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Rivaroxaban EP Impurity A

Rivaroxaban EP Impurity A

Product Description
CAT No.
ALN-R017017
CAS No.
865479-71-6
Mol. F.
C19H18CIN3O5S
Mol. Wt.
435.9
Stock
In Stock
Chemical Name : 5-chloro-N-[[(5R)-2-oxo-3-[4-(3-oxomorpholin-4-yl)phenyl]-1,3-oxazolidin-5-yl]methyl]thiophene-2-carboxamide (as per EP);(R)-5-Chloro-N-({2-oxo-3-[4-(3-oxomorpholino)phenyl]oxazolidin-5-yl}methyl)thiophene-2-carboxamide (as per USP)
Smiles : O=C(C1=CC=C(Cl)S1)NC[C@@H]2CN(C3=CC=C(N4C(COCC4)=O)C=C3)C(O2)=O
Inchi : InChI=1S/C22H19N3O6/c26-19-13-30-10-9-23(19)14-5-7-15(8-6-14)24-11-16(31-22(24)29)12-25-20(27)17-3-1-2-4-18(17)21(25)28/h1-8,16H,9-13H2/t16-/m1/s1
Synonym : Rivaroxaban R-enantiomer

Development and validation of stability indicating UPLC method for the determination of Rivaroxaban in bulk and finished products and identification of degradation products by LCMS

By Ali, Syed Mastan; Ramachandran, D.nFrom Journal of Applicable Chemistry (Lumami, India) (2021), 10(3), 291-301

Validated LC-MS/MS method for the determination of three genotoxic impurities in rivaroxaban drug substance

By Korlakunta, Vijaya Gouri; Dasari, Vijaya Bharathi; Sharma, Hemant Kumar; Nowduri, Annapurna; Bonige, Kishore Babu; Chavakula, Ramadas – From European Journal of Biomedical and Pharmaceutical Sciences (2020), 7(8), 492-500

Development of a stability-indicating HPLC method and a dissolution test for rivaroxaban dosage forms

By Souri, Effat; Mottaghi, Siavash; Zargarpoor, Mohammad; Ahmadkhaniha, Reza; Jalalizadeh, Hassan – From Acta Chromatographica (2016), 28(3), 347-361

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