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Details

Stereochemistry ACHIRAL
Molecular Formula C10H9NO7S2
Molecular Weight 319.311
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1-NAPHTHOL-8-AMINO-3,6-DISULFONIC ACID

SMILES

NC1=C2C(O)=CC(=CC2=CC(=C1)S(O)(=O)=O)S(O)(=O)=O

InChI

InChIKey=APRRQJCCBSJQOQ-UHFFFAOYSA-N
InChI=1S/C10H9NO7S2/c11-8-3-6(19(13,14)15)1-5-2-7(20(16,17)18)4-9(12)10(5)8/h1-4,12H,11H2,(H,13,14,15)(H,16,17,18)

HIDE SMILES / InChI

Molecular Formula C10H9NO7S2
Molecular Weight 319.311
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
A simple and sensitive spectrophotometric method for the determination of trace amounts of nitrite in environmental and biological samples using 4-amino-5-hydroxynaphthalene-2,7-disulphonic acid monosodium salt.
2010-05
Sensitive spectrophotometric methods for the assessment of nitrite in water sample.
2008-12
Determination of boron in water samples at nanograms per cubic decimeter levels by reversed-phase partition high-performance liquid chromatography with precolumn complexation reaction using salicylaldehyde and 1-amino-8-naphthol-3,6-disulfonate.
2008-06
Selective fluorescent Hg(II) detection in aqueous solutions with a dye intermediate.
2007-11
A coupled photocatalytic-biological process for degradation of 1-amino-8-naphthol-3, 6-disulfonic acid (H-acid).
2005-12
Treatment of H-acid wastewater by photo-Fenton reagent combined with a biotreatment process: a study on optimum conditions of pretreatment by a photo-Fenton process.
2002-09
[Study on the oxidative coupling of p-amino-N,N-dimethylaniline with 1-amino-8-naphthol-3,6-disulfonic acid and its application].
2002-08
Novel reagents for the sensitive spectrophotometric determination of flutamide, an anticancer drug in pharmaceutical preparations.
2002-03-20
Structure-activity relationship studies with symmetric naphthalenesulfonic acid derivatives. Synthesis and influence of spacer and naphthalenesulfonic acid moiety on anti-HIV-1 activity.
1993-07-09
Potential anti-AIDS naphthalenesulfonic acid derivatives. Synthesis and inhibition of HIV-1 induced cytopathogenesis and HIV-1 and HIV-2 reverse transcriptase activities.
1992-12-25
Inhibition of HIV replication by derivatives of naphthalenedisulfonic acids.
1990-08
Inhibition of HIV replication by naphthalenemonosulfonic acid derivatives and a bis naphthalenedisulfonic acid compound.
1990
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:08:11 GMT 2025
Edited
by admin
on Mon Mar 31 19:08:11 GMT 2025
Record UNII
4WUM31ES4U
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SULFONPHTHOL
Preferred Name English
1-NAPHTHOL-8-AMINO-3,6-DISULFONIC ACID
MI  
Common Name English
NSC-190492
Code English
C.I. 35570
Code English
2,7-NAPHTHALENEDISULFONIC ACID, 4-AMINO-5-HYDROXY-
Systematic Name English
H ACID
Common Name English
1-NAPHTHOL-8-AMINO-3,6-DISULFONIC ACID [MI]
Common Name English
8-HYDROXY-3,6-DISULFO-1-NAPHTHYLAMINE
Systematic Name English
4-AMINO-5-HYDROXY-2,7-NAPHTHALENEDISULFONIC ACID
Systematic Name English
Code System Code Type Description
NSC
190492
Created by admin on Mon Mar 31 19:08:11 GMT 2025 , Edited by admin on Mon Mar 31 19:08:11 GMT 2025
PRIMARY
EPA CompTox
DTXSID0046981
Created by admin on Mon Mar 31 19:08:11 GMT 2025 , Edited by admin on Mon Mar 31 19:08:11 GMT 2025
PRIMARY
MERCK INDEX
m7740
Created by admin on Mon Mar 31 19:08:11 GMT 2025 , Edited by admin on Mon Mar 31 19:08:11 GMT 2025
PRIMARY Merck Index
PUBCHEM
7009
Created by admin on Mon Mar 31 19:08:11 GMT 2025 , Edited by admin on Mon Mar 31 19:08:11 GMT 2025
PRIMARY
FDA UNII
4WUM31ES4U
Created by admin on Mon Mar 31 19:08:11 GMT 2025 , Edited by admin on Mon Mar 31 19:08:11 GMT 2025
PRIMARY
ECHA (EC/EINECS)
201-975-7
Created by admin on Mon Mar 31 19:08:11 GMT 2025 , Edited by admin on Mon Mar 31 19:08:11 GMT 2025
PRIMARY
CAS
90-20-0
Created by admin on Mon Mar 31 19:08:11 GMT 2025 , Edited by admin on Mon Mar 31 19:08:11 GMT 2025
PRIMARY