Certain New Chemicals; Receipt and Status Information for March 2019, 28799-28811 [2019-13099]
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Vallejo, in Solano County, California.
The sole purpose of a preliminary
permit, if issued, is to grant the permit
holder priority to file a license
application during the permit term. A
preliminary permit does not authorize
the permit holder to perform any landdisturbing activities or otherwise enter
upon lands or waters owned by others
without the owners’ express permission.
The proposed project would consist of
a floating power platform located at Cal
Maritime’s property and use marine
hydrokinetic technologies to generate
approximately 41,610 megawatt hours
annually. The floating platform would
measure 120-feet-long by 40-feet-wide,
and 14-feet-deep. Cal Maritime proposes
to use the power generated by the
project on its campus and distribute the
excess power through an interconnect
with Pacific Gas and Electric Company’s
Colgate-Oakland transmission line.
Applicant Contact: Franz Lozano,
Vice President & CFO, California State
University Maritime Academy, 200
Maritime Academy, Vallejo, CA 94590;
phone: (707) 654–1038; or via email at:
flozano@csum.edu.
FERC Contact: Kenneth Hogan;
phone: (202) 502–8434; or email at:
Kenneth.Hogan@ferc.gov.
Deadline for filing comments, motions
to intervene, competing applications
(without notices of intent), or notices of
intent to file competing applications: 60
days from the issuance of this notice.
Competing applications and notices of
intent must meet the requirements of 18
CFR 4.36.
The Commission strongly encourages
electronic filing. Please file comments,
motions to intervene, notices of intent,
and competing applications using the
Commission’s eFiling system at https://
www.ferc.gov/docs-filing/efiling.asp.
Commenters can submit brief comments
up to 6,000 characters, without prior
registration, using the eComment system
at https://www.ferc.gov/docs-filing/
ecomment.asp. You must include your
name and contact information at the end
of your comments. For assistance,
please contact FERC Online Support at
FERCOnlineSupport@ferc.gov, (866)
208–3676 (toll free), or (202) 502–8659
(TTY). In lieu of electronic filing, please
send a paper copy to: Secretary, Federal
Energy Regulatory Commission, 888
First Street NE, Washington, DC 20426.
The first page of any filing should
include docket number P–14986–000.
More information about this project,
including a copy of the application, can
be viewed or printed on the ‘‘eLibrary’’
link of Commission’s website at https://
www.ferc.gov/docs-filing/elibrary.asp.
Enter the docket number (P–14986–000)
in the docket number field to access the
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document. For assistance, contact FERC
Online Support.
Dated: June 14, 2019.
Nathaniel J. Davis, Sr.,
Deputy Secretary.
[FR Doc. 2019–13136 Filed 6–19–19; 8:45 am]
BILLING CODE 6717–01–P
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPPT–2019–0075; FRL–9992–77]
Certain New Chemicals; Receipt and
Status Information for March 2019
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
EPA is required under the
Toxic Substances Control Act (TSCA),
as amended by the Frank R. Lautenberg
Chemical Safety for the 21st Century
Act, to make information publicly
available and to publish information in
the Federal Register pertaining to
submissions under TSCA Section 5,
including notice of receipt of a
Premanufacture notice (PMN),
Significant New Use Notice (SNUN) or
Microbial Commercial Activity Notice
(MCAN), including an amended notice
or test information; an exemption
application (Biotech exemption); an
application for a test marketing
exemption (TME), both pending and/or
concluded; a notice of commencement
(NOC) of manufacture (including
import) for new chemical substances;
and a periodic status report on new
chemical substances that are currently
under EPA review or have recently
concluded review. This document
covers the period from 03/01/2019 to
03/31/2019.
DATES: Comments identified by the
specific case number provided in this
document must be received on or before
July 22, 2019.
ADDRESSES: Submit your comments,
identified by docket identification (ID)
number EPA–HQ–OPPT–2019–0075,
and the specific case number for the
chemical substance 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
SUMMARY:
PO 00000
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28799
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, Information Management
Division (7407M), Office of Pollution
Prevention and Toxics, Environmental
Protection Agency, 1200 Pennsylvania
Ave. NW, Washington, DC 20460–0001;
telephone number: (202) 564–8593;
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. Executive Summary
What action is the Agency taking?
This document provides the receipt
and status reports for the period from
03/01/2019 to 03/31/2019. The Agency
is providing notice of receipt of PMNs,
SNUNs and MCANs (including
amended notices and test information);
an exemption application under 40 CFR
part 725 (Biotech exemption); TMEs,
both pending and/or concluded; NOCs
to manufacture a new chemical
substance; and a periodic status report
on new chemical substances that are
currently under EPA review or have
recently concluded review.
EPA is also providing information on
its website about cases reviewed under
the amended TSCA, including the
section 5 PMN/SNUN/MCAN and
exemption notices received, the date of
receipt, the final EPA determination on
the notice, and the effective date of
EPA’s determination for PMN/SNUN/
MCAN notices on its website at: https://
www.epa.gov/reviewing-new-chemicalsunder-toxic-substances-control-act-tsca/
status-pre-manufacture-notices. This
information is updated on a weekly
basis.
B. What is the Agency’s authority for
taking this action?
Under the TSCA, 15 U.S.C. 2601 et
seq., a chemical substance may be either
an ‘‘existing’’ chemical substance or a
‘‘new’’ chemical substance. Any
chemical substance that is not on EPA’s
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TSCA Inventory of Chemical Substances
(TSCA Inventory) is classified as a ‘‘new
chemical substance,’’ while a chemical
substance that is listed on the TSCA
Inventory is classified as an ‘‘existing
chemical substance.’’ (See TSCA section
3(11).) For more information about the
TSCA Inventory go to: https://
www.epa.gov/tsca-inventory.
Any person who intends to
manufacture (including import) a new
chemical substance for a non-exempt
commercial purpose, or to manufacture
or process a chemical substance in a
non-exempt manner for a use that EPA
has determined is a significant new use,
is required by TSCA section 5 to
provide EPA with a PMN, MCAN or
SNUN, as appropriate, before initiating
the activity. EPA will review the notice,
make a risk determination on the
chemical substance or significant new
use, and take appropriate action as
described in TSCA section 5(a)(3).
TSCA section 5(h)(1) authorizes EPA
to allow persons, upon application and
under appropriate restrictions, to
manufacture or process a new chemical
substance, or a chemical substance
subject to a significant new use rule
(SNUR) issued under TSCA section
5(a)(2), for ‘‘test marketing’’ purposes,
upon a showing that the manufacture,
processing, distribution in commerce,
use, and disposal of the chemical will
not present an unreasonable risk of
injury to health or the environment.
This 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 and 8 and
EPA regulations, EPA is required to
publish in the Federal Register certain
information, including notice of receipt
of a PMN/SNUN/MCAN (including
amended notices and test information);
an exemption application under 40 CFR
part 725 (biotech exemption); an
application for a TME, both pending
and concluded; NOCs to manufacture a
new chemical substance; and a periodic
status report on the new chemical
substances that are currently under EPA
review or have recently concluded
review.
C. Does this action apply to me?
This action provides information that
is directed to the public in general.
D. Does this action have any
incremental economic impacts or
paperwork burdens?
No.
E. What should I consider as I prepare
my comments for EPA?
1. Submitting confidential business
information (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. Status Reports
In the past, EPA has published
individual notices reflecting the status
of TSCA section 5 filings received,
pending or concluded. In 1995, the
Agency modified its approach and
streamlined the information published
in the Federal Register after providing
notice of such changes to the public and
an opportunity to comment (See the
Federal Register of May 12, 1995, (60
FR 25798) (FRL–4942–7). Since the
passage of the Lautenberg amendments
to TSCA in 2016, public interest in
information on the status of section 5
cases under EPA review and, in
particular, the final determination of
such cases, has increased. In an effort to
be responsive to the regulated
community, the users of this
information, and the general public, to
comply with the requirements of TSCA,
to conserve EPA resources and to
streamline the process and make it more
timely, EPA is providing information on
its website about cases reviewed under
the amended TSCA, including the
section 5 PMN/SNUN/MCAN and
exemption notices received, the date of
receipt, the final EPA determination on
the notice, and the effective date of
EPA’s determination for PMN/SNUN/
MCAN notices on its website at: https://
www.epa.gov/reviewing-new-chemicalsunder-toxic-substances-control-act-tsca/
status-pre-manufacture-notices. This
information is updated on a weekly
basis.
III. Receipt Reports
For the PMN/SNUN/MCANs that
have passed an initial screening by EPA
during this period, Table I provides the
following information (to the extent that
such information is not subject to a CBI
claim) on the notices screened by EPA
during this period: The EPA case
number assigned to the notice that
indicates whether the submission is an
initial submission, or an amendment, a
notation of which version was received,
the date the notice was received by EPA,
the submitting manufacturer (i.e.,
domestic producer or importer), the
potential uses identified by the
manufacturer in the notice, and the
chemical substance identity.
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 this information in the
table is generic information because the
specific information provided by the
submitter was claimed as CBI.
Submissions which are initial
submissions will not have a letter
following the case number. Submissions
which are amendments to previous
submissions will have a case number
followed by the letter ‘‘A’’ (e.g., P–18–
1234A). The version column designates
submissions in sequence as ‘‘1’’, ‘‘2’’,
‘‘3’’, etc. Note that in some cases, an
initial submission is not numbered as
version 1; this is because earlier
version(s) were rejected as incomplete
or invalid submissions. Note also that
future versions of the following tables
may adjust slightly as the Agency works
to automate population of the data in
the tables.
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TABLE I—PMN/SNUN/MCANS APPROVED* FROM 03/01/2019 TO 03/31/2019
Case No.
Version
J–19–0018 ...........
2
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Manufacturer
Use
CBI ......................
(G) Protein production .....................
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Chemical substance
(G) Protein-producing modified
microorganism, with
chromosomally-borne modifications.
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TABLE I—PMN/SNUN/MCANS APPROVED* FROM 03/01/2019 TO 03/31/2019—Continued
Case No.
Version
J–19–0019 ...........
1
3/20/2019
Danisco US, Inc.
(G) Production of an enzyme substance.
J–19–0020 ...........
1
3/20/2019
Danisco US, Inc ..
(G) Production of an enzyme substance.
P–16–0225A ........
2
3/14/2019
International Flavors.
P–16–0422A ........
4
3/20/2019
Polymer Additives
Inc.
(S) The notified substance will be
used as a fragrance ingredient,
being blended (mixed) with other
fragrance ingredients to make fragrance oils that will be sold to industrial and commercial customers for their incorporation into
soaps, detergents, cleaners, air
fresheners, candles and other
similar industrial, household and
consumer products.
(G) Additive for Polymers ................
P–16–0493A ........
7
2/7/2019
CBI ......................
(G) Paint ..........................................
P–16–0593A ........
4
2/22/2019
Emery
Oleochemicals.
(S) Aromatic polyester polyol for
rigid foam.
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Use
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Chemical substance
(G) Genetically modified microorganism for the production of an enzyme substance.
(G) Genetically modified microorganism for the production of an enzyme substance.
(S) isomer mixture of Cyclohexanol,
4-ethylidene-2-propoxy- (CAS
1631145–48–6) (35–45%) and
Cyclohexanol, 5-ethylidene-2propoxy.
(S) 1,2-Cyclohexanedicarboxylic
acid, 1-(phenylmethyl) ester, ester
with 2,2,4-trimethyl-1,3pentanediol mono(2methylpropanoate).
(G) Dicarboxylic acids, polymers
with alkyl prop-2-enoate, alkyl 2methylprop-2-enoate, alkyl [(alkenyl) alkyl] alkanediol, alkanediol,
alkanedioic acid, alkyl 2methylprop-2-enoate, alkyl prop2-enoic acid, alkylene
[Isocyanatocarbomonocyle] and
alkanediol, alkanolamineblocked, compds with 2(alkylamino)alkanol.
(G) Aromatic Polyester Polyol.
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TABLE I—PMN/SNUN/MCANS APPROVED* FROM 03/01/2019 TO 03/31/2019—Continued
Case No.
Version
P–17–0108A ........
5
P–17–0240A ........
Manufacturer
Use
2/27/2019
Crison LLC ..........
2
3/1/2019
Ashland, Inc ........
(G) The product of this PMN is typically added at a rate of 3–5% of
the collector package. The product is added after the grinding of
the ore, along with copious
amounts of water to enable the
flotation of the desired mineral.
The product binds to the target
mineral and makes it hydrophobic, enabling the dissolved
gas flotation system to float the
target mineral. The collected target mineral concentrate (with the
product bound to them) is then
sent to a metullurgy plant for further purification. The high temperature processing results in all
the organics (including the product) being burned off. The resulting combustion products are
scrubbed as required by the
mettullurgical plants permits. A
very small amount of product settles with the larger particles of ore
that contain target mineral. This
product goes with the gangue to
the tailing ponds. The tailing
ponds have their own set of permits but are isolated with various
membrane and other groundwater
protection methods that are beyond the scope of this application. It is worth noting that only 3–
5% of the collector package at
this time is made up of the product of this PMN. The chemistry is
an incremental improvement on
the currently commercially practiced collection method, containing the same functional
groups and similar solubilities.
Thus, the product of this PMN is
readily detected or measured with
current monitoring at the use
sites. Because the product is
added at a stage where large
amounts of water are also added,
the current international users
wash the drums with large
amounts of water, and the wash
water is added to the process
with the prime material as it is
added.
(G) Encapsulanting polymer ............
P–17–0240A ........
3
3/7/2019
Ashland, Inc ........
(G) Encapsulanting polymer ............
P–17–0312A ........
7
2/20/2019
CBI ......................
(G)Additive for electrocoat formulas
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Chemical substance
(S) Carbonodithioic acid, O-[2[(dithiocarboxy)amino]-2methylpropyl] ester, sodium salt
(1:2).
(G) Alkenoic acid, polymer with
alkanepolyolpolyacrylate, 2,2′azobis[2-methylbutanenitrile]-initiated.
(G) Alkenoic acid, polymer with
alkanepolyolpolyacrylate, 2,2′azobis[2-methylbutanenitrile]-initiated.
(G) Organic acid, compds. with
bisphenol A-epichlorohydrin-polypropylene glycol diglycidyl ether
polymer-disubstituted polypropylene glycol reaction products.
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TABLE I—PMN/SNUN/MCANS APPROVED* FROM 03/01/2019 TO 03/31/2019—Continued
Case No.
Version
P–17–0313A ........
7
P–17–0314A ........
Manufacturer
Use
Chemical substance
2/20/2019
CBI ......................
(G)Additive for electrocoat formulas
7
2/20/2019
CBI ......................
(G)Additive for electrocoat formulas
P–17–0315A ........
7
2/20/2019
CBI ......................
(G)Additive for electrocoat formulas
P–17–0316A ........
7
2/20/2019
CBI ......................
(G)Additive for electrocoat formulas
P–17–0317A ........
7
2/20/2019
CBI ......................
(G)Additive for electrocoat formulas
P–17–0375A ........
4
2/8/2019
CBI ......................
(G) Paint additive .............................
P–17–0395A ........
P–18–0036A ........
4
5
2/7/2019
2/8/2019
CBI ......................
CBI ......................
(G) Water treatment additive ...........
(G) Water repellant ..........................
P–18–0064A ........
2
2/25/2019
CBI ......................
(G) Intermediate ...............................
P–18–0069A ........
2
2/20/2019
(G) Polymer performance additive ..
P–18–0085A ........
2
3/5/2019
Sasol Chemicals
(USA), LLC.
CBI ......................
(G) Phenol, 4,4′-(1methylethylidene) bis-, polymer
with 2-(chloromethyl) oxirane and
alpha-(2-oxiranylmethyl)-omega(2-oxiranylmethoxy)
poly[oxy(methyl-1,2-ethanediyl)],
reaction products with
disubstituted amine and
disubstituted polypropylene glycol, organic acid salts.
(G) Organic acid, 2-substituted-,
compds. with bisphenol Aepichlorohydrin-polypropylene glycol diglycidyl ether polymerdisubstituted aminedisubstituted
polypropylene glycol reaction
products.
(G) Phenol, 4,4′-(1methylethylidene) bis-, polymer
with alpha-(2-substitutedmethylethyl)-omega-(2-substituted-methylethoxy)
poly[oxy(methyl-1,2-ethanediyl)],
2-(chloromethyl) oxirane and
alpha-(2-oxiranylmethyl)-omega(2-oxiranylmethoxy)
poly[oxy(methyl-1,2-ethanediyl)],
alkylphenyl ethers, reaction products with disubstituted amine, organic acid salts.
(G) Organic acid, compds. with
bisphenol A-epichlorohydrindisubstituted polypropylene glycol-polypropylene glycol diglycidyl
ether polymer alkylphenyl ethersdisubstituted amine reaction products.
(G) Organic acid, compds. with
bisphenol A-epichlorohydrin-polypropylene glycol diglycidyl ether
polymer-disubstituted polypropylene glycol reaction products.
(G) 2-Oxepanone, polymer with
diisocyanatohexane, alkyl((hydroxyalkyl)-alkanediol and
isocyanato-(isocyanatoalkyl)trialkylcyclohexane, di-alkyl
malonate- and polyalkylene glycol
mono-Me ether-blocked, reaction
products with (methylalkyl)propanamine.
(G) Alkyl tri dithiocarbmate tri salt.
(S) Siloxanes and Silicones, di-Me,
3- [3-carboxy-2(or 3)- (octenyl)-1oxopropoxy] propyl group-terminated.
(G) Fluorinated carboxylate esters
and fluorinated alkoxyalkyl
heterocycles.
(G) Surface modified boehmite.
(G) Industrial use in oilfield ..............
P–18–0106A ........
3
2/25/2019
CBI ......................
(S) Process aid ................................
P–18–0120A ........
4
3/19/2019
Designer Molecules, Inc.
(G) Adhesive component .................
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(G) Fatty acids reaction products
with ethyleneamines and dialkyl
ester.
(G) Perfluoro[(alkenyl)oxy] alkane-,
manuf. of, by-products from,
distn. residues.
(S) 1H-Pyrrole-2,5-dione, 1,1′-C36alkylenebis-.
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TABLE I—PMN/SNUN/MCANS APPROVED* FROM 03/01/2019 TO 03/31/2019—Continued
Case No.
Version
Received date
P–18–0131A ........
4
3/5/2019
P–18–0169A ........
7
P–18–0175A ........
Manufacturer
Use
Chemical substance
Coim USA, Inc ....
(S) Polyol prepolymer in polyester
foam applications.
2/15/2019
C. L. Hauthaway
& Sons Corp.
(G) Protective coating ......................
6
2/12/2019
Hexion, Inc ..........
(S) Food can coating; ......................
(S) Non-food contact can coating ....
P–18–0219A ........
6
3/5/2019
CBI ......................
(G) Intermediate for topcoat ............
P–18–0247A ........
3
3/13/2019
CBI ......................
(S) Crosslinker for automotive
electrocoat.
P–18–0248A ........
3
3/13/2019
CBI ......................
(S) Crosslinker for automotive
electrocoat.
P–18–0249A ........
3
3/13/2019
CBI ......................
(S) Crosslinker for automotive
electrocoat.
P–18–0250A ........
3
3/13/2019
CBI ......................
(S) Crosslinker for automotive
electrocoat.
P–18–0251A ........
3
3/13/2019
CBI ......................
(S) Crosslinker for automotive
electrocoat.
P–18–0252A ........
3
3/13/2019
CBI ......................
(S) Crosslinker for automotive
electrocoat.
P–18–0258A ........
2
3/7/2019
CBI ......................
(G) Copolyamide for packaging
films; (G) Copolyamide for
monofilamen; (G) Copolyamide
for molding parts.
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(G) Soybean oil, polymer with
mixed difunctional glycols, glycerol, melamine, phthalic anhydride, poyethylene glycol, and
terephathalic acid.
(G) Propanoic acid, 3-hydroxy-2(hydroxymethyl)-2-methyl-, polymer with dimethyl carbonate, 1,6hexanediol, diamine and 1,1′methylenebis[4isocyanatocyclohexane], acrylateblocked, compds. with
triethylamine.
(S) Formaldehyde, polymer with 4(1,1-dimethylethyl) phenol and
phenol, Bu ether.
(G) Polythioether, short chain diol
polymer terminated with aliphatic
diisocyanate.
(G) Isocyanic acid,
polymethylenepolyphenylene
ester, polymer with 2-ethyl-2(hydroxymethyl)-1,3-propanediol,
polyetherpolyol, ¿, ¿′-[(1methylethylidene) di-4,1-phenylene] bis[¿-hydroxypoly(oxy-1,2ethanediyl)] and 1,2-propanediol,
iso-Bu alc.- and 2-butoxyethanoland 2-(2-butoxyethoxy) ethanoland Et alc.- and methanol- and 1methoxy-2-propanol-blocked.
(G) Isocyanic acid,
polymethylenepolyphenylene
ester, polymer with
polyetherpolyol, 2-butoxyethanoland 2-(2-butoxyethoxy) ethanoland methanolblocked.
(G) Isocyanic acid,
polymethylenepolyphenylene
ester, polymer with
polyetherpolyol, 2-butoxyethanoland 2-(2-butoxyethoxy) ethanoland methanoland 1-methoxy-2propanol-blocked.
(G) Isocyanic acid,
polymethylenepolyphenylene
ester, polymer with
polyetherpolyol, 2-butoxyethanoland 2-(2-butoxyethoxy) ethanoland 1(or2) -(2methoxymethylethoxy) propanolblocked.
(S) Isocyanic acid,
polymethylenepolyphenylene
ester, 2-butoxyethanol- and 2-(2butoxyethoxy) ethanol- and
methanol- and 1(or2) -(2methoxymethylethoxy) propanolblocked.
(S) Isocyanic acid,
polymethylenepolyphenylene
ester, 2-butoxyethanol- and 2-(2butoxyethoxy) ethanol- and
methanol- and 1-methoxy-2-propanol-blocked.
(G) Dioic acids, polymers with
caprolactam and alkyldiamines.
20JNN1
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TABLE I—PMN/SNUN/MCANS APPROVED* FROM 03/01/2019 TO 03/31/2019—Continued
Case No.
Version
P–18–0259A ........
2
P–18–0262A ........
Manufacturer
Use
3/7/2019
CBI ......................
4
2/14/2019
Seppic .................
(G) Copolyamide for packaging
films; (G) Copolyamide for
monofilamen; (G) Copolyamide
for molding parts.
(S) Function: Stabilizer of suspensions, Applications: Detergency,
treatment of physical surfaces,
development of soaps; (S) Function: thickener, Applications:
Paints, adhesive; (S) Function:
polishes, Applications: Wood
care, leather care.
P–18–0270A ........
4
3/8/2019
Specialty Elements, LLC.
P–18–0271A ........
4
3/8/2019
Specialty Elements, LLC.
P–18–0272A ........
2
2/26/2019
CBI ......................
P–18–0274A ........
5
3/13/2019
CBI ......................
P–18–0275A ........
2
3/13/2019
CBI ......................
(S) Chemical intermediate; (G) Additive.
(G) Polymer additive ........................
P–18–0282A ........
11
3/7/2019
Ashland, Inc ........
(G) Adhesive ....................................
P–18–0283A ........
4
3/1/2019
CBI ......................
(G)Open, non-dispersive use ..........
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Chemical substance
(G) Fatty acids, dimers, hydrogenated, polymers with
caprolactam and alkyl diamine.
(S) Active co-solvent for solventbased coatings; (S) Coalescent
for industrial water-based coatings; (S) Coupling agent and solvent in industrial cleaners, rust removers, hard surface cleaners,
and disinfectants; (S) Primary solvent in solvent-based silk screen
printing inks; (S) Coupling agent
for resins and dyes in waterbased printing inks; (S) Other
uses include a co- solvent for agricultural pesticides and may be
used in the production of a wide
variety of products and commodities such as polyester resins, engine coolants, latex paints, heat
transfer fluids and deicing compounds, lubricants, plasticizers
and cement grinding additives.
(S) Film forming coalescent for architectural coatings; (S) Film
forming coalescent for consumer
architectural coatings; (S) Film
forming coalescent for automotive
OEM coatings (electrodeposition
primers); (S) Film forming coalescent for can and coil coatings;
(S) Film forming coalescent for industrial wood coatings; (S) Film
forming coalescent for floor
polishes; (S) Film forming coalescent for industrial maintenance
coatings; (S) Film forming coalescent for marine and wood
coatings; (S) Film forming coalescent for consumer marine and
wood coatings; (S) Film forming
coalescent for transportation coatings; (S) Other uses include
Graphic Arts—Printing Inks (Lithographic and Letterpress oilbased inks), Reactive Intermediate—Ester Derivatives for
Plasticizers.
(G) Polymer composite additive ......
Fmt 4703
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E:\FR\FM\20JNN1.SGM
(S) 2-Propenoic acid, 2-methyl-,
dodecyl ester, polymer with ammonium 2-methyl-2-[(1-oxo-2propen-1-yl) amino]-1propanesulfonate (1:1), N, N-dimethyl-2-propenamide and.
alpha-(2-methyl-1-oxo-2-propen1-yl)-omega-(dodecyloxy)
poly(oxy-1,2-ethanediyl).
(G) Ethanol, 2-butoxy-, 1,1′-ester.
(G) 2-Propanol, 1-butoxy-, 2,2′ester.
(G) Metal, alkylcarboxylate oxo
complexes.
(G) Heterocycle fluoroalkyl sulfonyl.
(G) Methanone phenylene
fluoroalkyl sulfonyl heterocycle.
(G) Fatty acid ester, polyether,
diisocyanate polymer.
(G) Hydroxy alkanoic acid, compds.
with aminoalkoxyalcohol-epoxy
polymer-alkanolamine reaction
products.
20JNN1
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TABLE I—PMN/SNUN/MCANS APPROVED* FROM 03/01/2019 TO 03/31/2019—Continued
Case No.
Version
P–18–0283A ........
5
P–18–0284A ........
Manufacturer
Use
Chemical substance
3/11/2019
CBI ......................
(G)Open, non-dispersive use ..........
2
3/1/2019
CBI ......................
(G) Polymer composite additive ......
P–18–0292A ........
2
2/19/2019
CBI ......................
(G) Use in print resins .....................
P–18–0292A ........
3
3/21/2019
CBI ......................
(G) Use in print resins .....................
P–18–0300A ........
2
2/8/2019
CBI ......................
(S) Additive for automatic dishwashing detergent.
P–18–0313A ........
4
3/19/2019
Ashland Inc .........
(G) Adhesive ....................................
P–18–0322A ........
6
2/7/2019
CBI ......................
P–18–0327A ........
P–18–0341A ........
4
3
3/21/2019
3/15/2019
CBI ......................
CBI ......................
(G) The notified substance is used
as a fragrance ingredient in consumer products.
(G) Filler for non-dispersive resins ..
(G) Component in coatings .............
(G) Hydroxy alkanoic acid, compds.
with aminoalkoxyalcohol-epoxy
polymer-alkanolamine reaction
products.
(G) Inorganic acid, reaction products with alkyl alcohol.
(G) Alkanediol, polymer with 5isocyanato-1-(isocyanatomethyl)1,3,3-trimethylcyclohexane,
alkylaminoalkyl methacrylateblocked.
(G) Alkanediol, polymer with 5isocyanato-1-(isocyanatomethyl)1,3,3-trimethylcyclohexane,
alkylaminoalkyl methacrylateblocked.
(G) Heteromonocycle, alkenoic 1:1
salt, polymer with alpha-(2-methyl-1-oxo-2-propen-1-y) lomegamethoxypoly(oxy-1,2ethanediyl) and methyl-alkenoic
acid.
(G) Alkoxylated glycol ether with
1,2-propanediol, reaction products
with alkyl alcohol blocked 1,1′methylenebis [4isocyanatobenzene] homopolymer
and 1,1′-methylenebis [4isocyanatobenzene].
(G) Heteromonocycle, 4,6-dimethyl2-(1-phenylethyl)-.
P–18–0342A ........
3
3/15/2019
CBI ......................
(G) Component in coatings .............
P–18–0343A ........
3
3/15/2019
CBI ......................
(G) Component in coatings .............
P–18–0344A ........
3
3/15/2019
CBI ......................
(G) Component in coatings .............
P–18–0346A ........
3
3/4/2019
Chitec Technology Co., Ltd.
(S) Antioxidant compounded into
various polymers to be used in
extrusion processes to fabricate
articles.
P–18–0381A ........
2
3/19/2019
P–18–0387A ........
3
2/11/2019
The Shepherd
(G) For use in exterior paints and
Color Company.
plastics; (G) For use in coatings;
(G) For use in high temperature
engineering polymers; (G) For
use in artist materials.
CBI ...................... (G) Plastic additive ..........................
P–18–0388A ........
3
2/11/2019
CBI ......................
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17:47 Jun 19, 2019
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(G) Plastic additive ..........................
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(G) Mixed metal oxide.
(G) Alkane dicarboxylic acid, polymer with alkoxylated polyalcohol,
alkyl polyglycol, alkyl dialcohol,
and functionalized carboxylic
acid.
(G) Alkane dicarboxylic acid, polymer with alkyl polyglycol, alkyl
dialcohol, and functionalized carboxylic acid.
(G) Alkane dicarboxylic acid, polymer with alkoxylated polyalcohol,
and alkyl dialcohol, (hydroxy
alkyl) ester.
(G) Aromatic dicarboxylic acid, polymer with alkane dicarboxylic acid,
alkoxylated polyalcohol, and alkyl
dialcohol.
(S) 2,4,8,10-Tetraoxa-3,9diphosphaspiro [5.5] undecane,
3,9-bis-[2-(1-methyl-1phenylethyl)-4-(1,1,3,3tetramethylbutyl) phenoxy]-.
(S) Indium manganese yttrium
oxide.
(G) Alkanal, reaction products with
alkanediyl bis[alkyl-tris(alkylheterocycle)-1,3,5-triazine-2,4,6triamine and hydrogen peroxide.
(G) 1,3,5-triazine-2,4,6-triamine,
alkanediyl bis[alkyl-tris(alkylheterocycle)-, allyl derivs.,
oxidized, hydrogenated.
20JNN1
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TABLE I—PMN/SNUN/MCANS APPROVED* FROM 03/01/2019 TO 03/31/2019—Continued
Case No.
Version
P–18–0389A ........
2
P–18–0393A ........
Manufacturer
Use
Chemical substance
3/13/2019
CBI ......................
(G) Component in package coatings
2
3/15/2019
CBI ......................
(G) Paint ..........................................
P–18–0394A ........
2
2/25/2019
CBI ......................
(G) Chemical Intermediate ..............
P–18–0402A ........
3
3/11/2019
CBI ......................
(G) Fuel additive ..............................
P–19–0009A ........
4
2/7/2019
Allnex USA, Inc.
(S) The PMN substance is used as
a coating resin additive for corrosion protection.
P–19–0012A ........
9
3/11/2019
CBI ......................
P–19–0015A ........
3
3/1/2019
CBI ......................
P–19–0021A ........
2
2/13/2019
CBI ......................
(S) Resin component for the
polyisocyanurate; (S) Resin component in specialty polyurethane
kits and systems for aerospace
and military applications.
(S) Emulsifier for use in asphalt applications.
(G) Pigment ink ................................
(G) Alkenoic acid, alkyl-substituted,
epoxy ester, polymer with alkyl
alkenoate, alkene, and
polylactide.
(G) Alkenoic acid, alkyl, alkyl ester,
polymer with alkyl propenoate,
vinyl carbomonocyle, substituted
alkyl propenoate, alkyl 2-alkyl 2propenoate, alkanediol mono(2alkyl-2-propenoate) and
bicarbomonocylo alkyl 2-alkyl-2alkenoate, tertiary alkyl substituted alkane peroxoate initiated.
(G) Substituted benzylic ether polyethylene glycol alkyl ether derivative.
(G) Phenol, alkanepolyolbis
(heteroalkylene)bis-, polyalkylene
derivs.
(G) Carbonmonocycles, polymer
with haloalkyl substituted
heteromonocycle and hydrohydroxypoly[oxy(alkyl-alkanediyl)],
dialkyl-alkanediamineterminated,
hydroxyalkylated, acetates (salts).
(G) Benzenedicarboxylic acid,
rection products with
isobenzofurandione and
diethylene glycol.
P–19–0022A ........
2
2/13/2019
CBI ......................
(G) Pigment ink ................................
P–19–0025A ........
P–19–0026A ........
2
4
2/21/2019
2/27/2019
Bercen, Inc .........
Allnex USA, Inc.
P–19–0028A ........
P–19–0032A ........
6
4
2/22/2019
3/18/2019
CBI ......................
Presidium USA,
Inc.
(G) Hydrophobe formulation ............
(S) The PMN substance is an isolated intermediate incorporated as
a component in several imported
allnex coating resin products that
are only applied by Cathodic
Electrodeposition (CED) and used
as additives for corrosion protection.
(G) Lubricating oil additive ...............
(G) Polyol used in the manufacture
of articles made of a polyurethane thermoset material.
P–19–0034A ........
3
3/15/2019
CBI ......................
P–19–0038A ........
3
2/7/2019
P–19–0050A ........
3
3/11/2019
VerDate Sep<11>2014
18:52 Jun 19, 2019
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Jkt 247001
Allan Chemical
Corporation.
Kimes Technologies International, Inc.
PO 00000
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(G) Contained use as a component
of tires.
(S) Ink carrier for the ceramic industries.
(S) Rust preventative .......................
Fmt 4703
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E:\FR\FM\20JNN1.SGM
(G) Alkyl cyclic amide.
(G) Hydroxyalkyl carboxylic acid,
polymer with alkylamine, alkylene
carbonate, alkanediol, isocyanate,
compd. with alkylamine.
(G) Hydroxyalkyl carboxylic acid,
polymer with alkylamine, alkyl
carbonate, alkanediol, isocyanate,
compd. with alkylamine.
(S) 11-Docosene.
(G) Alkanoic acid, compds. with
substituted carbomonocycledialkyl-alkanediaminehalosubstitued heteromonocyclepolyalkylene glycol
polymerdialkanolamine reaction
products.
(G) Alkyl salicylate, metal salts.
(G) Carbonic dichloride, polymer
with 4,4′-(1-methylethylidene)
bis[phenol] ester, polymer with
tetrol and polyether tetrol.
(G) Metal, bis (2,4-pentanedionatokO2, kO4)-, (T-4)-.
(S) Fatty acids, coco, iso-Bu esters.
(S) Hydrocarbon waxes (petroleum),
oxidized, Bu esters.
20JNN1
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TABLE I—PMN/SNUN/MCANS APPROVED* FROM 03/01/2019 TO 03/31/2019—Continued
Case No.
Version
P–19–0053A ........
2
P–19–0064 ...........
Manufacturer
Use
3/13/2019
Wacker Chemical
Corporation.
1
3/4/2019
The Sherwin Williams Company.
(S) Used as a surface treatment,
sealant, caulk, and coating for
mineral building materials such as
concrete, brick, limestone, and
plaster, as well as on wood,
metal and other substrates. Formulations containing the crosslinker provide release and antigraffiti properties, water
repellency, weather proofing, and
improved bonding in adhesive/
sealant applications. The new
substance is a moisture curing
cross-linking agent which binds/
joins polymers together when
cured. Ethanol is released during
cure, and once the cure reaction
is complete, the product will remain bound in the cured polymer
matrix.
(G) Polymeric film former for coatings.
P–19–0064A ........
2
3/18/2019
The Sherwin Williams Company.
(G) Polymeric film former for coatings.
P–19–0065 ...........
4
3/22/2019
eScientia Technologies, LLC.
P–19–0066 ...........
4
3/22/2019
eScientia Technologies, LLC.
(S) Fire retardant for thermal plastics: Application: This product is
the environmental protection
Phosphazene flame retardant. It
does not produce pollutants after
burning. It is mainly used in PC
and ABS resins. It has good
flame retardancy on epoxy resin,
it can be used to make EMC for
IC Packaging, its flame
retardancy is much better than
Brominated flame retardant, the
flame retardancy can reach UL–
94V0 grade. Oxygen index could
reach 33.1%. When it is used in
Benzoxazine Resin glass cloth
laminate, if the HPCTP is 10%,
the grade of burning could reach
V–0 grade, the parallel breakdown voltage is 47KV. When it is
used in Polyethylene, the LOI of
final flame retardancy polyethylene could reach 30–33. After
used in viscose spinning solution,
we could get the flame retardant
viscose fiber with oxygen index
25.3–26.7. If the added amount is
12% in PC/ABS, it could pass the
UL–94 V0 test. It also can be
used in LED, powder coating,
potting material and polymers.
(S) Fire retardant .............................
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Chemical substance
(S) 1-Butanamine, N-butyl-N[(triethoxysilyl)methyl]-.
(G) 4,4′-methylenebis [2,6-dimethyl
phenol] polymer with 2(chloromethyl) oxirane, 1,4-benzyl
diol, 2-methyl-2-propenoic acid,
butyl 2-methyl 2-propenoate, ethyl
2-methyl 2-propenoate, and ethyl
2-propenoate, reaction products
with 2-(dimethylamino) ethanol.
(G) 4,4′-methylenebis [2,6-dimethyl
phenol] polymer with 2(chloromethyl) oxirane, 1,4-benzyl
diol, 2-methyl-2-propenoic acid,
butyl 2-methyl 2-propenoate, ethyl
2-methyl 2-propenoate, and ethyl
2-propenoate, reaction products
with 2-(dimethylamino) ethanol.
(S) 2lambda5, 4lambda5,
6lambda5—1,3,5,2,4,6
Triazatriphosphorine,
2,2,4,4,6,6—hexaphenoxy-.
(S) 2lambda5, 4lambda5,—
1,3,5,2,4,6 Triazatriphosphorine,
2,2,4,4,6,6, -hexaphenoxy.
20JNN1
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TABLE I—PMN/SNUN/MCANS APPROVED* FROM 03/01/2019 TO 03/31/2019—Continued
Case No.
Version
P–19–0067 ...........
2
P–19–0069 ...........
Received date
Manufacturer
Use
Chemical substance
3/19/2019
CBI ......................
(G) Triglyceride, reactions products
with diethylenetriamine.
1
3/19/2019
CBI ......................
(G) On site consumption as a raw
material in the production of
downstream chemicals, (G) Production of water-soluble corrosion
inhibitors; (G) Production of oil
soluble corrosion inhibitors..
(G) Curing agent for coatings ..........
P–19–0070 ...........
1
3/22/2019
CBI ......................
(G) Curing agent for coatings ..........
P–19–0071 ...........
1
3/22/2019
CBI ......................
P–19–0072 ...........
1
3/26/2019
CBI ......................
(S) Physical property modifier for
polymers.
(G) Raw material used in chemical
manufacture.
SN–18–0005A ......
3
3/3/2019
CBI ......................
(G) Monomer for industrial adhesives, coatings and inks.
SN–18–0013A ......
SN–18–0016A ......
2
4
2/27/2019
3/20/2019
CBI ......................
Hexion, Inc ..........
(G) Intermediate ...............................
(G) Reactive polymer; (S) Reactive
polyol for composites; (S) Reactive polyol for 2- part coatings; (S)
Reactive polyol for 1- part coatings; (S) Reactive polyol for
sealants; (S) Reactive modifier for
bonded abrasives; (S) Reactive
modifier for refractory; (S) Reactive modifier for glass inserts; (S)
Reactive modifier for coated abrasives; (S) Reactive modifier for
friction; (S) Reactive modifier for
fiber bonding; (S) Reactive modifier for carbon (liquid EPF); (S)
Reactive modifier for carbon
(powder EPF).
(G) Diisocyanatoalkane,
homopolymer, di-alkyl malonateand alkyl acetoacetate-blocked,
isoalkyl methylalkyl esters.
(G) Oxacyclanone, polymer with
diisocyanatoalkane, and alkyl(substitutedalkyl)-polyol, di-alkyl
malonate- and alkyl acetoacetateblocked, alkyl esters.
(G) Trimethylolpropane, alkenoic
acid, triester.
(S) 1-Butanol, reaction products
with 2-[(2-propen-1-yloxy)- methyl] oxirane.
(S) Butanoic acid, 3-mercapto-,1,1′[2,2-bis[(3-mercapto-1-oxobutoxy)
methyl]-1,3-propanediyl] ester.
(G) Lithiated metal oxide.
(G) Modified phenol-formaldehyde
resin.
*The term ‘Approved’ indicates that a submission has passed a quick initial screen ensuring all required information and documents have been
provided with the submission prior to the start of the 90-day review period, and in no way reflects the final status of a complete submission
review.
In Table II of this unit, EPA provides
the following information (to the extent
that such information is not claimed as
CBI) on the NOCs that have passed an
initial screening by EPA during this
period: The EPA case number assigned
to the NOC including whether the
submission was an initial or amended
submission, the date the NOC was
received by EPA, the date of
commencement provided by the
submitter in the NOC, a notation of the
type of amendment (e.g., amendment to
generic name, specific name, technical
contact information, etc.) and chemical
substance identity.
TABLE II—NOCS APPROVED * FROM 03/01/2019 TO 03/31/2019
jbell on DSK3GLQ082PROD with NOTICES
Case No.
Received date
Commencement date
If amendment,
type of
amendment
P–07–0541A .......
3/27/2019
11/14/2007
P–11–0294 .........
3/5/2019
3/24/2014
Generic chemical
name updated.
N ........................
P–11–0450 .........
P–11–0451 .........
2/28/2019
2/28/2019
2/17/2019
2/17/2019
N ........................
N ........................
P–11–0452 .........
P–14–0382 .........
2/28/2019
3/8/2019
2/17/2019
2/13/2019
N ........................
N ........................
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18:52 Jun 19, 2019
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Chemical substance
(G) Diaminodiol, polymer with diisocyanate, polyether alcohol,
polyether amine, benzyl chloride-quaternized.
(S) Carbonic dichloride, polymer with 4,4′-(1methylethylidene)bis(phenol) and 4,4′-(3,3,5trimethylcyclohexylidene)bis(phenol)), bis(4-(1,1dimethylethyl)phenyl) ester.
(S) Fatty acids, carnauba-wax.
(S) Fatty acids, carnauba wax, esters with 1,3-butanediol;
(S) Fatty acids, Carnauba-wax, calcium salts.
(S) Fatty acids, carnauba-wax, ethylene esters.
(G) Quaternary ammonium compounds, tri-C8–10-alkylmethyl, hydrogen sulfates.
Sfmt 4703
E:\FR\FM\20JNN1.SGM
20JNN1
28810
Federal Register / Vol. 84, No. 119 / Thursday, June 20, 2019 / Notices
TABLE II—NOCS APPROVED * FROM 03/01/2019 TO 03/31/2019—Continued
Case No.
Received date
Commencement date
If amendment,
type of
amendment
P–16–0360 .........
3/22/2019
3/17/2019
N ........................
P–16–0421 .........
P–17–0354 .........
P–18–0030 .........
3/18/2019
3/4/2019
3/22/2019
2/20/2019
2/4/2019
3/14/2019
N ........................
N ........................
N ........................
P–18–0123 .........
P–18–0124 .........
P–18–0136 .........
3/6/2019
3/6/2019
3/22/2019
2/20/2019
2/21/2019
2/22/2019
N ........................
N ........................
N ........................
P–18–0233 .........
3/4/2019
2/13/2019
N ........................
P–18–0318 .........
3/5/2019
3/4/2019
N ........................
Chemical substance
(S) Poly (oxy-1,2-ethanediyl), alpha- (1-oxodocosyl)- omega- [(1oxodocosyl)oxy]-.
(S) Flue dust, glass manufacturing, desulfurization.
(G) (substituted-dialkyl(C=1∼7)silyl) alkanenitrile.
(G) Poly[oxy(methyl-alkylendiyl)],alpha,alpha′,alpha″-1,2,3alkanetriyltris[omega-hydroxy-, polymer with 1,1′-alkylenebis[4isocyanatocarbomonocycle], 2-substituted ethyl acrylate- and 2-substituted ethyl metacrylate-blocked.
(S) Hydrogen lithium nickel oxide.
(S) Lithium nickel potassium oxide.
(G) 1-Butanaminium,N,N,N-tributyl-,2(or5)[[benzoyldihydrodioxo[(sulfophenyl)amino]heteropolycycle]oxy]5(or2)-(1,1-dimethylpropyl)benzenesulfonate (2:1).
(G) Alkyl Alkenoic acid, alkyl ester, telomer with alkylthiol, substituted
carbomonocycle, substituted alkyl alkyl alkenoate and hydroxyalkyl
alkenoate, tert-butyl alkyl peroxoate-initiated.
(S) 1-Octadecanaminium, N,N-dimethyl-N-[3-(triethoxysilyl)propyl]chloride.
* The term ‘Approved’ indicates that a submission has passed a quick initial screen ensuring all required information and documents have been
provided with the submission.
In Table III of this unit, EPA provides
the following information (to the extent
such information is not subject to a CBI
claim) on the test information that have
passed an initial screening by EPA
during this time period: The EPA case
number assigned to the test information;
the date the test information was
received by EPA, the type of test
information submitted, and chemical
substance identity.
TABLE III—TEST INFORMATION RECEIVED FROM 03/01/2019 TO 03/31/2019
jbell on DSK3GLQ082PROD with NOTICES
Case No.
Received date
Type of test information
Chemical substance
P–08–0087 .....
3/15/2019
Hydrolysis as a Function (OECD 111) ......................................................
P–08–0508 .....
3/25/2019
P–08–0509 .....
3/25/2019
P–10–0060 .....
3/21/2019
P–15–0450 .....
P–16–0543 .....
3/20/2019
3/14/2019
In Vitro Mammalian Cytogenetic Test (OECD 473), Mutagenicity Testing of H–2O421 in the Salmonella Typhimurium Plate Incorporation
Assay (OECD 473), Combined Two-Week Inhalation Toxicity and
Micronucleus Studies, Thermal Transformation Byproduct, Determination of the Water Solubility and Vapor Pressure of H–28327 (OECD
104–105), Determination of the n-Octanol/Water Partition Coefficient
of H–28327 (OPPTS 830.7560).
In Vitro Mammalian Cytogenetic Test (OECD 473), Mutagenicity Testing of H–2O421 in the Salmonella Typhimurium Plate Incorporation
Assay (OECD 473), Combined Two-Week Inhalation Toxicity and
Micronucleus Studies, Thermal Transformation Byproduct, Determination of the Water Solubility and Vapor Pressure of H–28327 (OECD
104–105), Determination of the n-Octanol/Water Partition Coefficient
of H–28327 (OPPTS 830.7560).
Studies for Triggered Testing: (OECD 421), Modified One-Generation
Reproduction Test (Mice) (OPPTS 850.3050).
90-Day Inhalation Toxicity Study (OECD 413) .........................................
Exposure Monitoring Report .....................................................................
P–18–0060 .....
3/26/2019
Sediment and Soil Adsorption/Desorption Isotherm (OECD 106), Acute
Dermal Toxicity (OECD 402), Mammalian Erythrocyte Micronucleus
Test (OECD 474).
P–18–0093 .....
3/1/2019
Dust Control, Analytical Test Results, Water Immersion Testing, H2O
Immersion with Proton Pulse Sequence, Plastic Abrasions SEM Summary and SEM Images, Risks Identified in Focus Report.
P–18–0177 .....
3/5/2019
Solubility in Alga Growth Media (OECD 201) ...........................................
P–18–0286 .....
3/8/2019
Supplemental Worker Exposure ...............................................................
P–18–0293 .....
3/21/2019
In Vitro Skin Sensitization Assays (OECD 422D) .....................................
P–18–0294 .....
3/21/2019
In Vitro Skin Sensitization Assays (OECD 422D) .....................................
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18:52 Jun 19, 2019
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(G) Alkyl acids, reaction products
with metal salt of an alkanol.
(S) Propanoic acid, 2,3,3,3tetrafluoro-2-(1,1,2,2,3,3,3heptafluoropropoxy).
(S) Propanoic acid, 2,3,3,3tetrafluoro-2-(1,1,2,2,3,3,3heptafluoropropoxy)-, ammonium
salt (1:1).
(G) Partially fluorinated alcohol substituted glycol.
(G) Lithium mixed metal oxide.
(G) Halogenophosphoric acid metal
salt.
(S) 1-butanaminium, 4-amino-N-(2hydroxy-3-sulfopropyl)-N, N-dimethyl-4-oxo-, N-coco alkyl
derivs., inner salts.
(G) Pentacyclo
[9.5.1.13,9.15,15.17,13]
octasiloxane, 1,3,5,7,9,11,13,15octakis (polyfluoroalkyl).
(S) Waxes and waxy substances,
rice bran, oxidized.
(S) Propane, 1,1,1,3,3,3-hexafluoro2-methoxy.
(S) Propanedioic acid, 2-methylene-, 1,3-dihexyl ester.
(S) Propanedioic acid, 2-methylene-, 1,3-dicyclohexyl ester.
20JNN1
Federal Register / Vol. 84, No. 119 / Thursday, June 20, 2019 / Notices
28811
TABLE III—TEST INFORMATION RECEIVED FROM 03/01/2019 TO 03/31/2019—Continued
Case No.
Received date
P–18–0325 .....
3/18/2019
SN–18–0003 ..
3/5/2019
Type of test information
Fish Acute Toxicity (OECD 203), Daphnia Acute Toxicity (OECD 202),
Algae Acute Toxicity (OECD 201), Acute Oral Toxicity (OECD 401),
Acute Dermal Toxicity (OECD 402), Dermal Irritation (OECD 404),
Eye Irritation (OECD 405), Ready Biodegradability (OECD 301B), Activated Sludge Respiration Inhibition Tests (OECD 209), Ames Test
(OECD 471), Skin Sensitization (OECD 406), Chromosome Aberration Test (OECD 473), 28-Day Oral Toxicity Study (OECD 407).
Algae Growth Inhibition Study (OECD 201) .............................................
If you are interested in information
that is not included in these tables, you
may contact EPA’s technical
information contact or general
information contact as described under
FOR FURTHER INFORMATION CONTACT to
access additional non-CBI information
that may be available.
Authority: 15 U.S.C. 2601 et seq.
Dated: June 6, 2019.
Megan Carroll,
Acting Director, Information Management
Division, Office of Pollution Prevention and
Toxics.
[FR Doc. 2019–13099 Filed 6–19–19; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
[FRL–9995–46–OAR]
Alternative Methods for Calculating
Off-Cycle Credits Under the Light-Duty
Vehicle Greenhouse Gas Emissions
Program: Application From Toyota
Motor North America, Inc.
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
EPA is requesting comment
on an application from Toyota Motor
North America, Inc. (‘‘Toyota’’) for offcycle carbon dioxide (CO2) credits
under EPA’s light-duty vehicle
greenhouse gas emissions standards.
‘‘Off-cycle’’ emission reductions can be
achieved by employing technologies
that result in real-world benefits, but
where that benefit is not adequately
captured on the test procedures used by
manufacturers to demonstrate
compliance with emission standards.
EPA’s light-duty vehicle greenhouse gas
program acknowledges these benefits by
giving automobile manufacturers several
options for generating ‘‘off-cycle’’ CO2
credits. Under the regulations, a
manufacturer may apply for CO2 credits
for off-cycle technologies that result in
off-cycle benefits. In these cases, a
manufacturer must provide EPA with a
proposed methodology for determining
jbell on DSK3GLQ082PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
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Chemical substance
Jkt 247001
the real-world off-cycle benefit. Toyota
has submitted an application that
describes methodologies for
determining off-cycle credits from
technologies described in their
application. Pursuant to applicable
regulations, EPA is making Toyota’s offcycle credit calculation methodologies
available for public comment.
Comments must be received on
or before July 22, 2019.
DATES:
Submit your comments,
identified by Docket ID No. EPA–HQ–
OAR–2019–0333, to the Federal
eRulemaking Portal: https://
www.regulations.gov. Follow the online
instructions for submitting comments.
Once submitted, comments cannot be
edited or withdrawn. The EPA may
publish any comment received to its
public docket. Do not submit
electronically any information you
consider to be Confidential Business
Information (CBI) or other information
whose disclosure is restricted by statute.
Multimedia submissions (audio, video,
etc.) must be accompanied by a written
comment. The written comment is
considered the official comment and
should include discussion of all points
you wish to make. The EPA will
generally not consider comments or
comment contents located outside of the
primary submission (i.e. on the web,
cloud, or other file sharing system). For
additional submission methods, the full
EPA public comment policy,
information about CBI or multimedia
submissions, and general guidance on
making effective comments, please visit
https://www2.epa.gov/dockets/
commenting-epa-dockets.
ADDRESSES:
FOR FURTHER INFORMATION CONTACT:
Roberts French, Environmental
Protection Specialist, Office of
Transportation and Air Quality,
Compliance Division, U.S.
Environmental Protection Agency, 2000
Traverwood Drive, Ann Arbor, MI
48105. Telephone: (734) 214–4380. Fax:
(734) 214–4869. Email address:
french.roberts@epa.gov.
SUPPLEMENTARY INFORMATION:
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(G) Benzenesulfonic acid, alkyl
derivs., compds. with
diisopropanolamine.
(S) Lithium nickel oxide (LiNiO2).
I. Background
EPA’s light-duty vehicle greenhouse
gas (GHG) program provides three
pathways by which a manufacturer may
accrue off-cycle carbon dioxide (CO2)
credits for those technologies that
achieve CO2 reductions in the real
world but where those reductions are
not adequately captured on the test used
to determine compliance with the CO2
standards, and which are not otherwise
reflected in the standards’ stringency.
The first pathway is a predetermined
list of credit values for specific off-cycle
technologies that may be used beginning
in model year 2014.1 This pathway
allows manufacturers to use
conservative credit values established
by EPA for a wide range of technologies,
with minimal data submittal or testing
requirements, if the technologies meet
EPA regulatory definitions. In cases
where the off-cycle technology is not on
the menu but additional laboratory
testing can demonstrate emission
benefits, a second pathway allows
manufacturers to use a broader array of
emission tests (known as ‘‘5-cycle’’
testing because the methodology uses
five different testing procedures) to
demonstrate and justify off-cycle CO2
credits.2 The additional emission tests
allow emission benefits to be
demonstrated over some elements of
real-world driving not adequately
captured by the GHG compliance tests,
including high speeds, hard
accelerations, and cold temperatures.
These first two methodologies were
completely defined through notice and
comment rulemaking and therefore no
additional process is necessary for
manufacturers to use these methods.
The third and last pathway allows
manufacturers to seek EPA approval to
use an alternative methodology for
determining the off-cycle CO2 credits.3
This option is only available if the
benefit of the technology cannot be
adequately demonstrated using the 5cycle methodology. Manufacturers may
1 See
40 CFR 86.1869–12(b).
40 CFR 86.1869–12(c).
3 See 40 CFR 86.1869–12(d).
2 See
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20JNN1
]]>Agencies
[Federal Register Volume 84, Number 119 (Thursday, June 20, 2019)]
[Notices]
[Pages 28799-28811]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-13099]
=======================================================================
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
[EPA-HQ-OPPT-2019-0075; FRL-9992-77]
Certain New Chemicals; Receipt and Status Information for March
2019
AGENCY: Environmental Protection Agency (EPA).
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: EPA is required under the Toxic Substances Control Act (TSCA),
as amended by the Frank R. Lautenberg Chemical Safety for the 21st
Century Act, to make information publicly available and to publish
information in the Federal Register pertaining to submissions under
TSCA Section 5, including notice of receipt of a Premanufacture notice
(PMN), Significant New Use Notice (SNUN) or Microbial Commercial
Activity Notice (MCAN), including an amended notice or test
information; an exemption application (Biotech exemption); an
application for a test marketing exemption (TME), both pending and/or
concluded; a notice of commencement (NOC) of manufacture (including
import) for new chemical substances; and a periodic status report on
new chemical substances that are currently under EPA review or have
recently concluded review. This document covers the period from 03/01/
2019 to 03/31/2019.
DATES: Comments identified by the specific case number provided in this
document must be received on or before July 22, 2019.
ADDRESSES: Submit your comments, identified by docket identification
(ID) number EPA-HQ-OPPT-2019-0075, and the specific case number for the
chemical substance 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, Information
Management Division (7407M), Office of Pollution Prevention and Toxics,
Environmental Protection Agency, 1200 Pennsylvania Ave. NW, Washington,
DC 20460-0001; telephone number: (202) 564-8593; email address:
[email protected].
For general information contact: The TSCA-Hotline, ABVI-Goodwill,
422 South Clinton Ave., Rochester, NY 14620; telephone number: (202)
554-1404; email address: [email protected].
SUPPLEMENTARY INFORMATION:
I. Executive Summary
What action is the Agency taking?
This document provides the receipt and status reports for the
period from 03/01/2019 to 03/31/2019. The Agency is providing notice of
receipt of PMNs, SNUNs and MCANs (including amended notices and test
information); an exemption application under 40 CFR part 725 (Biotech
exemption); TMEs, both pending and/or concluded; NOCs to manufacture a
new chemical substance; and a periodic status report on new chemical
substances that are currently under EPA review or have recently
concluded review.
EPA is also providing information on its website about cases
reviewed under the amended TSCA, including the section 5 PMN/SNUN/MCAN
and exemption notices received, the date of receipt, the final EPA
determination on the notice, and the effective date of EPA's
determination for PMN/SNUN/MCAN notices on its website at: https://www.epa.gov/reviewing-new-chemicals-under-toxic-substances-control-act-tsca/status-pre-manufacture-notices. This information is updated on a
weekly basis.
B. What is the Agency's authority for taking this action?
Under the TSCA, 15 U.S.C. 2601 et seq., a chemical substance may be
either an ``existing'' chemical substance or a ``new'' chemical
substance. Any chemical substance that is not on EPA's
[[Page 28800]]
TSCA Inventory of Chemical Substances (TSCA Inventory) is classified as
a ``new chemical substance,'' while a chemical substance that is listed
on the TSCA Inventory is classified as an ``existing chemical
substance.'' (See TSCA section 3(11).) For more information about the
TSCA Inventory go to: https://www.epa.gov/tsca-inventory.
Any person who intends to manufacture (including import) a new
chemical substance for a non-exempt commercial purpose, or to
manufacture or process a chemical substance in a non-exempt manner for
a use that EPA has determined is a significant new use, is required by
TSCA section 5 to provide EPA with a PMN, MCAN or SNUN, as appropriate,
before initiating the activity. EPA will review the notice, make a risk
determination on the chemical substance or significant new use, and
take appropriate action as described in TSCA section 5(a)(3).
TSCA section 5(h)(1) authorizes EPA to allow persons, upon
application and under appropriate restrictions, to manufacture or
process a new chemical substance, or a chemical substance subject to a
significant new use rule (SNUR) issued under TSCA section 5(a)(2), for
``test marketing'' purposes, upon a showing that the manufacture,
processing, distribution in commerce, use, and disposal of the chemical
will not present an unreasonable risk of injury to health or the
environment. This 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 and 8 and EPA regulations, EPA is required to
publish in the Federal Register certain information, including notice
of receipt of a PMN/SNUN/MCAN (including amended notices and test
information); an exemption application under 40 CFR part 725 (biotech
exemption); an application for a TME, both pending and concluded; NOCs
to manufacture a new chemical substance; and a periodic status report
on the new chemical substances that are currently under EPA review or
have recently concluded review.
C. Does this action apply to me?
This action provides information that is directed to the public in
general.
D. Does this action have any incremental economic impacts or paperwork
burdens?
No.
E. What should I consider as I prepare my comments for EPA?
1. Submitting confidential business information (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. Status Reports
In the past, EPA has published individual notices reflecting the
status of TSCA section 5 filings received, pending or concluded. In
1995, the Agency modified its approach and streamlined the information
published in the Federal Register after providing notice of such
changes to the public and an opportunity to comment (See the Federal
Register of May 12, 1995, (60 FR 25798) (FRL-4942-7). Since the passage
of the Lautenberg amendments to TSCA in 2016, public interest in
information on the status of section 5 cases under EPA review and, in
particular, the final determination of such cases, has increased. In an
effort to be responsive to the regulated community, the users of this
information, and the general public, to comply with the requirements of
TSCA, to conserve EPA resources and to streamline the process and make
it more timely, EPA is providing information on its website about cases
reviewed under the amended TSCA, including the section 5 PMN/SNUN/MCAN
and exemption notices received, the date of receipt, the final EPA
determination on the notice, and the effective date of EPA's
determination for PMN/SNUN/MCAN notices on its website at: https://www.epa.gov/reviewing-new-chemicals-under-toxic-substances-control-act-tsca/status-pre-manufacture-notices. This information is updated on a
weekly basis.
III. Receipt Reports
For the PMN/SNUN/MCANs that have passed an initial screening by EPA
during this period, Table I provides the following information (to the
extent that such information is not subject to a CBI claim) on the
notices screened by EPA during this period: The EPA case number
assigned to the notice that indicates whether the submission is an
initial submission, or an amendment, a notation of which version was
received, the date the notice was received by EPA, the submitting
manufacturer (i.e., domestic producer or importer), the potential uses
identified by the manufacturer in the notice, and the chemical
substance identity.
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 this information in the table is
generic information because the specific information provided by the
submitter was claimed as CBI. Submissions which are initial submissions
will not have a letter following the case number. Submissions which are
amendments to previous submissions will have a case number followed by
the letter ``A'' (e.g., P-18-1234A). The version column designates
submissions in sequence as ``1'', ``2'', ``3'', etc. Note that in some
cases, an initial submission is not numbered as version 1; this is
because earlier version(s) were rejected as incomplete or invalid
submissions. Note also that future versions of the following tables may
adjust slightly as the Agency works to automate population of the data
in the tables.
Table I--PMN/SNUN/MCANs Approved* From 03/01/2019 to 03/31/2019
--------------------------------------------------------------------------------------------------------------------------------------------------------
Case No. Version Received date Manufacturer Use Chemical substance
--------------------------------------------------------------------------------------------------------------------------------------------------------
J-19-0018............................ 2 3/5/2019 CBI..................... (G) Protein production....... (G) Protein-producing
modified microorganism, with
chromosomally-borne
modifications.
[[Page 28801]]
J-19-0019............................ 1 3/20/2019 Danisco US, Inc......... (G) Production of an enzyme (G) Genetically modified
substance. microorganism for the
production of an enzyme
substance.
J-19-0020............................ 1 3/20/2019 Danisco US, Inc......... (G) Production of an enzyme (G) Genetically modified
substance. microorganism for the
production of an enzyme
substance.
P-16-0225A........................... 2 3/14/2019 International Flavors... (S) The notified substance (S) isomer mixture of
will be used as a fragrance Cyclohexanol, 4-ethylidene-2-
ingredient, being blended propoxy- (CAS 1631145-48-6)
(mixed) with other fragrance (35-45%) and Cyclohexanol, 5-
ingredients to make ethylidene-2-propoxy.
fragrance oils that will be
sold to industrial and
commercial customers for
their incorporation into
soaps, detergents, cleaners,
air fresheners, candles and
other similar industrial,
household and consumer
products.
P-16-0422A........................... 4 3/20/2019 Polymer Additives Inc... (G) Additive for Polymers.... (S) 1,2-
Cyclohexanedicarboxylic
acid, 1-(phenylmethyl)
ester, ester with 2,2,4-
trimethyl-1,3-pentanediol
mono(2-methylpropanoate).
P-16-0493A........................... 7 2/7/2019 CBI..................... (G) Paint.................... (G) Dicarboxylic acids,
polymers with alkyl prop-2-
enoate, alkyl 2-methylprop-2-
enoate, alkyl [(alkenyl)
alkyl] alkanediol,
alkanediol, alkanedioic
acid, alkyl 2-methylprop-2-
enoate, alkyl prop-2-enoic
acid, alkylene
[Isocyanatocarbomonocyle]
and alkanediol, alkanolamine-
blocked, compds with 2-
(alkylamino)alkanol.
P-16-0593A........................... 4 2/22/2019 Emery Oleochemicals..... (S) Aromatic polyester polyol (G) Aromatic Polyester
for rigid foam. Polyol.
[[Page 28802]]
P-17-0108A........................... 5 2/27/2019 Crison LLC.............. (G) The product of this PMN (S) Carbonodithioic acid, O-
is typically added at a rate [2-[(dithiocarboxy)amino]-2-
of 3-5% of the collector methylpropyl] ester, sodium
package. The product is salt (1:2).
added after the grinding of
the ore, along with copious
amounts of water to enable
the flotation of the desired
mineral. The product binds
to the target mineral and
makes it hydrophobic,
enabling the dissolved gas
flotation system to float
the target mineral. The
collected target mineral
concentrate (with the
product bound to them) is
then sent to a metullurgy
plant for further
purification. The high
temperature processing
results in all the organics
(including the product)
being burned off. The
resulting combustion
products are scrubbed as
required by the
mettullurgical plants
permits. A very small amount
of product settles with the
larger particles of ore that
contain target mineral. This
product goes with the gangue
to the tailing ponds. The
tailing ponds have their own
set of permits but are
isolated with various
membrane and other
groundwater protection
methods that are beyond the
scope of this application.
It is worth noting that only
3-5% of the collector
package at this time is made
up of the product of this
PMN. The chemistry is an
incremental improvement on
the currently commercially
practiced collection method,
containing the same
functional groups and
similar solubilities. Thus,
the product of this PMN is
readily detected or measured
with current monitoring at
the use sites. Because the
product is added at a stage
where large amounts of water
are also added, the current
international users wash the
drums with large amounts of
water, and the wash water is
added to the process with
the prime material as it is
added.
P-17-0240A........................... 2 3/1/2019 Ashland, Inc............ (G) Encapsulanting polymer... (G) Alkenoic acid, polymer
with
alkanepolyolpolyacrylate,
2,2'-azobis[2-
methylbutanenitrile]-
initiated.
P-17-0240A........................... 3 3/7/2019 Ashland, Inc............ (G) Encapsulanting polymer... (G) Alkenoic acid, polymer
with
alkanepolyolpolyacrylate,
2,2'-azobis[2-
methylbutanenitrile]-
initiated.
P-17-0312A........................... 7 2/20/2019 CBI..................... (G)Additive for electrocoat (G) Organic acid, compds.
formulas. with bisphenol A-
epichlorohydrin-
polypropylene glycol
diglycidyl ether polymer-
disubstituted polypropylene
glycol reaction products.
[[Page 28803]]
P-17-0313A........................... 7 2/20/2019 CBI..................... (G)Additive for electrocoat (G) Phenol, 4,4'-(1-
formulas. methylethylidene) bis-,
polymer with 2-
(chloromethyl) oxirane and
alpha-(2-oxiranylmethyl)-
omega-(2-oxiranylmethoxy)
poly[oxy(methyl-1,2-
ethanediyl)], reaction
products with disubstituted
amine and disubstituted
polypropylene glycol,
organic acid salts.
P-17-0314A........................... 7 2/20/2019 CBI..................... (G)Additive for electrocoat (G) Organic acid, 2-
formulas. substituted-, compds. with
bisphenol A-epichlorohydrin-
polypropylene glycol
diglycidyl ether polymer-
disubstituted
aminedisubstituted
polypropylene glycol
reaction products.
P-17-0315A........................... 7 2/20/2019 CBI..................... (G)Additive for electrocoat (G) Phenol, 4,4'-(1-
formulas. methylethylidene) bis-,
polymer with alpha-(2-
substituted-methylethyl)-
omega-(2-substituted-
methylethoxy)
poly[oxy(methyl-1,2-
ethanediyl)], 2-
(chloromethyl) oxirane and
alpha-(2-oxiranylmethyl)-
omega-(2-oxiranylmethoxy)
poly[oxy(methyl-1,2-
ethanediyl)], alkylphenyl
ethers, reaction products
with disubstituted amine,
organic acid salts.
P-17-0316A........................... 7 2/20/2019 CBI..................... (G)Additive for electrocoat (G) Organic acid, compds.
formulas. with bisphenol A-
epichlorohydrin-
disubstituted polypropylene
glycol-polypropylene glycol
diglycidyl ether polymer
alkylphenyl ethers-
disubstituted amine reaction
products.
P-17-0317A........................... 7 2/20/2019 CBI..................... (G)Additive for electrocoat (G) Organic acid, compds.
formulas. with bisphenol A-
epichlorohydrin-
polypropylene glycol
diglycidyl ether polymer-
disubstituted polypropylene
glycol reaction products.
P-17-0375A........................... 4 2/8/2019 CBI..................... (G) Paint additive........... (G) 2-Oxepanone, polymer with
diisocyanatohexane, alkyl-
((hydroxyalkyl)-alkanediol
and isocyanato-
(isocyanatoalkyl)-
trialkylcyclohexane, di-
alkyl malonate- and
polyalkylene glycol mono-Me
ether-blocked, reaction
products with (methylalkyl)-
propanamine.
P-17-0395A........................... 4 2/7/2019 CBI..................... (G) Water treatment additive. (G) Alkyl tri dithiocarbmate
tri salt.
P-18-0036A........................... 5 2/8/2019 CBI..................... (G) Water repellant.......... (S) Siloxanes and Silicones,
di-Me, 3- [3-carboxy-2(or 3)-
(octenyl)-1-oxopropoxy]
propyl group-terminated.
P-18-0064A........................... 2 2/25/2019 CBI..................... (G) Intermediate............. (G) Fluorinated carboxylate
esters and fluorinated
alkoxyalkyl heterocycles.
P-18-0069A........................... 2 2/20/2019 Sasol Chemicals (USA), (G) Polymer performance (G) Surface modified
LLC. additive. boehmite.
P-18-0085A........................... 2 3/5/2019 CBI..................... (G) Industrial use in (G) Fatty acids reaction
oilfield. products with ethyleneamines
and dialkyl ester.
P-18-0106A........................... 3 2/25/2019 CBI..................... (S) Process aid.............. (G) Perfluoro[(alkenyl)oxy]
alkane-, manuf. of, by-
products from, distn.
residues.
P-18-0120A........................... 4 3/19/2019 Designer Molecules, Inc. (G) Adhesive component....... (S) 1H-Pyrrole-2,5-dione,
1,1'-C36-alkylenebis-.
[[Page 28804]]
P-18-0131A........................... 4 3/5/2019 Coim USA, Inc........... (S) Polyol prepolymer in (G) Soybean oil, polymer with
polyester foam applications. mixed difunctional glycols,
glycerol, melamine, phthalic
anhydride, poyethylene
glycol, and terephathalic
acid.
P-18-0169A........................... 7 2/15/2019 C. L. Hauthaway & Sons (G) Protective coating....... (G) Propanoic acid, 3-hydroxy-
Corp. 2-(hydroxymethyl)-2-methyl-,
polymer with dimethyl
carbonate, 1,6-hexanediol,
diamine and 1,1'-
methylenebis[4-
isocyanatocyclohexane],
acrylate-blocked, compds.
with triethylamine.
P-18-0175A........................... 6 2/12/2019 Hexion, Inc............. (S) Food can coating;........ (S) Formaldehyde, polymer
(S) Non-food contact can with 4-(1,1-dimethylethyl)
coating. phenol and phenol, Bu ether.
P-18-0219A........................... 6 3/5/2019 CBI..................... (G) Intermediate for topcoat. (G) Polythioether, short
chain diol polymer
terminated with aliphatic
diisocyanate.
P-18-0247A........................... 3 3/13/2019 CBI..................... (S) Crosslinker for (G) Isocyanic acid,
automotive electrocoat. polymethylenepolyphenylene
ester, polymer with 2-ethyl-
2-(hydroxymethyl)-1,3-
propanediol,
polyetherpolyol, [iquest],
[iquest]'-[(1-
methylethylidene) di-4,1-
phenylene] bis[[iquest]-
hydroxypoly(oxy-1,2-
ethanediyl)] and 1,2-
propanediol, iso-Bu alc.-
and 2-butoxyethanol- and 2-
(2-butoxyethoxy) ethanol-
and Et alc.- and methanol-
and 1-methoxy-2-propanol-
blocked.
P-18-0248A........................... 3 3/13/2019 CBI..................... (S) Crosslinker for (G) Isocyanic acid,
automotive electrocoat. polymethylenepolyphenylene
ester, polymer with
polyetherpolyol, 2-
butoxyethanol- and 2-(2-
butoxyethoxy) ethanol- and
methanolblocked.
P-18-0249A........................... 3 3/13/2019 CBI..................... (S) Crosslinker for (G) Isocyanic acid,
automotive electrocoat. polymethylenepolyphenylene
ester, polymer with
polyetherpolyol, 2-
butoxyethanol- and 2-(2-
butoxyethoxy) ethanol- and
methanoland 1-methoxy-2-
propanol-blocked.
P-18-0250A........................... 3 3/13/2019 CBI..................... (S) Crosslinker for (G) Isocyanic acid,
automotive electrocoat. polymethylenepolyphenylene
ester, polymer with
polyetherpolyol, 2-
butoxyethanol- and 2-(2-
butoxyethoxy) ethanol- and
1(or2) -(2-
methoxymethylethoxy)
propanol-blocked.
P-18-0251A........................... 3 3/13/2019 CBI..................... (S) Crosslinker for (S) Isocyanic acid,
automotive electrocoat. polymethylenepolyphenylene
ester, 2-butoxyethanol- and
2-(2-butoxyethoxy) ethanol-
and methanol- and 1(or2) -(2-
methoxymethylethoxy)
propanol-blocked.
P-18-0252A........................... 3 3/13/2019 CBI..................... (S) Crosslinker for (S) Isocyanic acid,
automotive electrocoat. polymethylenepolyphenylene
ester, 2-butoxyethanol- and
2-(2-butoxyethoxy) ethanol-
and methanol- and 1-methoxy-
2-propanol-blocked.
P-18-0258A........................... 2 3/7/2019 CBI..................... (G) Copolyamide for packaging (G) Dioic acids, polymers
films; (G) Copolyamide for with caprolactam and
monofilamen; (G) Copolyamide alkyldiamines.
for molding parts.
[[Page 28805]]
P-18-0259A........................... 2 3/7/2019 CBI..................... (G) Copolyamide for packaging (G) Fatty acids, dimers,
films; (G) Copolyamide for hydrogenated, polymers with
monofilamen; (G) Copolyamide caprolactam and alkyl
for molding parts. diamine.
P-18-0262A........................... 4 2/14/2019 Seppic.................. (S) Function: Stabilizer of (S) 2-Propenoic acid, 2-
suspensions, Applications: methyl-, dodecyl ester,
Detergency, treatment of polymer with ammonium 2-
physical surfaces, methyl-2-[(1-oxo-2-propen-1-
development of soaps; (S) yl) amino]-1-
Function: thickener, propanesulfonate (1:1), N, N-
Applications: Paints, dimethyl-2-propenamide and.
adhesive; (S) Function: alpha-(2-methyl-1-oxo-2-
polishes, Applications: Wood propen-1-yl)-omega-
care, leather care. (dodecyloxy) poly(oxy-1,2-
ethanediyl).
P-18-0270A........................... 4 3/8/2019 Specialty Elements, LLC. (S) Active co-solvent for (G) Ethanol, 2-butoxy-, 1,1'-
solvent-based coatings; (S) ester.
Coalescent for industrial
water-based coatings; (S)
Coupling agent and solvent
in industrial cleaners, rust
removers, hard surface
cleaners, and disinfectants;
(S) Primary solvent in
solvent-based silk screen
printing inks; (S) Coupling
agent for resins and dyes in
water-based printing inks;
(S) Other uses include a co-
solvent for agricultural
pesticides and may be used
in the production of a wide
variety of products and
commodities such as
polyester resins, engine
coolants, latex paints, heat
transfer fluids and deicing
compounds, lubricants,
plasticizers and cement
grinding additives.
P-18-0271A........................... 4 3/8/2019 Specialty Elements, LLC. (S) Film forming coalescent (G) 2-Propanol, 1-butoxy-,
for architectural coatings; 2,2'-ester.
(S) Film forming coalescent
for consumer architectural
coatings; (S) Film forming
coalescent for automotive
OEM coatings
(electrodeposition primers);
(S) Film forming coalescent
for can and coil coatings;
(S) Film forming coalescent
for industrial wood
coatings; (S) Film forming
coalescent for floor
polishes; (S) Film forming
coalescent for industrial
maintenance coatings; (S)
Film forming coalescent for
marine and wood coatings;
(S) Film forming coalescent
for consumer marine and wood
coatings; (S) Film forming
coalescent for
transportation coatings; (S)
Other uses include Graphic
Arts--Printing Inks
(Lithographic and
Letterpress oil-based inks),
Reactive Intermediate--Ester
Derivatives for Plasticizers.
P-18-0272A........................... 2 2/26/2019 CBI..................... (G) Polymer composite (G) Metal, alkylcarboxylate
additive. oxo complexes.
P-18-0274A........................... 5 3/13/2019 CBI..................... (S) Chemical intermediate; (G) Heterocycle fluoroalkyl
(G) Additive. sulfonyl.
P-18-0275A........................... 2 3/13/2019 CBI..................... (G) Polymer additive......... (G) Methanone phenylene
fluoroalkyl sulfonyl
heterocycle.
P-18-0282A........................... 11 3/7/2019 Ashland, Inc............ (G) Adhesive................. (G) Fatty acid ester,
polyether, diisocyanate
polymer.
P-18-0283A........................... 4 3/1/2019 CBI..................... (G)Open, non-dispersive use.. (G) Hydroxy alkanoic acid,
compds. with
aminoalkoxyalcohol-epoxy
polymer-alkanolamine
reaction products.
[[Page 28806]]
P-18-0283A........................... 5 3/11/2019 CBI..................... (G)Open, non-dispersive use.. (G) Hydroxy alkanoic acid,
compds. with
aminoalkoxyalcohol-epoxy
polymer-alkanolamine
reaction products.
P-18-0284A........................... 2 3/1/2019 CBI..................... (G) Polymer composite (G) Inorganic acid, reaction
additive. products with alkyl alcohol.
P-18-0292A........................... 2 2/19/2019 CBI..................... (G) Use in print resins...... (G) Alkanediol, polymer with
5-isocyanato-1-
(isocyanatomethyl)-1,3,3-
trimethylcyclohexane,
alkylaminoalkyl methacrylate-
blocked.
P-18-0292A........................... 3 3/21/2019 CBI..................... (G) Use in print resins...... (G) Alkanediol, polymer with
5-isocyanato-1-
(isocyanatomethyl)-1,3,3-
trimethylcyclohexane,
alkylaminoalkyl methacrylate-
blocked.
P-18-0300A........................... 2 2/8/2019 CBI..................... (S) Additive for automatic (G) Heteromonocycle, alkenoic
dishwashing detergent. 1:1 salt, polymer with alpha-
(2-methyl-1-oxo-2-propen-1-
y) l-omegamethoxypoly(oxy-
1,2-ethanediyl) and methyl-
alkenoic acid.
P-18-0313A........................... 4 3/19/2019 Ashland Inc............. (G) Adhesive................. (G) Alkoxylated glycol ether
with 1,2-propanediol,
reaction products with alkyl
alcohol blocked 1,1'-
methylenebis [4-
isocyanatobenzene]
homopolymer and 1,1'-
methylenebis [4-
isocyanatobenzene].
P-18-0322A........................... 6 2/7/2019 CBI..................... (G) The notified substance is (G) Heteromonocycle, 4,6-
used as a fragrance dimethyl-2-(1-phenylethyl)-.
ingredient in consumer
products.
P-18-0327A........................... 4 3/21/2019 CBI..................... (G) Filler for non-dispersive (G) Mixed metal oxide.
resins.
P-18-0341A........................... 3 3/15/2019 CBI..................... (G) Component in coatings.... (G) Alkane dicarboxylic acid,
polymer with alkoxylated
polyalcohol, alkyl
polyglycol, alkyl dialcohol,
and functionalized
carboxylic acid.
P-18-0342A........................... 3 3/15/2019 CBI..................... (G) Component in coatings.... (G) Alkane dicarboxylic acid,
polymer with alkyl
polyglycol, alkyl dialcohol,
and functionalized
carboxylic acid.
P-18-0343A........................... 3 3/15/2019 CBI..................... (G) Component in coatings.... (G) Alkane dicarboxylic acid,
polymer with alkoxylated
polyalcohol, and alkyl
dialcohol, (hydroxy alkyl)
ester.
P-18-0344A........................... 3 3/15/2019 CBI..................... (G) Component in coatings.... (G) Aromatic dicarboxylic
acid, polymer with alkane
dicarboxylic acid,
alkoxylated polyalcohol, and
alkyl dialcohol.
P-18-0346A........................... 3 3/4/2019 Chitec Technology Co., (S) Antioxidant compounded (S) 2,4,8,10-Tetraoxa-3,9-
Ltd. into various polymers to be diphosphaspiro [5.5]
used in extrusion processes undecane, 3,9-bis-[2-(1-
to fabricate articles. methyl-1-phenylethyl)-4-
(1,1,3,3-tetramethylbutyl)
phenoxy]-.
P-18-0381A........................... 2 3/19/2019 The Shepherd Color (G) For use in exterior (S) Indium manganese yttrium
Company. paints and plastics; (G) For oxide.
use in coatings; (G) For use
in high temperature
engineering polymers; (G)
For use in artist materials.
P-18-0387A........................... 3 2/11/2019 CBI..................... (G) Plastic additive......... (G) Alkanal, reaction
products with alkanediyl
bis[alkyl-tris(alkyl-
heterocycle)-1,3,5-triazine-
2,4,6-triamine and hydrogen
peroxide.
P-18-0388A........................... 3 2/11/2019 CBI..................... (G) Plastic additive......... (G) 1,3,5-triazine-2,4,6-
triamine, alkanediyl
bis[alkyl-tris(alkyl-
heterocycle)-, allyl
derivs., oxidized,
hydrogenated.
[[Page 28807]]
P-18-0389A........................... 2 3/13/2019 CBI..................... (G) Component in package (G) Alkenoic acid, alkyl-
coatings. substituted, epoxy ester,
polymer with alkyl
alkenoate, alkene, and
polylactide.
P-18-0393A........................... 2 3/15/2019 CBI..................... (G) Paint.................... (G) Alkenoic acid, alkyl,
alkyl ester, polymer with
alkyl propenoate, vinyl
carbomonocyle, substituted
alkyl propenoate, alkyl 2-
alkyl 2-propenoate,
alkanediol mono(2-alkyl-2-
propenoate) and
bicarbomonocylo alkyl 2-
alkyl-2-alkenoate, tertiary
alkyl substituted alkane
peroxoate initiated.
P-18-0394A........................... 2 2/25/2019 CBI..................... (G) Chemical Intermediate.... (G) Substituted benzylic
ether polyethylene glycol
alkyl ether derivative.
P-18-0402A........................... 3 3/11/2019 CBI..................... (G) Fuel additive............ (G) Phenol,
alkanepolyolbis(heteroalkyle
ne)bis-, polyalkylene
derivs.
P-19-0009A........................... 4 2/7/2019 Allnex USA, Inc......... (S) The PMN substance is used (G) Carbonmonocycles, polymer
as a coating resin additive with haloalkyl substituted
for corrosion protection. heteromonocycle and hydro-
hydroxypoly[oxy(alkyl-
alkanediyl)], dialkyl-
alkanediamineterminated,
hydroxyalkylated, acetates
(salts).
P-19-0012A........................... 9 3/11/2019 CBI..................... (S) Resin component for the (G) Benzenedicarboxylic acid,
polyisocyanurate; (S) Resin rection products with
component in specialty isobenzofurandione and
polyurethane kits and diethylene glycol.
systems for aerospace and
military applications.
P-19-0015A........................... 3 3/1/2019 CBI..................... (S) Emulsifier for use in (G) Alkyl cyclic amide.
asphalt applications.
P-19-0021A........................... 2 2/13/2019 CBI..................... (G) Pigment ink.............. (G) Hydroxyalkyl carboxylic
acid, polymer with
alkylamine, alkylene
carbonate, alkanediol,
isocyanate, compd. with
alkylamine.
P-19-0022A........................... 2 2/13/2019 CBI..................... (G) Pigment ink.............. (G) Hydroxyalkyl carboxylic
acid, polymer with
alkylamine, alkyl carbonate,
alkanediol, isocyanate,
compd. with alkylamine.
P-19-0025A........................... 2 2/21/2019 Bercen, Inc............. (G) Hydrophobe formulation... (S) 11-Docosene.
P-19-0026A........................... 4 2/27/2019 Allnex USA, Inc......... (S) The PMN substance is an (G) Alkanoic acid, compds.
isolated intermediate with substituted
incorporated as a component carbomonocycle-dialkyl-
in several imported allnex alkanediamine-halosubstitued
coating resin products that heteromonocycle-polyalkylene
are only applied by Cathodic glycol polymerdialkanolamine
Electrodeposition (CED) and reaction products.
used as additives for
corrosion protection.
P-19-0028A........................... 6 2/22/2019 CBI..................... (G) Lubricating oil additive. (G) Alkyl salicylate, metal
salts.
P-19-0032A........................... 4 3/18/2019 Presidium USA, Inc...... (G) Polyol used in the (G) Carbonic dichloride,
manufacture of articles made polymer with 4,4'-(1-
of a polyurethane thermoset methylethylidene)
material. bis[phenol] ester, polymer
with tetrol and polyether
tetrol.
P-19-0034A........................... 3 3/15/2019 CBI..................... (G) Contained use as a (G) Metal, bis (2,4-
component of tires. pentanedionato-kO2, kO4)-,
(T-4)-.
P-19-0038A........................... 3 2/7/2019 Allan Chemical (S) Ink carrier for the (S) Fatty acids, coco, iso-Bu
Corporation. ceramic industries. esters.
P-19-0050A........................... 3 3/11/2019 Kimes Technologies (S) Rust preventative........ (S) Hydrocarbon waxes
International, Inc. (petroleum), oxidized, Bu
esters.
[[Page 28808]]
P-19-0053A........................... 2 3/13/2019 Wacker Chemical (S) Used as a surface (S) 1-Butanamine, N-butyl-N-
Corporation. treatment, sealant, caulk, [(triethoxysilyl)methyl]-.
and coating for mineral
building materials such as
concrete, brick, limestone,
and plaster, as well as on
wood, metal and other
substrates. Formulations
containing the cross-linker
provide release and anti-
graffiti properties, water
repellency, weather
proofing, and improved
bonding in adhesive/sealant
applications. The new
substance is a moisture
curing cross-linking agent
which binds/joins polymers
together when cured. Ethanol
is released during cure, and
once the cure reaction is
complete, the product will
remain bound in the cured
polymer matrix.
P-19-0064............................ 1 3/4/2019 The Sherwin Williams (G) Polymeric film former for (G) 4,4'-methylenebis [2,6-
Company. coatings. dimethyl phenol] polymer
with 2-(chloromethyl)
oxirane, 1,4-benzyl diol, 2-
methyl-2-propenoic acid,
butyl 2-methyl 2-propenoate,
ethyl 2-methyl 2-propenoate,
and ethyl 2-propenoate,
reaction products with 2-
(dimethylamino) ethanol.
P-19-0064A........................... 2 3/18/2019 The Sherwin Williams (G) Polymeric film former for (G) 4,4'-methylenebis [2,6-
Company. coatings. dimethyl phenol] polymer
with 2-(chloromethyl)
oxirane, 1,4-benzyl diol, 2-
methyl-2-propenoic acid,
butyl 2-methyl 2-propenoate,
ethyl 2-methyl 2-propenoate,
and ethyl 2-propenoate,
reaction products with 2-
(dimethylamino) ethanol.
P-19-0065............................ 4 3/22/2019 eScientia Technologies, (S) Fire retardant for (S) 2lambda5, 4lambda5,
LLC. thermal plastics: 6lambda5--1,3,5,2,4,6
Application: This product is Triazatriphosphorine,
the environmental protection 2,2,4,4,6,6--hexaphenoxy-.
Phosphazene flame retardant.
It does not produce
pollutants after burning. It
is mainly used in PC and ABS
resins. It has good flame
retardancy on epoxy resin,
it can be used to make EMC
for IC Packaging, its flame
retardancy is much better
than Brominated flame
retardant, the flame
retardancy can reach UL-94V0
grade. Oxygen index could
reach 33.1%. When it is used
in Benzoxazine Resin glass
cloth laminate, if the HPCTP
is 10%, the grade of burning
could reach V-0 grade, the
parallel breakdown voltage
is 47KV. When it is used in
Polyethylene, the LOI of
final flame retardancy
polyethylene could reach 30-
33. After used in viscose
spinning solution, we could
get the flame retardant
viscose fiber with oxygen
index 25.3-26.7. If the
added amount is 12% in PC/
ABS, it could pass the UL-94
V0 test. It also can be used
in LED, powder coating,
potting material and
polymers.
P-19-0066............................ 4 3/22/2019 eScientia Technologies, (S) Fire retardant........... (S) 2lambda5, 4lambda5,--
LLC. 1,3,5,2,4,6
Triazatriphosphorine,
2,2,4,4,6,6, -hexaphenoxy.
[[Page 28809]]
P-19-0067............................ 2 3/19/2019 CBI..................... (G) On site consumption as a (G) Triglyceride, reactions
raw material in the products with
production of downstream diethylenetriamine.
chemicals, (G) Production of
water-soluble corrosion
inhibitors; (G) Production
of oil soluble corrosion
inhibitors..
P-19-0069............................ 1 3/19/2019 CBI..................... (G) Curing agent for coatings (G) Diisocyanatoalkane,
homopolymer, di-alkyl
malonate- and alkyl
acetoacetate-blocked,
isoalkyl methylalkyl esters.
P-19-0070............................ 1 3/22/2019 CBI..................... (G) Curing agent for coatings (G) Oxacyclanone, polymer
with diisocyanatoalkane, and
alkyl-(substitutedalkyl)-
polyol, di-alkyl malonate-
and alkyl acetoacetate-
blocked, alkyl esters.
P-19-0071............................ 1 3/22/2019 CBI..................... (S) Physical property (G) Trimethylolpropane,
modifier for polymers. alkenoic acid, triester.
P-19-0072............................ 1 3/26/2019 CBI..................... (G) Raw material used in (S) 1-Butanol, reaction
chemical manufacture. products with 2-[(2-propen-1-
yloxy)- methyl] oxirane.
SN-18-0005A.......................... 3 3/3/2019 CBI..................... (G) Monomer for industrial (S) Butanoic acid, 3-mercapto-
adhesives, coatings and inks. ,1,1'-[2,2-bis[(3-mercapto-1-
oxobutoxy) methyl]-1,3-
propanediyl] ester.
SN-18-0013A.......................... 2 2/27/2019 CBI..................... (G) Intermediate............. (G) Lithiated metal oxide.
SN-18-0016A.......................... 4 3/20/2019 Hexion, Inc............. (G) Reactive polymer; (S) (G) Modified phenol-
Reactive polyol for formaldehyde resin.
composites; (S) Reactive
polyol for 2- part coatings;
(S) Reactive polyol for 1-
part coatings; (S) Reactive
polyol for sealants; (S)
Reactive modifier for bonded
abrasives; (S) Reactive
modifier for refractory; (S)
Reactive modifier for glass
inserts; (S) Reactive
modifier for coated
abrasives; (S) Reactive
modifier for friction; (S)
Reactive modifier for fiber
bonding; (S) Reactive
modifier for carbon (liquid
EPF); (S) Reactive modifier
for carbon (powder EPF).
--------------------------------------------------------------------------------------------------------------------------------------------------------
*The term `Approved' indicates that a submission has passed a quick initial screen ensuring all required information and documents have been provided
with the submission prior to the start of the 90-day review period, and in no way reflects the final status of a complete submission review.
In Table II of this unit, EPA provides the following information
(to the extent that such information is not claimed as CBI) on the NOCs
that have passed an initial screening by EPA during this period: The
EPA case number assigned to the NOC including whether the submission
was an initial or amended submission, the date the NOC was received by
EPA, the date of commencement provided by the submitter in the NOC, a
notation of the type of amendment (e.g., amendment to generic name,
specific name, technical contact information, etc.) and chemical
substance identity.
Table II--NOCs Approved * From 03/01/2019 to 03/31/2019
--------------------------------------------------------------------------------------------------------------------------------------------------------
Commencement If amendment, type of
Case No. Received date date amendment Chemical substance
--------------------------------------------------------------------------------------------------------------------------------------------------------
P-07-0541A............................. 3/27/2019 11/14/2007 Generic chemical name (G) Diaminodiol, polymer with diisocyanate,
updated. polyether alcohol, polyether amine, benzyl
chloride-quaternized.
P-11-0294.............................. 3/5/2019 3/24/2014 N......................... (S) Carbonic dichloride, polymer with 4,4'-(1-
methylethylidene)bis(phenol) and 4,4'-(3,3,5-
trimethylcyclohexylidene)bis(phenol)), bis(4-(1,1-
dimethylethyl)phenyl) ester.
P-11-0450.............................. 2/28/2019 2/17/2019 N......................... (S) Fatty acids, carnauba-wax.
P-11-0451.............................. 2/28/2019 2/17/2019 N......................... (S) Fatty acids, carnauba wax, esters with 1,3-
butanediol;
(S) Fatty acids, Carnauba-wax, calcium salts.
P-11-0452.............................. 2/28/2019 2/17/2019 N......................... (S) Fatty acids, carnauba-wax, ethylene esters.
P-14-0382.............................. 3/8/2019 2/13/2019 N......................... (G) Quaternary ammonium compounds, tri-C8-10-
alkylmethyl, hydrogen sulfates.
[[Page 28810]]
P-16-0360.............................. 3/22/2019 3/17/2019 N......................... (S) Poly (oxy-1,2-ethanediyl), alpha- (1-
oxodocosyl)- omega- [(1-oxodocosyl)oxy]-.
P-16-0421.............................. 3/18/2019 2/20/2019 N......................... (S) Flue dust, glass manufacturing,
desulfurization.
P-17-0354.............................. 3/4/2019 2/4/2019 N......................... (G) (substituted-dialkyl(C=1~7)silyl)
alkanenitrile.
P-18-0030.............................. 3/22/2019 3/14/2019 N......................... (G) Poly[oxy(methyl-
alkylendiyl)],alpha,alpha',alpha''-1,2,3-
alkanetriyltris[omega-hydroxy-, polymer with 1,1'-
alkylenebis[4-isocyanatocarbomonocycle], 2-
substituted ethyl acrylate- and 2-substituted
ethyl metacrylate-blocked.
P-18-0123.............................. 3/6/2019 2/20/2019 N......................... (S) Hydrogen lithium nickel oxide.
P-18-0124.............................. 3/6/2019 2/21/2019 N......................... (S) Lithium nickel potassium oxide.
P-18-0136.............................. 3/22/2019 2/22/2019 N......................... (G) 1-Butanaminium,N,N,N-tributyl-,2(or5)-
[[benzoyldihydrodioxo[(sulfophenyl)amino]heteropol
ycycle]oxy]-5(or2)-(1,1-
dimethylpropyl)benzenesulfonate (2:1).
P-18-0233.............................. 3/4/2019 2/13/2019 N......................... (G) Alkyl Alkenoic acid, alkyl ester, telomer with
alkylthiol, substituted carbomonocycle,
substituted alkyl alkyl alkenoate and hydroxyalkyl
alkenoate, tert-butyl alkyl peroxoate-initiated.
P-18-0318.............................. 3/5/2019 3/4/2019 N......................... (S) 1-Octadecanaminium, N,N-dimethyl-N-[3-
(triethoxysilyl)propyl]- chloride.
--------------------------------------------------------------------------------------------------------------------------------------------------------
* The term `Approved' indicates that a submission has passed a quick initial screen ensuring all required information and documents have been provided
with the submission.
In Table III of this unit, EPA provides the following information
(to the extent such information is not subject to a CBI claim) on the
test information that have passed an initial screening by EPA during
this time period: The EPA case number assigned to the test information;
the date the test information was received by EPA, the type of test
information submitted, and chemical substance identity.
Table III--Test Information Received From 03/01/2019 to 03/31/2019
----------------------------------------------------------------------------------------------------------------
Case No. Received date Type of test information Chemical substance
----------------------------------------------------------------------------------------------------------------
P-08-0087................... 3/15/2019 Hydrolysis as a Function (OECD 111)..... (G) Alkyl acids,
reaction products with
metal salt of an
alkanol.
P-08-0508................... 3/25/2019 In Vitro Mammalian Cytogenetic Test (S) Propanoic acid,
(OECD 473), Mutagenicity Testing of H- 2,3,3,3-tetrafluoro-2-
2O421 in the Salmonella Typhimurium (1,1,2,2,3,3,3-
Plate Incorporation Assay (OECD 473), heptafluoropropoxy).
Combined Two-Week Inhalation Toxicity
and Micronucleus Studies, Thermal
Transformation Byproduct, Determination
of the Water Solubility and Vapor
Pressure of H-28327 (OECD 104-105),
Determination of the n-Octanol/Water
Partition Coefficient of H-28327 (OPPTS
830.7560).
P-08-0509................... 3/25/2019 In Vitro Mammalian Cytogenetic Test (S) Propanoic acid,
(OECD 473), Mutagenicity Testing of H- 2,3,3,3-tetrafluoro-2-
2O421 in the Salmonella Typhimurium (1,1,2,2,3,3,3-
Plate Incorporation Assay (OECD 473), heptafluoropropoxy)-,
Combined Two-Week Inhalation Toxicity ammonium salt (1:1).
and Micronucleus Studies, Thermal
Transformation Byproduct, Determination
of the Water Solubility and Vapor
Pressure of H-28327 (OECD 104-105),
Determination of the n-Octanol/Water
Partition Coefficient of H-28327 (OPPTS
830.7560).
P-10-0060................... 3/21/2019 Studies for Triggered Testing: (OECD (G) Partially
421), Modified One-Generation fluorinated alcohol
Reproduction Test (Mice) (OPPTS substituted glycol.
850.3050).
P-15-0450................... 3/20/2019 90-Day Inhalation Toxicity Study (OECD (G) Lithium mixed metal
413). oxide.
P-16-0543................... 3/14/2019 Exposure Monitoring Report.............. (G) Halogenophosphoric
acid metal salt.
P-18-0060................... 3/26/2019 Sediment and Soil Adsorption/Desorption (S) 1-butanaminium, 4-
Isotherm (OECD 106), Acute Dermal amino-N-(2-hydroxy-3-
Toxicity (OECD 402), Mammalian sulfopropyl)-N, N-
Erythrocyte Micronucleus Test (OECD dimethyl-4-oxo-, N-coco
474). alkyl derivs., inner
salts.
P-18-0093................... 3/1/2019 Dust Control, Analytical Test Results, (G) Pentacyclo
Water Immersion Testing, H2O Immersion [9.5.1.13,9.15,15.17,13
with Proton Pulse Sequence, Plastic ] octasiloxane,
Abrasions SEM Summary and SEM Images, 1,3,5,7,9,11,13,15-
Risks Identified in Focus Report. octakis
(polyfluoroalkyl).
P-18-0177................... 3/5/2019 Solubility in Alga Growth Media (OECD (S) Waxes and waxy
201). substances, rice bran,
oxidized.
P-18-0286................... 3/8/2019 Supplemental Worker Exposure............ (S) Propane, 1,1,1,3,3,3-
hexafluoro-2-methoxy.
P-18-0293................... 3/21/2019 In Vitro Skin Sensitization Assays (OECD (S) Propanedioic acid, 2-
422D). methyl- ene-, 1,3-
dihexyl ester.
P-18-0294................... 3/21/2019 In Vitro Skin Sensitization Assays (OECD (S) Propanedioic acid, 2-
422D). methyl- ene-, 1,3-
dicyclohexyl ester.
[[Page 28811]]
P-18-0325................... 3/18/2019 Fish Acute Toxicity (OECD 203), Daphnia (G) Benzenesulfonic
Acute Toxicity (OECD 202), Algae Acute acid, alkyl derivs.,
Toxicity (OECD 201), Acute Oral compds. with
Toxicity (OECD 401), Acute Dermal diisopropanolamine.
Toxicity (OECD 402), Dermal Irritation
(OECD 404), Eye Irritation (OECD 405),
Ready Biodegradability (OECD 301B),
Activated Sludge Respiration Inhibition
Tests (OECD 209), Ames Test (OECD 471),
Skin Sensitization (OECD 406),
Chromosome Aberration Test (OECD 473),
28-Day Oral Toxicity Study (OECD 407).
SN-18-0003.................. 3/5/2019 Algae Growth Inhibition Study (OECD 201) (S) Lithium nickel oxide
(LiNiO2).
----------------------------------------------------------------------------------------------------------------
If you are interested in information that is not included in these
tables, you may contact EPA's technical information contact or general
information contact as described under FOR FURTHER INFORMATION CONTACT
to access additional non-CBI information that may be available.
Authority: 15 U.S.C. 2601 et seq.
Dated: June 6, 2019.
Megan Carroll,
Acting Director, Information Management Division, Office of Pollution
Prevention and Toxics.
[FR Doc. 2019-13099 Filed 6-19-19; 8:45 am]
BILLING CODE 6560-50-P
