Amylamine

CoeflSeient of azpannon t 20-60 C ConBtnnt-boiling mixture n-AmyUmine Water 

Heat of vaporisation hfoltinf point Speeifie gravity at 20/20 C Speeific heat at 60 F Befraetive index at 19 C Surface tension at 13 C 

Viscosity at 20 C Vapa pressure at 26 C Weight per gallon at 20 C Color 

Distillation range Initial boiling point Not less than 05% 

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Pentyl amine, see n-Amylamine Iso-Pentyl nitrite, see Amyl nitrite Peracetic acid (40% acetic acid solution)... 

Pinene-nitrosochloride forms a series of compounds with various bases, such as propylamine, amylamine, benzylamine, etc., known as pinene-nitrolamines. If two molecules of benzylamine in alcoholic solution be allowed to act on one molecule of pinene-nitrosochloride, pinene nitrol-benzylamine separates on the addition of water, and on recrystallisation from a mixture of ether and alcohol, forms beautiful... 

Caprolactam is a thermally unstable compound which on distillation may form methyl-, ethyl-, propyl-, and n-amylamines. Also, at high temperatures, CL reacts widi oxygen to form hydroperoxides which in the presence of iron or cobalt ions are converted into adipimide. /V-alkoxy compounds are also formed by the reaction of CL with aldehydes during storage. 

Methylamine Ethylamine n-Propylamine Mo-Propylamine n-Butylamine. iso-Butylamiiie ec. -B utylamiiie n-Amylamine. i o-Amylamino n-Hexylamine. n-Heptylamine... 

Pentanone, see Methyl n-propyl ketone 3- Pentanone, see Diethyl ketone Pentene, see Amylene n-Pentyl acetate, see n-Amyl acetate sec-Pentyl acetate, see sec-Amyl acetate Pentyl alcohol, see n-Amyl alcohol Pentyl amine, see n-Amylamine iso-Pentyl nitrite, see Amyl nitrite Peracetic acid (40% acetic acid 1.23 41... 

Amyl alcohol, salicylic acid and, 22 6 n-Amyl alcohol. See 1-Pentanol sec-Amyl alcohol. See 2-Pentanol lerl-Amyl alcohol. See 2-Methyl-2-butanol Amylamine, 2 538t... 

Ehrlich showed that leucine, when heated to 200° C.,.was converted into d-amylamine with loss of CO2 —... 

Ethyl-3-methylpyridine (also known as aldehyde-collidine ) has been prepared by heating aldehyde-ammonia aldehyde-ammonia and acetaldehyde or paraldehyde aldol-ammonia and ammonia paraldehyde and ammonia <> 11,12 acetamide,1 or acetamide and phosphorus pentoxide ethylene glycol and ammonium chloride ethylidene chloride or bromide and ammonia ethylidene chloride and acetamide, ethylamine, or n-amylamine crotonic acid and a calcium chloride-ammonia complex 1 and by passage of acetylene or acetaldehyde and ammonia over alumina and other catalysts. 

The relative reaction rates of several amines with phenyl isocyanate in ether at 0°C have been determined. Aniline is about half as reactive as ethyl-, n-propyl-, n-butylamine, and n-amylamine is between eight and ten times as reactive as ammonia [28]. 

In one study, resorcinol increased the incidence of tongue and oesophageal tumours after initiation with A -nitrosomethyl-u-amylamine. 

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