Absorption of Deuterium-Labeled cis- and trans-Octadecenoic Acid Positional Isomers in Man *

2018 ◽  
pp. 159-176
Author(s):  
E.A. Emken
2013 ◽  
Vol 62 (10) ◽  
pp. 781-788 ◽  
Author(s):  
Kazuaki Yoshinaga ◽  
Masaharu Asanuma ◽  
Chao Xu ◽  
Hoyo Mizobe ◽  
Koichi Kojima ◽  
...  

1986 ◽  
Vol 86 (10) ◽  
pp. 1391-1394
Author(s):  
Mieke M. van den Reek ◽  
Margaret C. Craig-Schmidt ◽  
A.J. Clark

1978 ◽  
Vol 61 (3) ◽  
pp. 702-708
Author(s):  
Henry B S Conacher ◽  
Jagannath R Iyengar

Abstract Studies in our laboratories indicated that the trans contents of a number of commercial margarines, determined by gas-liquid chromatography (GLC) on a 15 ft column packed with 10% Silar IOC, were approximately 80-85% of those determined by infrared spectroscopy. This is mainly due to overlap of some of the trans positional isomers with the cis positional isomers in the octadecenoate fraction, shown by studies involving determination of the transoctadecenoate content of the margarines by silver ion thin layer chromatography/GLC, and by preparation and study of the GLC behavior of the cis and trans positional isomers of Δ6-, Δ9-, Δ12-, and Δl5-octadecenoates. The last 3 isomers were prepared by hydrazine reduction and nitrous acid isomerization of linoleic and linolenic acids. Since it is possible that longer, more efficient columns might result in better separation of the cis- and traru-octadecenoate isomers, it is recommended that studies be continued on longer packed columns (20 ft) and possibly on support-coated open tubular columns.


1953 ◽  
Vol 46 (2) ◽  
pp. 364-375 ◽  
Author(s):  
David G. Cornwell ◽  
Richard Backderf ◽  
Christopher L. Wilson ◽  
J.B. Brown

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