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Cyfluthrin is a pyrethroid insecticide and common household pesticide. It is a complex organic compound and the commercial product is sold as a mixture of isomers . Like most pyrethroids (MoA 3a), [ 1 ] it is highly toxic to fish and invertebrates , but it is far less toxic to humans. [ 2 ]
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)
Poisoning can occur if pyrethroid containing flea treatment products, which are intended for dogs, are used on cats. The livers of cats detoxify pyrethroids via glucuronidation more poorly than dogs, which is the cause of this difference. [15] Aside from cats, pyrethroids are typically not toxic to mammals or birds. [16]
Pyrethrins and Pyrethroids Fact Sheet - National Pesticide Information Center; Pyrethrins and pyrethroids on the EXTOXNET; Pyrethrin and Permethrin Toxicity in Dogs and Cats; Wagner, S. L. (2000). "Fatal asthma in a child after use of an animal shampoo containing pyrethrin". The Western Journal of Medicine. 173 (2): 86– 7. doi:10.1136/ewjm ...
Effects were also observed in the liver (rats, mice, and dogs), heart (dogs), and thyroid gland (rats). Some effects were also seen in the kidney (mice and rats). However, neurotoxicity was the most sensitive endpoint in the toxicology database, and other effects were generally seen in the presence of neurotoxicity and/or at higher doses.
In fact, even dogs' sleep patterns are considered to be similar to that of humans, with a Live Science report noting that the cycle typically includes "stages of wakefulness, rapid-eye-movement ...
Dinotefuran is an insecticide of the neonicotinoid class developed by Mitsui Chemicals for control of insect pests such as aphids, whiteflies, thrips, leafhoppers, leafminers, sawflies, mole cricket, white grubs, lacebugs, billbugs, beetles, mealybugs, and cockroaches on leafy vegetables, in residential and commercial buildings, and for professional turf management. [2]
Carbaryl is often inexpensively produced by direct reaction of methyl isocyanate with 1-naphthol. [5]C 10 H 7 OH + CH 3 NCO → C 10 H 7 OC(O)NHCH 3. Alternatively, 1-naphthol can be treated with excess phosgene to produce 1-naphthyl chloroformate, which is then converted to carbaryl by reaction with methylamine. [5]