Certain New Chemicals; Receipt and Status Information, 76029-76034 [2012-31063]

Download as PDF Federal Register / Vol. 77, No. 247 / Wednesday, December 26, 2012 / Notices Dated: December 17, 2012. Matthew G. Leopard, Director, Information Management Division, Office of Pollution Prevention and Toxics. [FR Doc. 2012–31094 Filed 12–21–12; 4:15 pm] BILLING CODE 6560–50–P ENVIRONMENTAL PROTECTION AGENCY [EPA–HQ–OPPT–2012–0881; FRL–9373–1] Certain New Chemicals; Receipt and Status Information Environmental Protection Agency (EPA). ACTION: Notice. AGENCY: The Toxic Substances Control Act (TSCA) requires any person who intends to manufacture (defined by statute to include import) a new chemical (i.e., a chemical not on the TSCA Chemical Substances Inventory (TSCA Inventory)) to notify EPA and comply with the statutory provisions pertaining to the manufacture of new chemicals. In addition under TSCA, EPA is required to publish in the Federal Register a notice of receipt of a premanufacture notice (PMN) or an application for a test marketing exemption (TME), and to publish in the Federal Register periodic status reports on the new chemicals under review and the receipt of notices of commencement (NOC) to manufacture those chemicals. This document, which covers the period from November 1, 2012 to November 30, 2012, and provides the required notice and status report, consists of the PMNs and TMEs, both pending or expired, and the NOC to manufacture a new chemical that the Agency has received under TSCA section 5 during this time period. DATES: Comments identified by the specific PMN number or TME number, must be received on or before January 25, 2013. ADDRESSES: Submit your comments, identified by docket identification (ID) number EPA–HQ–OPPT–2012–0881, and the specific PMN number or TME number for the chemical related to your comment, by one of the following methods: • Federal eRulemaking Portal: https:// www.regulations.gov. Follow the online instructions for submitting comments. • Mail: Document Control Office (7407M), Office of Pollution Prevention and Toxics (OPPT), Environmental Protection Agency, 1200 Pennsylvania Ave., NW., Washington, DC 20460– 0001. • Hand Delivery: OPPT Document Control Office (DCO), EPA East Bldg., tkelley on DSK3SPTVN1PROD with SUMMARY: VerDate Mar<15>2010 06:31 Dec 22, 2012 Jkt 229001 Rm. 6428, 1201 Constitution Ave., NW., Washington, DC. The DCO is open from 8 a.m. to 4 p.m., Monday through Friday, excluding legal holidays. The telephone number for the DCO is (202) 564–8930. Such deliveries are only accepted during the DCO’s normal hours of operation, and special arrangements should be made for deliveries of boxed information. Instructions: EPA’s policy is that all comments received will be included in the docket without change and may be made available online at https:// www.regulations.gov, including any personal information provided, unless the comment includes information claimed to be Confidential Business Information (CBI) or other information whose disclosure is restricted by statute. Do not submit information that you consider to be CBI or otherwise protected through regulations.gov or email. The regulations.gov Web site is an ‘‘anonymous access’’ system, which means EPA will not know your identity or contact information unless you provide it in the body of your comment. If you send an email comment directly to EPA without going through regulations.gov, your email address will be automatically captured and included as part of the comment that is placed in the docket and made available on the Internet. If you submit an electronic comment, EPA recommends that you include your name and other contact information in the body of your comment and with any disk or CD–ROM you submit. If EPA cannot read your comment due to technical difficulties and cannot contact you for clarification, EPA may not be able to consider your comment. Electronic files should avoid the use of special characters, any form of encryption, and be free of any defects or viruses. Docket: All documents in the docket are listed in the docket index available at https://www.regulations.gov. Although listed in the index, some information is not publicly available, e.g., CBI or other information whose disclosure is restricted by statute. Certain other material, such as copyrighted material, will be publicly available only in hard copy. Publicly available docket materials are available electronically at https://www.regulations.gov, or, if only available in hard copy, at the OPPT Docket. The OPPT Docket is located in the EPA Docket Center (EPA/DC) at Rm. 3334, EPA West Bldg., 1301 Constitution Ave., NW., Washington, DC. The EPA/DC Public Reading Room hours of operation are 8:30 a.m. to 4:30 p.m., Monday through Friday, excluding legal holidays. The telephone number of the EPA/DC Public Reading Room is PO 00000 Frm 00062 Fmt 4703 Sfmt 4703 76029 (202) 566–1744, and the telephone number for the OPPT Docket is (202) 566–0280. Docket visitors are required to show photographic identification, pass through a metal detector, and sign the EPA visitor log. All visitor bags are processed through an X-ray machine and subject to search. Visitors will be provided an EPA/DC badge that must be visible at all times in the building and returned upon departure. FOR FURTHER INFORMATION CONTACT: For technical information contact: Bernice Mudd, Information Management Division (7407M), Office of Pollution Prevention and Toxics, Environmental Protection Agency, 1200 Pennsylvania Ave., NW., Washington, DC 20460– 0001; telephone number: (202) 564– 8955; fax number: (202) 564–8951; email address: mudd.bernice@epa.gov. For general information contact: The TSCA-Hotline, ABVI-Goodwill, 422 South Clinton Ave., Rochester, NY 14620; telephone number: (202) 554– 1404; email address: TSCAHotline@epa.gov. SUPPLEMENTARY INFORMATION: I. General Information A. Does this action apply to me? This action is directed to the public in general. As such, the Agency has not attempted to describe the specific entities that this action may apply to. Although others may be affected, this action applies directly to the submitter of the PMNs addressed in this action. B. What should I consider as I prepare my comments for EPA? 1. Submitting CBI. Do not submit this information to EPA through regulations.gov or email. Clearly mark the part or all of the information that you claim to be CBI. For CBI information in a disk or CD–ROM that you mail to EPA, mark the outside of the disk or CD–ROM as CBI and then identify electronically within the disk or CD–ROM the specific information that is claimed as CBI. In addition to one complete version of the comment that includes information claimed as CBI, a copy of the comment that does not contain the information claimed as CBI must be submitted for inclusion in the public docket. Information so marked will not be disclosed except in accordance with procedures set forth in 40 CFR part 2. 2. Tips for preparing your comments. When submitting comments, remember to: i. Identify the document by docket ID number and other identifying information (subject heading, Federal Register date and page number). E:\FR\FM\26DEN1.SGM 26DEN1 76030 Federal Register / Vol. 77, No. 247 / Wednesday, December 26, 2012 / Notices ii. Follow directions. The Agency may ask you to respond to specific questions or organize comments by referencing a Code of Federal Regulations (CFR) part or section number. iii. Explain why you agree or disagree; suggest alternatives and substitute language for your requested changes. iv. Describe any assumptions and provide any technical information and/ or data that you used. v. If you estimate potential costs or burdens, explain how you arrived at your estimate in sufficient detail to allow for it to be reproduced. vi. Provide specific examples to illustrate your concerns and suggest alternatives. vii. Explain your views as clearly as possible, avoiding the use of profanity or personal threats. viii. Make sure to submit your comments by the comment period deadline identified. II. Why is EPA taking this action? EPA classifies a chemical substance as either an ‘‘existing’’ chemical or a ‘‘new’’ chemical. Any chemical substance that is not on EPA’s TSCA Inventory is classified as a ‘‘new chemical,’’ while those that are on the TSCA Inventory are classified as an ‘‘existing chemical.’’ For more information about the TSCA Inventory go to https://www.epa.gov/opptintr/ newchems/pubs/inventory.htm. Anyone who plans to manufacture or import a new chemical substance for a nonexempt commercial purpose is required by TSCA section 5 to provide EPA with a PMN, before initiating the activity. Section 5(h)(1) of TSCA authorizes EPA to allow persons, upon application, to manufacture (includes import) or process a new chemical substance, or a chemical substance subject to a significant new use rule (SNUR) issued under TSCA section 5(a), for ‘‘test marketing’’ purposes, which is referred to as a test marketing exemption, or TME. For more information about the requirements applicable to a new chemical go to: https://www.epa.gov/ oppt/newchems. Under TSCA sections 5(d)(2) and 5(d)(3), EPA is required to publish in the Federal Register a notice of receipt of a PMN or an application for a TME and to publish in the Federal Register periodic status reports on the new chemicals under review and the receipt of NOCs to manufacture those chemicals. This status report, which covers the period from November 1, 2012 to November 30, 2012, consists of the PMNs and TMEs, both pending or expired, and the NOCs to manufacture a new chemical that the Agency has received under TSCA section 5 during this time period. III. Receipt and Status Reports In Table I. of this unit, EPA provides the following information (to the extent that such information is not claimed as CBI) on the PMNs received by EPA during this period: The EPA case number assigned to the PMN, the date the PMN was received by EPA, the projected end date for EPA’s review of the PMN, the submitting manufacturer/ importer, the potential uses identified by the manufacturer/importer in the PMN, and the chemical identity. TABLE I—55 PMNS RECEIVED FROM 11/1/2012 TO 11/30/12 Received date Case No. Projected notice end date Manufacturer/importer Use Chemical (S) Hotmelt adhesive for panel lamination and other assemblies. (S) Coatings additive .. (G) Resin for non-dispersive use. (G) Acrylic modified polyether-ester polyurethane prepolymer. 11/2/2012 1/30/2013 Henkel Corp. ............... P–13–0083 ..... P–13–0090 ..... 11/1/2012 11/1/2012 1/29/2013 1/29/2013 CBI .............................. Cytec Industries, Inc. .. P–13–0091 ..... 11/5/2012 2/2/2013 Cray Valley USA, LLC P–13–0092 ..... 11/6/2012 2/3/2013 CBI .............................. P–13–0093 ..... 11/8/2012 2/5/2013 P–13–0094 ..... 11/6/2012 2/3/2013 The Goodyear Tire & Rubber Co. Department 100D. CBI .............................. P–13–0095 ..... tkelley on DSK3SPTVN1PROD with P–13–0082 ..... 11/6/2012 2/3/2013 Gelest, Inc. ................. P–13–0096 ..... 11/12/2012 2/9/2013 Cytec Industries, Inc. .. VerDate Mar<15>2010 06:31 Dec 22, 2012 Jkt 229001 PO 00000 Frm 00063 Fmt 4703 (G) Additive for rubber to improve properties. (G) Adhesive for electrical industry use. (S) Precursor to polymerization catalyst. (G) Additive for adhesives, pottings and sealants. (S) Further purified at one site; further purified material packaged and sent to end use for use in CVD LOWK dielectric barrier in microelectronic application.. (G) Coating resin ........ Sfmt 4703 (G) Epoxysilane homopolymer. (G) Alkenenitrile, polymer with alkadiene, substituted alkyl-terminated, polymers with substituted carbonomocycles, alkoxy-terminated-substituted alkyl-alkadiene polymer, substituted carbomoncycle and halogen substituted carbomonocycle. (G) Siloxane functional polybutadiene polymer. (G) Latex polymer. (S) Neodymium, butadiene neodecanoate complexes. iso-bu (G) Acrylic ester functionalized polyether polymer. (S) Silane, yldiethoxymethyl- bicyclo[2.2.1]hept-2- (G) Alkenoic acid, reaction product with alkylpolyol, polymers with substituted heteromonocycle. E:\FR\FM\26DEN1.SGM 26DEN1 Federal Register / Vol. 77, No. 247 / Wednesday, December 26, 2012 / Notices 76031 TABLE I—55 PMNS RECEIVED FROM 11/1/2012 TO 11/30/12—Continued Received date Case No. Projected notice end date Manufacturer/importer Use Chemical (G) Vinyl chloride emulsion (acrylic group emulsion type). 11/9/2012 2/6/2013 Shin ETSU Microsi ..... P–13–0098 ..... 11/12/2012 2/9/2013 CBI .............................. P–13–0099 ..... 11/13/2012 2/10/2013 H.B. Fuller Company .. (G) Non combustible coating for non woven fabric for automobile air filters and carpet flooring materials. (G) An open, non-dispersive use. (G) Industrial adhesive P–13–0100 ..... 11/13/2012 2/10/2013 H.B. Fuller Company .. (G) Industrial adhesive P–13–0101 ..... 11/13/2012 2/10/2013 H.B. Fuller Company .. (G) Industrial adhesive P–13–0102 ..... 11/13/2012 2/10/2013 H.B. Fuller Company .. (G) Industrial adhesive P–13–0103 ..... 11/13/2012 2/10/2013 H.B. Fuller Company .. (G) Industrial adhesive P–13–0104 ..... 11/13/2012 2/10/2013 H.B. Fuller Company .. (G) Industrial adhesive P–13–0105 ..... 11/13/2012 2/10/2013 Sika Corporation ......... P–13–0106 ..... 11/9/2012 2/6/2013 P–13–0107 ..... 11/14/2012 2/11/2013 P–13–0108 ..... 11/14/2012 2/11/2013 The Goodyear Tire & Rubber Company. Trinity Manufacturing, Inc.. CBI .............................. P–13–0109 ..... 11/14/2012 2/11/2013 Trinity Manufacturing, Inc.. P–13–0110 ..... tkelley on DSK3SPTVN1PROD with P–13–0097 ..... 11/14/2012 2/11/2013 CBI .............................. P–13–0111 ..... 11/15/2012 2/12/2013 CBI .............................. P–13–0112 ..... 11/15/2012 2/12/2013 CBI .............................. P–13–0113 ..... 11/15/2012 2/12/2013 CBI .............................. (G) Latent hardener for polyurethane roof membrane. (S) Precursor to polymerization catalyst. (S) Flame retardant for rubber products. (S) Feed for a bromine recovery unit. (S) Flame retardant in rubber products; extreme pressure additive in lubricants. (G) Additive, open, non-dispersive use. (G) Additive, open, non-dispersive use. (G) Additive, open, non-dispersive use. (G) Additive, open, non-dispersive use. VerDate Mar<15>2010 06:31 Dec 22, 2012 Jkt 229001 PO 00000 Frm 00064 Fmt 4703 Sfmt 4703 (G) Modified polyarylamide salt. (G) 1,4-benzenedicarboxylic acid, polymer with 2,2-dimethyl-1,3-propanediol, alkane diacid, 1,2-ethanediol, hexanedioic acid, alkanediol, .alpha.-hydro-.omega.hydroxypoly[oxy(methyl-1,2-ethanediyl)], 1,3-isobenzofurandione, 1,1’methylenebis[4-isocyanatobenzene], 2oxepanone and 2,2’-oxybis[ethanol]. (G) Alkane diacid, polymer with hexanedioic acid, alkanediol, .alpha.-hydro-.omega.hydroxypoly[oxy(methyl-1,2-ethanediyl)], 1,3-isobenzofurandione, 1,1’methylenebis[4-isocyanatobenzene], 2oxepanone and 2,2’-oxybis[ethanol]. (G) 1,3-benzenedicarboxylic acid, polymer with 1,4-benzenedicarboxylic acid, alkane diacid, 1,2-ethanediol, hexanedioic acid, alkanediol, .alpha.-hydro-.omega.hydroxypoly[oxy(methyl-1,2-ethanediyl)], 1,3-isobenzofurandione, 1,1’methylenebis[4-isocyanatobenzene], 2oxepanone and 2,2’-oxybis[ethanol]. (G) Alkane diacid, polymer with hexanedioic acid, alkanediol, .alpha.-hydro-.omega.hydroxypoly[oxy(methyl-1,2-ethanediyl)], 1,1’-methylenebis[4-isocyanatobenzene], 2oxepanone and .alpha.,.alpha.’,.alpha.-1. (G) Alkane diacid, polymer with 2,2-dimethyl1,3-propanediol, 1,2-ethanediol, hexanedioic acid, alkanediol, .alpha.-hydro.omega.-hydroxypoly[oxy(methyl-1,2ethanediyl)], 1,1’-methylenebis[4isocyanatobenzene], and.alpha.,.alpha.’,.alpha.-1. (G) Alkane diacid, polymer with 2,2-dimethyl1,3-propanediol, 1,2-ethanediol, hexanedioic acid, alkanediol, .alpha.-hydro.omega.-hydroxypoly[oxy(methyl-1,2ethanediyl)], 1,3-isobenzofurandione, 1,1’methylenebis[4-isocyanatobenzene], and 2,2’-oxybis[ethanol]. (G) Latent hardener for polyurethane. (G) Neodymium, Ziegler—Natta preformed stage 1 catalyst. (S) Alkanes, C22–30-branched and linear, chloro. (S) Bromine, manufacturer of, by-products from distant residues. (S) Alkanes, C24–28, chloro. (G) Hydroxyalkyl methacrylate, reaction product with cyclic ether. (G) Acrylfunctional polysiloxane, reaction product of alcohols with isocyanates. (G) Acrylfunctional polysiloxane, reaction product of alcohols with isocyanates. (G) Acrylfunctional polysiloxane, reaction product of alcohols with isocyanates. E:\FR\FM\26DEN1.SGM 26DEN1 76032 Federal Register / Vol. 77, No. 247 / Wednesday, December 26, 2012 / Notices TABLE I—55 PMNS RECEIVED FROM 11/1/2012 TO 11/30/12—Continued Case No. Received date P–13–0114 ..... 11/19/2012 P–13–0115 ..... Projected notice end date Use 2/16/2013 CBI .............................. 11/20/2012 2/17/2013 CBI .............................. (S) Reactant/intermediate for polymers and oligomers, polyesters, and other materials that might include personal care and pharmaceutical applications. (G) Pigment dispersant P–13–0116 ..... 11/20/2012 2/17/2013 CBI .............................. (G) Pigment dispersant P–13–0117 ..... P–13–0118 ..... 11/20/2012 11/20/2012 2/17/2013 2/17/2013 H.B. Fuller Company .. CBI .............................. (G) Industrial adhesive (G) Industrial adhesive P–13–0119 ..... 11/20/2012 2/17/2013 CBI .............................. P–13–0120 ..... 11/20/2012 2/17/2013 CBI .............................. P–13–0121 ..... 11/20/2012 2/17/2013 CBI .............................. (G) Polymer processing additive. (S) Catalyst for use in polyurethane coatings. (G) Polymeric colorant P–13–0122 ..... 11/20/2012 2/17/2013 CBI .............................. (G) Packaging material P–13–0123 ..... 11/20/2012 2/17/2013 CBI .............................. P–13–0124 ..... 11/20/2012 2/17/2013 P–13–0125 ..... 11/20/2012 2/17/2013 DIC International (USA) LLC. Soane Energy LLC ..... P–13–0126 ..... 11/20/2012 2/17/2013 Soane Energy LLC ..... P–13–0127 ..... 11/20/2012 2/17/2013 P–13–0128 ..... 11/21/2012 2/18/2013 Miwon North America, Inc.. CBI .............................. P–13–0129 ..... 11/21/2012 2/18/2013 CBI .............................. P–13–0130 ..... 11/20/2012 2/17/2013 CBI .............................. P–13–0131 ..... 11/26/2012 2/23/2013 CBI .............................. P–13–0132 ..... 11/26/2012 2/23/2013 Euticals, Inc. ............... P–13–0133 ..... 11/27/2012 2/24/2013 CBI .............................. P–13–0134 ..... 11/27/2012 2/24/2013 CBI .............................. P–13–0135 ..... 11/26/2012 2/23/2013 Euticals, Inc. ............... P–13–0136 ..... 11/28/2012 2/25/2013 Sika Corporation ......... P–13–0137 ..... P–13–0138 ..... 11/28/2012 11/28/2012 2/25/2013 2/25/2013 CBI .............................. CBI .............................. P–13–0139 ..... tkelley on DSK3SPTVN1PROD with Manufacturer/importer 11/28/2012 2/25/2013 CBI .............................. (G) Additive, open, non-dispersive use. (G) Polymer for coating. (G) Used in the upstream oil and gas industry. (G) Used in the upstream oil and gas industry. (S) Resin for industrial coating. (G) Additive, open, non-dispersive use. (G) Additive, open, non-dispersive use. (G) Flow improver for oilfield applications. (G) Inhibitor for oil field applications. (S) Monomer intermediate for use in the manufacture of a polymer. (G) Catalyst for silicone polymerization. (G) Catalyst for silicone polymerization. (S) Intermediate monomer for use in the manufacture of another monomer. (G) Roof membrane hardener. (G) Chemical additive (G) Textile processing additive. (G) Gasoline additive .. P–13–0140 ..... 11/29/2012 2/26/2013 CBI .............................. (G) Solvent ................. P–13–0141 ..... 11/29/2012 2/26/2013 Dow Chemical Company. (S) Hardener for epoxy thermosetting coatings. VerDate Mar<15>2010 06:31 Dec 22, 2012 Jkt 229001 PO 00000 Frm 00065 Fmt 4703 Sfmt 4703 Chemical (G) Sorbitan ester. (G) Fatty acids of natural oils, conjugated, maleated, substituted phenoxyalkyl ester. (G) Fatty acids of natural oils, conjugated, maleated, substituted phenoxyalkyl ester. (G) Vegetable oil, polymer with isocyanate. (G) Vegetable oil, polymer with isocyanate and propanol, oxybis-. (S) D-glucitol, 1,3:2,4-bis-o-[(4ethylphenyl)methylene]-. (G) Substituted dimethyltin. (G) Substituted polymeric aromatic amine azo colorant. (G) Acetic acid ethenyl ester, copolymer, hydrolyzed. (G) Salt of acidic polymers with monomeric and polymeric bases. (G) Coating polymer. (S) Poly(oxy-1,2-ethanediyl), .alpha.-hydro.omega.-hydroxy-, hydrogen 2–C15–20alkenylbutanediotes. (S) Poly(oxy-1,2-ethanediyl), .alpha.-hydro.omega.-hydroxy-, hydrogen 2–C15–20alkenylbutanediotes, sodium salts. (G) Monofunctional acrylate. (G) Polyether modified potassium polystyrene maleate. (G) Polyether modified fatty acid dimmer. (G) Formaldehyde, polymer with alklyphenols. (G) Tertiary ammonium compound. (S) Boronic acid, yl)amino]phenyl]-. b-[3-[(1-oxo-2-propen-1- (G) Dichlorophosphazene oligomers. (G) Partially hydrolyzed dichlorophosphazene oligomers. (G) Substituted benzenamine. (G) Latent hardener for polyurethane. (S) Butanedioic acid, 2-(2-octen-1-yl)-. (S) Butanedioic acid, 2-(2-octen-1-yl)-, potassium salt (1:2). (G) Fatty acids, alkyl-unsaturated, esters with polyol. (S) Pentanoic acid, 5-(dimethylamino)-2-methyl-5-oxo-, methyl ester. (G) Alkyl amines polymer with polyglycol ether, and bis a epoxy reaction products with aromatic epoxies. E:\FR\FM\26DEN1.SGM 26DEN1 Federal Register / Vol. 77, No. 247 / Wednesday, December 26, 2012 / Notices 76033 TABLE I—55 PMNS RECEIVED FROM 11/1/2012 TO 11/30/12—Continued Case No. P–13–0142 ..... Projected notice end date Received date 11/30/2012 2/27/2013 In Table II. of this unit, EPA provides the following information (to the extent that such information is not claimed as CBI) on the TMEs received by EPA Manufacturer/importer Use Chemical Scott Bader, Inc. ......... (G) Fabrication of composite articles. during this period: The EPA case number assigned to the TME, the date the TME was received by EPA, the projected end date for EPA’s review of (G) Unsaturated urethane methacrylate. the TME, the submitting manufacturer/ importer, the potential uses identified by the manufacturer/importer in the TME, and the chemical identity. TABLE II— 3 TMES RECEIVED FROM 11/1/12 TO 11/30/12 Projected notice end date Received date Case No. Manufacturer/importer Use Chemical (G) Alkenenitrile, polymer with alkadiene, substituted alkyl-terminated, polymers with substituted carbonomocycles, alkoxy-terminated-substituted alkyl-alkadiene polymer, substituted carbomonocycle and halogen substituted carbomonocycle. (G) Alkenoic acid, reaction product with alkylpolyol, polymers with substituted heteromonocycle. (G) Tertiary ammonium compound. T–13–0002 ...... 11/1/2012 12/15/2012 Cytec Industries, Inc. .. (G) Resin for non-dispersive use. T–13–0003 ...... 11/12/2012 12/26/2012 Cytec Industries, Inc. .. (G) Coating resin ........ T–13–0004 ...... 11/26/2012 1/9/2013 CBI .............................. (G) Inhibitor for oil field applications. In Table III. of this unit, EPA provides the following information (to the extent that such information is not claimed as CBI) on the NOCs received by EPA during this period: The EPA case number assigned to the NOC, the date the NOC was received by EPA, the projected end date for EPA’s review of the NOC, and chemical identity. TABLE III—32 NOCS RECEIVED FROM 11/1/12 TO 11/30/12 Case No. Received date Commencement notice end date 11/5/2012 11/20/2012 11/20/2012 11/27/2012 10/25/2012 5/7/2008 3/1/2009 11/14/2012 P–09–0107 ...... P–09–0263 ...... P–10–0014 ...... 11/1/2012 11/14/2012 11/26/2012 10/4/2012 10/24/2012 11/15/2012 P–10–0560 ...... P–10–0561 ...... P–11–0016 ...... 11/13/2012 11/19/2012 11/20/2012 10/4/2012 10/4/2012 11/1/2012 P–11–0368 ...... P–11–0557 ...... 11/20/2012 11/27/2012 8/11/2011 11/2/2012 P–12–0044 P–12–0143 P–12–0152 P–12–0174 P–12–0246 P–12–0247 tkelley on DSK3SPTVN1PROD with J–12–0004 ....... P–07–0101 ...... P–08–0654 ...... P–09–0106 ...... ...... ...... ...... ...... ...... ...... 11/30/2012 11/14/2012 11/13/2012 11/28/2012 11/19/2012 11/20/2012 11/1/2012 11/2/2012 10/31/2012 11/7/2012 11/7/2012 10/10/2012 P–12–0248 ...... P–12–0272 ...... 11/20/2012 11/6/2012 11/1/2012 11/2/2012 VerDate Mar<15>2010 06:31 Dec 22, 2012 Jkt 229001 PO 00000 Chemical (G) Saccharomyces cerevisiae, strain CBI. (G) Alkoxylate polymer. (G) Fatty acids, C18-unsaturated., dimers, polymers with diamines and monoacids. (G) Fatty acids, tall-oil, reaction products with modified fatty acids and polyalkanolamines, hydrochlorides. (G) Fatty acids, tall-oil, reaction products with modified fatty acids and polyalkanolamines. (S) 4-dodecenenitrile, (4z)-. (G) Quino[2,3-b]acridine-7, 14-dione, 2,9-dichloro-5, 12-dihydro[4-[[2(sulfooxy)ethyl]substituted]phenyl]-,sodium salt (1:1). (G) Silyl-modified polymer. (G) Silyl-modified polymer. (G) Adipic acid, polymer with benzenepolycarboxylic acids, polyakylene glycol, alkanediols, 1,1’-methylenebis[isocyanatobenzene] and a substituted-, trialkoxysilane. (G) Ipdi modified polyester resin. (G) 2-propenoic acid, 2-methyl-, 2-hydroxyethyl ester, telomers with C18–26 alkyl acrylate, 1-dodecanthiol, N-(hydroxymethyl)-2-methyl-2-propenamide, polyfluorooctyl methacrylate and vinylidene chloride, 2,2’-[1,2-diazenediylbis(1-methylethylidene)]-bis[4,5dihydro-1H-imidazole]hydrochloride (1:2)-initiated. (G) Multi-wall carbon nanotubes. (G) Poly(oxy-1,4-butanediyl), -hydro-hydroxy-, polymer with alkyldisocyanates. (G) Ester substituted bicyclic olefin. (G) Polyurethane. (G) Methyl, phenyl, amino-functional siloxanes and silsesquixane. (G) Alkyl carboxylic acid, oxiranyl alkyl ester, polymer with cycloalkyl dicarboxylic acid anhydride, alkyl alcohol ester. (G) Polyester type polyurethane resin. (S) 1,3-benzenedicarboylic acid, polymer with 1,4-benzenedicarboxylic acid,2,2-dimethyl1,3-propanediol, dodecanedioic acid, 1,2-ethanediol, hexanedioic acid, 1,6-hexanediol, .alpha.-hydroxy-.omega.-hydroxypoly[oxy(methyl-1,2-ethanediyl)] and 1,1’methylenebis[4-isocyanatobenzene]. Frm 00066 Fmt 4703 Sfmt 4703 E:\FR\FM\26DEN1.SGM 26DEN1 76034 Federal Register / Vol. 77, No. 247 / Wednesday, December 26, 2012 / Notices TABLE III—32 NOCS RECEIVED FROM 11/1/12 TO 11/30/12—Continued Case No. Received date Commencement notice end date P–12–0340 ...... 11/2/2012 10/23/2012 P–12–0363 ...... 11/6/2012 10/27/2012 ...... ...... ...... ...... 11/26/2012 11/9/2012 11/6/2012 11/27/2012 10/28/2012 11/7/2012 10/29/2012 11/21/2012 P–12–0483 ...... 11/2/2012 11/1/2012 P–12–0501 ...... 11/9/2012 11/8/2012 11/27/2012 11/20/2012 11/20/2012 11/20/2012 11/16/2012 11/16/2012 11/19/2012 11/19/2012 P–12–0381 P–12–0447 P–12–0476 P–12–0482 P–12–0507 P–12–0511 P–12–0515 P–12–0517 ...... ...... ...... ...... If you are interested in information that is not included in these tables, you may contact EPA as described in Unit II. to access additional non-CBI information that may be available. List of Subjects Environmental protection, Chemicals, Hazardous substances, Imports, Notice of commencement, Premanufacturer, Reporting and recordkeeping requirements, Test marketing exemptions. Dated: December 10, 2012. Chandler Sirmons, Acting Director, Information Management Division, Office of Pollution Prevention and Toxics. [FR Doc. 2012–31063 Filed 12–21–12; 4:15 pm] BILLING CODE 6560–50–P ENVIRONMENTAL PROTECTION AGENCY [EPA–HQ–OW–2011–0943; FRL9716–6] National Water Program 2012 Strategy: Response to Climate Change Environmental Protection Agency (EPA). ACTION: Notice of availability. AGENCY: The Environmental Protection Agency (EPA) is publishing the final ‘‘National Water Program 2012 Strategy: Response to Climate Change’’ (2012 Strategy). The Strategy describes a set of long-term visions and goals for the management of water resources in light of climate change and charts key tkelley on DSK3SPTVN1PROD with SUMMARY: VerDate Mar<15>2010 06:31 Dec 22, 2012 Jkt 229001 Chemical (G) Reaction product of bisphenol a diglycidyl ether and an amineterminated cycloaliphatic propoxylate. (G) Alkylcarboxyalkenyl polymer with carboxyalkenyl dihydroxyalkylate, carboxyalkenyl and alkylalkenyl sulfonate sodium salt. (G) Amido amine polyether polymer. (G) Hydrophobic modified acrylic swellable emulsion. (G) Aromatic polyester polyether polyol. (S) Flue dust, automotive metal recovery; definition: Flue dust collected from the hot gases released from a cupola furnace during a metal recovery process used by the automotive industry composed primarily of oxides of zinc, iron, manganese, aluminum, and silicon. (G) Siloxanes and silicones, substituted alkyl group-terminated, ethoxylated, polymers with 5-isocyanato-1-(isocyanatomethyl)-,1,3,3-trimethylcyclohexane and N-alkyl glycol, hydroxyethyl methacrylate-blocked. (S) Slimes and sludges, automotive phosphate conversion coating wastewater definition: The waste solution produced during the zinc phosphate conversion coating process of automobiles. It may contain oxides of iron, calcium, aluminum, zinc, nickel and magnesium. (G) Poly(oxyalkylene) alkylamine. (G) Poly(oxyalkylene) alkylamine. (G) Polycarboxylic acids, polymer with polyols. (G) Polycarboxylic acids, polymer with polyols. strategic actions to be taken to achieve the goals in 2012 and subsequent years. The Strategy will be a roadmap to inform the National Water Program planning process. The Strategy also includes goals and strategic actions for EPA in ten geographic climate regions, largely patterned after the climate regions established by the U.S. Global Change Research Program (USGCRP). The final version of the Strategy reflects public comments. The final Strategy, is available on the Internet at: https:// www.epa.gov/water/climatechange. ADDRESSES: Public comments received on the draft strategy and the final Strategy are available at the Water Docket, located at the EPA Docket Center (EPA/DC), EPA West 1301 Constitution Avenue NW., Washington, DC 20004. These documents are also available via the EPA Dockets at https:// www.regulations.gov under docket number EPA–HQ–OW–2012–0943. FOR FURTHER INFORMATION CONTACT: Ms. Elana Goldstein, Office of Water (4101M), Environmental Protection Agency, Ariel Rios Building, Mail Code 4101M, 1200 Pennsylvania Avenue NW., Washington, DC 20460; telephone number: 202–564–1800; email address: water_climate_change@epa.gov. For more information, visit: https:// www.epa.gov/water/climatechange. SUPPLEMENTARY INFORMATION: Climate change alters the hydrological background in which EPA’s water programs function. Climate change poses challenges to various aspects of water resource management, including PO 00000 Frm 00067 Fmt 4703 Sfmt 4703 how to: address risks to drinking water, wastewater and storm water infrastructure; protect the quality of surface water, ground water and drinking water; build resilience of watersheds, wetlands, and coastal and ocean waters; and work with tribal communities to understand the implications of climate change to their economy and culture. To remain effective and continue to fulfill its mission, the National Water Program will need to adapt to already observed and projected climatic changes. To that end, EPA will continue to collaborate with partners at the federal, state, tribal, and local levels to develop the requisite information, tools and strategies. Dated: December 17, 2012. Nancy K. Stoner, Acting Assistant Administrator for Water. [FR Doc. 2012–31089 Filed 12–21–12; 4:15 pm] BILLING CODE 6560–50–P ENVIRONMENTAL PROTECTION AGENCY [FRL–9764–2] Public Water System Supervision Program Approval for the State of Ohio Environmental Protection Agency (EPA). ACTION: Notice of tentative approval. AGENCY: Notice is hereby given that the EPA has tentatively approved revisions to the State of Ohio’s public water system supervision program. Ohio SUMMARY: E:\FR\FM\26DEN1.SGM 26DEN1

Agencies

ENVIRONMENTAL PROTECTION AGENCY

[Federal Register Volume 77, Number 247 (Wednesday, December 26, 2012)]
[Notices]
[Pages 76029-76034]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-31063]

-----------------------------------------------------------------------

ENVIRONMENTAL PROTECTION AGENCY

[EPA-HQ-OPPT-2012-0881; FRL-9373-1]

Certain New Chemicals; Receipt and Status Information

AGENCY: Environmental Protection Agency (EPA).

ACTION: Notice.

-----------------------------------------------------------------------

SUMMARY: The Toxic Substances Control Act (TSCA) requires any person
who intends to manufacture (defined by statute to include import) a new
chemical (i.e., a chemical not on the TSCA Chemical Substances
Inventory (TSCA Inventory)) to notify EPA and comply with the statutory
provisions pertaining to the manufacture of new chemicals. In addition
under TSCA, EPA is required to publish in the Federal Register a notice
of receipt of a premanufacture notice (PMN) or an application for a
test marketing exemption (TME), and to publish in the Federal Register
periodic status reports on the new chemicals under review and the
receipt of notices of commencement (NOC) to manufacture those
chemicals. This document, which covers the period from November 1, 2012
to November 30, 2012, and provides the required notice and status
report, consists of the PMNs and TMEs, both pending or expired, and the
NOC to manufacture a new chemical that the Agency has received under
TSCA section 5 during this time period.

DATES: Comments identified by the specific PMN number or TME number,
must be received on or before January 25, 2013.

ADDRESSES: Submit your comments, identified by docket identification
(ID) number EPA-HQ-OPPT-2012-0881, and the specific PMN number or TME
number for the chemical related to your comment, by one of the
following methods:
Federal eRulemaking Portal: https://www.regulations.gov.
Follow the online instructions for submitting comments.
Mail: Document Control Office (7407M), Office of Pollution
Prevention and Toxics (OPPT), Environmental Protection Agency, 1200
Pennsylvania Ave., NW., Washington, DC 20460-0001.
Hand Delivery: OPPT Document Control Office (DCO), EPA
East Bldg., Rm. 6428, 1201 Constitution Ave., NW., Washington, DC. The
DCO is open from 8 a.m. to 4 p.m., Monday through Friday, excluding
legal holidays. The telephone number for the DCO is (202) 564-8930.
Such deliveries are only accepted during the DCO's normal hours of
operation, and special arrangements should be made for deliveries of
boxed information.
Instructions: EPA's policy is that all comments received will be
included in the docket without change and may be made available online
at https://www.regulations.gov, including any personal information
provided, unless the comment includes information claimed to be
Confidential Business Information (CBI) or other information whose
disclosure is restricted by statute. Do not submit information that you
consider to be CBI or otherwise protected through regulations.gov or
email. The regulations.gov Web site is an ``anonymous access'' system,
which means EPA will not know your identity or contact information
unless you provide it in the body of your comment. If you send an email
comment directly to EPA without going through regulations.gov, your
email address will be automatically captured and included as part of
the comment that is placed in the docket and made available on the
Internet. If you submit an electronic comment, EPA recommends that you
include your name and other contact information in the body of your
comment and with any disk or CD-ROM you submit. If EPA cannot read your
comment due to technical difficulties and cannot contact you for
clarification, EPA may not be able to consider your comment. Electronic
files should avoid the use of special characters, any form of
encryption, and be free of any defects or viruses.
Docket: All documents in the docket are listed in the docket index
available at https://www.regulations.gov. Although listed in the index,
some information is not publicly available, e.g., CBI or other
information whose disclosure is restricted by statute. Certain other
material, such as copyrighted material, will be publicly available only
in hard copy. Publicly available docket materials are available
electronically at https://www.regulations.gov, or, if only available in
hard copy, at the OPPT Docket. The OPPT Docket is located in the EPA
Docket Center (EPA/DC) at Rm. 3334, EPA West Bldg., 1301 Constitution
Ave., NW., Washington, DC. The EPA/DC Public Reading Room hours of
operation are 8:30 a.m. to 4:30 p.m., Monday through Friday, excluding
legal holidays. The telephone number of the EPA/DC Public Reading Room
is (202) 566-1744, and the telephone number for the OPPT Docket is
(202) 566-0280. Docket visitors are required to show photographic
identification, pass through a metal detector, and sign the EPA visitor
log. All visitor bags are processed through an X-ray machine and
subject to search. Visitors will be provided an EPA/DC badge that must
be visible at all times in the building and returned upon departure.

FOR FURTHER INFORMATION CONTACT: For technical information contact:
Bernice Mudd, Information Management Division (7407M), Office of
Pollution Prevention and Toxics, Environmental Protection Agency, 1200
Pennsylvania Ave., NW., Washington, DC 20460-0001; telephone number:
(202) 564-8955; fax number: (202) 564-8951; email address:
mudd.bernice@epa.gov.
For general information contact: The TSCA-Hotline, ABVI-Goodwill,
422 South Clinton Ave., Rochester, NY 14620; telephone number: (202)
554-1404; email address: TSCA-Hotline@epa.gov.

SUPPLEMENTARY INFORMATION:

I. General Information

A. Does this action apply to me?

This action is directed to the public in general. As such, the
Agency has not attempted to describe the specific entities that this
action may apply to. Although others may be affected, this action
applies directly to the submitter of the PMNs addressed in this action.

B. What should I consider as I prepare my comments for EPA?

1. Submitting CBI. Do not submit this information to EPA through
regulations.gov or email. Clearly mark the part or all of the
information that you claim to be CBI. For CBI information in a disk or
CD-ROM that you mail to EPA, mark the outside of the disk or CD-ROM as
CBI and then identify electronically within the disk or CD-ROM the
specific information that is claimed as CBI. In addition to one
complete version of the comment that includes information claimed as
CBI, a copy of the comment that does not contain the information
claimed as CBI must be submitted for inclusion in the public docket.
Information so marked will not be disclosed except in accordance with
procedures set forth in 40 CFR part 2.
2. Tips for preparing your comments. When submitting comments,
remember to:
i. Identify the document by docket ID number and other identifying
information (subject heading, Federal Register date and page number).

[[Page 76030]]

ii. Follow directions. The Agency may ask you to respond to
specific questions or organize comments by referencing a Code of
Federal Regulations (CFR) part or section number.
iii. Explain why you agree or disagree; suggest alternatives and
substitute language for your requested changes.
iv. Describe any assumptions and provide any technical information
and/or data that you used.
v. If you estimate potential costs or burdens, explain how you
arrived at your estimate in sufficient detail to allow for it to be
reproduced.
vi. Provide specific examples to illustrate your concerns and
suggest alternatives.
vii. Explain your views as clearly as possible, avoiding the use of
profanity or personal threats.
viii. Make sure to submit your comments by the comment period
deadline identified.

II. Why is EPA taking this action?

EPA classifies a chemical substance as either an ``existing''
chemical or a ``new'' chemical. Any chemical substance that is not on
EPA's TSCA Inventory is classified as a ``new chemical,'' while those
that are on the TSCA Inventory are classified as an ``existing
chemical.'' For more information about the TSCA Inventory go to https://www.epa.gov/opptintr/newchems/pubs/inventory.htm. Anyone who plans to
manufacture or import a new chemical substance for a non-exempt
commercial purpose is required by TSCA section 5 to provide EPA with a
PMN, before initiating the activity. Section 5(h)(1) of TSCA authorizes
EPA to allow persons, upon application, to manufacture (includes
import) or process a new chemical substance, or a chemical substance
subject to a significant new use rule (SNUR) issued under TSCA section
5(a), for ``test marketing'' purposes, which is referred to as a test
marketing exemption, or TME. For more information about the
requirements applicable to a new chemical go to: https://www.epa.gov/oppt/newchems.
Under TSCA sections 5(d)(2) and 5(d)(3), EPA is required to publish
in the Federal Register a notice of receipt of a PMN or an application
for a TME and to publish in the Federal Register periodic status
reports on the new chemicals under review and the receipt of NOCs to
manufacture those chemicals. This status report, which covers the
period from November 1, 2012 to November 30, 2012, consists of the PMNs
and TMEs, both pending or expired, and the NOCs to manufacture a new
chemical that the Agency has received under TSCA section 5 during this
time period.

III. Receipt and Status Reports

In Table I. of this unit, EPA provides the following information
(to the extent that such information is not claimed as CBI) on the PMNs
received by EPA during this period: The EPA case number assigned to the
PMN, the date the PMN was received by EPA, the projected end date for
EPA's review of the PMN, the submitting manufacturer/importer, the
potential uses identified by the manufacturer/importer in the PMN, and
the chemical identity.

Table I--55 PMNs Received From 11/1/2012 to 11/30/12
----------------------------------------------------------------------------------------------------------------
Projected
Case No. Received notice end Manufacturer/ Use Chemical
date date importer
----------------------------------------------------------------------------------------------------------------
P-13-0082............ 11/2/2012 1/30/2013 Henkel Corp....... (S) Hotmelt (G) Acrylic modified
adhesive for polyether-ester
panel lamination polyurethane
and other prepolymer.
assemblies.
P-13-0083............ 11/1/2012 1/29/2013 CBI............... (S) Coatings (G) Epoxysilane
additive. homopolymer.
P-13-0090............ 11/1/2012 1/29/2013 Cytec Industries, (G) Resin for non- (G) Alkenenitrile,
Inc.. dispersive use. polymer with
alkadiene, substituted
alkyl-terminated,
polymers with
substituted
carbonomocycles,
alkoxy-terminated-
substituted alkyl-
alkadiene polymer,
substituted
carbomoncycle and
halogen substituted
carbomonocycle.
P-13-0091............ 11/5/2012 2/2/2013 Cray Valley USA, (G) Additive for (G) Siloxane functional
LLC. rubber to improve polybutadiene polymer.
properties.
P-13-0092............ 11/6/2012 2/3/2013 CBI............... (G) Adhesive for (G) Latex polymer.
electrical
industry use.
P-13-0093............ 11/8/2012 2/5/2013 The Goodyear Tire (S) Precursor to (S) Neodymium,
& Rubber Co. polymerization butadiene iso-bu
Department 100D. catalyst. neodecanoate
complexes.
P-13-0094............ 11/6/2012 2/3/2013 CBI............... (G) Additive for (G) Acrylic ester
adhesives, functionalized
pottings and polyether polymer.
sealants.
P-13-0095............ 11/6/2012 2/3/2013 Gelest, Inc....... (S) Further (S) Silane,
purified at one bicyclo[2.2.1]hept-2-
site; further yldiethoxymethyl-
purified material
packaged and sent
to end use for
use in CVD LOWK
dielectric
barrier in
microelectronic
application..
P-13-0096............ 11/12/2012 2/9/2013 Cytec Industries, (G) Coating resin. (G) Alkenoic acid,
Inc.. reaction product with
alkylpolyol, polymers
with substituted
heteromonocycle.

[[Page 76031]]

P-13-0097............ 11/9/2012 2/6/2013 Shin ETSU Microsi. (G) Non (G) Vinyl chloride
combustible emulsion (acrylic
coating for non group emulsion type).
woven fabric for
automobile air
filters and
carpet flooring
materials.
P-13-0098............ 11/12/2012 2/9/2013 CBI............... (G) An open, non- (G) Modified
dispersive use. polyarylamide salt.
P-13-0099............ 11/13/2012 2/10/2013 H.B. Fuller (G) Industrial (G) 1,4-
Company. adhesive. benzenedicarboxylic
acid, polymer with 2,2-
dimethyl-1,3-
propanediol, alkane
diacid, 1,2-
ethanediol,
hexanedioic acid,
alkanediol, .alpha.-
hydro-.omega.-
hydroxypoly[oxy(methyl-
1,2-ethanediyl)], 1,3-
isobenzofurandione,
1,1'-methylenebis[4-
isocyanatobenzene], 2-
oxepanone and 2,2'-
oxybis[ethanol].
P-13-0100............ 11/13/2012 2/10/2013 H.B. Fuller (G) Industrial (G) Alkane diacid,
Company. adhesive. polymer with
hexanedioic acid,
alkanediol, .alpha.-
hydro-.omega.-
hydroxypoly[oxy(methyl-
1,2-ethanediyl)], 1,3-
isobenzofurandione,
1,1'-methylenebis[4-
isocyanatobenzene], 2-
oxepanone and 2,2'-
oxybis[ethanol].
P-13-0101............ 11/13/2012 2/10/2013 H.B. Fuller (G) Industrial (G) 1,3-
Company. adhesive. benzenedicarboxylic
acid, polymer with 1,4-
benzenedicarboxylic
acid, alkane diacid,
1,2-ethanediol,
hexanedioic acid,
alkanediol, .alpha.-
hydro-.omega.-
hydroxypoly[oxy(methyl-
1,2-ethanediyl)], 1,3-
isobenzofurandione,
1,1'-methylenebis[4-
isocyanatobenzene], 2-
oxepanone and 2,2'-
oxybis[ethanol].
P-13-0102............ 11/13/2012 2/10/2013 H.B. Fuller (G) Industrial (G) Alkane diacid,
Company. adhesive. polymer with
hexanedioic acid,
alkanediol, .alpha.-
hydro-.omega.-
hydroxypoly[oxy(methyl-
1,2-ethanediyl)], 1,1'-
methylenebis[4-
isocyanatobenzene], 2-
oxepanone and
.alpha.,.alpha.',.alph
a.-1.
P-13-0103............ 11/13/2012 2/10/2013 H.B. Fuller (G) Industrial (G) Alkane diacid,
Company. adhesive. polymer with 2,2-
dimethyl-1,3-
propanediol, 1,2-
ethanediol,
hexanedioic acid,
alkanediol, .alpha.-
hydro-.omega.-
hydroxypoly[oxy(methyl-
1,2-ethanediyl)], 1,1'-
methylenebis[4-
isocyanatobenzene],
and.alpha.,.alpha.',.a
lpha.-1.
P-13-0104............ 11/13/2012 2/10/2013 H.B. Fuller (G) Industrial (G) Alkane diacid,
Company. adhesive. polymer with 2,2-
dimethyl-1,3-
propanediol, 1,2-
ethanediol,
hexanedioic acid,
alkanediol, .alpha.-
hydro-.omega.-
hydroxypoly[oxy(methyl-
1,2-ethanediyl)], 1,3-
isobenzofurandione,
1,1'-methylenebis[4-
isocyanatobenzene],
and 2,2'-
oxybis[ethanol].
P-13-0105............ 11/13/2012 2/10/2013 Sika Corporation.. (G) Latent (G) Latent hardener for
hardener for polyurethane.
polyurethane roof
membrane.
P-13-0106............ 11/9/2012 2/6/2013 The Goodyear Tire (S) Precursor to (G) Neodymium, Ziegler--
& Rubber Company. polymerization Natta preformed stage
catalyst. 1 catalyst.
P-13-0107............ 11/14/2012 2/11/2013 Trinity (S) Flame (S) Alkanes, C22 30-
Manufacturing, retardant for branched and linear,
Inc.. rubber products. chloro.
P-13-0108............ 11/14/2012 2/11/2013 CBI............... (S) Feed for a (S) Bromine,
bromine recovery manufacturer of, by-
unit. products from distant
residues.
P-13-0109............ 11/14/2012 2/11/2013 Trinity (S) Flame (S) Alkanes, C24 28,
Manufacturing, retardant in chloro.
Inc.. rubber products;
extreme pressure
additive in
lubricants.
P-13-0110............ 11/14/2012 2/11/2013 CBI............... (G) Additive, (G) Hydroxyalkyl
open, non- methacrylate, reaction
dispersive use. product with cyclic
ether.
P-13-0111............ 11/15/2012 2/12/2013 CBI............... (G) Additive, (G) Acrylfunctional
open, non- polysiloxane, reaction
dispersive use. product of alcohols
with isocyanates.
P-13-0112............ 11/15/2012 2/12/2013 CBI............... (G) Additive, (G) Acrylfunctional
open, non- polysiloxane, reaction
dispersive use. product of alcohols
with isocyanates.
P-13-0113............ 11/15/2012 2/12/2013 CBI............... (G) Additive, (G) Acrylfunctional
open, non- polysiloxane, reaction
dispersive use. product of alcohols
with isocyanates.

[[Page 76032]]

P-13-0114............ 11/19/2012 2/16/2013 CBI............... (S) Reactant/ (G) Sorbitan ester.
intermediate for
polymers and
oligomers,
polyesters, and
other materials
that might
include personal
care and
pharmaceutical
applications.
P-13-0115............ 11/20/2012 2/17/2013 CBI............... (G) Pigment (G) Fatty acids of
dispersant. natural oils,
conjugated, maleated,
substituted
phenoxyalkyl ester.
P-13-0116............ 11/20/2012 2/17/2013 CBI............... (G) Pigment (G) Fatty acids of
dispersant. natural oils,
conjugated, maleated,
substituted
phenoxyalkyl ester.
P-13-0117............ 11/20/2012 2/17/2013 H.B. Fuller (G) Industrial (G) Vegetable oil,
Company. adhesive. polymer with
isocyanate.
P-13-0118............ 11/20/2012 2/17/2013 CBI............... (G) Industrial (G) Vegetable oil,
adhesive. polymer with
isocyanate and
propanol, oxybis-.
P-13-0119............ 11/20/2012 2/17/2013 CBI............... (G) Polymer (S) D-glucitol, 1,3:2,4-
processing bis-o-[(4-
additive. ethylphenyl)methylene]-
.
P-13-0120............ 11/20/2012 2/17/2013 CBI............... (S) Catalyst for (G) Substituted
use in dimethyltin.
polyurethane
coatings.
P-13-0121............ 11/20/2012 2/17/2013 CBI............... (G) Polymeric (G) Substituted
colorant. polymeric aromatic
amine azo colorant.
P-13-0122............ 11/20/2012 2/17/2013 CBI............... (G) Packaging (G) Acetic acid ethenyl
material. ester, copolymer,
hydrolyzed.
P-13-0123............ 11/20/2012 2/17/2013 CBI............... (G) Additive, (G) Salt of acidic
open, non- polymers with
dispersive use. monomeric and
polymeric bases.
P-13-0124............ 11/20/2012 2/17/2013 DIC International (G) Polymer for (G) Coating polymer.
(USA) LLC. coating.
P-13-0125............ 11/20/2012 2/17/2013 Soane Energy LLC.. (G) Used in the (S) Poly(oxy-1,2-
upstream oil and ethanediyl), .alpha.-
gas industry. hydro-.omega.-hydroxy-
, hydrogen 2-C15 20-
alkenylbutanediotes.
P-13-0126............ 11/20/2012 2/17/2013 Soane Energy LLC.. (G) Used in the (S) Poly(oxy-1,2-
upstream oil and ethanediyl), .alpha.-
gas industry. hydro-.omega.-hydroxy-
, hydrogen 2-C15 20-
alkenylbutanediotes,
sodium salts.
P-13-0127............ 11/20/2012 2/17/2013 Miwon North (S) Resin for (G) Monofunctional
America, Inc.. industrial acrylate.
coating.
P-13-0128............ 11/21/2012 2/18/2013 CBI............... (G) Additive, (G) Polyether modified
open, non- potassium polystyrene
dispersive use. maleate.
P-13-0129............ 11/21/2012 2/18/2013 CBI............... (G) Additive, (G) Polyether modified
open, non- fatty acid dimmer.
dispersive use.
P-13-0130............ 11/20/2012 2/17/2013 CBI............... (G) Flow improver (G) Formaldehyde,
for oilfield polymer with
applications. alklyphenols.
P-13-0131............ 11/26/2012 2/23/2013 CBI............... (G) Inhibitor for (G) Tertiary ammonium
oil field compound.
applications.
P-13-0132............ 11/26/2012 2/23/2013 Euticals, Inc..... (S) Monomer (S) Boronic acid, b-[3-
intermediate for [(1-oxo-2-propen-1-
use in the yl)amino]phenyl]-.
manufacture of a
polymer.
P-13-0133............ 11/27/2012 2/24/2013 CBI............... (G) Catalyst for (G) Dichlorophosphazene
silicone oligomers.
polymerization.
P-13-0134............ 11/27/2012 2/24/2013 CBI............... (G) Catalyst for (G) Partially
silicone hydrolyzed
polymerization. dichlorophosphazene
oligomers.
P-13-0135............ 11/26/2012 2/23/2013 Euticals, Inc..... (S) Intermediate (G) Substituted
monomer for use benzenamine.
in the
manufacture of
another monomer.
P-13-0136............ 11/28/2012 2/25/2013 Sika Corporation.. (G) Roof membrane (G) Latent hardener for
hardener. polyurethane.
P-13-0137............ 11/28/2012 2/25/2013 CBI............... (G) Chemical (S) Butanedioic acid, 2-
additive. (2-octen-1-yl)-.
P-13-0138............ 11/28/2012 2/25/2013 CBI............... (G) Textile (S) Butanedioic acid, 2-
processing (2-octen-1-yl)-,
additive. potassium salt (1:2).
P-13-0139............ 11/28/2012 2/25/2013 CBI............... (G) Gasoline (G) Fatty acids, alkyl-
additive. unsaturated, esters
with polyol.
P-13-0140............ 11/29/2012 2/26/2013 CBI............... (G) Solvent....... (S) Pentanoic acid, 5-
(dimethylamino)-2-
methyl-5-oxo-, methyl
ester.
P-13-0141............ 11/29/2012 2/26/2013 Dow Chemical (S) Hardener for (G) Alkyl amines
Company. epoxy polymer with
thermosetting polyglycol ether, and
coatings. bis a epoxy reaction
products with aromatic
epoxies.

[[Page 76033]]

P-13-0142............ 11/30/2012 2/27/2013 Scott Bader, Inc.. (G) Fabrication of (G) Unsaturated
composite urethane methacrylate.
articles.
----------------------------------------------------------------------------------------------------------------

In Table II. of this unit, EPA provides the following information
(to the extent that such information is not claimed as CBI) on the TMEs
received by EPA during this period: The EPA case number assigned to the
TME, the date the TME was received by EPA, the projected end date for
EPA's review of the TME, the submitting manufacturer/importer, the
potential uses identified by the manufacturer/importer in the TME, and
the chemical identity.

Table II-- 3 TMEs Received From 11/1/12 to 11/30/12
----------------------------------------------------------------------------------------------------------------
Projected
Case No. Received notice end Manufacturer/ Use Chemical
date date importer
----------------------------------------------------------------------------------------------------------------
T-13-0002............ 11/1/2012 12/15/2012 Cytec Industries, (G) Resin for non- (G) Alkenenitrile,
Inc.. dispersive use. polymer with
alkadiene, substituted
alkyl-terminated,
polymers with
substituted
carbonomocycles,
alkoxy-terminated-
substituted alkyl-
alkadiene polymer,
substituted
carbomonocycle and
halogen substituted
carbomonocycle.
T-13-0003............ 11/12/2012 12/26/2012 Cytec Industries, (G) Coating resin. (G) Alkenoic acid,
Inc.. reaction product with
alkylpolyol, polymers
with substituted
heteromonocycle.
T-13-0004............ 11/26/2012 1/9/2013 CBI............... (G) Inhibitor for (G) Tertiary ammonium
oil field compound.
applications.
----------------------------------------------------------------------------------------------------------------

In Table III. of this unit, EPA provides the following information
(to the extent that such information is not claimed as CBI) on the NOCs
received by EPA during this period: The EPA case number assigned to the
NOC, the date the NOC was received by EPA, the projected end date for
EPA's review of the NOC, and chemical identity.

Table III--32 NOCs Received From 11/1/12 to 11/30/12
----------------------------------------------------------------------------------------------------------------
Commencement
Case No. Received date notice end date Chemical
----------------------------------------------------------------------------------------------------------------
J-12-0004....................... 11/5/2012 10/25/2012 (G) Saccharomyces cerevisiae, strain CBI.
P-07-0101....................... 11/20/2012 5/7/2008 (G) Alkoxylate polymer.
P-08-0654....................... 11/20/2012 3/1/2009 (G) Fatty acids, C18-unsaturated., dimers,
polymers with diamines and monoacids.
P-09-0106....................... 11/27/2012 11/14/2012 (G) Fatty acids, tall-oil, reaction products
with modified fatty acids and
polyalkanolamines, hydrochlorides.
P-09-0107....................... 11/1/2012 10/4/2012 (G) Fatty acids, tall-oil, reaction products
with modified fatty acids and
polyalkanolamines.
P-09-0263....................... 11/14/2012 10/24/2012 (S) 4-dodecenenitrile, (4z)-.
P-10-0014....................... 11/26/2012 11/15/2012 (G) Quino[2,3-b]acridine-7, 14-dione, 2,9-
dichloro-5, 12-dihydro[4-[[2-
(sulfooxy)ethyl]substituted]phenyl]-,sodium
salt (1:1).
P-10-0560....................... 11/13/2012 10/4/2012 (G) Silyl-modified polymer.
P-10-0561....................... 11/19/2012 10/4/2012 (G) Silyl-modified polymer.
P-11-0016....................... 11/20/2012 11/1/2012 (G) Adipic acid, polymer with
benzenepolycarboxylic acids, polyakylene
glycol, alkanediols, 1,1'-
methylenebis[isocyanatobenzene] and a
substituted-, trialkoxysilane.
P-11-0368....................... 11/20/2012 8/11/2011 (G) Ipdi modified polyester resin.
P-11-0557....................... 11/27/2012 11/2/2012 (G) 2-propenoic acid, 2-methyl-, 2-
hydroxyethyl ester, telomers with C18 26
alkyl acrylate, 1-dodecanthiol, N-
(hydroxymethyl)-2-methyl-2-propenamide,
polyfluorooctyl methacrylate and vinylidene
chloride, 2,2'-[1,2-diazenediylbis(1-
methylethylidene)]-bis[4,5-dihydro-1H-
imidazole]hydrochloride (1:2)-initiated.
P-12-0044....................... 11/30/2012 11/1/2012 (G) Multi-wall carbon nanotubes.
P-12-0143....................... 11/14/2012 11/2/2012 (G) Poly(oxy-1,4-butanediyl), -hydro-hydroxy-
, polymer with alkyldisocyanates.
P-12-0152....................... 11/13/2012 10/31/2012 (G) Ester substituted bicyclic olefin.
P-12-0174....................... 11/28/2012 11/7/2012 (G) Polyurethane.
P-12-0246....................... 11/19/2012 11/7/2012 (G) Methyl, phenyl, amino-functional
siloxanes and silsesquixane.
P-12-0247....................... 11/20/2012 10/10/2012 (G) Alkyl carboxylic acid, oxiranyl alkyl
ester, polymer with cycloalkyl dicarboxylic
acid anhydride, alkyl alcohol ester.
P-12-0248....................... 11/20/2012 11/1/2012 (G) Polyester type polyurethane resin.
P-12-0272....................... 11/6/2012 11/2/2012 (S) 1,3-benzenedicarboylic acid, polymer
with 1,4-benzenedicarboxylic acid,2,2-
dimethyl-1,3-propanediol, dodecanedioic
acid, 1,2-ethanediol, hexanedioic acid, 1,6-
hexanediol, .alpha.-hydroxy-.omega.-
hydroxypoly[oxy(methyl-1,2-ethanediyl)] and
1,1'-methylenebis[4-isocyanatobenzene].

[[Page 76034]]

P-12-0340....................... 11/2/2012 10/23/2012 (G) Reaction product of bisphenol a
diglycidyl ether and an amineterminated
cycloaliphatic propoxylate.
P-12-0363....................... 11/6/2012 10/27/2012 (G) Alkylcarboxyalkenyl polymer with
carboxyalkenyl dihydroxyalkylate,
carboxyalkenyl and alkylalkenyl sulfonate
sodium salt.
P-12-0381....................... 11/26/2012 10/28/2012 (G) Amido amine polyether polymer.
P-12-0447....................... 11/9/2012 11/7/2012 (G) Hydrophobic modified acrylic swellable
emulsion.
P-12-0476....................... 11/6/2012 10/29/2012 (G) Aromatic polyester polyether polyol.
P-12-0482....................... 11/27/2012 11/21/2012 (S) Flue dust, automotive metal recovery;
definition: Flue dust collected from the
hot gases released from a cupola furnace
during a metal recovery process used by the
automotive industry composed primarily of
oxides of zinc, iron, manganese, aluminum,
and silicon.
P-12-0483....................... 11/2/2012 11/1/2012 (G) Siloxanes and silicones, substituted
alkyl group-terminated, ethoxylated,
polymers with 5-isocyanato-1-
(isocyanatomethyl)-,1,3,3-
trimethylcyclohexane and N-alkyl glycol,
hydroxyethyl methacrylate-blocked.
P-12-0501....................... 11/9/2012 11/8/2012 (S) Slimes and sludges, automotive phosphate
conversion coating wastewater definition:
The waste solution produced during the zinc
phosphate conversion coating process of
automobiles. It may contain oxides of iron,
calcium, aluminum, zinc, nickel and
magnesium.
P-12-0507....................... 11/27/2012 11/16/2012 (G) Poly(oxyalkylene) alkylamine.
P-12-0511....................... 11/20/2012 11/16/2012 (G) Poly(oxyalkylene) alkylamine.
P-12-0515....................... 11/20/2012 11/19/2012 (G) Polycarboxylic acids, polymer with
polyols.
P-12-0517....................... 11/20/2012 11/19/2012 (G) Polycarboxylic acids, polymer with
polyols.
----------------------------------------------------------------------------------------------------------------

If you are interested in information that is not included in these
tables, you may contact EPA as described in Unit II. to access
additional non-CBI information that may be available.

List of Subjects

Environmental protection, Chemicals, Hazardous substances, Imports,
Notice of commencement, Premanufacturer, Reporting and recordkeeping
requirements, Test marketing exemptions.

Dated: December 10, 2012.
Chandler Sirmons,
Acting Director, Information Management Division, Office of Pollution
Prevention and Toxics.
[FR Doc. 2012-31063 Filed 12-21-12; 4:15 pm]
BILLING CODE 6560-50-P

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