Dimethylammonium Dimethyldithiocarbamate

CAS : 598-64-1

Ref. 3D-AAA59864

Informations sur le produit

• Nom: Dimethylammonium Dimethyldithiocarbamate
• Synonymes: Carbamic acid, dimethyldithio-, compd. with Me2NH, Carbamic acid, dimethyldithio-, compd. with dimethylamine (1:1), Carbamodithioic acid, N,N-dimethyl-, compd. with N-methylmethanamine (1:1), Carbamodithioic acid, dimethyl-, compd. with N-methylmethanamine (1:1), Dimethylamine, dimethyldithiocarbamate, Dimethylcarbamodithioic Acid, Dimethyldithiocarbamic acid compd. with dimethylamine (1:1), Dimethyldithiocarbamic acid diethylammonium salt, Dimethyldithiocarbamic acid dimethylamine salt, Dimethyldithiocarbamic acid dimethylammonium salt, Methanamine, N-methyl-, dimethylcarbamodithioate, N,N-Dimethylammonium N,N-dimethyldithiocarbamate, N,N-Dimethyldithiocarbamic acid dimethylammonium salt, N-methylmethanaminium dimethylcarbamodithioate, NSC 100885, NSC 6205

Description

Dimethylammonium dimethyldithiocarbamate is a nucleophilic aliphatic hydrocarbon that has been used as a fungicide. It inhibits the enzyme tyrosinase, which is involved in melanin synthesis. Dimethylammonium dimethyldithiocarbamate reacts with the phenol group of tyrosine to form an intermediate that undergoes a nucleophilic attack by the thiol group of carbon disulphide, leading to the formation of an adduct. The reaction mechanism for this process is shown below:

CH3C6H4OH + CH3N+S-R’ + CS2 → CH3N+S-R’CH2C6H4OCH3

This reaction results in the formation of the adduct, CH3N+S-R’CH2C6H4OCH3.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 166.3 g/mol
• Formule: C₅H₁₄N₂S₂
• Degré de pureté: Min. 95%