1959
DOI: 10.1016/s0021-9673(01)86340-8
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Gas-liquid chromatography: retention volumes of the methyl esters of fatty acids with special reference to n-odd-numbered ISO and (+)-Anteiso acids

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Cited by 68 publications
(18 citation statements)
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“…This conclusion was supported by the fact that the mass spectrum of peak a could be distinguished clearly from those of other methylbranched pentadecanoate, such as 12-methylpentadecanoate, 11-pentadecanoate etc [1]. The retention time of peak a by gas-liquid chromatography is identical with that of iso-pentadecanoic acid methyl ester [13]. Similarly, peak d (Fig.…”
Section: Methodsmentioning
confidence: 82%
See 1 more Smart Citation
“…This conclusion was supported by the fact that the mass spectrum of peak a could be distinguished clearly from those of other methylbranched pentadecanoate, such as 12-methylpentadecanoate, 11-pentadecanoate etc [1]. The retention time of peak a by gas-liquid chromatography is identical with that of iso-pentadecanoic acid methyl ester [13]. Similarly, peak d (Fig.…”
Section: Methodsmentioning
confidence: 82%
“…1). The peaks b,c and e were identified as the methyl esters of n-pentadecanoic acid, palmitic acid, and n-heptadecanoic acid respectively by the retention times of gas-liquid chromatographic [13] and mass spectrometric [1] analysis by using authentic materials. The mass spectrum of peak a (Fig.…”
Section: Methodsmentioning
confidence: 99%
“…The preparation of the columns and the operating parameters for the instrument have been described in detail by Vorbeck et al (1961). The techniques described by James (1959) and Hawke et al (1959), using the relative retention volume on a polar and nonpolar stationary phase and establishing a grid using known acids, were employed to identify the fatty acids. The acids were quantitated by peak-area integration.…”
Section: Lipid Fractionationmentioning
confidence: 99%
“…(Table I), but it is feasible t o group these acids in possible arrangements based on literature values (9,18) for the separation of iso, anteiso, and neo acids from the straight chain fatty acids with the same number of carbon atoms (Tables VI and VII). The final identification of the structures depends on determination of number of carbon atoms and on physicochemical (19) or chemical (20) examination, but the order of appearance in the urea separation and the groupings by separation from potential normal acids suggest t h a t B, D, and F are respectively CI5, C16, and C17 is0 acids; C and Y respectively C16 and C16 anteiso acids, although C16 and C17 neo acids cannot be entirely excluded as possibilities;…”
Section: Saturated Branch Chain Acidsmentioning
confidence: 99%
“…------ Odd-nz~mbercd Fatty A cids These acids may originate from microbiological activity (21) but are now accepted a s normal components of shark liver (18,22) and menhaden oils (9,23). In the seal oil there is clear evidence for the saturated C16, C17, and C19 acids, but not for the C21.…”
Section: Saturated Branch Chain Acidsmentioning
confidence: 99%