Maximum quantity allowed is 999
CAS RN: 74711-43-6 | 产品编码: Z0021
Zaltoprofen
![Zaltoprofen No-Image](/medias/Z0021.jpg?context=bWFzdGVyfHJvb3R8NDY4NzN8aW1hZ2UvanBlZ3xhRGxrTDJneVpDODRPVEl6TnpFeU9EUTNPVEF5TDFvd01ESXhMbXB3Wnd8YTRmODQzYzQ2M2YyZDc1Y2NmMzk2MTY3MDA0MDQ0N2YxMTIwMWI5MWJiNDk3OWQ2NTYxNzdiMjVjMzQ5YmU2Yw)
产品编码 | Z0021 |
纯度/分析方法 | >98.0%(T)(HPLC) |
分子式/分子量 | C__1__7H__1__4O__3S = 298.36 |
外观与形状(20°C) | 固体 |
储存温度 | 室温 (15°C以下阴凉干燥处) |
应避免的情况 | 光 |
包装和容器 | 1G-Glass Bottle with Plastic Insert (查看图片) |
CAS RN | 74711-43-6 |
Reaxys-RN | 6770548 |
PubChem物质ID | 160871191 |
Merck Index (14) | 10112 |
MDL编号 | MFCD00864323 |
Appearance | White to Light yellow powder to crystal |
Purity(HPLC) | min. 98.0 area% |
Purity(Neutralization titration) | min. 98.0 % |
Melting point | 135.0 to 139.0 °C |
熔点 | 137 °C |
水溶性 | 不溶 |
溶解性(可溶于) | 甲醇 |
溶解性(微溶于) | 苯, 乙醇 |
象形图 |
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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. |
RTECS# | HQ2526700 |
HS编码* | 2934.99-000 |
Comparison of cyclooxygenase-1 and -2 inhibitory activities of various nonsteroidal anti-inflammatory drugs using human platelets and synovial cells
Zaltoprofen inhibits bradykinin-induced responses by blocking the activation of second messenger signaling cascades in rat dorsal root ganglion cells
H. Tang, A. Inoue, K. Oshita, K. Hirate, Y. Nakata, Neuropharmacology 2005, 48, 1035.
Pharmacological investigations of the new antiinflammatory agent 2-(10,11-dihydro-10-oxodibenzo[b,f]thiepin-2-yl)propionic acid. 1st Communication: Inhibitory effects on rat paw edema
K. Tsurumi, K. Kyuki, M. Niwa, S. Kokuba, H. Fujimura, Arzneim.-Forsch. 1986, 36, 1796.
Analgesic and antiinflammatory effects of 2-(10,11-dihydro-10-oxo-dibenzo[b,f]thiepin-2-yl)propionic acid in rat and mouse
T. Kameyama, T. Nabeshima, S. Yamada, M. Sato, Arzneim.-Forsch. 1987, 37, 19.
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