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Revision as of 05:36, 20 March 2012

Sodium nonanoyloxybenzenesulfonate
Names
IUPAC name Sodium 4-nonanoyloxybenzenesulfonate
Other names 4-Sulfophenyl nonanoate sodium salt; Sodium p-nonanoyloxybenzenesulfonate; p-(Nonanoyloxy)benzenesulfonic acid sodium salt; p-Sodiosulfophenyl nonanoate
Identifiers
CAS Number
3D model (JSmol)
Abbreviations NOBS
ChemSpider
PubChem CID
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C15H22O5S.Na/c1-2-3-4-5-6-7-12-15(16)20-13-10-8-9-11-14(13)21(17,18)19;/h8-11H,2-7,12H2,1H3,(H,17,18,19);/q;+1/p-1Key: QSKQNALVHFTOQX-UHFFFAOYSA-M
  • InChI=1/C15H22O5S.Na/c1-2-3-4-5-6-7-12-15(16)20-13-10-8-9-11-14(13)21(17,18)19;/h8-11H,2-7,12H2,1H3,(H,17,18,19);/q;+1/p-1Key: QSKQNALVHFTOQX-REWHXWOFAO
SMILES
  • .O=C(Oc1ccccc1S()(=O)=O)CCCCCCCC
Properties
Chemical formula C15H21NaO5S
Molar mass 336.38 g·mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). checkY verify (what is  ?) Infobox references
Chemical compound

Sodium nonanoyloxybenzenesulfonate (NOBS) is an important component of detergents and bleaches. It is known as a bleaching activator for active oxygen sources, allowing formulas containing hydrogen peroxide releasing chemicals (specifically the sodium perborate, sodium percarbonate, sodium perphosphate, sodium persulfate, and urea peroxide. Unlike tetraacetylethylenediamine, NOBS can be used in a much lower temperature.

References

  1. Kuzel, P.; Lieser, T. (1990). "Bleach systems". Tenside, Surfactants, Detergents. 27 (1): 23–8.{{cite journal}}: CS1 maint: multiple names: authors list (link)
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