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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:
Pricing and availability is not currently available.
Recommended Products
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
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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
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
S D Bhattacharyya et al.
Infection and immunity, 57(10), 3053-3057 (1989-10-01)
Purified type A botulinum toxin of about 10(6) mouse 50% lethal doses per ml was greater than 99.9% inactivated when incubated at pH 7.4 for 30 min at 37 degrees C in 20 mM 1,10-phenanthroline (PTL) or 2,2'-dipyridyl (DPD) and
H Wang et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 57(12), 2403-2407 (2002-01-05)
The addition of thiol compounds to the fluorescence system of Zn(II)-8-hydroxyquinoline-5-sulphonic acid complex (Zn(II)-HQS) in H3BO3-Na2B4O7 buffer (pH 8.50) solution led to immediate fluorescence inhibition, which was proportional to their amounts. Based on this finding, a novel spectrofluorimetric method for
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