| CAS No. | 2962831-00-9 |
| 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 Isavuconazole Impurity 138.
As a process- or degradation-related impurity, Isavuconazole Impurity 138 (CAS 2962831-00-9, N/A) is essential for impurity profiling, related-substances testing, and forced-degradation studies in pharmaceutical development.
Isavuconazole Impurity 138 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).
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), Isavuconazole Impurity 138 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 |
| CAS Registry Year (est.) | 2004 |