The far infrared spectra of a number of aliphatic amines have been recorded as dilute solutions in cyclohexane. A characteristic band with center at 225 ± 10 cm<sup>−1</sup> is present in the spectra of aliphatic primary amines with a primary α-carbon atom. On the basis of the deuterium shift this band is assigned to the amino torsion. The effects of branching at the α-carbon, coupling of methyl and amino torsions, and intramolecular association on the frequencies of NH<sub>2</sub> torsions are discussed.

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