Rivaroxaban EP Impurity I

Name: Rivaroxaban EP Impurity I
Brand: Vaqora Chemicals
SKU: VQ-023663

About Rivaroxaban EP Impurity I

Rivaroxaban EP Impurity I (CAS 1151893-81-0) is a pharmacopeial impurity of Rivaroxaban offered by Vaqora Chemicals. Formula C24H21Cl2N3O7S2, molecular weight 598.5 g/mol. Common synonyms include Rivaroxaban Impurity and Rivaroxaban Impurity Vii(Potential Impurity).

It is supplied as a solid. Keep the vial tightly closed, protected from light and humidity, at the temperature stated on the Certificate of Analysis. Handle it with standard laboratory precautions and appropriate personal protective equipment.

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.

Standard pack sizes are 10 mg, 25 mg, 50 mg and 100 mg, and every batch ships with a Certificate of Analysis (COA) and we export worldwide.

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 I
Catalogue No.	VQ-023663
CAS Number	1151893-81-0
IUPAC name	2-[2-[N-(5-chlorothiophene-2-carbonyl)-4-[(5S)-5-[[(5-chlorothiophene-2-carbonyl)amino]methyl]-2-oxo-1,3-oxazolidin-3-yl]anilino]ethoxy]acetic acid
Molecular formula	C₂₄H₂₁Cl₂N₃O₇S₂
Molecular weight	598.5 g/mol
Exact mass	597.0198
Grade	Reference Standard
HSN code	38229090
InChIKey	XEOFNNZMYBBFPT-INIZCTEOSA-N
SMILES	C1[C@@H](OC(=O)N1C2=CC=C(C=C2)N(CCOCC(=O)O)C(=O)C3=CC=C(S3)Cl)CNC(=O)C4=CC=C(S4)Cl
PubChem CID	57572379

Physical properties
Physical form	Solid
LogP (XLogP3)	4.9
H-bond donors / acceptors	2 / 9
TPSA	182 Å²
Synonyms	Rivaroxaban Impurity, Rivaroxaban N-hydrolyse N-5-chlorothiophene-2-carbaldehyde, Rivaroxaban Impurity Vii(Potential Impurity), Rivaroxaban-10, Rivaroxaban impurity K: diamine

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 I?

The CAS Registry Number of Rivaroxaban EP Impurity I is 1151893-81-0. It is also known as Rivaroxaban Impurity, Rivaroxaban N-hydrolyse N-5-chlorothiophene-2-carbaldehyde, Rivaroxaban Impurity Vii(Potential Impurity).

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

Rivaroxaban EP Impurity I has the molecular formula C24H21Cl2N3O7S2 and a molecular weight of 598.5 g/mol. Its IUPAC name is 2-[2-[N-(5-chlorothiophene-2-carbonyl)-4-[(5S)-5-[[(5-chlorothiophene-2-carbonyl)amino]methyl]-2-oxo-1,3-oxazolidin-3-yl]anilino]ethoxy]acetic acid.

What is Rivaroxaban EP Impurity I used for?

Rivaroxaban EP Impurity I 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 I can I order?

We supply Rivaroxaban EP Impurity I in Reference Standard grade, in 10 mg, 25 mg, 50 mg, 100 mg packs. Larger bulk quantities and custom packing are quoted on request.

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

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

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