| CAS No. | 140459-96-7 |
| Molecular Formula | C10H16O4 |
| Molecular Weight | 200.23 g/mol |
| Category | Pharmacopoeial Impurity Standards / EP Impurities |
| Availability | In Stock |
Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including Lurasidone Impurity N87.
Lurasidone Impurity N87 (CAS 140459-96-7) is a certified pharmaceutical impurity reference standard with the molecular formula C10H16O4 and a molecular weight of 200.23 g/mol.
Owing to a carboxylic acid group, a hydroxyl group, an ether linkage, Lurasidone Impurity N87 is typically white to off-white crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 200.23 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 N87 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 | C10H16O4 |
| Molecular Weight | 200.23 g/mol |
| Purity | 97%+ |
| Storage | Store in a cool place (≤25°C), keep sealed and dry |
| Solubility (reference) | Soluble in methanol, ethanol, DMSO |
| Stability | May oxidize slowly on prolonged air exposure; Hygroscopic; reseal immediately after opening |
| Degree of Unsaturation (DBE) | 3.0 |
| UV Absorption | UV-absorbing |
| CAS Registry Year (est.) | 1997 |