Maximum quantity allowed is 999
请选择数量
CAS RN: 52-49-3 | 产品编码: T3303
Trihexyphenidyl Hydrochloride
×
![]()
×
技术规格
| Appearance | White to Almost white powder to crystal |
| Purity(HPLC) | min. 98.0 area% |
| Purity(Nonaqueous Titration) | min. 98.0 % |
| NMR | confirm to structure |
物性（参考值）
| 熔点 | 247 °C(dec.) |
| 水溶性 | 微溶 |
| 在水中的溶解度 | 10 g/l 25 °C |
| 溶解性（可溶于） | 醇, 氯仿 |
GHS
| 象形图 |
|
| 信号词 | Warning |
| 危险性说明 | H302 : Harmful if swallowed. |
| 防范说明 | P501 : Dispose of contents/ container to an approved waste disposal plant. P270 : Do not eat, drink or smoke when using this product. P264 : Wash skin thoroughly after handling. P301 + P312 + P330 : IF SWALLOWED: Call a POISON CENTER/doctor if you feel unwell. Rinse mouth. |
相关法规
| RTECS# | TN2625000 |
运输信息
| HS编码* | 2933.39-000 |
应用
Trihexyphenidyl Hydrochloride: A M1 Muscarinic Cholinergic Receptor Antagonist
Trihexyphenidyl hydrochloride is a M1 muscarinic cholinergic receptor antagonist, and is used for the treatment of parkinsonian syndrome. The exact mechanism of action in parkinsonian syndromes is not precisely understood, but it is known that trihexyphenidyl has a direct anti-spasmodic effect on smooth muscles and a control effect on extrapyramidal disorders which may be caused by certain drugs acting on the central nervous system. (The product is for research purpose only.)
References
- Parkinsonism. Clinical and neuropharmacologic aspects
- Binding and functional profiles of the selective M1 muscarinic receptor antagonists trihexyphenidyl and dicyclomine
- Comparative behavioral and neurochemical activities of cholinergic antagonists in rats
- Selective M1 muscarinic receptor antagonists disrupt memory consolidation of inhibitory avoidance in rats
参考文献
TCIMail
产品文档 (部分产品的分析图谱无法提供，敬请谅解。)
化学品安全说明书(SDS)
请选择语言。
如需更多帮助，请联系我 们。
技术规格
CoA及其他文档
请输入批号
批号输入有误。请输入中横线前的4-5个字母数字字符。
示例 CoA
可下载CoA示例。注：该示例不一定是最新批次的CoA。
目前没有该产品的 CoA 示例。
分析图谱
请输入批号
批号输入有误。请输入中横线前的4-5个字母数字字符。
很抱歉，您搜索的分析图谱无法提供。