Abstract
Several 1-alkoxymethyl-3-substituted-pyridinium chlorides with alkoxy chains including from 3 to 18 carbon atoms were prepared by the reaction of 3-substituted-pyridine with chloromethyl alkyl ethers. The prepared chlorides were examined for their antielectrostatic effects and their antimicrobial activities. 1-Dodecyloxymethyl-3-dimethylaminopyridinium chloride (23) exhibited strong antimicrobial activity and a wide antimicrobial spectrum, similar to the activity of benzalkonium chloride. We synthesized 1-alkoxymethyl-3-hydroxypyridinium chlorides possessing antielectrostatic properties, but lacking antimicrobial activity. The antielectrostatic effect and antimicrobial activities are strongly dependent on the kind of substituent at the 3-position in the pyridine ring and are greatly affected by an alkoxy chain. It was shown that dimethylamino group in position three must be present for a high antielectrostatic and antimicrobial activity of the agent.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
