Mm. Mossoba et al., SPECTRAL CONFIRMATION OF TRANS MONOUNSATURATED C-18 FATTY-ACID POSITIONAL ISOMERS, Journal of the American Oil Chemists' Society, 74(2), 1997, pp. 125-130
The trans octadecenoic acid methyl ester isomers were obtained from a
partially hydrogenated soybean oil sample and isolated by silver-ion h
igh-performance liquid chromatography. The double bond configuration w
as confirmed to be trans by using gas chromatography-direct deposition
-fourier transform infrared spectroscopy. The double bond positions fo
r nine individual trans octadecenoic acid positional isomers were conf
irmed by gas chromatography-electron ionization mass spectrometry afte
r derivatization to 2-alkenyl-4,4-dimethyloxazoline. These nine trans
positional isomers were resolved on either one of the two polar 100% c
yanopropylpolysiloxane 100-m capillary columns, SP 2560 and Cp-Sil 88,
at an isothermal temperature of 140 degrees C. These nine isomers wer
e confirmed to have double bonds at carbons C-8 through C-16. The pair
of trans octadecenoic acid positional isomers with double bonds at C-
13 and C-14 are reported for the first time to be resolved by gas chro
matography.