| CAS No. | CATO-C4X-155315 |
| Molecular Formula | - |
| Molecular Weight | N/A |
| Category | Pharmacopoeial Impurity Standards / EP Impurities |
| Availability | In Stock |
The occurrence of Bacitracin Impurity O is closely related to a structurally diverse molecular composition in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.
As a process- or degradation-related impurity, Bacitracin Impurity O (CAS CATO-C4X-155315, N/A) is essential for impurity profiling, related-substances testing, and forced-degradation studies in pharmaceutical development.
Bacitracin Impurity O 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.
The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.
| Molecular Formula | C7H18A2LuP C6H11A2N3S C4H8A2 C2H6 CH4 |
| Molecular Weight | 567.62 g/mol |
| Purity | 95% |
| Storage | Store at room temperature, protect from light |
| Solubility (reference) | Soluble in DMSO, DMF, methanol |
| Stability | Light-sensitive; avoid direct strong light |
| Degree of Unsaturation (DBE) | -1.0 |
| Nitrogen Atoms | 3 |
| Sulfur Atoms | 1 |