| CAS No. | 1012-29-9 |
| Molecular Formula | C11H22N2 |
| Molecular Weight | 182.31 g/mol |
| Category | Pharmacopoeial Impurity Standards / EP Impurities |
| Availability | In Stock |
The occurrence of Cefazolin Impurity 58 is closely related to a nitrile group in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.
CATO supplies Cefazolin Impurity 58 (CAS 1012-29-9), a pharmacopoeial impurity reference standard (molecular formula C11H22N2, MW 182.31 g/mol) used for the identification and quantification of trace impurities in APIs.
Cefazolin Impurity 58 (C11H22N2) contains a nitrile group. Its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.
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 Cefazolin Impurity 58 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 | C11H22N2 |
| Molecular Weight | 182.31 g/mol |
| Purity | >95% |
| Storage | Store at 2-8°C, protect from light |
| Solubility (reference) | Soluble in DMSO, DMF, methanol |
| Stability | Light-sensitive; avoid direct strong light |
| Degree of Unsaturation (DBE) | 2.0 |
| CAS Registry Year (est.) | 1957 |
| Nitrogen Atoms | 2 |