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

Rivaroxaban EP Impurity E

Synonyms: (S)-N-((2-Oxo-3-(4-(3-oxomorpholino)phenyl)oxazolidin-5-yl)methyl)thiophene-2-carboxamide · Dechloro-rivaroxaban · Rivaroxaban Deschloro Impurity · Rivaroxaban impurity E

CAS No.1415566-28-7
FormulaC19H19N3O5S
Mol. weight401.40
Catalogue No.VQ-006658
Purity99%
HSN38229090

Rivaroxaban EP Impurity E (CAS 1415566-28-7) – Rivaroxaban impurity standard, 99%. C19H19N3O5S, MW 401.4. Vaqora Chemicals: COA, global shipping.

Pack sizesPrice on quotation · bulk available
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25 mg
50 mg
100 mg
250 mg
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16-section GHS SDS
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About Rivaroxaban EP Impurity E

Listed under CAS 1415566-28-7, Rivaroxaban EP Impurity E is a pharmacopeial impurity of Rivaroxaban available from Vaqora Chemicals at a purity of 99%. With the molecular formula C19H19N3O5S, it has a molar mass of 401.4 g/mol. The IUPAC name is N-[[(5S)-2-oxo-3-[4-(3-oxomorpholin-4-yl)phenyl]-1,3-oxazolidin-5-yl]methyl]thiophene-2-carboxamide. It is also known as Dechloro-rivaroxaban or Rivaroxaban Deschloro Impurity.

It is supplied as a solid. Reference materials should be stored sealed and away from light and moisture, as specified on the accompanying COA. The GHS classification uses the signal word “Warning”, so appropriate gloves, eye protection and ventilation are recommended.

As a characterised impurity of Rivaroxaban, it is used for analytical method development, method validation (AMV) and routine quality-control testing, and it supports ANDA and DMF regulatory filings. Buyers come mainly from pharmaceutical manufacturing and academic and industrial research.

Vaqora Chemicals supplies Rivaroxaban EP Impurity E in 10 mg, 25 mg, 50 mg and 100 mg packs, each shipped with a Certificate of Analysis (COA), and exports 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 nameRivaroxaban EP Impurity E
Catalogue No.VQ-006658
CAS Number1415566-28-7
IUPAC nameN-[[(5S)-2-oxo-3-[4-(3-oxomorpholin-4-yl)phenyl]-1,3-oxazolidin-5-yl]methyl]thiophene-2-carboxamide
Molecular formulaC19H19N3O5S
Molecular weight401.4 g/mol
Exact mass401.1045
GradeReference Standard
Purity / assay99%
HSN code38229090
InChIKeySJVCANNMDYDYLN-HNNXBMFYSA-N
SMILESC1COCC(=O)N1C2=CC=C(C=C2)N3C[C@@H](OC3=O)CNC(=O)C4=CC=CS4
PubChem CID66926287
Physical properties
Physical formSolid
LogP (XLogP3)1.5
H-bond donors / acceptors1 / 6
TPSA116 Ų
Synonyms(S)-N-((2-Oxo-3-(4-(3-oxomorpholino)phenyl)oxazolidin-5-yl)methyl)thiophene-2-carboxamide, Dechloro-rivaroxaban, Rivaroxaban Deschloro Impurity, Rivaroxaban impurity E, Dechloro Rivaroxaban, Rivaroxaban Impurity C, CS-M1371, (S)-N-[[2-Oxo-3-[4-(3-oxomorpholino)phenyl]-5-oxazolidinyl]methyl]thiophene-2-carboxamide

Safety & hazard information (GHS)

GHS07 Harmful / irritant
Harmful / irritant

Signal word: Warning

Hazard statements

  • H302Harmful if swallowed

Precautionary statements: P264, P270, P301 + P317, P330, P501

Classification is indicative (aggregated GHS notifications) and may vary by grade and concentration. Always refer to the SDS supplied with your lot.

Documents

Frequently asked questions

What is the CAS number of Rivaroxaban EP Impurity E?

The CAS Registry Number of Rivaroxaban EP Impurity E is 1415566-28-7. It is also known as (S)-N-((2-Oxo-3-(4-(3-oxomorpholino)phenyl)oxazolidin-5-yl)methyl)thiophene-2-carboxamide, Dechloro-rivaroxaban, Rivaroxaban Deschloro Impurity.

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

Rivaroxaban EP Impurity E has the molecular formula C19H19N3O5S and a molecular weight of 401.4 g/mol. Its IUPAC name is N-[[(5S)-2-oxo-3-[4-(3-oxomorpholin-4-yl)phenyl]-1,3-oxazolidin-5-yl]methyl]thiophene-2-carboxamide.

What is Rivaroxaban EP Impurity E used for?

Rivaroxaban EP Impurity E 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 E can I order?

We supply Rivaroxaban EP Impurity E in Reference Standard (99%) 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 E?

Yes. Every lot of Rivaroxaban EP Impurity E 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 E be shipped internationally?

Yes. Rivaroxaban EP Impurity E is classified as hazardous, so it is packed in UN-approved packaging and shipped as dangerous goods under IATA/IMDG rules. We export worldwide on EXW, FOB, CIF and DAP terms.

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Why buyers choose Vaqora

  • Batch-traceable lots with COA
  • R&D packs to multi-tonne supply
  • IATA / IMDG dangerous-goods packing
  • EXW, FOB, CIF, DAP Incoterms
  • Custom synthesis & sourcing
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