進工業グリーン調達ガイドライン 規程文書番号： M3028025-03 改定日： 2015 年 8 月 8 日
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(EU) No 305/2014 of 25 March 2014 Concerning the Authorisation of Propionic Acid, Sodium Prop
L 90/12 EN Official Journal of the European Union 26.3.2014 COMMISSION IMPLEMENTING REGULATION (EU) No 305/2014 of 25 March 2014 concerning the authorisation of propionic acid, sodium propionate and ammonium propionate as feed additives for all animal species other than ruminants, pigs and poultry (Text with EEA relevance) THE EUROPEAN COMMISSION, that, under the proposed conditions of use, propionic acid, sodium propionate and ammonium propionate do Having regard to the Treaty on the Functioning of the European not have an adverse effect on animal health, human Union, health or the environment. It was also concluded that the substances improve the aerobic stability of easy to Having regard to Regulation (EC) No 1831/2003 of the ensile materials. The Authority does not consider that European Parliament and of the Council of 22 September there is a need for specific requirements of post-market 2003 on additives for use in animal nutrition ( 1 ), and in monitoring. It also verified the report on the methods of particular Article 9(2) thereof, analysis of the feed additives in feed submitted by the Reference Laboratory set up by Regulation (EC) No Whereas: 1831/2003. (1) Regulation (EC) No 1831/2003 provides for the auth (5) The assessment of the substances concerned shows that orisation of additives for use in animal nutrition and the conditions for authorisation, as provided for in for the grounds and procedures for granting such auth Article 5 of Regulation (EC) No 1831/2003, are satisfied. orisation. Accordingly, the use of those substances should be auth orised as specified in the Annex to this Regulation. -
United States Patent 1191 1111 3,931,208 Offermanns Et Al
United States Patent 1191 1111 3,931,208 Offermanns et al. [451 Jan. 6, 1976 [54] PROCESS FOR THE PRODUCTION OF formula: THlAZOLINES-( 3) [75] Inventors: lleribert Offermanns, Grossauheim; Friedrich Asinger, Rott; Wolf-Dieter Pfeifer, Grossauheim; Paul (l) Scherberich, Neu lsenburg; Gerd Schreyer, Grossauheim, all of Germany in which R‘, R2, and R3 and R4 are the same or differ [73] Assignee: Deutsche Gold- und _ ent, R‘ and R2 are straight or branched chain lower Silber-Scheideanstalt vormals alkyl, alkenyl ‘or aralkyl groups or together are a Roessler, Frankfurt am Main, straight or branched chain alkylene or ethylenically Germany unsaturated divalent aliphatic hydrocarbon group which joins with the adjacent carbon atom to form a 1221 Filed: Nov. 5, 1973 ring and R3 and R4 are similarly de?ned except R3 can 1211 Appl. No.: 413,048 also be hydrogen by reaching a 2,2’ dioxodisul?deof the formula ‘ [30] Foreign Application Priority Data Nov. 9, 1972 Germany .............. .... 2254701 ' [52] U.S. Cl ......................................... .. 260/306.7 R [5]] Int. Cl.2 ...................................... .. C07D 277/10 [58] Field of Search ............................ .. 260/306.7 R V[ 56] References Cited UNITED STATES PATENTS 2,879,273 3/1959 Asinger ct al .............. .. 260/3()6.7 R 3,004,981 l0/l96l Asingcr ct al .............. .. 26()/306.7 R 3.700.683 10/1972 Asinger ct al ............. .._. 260/306.7 R Primary Examiner—Richard J. Gallagher Assistant E.raminer—Anne Marie T. Tighe Attorney, Agent, or Firm——Cushman, Darby & Cushman and with ammonia and hydrogen sulfide in the pres ence of an amine and an ammonium salt. -
Ep 2385054 B1
(19) TZZ ¥Z_T (11) EP 2 385 054 B1 (12) EUROPEAN PATENT SPECIFICATION (45) Date of publication and mention (51) Int Cl.: of the grant of the patent: C07D 501/22 (2006.01) A61K 31/546 (2006.01) 02.10.2013 Bulletin 2013/40 A61P 31/04 (2006.01) (21) Application number: 09836052.2 (86) International application number: PCT/CN2009/076164 (22) Date of filing: 29.12.2009 (87) International publication number: WO 2010/075765 (08.07.2010 Gazette 2010/27) (54) CEFDINIR ACID DOUBLE SALT AND ITS PREPARATION CEFDINIRSÄURE-DOPPELSALZ UND SEINE ZUBEREITUNG DOUBLE SEL D’ACIDE DE CEFDINIR ET SA PRÉPARATION (84) Designated Contracting States: • YU, Baochun AT BE BG CH CY CZ DE DK EE ES FI FR GB GR Zhejiang 310011 (CN) HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL • YE, Tianjian PT RO SE SI SK SM TR Zhejiang 310011 (CN) • YU, Meiping (30) Priority: 31.12.2008 CN 200810164211 Zhejiang 310011 (CN) (43) Date of publication of application: (74) Representative: Hryszkiewicz, Danuta 09.11.2011 Bulletin 2011/45 Kancelaria Patentowa Matthias Scholl, Inc. (73) Proprietor: Zhejiang Adamerck Biopharmlabs Inc. Ul. Jana z Kolna 38 Zhejiang 310011 (CN) 75-204 Koszalin (PL) (72) Inventors: (56) References cited: • QI, Youmao EP-A2- 0 304 019 WO-A1-02/098884 Zhejiang 310011 (CN) WO-A1-2004/056835 CN-A- 1 251 590 • YE, Fengqi CN-A- 1 415 615 CN-A- 101 481 383 Zhejiang 310011 (CN) US-A- 4 559 334 •JIE,Qing Zhejiang 310011 (CN) Remarks: • QI, Yingbei Thefile contains technical information submitted after Zhejiang 310011 (CN) the application was filed and not included in this • ZHANG, Fengmin specification Zhejiang 310011 (CN) Note: Within nine months of the publication of the mention of the grant of the European patent in the European Patent Bulletin, any person may give notice to the European Patent Office of opposition to that patent, in accordance with the Implementing Regulations. -
American Chemical Society
VOL. XLI. No. IO. THE JOURNAL OF THE American Chemical Society with which has been incorporated the American Chemical Journal (Founded by Ira Reinsen) [CONTRIBUTIONPROM THE CHEMICALLABORATORY OF VANDERBILT UNIVERSITY.] A CRITICAL STUDY OF THE POTASSIUM AND SODIUM DOUBLE SALTS OF LEAD TETRAFLUORIDE AS SOURCES OF FLU0RINE.l BY GEORGEL. CLARK. Received April 9, 1919. The only strictly chemical method for the preparation of free fluorine which has shown satisfactory possibilities up to the present time is the decomposition of the double salt tripotassium lead hydrogen octafluoride 3KF.HF.PbF4, by heat. This compound was prepared in pure con- dition and studied for the first time by Brauner,2 who showed that the molecule of hydrogen fluoride could be completely removed at tem- peratures below 250', and that fluorine is evolved above 250'. In recent years doubts have been expressed by some chemists that such a discovery was really in accordance with the facts. By using this method, however, it has been found possible in the researches to be described 1 Published by permission of the Director of the Chemical Warfare Service. The general problem of the preparation and use of tripotassium hydrogen lead octafluoride was suggested by Captain A. B. Ray, and the investigations begun under his supervision and with the assistance of Messrs. I. M. Colbeth and J. H. Card, at the American University Experiment Station, Washington, D. C. The intensive solubility measurements, and all of the work on disodium lead hexafluoride were subsequently carried on by the author independently. J. Chenz. Soc., 65, 393 (1894). I478 GEORGE I,. -
Sds) (1272/2008/Ce)
SAFETY DATA SHEET (SDS) (1272/2008/CE) Trade Name: Edition: June 28, 2018 CALCIUM PROPIONATE Version: 7/en 1. IDENTIFICATION OF THE SUBSTANCE / PREPARATION AND COMPANY / UNDERTAKING Trade name Calcium Propionate Synonyms Calcium propanoate; calcium propianate; propionic acid, calcium salt; propanoic acid, calcium salt Recommended use Use as a preservative in food, feed and pharmaceutical applications. Use according to local and restriction on use regulations. Company Macco Organiques Inc., 100 McArthur, Suite 112, Salaberry-de-Valleyfield, Qc, Canada, J6S 4M5 Responsable service Tel: (450) 371-1066 Fax: (450) 371-5519 [email protected] http://www.macco.ca Emergency phone CANUTEC CHEMTREC, U.S. International numbers (613) 996-6666 (800) 424-9300 (703) 527-3887 2. HAZARDS IDENTIFICATION The substance is not classified as dangerous according to European Union (EU) directives 1272/2008, in replacement for 67/548/EEC including amendments and 1999/45/EC. Classification Not classified. Labeling type This product does not require any labeling according to EU directives and regulations of the instruction concerned country. Other hazards Combustible dust. May form explosive mixture with air. 3. COMPOSITION / INFORMATION ON INGREDIENTS Chemical name Calcium propionate 100% Synonyms Propionic acid, calcium salt; Calcium propanoate; calcium propianate; propanoic acid, calcium salt. Chemical formula Ca(C3H5O2)2 CAS no. 4075-81-4 EEC (CE) no. E 282 EINECS no. 223-795-8 4. FIRST-AID MEASURES DESCRIPTION OF FIRST AID EMERGENCIES General advices In case of accident or illness, immediately get medical attention (show the label if possible). Show this safety data sheet to the physician. Remove and wash contaminated clothing before reusing. -
United States Patent (19) 11 4,092,314 Vander Zwan Et Al
United States Patent (19) 11 4,092,314 Vander Zwan et al. 45 May 30, 1978 54 PREPARATION OF (56) References Cited 4,6-DIAMINO-5-ARYLAZOPYRIMIDINES AND A DENNE COMPOUNDS FOREIGN PATENT DOCUMENTS 81,394/74 8/1974 Japan. 75) Inventors: Michael C. Vander Zwan, Somerset; 28,497/73 4/1973 Japan. Donald F. Reinhold, North Plainfield, both of N.J. Primary Examiner-Paul M. Coughlan, Jr. Attorney, Agent, or Firm-Walter Patton 73 Assignee: Merck & Co., Inc., Rahway, N.J. 57 ABSTRACT 21) Appl. No.: 733,489 The present invention relates to a novel and useful pro 22) Filed: Oct. 18, 1976 cess for preparing 4,6-diamino-5-arylazopyrimidine from an arylazomalononitrile in the presence of ammo Related U.S. Application Data nium chloride and formamide. If desired, the 4,6- 63) Continuation-in-part of Ser. No. 593,910, Jul. 7, 1975, diamino-5-arylazopyrimidine may then be hydroge abandoned. nated to form 4,5,6-triaminopyrimidine which, when the hydrogenation is carried out in the presence of for (51) Int. Cl’............................................ CO7D 473/34 mic acid or its derivative, gives adenine. 52) 0 d d 544/277; 260/154 58) Field of Search ................................ 260/154, 252 10 Claims, No Drawings 4,092,314 1. 2 are generally used in amounts of at least 0.1% by weight PREPARATION OF based on the weight of the arylazomalononitrile and 4,6-DIAMNO-5-ARYLAZOPYRIMD NES AND more preferably from 5 to 100%. In a more preferred ADENINE COMPOUNDS embodiment the amount is 10 to 60%. This application is a continuation-in-part application The temperature to be employed for the reaction is of co-pending application U.S. -
Agricultural and Veterinary Chemicals Code Ingredient Determination 2015
Agricultural and Veterinary Chemicals Code Ingredient Determination 2015 Agricultural and Veterinary Chemicals Code Act 1994 I, Kareena Arthy, Chief Executive Officer of the Australian Pesticides and Veterinary Medicines Authority, make this Instrument under clause 9 of Division 3.3 of Part 3 of Schedule 3AA to the Agricultural and Veterinary Chemicals Code Regulations 1995. Dated 3 June 2015 Kareena Arthy Chief Executive Officer Federal Register of Legislative Instruments F2015L00785 Section 1 Name of instrument 1 Name of instrument This Instrument is the Agricultural and Veterinary Chemicals Code Ingredient Determination 2015. 2 Commencement This Instrument commences on the day after it is registered. 3 Authority This Instrument is made under clause 9 of Division 3.3 of Part 3 of Schedule 3AA to the Agricultural and Veterinary Chemicals Code Regulations 1995. 4 Interpretation (1) In this Instrument, unless the contrary intention appears: “Food Standards Code” has the meaning given in subsection 3 (1) of the National Food Authority Act 1991; “Regulations” means the Agricultural and Veterinary Chemicals Code Regulations 1995. (2) A reference in this Instrument to a salt, without reference to the level of hydration of that salt, includes all hydrated forms of that salt. 5 Authorisation of constituent For the purposes of item 8 in the table at subclause 5(3) of Schedule 3AA to the Regulations, a constituent listed in the Schedule is authorised to be used for the purpose or purposes set out in the heading of the Schedule under which that -
Pp-03-25-New Dots.Qxd 10/23/02 2:38 PM Page 464
pp-03-25-new dots.qxd 10/23/02 2:38 PM Page 464 464 LEAD CARBONATE, BASIC / LEAD CHROMATE LEAD CARBONATE, BASIC [1319-46-6] Formula: Pb(OH)2•2PbCO3; MW 775.60; phase rule study indicates the exis- tence of basic lead carbonates of other compositions: 3PbO•5PbCO3; PbO•PbCO3; 2PbO•PbCO3 Synonyms: white lead; basic carbonate Uses White lead, in the basic carbonate form, was used extensively as white pig- ment in paint until its toxic properties became known. At present, most of its pigment applications are as red-reflecting pigment in plastic sheets; in UV light-reflecting paints; in ceramic glaze; and in many temperature-sensitive inks that cause color change. Other applications include use as a catalyst in terephthalic acid reactions with diols; as a heat-sensitive stabilizer for poly vinyl chloride polymers; in lubricating grease, and as a curing agent to improve polyethylene wire insulation. Preparation Many commercial processes have been developed for manufacturing basic lead carbonate. These include: Thomson-Stewart process, Carter process, and Dutch process. The method of preparation involves treating lead with acetic acid vapors in the presence of carbon dioxide at 60°C. In the Thomson-Stewart process, finely divided lead monoxide or lead metal is mixed with water to give aqueous slurry, which is then mixed with acetic acid in the presence of air and carbon dioxide. All these processes are slow, taking weeks to obtain products of desired composition. Basic lead carbonate also is precipitated by dissolving lead monoxide in lead(II) acetate solution, and treating the solution with carbon dioxide. -
THE FLUORIDES of PLATINUM and R E L a T E D Compounds by DEREK HARRY LOHMANN B.Sc, University of London, 1953 M.Sc, Queen's Univ
THE FLUORIDES OF PLATINUM and related compounds by DEREK HARRY LOHMANN B.Sc, University of London, 1953 M.Sc, Queen's University, Ontario, 1959 A THESIS SUBMITTED IN PARTIAL FULFILMENT OF THE REQUIREMENTS FOR THE DEGREE OF DOCTOR OF PHILOSOPHY in the Department of CHEMISTRY We accept this thesis as conforming to the required standard. THE UNIVERSITY OF BRITISH COLUMBIA October 1961, In presenting this thesis in partial fulfilment of the requirements for an advanced degree at the University of British Columbia, I agree that the Library shall make it freely available for reference and study. I further agree that- permission for extensive copying of this thesis for scholarly purposes may be granted by the Head of my Department or by his representatives. It is understood that copying or publication of this thesis for financial gain shall not be allowed without my written permission. Department of CHEMISTRY The University of British Columbia, Vancouver 8, Canada. Date 31st October 1961. %\\t Pntesttg of ^irtttslj Columbia FACULTY OF GRADUATE STUDIES PROGRAMME OF THE FINAL ORAL EXAMINATION FOR THE DEGREE OF DOCTOR OF PHILOSOPHY PUBLICATIONS oi . I. "Polar effects in Hydrogen abstraction reactions," M. P. Godsay, DEREK HARRY LOHMANN D. H. Lohmann and K. E. Russell, Chem. and Ind., 1959, 1603. B.Sc, University of London, 1953 M.Sc, Queen's University, Ontario, 1959 2. "Two new fluorides of Platinum," N. Bartlett and D. H. Lohmann, Proc. Chem. Soc, 1960, 14. TUESDAY, NOVEMBER 28th, 1961, AT 1:00 P.M. 3. "The reaction of 2,2-Diphenyl-l-Picrylhydrazyl with 9,10-Dihy- droanthracene and 1,4-Dihydronaphthalene," I. -
Ammoneum Propionate and Ammonium. Lactate A3
— —— —— _— —— —— —- —— —_ .— .— —- —- AMMONEUM PROPIONATE AND —— —- A3 NITROGEN — AMMONIUM. LACTATE SOURCES FOR LACTATING DAiRY. COWS Thesis for the Degree of M. 3. MECHIGAN STATE UNIVERSW N. ALFRED DUTROW 1 97 3‘ 4 It“. ( HNS 1i "i LIBRIQR 1" L 5‘ Michfgtzn State {I:4: University (7;! .m. I 81/53," ' "p I HUM? 8: SflNS' 800K BINDERY [NJ A LIBRARY BINDERS ; gmsronnm OIISA _n >—‘“‘ “Q r“ ABSTRACT AMMONIUM PROPIONATE AND AMMONIUM LACTATE AS NITROGEN SOURCES FOR LACTATING DAIRY COWS BY N. Alfred Dutrow Four isonitrogenous concentrates using soybean meal, urea, ammonium propionate or ammonium lactate as supplemental nitrogen sources were fed to 36 cows (9 per treatment) at 1 kg per 2.5 kg milk for 84 days. Each cow's concentrate was mixed with sufficient corn silage to yield a 10% refusal of the complete feed. Rations were fed once daily. Intakes of urea, ammonium prOpionate, and ammonium lactate were 209, 1170, and 1151 g per day, respectively. Milk yields and composition were adjusted by co- variance using means of a 14-day standardization period. For soybean meal, urea, ammonium propionate, and ammonium lactate, milk yields averaged 23.3, 23.0, 23.8, and 22.7 kg per day; FCM, 19.6, 22.6, 21.8, and 20.6 kg per day; milk N. Alfred Dutrow fat, 3.0, 3.6, 3.5, and 3.5%; and milk solids-not-fat, 8.84, 3.92, 8.99, and 0.83%. FCM was higher (p < .05) for NPN treatments than soybean meal. Dry matter intakes were 18.i, 18.7, 17.7, and 17.9 kg per day for the respective treatments. -
D I C I O N Á R I O De Q U Í M I Ca
7 2 8 2 53 2 5 6 6 18 18 d I 7 c i o N á r i O Iodo Nitrogênio Oxigênio 126.90447 14.0067 126.90447 de 92 2 11 2 8 8 18 8 32 2 21 9 Q U 2 í m i Ca Urânio Cálcio 238.02891 40.078 Inglês - Português Fernando José Luna DICIONÁRIO DE QUÍMICA INGLÊS - PORTUGUÊS 0 8 Fernando José Luna 0 8 Seropédica 2019 Reitor Ricardo Luiz Louro Berbara Vice-Reitor Luiz Carlos de Oliveira Lima Pró-Reitor de Pesquisa e Pós-Graduação Alexandre Fortes Pró-Reitora Adjunta de Pesquisa e Pós-Graduação Lucia Helena Cunha dos Anjos Conselho Consultivo: Adriana T. M. Lessa Lúcia Valadares Sartório Ana Maria Marques dos Santos Luiz Alberto de Lima Leandro Ana Paula Perrota Franco Manlio Silvestre Fernandes Biancca Scarpeline de Castro Márcio Rufino Silva Carmen Andriolli Maria Gracinda Carvalho Teixeira Christian Dutilleux Marta Cioccari Cláudia Mazza Rebeca Gontijo Teixeira Clézio dos Santos Simone Batista Danilo Bilate Tania Mikaela Garcia Roberto Débora Lerrer Vladimyr Lombardo Jorge Janaína Machado Simões Yllan de Mattos Oliveira Lígia Fátima Lima Calixto EDUR Editora da Universidade Federal Rural do Rio de Janeiro Br 465, Km. 7, Seropédica – RJ - CEP: 23.897-000 Telefone: (21) 2681-4711 Site: www.editora.ufrrj.br E-mail: [email protected] Relação das abreviações usadas neste dicionário: abr., abrev. abreviação adj. adjetivo LALQ alquimia amer. inglês americano BIO biologia BIOTEC biotecnologia CATAL catálise cf. confira CG cromatografia a gás CROMAT cromatografia DH Dicionário Houaiss ENG.QUÍM engenharia química FÍS física FOTQ fotoquímica G.QUÍM guerra química GEOQUÍM geoquímica ing. -
Direct Contribution of Ammonia to CCN-Size Αlpha-Pinene Secondary Organic Aerosol Formation
https://doi.org/10.5194/acp-2020-457 Preprint. Discussion started: 14 May 2020 c Author(s) 2020. CC BY 4.0 License. Direct contribution of ammonia to CCN-size αlpha-pinene secondary organic aerosol formation Liqing Hao1, Eetu Kari1,a, Ari Leskinen1,2, Douglas R. Worsnop1,3, Annele Virtanen1 1Department of Applied Physics, University of Eastern Finland, Kuopio, Finland 5 2Finnish Meteorological Institute, Kuopio, Finland 3Aerodyne Research Inc., Billerica, MA 08121-3976, USA a now at: Neste Oyj, Porvoo, Finland Correspondence to: Liqing Hao ([email protected]) and Annele Virtanen ([email protected]) Abstract. Ammonia (NH3), a gasous compound ubiquitiously present in the atmosphere, is involved in the formation 10 of secondary organic aerosol (SOA), but the exact mechanisum is still not well known. This study presents the results of SOA experiments from the photooxidation of α-pinene in the presence of NH3 in the reaction chamber. SOA was formed in nucleation experiment and in seeded experiment with ammonium sulfate particles as seeds. The chemical composition and time-series of compounds in the gas- and particle- phase were characterized by an on-line high- resolution time-of-flight proton transfer reaction mass spectrometer (HR-ToF-PTRMS) and a high-resolution time- 15 of-flight aerosol mass spectrometer (HR-ToF-AMS), respectively. Our results show that for the aerosol particles in + cloud condensation nuclei (CCN) size, the mass concentration of ammonium (NH4 ) was still rising even after the mass concentration of organic component started to decrease due to aerosol wall deposition and evaporation, implying the continuous new formation of particle phase ammonium in the process.