| CAS No. | 20225-24-5 |
| Molecular Formula | C7H14O2 |
| Molecular Weight | 130.18 g/mol |
| Category | Pharmacopoeial Impurity Standards / EP Impurities |
| Availability | In Stock |
As a certified reference material (CRM), Sodium Valproate EP Impurity B 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.
Sodium Valproate EP Impurity B (CAS 20225-24-5) is a certified pharmaceutical impurity reference standard with the molecular formula C7H14O2 and a molecular weight of 130.18 g/mol.
Based on its molecular formula C7H14O2, Sodium Valproate EP Impurity B contains 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 130.18 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry.
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 | C7H14O2 |
| Molecular Weight | 130.18 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.) | 1962 |