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Saponification

Process that converts fat, oil, or lipid into soap and alcohol

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Through Alcohol (chemistry), Alkali and Sodium hydroxide

C2H5O2CCH3 + NaOH → C2H5OH + NaO2CCH3

Saponification of fats

Vegetable oils and animal fats are the traditional materials that are saponified. These greasy materials, triesters called triglycerides, are usually mixtures derived from diverse fatty acids. In the traditional saponification, the triglyceride is treated with lye, which cleaves the ester bonds, releasing fatty acid salts (soaps) and glycerol. In one simplified version, the saponification of stearin gives sodium stearate.

C3H5(O2C(CH2)16CH3)3 + 3 NaOH → C3H5(OH)3 + 3 NaO2C(CH2)16CH3

This process is the main industrial method for producing glycerol (C3H5(OH)3).

Some soap-makers leave the glycerol in the soap. Others precipitate the soap by salting it out with sodium chloride.

Fat in a corpse converts into adipocere, often called "grave wax". This process is more common where the amount of fatty tissue is high and the agents of decomposition are absent or only minutely present.

Saponification value

The saponification value is the amount of base required to saponify a fat sample. Soap makers formulate their recipes with a small deficit of lye to account for the unknown deviation of saponification value between their oil batch and laboratory averages.

Mechanism of basic hydrolysis

The hydroxide anion adds to the carbonyl group of the ester. The immediate product is called an orthoester.

Expulsion of the alkoxide generates a carboxylic acid:

The alkoxide ion is a strong base so the proton is transferred from the carboxylic acid to the alkoxide ion, creating an alcohol:

In a classic laboratory procedure, the triglyceride trimyristin is obtained by extracting it from nutmeg with diethyl ether. Saponification to the soap sodium myristate takes place using NaOH in water. Treating the soap with hydrochloric acid gives myristic acid.


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