Clopidogrel Bisulfate
| パラメータ | 仕様 |
|---|---|
| 製品名 | Clopidogrel Bisulfate |
| CAS番号 | 120202-66-6 |
| 分子式 | C16H16ClNO2S·H2SO4 |
| 分子量 | 419.9 g/mol |
| 外観 | 白色からオフホワイトの結晶性粉末 |
| 分析(HPLC) | 98.0% – 102.0% (on dried basis) |
| 溶解度 | Soluble in water, methanol, and dimethyl sulfoxide; practically insoluble in hexane |
| パッケージ | 25 kgの繊維製ドラム缶(ポリエチレン製ライナー2重仕様) |
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同義語: Clopidogrel hydrogen sulfate, Plavix, Iscover, SR-25990C, Clopidogrel bisulphate
Clopidogrel bisulfate is the hydrogen sulfate salt of clopidogrel, a thienopyridine-class antiplatelet agent used to prevent thrombotic events in patients with cardiovascular disease. It was developed by Sanofi and Bristol-Myers Squibb and first approved in 1997 under the brand name Plavix. As an API, it is a white to off-white crystalline powder that is slightly soluble in water and freely soluble in methanol. The bisulfate salt form was chosen for its improved stability and aqueous solubility compared to the free base.
Chemically, clopidogrel bisulfate is a prodrug that requires hepatic metabolism to generate its active metabolite. The parent molecule contains a thienopyridine core with a chiral center at the benzylic position; only the S-enantiomer is pharmacologically active. The bisulfate salt is the (S)-(+)-enantiomer, and the presence of the sulfuric acid moiety contributes to its crystallinity and handling properties. It is typically supplied as a white powder with a characteristic crystalline structure, and its purity is critical for ensuring consistent therapeutic performance.
In the pharmaceutical industry, clopidogrel bisulfate is classified as a high-potency API and is primarily used in the manufacture of oral tablets. It is often combined with aspirin in fixed-dose combinations for dual antiplatelet therapy. The API is subject to stringent quality control, including enantiomeric purity and residual solvent testing, to meet pharmacopeial standards such as USP and EP. Its market demand remains strong due to the widespread use of clopidogrel in secondary prevention of atherothrombotic events.
| Test Item | 仕様 |
|---|---|
| 識別 | IR and HPLC retention time match reference standard |
| 乾燥減量 | ≤ 0.5% |
| 焼失残渣 | ≤ 0.1% |
| 重金属 | ≤ 20 ppm |
| Organic Impurities | Meet USP/EP requirements |
| 残留溶剤 | Meet ICH Q3C limits |
| Microbial Limits | Total aerobic count ≤ 1000 CFU/g; absence of specified pathogens |
Our standard MOQ is 1 kg. For larger quantities, we can offer competitive pricing.
Yes, we can provide samples for quality evaluation. Please contact us for details.
Lead time is typically 3-5 business days after order confirmation, depending on quantity and destination.
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