Rivaroxaban EP Impurity E | CAS 1415566-28-7 - Request Quote
Rivaroxaban EP Impurity E
| SZ CAT No: | SZ-R017008 |
| CAS No | 1415566-28-7 |
| Mol.F. | C19H19N3O5S |
| Mol.Wt. | 401.4 |
| Inv. Status | In Stock |
| Shipping Condition | Room Temperature |
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Usage Note:
Rivaroxaban EP Impurity E is chemically N-[[(5S)-2-oxo-3-[4-(3-oxomorpholin-4-yl)phenyl]-1,3-oxazolidin-5-yl]methyl]thiophene-2-carboxamide (as per EP). It is also known as Rivaroxaban Deschloro Impurity. Rivaroxaban EP Impurity E is supplied with detailed characterization data compliant with regulatory guideline. Rivaroxaban EP Impurity E can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Rivaroxaban.
The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. SynZeal products are for analytical purpose only and not for human use.
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Rivaroxaban EP Impurity E for Method Validation
Rivaroxaban Reference Standard
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Rivaroxaban EP Impurity E for Forced Degradation Studies
Rivaroxaban EP Impurity E Identification Standards
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