(1R,3r,5S)-Ipratropium Impurity 35 CAS 88607-15-2

Description

Compared with other compounds in its class, the molecular weight of 287.40 g/mol gives (1R,3r,5S)-Ipratropium Impurity 35 distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies (1R,3r,5S)-Ipratropium Impurity 35 (CAS 88607-15-2), a pharmacopoeial impurity reference standard (molecular formula C18H25NO2, MW 287.40 g/mol) used for the identification and quantification of trace impurities in APIs.

Owing to a steroid core, an amide group, a hydroxyl group, an ether linkage, (1R,3r,5S)-Ipratropium Impurity 35 is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 287.40 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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), (1R,3r,5S)-Ipratropium Impurity 35 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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