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Benzenamine, 4-[(2,4-dimethylphenyl)azo]-2,5-dimethyl-

Base Information Edit
  • Chemical Name:Benzenamine, 4-[(2,4-dimethylphenyl)azo]-2,5-dimethyl-
  • CAS No.:136-21-0
  • Molecular Formula:C16H19 N3
  • Molecular Weight:253.347
  • Hs Code.:2927000090
  • European Community (EC) Number:205-231-2
  • DSSTox Substance ID:DTXSID0059663
  • Nikkaji Number:J30.258I
  • Mol file:136-21-0.mol
Benzenamine, 4-[(2,4-dimethylphenyl)azo]-2,5-dimethyl-

Synonyms:136-21-0;4-(2,4-Xylylazo)-2,5-xylidine;Benzenamine, 4-[(2,4-dimethylphenyl)azo]-2,5-dimethyl-;EINECS 205-231-2;4-[(2,4-dimethylphenyl)diazenyl]-2,5-dimethylaniline;Benzenamine, 4-((2,4-dimethylphenyl)azo)-2,5-dimethyl-;Benzenamine, 4-(2-(2,4-dimethylphenyl)diazenyl)-2,5-dimethyl-;DTXSID0059663;4-(2,4-Xylylazo)-2,5-dimethylbenzenamine

Suppliers and Price of Benzenamine, 4-[(2,4-dimethylphenyl)azo]-2,5-dimethyl-
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
Total 6 raw suppliers
Chemical Property of Benzenamine, 4-[(2,4-dimethylphenyl)azo]-2,5-dimethyl- Edit
Chemical Property:
  • Vapor Pressure:5.83E-08mmHg at 25°C 
  • Boiling Point:440.6°Cat760mmHg 
  • Flash Point:220.2°C 
  • PSA:50.74000 
  • Density:1.07g/cm3 
  • LogP:5.49900 
  • XLogP3:4.5
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:2
  • Exact Mass:253.157897619
  • Heavy Atom Count:19
  • Complexity:315
Purity/Quality:

98%min *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1=CC(=C(C=C1)N=NC2=CC(=C(C=C2C)N)C)C
Technology Process of Benzenamine, 4-[(2,4-dimethylphenyl)azo]-2,5-dimethyl-

There total 1 articles about Benzenamine, 4-[(2,4-dimethylphenyl)azo]-2,5-dimethyl- 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 sodium nitrite; man erwaermt die entstandene Diazoaminoverbindung mit p-Xylidin und salzsaures p-Xylidin auf dem Wasserbade;
Guidance literature:
Multi-step reaction with 2 steps
1: tin dichloride; hydrochloric acid
2: Oxydation
With hydrogenchloride; tin(ll) chloride;
Guidance literature:
With hydrogenchloride; tin(ll) chloride;
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