Vortioxetine Impurity 7 CAS CATO-C4X-10567

Purity 97%+In StockPharmacopoeial Impurity Standards
CAS No.CATO-C4X-10567
Molecular FormulaC22H22S2
Molecular Weight350.54 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Vortioxetine Impurity 7 CAS CATO-C4X-10567 chemical structure

Description

As a process- or degradation-related impurity, Vortioxetine Impurity 7 (CAS CATO-C4X-10567, C22H22S2) is essential for impurity profiling, related-substances testing, and forced-degradation studies in pharmaceutical development.

Owing to sulfur-containing functionality, a polycyclic aromatic system, Vortioxetine Impurity 7 is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 350.54 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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.

As a certified reference material (CRM), Vortioxetine Impurity 7 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.

Physical & Chemical Properties

Molecular FormulaC22H22S2
Molecular Weight350.54 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
Sulfur Atoms2

Related Vortioxetine Standards

Recommended Standards

Why CATO?