Msflk. Jie et al., C-13 NUCLEAR-MAGNETIC-RESONANCE SPECTROSCOPIC ANALYSIS OF THE TRIACYLGLYCEROL COMPOSITION OF SOME MARGARINES, Journal of the American Oil Chemists' Society, 73(8), 1996, pp. 1011-1017
The triacylglycerol fraction of three samples of margarine, namely ''F
lora'' (Holland), ''Kaliakra'' (Bulgaria), and ''Corona'' (Holland), w
ere studied by C-13 nuclear magnetic resonance spectroscopy. By examin
ing the various carbon chemi cal shifts of the saturated and unsaturat
ed carbon nuclei, ''Flora'' margarine was shown to contain a mixture o
f hydrogenated and unhydrogenated vegetable oils. This technique allow
ed all major acyl groups (saturated, oleate, linoleate, and linolenate
) and minor acyl components [different positional isomers of long-chai
n (E)- and (Z)-monoenoic moieties arising as by-products during cataly
tic hydrogenation] to be identified. The amount of each fatty acid pre
sent in the margarine was also estimated from the relative intensities
of the corresponding signals. ''Kaliakra'' margarine consisted of a b
lend of unhydrogenated natural fats and oils that contained saturated
fatty acids, oleate, and linoleate. There were no signs in the spectru
m of ''Kaliakra'' of any (E)-isomers, nor signals associated with posi
tional unsaturated acyl groups (other than oleate and linoleate). The
sample of ''Corona'' margarine consisted of a mixture of hydrogenated
and unhydrogenated vegetable oils and butter (1.3%). The presence of b
utter in this sample was identified by the characteristic carbon shift
s of the C-1 to C-4 carbon atoms of butyrate. The distribution of the
fatty acids on the glycerol ''backbone'' also was estimated by this te
chnique.