Paricalcitol lmpurity 40 CAS CATO-C4X-138740

Purity >95%In StockPharmacopoeial Impurity Standards
CAS No.CATO-C4X-138740
Molecular Formula2*C26H37O3PSi
Molecular WeightN/A
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Paricalcitol lmpurity 40 CAS CATO-C4X-138740 chemical structure

Description

As a certified reference material (CRM), Paricalcitol lmpurity 40 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.

As a process- or degradation-related impurity, Paricalcitol lmpurity 40 (CAS CATO-C4X-138740, C26H37O3PSi) is essential for impurity profiling, related-substances testing, and forced-degradation studies in pharmaceutical development.

The molecular framework of Paricalcitol lmpurity 40 (C26H37O3PSi) is characterized by a steroid core, a phosphonate group, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. 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 Formula2*C26H37O3PSi
Molecular Weight456.64 g/mol
AppearancePale yellow to yellow crystalline powder
Purity>95%
StorageStore at room temperature, protect from light, keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)8.5
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present

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