H1129
8-Hydroxyquinoline-5-sulfonic acid
crystalline
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About This Item
Fórmula empírica (notación de Hill):
C9H7NO4S
Número de CAS:
Peso molecular:
225.22
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
Productos recomendados
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
13 - Non Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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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
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
O M Mahmoud et al.
Journal of comparative pathology, 93(4), 551-558 (1983-10-01)
When sheep are injected subcutaneously with copper calcium edetate or copper oxyquinoline sulphonate there is a rapid increase in the concentration of copper in whole blood, serum and urine within the first 24 h. When sheep are injected with copper
Claude Amiard-Triquet et al.
Environmental toxicology, 21(1), 1-7 (2006-02-08)
Copper distribution has been examined in two microalgae (Haslea ostrearia, Diatom; Tetraselmis suecica, Prasinophyceae) exposed to Cu at 30 microg/L(-1). Exchangeable copper linked at the cell surface was desorbed using 8-hydroxyquinoline-5-sulfonate as complexing agent. Then, incorporated copper was separated between
K A Mookhtiar et al.
Archives of biochemistry and biophysics, 246(2), 645-649 (1986-05-01)
A series of chemical modification reactions has been carried out to identify functional constituents of the active site of human neutrophil collagenase. The enzyme is reversibly inhibited by the transition metal chelating agent 1,10-phenanthroline, and inhibition is fully reversed by
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