Lercanidipine Impurity 17 CAS CATO-C4X-136417

Description

Compared with other compounds in its class, the molecular weight of 690.28 g/mol gives Lercanidipine Impurity 17 distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies Lercanidipine Impurity 17 (CAS CATO-C4X-136417), a pharmacopoeial impurity reference standard (molecular formula C39H47N3O6HCl, MW 690.28 g/mol) used for the identification and quantification of trace impurities in APIs.

Lercanidipine Impurity 17 (C39H47N3O6HCl) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine 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).

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), Lercanidipine Impurity 17 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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