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Amyl amine

In the pyrolysis of pure amine oxides, temperature has a significant effect on the ratio of products obtained (22). The principal reaction during thermal decomposition of /V,/V-dimetby11 amyl amine oxide [1643-20-5] at 80—100°C is deoxygenation to /V,/V-dimetby11 amyl amine [112-18-5] (lauryl = dodecyl). [Pg.190]

Azidomethylbutane. See Amylazide under Amyl amine and Derivatives, p A3 95... [Pg.640]

Amylamine Aminopentme Aminomethyl-6ata c,C H, NH,. Several isomers are known, including /soamylaiwi e,(CH,),-CH-CHj -CH, NHj. They can be prepd by the reaction of amyl chlorides with ammonia in the presence of alcohol as a mutual solvent. Datta Chatterjee(Ref 2) detd expln temps of amylaminepicrate and amyl amine perchlorate and found them to be 270 and 262°, respectively... [Pg.395]

SYNS AMN METHYLAMYLNITROSAMN (GERMAN) METHYLAMYLNITROSAMINE METH-YL-N-AMYLNITROSAMINE N-METHYL-N-NITROSO-PENTYLAMINE METHYL-N-PENTYL-NITROSAMINE N-NITROSO-N-METHYL-N-AMYL-AMINE NITRO-SOMETHYL-N-PENTYLAMINE... [Pg.81]

A general method for the preparation of primary amines, free from secondary and tertiary amines, involves the interaction of Grignard reagents and O-methylhydroxylamine. The yields range from 45% to 90% for many amines including ethylamine (81%), t-butylamine (70%), n-amyl-amine (65%), and /3-phenylethylamine (68%)/ ... [Pg.792]

C9H20N2O N-butyl-N-nitroso amyl amine 16339-05-2 482.15 42.172 2 18313 C9H20O 2,2,4-trimethyl-3-hexanol 66793-89-3 442.15 42.819 1,2... [Pg.488]

Figure 26.8 Solid-state fluorescence spectra of the ADS salts with benzyl amine (solid line), n-amyl amine (dashed line), and n-butyl amine (dotted line). Their spectra in solution (inset). Figure 26.8 Solid-state fluorescence spectra of the ADS salts with benzyl amine (solid line), n-amyl amine (dashed line), and n-butyl amine (dotted line). Their spectra in solution (inset).
HjO almost insoluble in cold alcohol and ether soluble in boiling alcohol it is odorless and tasteless, and its solutions are neutral. It sublimes at 170° (338° P.) without decomposition if suddenly heated above 180° (356° F.), it is decomposed into amyl-amin and carbon dioxid. [Pg.283]

Amino-n-pentanol-l 5-Hydroxy-n-amyl amine, 5-amino-n-amyl alcohol, 5-pentanolamine)... [Pg.114]

C HuBr N Bi8-(y2.bn>m-butyl].ainin 4II636. Bia-[6-biom-batyI]-amin 4 II636. (v-nx>m-p[opyI]-[B-bfom.n-amyl]-amin 4,177. [Pg.276]

CjAaN Athyldiiaobiilylaiiim 4.166. Di-n-amyl-amin 4 1 378. II642. Bis-[x-methyl-biil ]-amin 4,178, II643. Bis-[x-5thyl-pcopyl]-anim 41379, II644. [Pg.507]

CigHgjNjO, Methjrl.bia.[E.dimethylamino-n-amyl]-amin.tna.hydTOxyraethylat 4T 422. [Pg.2747]

See other pages where Amyl amine is mentioned: [Pg.197]    [Pg.198]    [Pg.198]    [Pg.198]    [Pg.199]    [Pg.14]    [Pg.127]    [Pg.80]    [Pg.199]    [Pg.793]    [Pg.79]    [Pg.197]    [Pg.197]    [Pg.197]    [Pg.198]    [Pg.198]    [Pg.198]    [Pg.204]    [Pg.142]    [Pg.133]    [Pg.115]    [Pg.469]    [Pg.863]    [Pg.507]    [Pg.808]    [Pg.1399]    [Pg.15]    [Pg.788]    [Pg.205]   


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