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Pharmacopeial Impurities (EP / USP / BP)

Rivaroxaban EP Impurity E

Reference StandardIn stock

Buy Rivaroxaban EP Impurity E (CAS 1415566-28-7) from Zemixal. Request a quote with price, lead time and documents. Exported from India with full paperwork.

Pack sizes
Rivaroxaban EP Impurity E chemical structure
CAS number1415566-28-7
FormulaC19H19N3O5S
Molar mass401.4 g/mol
Physical formSolid
HS code38229090
Purity99%
InChIKeySJVCANNMDYDYLN-HNNXBMFYSA-N
IUPAC nameN-[[(5S)-2-oxo-3-[4-(3-oxomorpholin-4-yl)phenyl]-1,3-oxazolidin-5-yl]methyl]thiophene-2-carboxamide

About Rivaroxaban EP Impurity E

Rivaroxaban EP Impurity E is supplied by Zemixal as a characterised reference material for Rivaroxaban analysis. Key data (Reference Standard): CAS 1415566-28-7, formula C19H19N3O5S and molar mass 401.4 g/mol. It is handled as a solid.

Typical applications

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

Safe handling

Classified under GHS with signal word Warning and hazard statements H302. Read the SDS before first use.

Standard pack sizes are 10 mg, 25 mg, 50 mg, 100 mg and 250 mg, and custom quantities are quoted on request. Every shipment includes a certificate of analysis with characterisation data. Request pricing online and we confirm availability, documentation and freight to your country.

Reference standards for Rivaroxaban

See every impurity, metabolite and related compound we list for this API.

Rivaroxaban standards

Typical uses

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

Applications

Pharmaceutical Manufacturing and QCResearch Labs and Universities

Grade guides

Ph. Eur. Grade (European Pharmacopoeia)

Specifications and identifiers

Specifications of Rivaroxaban EP Impurity E
Product nameRivaroxaban EP Impurity E
Catalogue numberZX-005961
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
Molar mass401.4 g/mol
Exact mass401.1045
GradeReference Standard
Purity / assay99%
Physical formSolid
XLogP31.5
H-bond donors / acceptors1 / 6
Topological polar surface area116 Ų
HS code38229090
InChIKeySJVCANNMDYDYLN-HNNXBMFYSA-N
SMILESC1COCC(=O)N1C2=CC=C(C=C2)N3C[C@@H](OC3=O)CNC(=O)C4=CC=CS4
PubChem CID66926287
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

Lot values are stated on the batch certificate of analysis. Ask for a typical COA with your quotation.

Safety and GHS hazards

GHS07 Irritant or harmful
Irritant or harmful

Signal word Warning

  • H302Harmful if swallowed

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

Classification summarised from public GHS notifications. It can vary with grade and concentration, so always follow the SDS supplied with your lot.

Pack sizes

Pack sizes of Rivaroxaban EP Impurity E
10 mgQuoted on request
25 mgQuoted on request
50 mgQuoted on request
100 mgQuoted on request
250 mgQuoted on request

Need a different size? Bulk drums and custom packing are quoted on request through the quote form on this page.

Questions about Rivaroxaban EP Impurity E

Which CAS number identifies Rivaroxaban EP Impurity E?
Rivaroxaban EP Impurity E is registered under CAS 1415566-28-7. You may also see it listed as (S)-N-((2-Oxo-3-(4-(3-oxomorpholino)phenyl)oxazolidin-5-yl)methyl)thiophene-2-carboxamide, Dechloro-rivaroxaban, Rivaroxaban Deschloro Impurity. Our catalogue number for this item is ZX-005961.
What are the formula and molar mass of Rivaroxaban EP Impurity E?
For Rivaroxaban EP Impurity E, its formula is C19H19N3O5S and its molar mass is 401.4 g/mol. The systematic (IUPAC) name is N-[[(5S)-2-oxo-3-[4-(3-oxomorpholin-4-yl)phenyl]-1,3-oxazolidin-5-yl]methyl]thiophene-2-carboxamide. InChIKey SJVCANNMDYDYLN-HNNXBMFYSA-N lets you match it in any structure database.
How is Rivaroxaban EP Impurity E used in pharmaceutical QC?
Rivaroxaban EP Impurity E is a characterised reference material linked to Rivaroxaban. Laboratories use it to identify and quantify this impurity during method development and validation, stability work, batch release testing and regulatory submissions.
What grade and pack sizes are available for Rivaroxaban EP Impurity E?
This listing is Reference Standard grade with 99% purity. Standard packs are 10 mg, 25 mg, 50 mg, 100 mg, 250 mg. Larger quantities and custom packing can be quoted on request.
Which documents come with Rivaroxaban EP Impurity E?
Each lot ships with a batch certificate of analysis and a 16-section GHS safety data sheet. A typical COA or specification sheet can be shared with the quotation before you order.
Can Zemixal ship Rivaroxaban EP Impurity E to my country?
Yes. Because Rivaroxaban EP Impurity E is classed as hazardous, it travels in UN-approved packaging as dangerous goods under IATA or IMDG rules, with the export paperwork your broker needs.

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