1978
DOI: 10.1039/cs9780700473
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Synthetic pyrethroids ? a new class of insecticide

Abstract: CHa=CH--CHI PyrethrinI CH,--CHI CincrinI CHs-CHa--CHI Jasmolin I CHa=CH---COSCH, Pyrethrin I1 CH,--CO,CHs Cinerin I1 CHs-CHa--COpCHa Jasmolin I1 (a) natural esters (b) most active isomer in fenvalerate Figure 1 (a) TIte six natural esters; (6) a recent synthetic pyrethroid 2 DefinitionAlthough it is accepted that pyrethroids interfere with nerve action, the precise M. Elliott, in 'The Future for Insecticides: Needs and Prospects', ed. R. L. Metcalf and

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Cited by 303 publications
(88 citation statements)
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“…1) In 1977, cypermethrin was allowed for turnover as a very active synthetic pyrethrin insecticide, effective in the control of many pest species in agriculture, animal breeding and the household. 2,3) After household treatments, it persists in air and on walls and furniture for about three months. 4) In spite of the low toxicity of pyretroids, persistence of these compounds in mammalian tissues may be dangerous.…”
Section: Introductionmentioning
confidence: 99%
“…1) In 1977, cypermethrin was allowed for turnover as a very active synthetic pyrethrin insecticide, effective in the control of many pest species in agriculture, animal breeding and the household. 2,3) After household treatments, it persists in air and on walls and furniture for about three months. 4) In spite of the low toxicity of pyretroids, persistence of these compounds in mammalian tissues may be dangerous.…”
Section: Introductionmentioning
confidence: 99%
“…1) Pyrethroids are modified derivates of pyrethrins, natural substances obtained from the flowers of Pyrethrum species. 2,3) At present, they have broad-spectrum use in agriculture, domestic and veterinary applications due to their high bioefficacy, enhanced stability, and comparatively low mammalian toxicity. [4][5][6] Pyrethroid insecticides have been divided into types I and II based on behavioral profiles of toxicity.…”
Section: Introductionmentioning
confidence: 99%
“…Although the naturally occurring compounds are quite insecticidal in the natural form, they possess virtually no residual activity in the environment. A broader spectrum of activity against a large array of arthropod species and improved photostability were further developed by synthesizing analogs with aromatic rings and halogens (Elliot et al 1973, Elliot andJanes 1978;Elliot 1980). Indeed, many synthetic bioactive compounds on the market today were designed after naturally occurring compounds.…”
mentioning
confidence: 99%