3652-33-3

Basic information

• Product Name: 4-AMINO-4H-1,2,4-TRIAZOLE-3,5-DITHIOL
• Synonyms: 4H-1,2,4-Triazole-3,5-dithiol,4-amino- (7CI,8CI);4-Amino-3,5-dimercapto-1,2,4-triazole
• CAS NO: 3652-33-3
• Molecular Formula: C₂H₄N₄S₂
• Molecular Weight: 148.21
• Mol File: 3652-33-3.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 224.2 °C at 760 mmHg
• Flash Point: 89.4 °C
• Appearance: /
• Density: 1.85 g/cm³
• Vapor Pressure: 0.0926mmHg at 25°C
• Refractive Index: 1.94
• CAS DataBase Reference: 4-AMINO-4H-1,2,4-TRIAZOLE-3,5-DITHIOL(CAS DataBase Reference)
• NIST Chemistry Reference: 4-AMINO-4H-1,2,4-TRIAZOLE-3,5-DITHIOL(3652-33-3)
• EPA Substance Registry System: 4-AMINO-4H-1,2,4-TRIAZOLE-3,5-DITHIOL(3652-33-3)

Safety Data

• Hazardous Substances Data: 3652-33-3(Hazardous Substances Data)

Usage

General Description

4-Amino-4H-1,2,4-triazole-3,5-dithiol is a chemical compound with the molecular formula C2H4N4S2. It is a heterocyclic compound that contains both an amino group and dithiol group, and it is commonly used as a corrosion inhibitor and as a ligand in coordination chemistry. The compound has a range of applications in industrial processes, particularly in the control of metal corrosion in various environments. It is also used in the synthesis of other organic compounds and in the production of chemical reagents. Additionally, it has been studied for its potential pharmaceutical properties, such as antioxidant and anti-inflammatory effects. Overall, 4-Amino-4H-1,2,4-triazole-3,5-dithiol has diverse uses in various industries due to its unique chemical properties and potential biological activities.

InChI:InChI=1/C2H4N4S2/c3-6-1(7)4-5-2(6)8/h3H2,(H,4,7)(H,5,8)

Upstream product

• 142-46-1 bithiourea 
• 854654-87-8 N,N'-bis-isothiocyanato-thiourea 
• 20953-16-6 1-thiocarbamylthiocarbohydrazide 
• 253266-93-2 4-thioxo-3,5-dithia-heptanedioic acid dimethyl ester 
• 2231-57-4 Thiocarbohydrazide 
• 75-15-0 carbon disulfide 

Downstream Products

• 952417-84-4 6-(4-chlorophenyl)-2H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole-3-thione 

Relevant articles and documents

Synthesis and characterization of manganese, copper and zinc complexes derived from Schiff - base ligand

A Schiff base has been prepared by the condensation of 4- amino -3,5-dimercapto, 1,2,4-triazole with 2,4-diaminobenzaldehyde. The ligand has been used for complexation with Mn(II), Cu(II) and Zn(II) metal ions. The complexes have been characterized by their elemental analysis, molar conductivity, magnetic susceptibility, IR spectra and electronic spectra. The very low value of molar conductivity of complexes shows their non-electrolytic nature. The comparison of IR spectra of complexes with that of free ligand reveals that the ligand is coordinated through azomethine nitrogen and deprotonated thiol sulphur forming five membered heterochelates. The magnetic moment values and electronic spectral bands clearly indicate the octahedral geometry around metal ions in complexes.

Regioselective synthesis of 3-sulfanyl-5H-naphtho[2,3-e][1,3,4] triazino[3,4-b][1,3,4]thiadiazole-6,11-dione and its derivatives

Regioselective synthesis of novel 3-sulfanyl-5H-naphtho[2,3-e][1,3,4] triazino[3,4-b][1,3,4]thiadiazole-6,11-dione (3) has been achieved by the condensation of 2-bromo-3-hydroxynaphthalene-1,4-dione (1) with 4-amino-4H-1,2,4-triazole-3,5-dithiol (2) in DM