Oseltamivir Impurity 137 CAS CATO-C4X-1720137

Purity 97%+In StockPharmacopoeial Impurity Standards
CAS No.CATO-C4X-1720137
Molecular FormulaC17H31NO4
Molecular Weight313.43 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Oseltamivir Impurity 137 CAS CATO-C4X-1720137 chemical structure

Description

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 supplies Oseltamivir Impurity 137 (CAS CATO-C4X-1720137), a pharmacopoeial impurity reference standard (molecular formula C17H31NO4, MW 313.43 g/mol) used for the identification and quantification of trace impurities in APIs.

Oseltamivir Impurity 137 (C17H31NO4) contains an amide group, a carboxylic acid group, a hydroxyl group, an ether linkage. The carboxyl group imparts weak acidity; 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).

CATO manufactures Oseltamivir Impurity 137 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 FormulaC17H31NO4
Molecular Weight313.43 g/mol
AppearanceWhite to pale yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)3.0
UV AbsorptionUV-absorbing
Nitrogen Atoms1

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