Rivaroxaban
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Rivaroxaban EP Impurity D
| N° de SZ CAT: | SZ-R017018 |
| Número CAS | 1365267-35-1 |
| Mol.F. | C29H32N6O9 |
| Peso Molecular |
608.6 |
| Status de Fatura |
In Stock |
| Shipping Condition | Room Temperature |
Nome Químico: N,N′-bis[[(5S)-2-oxo-3-[4-(3-oxomorpholin-4-yl)phenyl]-1,3-oxazolidin-5-yl]methyl]urea (as per EP); 1,3-Bis({(S)-2-oxo-3-[4-(3-oxomorpholino)phenyl]oxazolidin-5-yl}methyl)urea (as per USP)
Sinônimo: Rivaroxaban USP Related Compound D ; Rivaroxaban Urea Dimer
Shipping Temperature: Room Temperature
HSN Code: 38229010
Country of Origin: India
Sorrisos: O=C(NC[C@H]1CN(C2=CC=C(N3C(COCC3)=O)C=C2)C(O1)=O)NC[C@H]4CN(C5=CC=C(N6C(COCC6)=O)C=C5)C(O4)=O
Rivaroxaban EP Impurity D is chemically N,N′-bis[[(5S)-2-oxo-3-[4-(3-oxomorpholin-4-yl)phenyl]-1,3-oxazolidin-5-yl]methyl]urea (as per EP); 1,3-Bis({(S)-2-oxo-3-[4-(3-oxomorpholino)phenyl]oxazolidin-5-yl}methyl)urea (as per USP). It is also known as Rivaroxaban USP Related Compound D ; Rivaroxaban Urea Dimer. Rivaroxaban EP Impurity D is supplied with detailed characterization data compliant with regulatory guideline. Rivaroxaban EP Impurity D 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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