Myclobutanil

CAS : 88671-89-0

Ref. 3D-FM159281

Informations sur le produit

• Nom: Myclobutanil
• Synonymes: (.+-.)-Myclobutanil, 2-p-Chlorophenyl-2-(1H-1,2,4-triazol-1-ylmethyl)hexanenitrile, Deccotanil, Eagle, Fungiben, Hoe 39304F, Laredo 25EC, Laredo 25EW, Myclobutanil [α-Butyl-α-(4-chlorophenyl)-1.ITAL.H.-1,2,4-triazole-1-propanenitrile], Mycloss Xtra, Nova, Nova (pesticide), Nova 40W, Nova W, Nu-Flow M, Rally, Rally 40 WP, Rally 40WSP, Rh 3866, Spectracide Immunox Multi-Purpose Fungicide, Systhane, Systhane 12E, Systhane 20EW, Systhane 40 W, Systhane 40W, Systhane 6 Flo, α-Butyl-α-(4-chlorophenyl)-1H-1,2,4-triazole-1-propanenitrile, 2-(4-chlorophenyl)-2-(1H-1,2,4-triazol-1-ylmethyl)hexanenitrile, 1H-1,2,4-Triazole-1-propanenitrile, α-butyl-α-(4-chlorophenyl)-, 1-(4-Chlorophenyl)-2-(hydro-1,2,4-triazole-1-methyl)-amylcyanide, alpha-Butyl-alpha-(4-chlorophenyl)-1H-1,2,4-triazole-1-propanenitrile

Description

Myclobutanil is a fungicide that inhibits the growth of fungi by inhibiting the synthesis of essential cell components, such as proteins and nucleic acids. Myclobutanil is absorbed through the skin or lungs, and is metabolized in the liver to form an inactive metabolite. The hydrogen bonding interactions between myclobutanil and enzymes are reversible, which allows for detoxification. It has been shown that myclobutanil affects the activity of detoxification enzymes in rat liver microsomes. Myclobutanil also inhibits polymerase chain reactions (PCRs) in model systems.
The analytical method used to measure myclobutanil concentrations in soil or water samples relies on gas chromatography with flame ionization detection (GC-FID). This technique measures myclobutanil concentrations by detecting it as a peak on a chromatogram. The sample preparation for this method involves extracting myclobutanil from soil or water samples with dichlor

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 288.78 g/mol
• Formule: C₁₅H₁₇ClN₄
• Degré de pureté: Min. 95%
• Couleur/Forme: Powder
• SMILES: CCCCC(C#N)(Cn1cncn1)c1ccc(Cl)cc1