Vortioxetine Impurity 114 CAS 86632-33-9

Purity >95%In StockPharmacopoeial Impurity Standards
CAS No.86632-33-9
Molecular FormulaC44H32O2P2
Molecular Weight654.67 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Vortioxetine Impurity 114 CAS 86632-33-9 chemical structure

Description

CATO manufactures Vortioxetine Impurity 114 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.

As a process- or degradation-related impurity, Vortioxetine Impurity 114 (CAS 86632-33-9, C44H32O2P2) is essential for impurity profiling, related-substances testing, and forced-degradation studies in pharmaceutical development.

Owing to organophosphorus functionality, a carboxylic acid group, a hydroxyl group, an ether linkage, a polycyclic aromatic system, Vortioxetine Impurity 114 is typically pale yellow to yellow amorphous powder. Its solid-state physicochemical attributes — including a molecular weight of 654.67 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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 FormulaC44H32O2P2
Molecular Weight654.67 g/mol
Purity>95%
StorageStore at room temperature, protect from light
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)29.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1981

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