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viomycin

Base Information Edit
  • Chemical Name:viomycin
  • CAS No.:32988-50-4
  • Molecular Formula:C25H43 N13 O10
  • Molecular Weight:685.698
  • Hs Code.:
  • Mol file:32988-50-4.mol
viomycin

Synonyms:Viomycin(8CI,9CI); 1,4,7,10,13-Pentaazacyclohexadecane, cyclic peptide deriv.;Celiomycin; Florimycin; Stereoisomer of3,6-diamino-N-[6-[[(aminocarbonyl)amino]methylene]-3-(2-amino-1,4,5,6-tetrahydro-6-hydroxy-4-pyrimidinyl)-9,12-bis(hydroxymethyl)-2,5,8,11,14-pentaoxo-1,4,7,10,13-pentaazacyclohexadec-15-yl]hexanamide;Tuberactinomycin B; Vinacetin A; Vioactane

Suppliers and Price of viomycin
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
  • Tocris
  • Viomycin
  • 10
  • $ 182.00
  • ApexBio Technology
  • Viomycin
  • 10mg
  • $ 274.00
  • American Custom Chemicals Corporation
  • VIOMYCIN 95.00%
  • 5MG
  • $ 500.54
Total 11 raw suppliers
Chemical Property of viomycin Edit
Chemical Property:
  • Melting Point:280 °C 
  • Refractive Index:1.6700 (estimate) 
  • Boiling Point:695.81°C (rough estimate) 
  • PKA:pKa 8.2 (Uncertain);10.3 (Uncertain) 
  • PSA:392.86000 
  • Density:1.8g/cm3 
  • LogP:-3.89140 
  • Storage Temp.:Store at -20°C 
Purity/Quality:

95-99% *data from raw suppliers

Viomycin *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Indications Viomycin is a complex polypeptide antibiotic that is active against MDR strains of tuberculosis. Cross-resistance between viomycin and kanamycin is less frequent than between viomycin and capreomycin.
  • Therapeutic Function Antitubercular
Technology Process of viomycin

There total 1 articles about viomycin which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

Guidance literature:
Mikrobiol. Herstellung durch Actinomyces floridae unter Zusatz von Phenylessigsaeure,Phenolphthalein und α-Naphthylessigsaeure;
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