Lipase catalyzed esterification of free hydroxyl groups of Beta-cyclodextrin and its derivatives.
IR@CSIR-CFTRI
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Relation |
http://ir.cftri.com/4560/
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Title |
Lipase catalyzed esterification of free hydroxyl groups of Beta-cyclodextrin and its derivatives.
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Creator |
Pattekhan, H. H.
Divakar, S. |
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Subject |
08 Food Chemistry
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Description |
Modification of hydroxyl groups of beta-cyclodextrin (beta-CD) and its n-heptane at 50 C has been carried out with acetic, propionic, butyric, isobutyric, valeric, isovaleric, lauric, octanoic, palmitic and stearic acids. Degree of modification is determined from 1H NMR. Although the ratio of beta-CD to organic acid employed is 1:50, 6.8 OH groups on an average are found to be modified with acetic acid, 0.38 with propionic acid and 2.43 with isobutyric acid. Heptakis-2,6-di-)-methyl-beta-cyclodextrin (DMbeta-CD) and hydroxypropyl-beta-cyclodextrin (HPbeta-CD) which are already substituted with methyl and hydroxypropyl groups, respectively show degrees of substitution to be 2.45 and 2.0 at the freely available 2-OH or 3-OH hydroxyl groups.
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Date |
2002
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Type |
Article
PeerReviewed |
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Format |
application/pdf
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Language |
en
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Rights |
—
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Identifier |
http://ir.cftri.com/4560/1/Ind_J_of_Chem_B_41_5_1025-1027.pdf
Pattekhan, H. H. and Divakar, S. (2002) Lipase catalyzed esterification of free hydroxyl groups of Beta-cyclodextrin and its derivatives. Indian Journal of Chemistry, 41B (5). pp. 1025-1027. |
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