Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C10H7O3S.Na |
| Molecular Weight | 230.216 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[Na+].[O-]S(=O)(=O)C1=CC=C2C=CC=CC2=C1
InChI
InChIKey=YWPOLRBWRRKLMW-UHFFFAOYSA-M
InChI=1S/C10H8O3S.Na/c11-14(12,13)10-6-5-8-3-1-2-4-9(8)7-10;/h1-7H,(H,11,12,13);/q;+1/p-1
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
| Title | Date | PubMed |
|---|---|---|
| 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 |
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| Separation and migration behavior of positional and structural naphthalenesulfonate isomers by cyclodextrin-mediated capillary electrophoresis. | 2004 Apr 9 |
|
| Adsorption mechanism in reversed-phase liquid chromatography. Effect of the surface coverage of a monomeric C18-silica stationary phase. | 2006 May 19 |
|
| The development of electrically conductive polycaprolactone fumarate-polypyrrole composite materials for nerve regeneration. | 2010 Aug |
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| Novel naphthalene-based inhibitors of Trypanosoma brucei RNA editing ligase 1. | 2010 Aug 24 |
|
| Microbial conversion of 5-sulfoisophthalic acid into 5-hydroxyisophthalic acid by Ochrobactrum anthropi S9. | 2010 Mar |
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EPA PESTICIDE CODE |
217202
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532-02-5
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1366947
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1366946
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PARENT (SALT/SOLVATE)
SUBSTANCE RECORD
