| CAS No. | 21003-56-5 |
| Molecular Formula | C16H19N |
| Molecular Weight | 225.33 g/mol |
| Category | Pharmacopoeial Impurity Standards / EP Impurities |
| Availability | In Stock |
Compared with other compounds in its class, the molecular weight of 225.33 g/mol gives Tamsulosin Impurity 16 distinctive chromatographic separation conditions and mass-spectrometry parameter settings.
Tamsulosin Impurity 16 (CAS 21003-56-5) is a certified pharmaceutical impurity reference standard with the molecular formula C16H19N and a molecular weight of 225.33 g/mol.
Owing to a nitrogen-containing heterocyclic scaffold, a nitrile group, Tamsulosin Impurity 16 is typically pale yellow to yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 225.33 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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.
As a certified reference material (CRM), Tamsulosin Impurity 16 meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.
| Molecular Formula | C16H19N |
| Molecular Weight | 225.33 g/mol |
| Purity | 97%+ |
| Storage | Store at 2-8°C, protect from light |
| Solubility (reference) | Soluble in chloroform, dichloromethane, ethyl acetate |
| Stability | Light-sensitive; avoid direct strong light |
| Degree of Unsaturation (DBE) | 8.0 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| CAS Registry Year (est.) | 1963 |
| Nitrogen Atoms | 1 |