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CAS RN: 50679-08-8 | 产品编码: T3977
Terfenadine

纯度/分析方法: >98.0%(HPLC)
别名:
- 特非那定
- α-[4-(1,1-二甲基乙基)苯基]-4-(羟基二苯基甲基)-1-哌啶丁醇
- 1-[4-(叔丁基)苯基]-4-[4-(羟基二苯基甲基)哌啶-1-基]丁-1-醇
- α-[4-(1,1-Dimethylethyl)phenyl]-4-(hydroxydiphenylmethyl)-1-piperidinebutanol
- 1-[4-(tert-butyl)phenyl]-4-[4-(hydroxydiphenylmethyl)piperidin-1-yl]butan-1-ol
产品文档:
产品编码 | T3977 |
纯度/分析方法 ![]() |
>98.0%(HPLC) |
分子式/分子量 | C__3__2H__4__1NO__2 = 471.69 |
外观与形状(20°C) | 固体 |
储存温度 ![]() |
冷藏 (0-10°C) |
储存在惰性气体下 | 存放于惰性气体之中 |
应避免的情况 | 空气,加热 |
包装和容器 ![]() |
1G-Glass Bottle with Plastic Insert (查看图片) |
CAS RN | 50679-08-8 |
Reaxys-RN | 5857899 |
PubChem物质ID | 468593048 |
MDL编号 | MFCD00079622 |
技术规格
Appearance | White to Light yellow powder to crystal |
Purity(HPLC) | min. 98.0 area% |
Melting point | 146.0 to 150.0 °C |
NMR | confirm to structure |
物性(参考值)
熔点 | 148 °C |
最大吸收波长 | 260 nm (EtOH) |
水溶性 | 不溶 |
在水中的溶解度 | 0.0963 mg/l 25 °C |
溶解性(可溶于) | 甲醇, 乙醇 |
GHS
相关法规
RTECS# | TM4969000 |
运输信息
HS编码* | 2933.39-000 |
应用
Terfenadine: A Prodrug of Fexofenadine with Selective H1-Receptor Antagonist Activity
Terfenadine is a prodrug of fexofenadine [F0698] (HCl salt) which is a non-sedative antihistamine with selective H1-receptor antagonist activity. Terfenadine is metabolized by intestinal CYP3A4 to fexofenadine which competitively binds peripheral H1-receptors, thereby stabilizing an inactive conformation of the receptor. Consequently, usual allergic responses as a result of mast-cell degranulation followed by the release of multiple inflammatory mediators, such as interleukins, prostaglandins, and leukotriene precursors, are blocked. In addition, it has been reported that terfenadine may reach excessive blood levels when the metabolism is too slow; and which can cause cardiac arrhythmias (prolongation of QT-interval). (The product is for research purpose only.)
References
- Fexofenadine: a review of its use in the management of seasonal allergic rhinitis and chronic idiopathic urticaria
- Terfenadine (A review on description, synthesis, physical properties, analysis, stability, polymorphism and crystal habits, and pharmacokinetics)
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