Chlorfenapyr Crystal Polymorphism and Insecticidal Activity.

Cryst Growth Des

Department of Chemistry and Molecular Design Institute, New York University, 29 Washington Place, New York City, New York 10003, United States.

Published: February 2024

Four crystalline polymorphs of the proinsecticide chlorfenapyr [4-bromo-2-(4-chlorophenyl)-1-ethoxymethyl-5-trifluoromethyl-1-pyrrole-3-carbonitrile] have been identified and characterized by polarized light optical microscopy, differential scanning calorimetry, Raman spectroscopy, X-ray diffraction, and electron diffraction. Three of the four structures were considered polytypic. Chlorfenapyr polymorphs show similar lethality against fruit flies () and mosquitoes () with the least stable polymorph showing slightly higher lethality. Similar activities may be expected to be consistent with structural similarities. Knockdown kinetics, however, depend on an internal metabolic activating step, which further complicates polymorph-dependent bioavailability.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10853905PMC
http://dx.doi.org/10.1021/acs.cgd.3c01257DOI Listing

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