| CAS No. | CATO-C4X-155317 |
| Molecular Formula | C9H17N3S |
| Molecular Weight | N/A |
| Category | Pharmacopoeial Impurity Standards / EP Impurities |
| Availability | In Stock |
Compared with other compounds in its class, the molecular weight of N/A g/mol gives Bacitracin Impurity Q distinctive chromatographic separation conditions and mass-spectrometry parameter settings.
Bacitracin Impurity Q (CAS CATO-C4X-155317) is a certified pharmaceutical impurity reference standard with the molecular formula N/A and a molecular weight of N/A g/mol.
Bacitracin Impurity Q 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.
CATO manufactures Bacitracin Impurity Q under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.
| Molecular Formula | C9H17N3S C6H15P C5H12 CH5N 2*C2H6 H2A3HeN CH4 |
| Molecular Weight | 486.82 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) | -3.0 |
| Nitrogen Atoms | 5 |
| Sulfur Atoms | 1 |