| CAS No. | CATO-CAB-1050 |
| Molecular Formula | - |
| Molecular Weight | N/A |
| 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 Amlodipine Impurity G.
Amlodipine Impurity G (CAS CATO-CAB-1050) is a certified pharmaceutical impurity reference standard with the molecular formula N/A and a molecular weight of N/A g/mol.
Amlodipine Impurity G is supplied as a fully characterized reference material; its structural identity, assigned purity, and stability data are documented in the batch-specific Certificate of Analysis (COA).
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.
As a certified reference material (CRM), Amlodipine Impurity G 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.
| Purity | 97%+ |
| Storage | Store at 2-8°C |
| Solubility (reference) | Freely soluble in water |
| Stability | Stable under recommended storage conditions |