Tenofovir disoproxil Impurity 17 CAS CATO-C4X-107617

Description

The occurrence of Tenofovir disoproxil Impurity 17 is closely related to a flavonoid core, an amide group, a phosphate ester group, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

Tenofovir disoproxil Impurity 17 (CAS CATO-C4X-107617) is a certified pharmaceutical impurity reference standard with the molecular formula C17H26N5O10PC4H4O4 and a molecular weight of 607.47 g/mol.

The molecular framework of Tenofovir disoproxil Impurity 17 (C17H26N5O10PC4H4O4) is characterized by a flavonoid core, an amide group, a phosphate ester group, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. 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).

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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

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