4.0 Article

Grafting of Chitosan with Fatty Acyl Derivatives

Journal

JOURNAL OF THE BRAZILIAN CHEMICAL SOCIETY
Volume 21, Issue 10, Pages 1910-1916

Publisher

SOC BRASILEIRA QUIMICA
DOI: 10.1590/S0103-50532010001000016

Keywords

chitosan; grafting; lauroyl chitosan; fatty acyl derivatives

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The internal plasticization of chitosan with covalently linked long aliphatic branches, typically 12C, was accomplished through the condensation of the amino groups of chitosan with acidic derivatives of lauric acid, as lauroyl anhydride or lauroyl chloride, that are more reactive than the fatty acid itself. The chemical pathway led to selective N-acylation. The degree of substitution was quantitatively determined by FTIR and H-1 NMR and varied between 3 and 35%. The FTIR quantitative analysis was based in a calibration mmethod with good accuracy. The modified chitosan products were soluble in neutral water and/or DMF according to the degree of substitution. The modified chitosan films were more flexible than the pristine, non-modified ones.

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