Rivaroxaban EP Impurity D

About Rivaroxaban EP Impurity D

Rivaroxaban EP Impurity D is a pharmacopeial impurity of Rivaroxaban carrying the CAS registry number 1365267-35-1 with a typical assay of 97.31%. Formula C29H32N6O9, molecular weight 608.6 g/mol. Systematically, it is named 1,3-bis[[(5S)-2-oxo-3-[4-(3-oxomorpholin-4-yl)phenyl]-1,3-oxazolidin-5-yl]methyl]urea. It is also known as Rivaroxaban USP Related Compound D or Rivaroxaban Urea Dimer.

The product is provided as a solid. Store the standard in its sealed vial, protected from light and moisture, and follow the storage condition printed on the COA. Good laboratory practice and suitable PPE are recommended during handling.

This Rivaroxaban impurity supports analytical method development and validation (AMV), batch release testing and the impurity sections of ANDA and DMF filings. Our customers for this product work in pharmaceutical manufacturing and academic and industrial research.

We offer Rivaroxaban EP Impurity D in 10 mg, 25 mg, 50 mg and 100 mg packs with a batch-specific COA, and ship to customers worldwide. Stock is available for quick dispatch.

Typical applications

Pharmacopeial method verification
Impurity profiling
QC release testing
ANDA / DMF filings

Industries

Related to Rivaroxaban

View every impurity, metabolite and intermediate we list for Rivaroxaban.

Rivaroxaban impurities

Grade guides

Specifications & identifiers

Chemical identifiers
Product name	Rivaroxaban EP Impurity D
Catalogue No.	VQ-006657
CAS Number	1365267-35-1
IUPAC name	1,3-bis[[(5S)-2-oxo-3-[4-(3-oxomorpholin-4-yl)phenyl]-1,3-oxazolidin-5-yl]methyl]urea
Molecular formula	C₂₉H₃₂N₆O₉
Molecular weight	608.6 g/mol
Exact mass	608.2231
Grade	Reference Standard
Purity / assay	97.31%
HSN code	38229090
InChIKey	RMYVVSKNFAMRGJ-ZEQRLZLVSA-N
SMILES	C1COCC(=O)N1C2=CC=C(C=C2)N3C[C@@H](OC3=O)CNC(=O)NC[C@H]4CN(C(=O)O4)C5=CC=C(C=C5)N6CCOCC6=O
PubChem CID	56943041

Physical properties
Physical form	Solid
H-bond donors / acceptors	2 / 9
TPSA	159 Å²
Synonyms	1,3-Bis(((S)-2-oxo-3-(4-(3-oxomorpholino)phenyl)oxazolidin-5-yl)methyl)urea, N,N′-Bis[[(5S)-2-oxo-3-[4-(3-oxo-4-morpholinyl)phenyl]-5-oxazolidinyl]methyl]urea, Rivaroxaban USP Related Compound D, Rivaroxaban Urea Dimer, N,N'-Bis[Des(5-chloro-2-carvoxythienyl) Rivaroxaban] Urea, Urea, N,N'-bis[[(5S)-2-oxo-3-[4-(3-oxo-4-morpholinyl)phenyl]-5-oxazolidinyl]methyl]-, N,N'-Bis[[(5S)-2-oxo-3-[4-(3-oxo-4-morpholinyl)phenyl]-5-oxazolidinyl]methyl]urea, Urea,N,N'-bis[[(5S)-2-oxo-3-[4-(3-oxo-4-Morpholinyl)phenyl]-5-oxazolidinyl]Methyl]-, N,N'-Bis(des(5-chloro-2-carvoxythienyl) rivaroxaban) urea, 1,3-Bis(((5S)-2-oxo-3-(4-(3-oxomorpholin-4-yl)phenyl)-1,3-oxazolidin-5-yl)methyl)urea, N,N'-Bis(((5S)-2-oxo-3-(4-(3-oxomorpholin-4-yl)phenyl)-1,3-oxazolidin-5-yl)methyl)urea, Urea, N,N'-bis(((5S)-2-oxo-3-(4-(3-oxo-4-morpholinyl)phenyl)-5-oxazolidinyl)methyl)-

Documents

Safety Data Sheet (SDS)16-section GHS · on request Certificate of AnalysisTypical / batch COA · on request Specification sheetTDS / MOA · on request

Frequently asked questions

What is the CAS number of Rivaroxaban EP Impurity D?

The CAS Registry Number of Rivaroxaban EP Impurity D is 1365267-35-1. It is also known as 1,3-Bis(((S)-2-oxo-3-(4-(3-oxomorpholino)phenyl)oxazolidin-5-yl)methyl)urea, N,N′-Bis[[(5S)-2-oxo-3-[4-(3-oxo-4-morpholinyl)phenyl]-5-oxazolidinyl]methyl]urea, Rivaroxaban USP Related Compound D.

What is the molecular formula and molecular weight of Rivaroxaban EP Impurity D?

Rivaroxaban EP Impurity D has the molecular formula C29H32N6O9 and a molecular weight of 608.6 g/mol. Its IUPAC name is 1,3-bis[[(5S)-2-oxo-3-[4-(3-oxomorpholin-4-yl)phenyl]-1,3-oxazolidin-5-yl]methyl]urea.

What is Rivaroxaban EP Impurity D used for?

Rivaroxaban EP Impurity D is supplied as a characterised reference material related to Rivaroxaban. It is used for analytical method development and validation (AMV), impurity profiling, stability studies and quality control, and in ANDA/DMF regulatory filings.

Which grade and pack sizes of Rivaroxaban EP Impurity D can I order?

We supply Rivaroxaban EP Impurity D in Reference Standard (97.31%) grade, in 10 mg, 25 mg, 50 mg, 100 mg, 250 mg packs. Larger bulk quantities and custom packing are quoted on request.

Do you provide a COA and SDS with Rivaroxaban EP Impurity D?

Yes. Every lot of Rivaroxaban EP Impurity D is shipped with a batch-specific Certificate of Analysis, and a 16-section GHS Safety Data Sheet is provided with the quotation and the shipment.

Can Rivaroxaban EP Impurity D be shipped internationally?

Yes. We export Rivaroxaban EP Impurity D worldwide by air and sea freight or express courier, on EXW, FOB, CIF, CFR or DAP Incoterms, with full export documentation.