| CAS No. | CATO-C4X-155313 |
| 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 Bacitracin Impurity M.
As a process- or degradation-related impurity, Bacitracin Impurity M (CAS CATO-C4X-155313, N/A) is essential for impurity profiling, related-substances testing, and forced-degradation studies in pharmaceutical development.
Bacitracin Impurity M 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), Bacitracin Impurity M 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 | C10H18A2BN3O2S C3H8APS C2H6 CH4 |
| Molecular Weight | 408.39 g/mol |
| Purity | 95% |
| Storage | Store in a cool place (≤25°C), protect from light, keep sealed and dry |
| Solubility (reference) | Soluble in DMSO, DMF, methanol |
| Stability | Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening |
| Degree of Unsaturation (DBE) | 0.5 |
| Nitrogen Atoms | 3 |
| Sulfur Atoms | 2 |