Amyl alcohol

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Amyl alcohol is an organic compound and an alcohol. There are eight isomers of amyl alcohol (C₅H₁₁OH):

**Isomers of amyl alcohol**
name	alcohol structure	IUPAC Name
normal amyl alcohol	primary	1-pentanol
isobutyl carbinol or isoamyl alcohol	primary	3-methyl-1-butanol
active amyl alcohol	primary	2-methyl-1-butanol
tertiary butyl carbinol or neopentyl alcohol	primary	2,2-dimethyl-1-propanol
diethyl carbinol	secondary	3-pentanol
methyl (n) propyl carbinol	secondary	2-pentanol
methyl isopropyl carbinol	secondary	3-methyl-2-butanol
dimethyl ethyl carbinol or tertiary amyl alcohol	tertiary	2-methyl-2-butanol

Three of these alcohols, active amyl alcohol, methyl (n) propyl carbinol, and methyl isopropyl carbinol, contain an asymmetric carbon atom and can consequently each exist in two optically active, and one optically inactive form.

The most important is isobutyl carbinol, this being the chief constituent of fermentation amyl alcohol, and consequently a constituent of fusel oil. It may be separated from fusel oil by shaking with strong brine solution, separating the oily layer from the brine layer and distilling it, the portion boiling between 125 °C and 140 °C. being collected. For further purification it may be shaken with hot lime water, the oily layer separated, dried with calcium chloride and fractionated, the fraction boiling between 128 °C and 132 °C only being collected. It may be synthetically prepared from isobutanol by conversion into isovaleraldehyde, which is subsequently reduced to isobutyl carbinol by means of sodium amalgam.

It is a colourless liquid of density 0.8247 g/cm³ (0 °C), boiling at 131.6 °C, slightly soluble in water, easily soluble in alcohol, ether, chloroform and benzene. It possesses a characteristic strong smell and a sharp burning taste. When perfectly pure, it is not a poison, although the impure product is. On passing its vapour through a red-hot tube, it undergoes decomposition with production of acetylene, ethylene, propylene, etc. It is oxidized by chromic acid mixture to isovaleraldehyde; and it forms crystalline addition compounds with calcium chloride and tin(IV) chloride.

The other amyl alcohols may be obtained synthetically. Of these, tertiary butyl carbinol has been the most difficult to obtain, its synthesis having first been accomplished in 1891, by L. Tissier (Comptes Rendus, 1891, 112, p. 1065) by the reduction of a mixture of trimethyl acetic acid and trimethylacetyl chloride with sodium amalgam. It is a solid which melts at 48 to 50 °C and boils at 112.3 °C.