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CAS RN: 3505-38-2 | 產品號碼: C3057
Carbinoxamine Maleate

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產品號碼 | C3057 |
純度/分析方法 ![]() |
>98.0%(T)(HPLC) |
分子式 / 分子量 | C__1__6H__1__9ClN__2O·C__4H__4O__4 = 406.86 |
外觀與形狀(20°C) | Solid |
儲存條件 ![]() |
Room Temperature (Recommended in a cool and dark place, <15°C) |
應避免的情況 | Light Sensitive |
CAS RN | 3505-38-2 |
相關CAS RN ![]() |
486-16-8 |
Reaxys-RN | 6557352 |
PubChem Substance ID | 253662526 |
Merck Index(14) | 1799 |
MDL編號 | MFCD00082461 |
產品規格
Appearance | White to Almost white powder to crystal |
Purity(HPLC) | min. 98.0 %(excluding counter anion) |
Purity(Nonaqueous Titration) | min. 98.0 % |
Melting point | 116.0 to 121.0 °C |
NMR | confirm to structure |
性質
熔點 | 119 °C |
GHS
圖形表示 |
![]() |
信號詞 | Danger |
危險性說明 | H301 : Toxic if swallowed. |
防範說明 | 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 + P310 + P330 : IF SWALLOWED: Immediately call a POISON CENTER/doctor. Rinse mouth. P405 : Store locked up. |
相關法規
RTECS # | US6350000 |
運輸資料
UN編號 | UN2811 |
類別 | 6.1 |
包裝類別 | III |
HS編碼* | 2933.39-000 |
Application
Carbinoxamine maleate: A Histamine H1-Receptor Antagonist.
Carbinoxamine maleate, a first generation antihistamine, is a histamine H1-receptor antagonist. Carbinoxamine competes with histamine (type H1) for receptor sites on effector cells in the gastrointestinal tract, blood vessels and respiratory tract.
References
- Comparison of the effects of eleven histamine H1-receptor antagonists on monoamine turnover in the mouse brain
- Screening procedure for the detection of alkanolamine antihistamines and their metabolites in urine using computerized gas chromatography-mass spectrometry
- Determination of pseudoephedrine hydrochloride and carbinoxamine maleate in combination drug formulation by liquid chromatography
- A. M. Mansour, J. AOAC Int. 1998, 81, 958.
- Quantitative chiral analysis of carbinoxamine, doxylamine, and orphenadrine by capillary zone electrophoresis
- Determination of carbinoxamine maleate in pharmaceuticals by direct and differential pulse polarography
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