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Stabilizing polymorphic transitions of tristearin using diacylglycerols and sucrose polyesters

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Journal of the American Oil Chemists' Society

Abstract

The polymorphic transitions of synthesized tristearin in the presence of selected DAG or commercial sucrose polyesters (SPE) were investigated using DSC and X-ray diffractiometry. The stabilizing effects of DAG and SPE on α to β transitions of tristearin were dependent on the chemical structures of additives such as FA chain length, saturation of FA, positions and number of FA on backbones. The addition of 1,2-distearin (DS) or SPE containing 70% stearic acid with a hydrophile-lipophile balance value of 1 (S-170) to tristearin resulted in a significant stabilizing effect on the α to β transition during constant heating and storage of α forms at 53°C. The addition of 1,2-DS or S-170 also stabilized the β′ to β transitions of tristearin during constant heating and storage at 59°C. The addition of S-170 exhibited greater stabilizing effects than the addition of 1,2-DS during early stages of storage of α or β′ forms of tristearin. This study provides evidence of potential uses for SPE as additives to improve the quality and shelf life of foods containing fats by stabilizing the desirable α or β′ forms of fats.

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Correspondence to Barry G. Swanson.

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Oh, JH., McCurdy, A.R., Clark, S. et al. Stabilizing polymorphic transitions of tristearin using diacylglycerols and sucrose polyesters. J Amer Oil Chem Soc 82, 13–19 (2005). https://doi.org/10.1007/s11746-005-1036-y

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  • DOI: https://doi.org/10.1007/s11746-005-1036-y

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