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Bifenthrin or (2-methyl-1,1-biphenyl-3-y1)-methyl-3-(2-chloro-3,3,3-trifluoro-1-propenyl)-2,2-dimethyl cyclopropanecarboxylate (CAS number 82657-04-3) is a pyrethroid insecticide that affects the nervous system of insects. Products containing bifenthrin include Talstar, Capture, Bifenthrine, Spinosad, and Ortho Home Defense Max.
Additional recommended knowledge
The material safety data sheet MSDS for Maxxthor (Bifenthrin's trade name) shows carcinogenic qualities to be virtually zero. It is highly toxic to fish, since it, like most pyrethroids, is also an ATPase inhibitor. Aquatic vertebrates are much more sensitive to ATPase inhibitors than terrestrial vertebrates due to their high dependence on ATP synthesis in the gills to maintain osmotic balance.
The United States Environmental Protection Agency (EPA) once classified bifenthrin in the past as a class C, although it no longer does so. It is probable that a one-time class "C" carcinogen (possible human carcinogen)designation was based on older data and lack of studies.
The last link contains the following statements about "Spinosad", a trade name (one of many) for Bifenthrin:
"4. Aggregate cancer risk for U.S. population. Spinosad has been classified as ``not likely to be carcinogenic in humans based on the results of a carcinogenicity study in mice and the combined chronic toxicity and carcinogenicity study in rats. Therefore, spinosad is not expected to pose a cancer risk to humans.
5. Determination of safety. Based on these risk assessments, EPA concludes that there is a reasonable certainty that no harm will result to the general population, and to infants and children from aggregate exposure to spinosad residues."
Based on the above findings, the "class C Carcinogen" designation was likely pre-2002, the date of this document.
Bifenthrins do have possible health impacts, however, and these should be understood.
|This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Bifenthrin". A list of authors is available in Wikipedia.|