## Abstract Conditions for separation of enantiomers of a mandelic acid derivative, methyl 2‐phenyl‐2‐(tetrahydropyranyloxy) acetate (the analyte) were studied. Because of the presence of two chiral carbons, the analyte consists of four stereoisomers stable at ambient temperature. Chiral HPLC of th
Retention behavior of trans isomers of eicosapentaenoic and docosahexaenoic acid methyl esters on a polyethylene glycol stationary phase
✍ Scribed by Svein A. Mjøs
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 376 KB
- Volume
- 110
- Category
- Article
- ISSN
- 1438-7697
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
A polyethylene glycol (PEG) stationary phase was evaluated for the separation of mono‐trans isomers of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) methyl esters. The resolution patterns were compared to patterns achieved with previously applied conditions on a cyanopropyl phase. There were no overlaps between all‐cis EPA/DHA and their mono‐trans isomers on the PEG phase. Because of overlap between 22:0 and 22:1 isomers, the PEG column is not a good choice for analyses of EPA trans isomers in crude fish oils. However, if the saturated and monounsaturated fatty acids are not present in significant amounts, PEG can be a better choice than cyanopropyl columns.
📜 SIMILAR VOLUMES