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Details

Stereochemistry ACHIRAL
Molecular Formula C10H7NO7S2.Na.H
Molecular Weight 341.293
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MONOSODIUM 8-AMINO-1-NAPHTHOL-3,6-DISULFONATE

SMILES

[H+].[Na+].NC1=CC(=CC2=C1C(O)=CC(=C2)S([O-])(=O)=O)S([O-])(=O)=O

InChI

InChIKey=QPILZZVXGUNELN-UHFFFAOYSA-M
InChI=1S/C10H9NO7S2.Na/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);/q;+1/p-1

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Inhibition of HIV replication by naphthalenemonosulfonic acid derivatives and a bis naphthalenedisulfonic acid compound.
1990
Inhibition of HIV replication by derivatives of naphthalenedisulfonic acids.
1990 Aug
Novel reagents for the sensitive spectrophotometric determination of flutamide, an anticancer drug in pharmaceutical preparations.
2002 Mar 20
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 Jun
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 May
Patents
Name Type Language
MONOSODIUM 8-AMINO-1-NAPHTHOL-3,6-DISULFONATE
Systematic Name English
MONOSODIUM 4-AMINO-5-HYDROXY-2,7-NAPHTHALENEDISULFONATE
Systematic Name English
NSC-8632
Code English
H ACID MONOSODIUM SALT
Common Name English
2,7-NAPHTHALENEDISULFONIC ACID, 4-AMINO-5-HYDROXY-, SODIUM SALT (1:1)
Systematic Name English
MONOSODIUM 1-NAPHTHOL-8-AMINO-3,6-DISULFONATE
Common Name English
Code System Code Type Description
PUBCHEM
23664361
Created by admin on Sat Dec 16 08:15:04 GMT 2023 , Edited by admin on Sat Dec 16 08:15:04 GMT 2023
PRIMARY
FDA UNII
BQX9B4J4FO
Created by admin on Sat Dec 16 08:15:04 GMT 2023 , Edited by admin on Sat Dec 16 08:15:04 GMT 2023
PRIMARY
NSC
8632
Created by admin on Sat Dec 16 08:15:04 GMT 2023 , Edited by admin on Sat Dec 16 08:15:04 GMT 2023
PRIMARY
CAS
5460-09-3
Created by admin on Sat Dec 16 08:15:04 GMT 2023 , Edited by admin on Sat Dec 16 08:15:04 GMT 2023
PRIMARY
ECHA (EC/EINECS)
226-736-4
Created by admin on Sat Dec 16 08:15:04 GMT 2023 , Edited by admin on Sat Dec 16 08:15:04 GMT 2023
PRIMARY
EPA CompTox
DTXSID4027600
Created by admin on Sat Dec 16 08:15:04 GMT 2023 , Edited by admin on Sat Dec 16 08:15:04 GMT 2023
PRIMARY