| CAS No. | 2044-27-1 |
| Molecular Formula | C6H7NS |
| Molecular Weight | 125.19 g/mol |
| Category | Pharmacopoeial Impurity Standards / EP Impurities |
| Availability | In Stock |
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.
CATO supplies Epinastine Impurity 37 (CAS 2044-27-1), a pharmacopoeial impurity reference standard (molecular formula C6H7NS, MW 125.19 g/mol) used for the identification and quantification of trace impurities in APIs.
Owing to a nitrile group, sulfur-containing functionality, an aromatic ring system, Epinastine Impurity 37 is typically off-white to pale yellow liquid. Its solid-state physicochemical attributes — including a molecular weight of 125.19 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.
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.
| Molecular Formula | C6H7NS |
| Molecular Weight | 125.19 g/mol |
| Purity | 97%+ |
| Storage | Store at 2-8°C, protect from light |
| Solubility (reference) | Soluble in methanol, acetonitrile, DMSO |
| Stability | Light-sensitive; avoid direct strong light |
| Degree of Unsaturation (DBE) | 4.0 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| CAS Registry Year (est.) | 1957 |
| Nitrogen Atoms | 1 |
| Sulfur Atoms | 1 |