Controlled Release of Covalently Bound Organic Molecules by Slow Hydrolysis for Potential Biocide Applications†

Author: Mosurkal Ravi   Kumar Jayant   Parmar Virinder   Watterson Arthur  

Publisher: Taylor & Francis Ltd

ISSN: 1060-1325

Source: Journal of Macromolecular Science, Part A: Pure and Applied Chemistry, Vol.44, Iss.12, 2007-12, pp. : 1289-1292

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

A study of the slow hydrolysis of labile acetal groups by low concentrations of lactic acid to release the active molecules is reported. A prototype molecule containing cyclic acetal groups, dimethyl-2,3-O-benzylidene-L-tartrate (DMTAc) and the same molecule incorporated as a pendant group in a polyamide were studied for their hydrolysis by low concentrations of lactic acid. The release of benzaldehyde during slow hydrolysis is monitored by UV-vis and 1H-NMR spectroscopy. This study is very useful to ultimately design and synthesize a polymer with covalently bound insecticidal/anti-microbial/anti-fungal materials for the development of controlled release formulations.