Metoprolol Tartrate
| Nombre del producto | Metoprolol Tartrate |
|---|---|
| Número CAS | 56392-17-7 |
| Fórmula molecular | C15H25NO3·½C4H6O6 |
| Peso molecular | 684.82 g/mol (as tartrate salt) |
| Apariencia | Polvo cristalino de color blanco a blanquecino |
| Ensayo (HPLC) | 98.5% – 101.5% (on dried basis) |
| Pérdida por secado | ≤ 0,51 TP3T |
| Residuo tras la combustión | ≤ 0,11 TP3T |
| Metales pesados | ≤ 20 ppm |
| Solubilidad | Soluble in water, methanol; slightly soluble in ethanol |
| Tamaño de las partículas | D90 ≤ 50 µm (customizable) |
| Paquete | 25 kg fiber drum with double polyethylene liner |
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Sinónimos: Metoprolol tartrate, 56392-17-7, 1-[4-(2-Methoxyethyl)phenoxy]-3-[(1-methylethyl)amino]-2-propanol tartrate, CGP 2175E, Lopressor, Seloken, Betaloc
Metoprolol tartrate is a cardioselective beta-1 adrenergic receptor blocker, structurally characterized by a phenoxypropanolamine core with a methoxyethyl side chain. This molecular configuration confers high affinity for beta-1 receptors located primarily in cardiac tissue, with minimal activity at beta-2 receptors in the lungs and vasculature. The tartrate salt enhances aqueous solubility, facilitating oral and parenteral formulation development.
As a second-generation beta-blocker, metoprolol tartrate is widely prescribed for hypertension, angina pectoris, and heart failure. It is also used in the management of arrhythmias and as an adjunct in myocardial infarction. The compound is available in immediate-release and extended-release forms, with the tartrate salt predominantly used in immediate-release tablets and injection solutions.
For pharmaceutical manufacturers, metoprolol tartrate API offers a well-established synthesis route and consistent crystalline form, ensuring reliable tableting and dissolution performance. Its compatibility with common excipients and stability under typical storage conditions make it a preferred choice for generic and branded formulations alike.
Metoprolol tartrate is a white to off-white crystalline powder with a molecular weight of 684.82 g/mol (as the tartrate salt). It is freely soluble in water and methanol, slightly soluble in ethanol, and practically insoluble in acetone. The tartrate counterion contributes to its stability and solubility profile, which is critical for injectable and oral solid dosage forms. The compound exists as a racemic mixture, with the S-enantiomer carrying the primary beta-blocking activity.
| Parámetro | Especificaciones |
|---|---|
| Ensayo (HPLC) | 98.5% – 101.5% |
| Pérdida por secado | ≤ 0,51 TP3T |
| Residuo tras la combustión | ≤ 0,11 TP3T |
| Metales pesados | ≤ 20 ppm |
| Sustancias relacionadas | Total impurities ≤ 0.5% |
| Disolventes residuales | Meets ICH Q3C limits |
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