Oleyl alcohol

[2] It can be produced by the hydrogenation of oleic acid esters by Bouveault–Blanc reduction, which avoids reduction of the C=C group (as would occur with usual catalytic hydrogenation).

The required oleate esters are obtained from beef fat, fish oil, and, in particular, olive oil (from which it gains its name).

The original procedure was reported by Louis Bouveault in 1904[3] and subsequently refined.

[4][5] It has uses as a nonionic surfactant, emulsifier, emollient and thickener in skin creams, lotions and many other cosmetic products including shampoos and hair conditioners.

It has also been investigated as a carrier for delivering medications through the skin or mucous membranes; particularly the lungs.

Space-filling model of oleyl alcohol
Structural model of oleyl alcohol
NFPA 704 four-colored diamond Health 1: Exposure would cause irritation but only minor residual injury. E.g. turpentine Flammability 0: Will not burn. E.g. water Instability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogen Special hazards (white): no code