方案
≥95.0% (GC)
表单
liquid
折射率
n20/D 1.612 (lit.)
沸点
105-107 °C/10 mmHg (lit.)
248 °C (lit.)
mp
−9-−3 °C (lit.)
溶解性
chloroform: soluble(lit.)
diethyl ether: soluble(lit.)
water: insoluble(lit.)
密度
1.058 g/mL at 25 °C (lit.)
SMILES字符串
Cc1ccc2ccccc2n1
InChI
1S/C10H9N/c1-8-6-7-9-4-2-3-5-10(9)11-8/h2-7H,1H3
InChI key
SMUQFGGVLNAIOZ-UHFFFAOYSA-N
基因信息
human ... CYP1A2(1544)
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一般描述
喹哪啶是一种有机化合物，由巴豆醛和苯胺在脱氢剂存在下与硫酸通过 Skraup 方法制备。以喹那啶为原料合成了几种染料，包括三聚辛氰染料、频哪腈染料、乙烯基染料、喹啉酮染料和喹那啶红。此外，它还用于生产药品、pH 指示剂、食品着色剂、油溶性染料和其他化合物。
应用
喹哪啶可用于：
- 在方胺染料（喹哪啶基方胺染料）的制备中，方胺染料具有重要的生物学意义，可作为金属离子传感器。
- 制备 pH 敏感的比色化学传感器。
特点和优势
2-甲基喹啉是可生物降解的。
免责声明
储存后可能变为棕色
警示用语：
Warning
危险分类
Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Muta. 2 - Skin Irrit. 2
储存分类代码
10 - Combustible liquids
WGK
WGK 3
闪点(°F)
174.2 °F - closed cup
闪点(°C)
79 °C - closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
D Ferri et al.
Journal of the American Chemical Society, 123(48), 12074-12084 (2001-11-29)
An in situ attenuated total reflection study of the chiral solid-liquid interface created by cinchonidine adsorption on a Pt/Al(2)O(3) model catalyst is presented. Experiments were performed in the presence of dissolved hydrogen, that is under conditions used for the heterogeneous
J Ortuño et al.
Fish & shellfish immunology, 12(1), 49-59 (2002-02-28)
Anaesthesia may depress the immune system in mammals, but there is no available information on this topic in fish. In the present work, four anaesthetics that are used in aquaculture, MS222 (0 19 mM), benzocaine (0.21 mM), 2-phenoxyethanol (16 mM)
M Naoi et al.
Life sciences, 40(11), 1075-1082 (1987-03-16)
Type A monoamine oxidase (MAO-A) in human placental mitochondria was competitively inhibited by naturally occurring substances, quinoline and quinaldine, using kynuramine as substrate. Quinoline had a higher affinity for MAO than kynuramine. MAO-A in human brain synaptosomal mitochondria was also
Yongmei Li et al.
Journal of hazardous materials, 173(1-3), 151-158 (2009-09-08)
The anaerobic degradation of quinoline, isoquinoline and 2-methylquinoline was investigated under nitrate-reducing conditions with acclimated activated sludge. Quinoline was completely transformed during degradation with an optimum COD/NO(3)-N ratio of 7. Isoquinoline and 2-methylquinoline were also completely transformed; however, nitrate consumption
J L Allen et al.
Veterinary and human toxicology, 28 Suppl 1, 21-24 (1986-01-01)
Residue concentrations of drugs that are administered to fish by bath immersion are related primarily to passage of the drugs across the gills. The elimination of these chemicals by fish can be mediated by biotransformation, but the route of elimination
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