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7-(Dimethylamino)-3,4-dihydroxy-1-(methoxycarbonyl)phenoxazin-5-ium chloride

Base Information Edit
  • Chemical Name:7-(Dimethylamino)-3,4-dihydroxy-1-(methoxycarbonyl)phenoxazin-5-ium chloride
  • CAS No.:6416-51-9
  • Molecular Formula:C16H15 N2 O5 . Cl
  • Molecular Weight:350.7537
  • Hs Code.:
  • European Community (EC) Number:229-126-6
  • UNII:71K50A0AXE
  • Wikidata:Q27265958
  • NCI Thesaurus Code:C72046
  • Mol file:6416-51-9.mol
7-(Dimethylamino)-3,4-dihydroxy-1-(methoxycarbonyl)phenoxazin-5-ium chloride

Synonyms:Prune Pure;Gallo Blue E;Solochrome Prune A;Solochrome Prune AS;Gallocyanine methyl ester;Violet PDH;C.I.Mordant Violet 54;UNII-71K50A0AXE;7-(Dimethylamino)-3,4-dihydroxy-1-(methoxycarbonyl)phenoxazin-5-ium chloride;71K50A0AXE;C.I. 51040;EINECS 229-126-6;6416-51-9;Phenoxazin-5-ium,7-(dimethylamino)-3,4-dihydroxy-1-(methoxycarbonyl)-, chloride;Prune;C.I. Mordant Violet 54;C16H15N2O5.Cl;C16-H15-N2-O5.Cl;CI 51040;Q27265958;Phenoxazin-5-ium, 7-(dimethylamino)-3,4-dihydroxy-1-(methoxycarbonyl)-, chloride;PHENOXAZIN-5-IUM, 7-(DIMETHYLAMINO)-3,4-DIHYDROXY-1-(METHOXYCARBONYL)-, CHLORIDE (1:1)

Suppliers and Price of 7-(Dimethylamino)-3,4-dihydroxy-1-(methoxycarbonyl)phenoxazin-5-ium chloride
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 2 raw suppliers
Chemical Property of 7-(Dimethylamino)-3,4-dihydroxy-1-(methoxycarbonyl)phenoxazin-5-ium chloride Edit
Chemical Property:
  • Vapor Pressure:8.05E-10mmHg at 25°C 
  • Boiling Point:474.8°C at 760 mmHg 
  • Flash Point:240.9°C 
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:3
  • Exact Mass:350.0669493
  • Heavy Atom Count:24
  • Complexity:647
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CN(C)C1=CC2=C(C=C1)[NH+]=C3C(=CC(=O)C(=C3O2)O)C(=O)OC.[Cl-]
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