Product Name

  • Name

    15(R)-15-METHYL PROSTAGLANDIN E2

  • EINECS
  • CAS No. 55028-70-1
  • Density 1.134g/cm3
  • Solubility
  • Melting Point
  • Formula C21H34 O5
  • Boiling Point 535.5°C at 760 mmHg
  • Molecular Weight 366.498
  • Flash Point 291.7°C
  • Transport Information
  • Appearance
  • Safety Human reproductive effects by intramuscular route: terminates pregnancy. Other experimental reproductive effects.
  • Risk Codes
  • Molecular Structure Molecular Structure of 55028-70-1 (15(R)-15-METHYL PROSTAGLANDIN E2)
  • Hazard Symbols
  • Synonyms (15R)-15-MethylprostaglandinE2; 15(R)-15-Methyl-PGE2; 15(R)-Methylprostaglandin E2; 15-MethylprostaglandinE2; Arbacet; Arbaprostil; CU 83; U 42842
  • PSA 94.83000
  • LogP 3.64120

Arbaprostil Chemical Properties

IUPAC name: (Z)-7-[(1R,3R)-3-hydroxy-2-[(E,3R)-3-hydroxy-3-methyloct-1-enyl]-5-oxocyclopentyl]hept-5-enoic acid 
Molecular Formula: C21H34O5
Molecular Weight: 366.491660 g/mol
Surface Tension: 52.2 dyne/cm
Index of Refraction: 1.556
Density: 1.134 g/cm3
Flash Point: 291.7 °C
Enthalpy of Vaporization: 93.38 kJ/mol
Boiling Point: 535.5 °C at 760 mmHg
Vapour Pressure: 1.06E-13 mmHg at 25 °C 
Following is the structure of Arbaprostil (CAS NO.55028-70-1):
     

Arbaprostil Safety Profile

Human reproductive effects by intramuscular route: terminates pregnancy. Other experimental reproductive effects.

Arbaprostil Specification

 Arbaprostil , its cas register number is 55028-70-1. It also can be called (15R)-15-Methylprostaglandin E2 ; 5A,11alpha,13E,15R)-11,15-Dihydroxy-15-methyl-9-oxo-5,13-prostadiensaeure ; (E,Z)-(1R,2R,3R)-7-(3-Hydroxy-2-((3R)-(3-hydroxy-3-methyl-1-octenyl))-5-oxocyclopentyl)-5-heptenoic acid ; 15(R)-15-Methyl prostaglandin E2 ; Arbacet ; Arbaprostil ; and Arbaprostilo .
 Arbaprostil (CAS NO.55028-70-1) is a synthetic prostaglandin E analog that protects the gastric mucosa, prevents ulceration, and promotes healing of peptic ulcers. The protective effect is independent of acid inhibition. It is also a potent inhibitor of pancreatic function and can inhibit the growth of experimental tumors.

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