| CAS No. | 43076-61-5 |
| Molecular Formula | C14H19ClO |
| Molecular Weight | 238.76 g/mol |
| Category | Pharmacopoeial Impurity Standards / EP Impurities |
| Availability | In Stock |
CATO manufactures Ebastine Impurity N2 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.
Ebastine Impurity N2 (CAS 43076-61-5) is a certified pharmaceutical impurity reference standard with the molecular formula C14H19ClO and a molecular weight of 238.76 g/mol.
Owing to a hydroxyl group, an ether linkage, chlorine substitution, an aromatic ring system, Ebastine Impurity N2 is typically off-white to pale yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 238.76 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).
Recommended for quantitative analysis by HPLC, GC, LC-MS/MS, or GC-MS as an external calibration standard; it can also be used for spiked-recovery experiments, LOD/LOQ determination, and LC-MS/MS multiple-reaction-monitoring (MRM) calibration.
| Molecular Formula | C14H19ClO |
| Molecular Weight | 238.76 g/mol |
| Purity | 97%+ |
| Storage | Store at room temperature, keep tightly closed to prevent evaporation |
| Solubility (reference) | Soluble in chloroform, dichloromethane, ethyl acetate, DMSO |
| Stability | May oxidize slowly on prolonged air exposure |
| Degree of Unsaturation (DBE) | 5.0 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| CAS Registry Year (est.) | 1969 |
| Halogen Content | Cl-containing |