Ad
related to: fipronil pesticide fact sheet printable pdf free
Search results
Results From The WOW.Com Content Network
Fipronil is a broad-spectrum insecticide that belongs to the phenylpyrazole insecticide class. [3] Fipronil disrupts the insect central nervous system by blocking the ligand-gated ion channel of the GABA A receptor (IRAC group 2B) and glutamate-gated chloride (GluCl) channels. This causes hyperexcitation of contaminated insects' nerves and muscles.
Chemical structure of fipronil, a common phenylpyrazole insecticide. Phenylpyrazole insecticides are a class of chemically-related broad-spectrum insecticides. [1] The chemical structures of these insecticides are characterized by a central pyrazole ring with a phenyl group attached to one of the nitrogen atoms of the pyrazole.
An active ingredient (AI) is the substance in a pesticide that is biologically active. To control colonies the roach bait may contain the active ingredients Fipronil.05% or Hydramethylnon 2%. Also there are indoxacarb versions. Residual pesticides turn the infected cockroaches and their fluids into bait themselves.
Chlorfenapyr was developed by American Cyanamid from the natural product dioxapyrrolomycin, which was isolated from Streptomyces fumanus. [2]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. [3]
Illinois Department of Public Health Pyrethroid Insecticides Fact Sheet. Retrieved October 26, 2005. World Health Organization (WHO) d-Allethrin. Retrieved October 26, 2005. Jim E. Riviere & Mark G. Papich Eds.: Veterinary Pharmacology and Therapeutics. Iowa State University Press, 2009. ISBN 9780813820613. (p. 1194)
According to its materials safety data sheet (MSDS), methoprene is a material that may be irritating to the mucous membranes and upper respiratory tract; may be harmful by inhalation, ingestion, or skin absorption; may cause eye, skin, or respiratory system irritation; and is very toxic to aquatic life. [5]
Chemical structure of Allethrin isomers Chemical structure of Permethrin isomers. A pyrethroid is an organic compound similar to the natural pyrethrins, which are produced by the flowers of pyrethrums (Chrysanthemum cinerariaefolium and C. coccineum).
Because the use of fipronil is illegal in the production of food for human consumption in Europe, a criminal investigation was initiated. [4] [9]Early investigation led to two companies: ChickFriend, a provider of pest control services in the Netherlands, suspected of knowingly using and selling DEGA-16 mixed with fipronil to hundreds of chicken farmers, and Poultry Vision in Belgium, accused ...