
(G) The anticipated use is as a
pigment dispersant.
P–16–0520 .......
9/26/2016
12/25/2016
CBI ...................
(G) The anticipated use is as a
deposit control agent.
P–16–0521 .......
asabaliauskas on DSK3SPTVN1PROD with NOTICES
P–16–0399 .......
9/26/2016
12/25/2016
CBI ...................
(G) The anticipated use is as a
deposit control agent.
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(S) Starch, polymer with 2-propenoic acid, potassium salt.
oxidized.
(S) Starch, polymer with 2-propenoic acid, potassium salt.
oxidized.
(G) Endcapped polysiloxane.
(G) Silane-treated aluminosilicate.
(G) Silane-treated aluminosilicate.
(G) Silane-treated aluminosilicate.
(G) Silane-treated aluminosilicate.
(G) Silane-treated aluminosilicate.
(G) Benzenesulfonic acid 1,2diazenediylbis[6-ethenyl]-3sulfophenyl diazenyl-2sulfophenyl ethenyl salt.
(G) 2-propenoic acid, polymer with
N-(alkyl)-2propenamide, sodium
alkyl alkene sulfonate (1:1) and
sodium 2-methyl-2-[(1-oxo-2propen-1-yl) amino]-1propanesulfonate (1:1),
peroxydisulfuric acid
([(ho)s(o)2]2o2) sodium salt
(1:2)-initiated.
(G) 2-propenoic acid, polymer with
N-(alkyl)-2propenamide, sodium
alkyl alkene sulfonate (1:1) and
sodium 2-methyl-2-[(1-oxo-2propen-1-yl) amino]-1propanesulfonate (1:1),
peroxydisulfuric acid
([(ho)s(o)2]2o2) sodium salt
(1:2)-initiated.
(G) 2-propenoic acid, polymer with
N-(alkyl)-2propenamide, sodium
alkyl alkene sulfonate (1:1) and
sodium 2-methyl-2-[(1-oxo-2propen-1-yl) amino]-1propanesulfonate (1:1),
peroxydisulfuric acid
([(ho)s(o)2]2o2) sodium salt
(1:2)-initiated.
(G) 2-propenoic acid, polymer with
N-(alkyl)-2propenamide, sodium
alkyl alkene sulfonate (1:1) and
sodium 2-methyl-2-[(1-oxo-2propen-1-yl) amino]-1propanesulfonate (1:1),
peroxydisulfuric acid
([(ho)s(o)2]2o2) sodium salt
(1:2)-initiated.
(G) 2-propenoic acid, polymer with
N-(alkyl)-2propenamide, sodium
alkyl alkene sulfonate (1:1) and
sodium 2-methyl-2-[(1-oxo-2propen-1-yl) amino]-1propanesulfonate (1:1), potassium salt, peroxydisulfuric acid
([(ho)s(o)2]2o2) sodium salt
(1:2)-initiated.
10NON1
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Federal Register / Vol. 81, No. 218 / Thursday, November 10, 2016 / Notices
TABLE 1—PMNS RECEIVED FROM SEPTEMBER 1, 2016 TO SEPTEMBER 30, 2016—Continued
Case No.
Received date
Projected
notice end
date
Manufacturer
importer
Use
Chemical
9/26/2016
12/25/2016
CBI ...................
(G) As described above, the notified polymer will be use as a
pigment dispersant.
P–16–0521 .......
9/26/2016
12/25/2016
CBI ...................
(G) The anticipated use is as a
deposit control agent and pigment dispersant.
P–16–0521 .......
9/26/2016
12/25/2016
CBI ...................
(G) The anticipated use is as a
pigment dispersant.
P–16–0522 .......
9/26/2016
12/25/2016
CBI ...................
(G) As described above, the notified polymer will be use as a
pigment dispersant.
P–16–0522 .......
9/26/2016
12/25/2016
CBI ...................
(G) The anticipated use is as a
pigment dispersant.
P–16–0522 .......
9/26/2016
12/25/2016
CBI ...................
(G) The anticipated use is as a
deposit control agent and pigment dispersant.
P–16–0522 .......
asabaliauskas on DSK3SPTVN1PROD with NOTICES
P–16–0521 .......
9/26/2016
12/25/2016
CBI ...................
(G) The anticipated use is as a
deposit control agent.
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(G) 2-propenoic acid, polymer with
N-(alkyl)-2propenamide, sodium
alkyl alkene sulfonate (1:1) and
sodium 2-methyl-2-[(1-oxo-2propen-1-yl) amino]-1propanesulfonate (1:1), potassium salt, peroxydisulfuric acid
([(ho)s(o)2]2o2) sodium salt
(1:2)-initiated.
(G) 2-propenoic acid, polymer with
N-(alkyl)-2propenamide, sodium
alkyl alkene sulfonate (1:1) and
sodium 2-methyl-2-[(1-oxo-2propen-1-yl) amino]-1propanesulfonate (1:1), potassium salt, peroxydisulfuric acid
([(ho)s(o)2]2o2) sodium salt
(1:2)-initiated.
(G) 2-propenoic acid, polymer with
N-(alkyl)-2propenamide, sodium
alkyl alkene sulfonate (1:1) and
sodium 2-methyl-2-[(1-oxo-2propen-1-yl) amino]-1propanesulfonate (1:1), potassium salt, peroxydisulfuric acid
([(ho)s(o)2]2o2) sodium salt
(1:2)-initiated.
(G) 2-propenoic acid, polymer with
N-(alkyl)-2propenamide, sodium
alkyl alkene sulfonate (1:1) and
sodium 2-methyl-2-[(1-oxo-2propen-1-yl) amino]-1propanesulfonate (1:1), sodium
salt, peroxydisulfuric acid
([(ho)s(o)2]2o2) sodium salt
(1:2)-initiated.
(G) 2-propenoic acid, polymer with
N-(alkyl)-2propenamide, sodium
alkyl alkene sulfonate (1:1) and
sodium 2-methyl-2-[(1-oxo-2propen-1-yl) amino]-1propanesulfonate (1:1), sodium
salt, peroxydisulfuric acid
([(ho)s(o)2]2o2) sodium salt
(1:2)-initiated.
(G) 2-propenoic acid, polymer with
N-(alkyl)-2propenamide, sodium
alkyl alkene sulfonate (1:1) and
sodium 2-methyl-2-[(1-oxo-2propen-1-yl) amino]-1propanesulfonate (1:1), sodium
salt, peroxydisulfuric acid
([(ho)s(o)2]2o2) sodium salt
(1:2)-initiated.
(G) 2-propenoic acid, polymer with
N-(alkyl)-2propenamide, sodium
alkyl alkene sulfonate (1:1) and
sodium 2-methyl-2-[(1-oxo-2propen-1-yl) amino]-1propanesulfonate (1:1), sodium
salt, peroxydisulfuric acid
([(ho)s(o)2]2o2) sodium salt
(1:2)-initiated.
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Federal Register / Vol. 81, No. 218 / Thursday, November 10, 2016 / Notices
TABLE 1—PMNS RECEIVED FROM SEPTEMBER 1, 2016 TO SEPTEMBER 30, 2016—Continued
Case No.
Received date
Projected
notice end
date
Manufacturer
importer
Use
Chemical
9/26/2016
12/25/2016
CBI ...................
(G) The anticipated use is as a
pigment dispersant.
P–16–0523 .......
9/26/2016
12/25/2016
CBI ...................
(G) As described above, the notified polymer will be use as a
pigment dispersant.
P–16–0523 .......
9/26/2016
12/25/2016
CBI ...................
(G) The anticipated use is as a
deposit control agent.
P–16–0523 .......
9/26/2016
12/25/2016
CBI ...................
(G) The anticipated use is as a
deposit control agent and pigment dispersant.
P–16–0528 .......
9/14/2016
12/13/2016
P–16–0528 .......
9/14/2016
12/13/2016
9/14/2016
12/13/2016
P–16–0528 .......
9/14/2016
12/13/2016
P–16–0528 .......
9/14/2016
12/13/2016
P–16–0537 .......
9/21/2016
12/20/2016
Shell Chemical
LP.
Shell Chemical
LP.
Shell Chemical
LP.
Shell Chemical
LP.
Shell Chemical
LP.
CBI ...................
(S) Metal workings fluids/rolling
oils.
(S) Coatings ...................................
P–16–0528 .......
P–16–0540 .......
9/28/2016
12/27/2016
CBI ...................
(G) Polymeric film former for coatings.
P–16–0541 .......
9/19/2016
12/18/2016
P–16–0545 .......
P–16–0546 .......
9/2/2016
9/16/2016
12/1/2016
12/15/2016
P–16–0547 .......
asabaliauskas on DSK3SPTVN1PROD with NOTICES
P–16–0523 .......
9/6/2016
12/5/2016
Specialty
Organics, Inc..
CBI ....................
Cardolite Corporation.
CBI ....................
(S) Adhesive for wood particle/
chip/fiberboard.
(G) Device chemical ......................
(S) GX–9203 is used for the adhesive application.
(G) Catalyst ...................................
P–16–0548 .......
P–16–0570 .......
9/8/2016
9/21/2016
12/7/2016
12/20/2016
CBI ....................
CBI ...................
P–16–0571 .......
9/14/2016
12/13/2016
CBI ...................
(G) Resin catalyst ..........................
(S) Aromatic polyester polyol for
rigid foam.
(G) Additive for coatings ................
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(S) Agrochemicals .........................
(S) Cleaning fluids .........................
(S) Sold as intermediate ................
(G) Masking photopolymer ............
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(G) 2-propenoic acid, polymer with
N-(alkyl)-2propenamide, sodium
alkyl alkene sulfonate (1:1) and
sodium 2-methyl-2-[(1-oxo-2propen-1-yl) amino]-1propanesulfonate (1:1), ammonium salt, peroxydisulfuric acid
([(ho)s(o)2]2o2) sodium salt
(1:2)-initiated.
(G) 2-propenoic acid, polymer with
N-(alkyl)-2propenamide, sodium
alkyl alkene sulfonate (1:1) and
sodium 2-methyl-2-[(1-oxo-2propen-1-yl) amino]-1propanesulfonate (1:1), ammonium salt, peroxydisulfuric acid
([(ho)s(o)2]2o2) sodium salt
(1:2)-initiated.
(G) 2-propenoic acid, polymer with
N-(alkyl)-2propenamide, sodium
alkyl alkene sulfonate (1:1) and
sodium 2-methyl-2-[(1-oxo-2propen-1-yl) amino]-1propanesulfonate (1:1), ammonium salt, peroxydisulfuric acid
([(ho)s(o)2]2o2) sodium salt
(1:2)-initiated.
(G) 2-propenoic acid, polymer with
N-(alkyl)-2propenamide, sodium
alkyl alkene sulfonate (1:1) and
sodium 2-methyl-2-[(1-oxo-2propen-1-yl) amino]-1propanesulfonate (1:1), ammonium salt, peroxydisulfuric acid
([(ho)s(o)2]2o2) sodium salt
(1:2)-initiated.
(S) Hydrocarbons, C16–22,
branched and linear.
(S) Hydrocarbons, C16–22,
branched and linear.
(S) Hydrocarbons, C16–22,
branched and linear.
(S) Hydrocarbons, C16–22,
branched and linear.
(S) Hydrocarbons, C16–22,
branched and linear.
(G) Formaldehyde phenol
isobenzofurandione polymer.
(G) Diphenolic compound, polymer
with 2-(chloromethyl)oxirane and
4,4′-methylenebis[di-alkyl-substituted phenol].
(S) Soybean meal, reaction products with phosphoric trichloride.
(G) Substituted siloxane polymer.
(G) Cashew, nutshell liquid, polymer with acid and halohydrin.
(G) Neodymium aluminum alkyl
catalyst.
(G) Triarylsulfonium salt.
(G) Aromatic polyester polyol.
(G) Alkyl alkenoate, alkanediyl,
polymer with alkyl alkenoate,
substituted carbomonocycle,
alkyl alkenoate and
heteromonocycle alkyl
alkenoate, diazene bis alkyl
heteromonocycle initiated.
10NON1
79025
Federal Register / Vol. 81, No. 218 / Thursday, November 10, 2016 / Notices
TABLE 1—PMNS RECEIVED FROM SEPTEMBER 1, 2016 TO SEPTEMBER 30, 2016—Continued
Case No.
Received date
Projected
notice end
date
Manufacturer
importer
Use
(S) Tackifier in hot melt adhesive
and pressure sensitive adhesive
formulation.
(G) Adhesive ingredient .................
(G) Adhesive for coating ...............
(G) Adhesive for coating particulate materials.
(G) Adhesive ingredient .................
(S) Tackifier in hot melt adhesive
and pressure sensitive adhesive
formulation.
(G) Adhesive for coating particulate materials.
(G) Adhesive for coating ...............
(S) Polymerization of glucose .......
Chemical
9/14/2016
12/13/2016
Hexion Inc ........
P–16–0572 .......
P–16–0572 .......
P–16–0572 .......
9/14/2016
9/14/2016
9/14/2016
12/13/2016
12/13/2016
12/13/2016
Hexion Inc ........
Hexion Inc ........
Hexion Inc ........
P–16–0573 .......
P–16–0573 .......
9/14/2016
9/14/2016
12/13/2016
12/13/2016
Hexion Inc ........
Hexion Inc ........
P–16–0573 .......
9/14/2016
12/13/2016
Hexion Inc ........
P–16–0573 .......
P–16–0575 .......
9/14/2016
9/15/2016
12/13/2016
12/14/2016
Hexion Inc ........
CBI ...................
P–16–0576 .......
P–16–0577 .......
P–16–0579 .......
9/16/2016
9/16/2016
9/19/2016
12/15/2016
12/15/2016
12/18/2016
CBI ...................
CBI ...................
Allnex USA Inc.
(G) Intermediate ............................
(G) Oil lubricant additive ................
(S) Ultraviolet (uv) curable coating
resin.
P–16–0580 .......
9/19/2016
12/18/2016
CBI ...................
P–16–0581
P–16–0581
P–16–0581
P–16–0581
P–16–0582
.......
.......
.......
.......
.......
9/19/2016
9/19/2016
9/19/2016
9/19/2016
9/20/2016
12/18/2016
12/18/2016
12/18/2016
12/18/2016
12/19/2016
CBI
CBI
CBI
CBI
CBI
(G) Synthetic aircraft engine lubricant for contained use industrial
lubricant.
(S) Polymer additive ......................
(S) Fiber additive ...........................
(S) Composite component .............
(S) Paper coating component .......
(S) Lubricity additive for industrial
oils And other lubricants.
P–16–0582 .......
9/20/2016
12/19/2016
CBI ...................
(S) Lubricity additive for automotive engine oil.
P–16–0583 .......
P–16–0584 .......
asabaliauskas on DSK3SPTVN1PROD with NOTICES
P–16–0572 .......
9/21/2016
9/22/2016
12/20/2016
12/21/2016
CBI ...................
CBI ...................
P–16–0585 .......
9/22/2016
12/21/2016
CBI ...................
P–16–0586 .......
9/22/2016
12/21/2016
CBI ...................
P–16–0587 .......
9/22/2016
12/21/2016
Kemira Chemicals.
(S) Sealant for head lamps of cars
(G) Additive used to impart specific physicochemical property(ies) to finished articles.
(G) Additive used to impart specific physicochemical property(ies) to finished articles.
(G) Additive used to impart specific physicochemical property(ies) to finished articles.
(S) Flocculant used in iron ore
processing plant.
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...................
...................
...................
...................
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(G) Polyamine polyacid adducts.
(G) Polyamine polyacid adducts.
(G) Polyamine polyacid adducts.
(G) Polyamine polyacid adducts.
(G) Polyamine polyacid adducts.
(G) Polyamine polyacid adducts.
(G) Polyamine polyacid adducts.
(G) Polyamine polyacid adducts.
(S) Glucosyltransferase—the
CASRN was determined using
the international union of biochemistry and molecular biology
(iubmb) enzyme nomenclature
recommendations for the noticed enzyme (see attachment—
iubmb nomenclature). reaction
catalyzed: sucrose+[(1--≤6)-?-dglucosyl]n = d-fructose + [(1--≤
6)-?-d-glucosyl]n+1iubmb number: 2.4.1.5 in addition to catalyzing the formation of alpha-1–
6-glucan linkages as specified in
the iubmb number 2.4.1.5, depending on the source organism
and gene, the
glycosyltransferase enzyme may
catalyze other alpha linkages including alpha 1–3 for the noticed enzyme and other linkages
(e.g. 1,4-, 1,6-).
(G) Modified alkyl polyamine.
(G) Alkyl polyamine.
(G) Waste plastics, poly(ethylene
terephthalate), depolymd. with
polypropylene glycol ether with
glycerol (3:1), polymers with
alkenoic and alkanoic acids.
(G) Trimethylolpropane ester of
mixed linear and branched carboxylic acids.
(G) Polysaccharide.
(G) Polysaccharide.
(G) Polysaccharide.
(G) Polysaccharide.
(G) Carboxylic acids, polyalkyl unsaturated, oligomers, polymers
with substituted alkyl alkenol
and alkylpolyol.
(G) Carboxylic acids, polyalkyl unsaturated, oligomers, polymers
with substituted alkyl alkenol
and alkylpolyol.
(G) Aromatic hydrocarbon resin.
(G) Multi-walled carbon
nanotubes.
(G) Multi-walled carbon
nanotubes.
(G) Muti-walled carbon nanotubes.
(S) Galactoarabinoxylan.
10NON1
79026
Federal Register / Vol. 81, No. 218 / Thursday, November 10, 2016 / Notices
TABLE 1—PMNS RECEIVED FROM SEPTEMBER 1, 2016 TO SEPTEMBER 30, 2016—Continued
Case No.
Received date
Projected
notice end
date
Manufacturer
importer
Use
Chemical
P–16–0588 .......
9/22/2016
12/21/2016
CBI ...................
(G) Additive for coatings ................
P–16–0589 .......
9/22/2016
12/21/2016
CBI ...................
P–16–0593 .......
9/28/2016
12/27/2016
CBI ...................
P–16–0594 .......
9/28/2016
12/27/2016
Chitec Technology Co.,
Ltd.
(G) Synthetic aircraft engine lubricant for contained use industrial
lubricant.
(S) Aromatic polyester polyol for
rigid foam.
(G) Ink additive ..............................
P–16–0595 .......
P–16–0596 .......
9/29/2016
9/29/2016
12/28/2016
12/28/2016
CBI ...................
Allnex USA Inc.
For the 21 NOCs received by EPA
during this period, Table 3 provides the
following information (to the extent that
such information is not claimed as CBI):
(G) Polymer ...................................
(S) Site limited intermediate used
for production of uv curable
coating resin.
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) Alkyl methacrylate, polymer
with alkyl acrylate and polyesters.
(G) Pentaerythritol ester of mixed
linear and branched carboxylic
acids.
(G) Aromatic polyester polyol.
(G) Alkanone, substituted oxyalkyl
substituted alkyl
carbomonocycle] substituted
dialkyl alkylcarbomonocycle.
(G) Polyether polyurethane.
(G) Alkenoic acid, reaction products with polyethylene glycol
ether with hydroxyalkyl substituted alkane.
submitter in the NOC; and the chemical
identity.
TABLE 2—NOCS RECEIVED FROM SEPTEMBER 1, 2016 TO SEPTEMBER 30, 2016
Case No.
Commencement
date
.......
.......
.......
.......
.......
9/9/2016
9/22/2016
9/1/2016
9/19/2016
9/21/2016
9/6/2016
8/23/2016
8/23/2016
8/25/2016
9/20/2016
P–13–0948 .......
P–15–0109 .......
9/9/2016
9/22/2016
8/31/2016
8/28/2016
P–15–0545 .......
P–15–0660 .......
9/28/2016
9/14/2016
9/19/2016
8/19/2016
P–15–0662 .......
9/14/2016
8/26/2016
P–15–0693 .......
9/2/2016
8/25/2016
P–15–0704 .......
9/6/2016
8/10/2016
P–15–0745 .......
9/12/2016
9/8/2016
P–16–0036
P–16–0094
P–16–0237
P–16–0263
P–16–0266
P–16–0272
P–16–0340
P–16–0392
asabaliauskas on DSK3SPTVN1PROD with NOTICES
P–05–0415
P–08–0724
P–11–0012
P–11–0424
P–12–0504
Received date
9/13/2016
9/27/2016
9/15/2016
9/8/2016
9/14/2016
9/9/2016
9/7/2016
9/23/2016
8/2/2016
9/24/2016
8/20/2016
8/11/2016
9/8/2016
8/24/2016
8/29/2016
9/6/2016
.......
.......
.......
.......
.......
.......
.......
.......
VerDate Sep<11>2014
17:46 Nov 09, 2016
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Chemical
(G) Acrylic polymer with styrene, peroxy-initiated.
(G) Cycloaliphatic anhydride, polymer with hydroxy alkyl diol, alkyl ester.
(G) Slump retainer in concrete.
(G) Alkenoyloxy arylphenone.
(G) Phosphinic acid, sodium salt (1:1), reaction products with alkenedioic anhydride
homopolymer, sodium salts.
(G) Amine phosphate.
(S) 1,2,4,5-benzenetetracarboxylic acid, mixed et and me esters, compds. with 4,4’methylenebis[benzeneamine]
mixed
et
and
me
4,4’-carbonylbis[1,2benzenedicarboxylate].
(G) Amine-functional acrylic polymer.
(G) Alicyclic anhydride, polymer with alkanepolyol, 2-(chloromethyl)oxirane, 4,4’-(1methylethylidene)bis[phenol] and cyclic ester.
(G) Alicyclic anhydride, polymer with alkanepolyol, 2-(chloromethyl)oxirane, ,
alkanediol,4,4’-(1-methylethylidene)bis[phenol] and cyclic ester.
(G) 1,2-ethanediamine, N1-(2-aminoethyl)-, reaction products with polyethylenimine
and polypropylene glycol -alkyl 3-(5-carboxy-1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)
ethers.
(S) Siloxanes and silicones, di-me, [(butylethenylmethylsilyl)oxy]- and hydrogen-terminated.
(G) Naturally-occurring minerals, reaction products with boron sodium oxide
(b4na2o7), hetero substituted alkyl acrylate polymer, kaolin and sodium silicate.
(G) Monohydroxy substituted heteropolycycle.
(G) Perfluoropolyether modified organosilane.
(S) 2-propenoic acid, dodecyl ester, polymer with 2-hydroxyethyl 2-propenoate.
(G) Alkene polymer with anhydride and imides.
(G) Polyester polyurethane polyol.
(S) Lecithins, soya, hydrogenated.
(G) Glycerides, C8–18 and C18 unsaturated, from algal fermentation.
(S) Soybean oil, mixed with hydrogenated soybean oil, interesterified.
Frm 00060
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10NON1
Federal Register / Vol. 81, No. 218 / Thursday, November 10, 2016 / Notices
Authority: 15 U.S.C. 2601 et seq.
Dated: October 27, 2016.
Pamela Myrick,
Director, Information Management Division,
Office of Pollution Prevention and Toxics.
[FR Doc. 2016–27195 Filed 11–9–16; 8:45 am]
BILLING CODE 6560–50–P
Nicholas_A._Fraser@omb.eop.gov; and
to Cathy Williams, FCC, via email PRA@
fcc.gov and to Cathy.Williams@fcc.gov.
Include in the comments the OMB
control number as shown in the
SUPPLEMENTARY INFORMATION section
below.
For
additional information or copies of the
information collection, contact Cathy
Williams at (202) 418–2918. To view a
copy of this information collection
request (ICR) submitted to OMB: (1) Go
to the Web page <https://
www.reginfo.gov/public/do/PRAMain>,
(2) look for the section of the Web page
called ‘‘Currently Under Review,’’ (3)
click on the downward-pointing arrow
in the ‘‘Select Agency’’ box below the
‘‘Currently Under Review’’ heading, (4)
select ‘‘Federal Communications
Commission’’ from the list of agencies
presented in the ‘‘Select Agency’’ box,
(5) click the ‘‘Submit’’ button to the
right of the ‘‘Select Agency’’ box, (6)
when the list of FCC ICRs currently
under review appears, look for the OMB
control number of this ICR and then
click on the ICR Reference Number. A
copy of the FCC submission to OMB
will be displayed.
SUPPLEMENTARY INFORMATION:
OMB Control No.: 3060–0360.
Title: Section 80.409, Station Logs
(Maritime Services).
Form No.: N/A.
Type of Review: Extension of a
currently approved collection.
Respondents: Business or other forprofit entities, not-for-profit institutions,
and state, local and tribal government.
Number of Respondents: 19,919
respondents; 19,919 responses.
Estimated Time per Response: 27.3–
95 hours.
Frequency of Response:
Recordkeeping requirement.
Obligation to Respond: Required to
obtain or retain benefits. The statutory
authority for this collection is contained
in 47 U.S.C. 151–155, 301–609.
Total Annual Burden: 561,188 hours.
Annual Cost Burden: None.
Privacy Act Impact Assessment: No
impact(s).
Nature and Extent of Confidentiality:
There is no need for confidentiality with
this collection of information.
Needs and Uses: The Commission
will submit this extension (no change in
the recordkeeping requirement) to the
OMB after this 60 day comment period
to obtain the full three-year clearance
from them. The information collection
requirements are as follows:
Section 80.409(c), Public Coast
Station Logs: This requirement is
necessary to document the operation
FOR FURTHER INFORMATION CONTACT:
FEDERAL COMMUNICATIONS
COMMISSION
[OMB 3060–0360]
Information Collection Being
Submitted for Review and Approval to
the Office of Management and Budget
Federal Communications
Commission.
ACTION: Notice and request for
comments.
AGENCY:
As part of its continuing effort
to reduce paperwork burdens, and as
required by the Paperwork Reduction
Act (PRA) of 1995 (44 U.S.C. 3501–
3520), the Federal Communication
Commission (FCC or Commission)
invites the general public and other
Federal agencies to take this
opportunity to comment on the
following information collections.
Comments are requested concerning:
Whether the proposed collection of
information is necessary for the proper
performance of the functions of the
Commission, including whether the
information shall have practical utility;
the accuracy of the Commission’s
burden estimate; ways to enhance the
quality, utility, and clarity of the
information collected; ways to minimize
the burden of the collection of
information on the respondents,
including the use of automated
collection techniques or other forms of
information technology; and ways to
further reduce the information
collection burden on small business
concerns with fewer than 25 employees.
The FCC may not conduct or sponsor
a collection of information unless it
displays a currently valid OMB control
number. No person shall be subject to
any penalty for failing to comply with
a collection of information subject to the
PRA that does not display a valid OMB
control number.
DATES: Written comments should be
submitted on or before December 12,
2016. If you anticipate that you will be
submitting comments, but find it
difficult to do so within the period of
time allowed by this notice, you should
advise the contacts below as soon as
possible.
ADDRESSES: Direct all PRA comments to
Nicholas A. Fraser, OMB, via email
asabaliauskas on DSK3SPTVN1PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
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79027
and public correspondence of public
coast radio telegraph, public coast
radiotelephone stations, and Alaska
public-fixed stations, including the
logging of distress and safety calls
where applicable. Entries must be made
giving details of all work performed
which may affect the proper operation
of the station. Logs must be retained by
the licensee for a period of two years
from the date of entry, and, where
applicable, for such additional periods
such as logs relating to a distress
situation or disaster must be retained for
three years from the date of entry in the
log. If the Commission has notified the
licensee of an investigation, the related
logs must be retained until the licensee
is specifically authorized in writing to
destroy them. Logs relating to any claim
or complaint of which the station
licensee has notice must be retained
until the claim or complaint has been
satisfied or barred by statute limiting the
time for filing suits upon such claims.
Section 80.409(d), Ship
Radiotelegraph Logs: Logs of ship
stations which are compulsorily
equipped for radiotelegraphy and
operating in the band 90 to 535 kHz
must contain specific information in log
entries according to this subsection.
Section 80.409(e), Ship
Radiotelephone Logs: Logs of ship
stations which are compulsorily
equipped for radiotelephony must
*62128 contain specific information in
applicable log entries and the time of
their occurrence.
The recordkeeping requirements
contained in section 80.409 is necessary
to document the operation and public
correspondence service of public coast
radiotelegraph, public coast
radiotelephone stations and Alaskapublic fixed stations, ship
radiotelegraph, ship radiotelephone and
applicable radiotelephone including the
logging of distress and safety calls
where applicable.
Federal Communications Commission.
Marlene H. Dortch,
Secretary, Office of the Secretary.
[FR Doc. 2016–27127 Filed 11–9–16; 8:45 am]
BILLING CODE 6712–01–P
FEDERAL ELECTION COMMISSION
Sunshine Act Meeting
Federal Election Commission.
Tuesday, November 15,
2016 at 10:00 a.m.
PLACE: 999 E Street NW., Washington,
DC.
STATUS: This meeting will be closed to
the public.
AGENCY:
DATE AND TIME:
E:\FR\FM\10NON1.SGM
10NON1
]]>Agencies
[Federal Register Volume 81, Number 218 (Thursday, November 10, 2016)]
[Notices]
[Pages 79020-79027]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-27195]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
[EPA-HQ-OPPT-2016-0484; FRL-9954-52]
Certain New Chemicals; Receipt and Status Information for
September 2016
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 notices
of commencement (NOC) to manufacture those chemicals. This document
covers the period from
[[Page 79021]]
September 1, 2016 to September 30, 2016.
DATES: Comments identified by the specific case number provided in this
document, must be received on or before December 12, 2016.
ADDRESSES: Submit your comments, identified by docket identification
(ID) number EPA-HQ-OPPT-2016-0484, 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 September 1, 2016 to September 30, 2016, 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, please 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 71 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 September 1, 2016 to September 30, 2016
----------------------------------------------------------------------------------------------------------------
Projected
Case No. Received date notice end Manufacturer Use Chemical
date importer
----------------------------------------------------------------------------------------------------------------
P-16-0379............ 9/26/2016 12/25/2016 CBI.................. (G) Intermediate (G) Vinyl
for polymer functional
synthesis. polymethylalkyl
polymer.
P-16-0399............ 9/16/2016 12/15/2016 Tryeco LLC........... (S) Compound to (S) Starch,
be used in polymer with 2-
preparation of propenoic acid,
advanced seed potassium salt.
coatings. oxidized.
[[Page 79022]]
P-16-0399............ 9/16/2016 12/15/2016 Tryeco LLC........... (S) Agricultural (S) Starch,
soil amendment polymer with 2-
for turf propenoic acid,
applications potassium salt.
and direct soil oxidized.
injection with
fertilizers.
P-16-0399............ 9/16/2016 12/15/2016 Tryeco LLC........... (S) Agricultural (S) Starch,
soil amendment polymer with 2-
for filed crops propenoic acid,
as ``agrisorb potassium salt.
plus'' granular oxidized.
soil amendment.
P-16-0429............ 9/20/2016 12/19/2016 CBI.................. (G) Universal (G) Endcapped
tint paste polysiloxane.
resin having
high solids.
P-16-0460............ 9/28/2016 12/27/2016 CBI.................. (G) Process aid. (G) Silane-
treated
aluminosilicate
.
P-16-0461............ 9/28/2016 12/27/2016 CBI.................. (G) Process aid. (G) Silane-
treated
aluminosilicate
.
P-16-0462............ 9/28/2016 12/27/2016 CBI.................. (G) Process aid. (G) Silane-
treated
aluminosilicate
.
P-16-0463............ 9/28/2016 12/27/2016 CBI.................. (G) Process aid. (G) Silane-
treated
aluminosilicate
.
P-16-0464............ 9/28/2016 12/27/2016 CBI.................. (G) Process aid. (G) Silane-
treated
aluminosilicate
.
P-16-0487............ 9/22/2016 12/21/2016 Jaychem LLC.......... (S) Mass (G)
coloration of Benzenesulfonic
paper. acid 1,2-
diazenediylbis[
6-ethenyl]-3-
sulfophenyl
diazenyl-2-
sulfophenyl
ethenyl salt.
P-16-0520............ 9/26/2016 12/25/2016 CBI.................. (G) As described (G) 2-propenoic
above, the acid, polymer
notified with N-(alkyl)-
polymer will be 2propenamide,
use as a sodium alkyl
pigment alkene
dispersant. sulfonate (1:1)
and sodium 2-
methyl-2-[(1-
oxo-2-propen-1-
yl) amino]-1-
propanesulfonat
e (1:1),
peroxydisulfuri
c acid
([(ho)s(o)2]2o2
) sodium salt
(1:2)-
initiated.
P-16-0520............ 9/26/2016 12/25/2016 CBI.................. (G) The (G) 2-propenoic
anticipated use acid, polymer
is as a deposit with N-(alkyl)-
control agent 2propenamide,
and pigment sodium alkyl
dispersant. alkene
sulfonate (1:1)
and sodium 2-
methyl-2-[(1-
oxo-2-propen-1-
yl) amino]-1-
propanesulfonat
e (1:1),
peroxydisulfuri
c acid
([(ho)s(o)2]2o2
) sodium salt
(1:2)-
initiated.
P-16-0520............ 9/26/2016 12/25/2016 CBI.................. (G) The (G) 2-propenoic
anticipated use acid, polymer
is as a pigment with N-(alkyl)-
dispersant. 2propenamide,
sodium alkyl
alkene
sulfonate (1:1)
and sodium 2-
methyl-2-[(1-
oxo-2-propen-1-
yl) amino]-1-
propanesulfonat
e (1:1),
peroxydisulfuri
c acid
([(ho)s(o)2]2o2
) sodium salt
(1:2)-
initiated.
P-16-0520............ 9/26/2016 12/25/2016 CBI.................. (G) The (G) 2-propenoic
anticipated use acid, polymer
is as a deposit with N-(alkyl)-
control agent. 2propenamide,
sodium alkyl
alkene
sulfonate (1:1)
and sodium 2-
methyl-2-[(1-
oxo-2-propen-1-
yl) amino]-1-
propanesulfonat
e (1:1),
peroxydisulfuri
c acid
([(ho)s(o)2]2o2
) sodium salt
(1:2)-
initiated.
P-16-0521............ 9/26/2016 12/25/2016 CBI.................. (G) The (G) 2-propenoic
anticipated use acid, polymer
is as a deposit with N-(alkyl)-
control agent. 2propenamide,
sodium alkyl
alkene
sulfonate (1:1)
and sodium 2-
methyl-2-[(1-
oxo-2-propen-1-
yl) amino]-1-
propanesulfonat
e (1:1),
potassium salt,
peroxydisulfuri
c acid
([(ho)s(o)2]2o2
) sodium salt
(1:2)-
initiated.
[[Page 79023]]
P-16-0521............ 9/26/2016 12/25/2016 CBI.................. (G) As described (G) 2-propenoic
above, the acid, polymer
notified with N-(alkyl)-
polymer will be 2propenamide,
use as a sodium alkyl
pigment alkene
dispersant. sulfonate (1:1)
and sodium 2-
methyl-2-[(1-
oxo-2-propen-1-
yl) amino]-1-
propanesulfonat
e (1:1),
potassium salt,
peroxydisulfuri
c acid
([(ho)s(o)2]2o2
) sodium salt
(1:2)-
initiated.
P-16-0521............ 9/26/2016 12/25/2016 CBI.................. (G) The (G) 2-propenoic
anticipated use acid, polymer
is as a deposit with N-(alkyl)-
control agent 2propenamide,
and pigment sodium alkyl
dispersant. alkene
sulfonate (1:1)
and sodium 2-
methyl-2-[(1-
oxo-2-propen-1-
yl) amino]-1-
propanesulfonat
e (1:1),
potassium salt,
peroxydisulfuri
c acid
([(ho)s(o)2]2o2
) sodium salt
(1:2)-
initiated.
P-16-0521............ 9/26/2016 12/25/2016 CBI.................. (G) The (G) 2-propenoic
anticipated use acid, polymer
is as a pigment with N-(alkyl)-
dispersant. 2propenamide,
sodium alkyl
alkene
sulfonate (1:1)
and sodium 2-
methyl-2-[(1-
oxo-2-propen-1-
yl) amino]-1-
propanesulfonat
e (1:1),
potassium salt,
peroxydisulfuri
c acid
([(ho)s(o)2]2o2
) sodium salt
(1:2)-
initiated.
P-16-0522............ 9/26/2016 12/25/2016 CBI.................. (G) As described (G) 2-propenoic
above, the acid, polymer
notified with N-(alkyl)-
polymer will be 2propenamide,
use as a sodium alkyl
pigment alkene
dispersant. sulfonate (1:1)
and sodium 2-
methyl-2-[(1-
oxo-2-propen-1-
yl) amino]-1-
propanesulfonat
e (1:1), sodium
salt,
peroxydisulfuri
c acid
([(ho)s(o)2]2o2
) sodium salt
(1:2)-
initiated.
P-16-0522............ 9/26/2016 12/25/2016 CBI.................. (G) The (G) 2-propenoic
anticipated use acid, polymer
is as a pigment with N-(alkyl)-
dispersant. 2propenamide,
sodium alkyl
alkene
sulfonate (1:1)
and sodium 2-
methyl-2-[(1-
oxo-2-propen-1-
yl) amino]-1-
propanesulfonat
e (1:1), sodium
salt,
peroxydisulfuri
c acid
([(ho)s(o)2]2o2
) sodium salt
(1:2)-
initiated.
P-16-0522............ 9/26/2016 12/25/2016 CBI.................. (G) The (G) 2-propenoic
anticipated use acid, polymer
is as a deposit with N-(alkyl)-
control agent 2propenamide,
and pigment sodium alkyl
dispersant. alkene
sulfonate (1:1)
and sodium 2-
methyl-2-[(1-
oxo-2-propen-1-
yl) amino]-1-
propanesulfonat
e (1:1), sodium
salt,
peroxydisulfuri
c acid
([(ho)s(o)2]2o2
) sodium salt
(1:2)-
initiated.
P-16-0522............ 9/26/2016 12/25/2016 CBI.................. (G) The (G) 2-propenoic
anticipated use acid, polymer
is as a deposit with N-(alkyl)-
control agent. 2propenamide,
sodium alkyl
alkene
sulfonate (1:1)
and sodium 2-
methyl-2-[(1-
oxo-2-propen-1-
yl) amino]-1-
propanesulfonat
e (1:1), sodium
salt,
peroxydisulfuri
c acid
([(ho)s(o)2]2o2
) sodium salt
(1:2)-
initiated.
[[Page 79024]]
P-16-0523............ 9/26/2016 12/25/2016 CBI.................. (G) The (G) 2-propenoic
anticipated use acid, polymer
is as a pigment with N-(alkyl)-
dispersant. 2propenamide,
sodium alkyl
alkene
sulfonate (1:1)
and sodium 2-
methyl-2-[(1-
oxo-2-propen-1-
yl) amino]-1-
propanesulfonat
e (1:1),
ammonium salt,
peroxydisulfuri
c acid
([(ho)s(o)2]2o2
) sodium salt
(1:2)-
initiated.
P-16-0523............ 9/26/2016 12/25/2016 CBI.................. (G) As described (G) 2-propenoic
above, the acid, polymer
notified with N-(alkyl)-
polymer will be 2propenamide,
use as a sodium alkyl
pigment alkene
dispersant. sulfonate (1:1)
and sodium 2-
methyl-2-[(1-
oxo-2-propen-1-
yl) amino]-1-
propanesulfonat
e (1:1),
ammonium salt,
peroxydisulfuri
c acid
([(ho)s(o)2]2o2
) sodium salt
(1:2)-
initiated.
P-16-0523............ 9/26/2016 12/25/2016 CBI.................. (G) The (G) 2-propenoic
anticipated use acid, polymer
is as a deposit with N-(alkyl)-
control agent. 2propenamide,
sodium alkyl
alkene
sulfonate (1:1)
and sodium 2-
methyl-2-[(1-
oxo-2-propen-1-
yl) amino]-1-
propanesulfonat
e (1:1),
ammonium salt,
peroxydisulfuri
c acid
([(ho)s(o)2]2o2
) sodium salt
(1:2)-
initiated.
P-16-0523............ 9/26/2016 12/25/2016 CBI.................. (G) The (G) 2-propenoic
anticipated use acid, polymer
is as a deposit with N-(alkyl)-
control agent 2propenamide,
and pigment sodium alkyl
dispersant. alkene
sulfonate (1:1)
and sodium 2-
methyl-2-[(1-
oxo-2-propen-1-
yl) amino]-1-
propanesulfonat
e (1:1),
ammonium salt,
peroxydisulfuri
c acid
([(ho)s(o)2]2o2
) sodium salt
(1:2)-
initiated.
P-16-0528............ 9/14/2016 12/13/2016 Shell Chemical LP.... (S) Metal (S)
workings fluids/ Hydrocarbons,
rolling oils. C16 22,
branched and
linear.
P-16-0528............ 9/14/2016 12/13/2016 Shell Chemical LP.... (S) Coatings.... (S)
Hydrocarbons,
C16 22,
branched and
linear.
P-16-0528............ 9/14/2016 12/13/2016 Shell Chemical LP.... (S) (S)
Agrochemicals. Hydrocarbons,
C16 22,
branched and
linear.
P-16-0528............ 9/14/2016 12/13/2016 Shell Chemical LP.... (S) Cleaning (S)
fluids. Hydrocarbons,
C16 22,
branched and
linear.
P-16-0528............ 9/14/2016 12/13/2016 Shell Chemical LP.... (S) Sold as (S)
intermediate. Hydrocarbons,
C16 22,
branched and
linear.
P-16-0537............ 9/21/2016 12/20/2016 CBI.................. (G) Masking (G) Formaldehyde
photopolymer. phenol
isobenzofurandi
one polymer.
P-16-0540............ 9/28/2016 12/27/2016 CBI.................. (G) Polymeric (G) Diphenolic
film former for compound,
coatings. polymer with 2-
(chloromethyl)o
xirane and 4,4'-
methylenebis[di-
alkyl-
substituted
phenol].
P-16-0541............ 9/19/2016 12/18/2016 Specialty Organics, (S) Adhesive for (S) Soybean
Inc.. wood particle/ meal, reaction
chip/fiberboard. products with
phosphoric
trichloride.
P-16-0545............ 9/2/2016 12/1/2016 CBI.................. (G) Device (G) Substituted
chemical. siloxane
polymer.
P-16-0546............ 9/16/2016 12/15/2016 Cardolite Corporation (S) GX-9203 is (G) Cashew,
used for the nutshell
adhesive liquid, polymer
application. with acid and
halohydrin.
P-16-0547............ 9/6/2016 12/5/2016 CBI.................. (G) Catalyst.... (G) Neodymium
aluminum alkyl
catalyst.
P-16-0548............ 9/8/2016 12/7/2016 CBI.................. (G) Resin (G)
catalyst. Triarylsulfoniu
m salt.
P-16-0570............ 9/21/2016 12/20/2016 CBI.................. (S) Aromatic (G) Aromatic
polyester polyester
polyol for polyol.
rigid foam.
P-16-0571............ 9/14/2016 12/13/2016 CBI.................. (G) Additive for (G) Alkyl
coatings. alkenoate,
alkanediyl,
polymer with
alkyl
alkenoate,
substituted
carbomonocycle,
alkyl alkenoate
and
heteromonocycle
alkyl
alkenoate,
diazene bis
alkyl
heteromonocycle
initiated.
[[Page 79025]]
P-16-0572............ 9/14/2016 12/13/2016 Hexion Inc........... (S) Tackifier in (G) Polyamine
hot melt polyacid
adhesive and adducts.
pressure
sensitive
adhesive
formulation.
P-16-0572............ 9/14/2016 12/13/2016 Hexion Inc........... (G) Adhesive (G) Polyamine
ingredient. polyacid
adducts.
P-16-0572............ 9/14/2016 12/13/2016 Hexion Inc........... (G) Adhesive for (G) Polyamine
coating. polyacid
adducts.
P-16-0572............ 9/14/2016 12/13/2016 Hexion Inc........... (G) Adhesive for (G) Polyamine
coating polyacid
particulate adducts.
materials.
P-16-0573............ 9/14/2016 12/13/2016 Hexion Inc........... (G) Adhesive (G) Polyamine
ingredient. polyacid
adducts.
P-16-0573............ 9/14/2016 12/13/2016 Hexion Inc........... (S) Tackifier in (G) Polyamine
hot melt polyacid
adhesive and adducts.
pressure
sensitive
adhesive
formulation.
P-16-0573............ 9/14/2016 12/13/2016 Hexion Inc........... (G) Adhesive for (G) Polyamine
coating polyacid
particulate adducts.
materials.
P-16-0573............ 9/14/2016 12/13/2016 Hexion Inc........... (G) Adhesive for (G) Polyamine
coating. polyacid
adducts.
P-16-0575............ 9/15/2016 12/14/2016 CBI.................. (S) (S)
Polymerization Glucosyltransfe
of glucose. rase--the CASRN
was determined
using the
international
union of
biochemistry
and molecular
biology (iubmb)
enzyme
nomenclature
recommendations
for the noticed
enzyme (see
attachment--iub
mb
nomenclature).
reaction
catalyzed:
sucrose+[(1--
>6)-?-d-
glucosyl]n = d-
fructose + [(1--
>6)-?-d-
glucosyl]n+1iub
mb number:
2.4.1.5 in
addition to
catalyzing the
formation of
alpha-1-6-
glucan linkages
as specified in
the iubmb
number 2.4.1.5,
depending on
the source
organism and
gene, the
glycosyltransfe
rase enzyme may
catalyze other
alpha linkages
including alpha
1-3 for the
noticed enzyme
and other
linkages (e.g.
1,4-, 1,6-).
P-16-0576............ 9/16/2016 12/15/2016 CBI.................. (G) Intermediate (G) Modified
alkyl
polyamine.
P-16-0577............ 9/16/2016 12/15/2016 CBI.................. (G) Oil (G) Alkyl
lubricant polyamine.
additive.
P-16-0579............ 9/19/2016 12/18/2016 Allnex USA Inc....... (S) Ultraviolet (G) Waste
(uv) curable plastics,
coating resin. poly(ethylene
terephthalate),
depolymd. with
polypropylene
glycol ether
with glycerol
(3:1), polymers
with alkenoic
and alkanoic
acids.
P-16-0580............ 9/19/2016 12/18/2016 CBI.................. (G) Synthetic (G)
aircraft engine Trimethylolprop
lubricant for ane ester of
contained use mixed linear
industrial and branched
lubricant. carboxylic
acids.
P-16-0581............ 9/19/2016 12/18/2016 CBI.................. (S) Polymer (G)
additive. Polysaccharide.
P-16-0581............ 9/19/2016 12/18/2016 CBI.................. (S) Fiber (G)
additive. Polysaccharide.
P-16-0581............ 9/19/2016 12/18/2016 CBI.................. (S) Composite (G)
component. Polysaccharide.
P-16-0581............ 9/19/2016 12/18/2016 CBI.................. (S) Paper (G)
coating Polysaccharide.
component.
P-16-0582............ 9/20/2016 12/19/2016 CBI.................. (S) Lubricity (G) Carboxylic
additive for acids,
industrial oils polyalkyl
And other unsaturated,
lubricants. oligomers,
polymers with
substituted
alkyl alkenol
and
alkylpolyol.
P-16-0582............ 9/20/2016 12/19/2016 CBI.................. (S) Lubricity (G) Carboxylic
additive for acids,
automotive polyalkyl
engine oil. unsaturated,
oligomers,
polymers with
substituted
alkyl alkenol
and
alkylpolyol.
P-16-0583............ 9/21/2016 12/20/2016 CBI.................. (S) Sealant for (G) Aromatic
head lamps of hydrocarbon
cars. resin.
P-16-0584............ 9/22/2016 12/21/2016 CBI.................. (G) Additive (G) Multi-walled
used to impart carbon
specific nanotubes.
physicochemical
property(ies)
to finished
articles.
P-16-0585............ 9/22/2016 12/21/2016 CBI.................. (G) Additive (G) Multi-walled
used to impart carbon
specific nanotubes.
physicochemical
property(ies)
to finished
articles.
P-16-0586............ 9/22/2016 12/21/2016 CBI.................. (G) Additive (G) Muti-walled
used to impart carbon
specific nanotubes.
physicochemical
property(ies)
to finished
articles.
P-16-0587............ 9/22/2016 12/21/2016 Kemira Chemicals..... (S) Flocculant (S)
used in iron Galactoarabinox
ore processing ylan.
plant.
[[Page 79026]]
P-16-0588............ 9/22/2016 12/21/2016 CBI.................. (G) Additive for (G) Alkyl
coatings. methacrylate,
polymer with
alkyl acrylate
and polyesters.
P-16-0589............ 9/22/2016 12/21/2016 CBI.................. (G) Synthetic (G)
aircraft engine Pentaerythritol
lubricant for ester of mixed
contained use linear and
industrial branched
lubricant. carboxylic
acids.
P-16-0593............ 9/28/2016 12/27/2016 CBI.................. (S) Aromatic (G) Aromatic
polyester polyester
polyol for polyol.
rigid foam.
P-16-0594............ 9/28/2016 12/27/2016 Chitec Technology (G) Ink additive (G) Alkanone,
Co., Ltd. substituted
oxyalkyl
substituted
alkyl
carbomonocycle]
substituted
dialkyl
alkylcarbomonoc
ycle.
P-16-0595............ 9/29/2016 12/28/2016 CBI.................. (G) Polymer..... (G) Polyether
polyurethane.
P-16-0596............ 9/29/2016 12/28/2016 Allnex USA Inc....... (S) Site limited (G) Alkenoic
intermediate acid, reaction
used for products with
production of polyethylene
uv curable glycol ether
coating resin. with
hydroxyalkyl
substituted
alkane.
----------------------------------------------------------------------------------------------------------------
For the 21 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 2--NOCs Received From September 1, 2016 to September 30, 2016
----------------------------------------------------------------------------------------------------------------
Commencement
Case No. Received date date Chemical
----------------------------------------------------------------------------------------------------------------
P-05-0415............................ 9/9/2016 9/6/2016 (G) Acrylic polymer with styrene,
peroxy-initiated.
P-08-0724............................ 9/22/2016 8/23/2016 (G) Cycloaliphatic anhydride, polymer
with hydroxy alkyl diol, alkyl
ester.
P-11-0012............................ 9/1/2016 8/23/2016 (G) Slump retainer in concrete.
P-11-0424............................ 9/19/2016 8/25/2016 (G) Alkenoyloxy arylphenone.
P-12-0504............................ 9/21/2016 9/20/2016 (G) Phosphinic acid, sodium salt
(1:1), reaction products with
alkenedioic anhydride homopolymer,
sodium salts.
P-13-0948............................ 9/9/2016 8/31/2016 (G) Amine phosphate.
P-15-0109............................ 9/22/2016 8/28/2016 (S) 1,2,4,5-benzenetetracarboxylic
acid, mixed et and me esters,
compds. with 4,4'-
methylenebis[benzeneamine] mixed et
and me 4,4'-carbonylbis[1,2-
benzenedicarboxylate].
P-15-0545............................ 9/28/2016 9/19/2016 (G) Amine-functional acrylic polymer.
P-15-0660............................ 9/14/2016 8/19/2016 (G) Alicyclic anhydride, polymer with
alkanepolyol, 2-
(chloromethyl)oxirane, 4,4'-(1-
methylethylidene)bis[phenol] and
cyclic ester.
P-15-0662............................ 9/14/2016 8/26/2016 (G) Alicyclic anhydride, polymer with
alkanepolyol, 2-
(chloromethyl)oxirane, ,
alkanediol,4,4'-(1-
methylethylidene)bis[phenol] and
cyclic ester.
P-15-0693............................ 9/2/2016 8/25/2016 (G) 1,2-ethanediamine, N1-(2-
aminoethyl)-, reaction products with
polyethylenimine and polypropylene
glycol -alkyl 3-(5-carboxy-1,3-
dihydro-1,3-dioxo-2H-isoindol-2-yl)
ethers.
P-15-0704............................ 9/6/2016 8/10/2016 (S) Siloxanes and silicones, di-me,
[(butylethenylmethylsilyl)oxy]- and
hydrogen-terminated.
P-15-0745............................ 9/12/2016 9/8/2016 (G) Naturally-occurring minerals,
reaction products with boron sodium
oxide (b4na2o7), hetero substituted
alkyl acrylate polymer, kaolin and
sodium silicate.
P-16-0036............................ 9/13/2016 8/2/2016 (G) Monohydroxy substituted
heteropolycycle.
P-16-0094............................ 9/27/2016 9/24/2016 (G) Perfluoropolyether modified
organosilane.
P-16-0237............................ 9/15/2016 8/20/2016 (S) 2-propenoic acid, dodecyl ester,
polymer with 2-hydroxyethyl 2-
propenoate.
P-16-0263............................ 9/8/2016 8/11/2016 (G) Alkene polymer with anhydride and
imides.
P-16-0266............................ 9/14/2016 9/8/2016 (G) Polyester polyurethane polyol.
P-16-0272............................ 9/9/2016 8/24/2016 (S) Lecithins, soya, hydrogenated.
P-16-0340............................ 9/7/2016 8/29/2016 (G) Glycerides, C8 18 and C18
unsaturated, from algal
fermentation.
P-16-0392............................ 9/23/2016 9/6/2016 (S) Soybean oil, mixed with
hydrogenated soybean oil,
interesterified.
----------------------------------------------------------------------------------------------------------------
[[Page 79027]]
Authority: 15 U.S.C. 2601 et seq.
Dated: October 27, 2016.
Pamela Myrick,
Director, Information Management Division, Office of Pollution
Prevention and Toxics.
[FR Doc. 2016-27195 Filed 11-9-16; 8:45 am]
BILLING CODE 6560-50-P
