Uridine-5'-triphosp...

Uridine-5'-triphosphoric acid trisodium salt

Uridine-5'-triphosphoric acid trisodium salt

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1 Kilogram

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  • Min.Order :1 Kilogram
  • Purity: 99%
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Keywords

19817-92-6 Uridine-5'-triphosphoric acid trisodium salt C9H12N2Na3O15P3

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  • Appearance:conform
  • Application:intermediate
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  • ProductionCapacity:1|Metric Ton|Day
  • Storage:R.T.
  • Transportation:by air/sea

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1.Noble Metal Catalysts (Pt.Pd...)

2.Organic Phosphine Ligands (Tert-butyl-phosphine.Cyclohexyl-phosphine...)

3.OLED intermediates (Fluorene,Carbazole,Boric acid...)

4.Customs Synthesis

 

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Details:

Uridine-5'-triphosphoric acid trisodium salt Basic information
Product Name: Uridine-5'-triphosphoric acid trisodium salt
Synonyms: Uridine 5'-triphosphatetrisodium salthydrate;URIDINE 5'-TRIPHOSPHATE TETRASODIUM;URIDINE-5'-TRIPHOSPHATE TETRASODIUM SALT;Uridine-5'-triphosphoric acid trisodium salt;uridine 5'-(disodium dihydrogen triphosphate);URIDINE 5'-TRIPHOSPHATE TRISODIUM*100 MM SOLUTION M;URIDINE 5'-TRIPHOSPHATE TYPE IV*TRISODIU M;URIDINE 5'-TRIPHOSPHATE SODIUM FROM*YEAS T TYPE III
CAS: 19817-92-6
MF: C9H12N2Na3O15P3
MW: 550.09
EINECS: 243-347-5
Product Categories: Biochemistry;Nucleosides, Nucleotides & Related Reagents;Nucleotides and their analogs;Bases & Related Reagents;Carbohydrates & Derivatives;Heterocycles;Intermediates & Fine Chemicals;Nucleotides;Pharmaceuticals;Material
Mol File: 19817-92-6.mol
Uridine-5'-triphosphoric acid trisodium salt Structure
 
Uridine-5'-triphosphoric acid trisodium salt Chemical Properties
mp  140 °C
Fp  113 °C
storage temp.  −20°C
Water Solubility  75 g/100 mL (20 ºC)
CAS DataBase Reference 19817-92-6(CAS DataBase Reference)
 
Safety Information
Hazard Codes  Xn,Xi
Risk Statements  20/21/22-68/20/21/22-68-36/37/38
Safety Statements  22-26-36-36/37
WGK Germany  1
MSDS Information
 
 
Uridine-5'-triphosphoric acid trisodium salt Usage And Synthesis
Chemical Properties White crystalline powder
Usage
Usage psychostimulant
Usage A polyphosphate analogue of the nucleoside uridine used in the preparation of potent and selective agonists at the G-protein-coupled P2Y receptors.

 

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