The development by collaborative study of a standardised method for the det
ermination of the stigmastadienes content in vegetable oils is described. T
he procedure involves the isolation of the unsaponifiable matter in the oil
ands its fractioning on a silica gel column. The fraction containing the s
teroidal hydrocarbons is then analysed by capillary gas chromatography and
the quantitative assessment made by the use of an internal standard/cholest
an-3,5-stadiene. The procedure is very sensitive allowing determination at
levels of 0.01-4.0 mg/kg.