Oseltamivir Impurity 161 CAS CATO-C4X-1720161

Purity >95%In StockPharmacopoeial Impurity Standards
CAS No.CATO-C4X-1720161
Molecular FormulaC8H12O7S
Molecular Weight252.24 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Oseltamivir Impurity 161 CAS CATO-C4X-1720161 chemical structure

Description

The molecular framework of Oseltamivir Impurity 161 (C8H12O7S) is characterized by a carbohydrate-derived structure, a sulfone group. In reversed-phase chromatography, its retention is governed primarily by the polarity and ionization state of its functional groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. 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 supplies Oseltamivir Impurity 161 (CAS CATO-C4X-1720161), a pharmacopoeial impurity reference standard (molecular formula C8H12O7S, MW 252.24 g/mol) used for the identification and quantification of trace impurities in APIs.

Recommended for quantitative analysis by HPLC, GC, LC-MS/MS, or GC-MS as an external calibration standard; it can also be used for spiked-recovery experiments, LOD/LOQ determination, and LC-MS/MS multiple-reaction-monitoring (MRM) calibration.

CATO manufactures Oseltamivir Impurity 161 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 FormulaC8H12O7S
Molecular Weight252.24 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 Atoms1

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