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Pharmacopeial Impurities (EP / USP / BP)Reference Standard In stock

Rivaroxaban EP Impurity D

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

CAS No.1365267-35-1
FormulaC29H32N6O9
Mol. weight608.60
Catalogue No.VQ-006657
Purity97.31%
HSN38229090

Rivaroxaban EP Impurity D (CAS 1365267-35-1) – Rivaroxaban impurity standard, 97.31%. C29H32N6O9, MW 608.6. Vaqora Chemicals: COA, global shipping.

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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

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Related to Rivaroxaban

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

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Specifications & identifiers

Chemical identifiers
Product nameRivaroxaban EP Impurity D
Catalogue No.VQ-006657
CAS Number1365267-35-1
IUPAC name1,3-bis[[(5S)-2-oxo-3-[4-(3-oxomorpholin-4-yl)phenyl]-1,3-oxazolidin-5-yl]methyl]urea
Molecular formulaC29H32N6O9
Molecular weight608.6 g/mol
Exact mass608.2231
GradeReference Standard
Purity / assay97.31%
HSN code38229090
InChIKeyRMYVVSKNFAMRGJ-ZEQRLZLVSA-N
SMILESC1COCC(=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 CID56943041
Physical properties
Physical formSolid
H-bond donors / acceptors2 / 9
TPSA159 Ų
Synonyms1,3-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)-

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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.

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