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359785

8-Quinolinethiol hydrochloride

Name: 8-Quinolinethiol hydrochloride
Brand: ALDRICH

97%

Synonym(s):

8-Mercaptoquinoline hydrochloride, Thiooxine hydrochloride

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About This Item

Empirical Formula (Hill Notation):

C₉H₇NS · HCl

CAS Number:

34006-16-1

Molecular Weight:

197.68

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24862107

EC Number:

251-785-3

Beilstein/REAXYS Number:

3694939

MDL number:

MFCD00043261

Assay:

97%

Form:

solid

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Properties

assay

97%

form

solid

mp

165 °C (dec.) (lit.)

solubility

ethanol: soluble 50 mg/mL, clear, dark orange-brown

SMILES string

Cl[H].Sc1cccc2cccnc12

InChI

1S/C9H7NS.ClH/c11-8-5-1-3-7-4-2-6-10-9(7)8;/h1-6,11H;1H

InChI key

RWBSBQAUAJSGHY-UHFFFAOYSA-N

Description

Application

8-Quinolinethiol hydrochloride may be used in the synthesis of N₂S₂-donor tetradentate ligands.

pictograms

GHS07

signalword

Warning

hcodes

H315,H319,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Effect of 8-hydroxy-, 8-mercapto- and 5-chloro-7-iodo-8-hydroxy-quinoline on the uptake and distribution of nickel in mice.

K Borg-Neczak et al.

Pharmacology & toxicology, 74(3), 185-192 (1994-03-01)

Oral administration of Ni2+ together with 8-hydroxyquinoline (8-OH-quinoline), 8-mercaptoquinoline (8-SH-quinoline) or 5-chloro-7-iodo-8-hydroxyquinoline (clioquinol) resulted in increased tissue levels of the metal in several tissues of mice in comparison with animals given the Ni2+ alone. Ni2+ forms lipophilic complexes with these

Assay of the antiangiogenic compound TNP-470, and one of its metabolites, AGM-1883, by reversed-phase high-performance liquid chromatography in plasma.

W D Figg et al.

Journal of chromatography, 652(2), 187-194 (1994-02-11)

This paper describes a reversed-phase, high-performance liquid chromatographic (HPLC) method for the isolation, detection, and quantification of TNP-470 (I) and one of its active metabolites, AGM-1883 (II), from plasma. These compounds are initially extracted from plasma with an organic solvent

Inhibitory activities of metal chelators on endothelin-converting enzyme. II. In vivo studies.

N Ashizawa et al.

Biological & pharmaceutical bulletin, 17(2), 212-216 (1994-02-01)

The effects of metal chelators on endothelin (ET)-converting enzyme (ECE) activity in vivo were examined. Three compounds, (2,3-dimercapto-1-propanol (DMP), toluene-3,4-dithiol (TDT) and 8-mercaptoquinoline (8-MQ)), which inhibited ECE in in vitro studies, exhibited inhibitory activity towards big ET-1-induced sudden death in

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Global Trade Item Number

SKU	GTIN
359785-1G	04061826258040