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Details

Stereochemistry ACHIRAL
Molecular Formula C14H7O5S.Na
Molecular Weight 310.257
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1-Anthracenesulfonic acid, 9,10-dihydro-9,10-dioxo-, sodium salt

SMILES

[Na+].[O-]S(=O)(=O)C1=C2C(=O)C3=C(C=CC=C3)C(=O)C2=CC=C1

InChI

InChIKey=SDKPSXWGRWWLKR-UHFFFAOYSA-M
InChI=1S/C14H8O5S.Na/c15-13-8-4-1-2-5-9(8)14(16)12-10(13)6-3-7-11(12)20(17,18)19;/h1-7H,(H,17,18,19);/q;+1/p-1

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Enhancement by anthraquinone-2-sulphonate of the photonitration of phenol by nitrite: implication for the photoproduction of nitrogen dioxide by coloured dissolved organic matter in surface waters.
2010-12
Bacterial growth response to photoactive quinones.
2010-10-07
Enhanced biodecolorization of azo dyes by anthraquinone-2-sulfonate immobilized covalently in polyurethane foam.
2010-09
Anthraquinone sulfonate modified, layered double hydroxide nanosheets for dye-sensitized solar cells.
2010-07-26
Bacterial and iron oxide aggregates mediate secondary iron mineral formation: green rust versus magnetite.
2010-06-01
Voltammetric characterization of DNA intercalators across the full pH range: anthraquinone-2,6-disulfonate and anthraquinone-2-sulfonate.
2010-03-25
Studies on the formation of a complex of Cu(II) with sodium 1,4-dihydroxy-9,10-anthraquinone-2-sulphonate - an analogue of the core unit of anthracycline anticancer drugs and its interaction with calf thymus DNA.
2009-12
Metabolism of sulphonated anthraquinones in rhubarb, maize and celery: the role of cytochromes P450 and peroxidases.
2009-11
Thermodynamic targeting of microbial perchlorate reduction by selective electron donors.
2009-04
Soda-anthraquinone pulping of palm oil empty fruit bunches and beating of the resulting pulp.
2009-02
Expression analysis of G Protein-Coupled Receptors in mouse macrophages.
2008-04-29
Transformation of phenolic compounds upon UVA irradiation of anthraquinone-2-sulfonate.
2008-03
Influence of sediment components on the immobilization of Zn during microbial Fe-(hydr)oxide reduction.
2006-06-15
Superquenching as a detector for microsphere-based flow cytometric assays.
2006-05
Charge transfer through DNA: A selective electrochemical DNA biosensor.
2006-04-01
Methionine radical cation: structural studies as a function of pH using X- and Q-band time-resolved electron paramagnetic resonance spectroscopy.
2005-07-07
Photooxidation of diglycine in confined media. Application of the microreactor model for spin-correlated radical pairs in reverse micelles and water-in-oil microemulsions.
2005-03-29
Evaluation of an integrated anaerobic/aerobic SBR system for the treatment of wool dyeing effluents. Purification of wool dyeing effluent in a SBR.
2005-02
Waste sizing solution as co-substrate for anaerobic decolourisation of textile dyeing wastewaters.
2005
Effect of different redox mediators during thermophilic azo dye reduction by anaerobic granular sludge and comparative study between mesophilic (30 degrees C) and thermophilic (55 degrees C) treatments for decolourisation of textile wastewaters.
2004-06
A comparative study on direct and indirect electrochemical oxidation of polyaromatic compounds.
2003-12
Evaluation of anthraquinone-2-sulfonyl chloride for determination of phenol in water by liquid chromatography using pre-column phase-transfer catalysed derivatization.
2002-11
Cyclic voltammetry study of glucose and insulin interactions with supported lipid membrane.
2002-05-15
Capillary electrophoresis of phytochemical substances.
2002-02-01
Removal of organic pollutants from industrial wastewater by electrogenerated Fenton's reagent.
2001-11
Patents
Name Type Language
1-Anthracenesulfonic acid, 9,10-dihydro-9,10-dioxo-, sodium salt
Systematic Name English
NSC-7575
Preferred Name English
Sodium anthraquinone-1-sulfonate
Systematic Name English
1-Anthracenesulfonic acid, 9,10-dihydro-9,10-dioxo-, sodium salt (1:1)
Systematic Name English
Code System Code Type Description
PUBCHEM
517266
Created by admin on Tue Apr 01 20:15:13 GMT 2025 , Edited by admin on Tue Apr 01 20:15:13 GMT 2025
PRIMARY
EPA CompTox
DTXSID50883320
Created by admin on Tue Apr 01 20:15:13 GMT 2025 , Edited by admin on Tue Apr 01 20:15:13 GMT 2025
PRIMARY
FDA UNII
F8Q2GUT8LB
Created by admin on Tue Apr 01 20:15:13 GMT 2025 , Edited by admin on Tue Apr 01 20:15:13 GMT 2025
PRIMARY
NSC
7575
Created by admin on Tue Apr 01 20:15:13 GMT 2025 , Edited by admin on Tue Apr 01 20:15:13 GMT 2025
PRIMARY
CAS
128-56-3
Created by admin on Tue Apr 01 20:15:13 GMT 2025 , Edited by admin on Tue Apr 01 20:15:13 GMT 2025
PRIMARY
HSDB
6386
Created by admin on Tue Apr 01 20:15:13 GMT 2025 , Edited by admin on Tue Apr 01 20:15:13 GMT 2025
PRIMARY
ECHA (EC/EINECS)
204-894-5
Created by admin on Tue Apr 01 20:15:13 GMT 2025 , Edited by admin on Tue Apr 01 20:15:13 GMT 2025
PRIMARY