Separation behavior of octadecadienoic acid isomers and identification of cis- and trans-isomers using gas chromatography

Shibamoto, S; Gooley, A; Yamamoto, K

HERO ID

2902339

Reference Type

Journal Article

Year

2015

Language

English

PMID

25466915

HERO ID 2902339
In Press No
Year 2015
Title Separation behavior of octadecadienoic acid isomers and identification of cis- and trans-isomers using gas chromatography
Authors Shibamoto, S; Gooley, A; Yamamoto, K
Journal Lipids
Volume 50
Issue 1
Page Numbers 85-100
Abstract Using a strongly polar cyanopropyl capillary column we have investigated the gas chromatography (GC) separation behaviors of 24 octadecadienoic acid methyl ester (18:2ME) isomers compared against saturated methyl stearate (18:0ME) and arachidic acid methyl ester (20:0ME), and the dependency on the GC column temperature. The 24 isomers were obtained by performing cis-to trans-isomerization of six regioisomers: five of the 18:2ME isomers were prepared by the partial reduction of methyl α-linolenate and methyl γ-linolenate C18 trienoic acids with different double bond positions, whereas the sixth isomer, 18:2ME (c5, c9), was obtained from a raw constituent fatty acid methyl ester (FAME) sample extracted from Japanese yew seeds. There are no reference standards commercially available for 18:2ME isomers, and in elucidating the elution order of these isomers this study should help the future identification of cis- and trans-type of 18:2ME. We also report the identification method of cis- and trans-type of FAME using equivalent chain lengths and attempt the identification of cis- and trans-type of 18:2ME isomers from partially hydrogenated canola oil.
Doi 10.1007/s11745-014-3966-8
Pmid 25466915
Is Certified Translation No
Dupe Override No
Is Public Yes
Language Text English