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(Redirected from Amyl Alcohol)
'Amyl alcohol' is an organic compound with the formula C₅H₁₁OH. All eight isomers of amyl alcohol are known:

'Isomers of amyl alcohol'

name	formula	alcohol structure	IUPAC Name
normal amyl alcohol		primary	1-pentanol
isobutyl carbinol or isoamyl alcohol or isopentyl 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, are optically active, as they contain an asymmetric carbon atom. The most important is isobutyl carbinol, this being the chief constituent of fermentation amyl alcohol, and consequently a constituent of fusel oil. It can 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 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 and 132 °C only being collected. It may be synthezed 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 organic solvents. It possesses a characteristic strong smell and a sharp burning taste. When pure, it is nontoxic, although the impure product is. On passing its vapour through a red-hot tube, it decomposs with production of acetylene, ethylene, propylene, and other compounds. It is oxidized by chromic acid 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 reported 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.

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