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High‐resolution 1 H and 2 H NMR spectroscopy of pure essential fatty acids for plants and animals
Author(s) -
Aursand M.,
Mabon F.,
Martin G. J.
Publication year - 1997
Publication title -
magnetic resonance in chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.483
H-Index - 72
eISSN - 1097-458X
pISSN - 0749-1581
DOI - 10.1002/(sici)1097-458x(199712)35:13<s91::aid-omr201>3.0.co;2-g
Subject(s) - chemistry , polyunsaturated fatty acid , deuterium , deuterium nmr , nuclear magnetic resonance spectroscopy , spectroscopy , nmr spectra database , high resolution , fatty acid , carbon 13 nmr , isotopic labeling , analytical chemistry (journal) , spectral line , chromatography , organic chemistry , physics , remote sensing , quantum mechanics , astronomy , geology
High‐resolution 1 H and 2 H NMR spectroscopy were used to study the most important saturated (C14:0, C16:0, C18:0), monounsaturated (C16:1n‐7, C18:1n‐7, C18:1n‐9, C20:1n‐9, C22:1n‐9) and polyunsaturated [C18:3n‐3, C20:5n‐3 (EPA), C22:6n‐3 (DHA)] fatty acids which may be found in fish lipids, in order to prepare the tools for a subsequent study of the recognition of the origin of fish oils by isotopic analysis. The interpretation of the 1 H and 2 H NMR spectra of the different acids is reported. Additionally, the overall D/H and the 13 C/ 12 C isotope ratios are given. The overall D/H ratio ranges from 114.0 to 137.2 ppm/V.SMOW (V.SMOW=water standard) and the 13 C/ 12 C ratio from ‐23.5 to ‐33.2‰. From the 2 H NMR spectra, an investigation of the internal deuterium distribution in the saturated and mono‐ and polyunsaturated fatty acids was made. The deuterium distribution can be given for nearly all the chemical sites, except for the different double bonds, in EPA and DHA. The precision of the measurements was of the order of 0.5–4% depending on the nature of the cluster considered. © 1997 John Wiley & Sons, Ltd.