Chlorfenapyr

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Chlorfenapyr
File:Chlorfenapyr.png
style="background: #F8EABA; text-align: center;" colspan="2" | Identifiers
CAS number 122453-73-0
ChemSpider 82875
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InChI key CWFOCCVIPCEQCK-UHFFFAOYAO
style="background: #F8EABA; text-align: center;" colspan="2" | Properties
Molecular formula C15H11BrClF3N2O
Molar mass 407.6 g/mol
Density 0.543 g/ml tapped bulk density
Melting point

100-101 °C

Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

Chlorfenapyr is a pesticide, and specifically a pro-insecticide (meaning it is metabolized into an active insecticide after entering the host), derived from a class of microbially produced compounds known as halogenated pyrroles. The United States Environmental Protection Agency initially denied registration in 2000 for use on cotton primarily because of concerns that the insecticide was toxic to birds and because effective alternatives were available. However, it was registered by EPA in January, 2001 for use on non-food crops in greenhouses. In 2005, EPA established a tolerance for residues of chlorfenapyr in or on all food commodities. Chlorfenapyr works by disrupting the production of Adenosine triphosphate, specifically, "Oxidative removal of the N-ethoxymethyl group of chlorfenapyr by mixed function oxidases forms the compound CL 303268. CL 303268 uncouples oxidative phosphorylation at the mitochondria, resulting in disruption of production of ATP, cellular death, and ultimately organism mortality."

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