Edoxaban Impurity 32 CAS 1461714-66-8

Purity 97%+In StockPharmacopoeial Impurity Standards
CAS No.1461714-66-8
Molecular FormulaC15H18N4OS2
Molecular Weight334.46 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Edoxaban Impurity 32 CAS 1461714-66-8 chemical structure

Description

CATO supplies Edoxaban Impurity 32 (CAS 1461714-66-8), a pharmacopoeial impurity reference standard (molecular formula C15H18N4OS2, MW 334.46 g/mol) used for the identification and quantification of trace impurities in APIs.

Edoxaban Impurity 32 (C15H18N4OS2) contains a nitrogen-containing heterocyclic scaffold, an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage. Its physicochemical properties are representative of its class; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

This reference standard supports related-substances testing and method development in line with ICH Q3A/Q3B guidance on impurity control, and is suitable for system suitability testing and forced-degradation studies.

CATO manufactures Edoxaban Impurity 32 under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC15H18N4OS2
Molecular Weight334.46 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1992
Nitrogen Atoms4
Sulfur Atoms2

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