Description

3,4-Diamino-1,2,4-triazole (CAS No. 38104-45-9) is a high-purity heterocyclic organic compound with the molecular formula C₂H₅N₅. This versatile triazole derivative is widely utilized in pharmaceutical research, agrochemical synthesis, and material science due to its unique reactivity and structural properties. The compound features two amino groups attached to a 1,2,4-triazole ring, making it a valuable building block for the development of novel bioactive molecules, coordination complexes, and advanced polymers. Our product is rigorously tested to ensure >98% purity (HPLC) and is supplied as a stable, off-white to light yellow crystalline powder. Proper storage at 2-8°C in a tightly sealed container is recommended to maintain optimal stability. Hazard information and handling protocols are provided in accordance with GHS standards.

Properties

• CAS Number: 38104-45-9
• Complexity: 63.1
• IUPAC Name: 1,2,4-triazole-3,4-diamine
• InChI: InChI=1S/C2H5N5/c3-2-6-5-1-7(2)4/h1H,4H2,(H2,3,6)
• InChI Key: VVICLQXCPOEFTM-UHFFFAOYSA-N
• Exact Mass: 99.05449518
• Molecular Formula: C2H5N5
• Molecular Weight: 99.10
• SMILES: C1=NN=C(N1N)N
• Topological: 82.8
• Monoisotopic Mass: 99.05449518
• Synonyms: 3,4-Diamino-1,2,4-triazole, 3,4-Diamino-1,2,4(4H)-triazole, vviclqxcpoeftm-uhfffaoysa-n, 4H-1,2,4-Triazole-3,4-diamine, 38104-45-9, 1,2,4-triazole-3,4-diamine, 5-Imino-1,5-dihydro-4H-1,2,4-triazol-4-amine, SCHEMBL971367, DTXSID60959060, ALBB-030352, 3,4-diamino-4H-1,2,4-triazole, STL436398, AKOS001487792, 4H-1,2,4-Triazole-3,4-diamine #, DB-069638, CS-0271106, EN300-143890, F0915-7974

3,4-Diamino-1,2,4-triazole serves as a key intermediate in the synthesis of nitrogen-rich heterocyclic compounds for pharmaceutical applications. Researchers employ this compound in the development of potential anticancer and antimicrobial agents due to its ability to form hydrogen-bonded networks. In materials science, it acts as a precursor for high-energy materials and coordination polymers with interesting luminescent properties. The compound’s bifunctional amino groups make it particularly valuable for creating Schiff base ligands in catalytic systems.

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