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Name |
Rivaroxaban |
Alias |
(S)-Rivaroxaban;(S)-5-Chloro-N-((2-oxo-3-(4-(3-oxomorpholino)phenyl)-oxazolidin-5-yl)methyl)thiophene-2-carbox;RIVAROXABAN STAGE-IV [5-CHLORO-N-({5S)-2-OXO-3-[4-(3-OXO-4-MORPHOLINYL)PHENYL]-1,3-OXAZOLIDIN-5-YL}-METHYL)-2(AS PER INV;Rivaroxaban Isomer;5-Chloro-N-[[(5S)-2-oxo-3-[4-(3-oxo-4-morpholinyl)phenyl]-5-oxazolidinyl]methyl]-2-thiophenecarboxamide;BAY 59-7939; 5-Chloro-N-(((5S)-2-oxo-3-(4-(3-oxomorpholin-4-yl)phenyl)-1,3-oxazolidin-5-yl)methyl)thiophene-2-carboxamide |
CAS NO. |
366789-02-8 |
Molecular Formula |
C19H18ClN3O5S |
Molecular Weight |
435.88 |
Brief Introduction |
Rivaroxaban is an oral, bioavailable Factor Xa inhibitor that selectively blocks the active site of Factor Xa and does not require a cofactor (eg, antithrombin III) to exert activity. Activation of factor X by factor Xa (FXa) by endogenous and exogenous pathways plays an important role in the coagulation cascade. Rivaroxaban dose-dependently inhibits factor Xa activity in humans, with dose-dependent prolongation of prothrombin time (PT), activated partial thromboplastin time (aPTT), and HepTest® heparin quantitative determination using Neoplastin® reagent. Anti-factor Xa activity is also affected by rivaroxaban. |
Storage condition |
Room temperature, seal. |
Items |
Standard |
Results |
Appearance |
White or almost white powder |
White powder |
Melting point |
229~ 234℃ |
230.0~231.5℃ |
Residue on ignition |
NMT0.1% |
0.03% |
Related substances
|
Any other impurity: NMT0.2% Total of impurity: NMT0.5 % |
0.1% 0.19% |
Loss on drying |
NMT1.0% |
0.13% |
Heavy metal |
NMT20ppm |
Conforms |
Purity |
More than 99.50% |
99.81% |
Conclusion: The results show that the product complies with the Enterprise standard. |
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