2608-11-9

Basic information

• Product Name: HEXAMETHYLENEAMMONIUM HEXAMETHYLENEDITHIOCARBAMATE
• Synonyms: HEXAMETHYLENEDITHIOCARBAMIC ACID HEXAMETHYLENEAMMONIUM SALT;HEXAMETHYLENEAMMONIUM HEXAMETHYLENEDITHIOCARBAMATE;hexahydro-1h-azepine-1-carbodithioicacicompd.withhexahydro-1h-azepine(;hexahydro-1H-azepine-1-dithiocarboxylic acid, compound with hexahydro-1H-azepine (1:1);Hexamethylenedithiocarbamicacidhexamethyleneimin;N,N-Hexamethylenedithiocarbamicacidhexamethyleneiminiumsalt=HexamethyleneammoniumHexamethylenedithiocarbamate;1H-Azepine-1-carbodithioic acid, hexahydro-, compd. with hexahydro-1H-azepine (1:1);Hexahydro-1H-azepine·hexahydro-1H-azepine-1-dithiocarboxylic acid
• CAS NO: 2608-11-9
• Molecular Formula: C₆H₁₃N*C₇H₁₃NS₂
• Molecular Weight: 274.49
• EINECS: 220-023-1
• Mol File: 2608-11-9.mol
• Article Data: 4

Chemical Properties

• Melting Point: 146.0 to 149.0 °C
• Boiling Point: 242.7°Cat760mmHg
• Flash Point: 100.6°C
• Appearance: /
• Density: g/cm³
• Vapor Pressure: 0.0335mmHg at 25°C
• CAS DataBase Reference: HEXAMETHYLENEAMMONIUM HEXAMETHYLENEDITHIOCARBAMATE(CAS DataBase Reference)
• NIST Chemistry Reference: HEXAMETHYLENEAMMONIUM HEXAMETHYLENEDITHIOCARBAMATE(2608-11-9)
• EPA Substance Registry System: HEXAMETHYLENEAMMONIUM HEXAMETHYLENEDITHIOCARBAMATE(2608-11-9)

Safety Data

• Hazardous Substances Data: 2608-11-9(Hazardous Substances Data)

Usage

General Description

HEXAMETHYLENEAMMONIUM HEXAMETHYLENEDITHIOCARBAMATE is a chemical compound that is commonly used as a fungicide and bactericide in agricultural applications. It is known for its strong antimicrobial properties and is effective against a wide range of plant pathogens. This chemical works by inhibiting the growth and reproduction of fungi and bacteria, making it an important tool in disease control and crop protection. It is often used in combination with other chemicals to provide a comprehensive and integrated approach to pest and disease management in agriculture. Additionally, it has low toxicity to humans and animals, making it a safe and reliable choice for agricultural use.

InChI:InChI=1/C7H13NS2.C6H13N/c9-7(10)8-5-3-1-2-4-6-8;1-2-4-6-7-5-3-1/h1-6H2,(H,9,10);7H,1-6H2

Upstream product

• 111-49-9 hexamethylene imine 
• 75-15-0 carbon disulfide 
• 105-60-2 caprolactam 

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.

Investigation of the reaction of dithiocarbamic acid salts with trimethyl orthoformate and styrene epoxide

The reaction of dithiocarbamic acid salts with trimethyl orthoformate in the presence of BF3·OEt2 was investigated to give 4-(N,N-dialkyldithiocarbamato)-2-dialkyliminio-1,3-dithietane tetrafluoroborates in good yields. Additionally, a one-pot procedure for the synthesis of 2-iminium-1,3-dithiolanes from the BF3·OEt2 catalyzed reaction of dithiocarbamic acid salts with styrene epoxide is described.