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Desacetyl Acetaminophen Glutathione

Base Information
  • Chemical Name:Desacetyl Acetaminophen Glutathione
  • CAS No.:129762-76-1
  • Molecular Formula:C16H22 N4 O7 S
  • Molecular Weight:414.4335
  • Hs Code.:
  • Mol file:129762-76-1.mol
Desacetyl Acetaminophen Glutathione

Synonyms:Desacetyl Acetaminophen Glutathione;

Suppliers and Price of Desacetyl Acetaminophen Glutathione
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
  • Usbiological
  • Desacetyl Acetaminophen Glutathione||
  • 500ug
  • $ 602.00
  • TRC
  • DesacetylAcetaminophenGlutathione
  • 10mg
  • $ 3765.00
  • Biosynth Carbosynth
  • Desacetyl acetaminophen glutathione
  • 10 mg
  • $ 5200.00
  • Biosynth Carbosynth
  • Desacetyl acetaminophen glutathione
  • 5 mg
  • $ 3250.00
  • Biosynth Carbosynth
  • Desacetyl acetaminophen glutathione
  • 2 mg
  • $ 1500.00
  • Biosynth Carbosynth
  • Desacetyl acetaminophen glutathione
  • 1 mg
  • $ 900.00
Total 6 raw suppliers
Chemical Property of Desacetyl Acetaminophen Glutathione
Chemical Property:
  • Vapor Pressure:1.47E-33mmHg at 25°C 
  • Melting Point:>150°C (dec.) 
  • Boiling Point:884.8°Cat760mmHg 
  • Flash Point:488.9°C 
  • PSA:237.35000 
  • Density:1.53g/cm3 
  • LogP:1.90630 
  • Storage Temp.:Hygroscopic, -20°C Freezer, Under Inert Atmosphere 
  • Solubility.:Methanol (Slightly), Water (Slightly) 
Purity/Quality:

98%min *data from raw suppliers

Desacetyl Acetaminophen Glutathione|| *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Uses Desacetyl Acetaminophen Glutathione is a hepatic metabolite of p-Aminophenol (1,2). The aminophenol glutathione S-conjugates formed induce p-Aminophenol nephrotoxicity by a pathway dependent on γ-glutamyl transpeptidase. The hepatic metabolite of p-Aminophenol. The aminophenol glutathione S-conjugates formed induce p-Aminophenol nephrotoxicity by a pathway dependent on γ-glutamyl transpeptidase.
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