2391-78-8

Basic information

• Product Name: DIETHYLDITHIOCARBAMIC ACID DIETHYL-
• Synonyms: triethylammonium diethyldithiocarbamate;diethylcarbamodithioic acid;DIETHYLDITHIOCARBAMIC ACID DIETHYL-
• CAS NO: 2391-78-8
• Molecular Formula: C₅H₁₁NS₂*C₆H₁₅N
• Molecular Weight: 250.46754
• EINECS: 219-240-4
• Mol File: 2391-78-8.mol
• Article Data: 8

Chemical Properties

• Melting Point: 82-84 °C(lit.)
• Boiling Point: 176.4°Cat760mmHg
• Flash Point: 60.5°C
• Appearance: /
• Density: g/cm³
• Vapor Pressure: 1.1mmHg at 25°C
• Sensitive: Hygroscopic
• CAS DataBase Reference: DIETHYLDITHIOCARBAMIC ACID DIETHYL-(CAS DataBase Reference)
• NIST Chemistry Reference: DIETHYLDITHIOCARBAMIC ACID DIETHYL-(2391-78-8)
• EPA Substance Registry System: DIETHYLDITHIOCARBAMIC ACID DIETHYL-(2391-78-8)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-37/39
• WGK Germany: 3
• RTECS: EZ5425000
• Hazardous Substances Data: 2391-78-8(Hazardous Substances Data)

Usage

General Description

Diethyldithiocarbamic Acid Diethyl- (DEDTCA) is a chemical compound known for its widespread use in the rubber industry as a vulcanization accelerator. Chemically, it is an ester that belongs to the group of dithiocarbamic acids and dithiocarbamates. It is also known by names such as Diethyldithiocarbamic acid diethyl ester, Aethyl-Dithiokohlensaureaethylester, and UNII-DJW1K3TVG8, among others. Highly flammable and corrosive, DEDTCA can pose significant hazards. Therefore, users should handle this chemical very carefully, making sure to use the necessary protective equipment to prevent skin or eye contact. Furthermore, its environmental impact and danger to aquatic life should also be considered. It is recommended that users always refer to the Material Safety Data Sheet (MSDS) for further information.

InChI:InChI=1/C6H15N.C5H11NS2/c1-4-7(5-2)6-3;1-3-6(4-2)5(7)8/h4-6H2,1-3H3;3-4H2,1-2H3,(H,7,8)

Upstream product

• 75-15-0 carbon disulfide 
• 109-89-7 diethylamine 
• 121-44-8 triethylamine 

Downstream Products

• 95-05-6 tetraethylthiuram monosulfide 
• 19200-30-7 S-(β-D-glucopyranosyl) N,N-diethyldithiocarbamate 
• 686-07-7 methyl diethyldithiocarbamate 
• 192883-67-3 (4R,5S,6S)-3-Diethylthiocarbamoylsulfanyl-6-((R)-1-hydroxy-ethyl)-4-methyl-7-oxo-1-aza-bicyclo[3.2.0]hept-2-ene-2-carboxylic acid 4-nitro-benzyl ester 
• 97-77-8 disulfiram 

Relevant articles and documents

A facile synthesis, crystallographic, spectral, thermal, and electrochemical investigations of neutral [Cu2(Et2dtc) 4] dimer

A neutral dimeric complex [Cu2(Et2dtc)4] (dtc = dithiocarbamate) (1) was synthesized in single step under mild conditions. Structure of 1 has been studied using single-crystal XRD to gauge the influence of CH3 and CH2 groups of coordinated dithiocarbamate ligands on the association of the molecules in solid state. Evidently 1 features the ability of these groups to form intermolecular (sp 3)CHΠ(chelate ring) and (sp3)CHS stacking interactions leading to fascinating 3D infinite network. Complex has been completely characterized by spectrophotometric methods, optical behavior, and thermal and cyclic voltammetry studies. Cyclic voltammetric study confirmed the binding affinity of 1 toward H2PO-4. Supplemental materials are available for this article. Go to the publisher's online edition of Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry to view the supplemental file. Copyright Taylor & Francis Group, LLC.

Protection-free synthesis of glycosyl dithiocarbamates in aqueous media by using 2-chloroimidazolinium reagent

Glycosyl dithiocarbamates (GDTCs) have been synthesized directly from the corresponding unprotected sugars and dithiocarbamate salts in good yields by using 2-chloro-1,3-dimethylimidazolinium chloride (DMC) as condensing agent in aqueous media. The three-component one-pot synthesis of GDTCs starting from unprotected sugars, carbon disulfide, and secondary amines has also been successfully demonstrated. This is the first report on the direct synthesis of GDTCs from unprotected sugars without using any protecting groups.

Bis(dialkylaminethiocarbonyl)disulfides as potent and selective monoglyceride lipase inhibitors

Monoglyceride lipase (MGL) inhibition may offer an approach in treating diseases in which higher 2-arachidonoyglycerol activity would be beneficial. We report here the synthesis and pharmacological evaluation of bis(dialkylaminethiocarbonyl)disulfide derivatives as irreversible MGL inhibitors. Inhibition occurs through interactions with MGL C208 and C242 residues, and these derivatives exhibit high inhibition selectivity over fatty acid amide hydrolase, another endocannabinoid-hydrolyzing enzyme. 2009 American Chemical Society.