Prednisone EP Impurity D CAS 10184-69-7

Description

Compared with other compounds in its class, the molecular weight of 342.43 g/mol gives Prednisone EP Impurity D distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies Prednisone EP Impurity D (CAS 10184-69-7), a pharmacopoeial impurity reference standard (molecular formula C21H26O4, MW 342.43 g/mol) used for the identification and quantification of trace impurities in APIs.

The molecular framework of Prednisone EP Impurity D (C21H26O4) is characterized by a flavonoid core, 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).

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.

CATO manufactures Prednisone EP Impurity D under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Why CATO?

• ISO 17034 accredited reference material producer (CNAS + ANAB dual accreditation)
• 130,000+ catalog items in stock, COA supplied with every batch
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• Technical support: +86 18665070610 / Nicole.chen@cato-chem.com