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Details

Stereochemistry ACHIRAL
Molecular Formula C10H8O3S
Molecular Weight 208.234
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-NAPHTHALENESULFONIC ACID

SMILES

OS(=O)(=O)C1=CC=C2C=CC=CC2=C1

InChI

InChIKey=KVBGVZZKJNLNJU-UHFFFAOYSA-N
InChI=1S/C10H8O3S/c11-14(12,13)10-6-5-8-3-1-2-4-9(8)7-10/h1-7H,(H,11,12,13)

HIDE SMILES / InChI
Sodium 2-naphthalenesulfonate is a sodium salt of naphthalene sulfonic acid. Sodium 2-naphthalenesulfonate is a surfactant-hydrotrope used in cosmetics. Use concentrations would be typically below 2%. In clinical studies, Sodium 2-naphthalenesulfonate was neither an irritant (tested up to 2%), cumulative irritant (tested up to 1%), nor a sensitizer (tested up to 1%). Sodium 2-naphthalenesulfonate is considered safe as used in cosmetic formulations intended to be applied to the skin.

Approval Year

PubMed

PubMed

TitleDatePubMed
Binding affinity properties of dendritic glycosides based on a beta-cyclodextrin core toward guest molecules and concanavalin A.
2001 Nov 16
Investigation of naphtalene sulfonate compounds sorption in a soil artificially contaminated using batch and column assays.
2002
Stability study and determination of benzene- and naphthalenesulfonates following an on-line solid-phase extraction method using the new programmable field extraction system.
2002 Apr
Development of generic liquid chromatography-mass spectrometry methods using experimental design.
2002 Jan
Isotachophoretic focusing and mass spectrometry detection as tools for improving the determination of aromatic sulfonates in capillary electrophoresis.
2002 Jul
Final report on the amended safety assessment of sodium polynaphthalenesulfonate and sodium naphthalenesulfonate.
2003
Depolymerisation and biodegradation of a synthetic tanning agent by activated sludges, the bacteria Arthrobacter globiformis and Comamonas testosteroni, and the fungus Cunninghamella polymorpha.
2005 Aug
Sorption enhancement of aromatic sulfonates onto an aminated hyper-cross-linked polymer.
2005 May 1
Adsorption mechanism in reversed-phase liquid chromatography. Effect of the surface coverage of a monomeric C18-silica stationary phase.
2006 May 19
The role of cross-linking structures to the formation of one-dimensional nano-organized polyaniline and their Raman fingerprint.
2008 Dec 1
trans-Diaqua-bis(ethyl-enediamine-κN,N')copper(II) bis[3-(3-pyrid-yl)propionate] dihydrate.
2008 Mar 5
Efficient removal of aromatic sulfonates from wastewater by a recyclable polymer: 2-naphthalene sulfonate as a representative pollutant.
2008 Oct 1
Influence of anionic sulfonate-containing co-ligands on the solid structures of silver complexes supported by 4,4'-bipyridine bridges.
2008 Oct 21
Rich aggregate morphologies induced by organic salts in aqueous solutions of a cationic gemini surfactant with a short spacer.
2009 Dec 1
Patents

Sample Use Guides

In clinical studies, Sodium 2-naphthalenesulfonate was neither an irritant (tested up to 2%), cumulative irritant (tested up to 1%), nor a sensitizer (tested up to 1%).
Route of Administration: Topical
Name Type Language
2-NAPHTHALENESULFONIC ACID
MI  
Systematic Name English
NAPHTHALENE-2-SULPHONIC ACID
Systematic Name English
.BETA.-NAPHTHALENESULFONIC ACID
Systematic Name English
NAPHTHALENE-2-SULFONIC ACID
Systematic Name English
2-NAPHTHALENESULFONIC ACID, MONOHYDRATE
Common Name English
2-NAPHTHALENESULFONIC ACID [MI]
Common Name English
Code System Code Type Description
CAS
120-18-3
Created by admin on Fri Dec 15 18:38:05 GMT 2023 , Edited by admin on Fri Dec 15 18:38:05 GMT 2023
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ECHA (EC/EINECS)
204-375-3
Created by admin on Fri Dec 15 18:38:05 GMT 2023 , Edited by admin on Fri Dec 15 18:38:05 GMT 2023
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CHEBI
44229
Created by admin on Fri Dec 15 18:38:05 GMT 2023 , Edited by admin on Fri Dec 15 18:38:05 GMT 2023
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WIKIPEDIA
Naphthalene-2-sulfonic acid
Created by admin on Fri Dec 15 18:38:05 GMT 2023 , Edited by admin on Fri Dec 15 18:38:05 GMT 2023
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PUBCHEM
8420
Created by admin on Fri Dec 15 18:38:05 GMT 2023 , Edited by admin on Fri Dec 15 18:38:05 GMT 2023
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MERCK INDEX
m7732
Created by admin on Fri Dec 15 18:38:05 GMT 2023 , Edited by admin on Fri Dec 15 18:38:05 GMT 2023
PRIMARY Merck Index
MESH
C534215
Created by admin on Fri Dec 15 18:38:05 GMT 2023 , Edited by admin on Fri Dec 15 18:38:05 GMT 2023
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FDA UNII
O9S4K2S25E
Created by admin on Fri Dec 15 18:38:05 GMT 2023 , Edited by admin on Fri Dec 15 18:38:05 GMT 2023
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EPA CompTox
DTXSID5044788
Created by admin on Fri Dec 15 18:38:05 GMT 2023 , Edited by admin on Fri Dec 15 18:38:05 GMT 2023
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DRUG BANK
DB08254
Created by admin on Fri Dec 15 18:38:05 GMT 2023 , Edited by admin on Fri Dec 15 18:38:05 GMT 2023
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