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Technology Process of Benzenediazonium, 4-chloro-2-methyl-, 1,5-naphthalenedisulfonate (1:1)

Benzenediazonium, 4-chloro-2-methyl-, 1,5-naphthalenedisulfonate (1:1)

Base Information
  • Chemical Name:Benzenediazonium, 4-chloro-2-methyl-, 1,5-naphthalenedisulfonate (1:1)
  • CAS No.:51503-28-7
  • Molecular Formula:C10H6O6S2.2(C7H6ClN2)
  • Molecular Weight:593.46
  • Hs Code.:
  • DSSTox Substance ID:DTXSID50890872
  • Mol file:51503-28-7.mol
Benzenediazonium, 4-chloro-2-methyl-, 1,5-naphthalenedisulfonate (1:1)

Synonyms:Benzenediazonium, 4-chloro-2-methyl-, 1,5-naphthalenedisulfonate (1:1);DTXSID50890872;AKOS016364160;Fast Red TR 1,5-naphthalenedisulfonate salt

Suppliers and Price of Benzenediazonium, 4-chloro-2-methyl-, 1,5-naphthalenedisulfonate (1:1)
Supply Marketing:
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
  • Sigma-Aldrich
  • Fast Red TR Salt 1,5-naphthalenedisulfonate salt
  • 5g
  • $ 142.00
  • Sigma-Aldrich
  • Fast Red TR Salt 1,5-naphthalenedisulfonate salt
  • 1g
  • $ 42.60
  • American Custom Chemicals Corporation
  • 4-CHLORO-2-METHYLBENZENEDIAZONIUM-1,5-NAPHTHALENEDISULFONATE 95.00%
  • 5G
  • $ 934.78
Total 23 raw suppliers
Chemical Property of Benzenediazonium, 4-chloro-2-methyl-, 1,5-naphthalenedisulfonate (1:1)
Chemical Property:
  • Appearance/Colour:yellow to buff crystalline powder 
  • Storage Temp.:−20°C 
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:1
  • Exact Mass:439.9903562
  • Heavy Atom Count:28
  • Complexity:644
Purity/Quality:

99% *data from raw suppliers

Fast Red TR Salt 1,5-naphthalenedisulfonate salt *data from reagent suppliers

Safty Information:
  • Pictogram(s): IrritantXi 
  • Hazard Codes:Xi,Xn 
  • Statements: 36/37/38-68/20/21/22-20/21/22 
  • Safety Statements: 26-36-37/39-36/37 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1=C(C=CC(=C1)Cl)[N+]#N.C1=CC2=C(C=CC=C2S(=O)(=O)[O-])C(=C1)S(=O)(=O)O
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