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VAQORARivaroxaban EP Impurity G
Synonyms: (S)-2-((2-Oxo-3-(4-(3-oxomorpholino)phenyl)oxazolidin-5-yl)methyl)isoindoline-1,3-dione · Rivaroxaban Phthalimido Impurity · [3-(4-Chlorophenyl)phenyl]methylamine, HCl · 4-[4-[(5S)-5-Phthalimidomethyl-2-oxo-3-oxazolidinyl]phenyl]-3-morpholinone
CAS No.446292-08-6
FormulaC22H19N3O6
Mol. weight421.40
Catalogue No.VQ-006661
PurityReference Standard
HSN38229090
Rivaroxaban EP Impurity G (CAS 446292-08-6) – Rivaroxaban impurity standard. C22H19N3O6, MW 421.4. Supplied by Vaqora Chemicals with COA, exported worldwide.
Pack sizesPrice on quotation · bulk available
10 mg
25 mg
50 mg
100 mg
250 mg
500 mg
1 g
Bulk / custom pack · kg to MT
Enquire Batch COA with every lot
16-section GHS SDS
Export to 120+ countries
DG-compliant packing
About Rivaroxaban EP Impurity G
Rivaroxaban EP Impurity G (CAS 446292-08-6) is a pharmacopeial impurity of Rivaroxaban offered by Vaqora Chemicals. Its molecular formula is C22H19N3O6 and its molecular weight is 421.4 g/mol. Systematically, it is named 2-[[(5S)-2-oxo-3-[4-(3-oxomorpholin-4-yl)phenyl]-1,3-oxazolidin-5-yl]methyl]isoindole-1,3-dione. Alternative names: Rivaroxaban Phthalimido Impurity and [3-(4-Chlorophenyl)phenyl]methylamine, HCl.
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.
Pharmaceutical QC and development laboratories use this impurity standard of Rivaroxaban to develop and validate HPLC methods, to set specification limits and to document impurity profiles in ANDA and DMF submissions. Typical end-use sectors are pharmaceutical manufacturing and academic and industrial research.
Available in 10 mg, 25 mg, 50 mg and 100 mg packs, Rivaroxaban EP Impurity G is dispatched with a Certificate of Analysis (COA) to destinations worldwide. This item is currently in stock for prompt 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 impuritiesGrade guides
Specifications & identifiers
| Product name | Rivaroxaban EP Impurity G |
|---|---|
| Catalogue No. | VQ-006661 |
| CAS Number | 446292-08-6 |
| IUPAC name | 2-[[(5S)-2-oxo-3-[4-(3-oxomorpholin-4-yl)phenyl]-1,3-oxazolidin-5-yl]methyl]isoindole-1,3-dione |
| Molecular formula | C22H19N3O6 |
| Molecular weight | 421.4 g/mol |
| Exact mass | 421.1274 |
| Grade | Reference Standard |
| HSN code | 38229090 |
| InChIKey | KUQNYAUTIWQAKY-MRXNPFEDSA-N |
| SMILES | C1COCC(=O)N1C2=CC=C(C=C2)N3C[C@@H](OC3=O)CN4C(=O)C5=CC=CC=C5C4=O |
| PubChem CID | 11690317 |
| Physical form | Solid |
|---|---|
| LogP (XLogP3) | 1.2 |
| H-bond donors / acceptors | 0 / 6 |
| TPSA | 96.5 Ų |
| Synonyms | (S)-2-((2-Oxo-3-(4-(3-oxomorpholino)phenyl)oxazolidin-5-yl)methyl)isoindoline-1,3-dione, Rivaroxaban Phthalimido Impurity, [3-(4-Chlorophenyl)phenyl]methylamine, HCl, 4-[4-[(5S)-5-Phthalimidomethyl-2-oxo-3-oxazolidinyl]phenyl]-3-morpholinone, (S)-2-({2-oxo-3-[4-(3-oxomorpholino)phenyl]oxazolidin-5-yl}methyl)isoindoline-1,3-dione, Rivaroxaban Impurity D, Rivaroxaban Intermediates II, Rivaroxaban Related Compound G, CS-M0563, (S)-2-((2-Oxo-3-(4-(3-oxomorph, (S)-2 ((2-oxo-3-(4-(3-oxomorpholino)phenyl)oxazolidin-5-yl)methyl)isoindoline-1,3-dione, (S)-2((2-oxo-3-(4-(3-oxomorpholino)phenyl)oxazolidin-5-yl)methyl)isoindoline-1,3-dione |
Safety & hazard information (GHS)
Hazard statements
H411Toxic to aquatic life with long lasting effects
Precautionary statements: P273, P391, 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 G?
The CAS Registry Number of Rivaroxaban EP Impurity G is 446292-08-6. It is also known as (S)-2-((2-Oxo-3-(4-(3-oxomorpholino)phenyl)oxazolidin-5-yl)methyl)isoindoline-1,3-dione, Rivaroxaban Phthalimido Impurity, [3-(4-Chlorophenyl)phenyl]methylamine, HCl.
What is the molecular formula and molecular weight of Rivaroxaban EP Impurity G?
Rivaroxaban EP Impurity G has the molecular formula C22H19N3O6 and a molecular weight of 421.4 g/mol. Its IUPAC name is 2-[[(5S)-2-oxo-3-[4-(3-oxomorpholin-4-yl)phenyl]-1,3-oxazolidin-5-yl]methyl]isoindole-1,3-dione.
What is Rivaroxaban EP Impurity G used for?
Rivaroxaban EP Impurity G 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 G can I order?
We supply Rivaroxaban EP Impurity G in Reference Standard grade, in 10 mg, 25 mg, 50 mg, 100 mg, 250 mg, 500 mg packs. Larger bulk quantities and custom packing are quoted on request.
Do you provide a COA and SDS with Rivaroxaban EP Impurity G?
Yes. Every lot of Rivaroxaban EP Impurity G 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 G be shipped internationally?
Yes. Rivaroxaban EP Impurity G 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.
Enquire about Rivaroxaban EP Impurity G
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