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CAS RN: 74103-07-4 | 产品编码: K0053

Ketorolac Tromethamine


纯度/分析方法: >98.0%(T)(HPLC)
别名:
  • 酮咯酸氨丁三醇
  • 酮咯酸丁三醇铵盐
  • (±)-5-苯甲酰基-2,3-二氢-1H-吡咯里嗪-1-羧酸丁三醇氨盐
  • Ketorolac Tris Salt
  • (±)-5-Benzoyl-2,3-dihydro-1H-pyrrolizine-1-carboxylic Acid Tris Salt
产品文档:
1G
S$78.00
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5G
S$283.50
10   1   请联系我们

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产品编码 K0053
纯度/分析方法 >98.0%(T)(HPLC)
分子式/分子量 C__1__5H__1__3NO__3·C__4H__1__1NO__3 = 376.41 
外观与形状(20°C) 固体
储存温度 室温 (15°C以下阴凉干燥处)
包装和容器 1G-Glass Bottle with Plastic Insert (查看图片)
CAS RN 74103-07-4
相关CAS RN 74103-06-3
Reaxys-RN 6463165
PubChem物质ID 253661330
Merck Index (14) 5306
MDL编号

MFCD00887595

技术规格
Appearance White to Light yellow powder to crystal
Purity(HPLC) min. 98.0 area%
Purity(Neutralization titration) min. 98.0 %
物性(参考值)
熔点 167 °C
最大吸收波长 322 nm (MeOH)
GHS
象形图 Pictogram
信号词 Danger
危险性说明 H301 : Toxic if swallowed.
H315 : Causes skin irritation.
H319 : Causes serious eye irritation.
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.
P280 : Wear protective gloves/ eye protection/ face protection.
P302 + P352 : IF ON SKIN: Wash with plenty of water.
P337 + P313 : If eye irritation persists: Get medical advice/ attention.
P305 + P351 + P338 : IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
P362 + P364 : Take off contaminated clothing and wash it before reuse.
P332 + P313 : If skin irritation occurs: Get medical advice/ attention.
P301 + P310 + P330 : IF SWALLOWED: Immediately call a POISON CENTER/doctor. Rinse mouth.
P405 : Store locked up.
相关法规
RTECS# UY7759900
运输信息
UN编号 UN2811
类别 6.1
包装类别 III
HS编码* 2933.99-000
*此H.S.编码用于日本出口报关,不适用于您所在国家或地区的进口申报
应用
Ketorolac Tromethamine: A Non-Selective Cyclooxygenase (COX) Inhibitor with Strong Analgesic Activity

Ketorolac tromethamine is a non-steroidal anti-inflammatory drug (NSAID) with strong analgesic activity. Ketorolac is a non-selective cyclooxygenase (COX) inhibitor. Thus, it reduces prostaglandin synthesis. Ketorolac is the racemic mixture of (-)-S and (+)-R enantiomers. Most of its analgesic and COX inhibitory activity is retained in the S-isomer. Besides, some formulations for controlled release of ketorolac tromethamine have been reported. Ketorolac and its metabolites are excreted primarily by the kidneys. For your reference, [B4934] is used as a synthetic intermediate of ketorolac. (The product is for research purpose only.)

References


参考文献


技术文章
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