| CAS No. | CATO-C4X-224038 |
| Molecular Formula | C12H13N3 |
| Molecular Weight | 199.25 g/mol |
| Category | Pharmacopoeial Impurity Standards / EP Impurities |
| Availability | In Stock |
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.
Anagrelide Impurity 38 (CAS CATO-C4X-224038) is a certified pharmaceutical impurity reference standard with the molecular formula C12H13N3 and a molecular weight of 199.25 g/mol.
Owing to a nitrogen-containing heterocyclic scaffold, a nitrile group, Anagrelide Impurity 38 is typically pale yellow to yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 199.25 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).
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 | C12H13N3 |
| Molecular Weight | 199.25 g/mol |
| Purity | 97%+ |
| 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) | 8.0 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| Nitrogen Atoms | 3 |