| CAS No. | 75172-11-1 |
| Molecular Formula | C4H8O2S |
| Molecular Weight | 120.17 g/mol |
| Category | Pharmacopoeial Impurity Standards / EP Impurities |
| Availability | In Stock |
As a certified reference material (CRM), Captopril Impurity 36 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.
As a process- or degradation-related impurity, Captopril Impurity 36 (CAS 75172-11-1, C4H8O2S) is essential for impurity profiling, related-substances testing, and forced-degradation studies in pharmaceutical development.
Owing to a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, Captopril Impurity 36 is typically white to off-white liquid. Its solid-state physicochemical attributes — including a molecular weight of 120.17 g/mol — guide the selection of appropriate sample preparation and analytical techniques.
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 | C4H8O2S |
| Molecular Weight | 120.17 g/mol |
| Purity | 97%+ |
| 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.) | 1978 |
| Sulfur Atoms | 1 |