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CAS RN: 87848-99-5 | 產品號碼: A2764
| 產品號碼 | A2764 |
| 純度/分析方法 | >98.0%(HPLC) |
| 分子式 / 分子量 | C__2__2H__2__4N__2O__2 = 348.45 |
| 外觀與形狀（20°C） | Solid |
| 儲存條件 | Refrigerated (0-10°C) |
| 應避免的情況 | Heat Sensitive |
| 包裝和容器 | 100MG-Glass Bottle with Plastic Insert （閲覽圖片）, 20MG-Glass Bottle with Plastic Insert （閲覽圖片） |
| CAS RN | 87848-99-5 |
| Reaxys-RN | 6739893 |
| Merck Index(14) | 127 |
| MDL編號 | MFCD00869830 |
產品規格
| Appearance | White to Almost white powder to crystal |
| Purity(HPLC) | min. 98.0 area% |
| Elemental analysis(Nitrogen) | 7.50 to 8.50 % |
性質
| 熔點 | 215 °C(dec.) |
GHS
| 危險性說明 | H413 : May cause long lasting harmful effects to aquatic life. |
| 防範說明 | P501 : Dispose of contents/ container to an approved waste disposal plant. P273 : Avoid release to the environment. |
相關法規
| RTECS # | UD3474000 |
運輸資料
| HS編碼* | 2933.39-000 |
Application
Acrivastine: A Short Acting Histamine H1-Receptor Antagonist
Acrivastine is a short acting histamine H1-receptor antagonist. It has been reported that acrivastine have a short terminal elimination half-life [1.7-h] and an 8-h duration of action in humans. (The product is for research purpose only.)
References
- The acute effects of acrivastine (BW825C), a new antihistamine, compared with triprolidine on measures of central nervous system performance and subjective effects
- Clinical pharmacology of new histamine H1 receptor antagonists (a review)
- Delineation of receptor-ligand interactions at the human histamine H1 receptor by a combined approach of site-directed mutagenesis and computational techniques - or - how to bind the H1 receptor
- Simultaneous analysis of the H1-antihistamine acrivastine and the decongestant pseudoephedrine hydrochloride by high-performance liquid chromatography
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