| CAS No. | 186204-35-3 |
| Molecular Formula | C10H20O6S2 |
| Molecular Weight | 300.39 g/mol |
| Category | Pharmacopoeial Impurity Standards / EP Impurities |
| Availability | In Stock |
The occurrence of Lurasidone Impurity 40 is closely related to a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.
CATO supplies Lurasidone Impurity 40 (CAS 186204-35-3), a pharmacopoeial impurity reference standard (molecular formula C10H20O6S2, MW 300.39 g/mol) used for the identification and quantification of trace impurities in APIs.
Based on its molecular formula C10H20O6S2, Lurasidone Impurity 40 contains a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage; these features give the compound characteristic functional-group stretching vibrations in infrared spectroscopy. The molecular weight of 300.39 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry.
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), Lurasidone Impurity 40 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.
| Molecular Formula | C10H20O6S2 |
| Molecular Weight | 300.39 g/mol |
| Purity | >95% |
| Storage | Store in a cool place (≤25°C), keep sealed and dry |
| Solubility (reference) | Soluble in methanol, ethanol, DMSO |
| Stability | Hygroscopic; reseal immediately after opening |
| Degree of Unsaturation (DBE) | 1.0 |
| CAS Registry Year (est.) | 2010 |
| Sulfur Atoms | 2 |