Merck
CN
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文件

275581

Sigma-Aldrich

6-氨基喹啉

98%

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别名:
6-喹啉胺
经验公式（希尔记法）:
C9H8N2
CAS号:
580-15-4
分子量:
144.17
Beilstein:
113320
EC 号:
209-453-0
MDL编号:
MFCD00006803
PubChem化学物质编号:
24856657
NACRES:
NA.22

检测方案

98%

形式

solid

bp

146 °C/0.3 mmHg (lit.)

mp

115-119 °C (lit.)

SMILES string

Nc1ccc2ncccc2c1

InChI

1S/C9H8N2/c10-8-3-4-9-7(6-8)2-1-5-11-9/h1-6H,10H2

InChI key

RJSRSRITMWVIQT-UHFFFAOYSA-N

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相关类别

应用

6-氨基喹啉可作为通过使用高效液相色谱（HPLC）-荧光检测（带柱后紫外光照射系统）同时测定血清尼古丁和可替宁的内标。它也可用作检测生物化学物质的荧光衍生剂，以及合成 N-甲基化烯胺酮叔胺。

象形图

Exclamation mark
GHS07

警示用语：

Warning

危险声明

H315 - H319

危险分类

Eye Irrit. 2 - Skin Irrit. 2

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

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Bryan P Ruddy et al.
Journal of controlled release : official journal of the Controlled Release Society, 306, 83-88 (2019-06-01)
Subcutaneous delivery of nicotine was performed using a novel electrically-operated needle-free jet injector, and compared to hypodermic needle delivery in a porcine model. Nicotine was delivered as a single, one-milligram dose into the abdominal skin, formulated as a 50 microliter
Pierre-Jean Aragon et al.
Chemical & pharmaceutical bulletin, 52(6), 659-663 (2004-06-10)
Indoloquinoline alkaloid cryptolepine and pyridocarbazole alkaloid ellipticine are of great interest because in vitro and in vivo studies revealed their good cytotoxic properties. In order to obtain some biologically active analogs of these compounds, we developped a synthesis based on
W Nashabeh et al.
Journal of chromatography, 600(2), 279-287 (1992-05-29)
The electrophoretic behavior of derivatized linear and branched oligosaccharides from various sources was examined in capillary zone electrophoresis with polyether-coated fused-silica capillaries. Two UV-absorbing (also fluorescent) derivatizing agents (2-aminopyridine and 6-aminoquinoline) were utilized for the electrophoresis and sensitive detection of
S A Cohen et al.
Analytical biochemistry, 211(2), 279-287 (1993-06-01)
A highly reactive amine derivatizing reagent, 6-aminoquinolyl-N-hydroxysuccinimidyl carbamate, has been synthesized. In a rapid, one-step procedure, the compound reacts with amino acids to form stable unsymmetric urea derivatives which are readily amenable to analysis by reversed phase HPLC. Studies on
Jong Bae Seo et al.
PloS one, 10(12), e0144432-e0144432 (2015-12-15)
Hydrolysis of phosphatidylinositol 4,5-bisphosphate (PIP2) of the plasma membrane by phospholipase C (PLC) generates two critical second messengers, inositol-1,4,5-trisphosphate and diacylglycerol. For the enzymatic reaction, PIP2 binds to positively charged amino acids in the pleckstrin homology domain of PLC. Here
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