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Encyclopedia

Diminazene

Base Information Edit
  • Chemical Name:Diminazene
  • CAS No.:536-71-0
  • Molecular Formula:C14H15N7
  • Molecular Weight:281.32
  • Hs Code.:2927000090
  • European Community (EC) Number:208-644-6
  • UNII:Y5G36EEA5Z
  • DSSTox Substance ID:DTXSID7043792
  • Nikkaji Number:J6.355J
  • Wikipedia:Diminazene
  • Wikidata:Q410958
  • NCI Thesaurus Code:C65409
  • Pharos Ligand ID:CR56XC951T8Y
  • Metabolomics Workbench ID:148110
  • ChEMBL ID:CHEMBL35241
  • Mol file:536-71-0.mol
Diminazene

Synonyms:4,4' Diazoaminobenzamidine;4,4'-Diazoaminobenzamidine;Diminazene

Suppliers and Price of Diminazene
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Crysdot
  • 4,4'-(Triaz-1-ene-1,3-diyl)dibenzimidamide 97%
  • 100g
  • $ 701.00
  • American Custom Chemicals Corporation
  • DIMINAZENE 95.00%
  • 5G
  • $ 210.00
Total 107 raw suppliers
Chemical Property of Diminazene Edit
Chemical Property:
  • Appearance/Colour:yellow to orange powder 
  • Vapor Pressure:9.21E-09mmHg at 25°C 
  • Melting Point:212 - 214oC 
  • Refractive Index:1.707 
  • Boiling Point:463.3 °C at 760 mmHg 
  • PKA:12.11±0.50(Predicted) 
  • Flash Point:234 °C 
  • PSA:136.49000 
  • Density:1.39 g/cm3 
  • LogP:4.03860 
  • XLogP3:1.9
  • Hydrogen Bond Donor Count:5
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:5
  • Exact Mass:281.13889351
  • Heavy Atom Count:21
  • Complexity:390
Purity/Quality:

99% *data from raw suppliers

4,4'-(Triaz-1-ene-1,3-diyl)dibenzimidamide 97% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC(=CC=C1C(=N)N)NN=NC2=CC=C(C=C2)C(=N)N
Technology Process of Diminazene

There total 3 articles about Diminazene which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With cytochrome b5; mitochondrial amidoxime reducing component 1; NADH cytochrome b5 reductase; NADH; at 37 ℃; pH=6; aq. phosphate buffer; Enzymatic reaction;
DOI:10.1021/jm8010417
Guidance literature:
With cytochrome b5; mitochondrial amidoxime reducing component 1; NADH cytochrome b5 reductase; NADH; at 37 ℃; pH=6; aq. phosphate buffer; Enzymatic reaction;
DOI:10.1021/jm8010417
Guidance literature:
With hydrogenchloride; sodium nitrite;
Refernces Edit
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