Oseltamivir Impurity 158 CAS CATO-C4X-1720158

Purity >95%In StockPharmacopoeial Impurity Standards
CAS No.CATO-C4X-1720158
Molecular FormulaC9H14O9S2
Molecular Weight330.33 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Oseltamivir Impurity 158 CAS CATO-C4X-1720158 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.

As a process- or degradation-related impurity, Oseltamivir Impurity 158 (CAS CATO-C4X-1720158, C9H14O9S2) is essential for impurity profiling, related-substances testing, and forced-degradation studies in pharmaceutical development.

Oseltamivir Impurity 158 (C9H14O9S2) contains a carbohydrate-derived structure, a sulfone group. It is notably hygroscopic, 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 158 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 FormulaC9H14O9S2
Molecular Weight330.33 g/mol
Purity>95%
StorageStore in a cool place (≤25°C), keep sealed and dry
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)3.0
UV AbsorptionUV-absorbing
Sulfur Atoms2

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