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Enzymatic preparation of ricinoleic acid esters of long-chain monohydric alcohols and properties of the esters

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Journal of the American Oil Chemists Society

Abstract

Apart from the conventional chemical esterification process, long-chain alkyl ricinoleates also can be prepared by enzymatic esterification or by enzymatic alcoholysis with high yield and without undesirable side reactions. On sulfonation to the hydroxyl group, the alkyl ricinoleates produce surface-active compounds. The tetradecyl ricinoleate shows the best surface-active behavior and seems to be much better than that of sulfonated castor oil commonly known as “Turkey Red Oil”.

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Ghoshray, S., Bhattacharya, D.K. Enzymatic preparation of ricinoleic acid esters of long-chain monohydric alcohols and properties of the esters. J Am Oil Chem Soc 69, 85–88 (1992). https://doi.org/10.1007/BF02635882

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  • DOI: https://doi.org/10.1007/BF02635882

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