Pyridaben

CAS: 96489-71-3

Ref. 3D-FP27294

Informação sobre produto

• Nome: Pyridaben
• Sinónimos: 4-Chloro-2-(1,1-dimethylethyl)-5-[[[4-(1,1-dimethylethyl)phenyl]methyl]thio]-3(2H)-pyridazinone2-tert-Butyl-5-(4-tert-butylbenzylth io)-4-chloropyridazin-3(2H)-oneBAS 300, 2-tert-butyl-5-(4-tert-butylbenzylthio)-4-chloropyridazin-3(2H)-one, 2-tert-butyl-5-(4-tert-butylbenzylthio)-chloropyridazin-3(2H)-3-one, 2-tert-butyl-5-[(4-tert-butylbenzyl)sulfanyl]-4-chloropyridazin-3(2H)-one, 3(2H)-Pyridazinone, 4-chloro-2-(1,1-dimethylethyl)-5-[[[4-(1,1-dimethylethyl)phenyl]methyl]thio]-, 4-Chloro-2-(1,1-dimethylethyl)-5-(((4-(1,1-dimethylethyl)phenyl)methyl)thio)-3(2H)-pyridazinone, Altair Miticide, Bas 300, Damanjing, Damanlin, Damantong, Gwn 1715, Nc 129, Nci 129, Nexter, Pyramite, Pyridazinone, Sanmite, Sumantong

Descrição

Pyridaben is a pesticide that is classified as an insecticide. It has been shown to have a synergic effect with monoclonal antibodies which are used to detect and identify the presence of specific proteins in vitro. Pyridaben's high resistance to degradation by enzymes such as esterases, glucuronidases, and lipases makes it suitable for use in sample preparation. This compound also has been shown to inhibit cell signaling pathways, including those involved in the production of fatty acids and the metabolism of drugs by cytochrome P450 enzymes. Pyridaben has not been found to be toxic when administered orally or topically in animal studies, but some toxicity may be seen at higher doses due to its ability to inhibit fatty acid synthesis. The detection sensitivity of pyridaben can be increased by gas chromatography-mass spectroscopy (GC-MS) or liquid chromatography-tandem mass spectroscopy (LC-MS/MS).

• Marca: Biosynth

Propriedades químicas

• Peso molecular: 364.93 g/mol
• Fórmula: C₁₉H₂₅ClN₂OS
• Pureza: Min. 95%
• InChI: InChI=1S/C19H25ClN2OS/c1-18(2,3)14-9-7-13(8-10-14)12-24-15-11-21-22(19(4,5)6)17(23)16(15)20/h7-11H,12H2,1-6H3
• Chave InChI: InChIKey=DWFZBUWUXWZWKD-UHFFFAOYSA-N
• SMILES: CC(C)(C)c1ccc(CSc2cnn(C(C)(C)C)c(=O)c2Cl)cc1