๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

High-resolution 13C-NMR olefinic spectra of DHA and EPA acids, methyl esters and triacylglycerols

โœ Scribed by R. Sacchi; I. Medina; L. Paolillo; F. Addeo


Publisher
Elsevier Science
Year
1994
Tongue
English
Weight
574 KB
Volume
69
Category
Article
ISSN
0009-3084

No coin nor oath required. For personal study only.

โœฆ Synopsis


The high-resolution 13C-NMR spectra of the olefinic carbons of two major n-3 polyunsaturated fatty acids of fish oils, DHA (22:6, n-3) and EPA (20:5, n-3), were recorded at 100.64 MHz in chloroform-d solutions on standard free acids, methyl esters, Atlantic tuna (Thunnus alalunga) triacylglycerols and methyl esters. All olefinic resonances were resolved in DHA and EPA acids and methyl esters, the number of olefinic signals corresponding to that of unsaturated carbons. The order of the spin-lattice relaxation times (T 0 and the chemical shift differences (A,5) between signal pairs related to the same double bond led to the complete assignment of DHA and EPA olefinic carbons in acids and methyl esters. The DHA and EPA olefinic shifts of Thunnus alalunga triacylglycerois were also studied and compared with those of methyl esters. The possibility of using ]3C-NMR olefinic carbons for the analysis of fish lipids and oils is discussed.


๐Ÿ“œ SIMILAR VOLUMES


High-resolution 13C NMR spectra of long-
โœ F.D. Gunstone ๐Ÿ“‚ Article ๐Ÿ“… 1993 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 281 KB

Chemical shifts are reported for long-chain acids, methyl esters, glycerol esters, wax esters, nitriles, amides, alcohols and acetates. These indicate the possibility of using high-resolution ]3C NMR spectroscopy for the analysis of mixtures of these types of compound.

The 13C NMR spectrum of abietic acid and
โœ William B. Smith ๐Ÿ“‚ Article ๐Ÿ“… 1978 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 155 KB

## Abstract The assignment of lines in the ^13^C NMR spectrum of abietic acid and its methyl ester have been made using carbon __T__~1~ values and lanthanide induced shift effects. Structureโ€“NMR parameter values are briefly discussed.

IR, 1H NMR and 13C NMR spectra of isomer
โœ Pรกl Sohรกr; ร–dรถn Fehรฉr; Endre Tihanyi ๐Ÿ“‚ Article ๐Ÿ“… 1979 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 371 KB

## Abstract The IR, ^1^H and ^13^C NMR spectra of six esters of 1โ€arylโ€4โ€methylโ€3โ€ and 5โ€pyrazolecarboxylic acids are reported. On the basis of their spectra the 3โ€ or 5โ€position of the substituent in such structural isomeric pairs can be established without recourse to the spectrum of the other me

13C-NMR of double and triple bond carbon
โœ Jan Bus; Izaรคk Sies; Marcel S.F. Lie Ken Jie ๐Ÿ“‚ Article ๐Ÿ“… 1977 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 562 KB

Fhe carbon magnetic resonance spectra of many fatty acid methyl esters with cis and trans double bonds and triple bonds at various positions and in many different combinations have been investigated. The influence of the ester group on double and triple bonds in the fatty acid chain depends strongl