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Merck

252565

Sigma-Aldrich

8-Quinolinol

ACS reagent, 98.5%

Sinónimos:

8-Quinolinol, 8-Hydroxyquinoline, 8-Oxychinolin, Oxine

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About This Item

Fórmula empírica (notación de Hill):
C9H7NO
Número de CAS:
Peso molecular:
145.16
Beilstein/REAXYS Number:
114512
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.21

grade

ACS reagent

Quality Level

assay

98.5%

ign. residue

≤0.05%

mp

72.5-74.0 °C

anion traces

sulfate (SO42-): ≤0.02%

antibiotic activity spectrum

fungi

mode of action

DNA synthesis | interferes
enzyme | inhibits

SMILES string

Oc1cccc2cccnc12

InChI

1S/C9H7NO/c11-8-5-1-3-7-4-2-6-10-9(7)8/h1-6,11H

Inchi Key

MCJGNVYPOGVAJF-UHFFFAOYSA-N

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General description

Chemical structure: quinolone

Application

8-Hydroxyquinoline may be used as a chelating ligand in the preparation of tris-(8-hydroxyquinoline)aluminum (Alq3), an organic electroluminescent compound used in organic light-emitting devices (OLEDs).

signalword

Danger

Hazard Classifications

Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Repr. 1B - Skin Sens. 1

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Preconcentration of trace elements in sea water by complexation with 8-hydroxyquinoline and adsorption on C18 bonded silica gel.
Watanabe H, et al.
Analytical Chemistry, 53(4), 738-739 (1981)
A Simple RNA Preparation Procedure from Yeast for Northern Blot Using Hot Phenol.
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Bio-protocol, 2(12) (2012)
Infra-red absorption spectra of metal chelates derived from 8-hydroxyquinoline, 2-methyl-8-hydroxyquinoline, and 4-methyl-8-hydroxyquinoline.
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Spectrochimica Acta Part A: Molecular Spectroscopy, 8(1), 1-8 (1956)
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