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2-Amino-5-nitrobenzenesulfonic acid ammonium salt

Base Information Edit
  • Chemical Name:2-Amino-5-nitrobenzenesulfonic acid ammonium salt
  • CAS No.:4346-51-4
  • Molecular Formula:C6H6 N2 O5 S . H3 N
  • Molecular Weight:235.24
  • Hs Code.:
  • European Community (EC) Number:224-408-5
  • DSSTox Substance ID:DTXSID2063424
  • Mol file:4346-51-4.mol
2-Amino-5-nitrobenzenesulfonic acid ammonium salt

Synonyms:4346-51-4;2-Amino-5-nitrobenzenesulfonic acid ammonium salt;ammonium 2-amino-5-nitrobenzenesulfonate;azanium;2-amino-5-nitrobenzenesulfonate;ammonium 2-amino-5-nitrobenzene-1-sulfonate;Benzenesulfonic acid, 2-amino-5-nitro-, monoammonium salt;2-amino-5-nitrobenzenesulfonic acid;azane;DTXSID2063424;AKOS003398347;NS00081716;W-109965;F8880-6345

Suppliers and Price of 2-Amino-5-nitrobenzenesulfonic acid ammonium salt
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
  • Matrix Scientific
  • Ammonium2-amino-5-nitrobenzene-1-sulfonate 95%+
  • 2.500g
  • $ 215.00
  • Matrix Scientific
  • Ammonium2-amino-5-nitrobenzene-1-sulfonate 95%+
  • 500mg
  • $ 87.00
  • Matrix Scientific
  • Ammonium2-amino-5-nitrobenzene-1-sulfonate 95%+
  • 100mg
  • $ 53.00
Total 51 raw suppliers
Chemical Property of 2-Amino-5-nitrobenzenesulfonic acid ammonium salt Edit
Chemical Property:
  • Vapor Pressure:1.82E-14mmHg at 25°C 
  • Boiling Point:583.7°Cat760mmHg 
  • Flash Point:306.8°C 
  • PSA:137.83000 
  • Density:g/cm3 
  • LogP:2.93280 
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:0
  • Exact Mass:235.02629157
  • Heavy Atom Count:15
  • Complexity:303
Purity/Quality:

99% *data from raw suppliers

Ammonium2-amino-5-nitrobenzene-1-sulfonate 95%+ *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC(=C(C=C1[N+](=O)[O-])S(=O)(=O)[O-])N.[NH4+]
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