69) Irak'ta Mayis-Eylul 2003 tarihleri arasinda 62 kez gece ULV calismasi malathion, resmethrin
ve permethrin kullanilarak gerceklestirilmistir.
According to Dan Strickman, a senior program officer in vector control at the Bill and Melinda Gates Foundation, that is what happened with resmethrin
and allethrin, two pyrethroids used in mosquito control.
The type segment is further classified in to bifenthrin, deltamethrin, permethrin, cypermethrin, cyfluthrin, lambda-cyhalothrin and other pyrethroids (fenvalerate, resmethrin
, tetramethrin, allethrin, phenothrin, barthrin, dimethrin, and bioresmethrin).
allethrin, bioallethrin, tetramethrin, phenothrin, resmethrin
, bioresmethrin, kadethrin, permethrin, cypermethrin, fenvalerate, deltamethrin and flumethrin.
1) In Canada, the natural pyrethrins and the synthetic pyrethroids permethrin, allethrin, tetramethrin, phenothrin and resmethrin
are registered for residential use.
Acute toxicity of resmethrin
, malathion and methoprene to larval and juvenile American lobsters (Homarus americanus) and analysis of pesticide levels in surface waters after Scourge, Anvil and Altosid application.
Peter Montague, writing for the Environmental Research Foundation, says there seems to be a strong link between brain cancers and products used to kill fleas and ticks like pyrethrins (natural) and pyrethroids (synthetic pyrethrins: permethrin, tetramethrin, allethrin, resmethrin
, and fenvalerate), and chlorpyrifos (known as Dursban).
Two of the most commonly used insecticides were Scourge (aa) (Bayer CropScience LP, Montvale, NJ) containing 4% resmethrin
and 12% piperonyl butoxide, and Anvil 10+10 ULV (bb) (Clarke Inc, Roselle, Illinois) with 10% 3-Phenoxybenzyl-(1RS, 3RS; 1RS, 3SR)-2,2-dimethyl -3-(2-methylprop-1-enyl) cyclopropanecarboxylate.
A dietary risk assessment of the pyrethroid insecticide resmethrin
associated with its use for West Nile virus mosquito vector control in California.
Pyrethroids, such as permethrin, allethrin, resmethrin
, and tetramethrin, are synthetic insecticides that chemically resemble natural pyrethrins.
While working at the Rothamsted Experimental Station at Harpenden, Hertfordshire, he embarked on a program to develop synthetic analogues of the naturally occurring compounds and developed two, resmethrin
(1962) and bioresmethrin (1967) which were more potent than their natural equivalents and targeted specific insect species, while being harmless to mammals and birds.
THE DEVELOPMENTAL TOXICITY OF RESMETHRIN
TO EMBRYOS OF XENOPUS LAEVIS.