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

6-Aminoquinoline, 98%

CAS: 580-15-4 | C9H8N2 | 144.177 g/mol
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25 g
Catalog number L13819.14
also known as L13819-14
Price (USD)
423.65
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470.00
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Quantity:
25 g
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Price (USD)
423.65
Online Exclusive
470.00
Save 46.35 (10%)
Each
Chemical Identifiers
CAS580-15-4
IUPAC Namequinolin-6-amine
Molecular FormulaC9H8N2
InChI KeyRJSRSRITMWVIQT-UHFFFAOYSA-N
SMILESNC1=CC=C2N=CC=CC2=C1
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SpecificationsSpecification SheetSpecification Sheet
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.