Sodium nonanoyloxybenzenesulfonate

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	89740-11-4 N
3D model (Jmol)	Interactive image
Abbreviations	NOBS
ChemSpider	152449 Y
PubChem	174822
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-1 Y Key: QSKQNALVHFTOQX-UHFFFAOYSA-M Y 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-1 Key: QSKQNALVHFTOQX-REWHXWOFAO
SMILES [Na+].O=C(Oc1ccccc1S([O-])(=O)=O)CCCCCCCC
Properties
Chemical formula	C15H21NaO5S
Molar mass	336.38 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YN ?)
Infobox references

Sodium nonanoyloxybenzenesulfonate (NOBS) is an important component of laundry detergents and bleaches. It is known as a bleach activator for active oxygen sources, allowing formulas containing hydrogen peroxide releasing chemicals (specifically sodium perborate, sodium percarbonate, sodium perphosphate, sodium persulfate, and urea peroxide to effect bleaching at lower temperatures.^[1] NOBS was developed by Procter & Gamble in 1983^[2] and was first used in American laundry detergents in 1988.^[3] NOBS is the main bleach activator used in the U.S.A. and Japan.^[4] Compared to TAED, which is the predominant bleach activator used in Europe, NOBS is efficient at much lower temperatures. At 20 °C NOBS is 100 times more soluble than TAED in water.^[5] When attacked by the perhydroxyl anion (from hydrogen peroxide), NOBS forms the peroxy acid peroxynonanoic acid and releases the leaving group sodium 4-hydroxybenzene sulfonate, which is an inert by-product.

References