Enzymatic synthesis of kojic acid esters and their potential industrial applications
β Scribed by Lajis, Ahmad Firdaus B.; Basri, Mahiran; Mohamad, Rosfarizan; Hamid, Muhajir; Ashari, Siti Efliza; Ishak, Nurazwa; Zookiflie, Azulia; Ariff, Arbakariya B.
- Book ID
- 120377464
- Publisher
- Versita
- Year
- 2013
- Tongue
- English
- Weight
- 233 KB
- Volume
- 67
- Category
- Article
- ISSN
- 0366-6352
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β¦ Synopsis
Abstract
In this paper, enzymatic methods for the synthesis of 5-hydroxy-2-(hydroxymethyl)-4H-pyran-4-one (kojic acid) esters are reviewed. Important process parameters related to the synthesis of kojic acid esters such as the type of immobilized lipase, solvent, temperature, initial water activity, water content, pH, metal salts, enzyme loading, substrates mole ratio, and acyl donors are highlighted and discussed. The properties of kojic acid esters related to their solubility, stability, cytotoxicity, depigmenting activity, tyrosinase inhibitory, metal-chelating, anti-oxidant, and other biological activities are also highlighted. At present, kojic acid and its esters are widely used in cosmetic and skin health industries as skin whitening agents. The advantages and disadvantages of various kojic acid esters are compared and possible industrial applications of these derivatives are also discussed.
π SIMILAR VOLUMES
## Abstract For Abstract see ChemInform Abstract in Full Text.
Unsaturated fatty acid β£-butylglucoside esters were prepared by enzymatic esterification of β£-butylglucoside in nonaqueous media. Conditions were firstly optimized using oleic acid as acyl group. Synthesis was possible in several solvents but the presence of water co-product in the medium limited th