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H1129

Sigma-Aldrich

8-Hydroxyquinoline-5-sulfonic acid

crystalline

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About This Item

Empirical Formula (Hill Notation):
C9H7NO4S
CAS Number:
Molecular Weight:
225.22
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

form

crystalline

color

yellow to green

SMILES string

Oc1ccc(c2cccnc12)S(O)(=O)=O

InChI

1S/C9H7NO4S/c11-7-3-4-8(15(12,13)14)6-2-1-5-10-9(6)7/h1-5,11H,(H,12,13,14)

InChI key

LGDFHDKSYGVKDC-UHFFFAOYSA-N

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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G Jourquin et al.
Journal of pharmaceutical and biomedical analysis, 14(8-10), 967-975 (1996-06-01)
The fluorescence of tin(IV) complexed by 8-hydroxyquinoline-5-sulfonic acid (8-HQSA) has been studied in both aqueous and hydroorganic (acetate buffer and dimethylsulfoxide) media. Several experimental parameters such as pH, DMSO/water ratio and reactant concentration have been investigated to increase the fluorescence
M H Lee et al.
Archives of biochemistry and biophysics, 248(1), 368-378 (1986-07-01)
Dihydropyrimidine amidohydrolase (EC 3.5.2.2) catalyzes the reversible hydrolysis of 5,6-dihydropyrimidines to the corresponding beta-ureido acids. Previous work has shown that incubation of this Zn2+ metalloenzyme with 2,6-dipicolinic acid, 8-hydroxyquinoline-5-sulfonic acid, or o-phenanthroline results in inactivation by Zn2+ removal by a
M Luísa Ramos et al.
Dalton transactions (Cambridge, England : 2003), 40(44), 11732-11741 (2011-10-04)
Multinuclear ((1)H, (13)C) magnetic resonance spectroscopy, DFT calculations and luminescence techniques have been used to study 8-hydroxyquinoline-5-sulfonate (8-HQS) and its complexes with Zn(ii), in aqueous solution. The study combines the high sensitivity of luminescence techniques, the selectivity of multinuclear NMR
Amruta R Poreddy et al.
Journal of combinatorial chemistry, 6(2), 239-254 (2004-03-09)
This article describes the solid-phase combinatorial methods developed for the synthesis of polyhydroxamate-based siderophores. This strategy was applied to generate several libraries of structural DFO (1a) analogues that include DFO variants, non-amide analogues, C-terminal modified analogues, reverse-amide analogues, and hybrid
Luciano Vitali et al.
International journal of biological macromolecules, 42(2), 152-157 (2007-12-07)
In the present study, a new chelating adsorbent was prepared from chitosan microspheres cross-linked with glutaraldehyde by spray drying using 8-hydroxyquinoline -5 sulphonic acid as chelant agent (CTS-SX-CL). Microspheres of the new adsorbent were characterized by Raman spectroscopy, scanning electron

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