MONOSODIUM 8-AMINO-1-NAPHTHOL-3,6-DISULFONATE

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

Structure Search

SMILES

[H+].[Na+].NC1=C2C(O)=CC(=CC2=CC(=C1)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

Molecular Formula	Na
Molecular Weight	22.98976928
Charge	1
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Molecular Formula	C10H8NO7S2
Molecular Weight	318.303
Charge	-1
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Approval Year

PubMed

Title	Date	PubMed
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	20207190
Sensitive spectrophotometric methods for the assessment of nitrite in water sample.	2008-12	18204910
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	18415086
Selective fluorescent Hg(II) detection in aqueous solutions with a dye intermediate.	2007-11	17418629
A coupled photocatalytic-biological process for degradation of 1-amino-8-naphthol-3, 6-disulfonic acid (H-acid).	2005-12	16310240
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	12177766
[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	12938382
Novel reagents for the sensitive spectrophotometric determination of flutamide, an anticancer drug in pharmaceutical preparations.	2002-03-20	11879746
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	8336338
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	1282569
Inhibition of HIV replication by derivatives of naphthalenedisulfonic acids.	1990-08	2261142
Inhibition of HIV replication by naphthalenemonosulfonic acid derivatives and a bis naphthalenedisulfonic acid compound.	1990	2122146

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 21:57:31 GMT 2025` Edited by `admin` on `Mon Mar 31 21:57:31 GMT 2025`
Record UNII	BQX9B4J4FO
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

MONOSODIUM 8-AMINO-1-NAPHTHOL-3,6-DISULFONATE

Systematic Name

English

NSC-8632

Preferred Name

English

MONOSODIUM 4-AMINO-5-HYDROXY-2,7-NAPHTHALENEDISULFONATE

Systematic Name

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