| CAS No. | 86632-33-9 |
| Molecular Formula | C44H32O2P2 |
| Molecular Weight | 654.67 g/mol |
| Category | Pharmacopoeial Impurity Standards / EP Impurities |
| Availability | In Stock |
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.
| Molecular Formula | C44H32O2P2 |
| Molecular Weight | 654.67 g/mol |
| Purity | >95% |
| Storage | Store at room temperature, protect from light |
| Solubility (reference) | Soluble in chloroform, dichloromethane, ethyl acetate, DMSO |
| Stability | May oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light |
| Degree of Unsaturation (DBE) | 29.0 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| CAS Registry Year (est.) | 1981 |