Dexchlorpheniramine Impurity 6 CAS CATO-C4X-16116

Description

Compared with other compounds in its class, the molecular weight of 289.76 g/mol gives Dexchlorpheniramine Impurity 6 distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies Dexchlorpheniramine Impurity 6 (CAS CATO-C4X-16116), a pharmacopoeial impurity reference standard (molecular formula C15H16ClN3O, MW 289.76 g/mol) used for the identification and quantification of trace impurities in APIs.

Dexchlorpheniramine Impurity 6 (C15H16ClN3O) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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.

As a certified reference material (CRM), Dexchlorpheniramine Impurity 6 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.

Physical & Chemical Properties

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