82882-12-0

Basic information

• Product Name: 4H-1,2,4-triazole-3,4,5-triamine
• CAS NO: 82882-12-0
• Molecular Formula: C₂H₆N₆
• Molecular Weight: 114.1092
• Mol File: 82882-12-0.mol

Chemical Properties

• Boiling Point: 505.2°C at 760 mmHg
• Flash Point: 259.3°C
• Density: 2.45g/cm³
• Vapor Pressure: 2.49E-10mmHg at 25°C
• Refractive Index: 2.122
• CAS DataBase Reference: 4H-1,2,4-triazole-3,4,5-triamine(CAS DataBase Reference)
• NIST Chemistry Reference: 4H-1,2,4-triazole-3,4,5-triamine(82882-12-0)
• EPA Substance Registry System: 4H-1,2,4-triazole-3,4,5-triamine(82882-12-0)

Safety Data

• Hazardous Substances Data: 82882-12-0(Hazardous Substances Data)

Upstream product

• 35600-34-1 S-methyl isothiosemicarbazide hydroiodide 
• 1467-79-4 NCNMe₂ 
• 79-19-6 thiosemicarbazide 

Relevant articles and documents

1,3,4,5-Tetraamino-1,2,4-triazolium Cation: An Energetic Moiety

The amination of 3,4,5-triamino-1,2,4-triazole with O-tosylhydroxylamine yielded the nitrogen-rich 1,3,4,5-tetraamino-1,2,4-triazolium cation as its tosylate salt. Subsequent metathesis reactions produced energetic salts with various energetic anions, inc

Facile entry into the 3H,9H-bis[1,2,4]triazolo-[1,5-a:5′,1′-d][1,3,5]triazinium (5/6/5 tricyclic NNN) system

A facile, one-pot reaction between 3,4,5-triamino-1,2,4-triazole (guanazine) and cyanogen bromide provides a new high-nitrogen example of the 3H,9H-bis[1,2,4]triazolo[1,5-a:5′,1′-d][1,3,5]triazinium system, the 2,3,5,6-tetraamino-9-imino derivative (3) as a quaternary bromide salt.

Synthesis of 3,4,5-Triamino-4H-1,2,4-triazole (Guanazine) and its 4-Arylideneamino Derivatives

Synthetic methods for the preparation of 3,4,5-triamino-4H-1,2,4-triazole (guanazine) and its 4-arylideneamino derivatives are described.Guanazine, which can be used as an appropriate starting material in the syntheses of different bicyclic heterocycles, was readily obtained from thiosemicarbazide by treatment with mercuric oxide.Guanazine was also obtained from the S-methylisothio ether of thiosemicarbazide via a pyrolytic reaction.The 4-arylideneamino derivatives were either prepared by treatment of guanazine with an appropriate aromatic aldehyde, or by methods in which 1-arylidene-5-thiocarbamoyldiaminoguanidines are used as starting materials.