Inhibition of Clostridium botulinum by p -Hydroxybenzoic Acid n -Alkyl Esters
Open Access
- 1 June 1979
- journal article
- research article
- Published by American Society for Microbiology in Antimicrobial Agents and Chemotherapy
- Vol. 15 (6), 798-801
- https://doi.org/10.1128/aac.15.6.798
Abstract
Twelve straight-chain esters, C 5 to C 14 , C 16 , and C 18 , of p -hydroxybenzoic acid were prepared, and their melting points, solubilities in water at 25°C, infrared spectra, dissociation constants ( pK a ), and activities against Clostridium botulinum were determined. These studies also included four commercial straight-chain esters, C 1 to C 4 . The most potent activity was exhibited by undecyl and dodecyl esters, which are about 300 times as active as sodium nitrite. Quadratic and cubic equations were developed correlating the activity with pK a values and chain length of the esters, respectively.This publication has 1 reference indexed in Scilit:
- INFLUENCE OF PARA‐HYDROXYBENZOIC ACID ESTERS ON THE GROWTH AND TOXIN PRODUCTION OF Clostridium botulinum 10755AJournal of Food Science, 1978