| CAS No. | 31599-25-4 |
| Molecular Formula | C12H10N6 |
| Molecular Weight | 238.25 g/mol |
| Category | Pharmacopoeial Impurity Standards / EP Impurities |
| Availability | In Stock |
Compared with other compounds in its class, the molecular weight of 238.25 g/mol gives Topiroxostat Impurity 25 distinctive chromatographic separation conditions and mass-spectrometry parameter settings.
Topiroxostat Impurity 25 (CAS 31599-25-4) is a certified pharmaceutical impurity reference standard with the molecular formula C12H10N6 and a molecular weight of 238.25 g/mol.
Owing to a nitrogen-containing heterocyclic scaffold, a nitrile group, Topiroxostat Impurity 25 is typically pale yellow to yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 238.25 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).
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 Topiroxostat Impurity 25 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 | C12H10N6 |
| Molecular Weight | 238.25 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) | 11.0 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| CAS Registry Year (est.) | 1966 |
| Nitrogen Atoms | 6 |