| CAS No. | CATO-C4X-214429 |
| Molecular Formula | HRbS |
| Molecular Weight | N/A |
| Category | Pharmacopoeial Impurity Standards / EP Impurities |
| Availability | In Stock |
The occurrence of Relebactam Impurity 29 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, Relebactam Impurity 29 (CAS CATO-C4X-214429, N/A) is essential for impurity profiling, related-substances testing, and forced-degradation studies in pharmaceutical development.
Relebactam Impurity 29 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 Relebactam Impurity 29 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 | HRbS C4H9NS C7H16 C7H15A2 C2H6 |
| Molecular Weight | 451.19 g/mol |
| Purity | 95% |
| Storage | Store at room temperature, protect from light |
| Solubility (reference) | Soluble in chloroform, dichloromethane, ethyl acetate |
| Stability | Light-sensitive; avoid direct strong light |
| Degree of Unsaturation (DBE) | -2.0 |
| Nitrogen Atoms | 1 |
| Sulfur Atoms | 2 |