598-64-1

Basic information

• Product Name: DIMETHYLDITHIOCARBAMIC ACID DIMETHYLAMMONIUM SALT
• Synonyms: dimethyldithiocarbamicaciddimethylaminesalt;dimethyldithio-carbamicacidimethylaminesalt(1:1);DIMETHYLAMMONIUM DIMETHYLDITHIOCARBAMATE;DIMETHYLDITHIOCARBAMIC ACID DIMETHYLAMMONIUM SALT;Dimethyldithiocarbamic acid diethylammonium salt;Dimethylamine dimethyldithiocarbamate;Carbamodithioic acid, dimethyl-, compd. with N-methylmethanamine (1:1);DIMETHYLDITHIOCARBAMICACIDDIMETHYLAMMLONIUMSALT
• CAS NO: 598-64-1
• Molecular Formula: C₂H₈N*C₃H₆NS₂
• Molecular Weight: 166.31
• EINECS: 209-945-5
• Mol File: 598-64-1.mol
• Article Data: 6

Chemical Properties

• Melting Point: 132°C
• Boiling Point: 129.4°Cat760mmHg
• Flash Point: 32°C
• Appearance: /
• Density: 1.117 (estimate)
• Vapor Pressure: 10.2mmHg at 25°C
• Refractive Index: 1.5300 (estimate)
• CAS DataBase Reference: DIMETHYLDITHIOCARBAMIC ACID DIMETHYLAMMONIUM SALT(CAS DataBase Reference)
• NIST Chemistry Reference: DIMETHYLDITHIOCARBAMIC ACID DIMETHYLAMMONIUM SALT(598-64-1)
• EPA Substance Registry System: DIMETHYLDITHIOCARBAMIC ACID DIMETHYLAMMONIUM SALT(598-64-1)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• RTECS: FA0250000
• Hazardous Substances Data: 598-64-1(Hazardous Substances Data)

Usage

General Description

DIMETHYLDITHIOCARBAMIC ACID DIMETHYLAMMONIUM SALT is a chemical compound with the formula (CH3)2NCS2–CH3. It is commonly used as a fungicide and bactericide in agricultural and industrial applications. The compound works by inhibiting the growth and reproduction of microorganisms, making it effective in controlling fungal and bacterial infections in crops and other plants. It is also employed as a biocide in industrial water treatment and in the preservation of wood and other materials. However, it is important to handle this compound with care, as it can be toxic if ingested or absorbed through the skin, and can be harmful to aquatic organisms if it enters waterways.

InChI:InChI=1/C3H7NS2.C2H7N/c1-4(2)3(5)6;1-3-2/h1-2H3,(H,5,6);3H,1-2H3

Upstream product

• 75-15-0 carbon disulfide 
• 124-40-3 dimethyl amine 
• 137-26-8 Thiram 

Downstream Products

• 19204-12-7 1-(dimethylaminothiocarbonylthio)propan-2-one 
• 76539-77-0 6-(3,4-Dimethoxy-phenyl)-4-dimethylamino-5,6-dihydro-thiopyran-2-thione 
• 76539-85-0 4-Dimethylamino-5-methyl-6-phenyl-5,6-dihydro-thiopyran-2-thione 
• 180746-53-6 Dimethyl-dithiocarbamic acid 2-biphenyl-4-yl-2-oxo-1-phenyl-ethyl ester 
• 180746-51-4 Dimethyl-dithiocarbamic acid 2-naphthalen-1-yl-2-oxo-1-phenyl-ethyl ester 
• 23839-34-1 2-oxo-2-phenylethyl dimethylcarbamodithioate 
• 137-26-8 Thiram 
• 5310-10-1 N-methylthioacetamide 
• 1803-14-1 (C₆H₅)2SbS₂CN(CH₃)2 
• 42139-17-3 Benzoylethylene Dimethyldithiocarbamate 
• 42139-08-2 2-nitro-1-phenyltrimethylene dimethyldithiocarbamate 
• 58350-72-4 3-[2-(dimethyl-thiocarbamoylsulfanyl)-ethyl]-2-methylsulfanyl-4-phenyl-thiazolium; iodide 
• 98121-86-9 2-(4-bromophenyl)-2-oxoethyl dimethylcarbamodithioate 
• 51-82-1 dimethyl-dithiocarbamic acid dimethylaminomethyl ester 

Relevant articles and documents

Cu-mediated one-pot three-component synthesis of 3-N-substituted 1,4,2-benzodithiazine 1,1-dioxide derivatives

A novel and efficient copper-catalyzed one-pot procedure for the synthesis of 3-N-substituted 1,4,2-benzodithiazine 1,1-dioxide derivatives from 2-halobenzenesulfonamides, amines and CS2 is described. The reaction proceeds through Ullmann-type S-arylation, intramolecular addition of NH2 with C[dbnd]S and dehydrosulfide, which provides a new and useful strategy for construction of cyclic aromatic sulfonamides.

Utilization of carbon disulfide as a powerful building block for the synthesis of 2-aminobenzoxazoles

This protocol describes a novel, mild and convenient route to afford 2-aminobenzoxazoles in high yields, and represents a significant advance towards an environmentally friendly strategy. Aliphatic amines are made to react with carbon disulfide to provide intermediate dithiocarbamates (DTC), which in the presence of 2-aminophenol, subsequently undergo successive intermolecular nucleophilic attack and desulfurization to produce 2-aminobenzoxazoles within 3 h.

Thiocarbamoylation of amine-containing compounds 4. Reactions of tetramethylthiuram disulfide with aliphatic amines

Thiocarbamoylation of primary and secondary aliphatic amines with tetramethylthiuram disulfide in various solvents at different temperatures was studied. At 110 °C, the reactions with primary amines afforded mixed N,N-dimethyl-N′-alkyl(cycloalkyl)thiourea