| CAS No. | 2819-48-9 |
| Molecular Formula | C8H12 |
| Molecular Weight | 108.18 g/mol |
| Category | Pharmacopoeial Impurity Standards / EP Impurities |
| Availability | In Stock |
The occurrence of Lurasidone Impurity 16 is closely related to an organic framework in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.
CATO supplies Lurasidone Impurity 16 (CAS 2819-48-9), a pharmacopoeial impurity reference standard (molecular formula C8H12, MW 108.18 g/mol) used for the identification and quantification of trace impurities in APIs.
Owing to an organic framework, Lurasidone Impurity 16 is typically white to off-white liquid. Its solid-state physicochemical attributes — including a molecular weight of 108.18 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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 Lurasidone Impurity 16 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.
| Molecular Formula | C8H12 |
| Molecular Weight | 108.18 g/mol |
| Purity | ~75% |
| Storage | Store at 2-8°C |
| Solubility (reference) | Soluble in methanol, acetonitrile, DMSO |
| Stability | Stable under recommended storage conditions |
| Degree of Unsaturation (DBE) | 3.0 |
| UV Absorption | UV-absorbing |
| CAS Registry Year (est.) | 1957 |