Siponimod impurity 34 CAS CATO-C4X-247234

Purity 97%+In StockPharmacopoeial Impurity Standards
CAS No.CATO-C4X-247234
Molecular FormulaC33H39F3N2O7
Molecular WeightN/A
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Siponimod impurity 34 CAS CATO-C4X-247234 chemical structure

Description

As a certified reference material (CRM), Siponimod impurity 34 meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

CATO supplies Siponimod impurity 34 (CAS CATO-C4X-247234), a pharmacopoeial impurity reference standard (molecular formula C33H39F3N2O7C2HF3O2, MW 746.70 g/mol) used for the identification and quantification of trace impurities in APIs.

Siponimod impurity 34 (C33H39F3N2O7C2HF3O2) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine substitution. It is notably hygroscopic, halogen substitution raises its density and boiling point, 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).

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.

Physical & Chemical Properties

Molecular FormulaC33H39F3N2O7 C2HF3O2
Molecular Weight746.70 g/mol
Purity97%+
StorageStore in a cool place (≤25°C), protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)14.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
Halogen ContentF-containing
Nitrogen Atoms2

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