Penehyclidine Impurity 1 CAS 151673-92-6

Description

The occurrence of Penehyclidine Impurity 1 is closely related to a hydroxyl group, an ether linkage, an aromatic ring system in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies Penehyclidine Impurity 1 (CAS 151673-92-6), a pharmacopoeial impurity reference standard (molecular formula C13H16O, MW 188.27 g/mol) used for the identification and quantification of trace impurities in APIs.

Penehyclidine Impurity 1 (C13H16O) contains a hydroxyl group, an ether linkage, an aromatic ring system. Its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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.

As a certified reference material (CRM), Penehyclidine Impurity 1 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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