Rowe R C
J Pharm Pharmacol. 1987 Jan;39(1):50-2. doi: 10.1111/j.2042-7158.1987.tb07162.x.
The reactivity of the fatty alcohols with cetrimide has been quantitatively assessed using immersion calorimetry. In all cases the reaction was endothermic i.e. it had a positive enthalpy. For the n-alcohols the reactivity, as evaluated by the rate of enthalpy change, decreased with increasing chain length although branching on the tetradecanol and hexadecanol resulted in a higher reactivity. Adding 1-octadecanol to 1-hexadecanol resulted in an increased reactivity rising to a maximum for mixtures containing 20-40% w/w 1-octadecanol. The results have been interpreted in terms of the polymorphic form of the alcohol.