Certain New Chemicals; Receipt and Status Information, 11871-11877 [2013-03765]

Download as PDF srobinson on DSK4SPTVN1PROD with NOTICES Federal Register / Vol. 78, No. 34 / Wednesday, February 20, 2013 / Notices biofuel feedstock producers by way of the Agency’s Central Data Exchange (CDX). The recordkeeping and reporting of this regulation will allow EPA to monitor compliance with the RFS program. We inform respondents that they may assert claims of business confidentiality (CBI) for information they submit in accordance with 40 CFR 2.203. Form Numbers: RFS0103: RFS2 Q1 2012 Activity Report RFS0104: RFS2 Activity Report RFS0201: RFS1 RIN Transaction Report (only if RFS1 RINs were bought, sold, retired, or reinstated) RFS0600: RFS2 Renewable Fuel Producer Supplemental Report (if applicable) RFS0701: RFS2 Renewable Fuel Producer Co-products Report RFS0801: RFS2 Renewable Biomass Report RFS0901: RFS2 Production Outlook Report EMTS: RFS2 RIN Transaction Report EMTS: RFS2 RIN Generation Report (Equivalent to RFS0400) RFS0301: RFS2 2010 Annual Compliance Report RFS0302: RFS2 2011 Annual Compliance Report EMTS: RFS2 RIN Transaction Report Respondents/affected entities: Producers of Renewable Fuels, Importers, Obligated Parties, Parties who own RINS (including foreign RIN owners). Respondent’s obligation to respond: mandatory Sections 114 and 208 of the Clean Air Act (CAA), 42 U.S.C. 7414 and 7542. Estimated number of respondents: 2,092,731. Frequency of response: Quarterly. Total estimated burden: 6,379,263 hours (per year). Burden is defined at 5 CFR 1320.03(b). Total estimated cost: $60,459,623 (per year), includes $ 320 annualized capital or operation & maintenance costs. Changes in Estimates: EMTS was introduced at the onset of the RFS2 program and was not a feature of RFS1. For the new EMTS system, all parties who owned RINs were required to reregister, disclose feedstock sources, prepare quarterly reports on RIN activity and submit annual compliance reports (obligated party only). Re-submittal provisions utilized in RFS1 are no longer required, resulting in a decrease in total responses for this ICR. The total responses for industry dropped from 4,525,625 to 2,092,731 a difference of 2,432,894 responses. Currently, biofuels producers and importers submit required quarterly reports along with VerDate Mar<15>2010 16:13 Feb 19, 2013 Jkt 229001 their third party disclosure on feedstock producers to EPA. All users of the EMTS system are required to submit quarterly RIN reports. The number of respondents or users of the EMTS system has more than doubled from 1,059,326 to 2,092,731 an increase of 1,639,992 users due to the additional response burden for mapping foreign and domestic plantation/forest land owners and foreign biofuel feedstock producers which were not reflected in the previous ICR reporting period. With an increase in the number of respondents, total burden hours have increased by more than 4 million costing the industry $60,459,623; however, a decrease of $47,882,366 was realized. The reduction in the total cost for this renewal is due to the fact that the EMTS system is automated and more efficient and helps users to prepare reports instantly, reducing the amount of time and the cost associated with responding, even with more than a million added users. This notable factor increased the industry burden hours, but will lower the total cost of this information collection request if renewed. Dated: February 13, 2013. Byron Bunker, Director, Transportation and Regional Programs Division. [FR Doc. 2013–03840 Filed 2–19–13; 8:45 am] BILLING CODE 6560–50–P ENVIRONMENTAL PROTECTION AGENCY [EPA–HQ–OPPT–2013–0053; FRL–9377–4] 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. SUMMARY: PO 00000 Frm 00058 Fmt 4703 Sfmt 4703 11871 This document, which covers the period from December 1, 2012 to January 11, 2013, and provides the required notice and status report, consists of the PMNs and TME, 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 March 22, 2013. ADDRESSES: Submit your comments, identified by docket identification (ID) number EPA–HQ–OPPT–2013–0053, 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 E:\FR\FM\20FEN1.SGM 20FEN1 11872 Federal Register / Vol. 78, No. 34 / Wednesday, February 20, 2013 / Notices 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 technical information contact: Bernice Mudd, Information Management Division, Records Docket Management Division (7407M), Office of Pollution Prevention and Toxics, Environmental Protection Agency, 1200 Pennsylvania Ave. NW., Washington, DC 20460–0001; telephone number: (202) 564–8951; fax number: (202) 564–8955; email address: mudd.bernice@epa.gov. For general information contact: The TSCA-Hotline, ABVI-Goodwill, 422 South Clinton Ave., Rochester, NY 14620; telephone number: (202) 554– 1404; email address: TSCAHotline@epa.gov. srobinson on DSK4SPTVN1PROD with NOTICES FOR FURTHER INFORMATION CONTACT: SUPPLEMENTARY INFORMATION: VerDate Mar<15>2010 16:13 Feb 19, 2013 Jkt 229001 I. General Information II. Why is EPA taking this action? 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. 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 December 1, 2012 to January 11,2013, consists of the PMNs and TME, 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. B. What should I consider as I prepare my comments for EPA? 1. Submitting CBI. Do not submit this information to EPA through regulations.gov or email. Clearly mark the part or all of the information that you claim to be CBI. For CBI information in a disk or CD–ROM that you mail to EPA, mark the outside of the disk or CD–ROM as CBI and then identify electronically within the disk or CD–ROM the specific information that is claimed as CBI. In addition to one complete version of the comment that includes information claimed as CBI, a copy of the comment that does not contain the information claimed as CBI must be submitted for inclusion in the public docket. Information so marked will not be disclosed except in accordance with procedures set forth in 40 CFR part 2. 2. Tips for preparing your comments. When submitting comments, remember to: i. Identify the document by docket ID number and other identifying information (subject heading, Federal Register date and page number). ii. Follow directions. The Agency may ask you to respond to specific questions or organize comments by referencing a Code of Federal Regulations (CFR) part or section number. iii. Explain why you agree or disagree; suggest alternatives and substitute language for your requested changes. iv. Describe any assumptions and provide any technical information and/ or data that you used. v. If you estimate potential costs or burdens, explain how you arrived at your estimate in sufficient detail to allow for it to be reproduced. vi. Provide specific examples to illustrate your concerns and suggest alternatives. vii. Explain your views as clearly as possible, avoiding the use of profanity or personal threats. viii. Make sure to submit your comments by the comment period deadline identified. PO 00000 Frm 00059 Fmt 4703 Sfmt 4703 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. E:\FR\FM\20FEN1.SGM 20FEN1 11873 Federal Register / Vol. 78, No. 34 / Wednesday, February 20, 2013 / Notices TABLE I—74 PMNS RECEIVED FROM 12/1/12 TO 1/11/13 Received date P–13–0142 ................ Projected notice end date 11/30/2012 P–13–0143 ................ Manufacturer/ importer Use Chemical 2/27/2013 Scott Bader, Inc ....... 11/30/2012 2/27/2013 12/3/2012 3/2/2013 Dover Chemical Corporation. CBI ........................... (G) Fabrication of composite articles. (G) Water emulsifier .................. P–13–0144 ................ (G) Unsaturated urethane methacrylate (G) Polyalkylene acid, alkanol amine derivative (G) polymer of substituted sulfonamide & didlycidylether P–13–0145 ................ 12/3/2012 3/2/2013 Corsitech .................. P–13–0146 ................ 12/4/2012 3/3/2013 CBI ........................... P–13–0147 ................ 12/5/2012 3/4/2013 Sika Corporation ...... P–13–0148 ................ 12/5/2012 3/4/2013 CBI ........................... P–13–0149 ................ 12/5/2012 3/4/2013 Ashland, Inc ............. P–13–0150 ................ 12/6/2012 3/5/2013 CBI ........................... P–13–0151 ................ 12/6/2012 3/5/2013 CBI ........................... (G) Chemical intermediate ........ P–13–0152 ................ 12/7/2012 3/6/2013 CBI ........................... (G) Contained use ..................... P–13–0153 ................ 12/7/2012 3/6/2013 CBI ........................... P–13–0154 ................ 12/7/2012 3/6/2013 CBI ........................... (G) Destructive and contained use. (G) Destructive use ................... P–13–0155 ................ 12/7/2012 3/6/2013 CBI ........................... (G) Contained use ..................... P–13–0156 ................ 12/7/2012 3/6/2013 CBI ........................... (G) Acrylic emulsion for waterborne exterior coatings. P–13–0157 ................ 12/7/2012 3/6/2013 CBI ........................... (G) Acrylic emulsion for waterborne exterior coatings. P–13–0158 ................ 12/7/2012 3/6/2013 CBI ........................... (G) Acrylic emulsion for waterborne exterior coatings. P–13–0159 ................ 12/7/2012 3/6/2013 CBI ........................... (G) Acrylic emulsion for waterborne exterior coatings. P–13–0160 ................ 12/7/2012 3/6/2013 CBI ........................... (G) Acrylic emulsion for waterborne exterior coatings. P–13–0161 ................ srobinson on DSK4SPTVN1PROD with NOTICES Case no. 12/7/2012 3/6/2013 CBI ........................... (G) Acrylic emulsion for waterborne exterior coatings. P–13–0162 ................ 12/7/2012 3/6/2013 Univation Technologies, LLC. (G) Catalyst in polymer synthesis. VerDate Mar<15>2010 16:13 Feb 19, 2013 Jkt 229001 PO 00000 Frm 00060 Fmt 4703 (G) Additive (generally 2–20% of the coating formulation) to enhance adhesion and gloss.. (G) Fuel additive—destructive use. (S) Acrylic resin used in the manufacture of ultra violet curable inks and coatings. (G) Hardener for roofing adhesive. (G) Crosslinker for radiation cured coatings. (G) Monomer for use in manufacturing polymers. (G) Reactant in polymer synthesis. Sfmt 4703 E:\FR\FM\20FEN1.SGM 20FEN1 (G) 2,5-furandione, polymer with alkene and alkyldiamine (G) Aromatic urethane acrylate composed of aliphatic glycol, aliphatic ester, aliphatic acid and aromatic isocyanate (G) Latent hardener for polyurethane (G) Urethane acrylate (G) Substituted hydroxyalkyl methacrylate (G) Aluminoxanes, alkyl, reaction products with dichloro substituted alkanediyl substituted heteropolycycle alkyl biphneyl zirconium and silica complex (G) Vegetable oil based polyol polyester (G) Metal, substituted heteropolycyclic (G) Aromatic hydrocarbon (G) Substituted carbomonocycle boron salt (G) Substituted carbomonocycle derivative metal (G) Alkyl methacrylate polymer with alkyl acrylate, amino acrylate and alkyl methacrylate (G) Acidic methacrylate polymer with alkyl methyacrylate, alkyl acrylate, amino acrylate and alkyl methacrylate (G) Acidic methacrylate polymer with alkyl methyacrylate, alkyl acrylate, amino acrylate, alkyl methacrylate, ammonium salt (G) Alkyl methacrylate polymer with alkyl acrylate, amino acrylate, alkyl hydroxy methacrylate, hydroxy alkyl methacrylate and alkyl methacrylate (G) Acidic methacrylate polymer with alkyl methacrylate, alkyl acrylate, amino acrylate, hydroxy alkyl methacrylate, and alkyl methacrylate (G) Acidic methacrylate polymer with alkyl methacrylate, alkyl acrylate, amino acrylate, hydroxy alkyl methacrylate, alkyl methacrylate, ammonium salt (G) Substituted cyclopentadienyl silico aluminoxanes 11874 Federal Register / Vol. 78, No. 34 / Wednesday, February 20, 2013 / Notices TABLE I—74 PMNS RECEIVED FROM 12/1/12 TO 1/11/13—Continued Received date P–13–0163 ................ Projected notice end date 12/10/2012 P–13–0164 ................ P–13–0165 ................ Manufacturer/ importer Use Chemical 3/9/2013 CBI ........................... (S) Textile finishing resin & industrial water-based ink vehicle. 12/10/2012 12/10/2012 3/9/2013 3/9/2013 CBI ........................... CBI ........................... (G) Chemical intermediate ........ (G) Paint component ................. P–13–0166 ................ 12/11/2012 3/10/2013 CBI ........................... 12/11/2012 12/12/2012 3/10/2013 3/11/2013 Sika Corporation ...... CBI ........................... P–13–0169 ................ 12/12/2012 3/11/2013 CBI ........................... (G) Electronic industry contained use. (G) Roof membrane hardener .. (S) Reactant for a lubricant additive. (G) Lubricant additive ................ (G) Alkyldioic acid, polymer with [(2Aminoalkyl)amino]alkylsulfonic acid monosodium salt. alkyldiol, alkyldiol, cycloaliphatic diisocyanate and cycloaliphatic diisocyanate, polyalkylene glycol monoalkyl ether-blocked (G) Benzotriazole derivative (G) Organic derivative of hydrotalcite (G) Carbopolycyclic P–13–0167 ................ P–13–0168 ................ P–13–0170 ................ 12/12/2012 3/11/2013 P–13–0171 ................ 12/13/2012 3/12/2013 P–13–0172 ................ 12/13/2012 3/12/2013 P–13–0173 ................ P–13–0174 ................ 12/14/2012 12/17/2012 3/13/2013 3/16/2013 Amfine Chemical Corporation. Dow Chemical U.S.A. Dow Chemical U.S.A. CBI ........................... Cytec Industries, Inc. P–13–0175 ................ 12/18/2012 3/17/2013 CBI ........................... P–13–0176 ................ 12/18/2012 3/17/2013 CBI ........................... P–13–0177 ................ 12/18/2012 3/17/2013 DIC International (USA), LLC. P–13–0178 ................ 12/18/2012 3/17/2013 Mane, USA ............... P–13–0179 ................ 12/19/2012 3/18/2013 CBI ........................... P–13–0180 ................ srobinson on DSK4SPTVN1PROD with NOTICES Case no. 12/19/2012 3/18/2013 CBI ........................... P–13–0181 ................ 12/19/2012 3/18/2013 CBI ........................... P–13–0182 ................ 12/19/2012 3/18/2013 CBI ........................... VerDate Mar<15>2010 16:13 Feb 19, 2013 Jkt 229001 PO 00000 Frm 00061 Fmt 4703 (G) Plastic additive .................... (G) Polymer used for adhesive formuation. (G) Polymer used for adhesive formuation. (G) Chemical intermediate ........ (S) Resin for ultra violet cured ink formulations. (S) Use as a coating additive in paper and paperboard to impart grease, alcohol, and solvent resistance. (S) Intermediate for use in the manufacture of a polymer. (G) A polymer component of industrial paint for coating/spray coating building materials, automotive materials and aero materials. (S) Fragrance in a fine fragrance; fragrance in a cosmetic product; fragrance in non cosmetic products. (G) The notified substance, nppt, is a new urea fertiliser additive that temporarily retards the enzymatic breakdown of urea by inhibition of urease. This provides an effective means of managing losses of nitrogen in the form of ammonia from surface-applied urea containing fertilizers. (S) Adhesion promoter for use in aphalt applications; emulsifier for use in asphalt applications. (S) Adhesion promoter for use in aphalt applications; emulsifier for use in asphalt applications. (S) Adhesion promoter for use in aphalt applications; emulsifier for use in asphalt applications. Sfmt 4703 E:\FR\FM\20FEN1.SGM 20FEN1 (G) Roofing adhesive (G) Alkylphenol (G) Sulfurized fatty acid derivative (G) Phosphoric acid, mixed esters (G) Silanated urethane polymer (G) Silanated urethane polymer (G) Alkenoic acid ester (G) Substituted carbomoncycles, polymer with alkyldiol (G) Perfluoro epoxide copolymer (G) Fluorinated oxirane polymer (G) Polyxiloxane acrylic resin (S) Cyclopentanol, 2-methyl-5(1-methylethyl), 1propanoate (G) Alkyl-substituted thiophosphoric acid triamide (G) Fatty acid amide (G) Fatty acid amide (G) Fatty acid amide 11875 Federal Register / Vol. 78, No. 34 / Wednesday, February 20, 2013 / Notices TABLE I—74 PMNS RECEIVED FROM 12/1/12 TO 1/11/13—Continued Received date P–13–0183 ................ Projected notice end date 12/19/2012 P–13–0184 ................ Manufacturer/ importer Use 3/18/2013 CBI ........................... 12/19/2012 3/18/2013 CBI ........................... P–13–0185 ................ 12/19/2012 3/18/2013 CBI ........................... P–13–0186 ................ 12/19/2012 3/18/2013 CBI ........................... (S) Adhesion promoter for use in aphalt applications; emulsifier for use in asphalt applications. (S) Adhesion promoter for use in aphalt applications; emulsifier for use in asphalt applications. (S) Adhesion promoter for use in aphalt applications; emulsifier for use in asphalt applications. (G) Lubricant additive ................ P–13–0187 ................ 12/18/2012 3/17/2013 CBI ........................... P–13–0188 ................ 12/21/2012 3/20/2013 Colonial Chemical, Inc. P–13–0189 ................ 12/23/2012 3/22/2013 CBI ........................... P–13–0190 ................ 12/26/2012 3/25/2013 CBI ........................... (S) Intermediate for use in the manufacture of polymers. (G) Pigment formulation additive P–13–0191 ................ P–13–0192 ................ 12/28/2012 12/28/2012 3/27/2013 3/27/2013 Zeon Chemicals, L.P. Zeon Chemicals, L.P. (S) Rubber compounds ............. (S) Rubber compounds ............. P–13–0193 ................ 1/2/2013 4/1/2013 Sika Corporation ...... P–13–0194 ................ 1/3/2013 4/2/2013 CBI ........................... P–13–0195 ................ 1/3/2013 4/2/2013 P–13–0196 ................ 1/3/2013 4/2/2013 P–13–0197 ................ 1/7/2013 4/6/2013 P–13–0198 ................ 1/7/2013 4/6/2013 Praxair Specialty Ceramics. Praxair Specialty Ceramics. Dow Chemical Company. Dow Chemical Company. (G) Hardener for roofing adhesive. (G) Coupling agent & film former. (G) Catalysts used in closed processes. (G) Catalysts used in closed processes. (G) Raw material for organic synthesis. (G) Coating curing agent .......... P–13–0199 ................ 1/7/2013 4/6/2013 Dow Chemical Company. (G) Coating curing agent .......... P–13–0200 ................ srobinson on DSK4SPTVN1PROD with NOTICES Case no. 1/8/2013 4/7/2013 CBI ........................... P–13–0201 ................ 1/8/2013 4/7/2013 CBI ........................... P–13–0202 ................ 1/8/2013 4/7/2013 CBI ........................... P–13–0203 ................ 1/8/2013 4/7/2013 CBI ........................... P–13–0204 ................ 1/8/2013 4/7/2013 CBI ........................... (S) Surfactant emulsions. (S) Surfactant emulsions. (S) Surfactant emulsions. (S) Surfactant emulsions. (S) Surfactant emulsions. VerDate Mar<15>2010 16:13 Feb 19, 2013 Jkt 229001 PO 00000 Frm 00062 Fmt 4703 Chemical (G) Industrial feedstock chemical. (S) Fire-fighting foams .............. Sfmt 4703 for use in asphalt for use in asphalt for use in asphalt for use in asphalt for use in asphalt E:\FR\FM\20FEN1.SGM 20FEN1 (G) Fatty acid amide (G) Fatty acid amide (G) Fatty acid amide (G) Substituted 2,5pyrrolidinedione, alkyl derivates (G) Algal biomass from a fermentation (S) Siloxanes and silicones, dime, 3-hydroxypropyl me, ethoxylated, ethers with oligomeric C10–16-alkyl Dglycopyranosides and oligomeric decyl octyl Dglycopyranosides and oligomeric decyl octyl Dglycopryanosides (G) Depolymerized waste plastics (G) 2-Oxepanone, homopolymer, ester with -alkyl—hydroxypoly (oxy-1,2ethanediyl), phosphate (G) alicyclic hydrocarbon resin (S) 4, 7-methano-1H-indene, 3a, 4, 7, 7a-tetrahydro-, polymer with 2-methyl-1, 3-butadiene and 5-(1methylethenyl)bicyclo[2.2.2.1]hept-2-ene (G) Amine adduct (G) Silylated polyazamide (G) Lanthanide group, groupiia, mn, oxide (G) Ni, lanthanide group, oxides (G) Alkyl substituted catechol (G) Alkyl hydroxyamine polymer with 2,2’-[(1methylethylidene)bis(4,1phenyleneoxymethylene)]bis[oxirane] (G) Alkyl hydroxyamine polymer with 2,2’-[(1methylethylidene)bis(4,1phenyleneoxymethylene)]bis[oxirane] (G) Fatty acid amide hydrochloride (G) Fatty acid amide hydrochloride (G) Fatty acid amide hydrochloride (G) Fatty acid amide hydrochloride (G) Fatty acid amide hydrochloride 11876 Federal Register / Vol. 78, No. 34 / Wednesday, February 20, 2013 / Notices TABLE I—74 PMNS RECEIVED FROM 12/1/12 TO 1/11/13—Continued Case no. Received date Projected notice end date Manufacturer/ importer Use Chemical (G) Fatty acid amide hydrochloride (G) Fatty acid amide hydrochloride (G) Fatty acid amide hydrochloride (G) Fatty acid amide hydrochloride (G) Fatty acid amide hydrochloride (G) Styrene acrylate polymer (G) Styrene acrylate polymer (G) Alkenyl succinate, amine salt P–13–0205 ................ 1/8/2013 4/7/2013 CBI ........................... P–13–0206 ................ 1/8/2013 4/7/2013 CBI ........................... P–13–0207 ................ 1/8/2013 4/7/2013 CBI ........................... P–13–0208 ................ 1/8/2013 4/7/2013 CBI ........................... P–13–0209 ................ 1/8/2013 4/7/2013 CBI ........................... P–13–0210 ................ P–13–0211 ................ P–13–0212 ................ 1/8/2013 1/8/2013 1/8/2013 4/7/2013 4/7/2013 4/7/2013 CBI ........................... CBI ........................... The Lubrizol Corporation. P–13–0213 ................ 1/8/2013 4/7/2013 The Lubrizol Corporation. P–13–0214 ................ 1/10/2013 4/9/2013 CBI ........................... (S) Surfactant for use in asphalt emulsions. (S) Surfactant for use in asphalt emulsions. (S) Surfactant for use in asphalt emulsions. (S) Surfactant for use in asphalt emulsions. (S) Surfactant for use in asphalt emulsions. (G) Thermoplastic binder .......... (G) Thermoplastic binder .......... (S) Metalworking fluid additive (lubricity and corrosion protection). (S) Metalworking fluid additive (lubricity and corrosion protection). (G) Coating resin ....................... P–13–0215 ................ 1/11/2013 4/10/2013 3M Company ............ (G) Adhesive ............................. 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 (G) Alkenyl succinate, amine salt (G) Polymer reaction product of formaldehyde, chloromethyl oxirane, phenol, 1,3isobenzofurandione, with n(2-aminoethyl)-1,2ethanediamine and phenol with tetrahydro-methano-indene glycidyl ether (G) Hetero substituted alkyl acrylate polymer the TME, the submitting manufacturer/ importer, the potential uses identified by the manufacturer/importer in the TME, and the chemical identity. TABLE II—1 TMES RECEIVED FROM 12/1/12 TO 1/11/13 Case No. T–13–5 ...................... Received date Projected notice end date 12/10/12 3/16/13 In Table III. of this unit, EPA provides the following information (to the extent that such information is not claimed as Manufacturer/ Importer Use Chemical Cytec Industries, Inc. (S)Resin for ultra violet formations. (G)Substituted carbomoncycles, polymer with alkyldiol. 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—33 NOCS RECEIVED FROM 12/1/12 TO 1/11/13 srobinson on DSK4SPTVN1PROD with NOTICES Case no. Received date Commencement notice end date P–06–0203 P–07–0072 P–09–0402 P–10–0361 P–10–0439 ....................................... ....................................... ....................................... ....................................... ....................................... 1/3/2013 12/14/2012 12/11/2012 12/12/2012 12/4/2012 12/31/2012 11/19/2012 11/19/2012 12/1/2012 10/25/2012 P–10–0442 P–12–0044 P–12–0064 P–12–0196 P–12–0245 P–12–0264 ....................................... ....................................... ....................................... ....................................... ....................................... ....................................... 12/18/2012 11/30/2012 12/14/2012 12/19/2012 12/27/2012 1/10/2013 12/17/2012 11/1/2012 11/16/2012 10/5/2012 12/13/2012 12/10/2012 VerDate Mar<15>2010 16:13 Feb 19, 2013 Jkt 229001 PO 00000 Frm 00063 Fmt 4703 Chemical (G) Polyisobutenyl succinimide (G) Alkanoic acid potassium salt (G) Oxoalkyl amino acid reaction product, sodium salt (G) Substituted phenol (S) Benzenesulfonic acid, 4-chloro-2-{[4,5-dihydro-3-methyl-5-oxo-1-(3sulfophenyl)-1h-pyrazole-4-yl)azo]-5-methyl,calcium salt (1:1) (G) MDI modified resin (G) Multi-wall carbon nanotubes (G) Green line emitting phosphor (G) Aromatic distillation bottoms (S) Niobium sulfur tin zinc oxide (G) Substituted, 2-hydroxy-N,N-dimethyl-N-[3-[[(13z)-1-oxo-13-docosen1-yl]amino]propyl]-3-sulfo-, inner salt Sfmt 4703 E:\FR\FM\20FEN1.SGM 20FEN1 Federal Register / Vol. 78, No. 34 / Wednesday, February 20, 2013 / Notices 11877 TABLE III—33 NOCS RECEIVED FROM 12/1/12 TO 1/11/13—Continued Case no. Received date Commencement notice end date P–12–0321 ....................................... P–12–0378 ....................................... 12/6/2012 1/3/2013 11/16/2012 12/28/2012 P–12–0398 ....................................... P–12–0444 ....................................... 12/7/2012 1/2/2013 11/7/2012 12/18/2012 ....................................... ....................................... ....................................... ....................................... ....................................... ....................................... 1/2/2013 1/2/2013 12/6/2012 12/6/2012 12/12/2012 12/6/2012 12/18/2012 12/18/2012 11/27/2012 11/9/2012 11/23/2012 11/21/2012 P–12–0519 ....................................... P–12–0521 ....................................... 12/13/2012 12/6/2012 12/8/2012 12/3/2012 P–12–0523 ....................................... P–12–0524 ....................................... 12/13/2012 12/6/2012 11/27/2012 12/3/2012 P–12–0526 ....................................... 1/2/2013 12/27/2012 P–12–0527 ....................................... P–12–0528 ....................................... 12/6/2012 12/11/2012 12/3/2012 12/10/2012 P–12–0529 ....................................... P–12–0540 ....................................... P–12–0542 ....................................... 12/5/2012 12/18/2012 12/19/2012 12/4/2012 12/5/2012 12/17/2012 P–12–0544 ....................................... 1/3/2013 12/24/2012 P–12–0564 ....................................... 1/10/2013 1/4/2013 P–12–0445 P–12–0446 P–12–0468 P–12–0469 P–12–0473 P–12–0485 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 srobinson on DSK4SPTVN1PROD with NOTICES Environmental protection, Chemicals, Hazardous substances, Imports, Notice of commencement, Premanufacturer, Reporting and recordkeeping requirements, Test marketing exemptions. Dated: February 4, 2013. Chandler Sirmons, Acting Director, Information Management Division, Office of Pollution Prevention and Toxics. [FR Doc. 2013–03765 Filed 2–19–13; 8:45 am] BILLING CODE 6560–50–P VerDate Mar<15>2010 16:13 Feb 19, 2013 Jkt 229001 Chemical (G) Aliphatic acrylate mixture (G) Diacrylate polymer with alkane esterdiol, alkane diol, alkane acid diol and diisocyanates (S) 1,2,4-benzenetricarboxylic acid, mixed lauryl and octyl triesters (G) Carbopolycyclic-alkyl-[[[[[[(haloalkyl-aryl]diazenyl]aryl]diazenyl]carbopolycyclic]diazenyl (G) Morpholine, [[[[(haloaryl)diazenyl]-alkylaryl]-diazenyl]aryl](G) Morpholine, [[[[(haloaryl)diazenyl]-alkylaryl]-diazenyl]aryl](G) Doped yttrium oxalate (G) Yttrium europium oxalate (S) Phenol 4-(ethoxymethyl)-2-methoxy-l (G) Oxirane, alkyl, polymer with aromatic isocyanate, alkyloxirane polymer with oxirane ether with alkyltriol, and oxirane, polyethylene glycol mono(alkylaromatic) ether-blocked (G) Alkyd polyester polyurethane (G) 2-Propenoic acid, 2-methyl-, alkyl esters, polymer with substituted methacrylate, substituted methacrylate, me methacrylate and polyalkene glycol alkyl ether, tert-bu 2-ethylhexaneperoxoate-initiated (G) Alkyl ketimines; polymeric ketimines (G) Vegetable-oil fatty acids, conjugated, polymers with ethylene glycol, substituted propanoic acid, anhydride, polyethylene glycol and trimethylolpropane, compounds with substituted alkanol (G) Siloxanes and silicones, substituted alkyl group-terminated ethers with polyethylene glycol and polyethylene glycol anhydride ester (G) Fatty acids of natural oils, conjugated, maleated (G) Substituted heteromonocycle, polymer with substituted alkane and substituted alkanediol, alkanoic acid substituted ester and substituted hetermonocyle homopolymer (G) Hydrogenated modified rosin (G) Styrenic anhydride maleimide terpolymer (G) Polyethyleneglycol modified polyacrylate block polypyridine polymer, hydrolyzed, sodium salts (G) Alkenoic acid, polymers with acrylate and polyalkandiol alkane ether alkyl alkenoate and polyalkene alkandiol alkane ether alkenoic alkyl ethers (G) 2-Propenoic acid 2-methyl, alkyl ester, polymer with heteromonocycle, substituted carbomonocycle, substituted alkyl propenoate, alkyl propenoate, alkyl propenoate, tert-bu benzenecarboperoxoate-initiated ENVIRONMENTAL PROTECTION AGENCY [EPA–HQ–RCRA–2013–0063; FRL–9782–5] Announcement of Requirements Gathering Meetings for the Electronic Manifest (e-Manifest) System Environmental Protection Agency (EPA). ACTION: Notice of public meetings. AGENCY: EPA’s Office of Resource Conservation and Recovery (ORCR) is holding public meetings in Arlington, Virginia; Chicago, Illinois; and Denver, Colorado to discuss and obtain public input from stakeholders on a national electronic manifest (‘‘e-Manifest’’) system to capture information regarding the shipment of hazardous waste from the time it leaves the generator facility where it was produced, until it reaches the off-site waste management facility that will store, treat, or dispose of the SUMMARY: PO 00000 Frm 00064 Fmt 4703 Sfmt 4703 hazardous waste. Specifically, the purpose of these meetings is to engage the states, industry, communities, nongovernmental organizations, and other stakeholders on what expectations and technical requirements EPA should consider as the agency begins the planning stage of the e-Manifest system development process. EPA envisions that e-Manifest will facilitate the electronic transmittal of manifests throughout the hazardous waste shipping process, including enabling better transparency by sharing data with the public at appropriate stages. Each meeting will be approximately one and one-half days. In order to meet the goals of the meetings, we encourage meeting participants from a variety of professional backgrounds to attend, such as state governmental staff, hazardous waste handlers (generators, transporters, waste management firms) staff, and each of their information technology (IT) staff. EPA will use E:\FR\FM\20FEN1.SGM 20FEN1

Agencies

ENVIRONMENTAL PROTECTION AGENCY

[Federal Register Volume 78, Number 34 (Wednesday, February 20, 2013)]
[Notices]
[Pages 11871-11877]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-03765]

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

ENVIRONMENTAL PROTECTION AGENCY

[EPA-HQ-OPPT-2013-0053; FRL-9377-4]

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 December 1, 2012
to January 11, 2013, and provides the required notice and status
report, consists of the PMNs and TME, 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 March 22, 2013.

ADDRESSES: Submit your comments, identified by docket identification
(ID) number EPA-HQ-OPPT-2013-0053, 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

[[Page 11872]]

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

SUPPLEMENTARY INFORMATION:

I. General Information

A. Does this action apply to me?

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

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

1. Submitting CBI. Do not submit this information to EPA through
regulations.gov or email. Clearly mark the part or all of the
information that you claim to be CBI. For CBI information in a disk or
CD-ROM that you mail to EPA, mark the outside of the disk or CD-ROM as
CBI and then identify electronically within the disk or CD-ROM the
specific information that is claimed as CBI. In addition to one
complete version of the comment that includes information claimed as
CBI, a copy of the comment that does not contain the information
claimed as CBI must be submitted for inclusion in the public docket.
Information so marked will not be disclosed except in accordance with
procedures set forth in 40 CFR part 2.
2. Tips for preparing your comments. When submitting comments,
remember to:
i. Identify the document by docket ID number and other identifying
information (subject heading, Federal Register date and page number).
ii. Follow directions. The Agency may ask you to respond to
specific questions or organize comments by referencing a Code of
Federal Regulations (CFR) part or section number.
iii. Explain why you agree or disagree; suggest alternatives and
substitute language for your requested changes.
iv. Describe any assumptions and provide any technical information
and/or data that you used.
v. If you estimate potential costs or burdens, explain how you
arrived at your estimate in sufficient detail to allow for it to be
reproduced.
vi. Provide specific examples to illustrate your concerns and
suggest alternatives.
vii. Explain your views as clearly as possible, avoiding the use of
profanity or personal threats.
viii. Make sure to submit your comments by the comment period
deadline identified.

II. Why is EPA taking this action?

EPA classifies a chemical substance as either an ``existing''
chemical or a ``new'' chemical. Any chemical substance that is not on
EPA's TSCA Inventory is classified as a ``new chemical,'' while those
that are on the TSCA Inventory are classified as an ``existing
chemical.'' For more information about the TSCA Inventory go to: https://www.epa.gov/opptintr/newchems/pubs/inventory.htm. Anyone who plans to
manufacture or import a new chemical substance for a non-exempt
commercial purpose is required by TSCA section 5 to provide EPA with a
PMN, before initiating the activity. Section 5(h)(1) of TSCA authorizes
EPA to allow persons, upon application, to manufacture (includes
import) or process a new chemical substance, or a chemical substance
subject to a significant new use rule (SNUR) issued under TSCA section
5(a), for ``test marketing'' purposes, which is referred to as a test
marketing exemption, or TME. For more information about the
requirements applicable to a new chemical go to: https://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 December 1, 2012 to January 11,2013, consists of the PMNs
and TME, 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.

[[Page 11873]]

Table I--74 PMNs Received From 12/1/12 to 1/11/13
----------------------------------------------------------------------------------------------------------------
Projected
Case no. Received notice end Manufacturer/ Use Chemical
date date importer
----------------------------------------------------------------------------------------------------------------
P-13-0142..................... 11/30/2012 2/27/2013 Scott Bader, Inc. (G) Fabrication (G) Unsaturated
of composite urethane
articles. methacrylate
P-13-0143..................... 11/30/2012 2/27/2013 Dover Chemical (G) Water (G) Polyalkylene
Corporation. emulsifier. acid, alkanol
amine
derivative
P-13-0144..................... 12/3/2012 3/2/2013 CBI.............. (G) Additive (G) polymer of
(generally 2-20% substituted
of the coating sulfonamide &
formulation) to didlycidylether
enhance adhesion
and gloss..
P-13-0145..................... 12/3/2012 3/2/2013 Corsitech........ (G) Fuel (G) 2,5-
additive--destru furandione,
ctive use. polymer with
alkene and
alkyldiamine
P-13-0146..................... 12/4/2012 3/3/2013 CBI.............. (S) Acrylic resin (G) Aromatic
used in the urethane
manufacture of acrylate
ultra violet composed of
curable inks and aliphatic
coatings. glycol,
aliphatic
ester,
aliphatic acid
and aromatic
isocyanate
P-13-0147..................... 12/5/2012 3/4/2013 Sika Corporation. (G) Hardener for (G) Latent
roofing adhesive. hardener for
polyurethane
P-13-0148..................... 12/5/2012 3/4/2013 CBI.............. (G) Crosslinker (G) Urethane
for radiation acrylate
cured coatings.
P-13-0149..................... 12/5/2012 3/4/2013 Ashland, Inc..... (G) Monomer for (G) Substituted
use in hydroxyalkyl
manufacturing methacrylate
polymers.
P-13-0150..................... 12/6/2012 3/5/2013 CBI.............. (G) Reactant in (G)
polymer Aluminoxanes,
synthesis. alkyl, reaction
products with
dichloro
substituted
alkanediyl
substituted
heteropolycycle
alkyl biphneyl
zirconium and
silica complex
P-13-0151..................... 12/6/2012 3/5/2013 CBI.............. (G) Chemical (G) Vegetable
intermediate. oil based
polyol
polyester
P-13-0152..................... 12/7/2012 3/6/2013 CBI.............. (G) Contained use (G) Metal,
substituted
heteropolycycli
c
P-13-0153..................... 12/7/2012 3/6/2013 CBI.............. (G) Destructive (G) Aromatic
and contained hydrocarbon
use.
P-13-0154..................... 12/7/2012 3/6/2013 CBI.............. (G) Destructive (G) Substituted
use. carbomonocycle
boron salt
P-13-0155..................... 12/7/2012 3/6/2013 CBI.............. (G) Contained use (G) Substituted
carbomonocycle
derivative
metal
P-13-0156..................... 12/7/2012 3/6/2013 CBI.............. (G) Acrylic (G) Alkyl
emulsion for methacrylate
waterborne polymer with
exterior alkyl acrylate,
coatings. amino acrylate
and alkyl
methacrylate
P-13-0157..................... 12/7/2012 3/6/2013 CBI.............. (G) Acrylic (G) Acidic
emulsion for methacrylate
waterborne polymer with
exterior alkyl
coatings. methyacrylate,
alkyl acrylate,
amino acrylate
and alkyl
methacrylate
P-13-0158..................... 12/7/2012 3/6/2013 CBI.............. (G) Acrylic (G) Acidic
emulsion for methacrylate
waterborne polymer with
exterior alkyl
coatings. methyacrylate,
alkyl acrylate,
amino acrylate,
alkyl
methacrylate,
ammonium salt
P-13-0159..................... 12/7/2012 3/6/2013 CBI.............. (G) Acrylic (G) Alkyl
emulsion for methacrylate
waterborne polymer with
exterior alkyl acrylate,
coatings. amino acrylate,
alkyl hydroxy
methacrylate,
hydroxy alkyl
methacrylate
and alkyl
methacrylate
P-13-0160..................... 12/7/2012 3/6/2013 CBI.............. (G) Acrylic (G) Acidic
emulsion for methacrylate
waterborne polymer with
exterior alkyl
coatings. methacrylate,
alkyl acrylate,
amino acrylate,
hydroxy alkyl
methacrylate,
and alkyl
methacrylate
P-13-0161..................... 12/7/2012 3/6/2013 CBI.............. (G) Acrylic (G) Acidic
emulsion for methacrylate
waterborne polymer with
exterior alkyl
coatings. methacrylate,
alkyl acrylate,
amino acrylate,
hydroxy alkyl
methacrylate,
alkyl
methacrylate,
ammonium salt
P-13-0162..................... 12/7/2012 3/6/2013 Univation (G) Catalyst in (G) Substituted
Technologies, polymer cyclopentadieny
LLC. synthesis. l silico
aluminoxanes

[[Page 11874]]

P-13-0163..................... 12/10/2012 3/9/2013 CBI.............. (S) Textile (G) Alkyldioic
finishing resin acid, polymer
& industrial with [(2-
water-based ink Aminoalkyl)amin
vehicle. o]alkylsulfonic
acid monosodium
salt.
alkyldiol,
alkyldiol,
cycloaliphatic
diisocyanate
and
cycloaliphatic
diisocyanate,
polyalkylene
glycol mono-
alkyl ether-
blocked
P-13-0164..................... 12/10/2012 3/9/2013 CBI.............. (G) Chemical (G)
intermediate. Benzotriazole
derivative
P-13-0165..................... 12/10/2012 3/9/2013 CBI.............. (G) Paint (G) Organic
component. derivative of
hydrotalcite
P-13-0166..................... 12/11/2012 3/10/2013 CBI.............. (G) Electronic (G)
industry Carbopolycyclic
contained use.
P-13-0167..................... 12/11/2012 3/10/2013 Sika Corporation. (G) Roof membrane (G) Roofing
hardener. adhesive
P-13-0168..................... 12/12/2012 3/11/2013 CBI.............. (S) Reactant for (G) Alkylphenol
a lubricant
additive.
P-13-0169..................... 12/12/2012 3/11/2013 CBI.............. (G) Lubricant (G) Sulfurized
additive. fatty acid
derivative
P-13-0170..................... 12/12/2012 3/11/2013 Amfine Chemical (G) Plastic (G) Phosphoric
Corporation. additive. acid, mixed
esters
P-13-0171..................... 12/13/2012 3/12/2013 Dow Chemical (G) Polymer used (G) Silanated
U.S.A. for adhesive urethane
formuation. polymer
P-13-0172..................... 12/13/2012 3/12/2013 Dow Chemical (G) Polymer used (G) Silanated
U.S.A. for adhesive urethane
formuation. polymer
P-13-0173..................... 12/14/2012 3/13/2013 CBI.............. (G) Chemical (G) Alkenoic
intermediate. acid ester
P-13-0174..................... 12/17/2012 3/16/2013 Cytec Industries, (S) Resin for (G) Substituted
Inc.. ultra violet carbomoncycles,
cured ink polymer with
formulations. alkyldiol
P-13-0175..................... 12/18/2012 3/17/2013 CBI.............. (S) Use as a (G) Perfluoro
coating additive epoxide
in paper and copolymer
paperboard to
impart grease,
alcohol, and
solvent
resistance.
P-13-0176..................... 12/18/2012 3/17/2013 CBI.............. (S) Intermediate (G) Fluorinated
for use in the oxirane polymer
manufacture of a
polymer.
P-13-0177..................... 12/18/2012 3/17/2013 DIC International (G) A polymer (G) Polyxiloxane
(USA), LLC. component of acrylic resin
industrial paint
for coating/
spray coating
building
materials,
automotive
materials and
aero materials.
P-13-0178..................... 12/18/2012 3/17/2013 Mane, USA........ (S) Fragrance in (S)
a fine Cyclopentanol,
fragrance; 2-methyl-5-(1-
fragrance in a methylethyl)- ,
cosmetic 1-propanoate
product;
fragrance in non
cosmetic
products.
P-13-0179..................... 12/19/2012 3/18/2013 CBI.............. (G) The notified (G) Alkyl-
substance, nppt, substituted
is a new urea thiophosphoric
fertiliser acid triamide
additive that
temporarily
retards the
enzymatic
breakdown of
urea by
inhibition of
urease. This
provides an
effective means
of managing
losses of
nitrogen in the
form of ammonia
from surface-
applied urea
containing
fertilizers.
P-13-0180..................... 12/19/2012 3/18/2013 CBI.............. (S) Adhesion (G) Fatty acid
promoter for use amide
in aphalt
applications;
emulsifier for
use in asphalt
applications.
P-13-0181..................... 12/19/2012 3/18/2013 CBI.............. (S) Adhesion (G) Fatty acid
promoter for use amide
in aphalt
applications;
emulsifier for
use in asphalt
applications.
P-13-0182..................... 12/19/2012 3/18/2013 CBI.............. (S) Adhesion (G) Fatty acid
promoter for use amide
in aphalt
applications;
emulsifier for
use in asphalt
applications.

[[Page 11875]]

P-13-0183..................... 12/19/2012 3/18/2013 CBI.............. (S) Adhesion (G) Fatty acid
promoter for use amide
in aphalt
applications;
emulsifier for
use in asphalt
applications.
P-13-0184..................... 12/19/2012 3/18/2013 CBI.............. (S) Adhesion (G) Fatty acid
promoter for use amide
in aphalt
applications;
emulsifier for
use in asphalt
applications.
P-13-0185..................... 12/19/2012 3/18/2013 CBI.............. (S) Adhesion (G) Fatty acid
promoter for use amide
in aphalt
applications;
emulsifier for
use in asphalt
applications.
P-13-0186..................... 12/19/2012 3/18/2013 CBI.............. (G) Lubricant (G) Substituted
additive. 2,5-
pyrrolidinedion
e, alkyl
derivates
P-13-0187..................... 12/18/2012 3/17/2013 CBI.............. (G) Industrial (G) Algal
feedstock biomass from a
chemical. fermentation
P-13-0188..................... 12/21/2012 3/20/2013 Colonial (S) Fire-fighting (S) Siloxanes
Chemical, Inc. foams. and silicones,
di-me, 3-
hydroxypropyl
me,
ethoxylated,
ethers with
oligomeric
C10 16-alkyl D-
glycopyranoside
s and
oligomeric
decyl octyl D-
glycopyranoside
s and
oligomeric
decyl octyl D-
glycopryanoside
s
P-13-0189..................... 12/23/2012 3/22/2013 CBI.............. (S) Intermediate (G)
for use in the Depolymerized
manufacture of waste plastics
polymers.
P-13-0190..................... 12/26/2012 3/25/2013 CBI.............. (G) Pigment (G) 2-Oxepanone,
formulation homopolymer,
additive. ester with -
alkyl--hydroxyp
oly (oxy-1,2-
ethanediyl),
phosphate
P-13-0191..................... 12/28/2012 3/27/2013 Zeon Chemicals, (S) Rubber (G) alicyclic
L.P.. compounds. hydrocarbon
resin
P-13-0192..................... 12/28/2012 3/27/2013 Zeon Chemicals, (S) Rubber (S) 4, 7-methano-
L.P.. compounds. 1H-indene, 3a,
4, 7, 7a-
tetrahydro-,
polymer with 2-
methyl-1, 3-
butadiene and 5-
(1-
methylethenyl)b
icyclo[2.2.2.1]
hept-2-ene
P-13-0193..................... 1/2/2013 4/1/2013 Sika Corporation. (G) Hardener for (G) Amine adduct
roofing adhesive.
P-13-0194..................... 1/3/2013 4/2/2013 CBI.............. (G) Coupling (G) Silylated
agent & film polyazamide
former.
P-13-0195..................... 1/3/2013 4/2/2013 Praxair Specialty (G) Catalysts (G) Lanthanide
Ceramics. used in closed group,
processes. groupiia, mn,
oxide
P-13-0196..................... 1/3/2013 4/2/2013 Praxair Specialty (G) Catalysts (G) Ni,
Ceramics. used in closed lanthanide
processes. group, oxides
P-13-0197..................... 1/7/2013 4/6/2013 Dow Chemical (G) Raw material (G) Alkyl
Company. for organic substituted
synthesis. catechol
P-13-0198..................... 1/7/2013 4/6/2013 Dow Chemical (G) Coating (G) Alkyl
Company. curing agent. hydroxyamine
polymer with
2,2'-[(1-
methylethyliden
e)bis(4,1-
phenyleneoxymet
hylene)]bis[oxi
rane]
P-13-0199..................... 1/7/2013 4/6/2013 Dow Chemical (G) Coating (G) Alkyl
Company. curing agent. hydroxyamine
polymer with
2,2'-[(1-
methylethyliden
e)bis(4,1-
phenyleneoxymet
hylene)]bis[oxi
rane]
P-13-0200..................... 1/8/2013 4/7/2013 CBI.............. (S) Surfactant (G) Fatty acid
for use in amide
asphalt hydrochloride
emulsions.
P-13-0201..................... 1/8/2013 4/7/2013 CBI.............. (S) Surfactant (G) Fatty acid
for use in amide
asphalt hydrochloride
emulsions.
P-13-0202..................... 1/8/2013 4/7/2013 CBI.............. (S) Surfactant (G) Fatty acid
for use in amide
asphalt hydrochloride
emulsions.
P-13-0203..................... 1/8/2013 4/7/2013 CBI.............. (S) Surfactant (G) Fatty acid
for use in amide
asphalt hydrochloride
emulsions.
P-13-0204..................... 1/8/2013 4/7/2013 CBI.............. (S) Surfactant (G) Fatty acid
for use in amide
asphalt hydrochloride
emulsions.

[[Page 11876]]

P-13-0205..................... 1/8/2013 4/7/2013 CBI.............. (S) Surfactant (G) Fatty acid
for use in amide
asphalt hydrochloride
emulsions.
P-13-0206..................... 1/8/2013 4/7/2013 CBI.............. (S) Surfactant (G) Fatty acid
for use in amide
asphalt hydrochloride
emulsions.
P-13-0207..................... 1/8/2013 4/7/2013 CBI.............. (S) Surfactant (G) Fatty acid
for use in amide
asphalt hydrochloride
emulsions.
P-13-0208..................... 1/8/2013 4/7/2013 CBI.............. (S) Surfactant (G) Fatty acid
for use in amide
asphalt hydrochloride
emulsions.
P-13-0209..................... 1/8/2013 4/7/2013 CBI.............. (S) Surfactant (G) Fatty acid
for use in amide
asphalt hydrochloride
emulsions.
P-13-0210..................... 1/8/2013 4/7/2013 CBI.............. (G) Thermoplastic (G) Styrene
binder. acrylate
polymer
P-13-0211..................... 1/8/2013 4/7/2013 CBI.............. (G) Thermoplastic (G) Styrene
binder. acrylate
polymer
P-13-0212..................... 1/8/2013 4/7/2013 The Lubrizol (S) Metalworking (G) Alkenyl
Corporation. fluid additive succinate,
(lubricity and amine salt
corrosion
protection).
P-13-0213..................... 1/8/2013 4/7/2013 The Lubrizol (S) Metalworking (G) Alkenyl
Corporation. fluid additive succinate,
(lubricity and amine salt
corrosion
protection).
P-13-0214..................... 1/10/2013 4/9/2013 CBI.............. (G) Coating resin (G) Polymer
reaction
product of
formaldehyde,
chloromethyl
oxirane,
phenol, 1,3-
isobenzofurandi
one, with n-(2-
aminoethyl)-1,2-
ethanediamine
and phenol with
tetrahydro-
methano-indene
glycidyl ether
P-13-0215..................... 1/11/2013 4/10/2013 3M Company....... (G) Adhesive..... (G) Hetero
substituted
alkyl acrylate
polymer
----------------------------------------------------------------------------------------------------------------

In Table II. of this unit, EPA provides the following information
(to the extent that such information is not claimed as CBI) on the TMEs
received by EPA during this period: The 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--1 TMEs Received From 12/1/12 to 1/11/13
----------------------------------------------------------------------------------------------------------------
Projected
Case No. Received notice end Manufacturer/ Use Chemical
date date Importer
----------------------------------------------------------------------------------------------------------------
T-13-5........................ 12/10/12 3/16/13 Cytec Industries, (S)Resin for (G)Substituted
Inc. ultra violet carbomoncycles,
formations. polymer with
alkyldiol.
----------------------------------------------------------------------------------------------------------------

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--33 NOCs Received From 12/1/12 to 1/11/13
----------------------------------------------------------------------------------------------------------------
Commencement
Case no. Received date notice end Chemical
date
----------------------------------------------------------------------------------------------------------------
P-06-0203.................................. 1/3/2013 12/31/2012 (G) Polyisobutenyl succinimide
P-07-0072.................................. 12/14/2012 11/19/2012 (G) Alkanoic acid potassium salt
P-09-0402.................................. 12/11/2012 11/19/2012 (G) Oxoalkyl amino acid reaction
product, sodium salt
P-10-0361.................................. 12/12/2012 12/1/2012 (G) Substituted phenol
P-10-0439.................................. 12/4/2012 10/25/2012 (S) Benzenesulfonic acid, 4-chloro-
2-{[4,5-dihydro-3-methyl-5-oxo-1-
(3-sulfophenyl)-1h-pyrazole-4-
yl)azo]-5-methyl,calcium salt
(1:1)
P-10-0442.................................. 12/18/2012 12/17/2012 (G) MDI modified resin
P-12-0044.................................. 11/30/2012 11/1/2012 (G) Multi-wall carbon nanotubes
P-12-0064.................................. 12/14/2012 11/16/2012 (G) Green line emitting phosphor
P-12-0196.................................. 12/19/2012 10/5/2012 (G) Aromatic distillation bottoms
P-12-0245.................................. 12/27/2012 12/13/2012 (S) Niobium sulfur tin zinc oxide
P-12-0264.................................. 1/10/2013 12/10/2012 (G) Substituted, 2-hydroxy-N,N-
dimethyl-N-[3-[[(13z)-1-oxo-13-
docosen-1-yl]amino]propyl]-3-sulfo-
, inner salt

[[Page 11877]]

P-12-0321.................................. 12/6/2012 11/16/2012 (G) Aliphatic acrylate mixture
P-12-0378.................................. 1/3/2013 12/28/2012 (G) Diacrylate polymer with alkane
esterdiol, alkane diol, alkane
acid diol and diisocyanates
P-12-0398.................................. 12/7/2012 11/7/2012 (S) 1,2,4-benzenetricarboxylic
acid, mixed lauryl and octyl
triesters
P-12-0444.................................. 1/2/2013 12/18/2012 (G) Carbopolycyclic-alkyl-
[[[[[[(haloalkyl-
aryl]diazenyl]aryl]diazenyl]-
carbopolycyclic]diazenyl
P-12-0445.................................. 1/2/2013 12/18/2012 (G) Morpholine,
[[[[(haloaryl)diazenyl]-alkylaryl]-
diazenyl]aryl]-
P-12-0446.................................. 1/2/2013 12/18/2012 (G) Morpholine,
[[[[(haloaryl)diazenyl]-alkylaryl]-
diazenyl]aryl]-
P-12-0468.................................. 12/6/2012 11/27/2012 (G) Doped yttrium oxalate
P-12-0469.................................. 12/6/2012 11/9/2012 (G) Yttrium europium oxalate
P-12-0473.................................. 12/12/2012 11/23/2012 (S) Phenol 4-(ethoxymethyl)-2-
methoxy-l
P-12-0485.................................. 12/6/2012 11/21/2012 (G) Oxirane, alkyl, polymer with
aromatic isocyanate, alkyloxirane
polymer with oxirane ether with
alkyltriol, and oxirane,
polyethylene glycol
mono(alkylaromatic) ether-blocked
P-12-0519.................................. 12/13/2012 12/8/2012 (G) Alkyd polyester polyurethane
P-12-0521.................................. 12/6/2012 12/3/2012 (G) 2-Propenoic acid, 2-methyl-,
alkyl esters, polymer with
substituted methacrylate,
substituted methacrylate, me
methacrylate and polyalkene glycol
alkyl ether, tert-bu 2-
ethylhexaneperoxoate-initiated
P-12-0523.................................. 12/13/2012 11/27/2012 (G) Alkyl ketimines; polymeric
ketimines
P-12-0524.................................. 12/6/2012 12/3/2012 (G) Vegetable-oil fatty acids,
conjugated, polymers with ethylene
glycol, substituted propanoic
acid, anhydride, polyethylene
glycol and trimethylolpropane,
compounds with substituted alkanol
P-12-0526.................................. 1/2/2013 12/27/2012 (G) Siloxanes and silicones,
substituted alkyl group-terminated
ethers with polyethylene glycol
and polyethylene glycol anhydride
ester
P-12-0527.................................. 12/6/2012 12/3/2012 (G) Fatty acids of natural oils,
conjugated, maleated
P-12-0528.................................. 12/11/2012 12/10/2012 (G) Substituted heteromonocycle,
polymer with substituted alkane
and substituted alkanediol,
alkanoic acid substituted ester
and substituted hetermonocyle
homopolymer
P-12-0529.................................. 12/5/2012 12/4/2012 (G) Hydrogenated modified rosin
P-12-0540.................................. 12/18/2012 12/5/2012 (G) Styrenic anhydride maleimide
terpolymer
P-12-0542.................................. 12/19/2012 12/17/2012 (G) Polyethyleneglycol modified
polyacrylate block polypyridine
polymer, hydrolyzed, sodium salts
P-12-0544.................................. 1/3/2013 12/24/2012 (G) Alkenoic acid, polymers with
acrylate and polyalkandiol alkane
ether alkyl alkenoate and
polyalkene alkandiol alkane ether
alkenoic alkyl ethers
P-12-0564.................................. 1/10/2013 1/4/2013 (G) 2-Propenoic acid 2-methyl,
alkyl ester, polymer with
heteromonocycle, substituted
carbomonocycle, substituted alkyl
propenoate, alkyl propenoate,
alkyl propenoate, tert-bu
benzenecarboperoxoate-initiated
----------------------------------------------------------------------------------------------------------------

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: February 4, 2013.
Chandler Sirmons,
Acting Director, Information Management Division, Office of Pollution
Prevention and Toxics.
[FR Doc. 2013-03765 Filed 2-19-13; 8:45 am]
BILLING CODE 6560-50-P

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