The glycerol backbone on the left is bound (ester OH binding) to three fatty
acids, shown here with palmitic acid, oleic acid and alpha-linolenic acid and
a total carbon number of 55.
This molecule is broken down to individual alkyl esters through a chemical
process called transesterification, whereby the glycerin is separated from the
fatty acids. Methanol (CH
3
OH) is added to the lipids and heated. Any strong
base capable of deprotonating the alcohol, such as NaOH or KOH is used as
catalyst.
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The process leaves behind methyl esters (with a CH
3
group on the ester
binding) and glycerin (a valuable byproduct used in soaps, explosives and
other products).