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Technology Process of STILBAZO

STILBAZO

Base Information
  • Chemical Name:STILBAZO
  • CAS No.:1571-36-4
  • Molecular Formula:C26H20 N4 O10 S2 . 2 H3 N
  • Molecular Weight:612.5878
  • Hs Code.:
  • Mol file:1571-36-4.mol
STILBAZO

Synonyms:2,2'-Stilbenedisulfonicacid, 4,4'-bis[(3,4-dihydroxyphenyl)azo]-, diammonium salt (6CI,8CI);Benzenesulfonic acid, 2,2'-(1,2-ethenediyl)bis[5-[(3,4-dihydroxyphenyl)azo]-,diammonium salt (9CI); Stilbazo; Stilbazo R

Suppliers and Price of STILBAZO
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
  • TRC
  • Stilbazo
  • 500mg
  • $ 95.00
  • TCI Chemical
  • Stilbazo [Spectrophotometric reagent for Al and other metals]
  • 1g
  • $ 73.00
  • TCI Chemical
  • Stilbazo [Spectrophotometric reagent for Al and other metals]
  • 5g
  • $ 217.00
  • Crysdot
  • Ammonium6,6'-(ethene-1,2-diyl)bis(3-((3,4-dihydroxyphenyl)diazenyl)benzenesulfonate) 95+%
  • 10g
  • $ 314.00
  • Crysdot
  • Ammonium6,6'-(ethene-1,2-diyl)bis(3-((3,4-dihydroxyphenyl)diazenyl)benzenesulfonate) 95+%
  • 25g
  • $ 620.00
  • American Custom Chemicals Corporation
  • STILBAZO 95.00%
  • 5G
  • $ 968.26
  • American Custom Chemicals Corporation
  • STILBAZO 95.00%
  • 1G
  • $ 655.49
  • AK Scientific
  • Stilbazo
  • 5g
  • $ 355.00
Total 21 raw suppliers
Chemical Property of STILBAZO
Chemical Property:
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • PSA：262.34000 
  • Density:1.72 g/cm3 
  • LogP:8.81300 
  • Water Solubility.:Soluble in water 
Purity/Quality:

98%,99%, *data from raw suppliers

Stilbazo *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
  • Statements: 36/37/38 
  • Safety Statements: 26-36/37/39 
MSDS Files:

SDS file from LookChem

Useful:
  • Uses Stilbazo is a azo dye; in determination of a polymer surfactant by potentiometry with ion-selective electrode membrane using inorganic or organic anions as counterions of electrode-active compound.
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