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N-phenyl-2-naphthylamine - CAS # 135-88-6 Information provided on N-phenyl-2-naphthylamine (135-88-6) is for reference only and is subject to change. There is no warranty of accuracy or completeness of any information contained herein.
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N-Phenyl-2-naphthylamine is probably released to the environment in waste streams from its production and use. In the atmosphere, it should exist in the vapor and particulate phases. Vapor phase N-phenyl-2-naphthylamine is expected to degrade rapidly (estimated half-life of 55 minutes) by reaction with photochemically produced hydroxyl radicals ...
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1.2. Limit defining parameters . 1.2.1. Detection limit of the analytical procedure. The detection limits of the analytical procedure are 180 and 32.5 pg per injection for N-phenyl-1-naphthylamine and N-phenyl-2-naphthylamine respectively.These are the amounts of each analyte that will produce peaks with heights that are approximately five times the baseline noise.
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It is also used as a stabilizer in electrical-insulating enamels and as an antioxidant in other polymers, in greases, and in lubricating and transformer oils. It is used as a chemical intermediate in the production of the rubber antioxidant, N-phenyl-2-naphthylamine-acetone condensate, and in the
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This chapter discusses the common name, mass spectrum, structure, Merck index reference, analytical artifacts, and spectra of derivatives, of several compounds in alphabetical order.
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United States EPA 560n"IIS-84-001a Environmental Protection Agency Toxic Integration Information Series Chemical Activities Status Report Fourth Edition Volume I Compiled under the direction of: Eleanor T. Merrick With the assistance of: Patricia Grim Data in this publication are current as of February 1984
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88) CAS No.: 309-00-2 A. Evidence for carcinogenicity to humans (inadequate) Specific mention of aldrin in analytical epidemiological studies is limited to reports of follow-up of two cohorts of men employed in its manufacture in plants where dieldrin and endrin (and, in one, telodrin) were also manufactured [ref: 1-4].
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40 CFR 721.10300 - Benzeneacetic acid, .alpha.-chloro-.alpha.-phenyl-, ethyl ester. Code of Federal Regulations, 2014 CFR. 2014-07-01... 40 Protection of Environment 31 2014-07-01
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The kinetics of 5-exo and 6-endo acyl radical cyclizations have been investigated under a variety of reaction conditions.28 The presence of the 6-endo product was found to arise either by a direct cyclization (2:0 104 s 1 ) or by a ring expansion (4:2 103 s 1 ) from the 5-exo radical product (1:6 105 s 1 ).
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Rates of acetolysis have been measured for methyl 2,3,6-tri-O-methyl-a-D-galacto(11a) and -gluco-pyranoside (11b), with substituents X OMe, OAc, and NHAc in the 4-position.14 In both series, the most electronegative substituent (methoxy) is associated with the fast rates, and the least electronegative (acetamido) is the slowest.
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Hypochlorous and peracetic acid induced oxidation of dairy proteins. PubMed. Kerkaert, Barbara; Mestdagh, Frédéric; Cucu, Tatiana; Aedo, Philip Roger; Ling, Shen ...
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Rates of acetolysis have been measured for methyl 2,3,6-tri-O-methyl-a-D-galacto(11a) and -gluco-pyranoside (11b), with substituents X OMe, OAc, and NHAc in the 4-position.14 In both series, the most electronegative substituent (methoxy) is associated with the fast rates, and the least electronegative (acetamido) is the slowest.
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VII Giornate Italo-Francesi di Chimica 7 èmes Journées Franco-Italiennes de Chimie Torino 5-6 maggio/mai 2014 Università di Torino Le sezioni del Piemonte-Valle d'aosta e della Liguria della Societá Chimica
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