Federal Register/Vol. 82, No. 248/Thursday
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
NITROGEN by Raymond L
NITROGEN By Raymond L. Cantrell In 1994, nitrogen compound supplies in the second in discharges to surface water, and third per-year ammonia plant based on methane gas United States reached an all time record high in terms of the largest emissions to the air. feedstock derived from lignite. A used because of strong domestic demand for Ammonium nitrate solution, nitric acid, ammonia plant was to be moved from Freeport- agricultural and industrial products; an acetonitrile, and ammonium sulfate solution McMoRan's idle Fort Madison, IA, facility. extremely tight supply situation was were also listed in the top 50 TRI releases, in Total ammonia capacity, including that already experienced. The total value of the U.S. order of importance.6 onsite, should approximate 310,000 tons per nitrogen compound supply, f.o.b. U.S. Gulf, year. The first flue gas desulfurization unit nearly doubled to an impressive $5.0 billion, Production based on ammoniation of sulfur dioxide to compared with $2.7 billion during the previous produce salable ammonium sulfate, was to be year. U.S. ammonia producers operated at more constructed using General Electric A unique combination of strong upward than 100% of design capacity in 1994. Environmental Systems' Inc. technology. The movement in the domestic nitrogen market led Ammonia ranked as the sixth largest volume unit was designed to produce 180,000 tons per to several new all time record highs, including chemical produced in the United States, year of salable ammonium sulfate, to be nitrogen fertilizer consumption1 and agricultural according to information published by Chemical marketed under contract by H. -
2010 Minerals Yearbook
2010 Minerals Yearbook EXPLOSIVES U.S. Department of the Interior October 2012 U.S. Geological Survey EXPLOSIVES By Lori E. Apodaca In 2010, U.S. explosives consumption was 2.68 million metric Vet’s Explosives Inc. tons (Mt), about an 18% increase from that of 2009; sales of Viking Explosives and Supply Inc. explosives were reported in all States except Delaware. Coal W.A. Murphy, Inc. mining, with about 71% of total consumption, continued to be El Dorado Chemical Co. (a subsidiary of LSB Industries Inc.) the dominant use for explosives in the United States. Wyoming, signed a 5-year agreement with Orica International Pte Ltd. West Virginia, and Kentucky, in descending order, led the (Orica) to supply Orica with 230,000 metric tons per year (t/yr) Nation in coal production, accounting for 63% of the total. of industrial-grade ammonium nitrate. The new agreement These States were also the leading explosives-consuming States, replaces the previous agreement to supply 190,000 t/yr of accounting for 46% of total U.S. explosives sales. ammonium nitrate to Orica (Green Markets, 2010b). Apache Nitrogen Products Inc. was investing $5.5 million to Legislation and Government Programs upgrade its Arizona ammonium nitrate prill plant. They were replacing the dry end of the prill ammonium nitrate process Effective February 3, the Occupational Safety and Health in order to reduce moisture problems. Sixty percent of the Administration (OSHA) terminated the rulemaking that had liquid ammonium nitrate produced onsite was used to produce been proposed in 2007 to amend its Explosives and Blasting low-density ammonium nitrate prill for use in the mining Agents Standard (CFR 1910.109). -
Potentially Explosive Chemicals*
Potentially Explosive Chemicals* Chemical Name CAS # Not 1,1’-Diazoaminonaphthalene Assigned 1,1-Dinitroethane 000600-40-8 1,2,4-Butanetriol trinitrate 006659-60-5 1,2-Diazidoethane 000629-13-0 1,3,5-trimethyl-2,4,6-trinitrobenzene 000602-96-0 1,3-Diazopropane 005239-06-5 Not 1,3-Dinitro-4,5-dinitrosobenzene Assigned Not 1,3-dinitro-5,5-dimethyl hydantoin Assigned Not 1,4-Dinitro-1,1,4,4-tetramethylolbutanetetranitrate Assigned Not 1,7-Octadiene-3,5-Diyne-1,8-Dimethoxy-9-Octadecynoic acid Assigned 1,8 –dihydroxy 2,4,5,7-tetranitroanthraquinone 000517-92-0 Not 1,9-Dinitroxy pentamethylene-2,4,6,8-tetramine Assigned 1-Bromo-3-nitrobenzene 000585-79-5 Not 2,2',4,4',6,6'-Hexanitro-3,3'-dihydroxyazobenzene Assigned 2,2-di-(4,4,-di-tert-butylperoxycyclohexyl)propane 001705-60-8 2,2-Dinitrostilbene 006275-02-1 2,3,4,6- tetranitrophenol 000641-16-7 Not 2,3,4,6-tetranitrophenyl methyl nitramine Assigned Not 2,3,4,6-tetranitrophenyl nitramine Assigned Not 2,3,5,6- tetranitroso nitrobenzene Assigned Not 2,3,5,6- tetranitroso-1,4-dinitrobenzene Assigned 2,4,6-Trinitro-1,3,5-triazo benzene 029306-57-8 Not 2,4,6-trinitro-1,3-diazabenzene Assigned Not 2,4,6-Trinitrophenyl trimethylol methyl nitramine trinitrate Assigned Not 2,4,6-Trinitroso-3-methyl nitraminoanisole Assigned 2,4-Dinitro-1,3,5-trimethyl-benzene 000608-50-4 2,4-Dinitrophenylhydrazine 000119-26-6 2,4-Dinitroresorcinol 000519-44-8 2,5-dimethyl-2,5-diydroperoxy hexane 2-Nitro-2-methylpropanol nitrate 024884-69-3 3,5-Dinitrosalicylic acid 000609-99-4 Not 3-Azido-1,2-propylene glycol dinitrate -
Pharmaceutical Appendix to the Tariff Schedule 2
Harmonized Tariff Schedule of the United States (2007) (Rev. 2) Annotated for Statistical Reporting Purposes PHARMACEUTICAL APPENDIX TO THE HARMONIZED TARIFF SCHEDULE Harmonized Tariff Schedule of the United States (2007) (Rev. 2) Annotated for Statistical Reporting Purposes PHARMACEUTICAL APPENDIX TO THE TARIFF SCHEDULE 2 Table 1. This table enumerates products described by International Non-proprietary Names (INN) which shall be entered free of duty under general note 13 to the tariff schedule. The Chemical Abstracts Service (CAS) registry numbers also set forth in this table are included to assist in the identification of the products concerned. For purposes of the tariff schedule, any references to a product enumerated in this table includes such product by whatever name known. ABACAVIR 136470-78-5 ACIDUM LIDADRONICUM 63132-38-7 ABAFUNGIN 129639-79-8 ACIDUM SALCAPROZICUM 183990-46-7 ABAMECTIN 65195-55-3 ACIDUM SALCLOBUZICUM 387825-03-8 ABANOQUIL 90402-40-7 ACIFRAN 72420-38-3 ABAPERIDONUM 183849-43-6 ACIPIMOX 51037-30-0 ABARELIX 183552-38-7 ACITAZANOLAST 114607-46-4 ABATACEPTUM 332348-12-6 ACITEMATE 101197-99-3 ABCIXIMAB 143653-53-6 ACITRETIN 55079-83-9 ABECARNIL 111841-85-1 ACIVICIN 42228-92-2 ABETIMUSUM 167362-48-3 ACLANTATE 39633-62-0 ABIRATERONE 154229-19-3 ACLARUBICIN 57576-44-0 ABITESARTAN 137882-98-5 ACLATONIUM NAPADISILATE 55077-30-0 ABLUKAST 96566-25-5 ACODAZOLE 79152-85-5 ABRINEURINUM 178535-93-8 ACOLBIFENUM 182167-02-8 ABUNIDAZOLE 91017-58-2 ACONIAZIDE 13410-86-1 ACADESINE 2627-69-2 ACOTIAMIDUM 185106-16-5 ACAMPROSATE 77337-76-9 -
Prediction of the Crystalline Densities of Aliphatic Nitrates by Quantum Chemistry Methods
Central European Journal of Energetic Materials ISSN 1733-7178; e-ISSN 2353-1843 Copyright © 2019 Sieć Badawcza Łukasiewicz – Institute of Industrial Organic Chemistry, Poland Cent. Eur. J. Energ. Mater. 2019, 16(3): 412-432; DOI 10.22211/cejem/112306 Article is available in PDF-format, in colour, at: http://www.wydawnictwa.ipo.waw.pl/cejem/Vol-16-Number3-2019/CEJEM_00978.pdf Article is available under the Creative Commons Attribution-Noncommercial-NoDerivs 3.0 license CC BY-NC-ND 3.0. Research paper Prediction of the Crystalline Densities of Aliphatic Nitrates by Quantum Chemistry Methods Guixiang Wang,* Yimin Xu, Chuang Xue, Zhiyuan Ding, Yan Liu, Hui Liu, Xuedong Gong** Computation Institute for Molecules and Materials, Department of Chemistry, Nanjing University of Science and Technology, Nanjing 210094, China E-mails: * [email protected]; ** [email protected] Abstract: Crystal density is a basic and important parameter for predicting the detonation performance of explosives, and nitrate esters are a type of compound widely used in the military context. In this study, thirty-one aliphatic nitrates were investigated using the density functional theory method (B3LYP) in combination with six basis sets (3-21G, 6-31G, 6-31G*, 6-31G**, 6-311G* and 6-31+G**) and the semiempirical molecular orbital method (PM3). Based on the geometric optimizations at various theoretical levels, the molecular volumes and densities were calculated. Compared with the available experimental data, the densities calculated by various methods are all overestimated, and the errors of the PM3 and B3LYP/3-21G methods are larger than those of other methods. Considering the results and the computer resources required by the calculations, the B3LYP/6-31G* method is recommended for predicting the crystalline densities of organic nitrates using a fitting equation. -
Compositions Comprising Nebivolol
(19) TZZ ZZ__T (11) EP 2 808 015 A1 (12) EUROPEAN PATENT APPLICATION (43) Date of publication: (51) Int Cl.: 03.12.2014 Bulletin 2014/49 A61K 31/34 (2006.01) A61K 31/502 (2006.01) A61K 31/353 (2006.01) A61P 9/00 (2006.01) (21) Application number: 14002458.9 (22) Date of filing: 16.11.2005 (84) Designated Contracting States: • O’Donnell, John AT BE BG CH CY CZ DE DK EE ES FI FR GB GR Morgantown, WV 26505 (US) HU IE IS IT LI LT LU LV MC NL PL PT RO SE SI • Bottini, Peter Bruce SK TR Morgantown, WV 26505 (US) • Mason, Preston (30) Priority: 31.05.2005 US 141235 Morgantown, WV 26504 (US) 10.11.2005 US 272562 • Shaw, Andrew Preston 15.11.2005 US 273992 Morgantown, WV 26504 (US) (62) Document number(s) of the earlier application(s) in (74) Representative: Samson & Partner accordance with Art. 76 EPC: Widenmayerstraße 5 09015249.7 / 2 174 658 80538 München (DE) 05848185.4 / 1 890 691 Remarks: (71) Applicant: MYLAN LABORATORIES, INC This application was filed on 16-07-2014 as a Morgantown, NV 26504 (US) divisional application to the application mentioned under INID code 62. (72) Inventors: • Davis, Eric Morgantown, WV 26508 (US) (54) Compositions comprising nebivolol (57) The active ingredients of the pharmaceutical composition described consist of nebivolol, one or more ACE inhibitors and one or more ARB. EP 2 808 015 A1 Printed by Jouve, 75001 PARIS (FR) EP 2 808 015 A1 Description [0001] This application is a continuation-in-part of application Ser. -
United States Patent (10) Patent No.: US 7,235,237 B2 L0scalz0 Et Al
USOO7235237B2 (12) United States Patent (10) Patent No.: US 7,235,237 B2 L0ScalZ0 et al. (45) Date of Patent: Jun. 26, 2007 (54) METHODS OF TREATING VASCULAR 5,968,983 A 10/1999 Kaesemeyer DISEASES CHARACTERIZED BY NITRC 5,973,011 A 10/1999 Noack et al. OXIDE INSUFFICIENCY 6,103,769 A 8, 2000 Kelm 6,117,872 A 9, 2000 Maxwell et al. (75) Inventors: Joseph Loscalzo, Dover, MA (US); 6,319,515 B1 1 1/2001 Hidaka et al. Joseph A. Vita, Hingham, MA (US); 6,458,797 B1 10/2002 Adams et al. Michael D. Loberg, Boston, MA (US); 2004, OO63719 A1 4/2004 Adams et al. Manuel Worcel, Boston, MA (US) FOREIGN PATENT DOCUMENTS (73) Assignee: NitroMed, Inc., Lexington, MA (US) EP O327263 A 8, 1989 (*) Notice: Subject to any disclaimer, the term of this EP O 968 713 A1 5, 1998 patent is extended or adjusted under 35 JP O905915.2 3, 1997 U.S.C. 154(b) by 492 days. WO WO95/26725 10, 1995 WO WO 98.21 193 5, 1998 (21) Appl. No.: 10/415,136 WO WO 99.00361 1, 1999 WO WO 99,66921 12/1999 (22) PCT Filed: May 2, 2001 WO WO 99,67231 12/1999 WO WO O1/35961 A 5, 2001 (86). PCT No.: PCT/USO1A14245 OTHER PUBLICATIONS S 371 (c)(1), (2), (4) Date: Apr. 25, 2003 Dupuis, Cardiovascular Drugs and Therapy, 8(3):501-507 (1994). Cohn et al. The New England Journal of Medicine, 325(5):303-310 (87) PCT Pub. -
Commerce in Explosives; 2020 Annual Those on the Annual List
Federal Register / Vol. 85, No. 247 / Wednesday, December 23, 2020 / Notices 83999 inspection at the Office of the Secretary or synonyms in brackets. This list Black powder substitutes. and on EDIS.3 supersedes the List of Explosive *Blasting agents, nitro-carbo-nitrates, This action is taken under the Materials published in the Federal including non-cap sensitive slurry and authority of section 337 of the Tariff Act Register on January 2, 2020 (Docket No. water gel explosives. of 1930, as amended (19 U.S.C. 1337), 2019R–04, 85 FR 128). Blasting caps. and of §§ 201.10 and 210.8(c) of the The 2020 List of Explosive Materials Blasting gelatin. Commission’s Rules of Practice and is a comprehensive list, but is not all- Blasting powder. Procedure (19 CFR 201.10, 210.8(c)). inclusive. The definition of ‘‘explosive BTNEC [bis (trinitroethyl) carbonate]. materials’’ includes ‘‘[e]xplosives, BTNEN [bis (trinitroethyl) nitramine]. By order of the Commission. BTTN [1,2,4 butanetriol trinitrate]. Issued: December 18, 2020. blasting agents, water gels and detonators. Explosive materials, Bulk salutes. William Bishop, include, but are not limited to, all items Butyl tetryl. Supervisory Hearings and Information in the ‘List of Explosive Materials’ Officer. C provided for in § 555.23.’’ 27 CFR Calcium nitrate explosive mixture. [FR Doc. 2020–28458 Filed 12–22–20; 8:45 am] 555.11. Accordingly, the fact that an BILLING CODE 7020–02–P Cellulose hexanitrate explosive explosive material is not on the annual mixture. list does not mean that it is not within Chlorate explosive mixtures. coverage of the law if it otherwise meets DEPARTMENT OF JUSTICE Composition A and variations. -
Characterization of Explosives & Precursors
Appendix A: Project Reports ALERT Thrust R1: Characterization & Elimination of Illicit Explosives Phase 2 Year 7 Annual Report Project R1-A.1 R1-A.1: Characterization of Explosives & Precursors I. PARTICIPANTS INVOLVED FROM JULY 1, 2019 TO JUNE 30, 2020 Faculty/Staff Name Title Institution Email Jimmie Oxley Co-PI URI [email protected] Jim Smith Co-PI URI [email protected] Gerald Kagan Post-Doc URI [email protected] Graduate, Undergraduate and REU Students Name Degree Pursued Institution Month/Year of Graduation Taylor Busby PhD URI 5/2021 Lindsay McLennan PhD URI 5/2020 Robert Ichiyama PhD URI 5/2023 II. PROJECT DESCRIPTION A. Project Overview This project sought to determine the physical properties, synthesis, and destruction mechanisms of improvised explosives, often called homemade explosives (HMEs). In Year 7, we performed further characterization on erythritol tetranitrate (ETN) and on the nitro-sugars mannitol and sorbitol hexanitrate and HMTD. For ETN, we examined its synthesis and sought stable isotope signatures that might allow attribution to particular groups. For the sugars we are attempting to establish basic properties and observing different polymorphs. The existence of polymorphs was also found with HMTD. B. State of the Art and Technical Approach Stable isotope analysis is a technique capable of determining the subtle differences between the stable isotope ratios of hydrogen (2H/1H), carbon (13C/12C), nitrogen (15N/14N), oxygen (18O/16O), and, with special modifications, sulfur (34S/32S). Stable isotope analyses are important for provenance studies, where minute differences in isotope ratios can determine production location. Stable isotope ratio mass spectrometry (IRMS) has been considered as a forensic science technique for attribution that has been applied to illicit drugs, chemical weapon agents, and recently to explosives. -
2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27
Case 4:20-cv-00463-BGM Document 1 Filed 10/28/20 Page 1 of 20 1 Ellen M. Mahan Deputy Section Chief 2 Deborah A. Gitin 3 Senior Counsel Environmental Enforcement Section 4 Environment and Natural Resources Division U.S. Department of Justice 5 450 Golden Gate Avenue, Room 7-6714 6 San Francisco, California 94102 (CA Bar # 284947) 7 Telephone: (415) 744-6488 Facsimile: (415) 744-6476 8 Email: [email protected] 9 Attorneys for the United States of America 10 11 IN THE UNITED STATES DISTRICT COURT 12 FOR THE DISTRICT OF ARIZONA 13 United States of America, 14 15 Plaintiff, 16 v. COMPLAINT 17 Apache Nitrogen Products, Inc., an Arizona 18 corporation, 19 Defendant. 20 21 22 23 24 25 26 27 28 1 COMPLAINT United States of America v. Apache Nitrogen Products, Inc. (D. Ariz.) Case 4:20-cv-00463-BGM Document 1 Filed 10/28/20 Page 2 of 20 1 Plaintiff, the United States of America (“United States”), by the authority of the 2 Attorney General, through its undersigned attorneys, and at the request of the 3 Administrator of the United States Environmental Protection Agency (“EPA”), hereby 4 alleges: 5 I. PRELIMINARY STATEMENT 6 1. This is a civil action for penalties and injunctive relief brought pursuant to 7 Section 113(b)(2) of the Clean Air Act (“CAA”), 42 U.S.C. § 7413(b)(2); Section 325 of 8 the Emergency Planning and Community Right-to-Know Act (“EPCRA”), 42 U.S.C. 9 § 11045; and Section 109(c) of the Comprehensive Environmental Response, 10 Compensation and Liability Act (“CERCLA”), 42 U.S.C. -
Federal Register / Vol. 60, No. 80 / Wednesday, April 26, 1995 / Notices DIX to the HTSUS—Continued
20558 Federal Register / Vol. 60, No. 80 / Wednesday, April 26, 1995 / Notices DEPARMENT OF THE TREASURY Services, U.S. Customs Service, 1301 TABLE 1.ÐPHARMACEUTICAL APPEN- Constitution Avenue NW, Washington, DIX TO THE HTSUSÐContinued Customs Service D.C. 20229 at (202) 927±1060. CAS No. Pharmaceutical [T.D. 95±33] Dated: April 14, 1995. 52±78±8 ..................... NORETHANDROLONE. A. W. Tennant, 52±86±8 ..................... HALOPERIDOL. Pharmaceutical Tables 1 and 3 of the Director, Office of Laboratories and Scientific 52±88±0 ..................... ATROPINE METHONITRATE. HTSUS 52±90±4 ..................... CYSTEINE. Services. 53±03±2 ..................... PREDNISONE. 53±06±5 ..................... CORTISONE. AGENCY: Customs Service, Department TABLE 1.ÐPHARMACEUTICAL 53±10±1 ..................... HYDROXYDIONE SODIUM SUCCI- of the Treasury. NATE. APPENDIX TO THE HTSUS 53±16±7 ..................... ESTRONE. ACTION: Listing of the products found in 53±18±9 ..................... BIETASERPINE. Table 1 and Table 3 of the CAS No. Pharmaceutical 53±19±0 ..................... MITOTANE. 53±31±6 ..................... MEDIBAZINE. Pharmaceutical Appendix to the N/A ............................. ACTAGARDIN. 53±33±8 ..................... PARAMETHASONE. Harmonized Tariff Schedule of the N/A ............................. ARDACIN. 53±34±9 ..................... FLUPREDNISOLONE. N/A ............................. BICIROMAB. 53±39±4 ..................... OXANDROLONE. United States of America in Chemical N/A ............................. CELUCLORAL. 53±43±0 -
Endothelial Dysfunction in Heart Failure and Ischemic Heart Disease: Rationale for the Clinical Use of Mononitrates
Heart International / Vol. 3 no. 3-4, 2007 / pp. 86-97 © Wichtig Editore, 2007 Endothelial dysfunction in heart failure and ischemic heart disease: rationale for the clinical use of mononitrates OBERDAN PARODI, RENATA DE MARIA, ELÈNA ROUBINA CNR Clinical Physiology Institute of Milan, Cardiology Department, Niguarda Cà Granda Hospital, Milan - Italy ABSTRACT: The clinical observation that heart failure can progress independently of the pa- tient’s hemodynamic status has focused interest on new, potential mechanisms underlying the progression of cardiac insufficiency. It has been shown that in both ischemic and non-ischemic heart failure, endothelial dysfunction and reduced bioavailability of NO can contribute to the process of left ventricular remodelling. The endothelial dysfunction contributes to increasing pe- ripheral vascular resistance, limiting blood flow to skeletal muscles, particularly during exercise, and compromising the regulation of pulmonary blood flow, leading to a flow-perfusion mis- match. The nitroderivates are a heterogeneous class of compounds that have in common their pharmacodynamic action, which is mediated through the production of NO. Isosorbide-2-mononitrate (IS-2-MN) and isosorbide-5-mononitrate (IS-5-MN) are the two main metabolites of isosorbide dinitrate (ISDN) and both act on the smooth muscle cells of vessel walls, causing generalized peripheral vasodilation, which is more marked in the venous system, reduced venous return to the heart and a reduction in peripheral resistance. The shorter half-life of IS-2-MN compared to that of IS-5-MN allows greater fluctuation of the blood levels of the drug; it can, therefore, be hypothesized that tolerance would develop more slowly.