Cyfluthrin

CAS: 68359-37-5

Ref. 3D-FC39572

Product Information

• Name: Cyfluthrin
• Synonyms: 3-(2,2-Dichlorovinyl)-2,2-Dimethylcyclopropanecarboxylate De Α-Cyano-4-Fluoro-3-Phenoxybenzyle, 3-(2,2-Diclorovinil)-2,2-Dimetilciclopropanocarboxilato De Α-Ciano-3-Fenoxi-4-Fluorobencilo, Adalticid Solfak, BAY-Vl 1704, Bay-Fcr 1272, Baythroid, Baythroid XL, Beta-Baythroid, Beta-cyfluthrin, Bulldock, Bulldock 125SC, CYANO(4-FLUORO-3-PHENOXYPHENYL)METHYL 3-(2,2- DICHLOROETHENYL)-2,2-DIMETHYLCYCLOPROPANECARBOXylic acid, Cyfloxylate, Cyfoxylate, Eulan SP, Fcr 1272, Fcr 4545, Optem PT 600, Preventol HS 12, Renounce, Responsar, Solfac, Solfac 050EW, Syfrutrin, Tempo 2, Tempo 20WP, Tempo Ultra, Tombstone, Tombstone Helios, Α-Cyano-4-Fluoro-3-Phenoxybenzyl 3-(2,2-Dichlorovinyl)-2,2-Dimethylcyclopropanecarboxylate, α-Cyan-4-fluor-3-phenoxybenzyl-3-(2,2-dichlorvinyl)-2,2-dimethylcyclopropancarboxylat, α-Cyano-3-phenoxy-4-fluorobenzyl 2,2-dimethyl-3-(2,2-dichlorovinyl)cyclopropanecarboxylate, α-Cyano-4-fluoro-3-phenoxybenzyl (1R,S)-cis,trans-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropancarboxylate

Description

Cyfluthrin is a pyrethroid insecticide that inhibits the activity of various enzymes, including those involved in the synthesis of proteins and nucleic acids. Cyfluthrin has been shown to synergize with other insecticides, such as carbamate or organophosphate compounds. It also has a sublethal effect on insects at low doses. Cyfluthrin is not genotoxic, but can cause biochemical and metabolic disorders in vertebrates. The toxicity of cyfluthrin can be determined by measuring its fluorescence spectrum using fluorescence spectrometry. The absorption spectrum and fluorescence emission spectra are then used to determine the chemical structure of cyfluthrin. Sodium citrate is used as an analytical reagent for cyfluthrin because it has been shown to increase the solubility of this compound in water.

• Brand: Biosynth

Chemical properties

• Molecular weight: 434.29 g/mol
• Formula: C₂₂H₁₈Cl₂FNO₃
• Purity: Min. 95%
• SMILES: CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)c1ccc(F)c(Oc2ccccc2)c1