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Uridine 5'-triphosphate tetrasodium

Base Information
  • Chemical Name:Uridine 5'-triphosphate tetrasodium
  • CAS No.:14264-46-1
  • Molecular Formula:C9H12N2O15P3*3Na
  • Molecular Weight:550.089
  • Hs Code.:
  • UNII:KP113C7B9H
  • Wikidata:Q27282360
Uridine 5'-triphosphate tetrasodium

Synonyms:Uridine 5'-triphosphate tetrasodium;Uridine STP;UNII-KP113C7B9H;KP113C7B9H;Uridine 5'-(tetrahydrogen triphosphate), tetrasodium salt;Uridine 5'-triphosphate sodium salt;14264-46-1;C9H15N2O15P3.3Na;C9-H15-N2-O15-P3.3Na;C9H15N2O15P3.4Na;C9-H15-N2-O15-P3.4Na;Uridine 5'-(tetrahydrogen triphosphate), trisodium salt;SODIUM UTP;AKOS025312540;URIDINE TRIPHOSPHATE SODIUM [WHO-DD];Q27282360;URIDINE 5'-(TETRAHYDROGEN TRIPHOSPHATE), SODIUM SALT (1:4);tetrasodium;[[[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-oxidophosphoryl]oxy-oxidophosphoryl] phosphate

Suppliers and Price of Uridine 5'-triphosphate tetrasodium
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
Total 2 raw suppliers
Chemical Property of Uridine 5'-triphosphate tetrasodium
Chemical Property:
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • Density:g/cm3 
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:15
  • Rotatable Bond Count:7
  • Exact Mass:571.89630577
  • Heavy Atom Count:33
  • Complexity:811
Purity/Quality:

97% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CN(C(=O)NC1=O)C2C(C(C(O2)COP(=O)([O-])OP(=O)([O-])OP(=O)([O-])[O-])O)O.[Na+].[Na+].[Na+].[Na+]
  • Isomeric SMILES:C1=CN(C(=O)NC1=O)[C@H]2[C@@H]([C@@H]([C@H](O2)COP(=O)([O-])OP(=O)([O-])OP(=O)([O-])[O-])O)O.[Na+].[Na+].[Na+].[Na+]
Technology Process of Uridine 5'-triphosphate tetrasodium

There total 2 articles about Uridine 5'-triphosphate tetrasodium 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:
Guidance literature:
UMP tetra-n-butylammonium salt; With 1-(benzenesulfonyl)-3-methylimidazolium triflate; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20 ℃; for 0.0166667h;
With magnesium chloride; bis(tetra-n-butylammonium) dihydrogen pyrophosphate; In N,N-dimethyl-formamide; at 0 - 20 ℃;
DOI:10.1021/ol203178k
Guidance literature:
Multi-step reaction with 2 steps
1.1: Dowex-50W ion exchange column [H(+) form]
1.2: pH 7
2.1: 1-(benzenesulfonyl)-3-methylimidazolium triflate; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 0.02 h / 20 °C
2.2: 0 - 20 °C
2.3: Dowex-50-W ion-exchange resin [Na(+) form]
With 1-(benzenesulfonyl)-3-methylimidazolium triflate; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide;
DOI:10.1021/ol203178k
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