| CAS No. | 3205-34-3 |
| Molecular Formula | C8H16O2 |
| Molecular Weight | 144.21 g/mol |
| Category | Pharmacopoeial Impurity Standards / EP Impurities |
| Availability | In Stock |
Owing to a carboxylic acid group, a hydroxyl group, an ether linkage, Lurasidone Impurity 41 is typically white to off-white liquid. Its solid-state physicochemical attributes — including a molecular weight of 144.21 g/mol — guide the selection of appropriate sample preparation and analytical techniques.
Lurasidone Impurity 41 (CAS 3205-34-3) is a certified pharmaceutical impurity reference standard with the molecular formula C8H16O2 and a molecular weight of 144.21 g/mol.
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 41 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 | C8H16O2 |
| Molecular Weight | 144.21 g/mol |
| Purity | >95% |
| Storage | Store at 2-8°C |
| Solubility (reference) | Soluble in methanol, acetonitrile, DMSO, water (slightly soluble) |
| Stability | Stable under recommended storage conditions |
| Degree of Unsaturation (DBE) | 1.0 |
| CAS Registry Year (est.) | 1957 |