Skip to Content
MilliporeSigma
All Photos(2)

Documents

C47000

Sigma-Aldrich

5-Chloro-8-quinolinol

95%

Synonym(s):

5-Chloro-8-hydroxyquinoline

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Empirical Formula (Hill Notation):
C9H6ClNO
CAS Number:
130-16-5
Molecular Weight:
179.60
Beilstein/REAXYS Number:
5289
EC Number:
204-978-1
MDL number:
MFCD00006788
UNSPSC Code:
12352100
PubChem Substance ID:
24892714
NACRES:
NA.22

assay

95%

form

crystals

mp

122-124 °C (lit.)

SMILES string

Oc1ccc(Cl)c2cccnc12

InChI

1S/C9H6ClNO/c10-7-3-4-8(12)9-6(7)2-1-5-11-9/h1-5,12H

InChI key

CTQMJYWDVABFRZ-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Sens. 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

V Arjunan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 72(4), 783-788 (2008-12-30)
The Fourier transform infrared (FTIR) and FT-Raman spectra of 7-bromo-5-chloro-8-hydroxyquinoline (BCHQ) have been measured in the range 4000-400 and 4000-100cm(-1), respectively. Complete vibrational assignment and analysis of the fundamental modes of the compound were carried out using the observed FTIR
E J Wojtowicz
Journal of pharmaceutical sciences, 73(10), 1430-1433 (1984-10-01)
A reverse-phase high-performance liquid chromatographic (HPLC) method was developed for determining iodochlorhydroxyquin, 5,7-dichloro-8-hydroxyquinoline, and 5,7-diiodo-8-hydroxyquinoline in creams, ointments, shampoos, tablets, and bulk drugs. A column packed with 10-micron phenyl-silica and a mobile phase of 0.001 M NiCl2 in acetonitrile-methanol-water (30:20:50)
Poonpilas Hongmanee et al.
Antimicrobial agents and chemotherapy, 51(3), 1105-1106 (2006-12-21)
The in vitro activities of cloxyquin (5-chloroquinolin-8-ol) against 9 standard strains and 150 clinical isolates of Mycobacterium tuberculosis were studied. The MICs ranged from 0.062 to 0.25 microg/ml. The MIC(50) and MIC(90) were 0.125 and 0.25 microg/ml, respectively. These indicate
Oleg V Larionov et al.
Organic letters, 16(3), 864-867 (2014-01-15)
A one-step transformation of heterocyclic N-oxides to 2-alkyl-, aryl-, and alkenyl-substituted N-heterocycles is described. The success of this broad-scope methodology hinges on the combination of copper catalysis and activation by lithium fluoride or magnesium chloride. The utility of this method
Marcos N Soares et al.
Materials science & engineering. C, Materials for biological applications, 33(4), 2213-2220 (2013-03-19)
A innovative 5-Cl-8-oxyquinolinepropoxycalix[4]arene ligand (2) have been prepared, exhibiting, at room temperature, blue fluorescent light emission and resulting in shift band to green fluorescent light (fluorescence mode) in the presence of coordinated Eu(III) and Tb(III) ions. Terbium complex presented phosphorescence
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service