Cyfluthrin

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Cyfluthrin
Cyfluthrin.png
Identifiers
CAS number 68359-37-5 YesY
PubChem 50153
ChemSpider 45482 YesY
UNII SCM2QLZ6S0 YesY
KEGG C10982 YesY
ChEMBL CHEMBL2104608
ATC code P03BA01,QP53AC12
Jmol-3D images Image 1
Properties
Molecular formula C22H18Cl2FNO3
Molar mass 434.29 g mol−1
Melting point 60 °C (140 °F; 333 K)
Solubility in water 2 μg/L
Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
 YesY (verify) (what is: YesY/N?)
Infobox references

Cyfluthrin is a synthetic 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, it is highly toxic to fish, invertebrates, and insects, but it is far less toxic to humans.[1] It is generally supplied as a 10-25% liquid concentrate for commercial use and is diluted prior to spraying onto agricultural crops and outbuildings.

Safety[edit]

In rats, the LD50s are 500, 800 (oral), and 600 (skin) mg/kg.[1]

Excessive exposure can cause nausea, headache, muscle weakness, salivation, shortness of breath and seizures. In humans, it is deactivated by enzymatic hydrolysis to several carboxylic acid metabolites, whose urinary excretion half-lives are in a range of 5–7 hours. Worker exposure to the chemical can be monitored by measurement of the urinary metabolites, while severe overdosage may be confirmed by quantification of cyfluthrin in blood or plasma.[2]

Health and safety risks are controlled by right to know laws that exist in most developed countries. Cyfluthrin is regulated in the US by the EPA.[3]

Commercial use[edit]

Cyfluthrin is used in insecticidal sprays such as Temprid (Bayer) which uses a combination of (beta-) cyfluthrin and imidacloprid.

See also[edit]

References[edit]

  1. ^ a b Robert L. Metcalf (2002). "Insect Control". Ullmann’s Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a14_263. 
  2. ^ R. Baselt (2008). Disposition of Toxic Drugs and Chemicals in Man (8th ed.). Foster City, CA: Biomedical Publications. pp. 388–389. 
  3. ^ "Pyrethroids and Pyrethrins". United States Environmental Protection Agency.