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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

Molecular Formula C10H8O3S
Molecular Weight 208.234
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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
Determination of cyclodextrins and their derivatives by capillary electrophoresis with indirect UV and conductivity detection.
2001 Apr
Determination of naphthalenesulfonic acid isomers by large-volume on-line derivatization and gas chromatography-mass spectrometry.
2001 Aug 17
Development of generic liquid chromatography-mass spectrometry methods using experimental design.
2002 Jan
Amplification of small analytes in polymer solution by capillary electrophoresis.
2002 Jun
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
Treatment of naphthalene-2-sulfonic acid from tannery wastewater by a granular activated carbon fixed bed inoculated with bacterial isolates Arthrobacter globiformis and Comamonas testosteroni.
2006 Feb
A chromatographic estimate of the degree of heterogeneity of RPLC packing materials. 1. Non-endcapped polymeric C30-bonded stationary phase.
2006 Jan 20
Adsorption mechanism in reversed-phase liquid chromatography. Effect of the surface coverage of a monomeric C18-silica stationary phase.
2006 May 19
Influence of anionic sulfonate-containing co-ligands on the solid structures of silver complexes supported by 4,4'-bipyridine bridges.
2008 Oct 21
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
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:38:05 GMT 2023
Edited
by admin
on Fri Dec 15 18:38:05 GMT 2023
Record UNII
O9S4K2S25E
Record Status Validated (UNII)
Record Version
  • Download
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
PRIMARY
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
PRIMARY
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
PRIMARY
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
PRIMARY
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
PRIMARY
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
PRIMARY
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
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT