Deucravacitinib Impurity 6 CAS CATO-C4X-31386

Purity 97%+In StockPharmacopoeial Impurity Standards
CAS No.CATO-C4X-31386
Molecular FormulaC10H12N4O
Molecular Weight204.23 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Deucravacitinib Impurity 6 CAS CATO-C4X-31386 chemical structure

Description

CATO supplies Deucravacitinib Impurity 6 (CAS CATO-C4X-31386), a pharmacopoeial impurity reference standard (molecular formula C10H12N4O, MW 204.23 g/mol) used for the identification and quantification of trace impurities in APIs.

Deucravacitinib Impurity 6 (C10H12N4O) contains a nitrogen-containing heterocyclic scaffold, an amide group, 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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC10H12N4O
Molecular Weight204.23 g/mol
AppearanceOff-white to pale yellow crystalline powder. (faint amine-like odor)
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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
Nitrogen Atoms4

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