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Merck
CN

260789

Sigma-Aldrich

8-氨基喹啉

98%

别名:

8-喹啉胺

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About This Item

经验公式(希尔记法):
C9H8N2
CAS号:
分子量:
144.17
Beilstein:
114474
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

98%

形式

solid

反应适用性

reaction type: C-H Activation
reagent type: catalyst

bp

174 °C/26 mmHg (lit.)

mp

60-65 °C (lit.)

SMILES字符串

Nc1cccc2cccnc12

InChI

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

InChI key

WREVVZMUNPAPOV-UHFFFAOYSA-N

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一般描述

8-氨基喹啉在低介电常数的介质中发出中等到微弱的荧光,但在强氢键或酸性水介质中不发出荧光 。研究了 8-氨基喹啉与铬 (Ⅲ)、锰 (Ⅱ)、铁 (Ⅱ) 和 (Ⅲ)、钴 (Ⅱ)、镍 (Ⅱ)、铜 (Ⅱ)、锌 (Ⅱ)、镉 (Ⅱ) 和铂 (Ⅱ) 盐的反应

应用

8-氨基喹啉已用于:
  • 制备锇碱基稳定的末端硼烯配合物
  • 分光光度法测定二价钯

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2

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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Paul Abu-Rabie et al.
Analytical chemistry, 83(22), 8779-8786 (2011-10-07)
A novel technique is presented that addresses the issue of how to apply internal standard (IS) to dried matrix spot (DMS) samples that allows the IS to integrate with the sample prior to extraction. The TouchSpray, a piezo electric spray
A Base-Stabilized Terminal Borylene Complex of Osmium Derived from Reaction between a Dichloroboryl Complex and 8-Aminoquinoline This work was supported by the Marsden Fund administered by The Royal Society of New Zealand.
Irvine et al.
Angewandte Chemie (International ed. in English), 39(5), 948-950 (2000-04-13)
Fluorescence and phosphorescence of 5- and 8-aminoquinoline.
S G Schulman et al.
Analytica chimica acta, 56(1), 83-89 (1971-08-01)
Liangliang Yan et al.
Journal of inorganic biochemistry, 106(1), 46-51 (2011-11-25)
Palladium(II) complexes are potential antitumor metallodrugs for their chemical resemblance to platinum(II) complexes. Two palladium(II) complexes (1 and 2) in the formula of [PdL(n)Cl] [L(1) = N-(tert-butoxycarbonyl)-l-methionine-N'-8-quinolylamide, L(2) = L-alanine-N'-8-quinolylamide] have been synthesized accordingly. The structures of the complexes were
Paul Abu-Rabie et al.
Bioanalysis, 3(24), 2769-2781 (2011-12-22)
The surge in interest in switching from traditionally used wet plasma to dried matrix spot (DMS) sampling and analysis to support pharmaceutical drug development is due to the significant ethical, financial and data quality advantages on offer. Unfortunately these advantages

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