Metoprolol Tartrate
| Tên sản phẩm | Metoprolol Tartrate |
|---|---|
| Số CAS | 56392-17-7 |
| Công thức phân tử | C15H25NO3·½C4H6O6 |
| Trọng lượng phân tử | 684.82 g/mol (as tartrate salt) |
| Hình thức | Bột tinh thể màu trắng đến trắng ngà |
| Phương pháp phân tích (HPLC) | 98.5% – 101.5% (on dried basis) |
| Mất mát khi sấy khô | ≤ 0,5% |
| Hàm lượng tro sau khi đốt | ≤ 0,1% |
| Kim loại nặng | ≤ 20 ppm |
| Độ hòa tan | Soluble in water, methanol; slightly soluble in ethanol |
| Kích thước hạt | D90 ≤ 50 µm (customizable) |
| Gói | 25 kg fiber drum with double polyethylene liner |
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Từ đồng nghĩa: 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.
| Tham số | Thông số kỹ thuật |
|---|---|
| Phương pháp phân tích (HPLC) | 98.5% – 101.5% |
| Mất mát khi sấy khô | ≤ 0,5% |
| Hàm lượng tro sau khi đốt | ≤ 0,1% |
| Kim loại nặng | ≤ 20 ppm |
| Các chất liên quan | Total impurities ≤ 0.5% |
| Chất dung môi còn lại | Meets ICH Q3C limits |
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