6-Aminoquinoline, 98%
6-Aminoquinoline, 98%
6-Aminoquinoline, 98%
Thermo Scientific Chemicals

6-Aminoquinoline, 98%

CAS: 580-15-4 | C9H8N2 | 144.177 g/mol
製品番号(カタログ番号) L13819.03
または、製品番号L13819-03
価格(JPY)
-
数量:
1 g
一括またはカスタム形式をリクエストする
化学物質識別子
CAS580-15-4
IUPAC Namequinolin-6-amine
Molecular FormulaC9H8N2
InChI KeyRJSRSRITMWVIQT-UHFFFAOYSA-N
SMILESNC1=CC=C2N=CC=CC2=C1
さらに表示
Appearance (Color)Dark cream to cream to yellow to brown to dark gray to gray
FormCrystals or powder or crystalline powder
Assay (GC)≥97.5%
6-Aminoquinoline was used as an internal standard in determining serum nicotine and cotinine simultaneously by using high-performance liquid chromatography (HPLC)-fluorometric detection with a postcolumn ultraviolet-photo irradiation system. It was also used as a fluorescent derivatizing agent for the detection of biochemicals and in the synthesis of tertiary N-methylated enaminonesa.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
6-Aminoquinoline was used as an internal standard in determining serum nicotine and cotinine simultaneously by using high-performance liquid chromatography (HPLC)-fluorometric detection with a postcolumn ultraviolet-photo irradiation system. It was also used as a fluorescent derivatizing agent for the detection of biochemicals and in the synthesis of tertiary N-methylated enaminonesa.

Solubility
Soluble in methanol, chloroform, ethanol, and benzene. Insoluble in water.

Notes
Air sensitive. Store under inert gas. Store away from oxidizing agents, air.
RUO – Research Use Only

General References:

  1. W Nashabeh; Z el Rassi. Capillary zone electrophoresis of linear and branched oligosaccharides. Journal of Chromatography A. 1992, 600, (2), 279-287.
  2. Eyal Danieli; Doron Shabat. Molecular probe for enzymatic activity with dual output. Bioorganic & Medicinal Chemistry. 2007, 15, (23), 7318-7324.