Tenofovir disoproxil Impurity 116 CAS 2241284-68-2

Description

The occurrence of Tenofovir disoproxil Impurity 116 is closely related to a nitrogen-containing heterocyclic scaffold, 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 116 (CAS 2241284-68-2) is a certified pharmaceutical impurity reference standard with the molecular formula C39H60N10O20P2 and a molecular weight of 1050.90 g/mol.

Based on its molecular formula C39H60N10O20P2, Tenofovir disoproxil Impurity 116 contains a nitrogen-containing heterocyclic scaffold, an amide group, a phosphate ester group, a hydroxyl group, an ether linkage; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 1050.90 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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.

CATO manufactures Tenofovir disoproxil Impurity 116 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

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