Vonoprazan Impurity 229 CAS CATO-C4X-1020229

Purity 97%+In StockPharmacopoeial Impurity Standards
CAS No.CATO-C4X-1020229
Molecular FormulaC12H13FN2
Molecular WeightN/A
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Vonoprazan Impurity 229 CAS CATO-C4X-1020229 chemical structure

Description

CATO manufactures Vonoprazan Impurity 229 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.

CATO supplies Vonoprazan Impurity 229 (CAS CATO-C4X-1020229), a pharmacopoeial impurity reference standard (molecular formula C12H13FN2HCl, MW 240.71 g/mol) used for the identification and quantification of trace impurities in APIs.

Structurally, Vonoprazan Impurity 229 (C12H13FN2HCl) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, fluorine/chlorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 6.0, corresponding to approximately 6 ring(s) or double-bond equivalent(s). With a molecular weight of 240.71 g/mol, it falls into the medium-molecular-weight range. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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 FormulaC12H13FN2 HCl
Molecular Weight240.71 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
Halogen ContentF/Cl-containing
Nitrogen Atoms2

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