Sodium nonanoyloxybenzenesulfonate

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Sodium nonanoyloxybenzenesulfonate
Sodium nonanoyloxybenzenesulfonate.png
Names
Preferred IUPAC name
Sodium 4-(nonanoyloxy)benzene-1-sulfonate
Other names
4-Sulfophenyl nonanoate sodium salt; Sodium p-nonanoyloxybenzenesulfonate; p-(Nonanoyloxy)benzenesulfonic acid sodium salt; p-Sodiosulfophenyl nonanoate
Identifiers
3D model (JSmol)
AbbreviationsNOBS
ChemSpider
PubChem CID
UNII
  • 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 Yes check.svgY
    Key: QSKQNALVHFTOQX-UHFFFAOYSA-M Yes check.svgY
  • 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
  • [Na+].O=C(Oc1ccccc1S([O-])(=O)=O)CCCCCCCC
Properties
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).
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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]

Contents

Synthesis

NOBS is formed by the reaction of nonanoic acid (or its esters) with phenol followed by aromatic sulfonation using SO3 to form a sulfonic acid at the para-position.

Bleach activation

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 peroxynonanoic acid (a peroxy acid) and releases the leaving group sodium 4-hydroxybenzene sulfonate, which is an inert by-product.

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References

  1. ↑ Kuzel, P.; Lieser, T. (1990). "Bleach systems". Tenside, Surfactants, Detergents. 27 (1): 23–8. doi:10.1515/tsd-1990-270109. S2CID   235325050.
  2. ↑ Chung, S. Y.; Spadini, G. L. (1983). US4412934.
  3. ↑ Arno Cahn (30 January 1994). Proceedings of the 3rd World Conference on Detergents: Global Perspectives. The American Oil Chemists Society. pp. 64–70. ISBN   978-0-935315-52-3.
  4. ↑ Hirschen, M. (2005). Handbook of Detergents Part C: Analysis. Marcel Dekker. pp. 439–470. ISBN   9780824703516.
  5. ↑ Reinhardt, G.; Borchers, G. (2009). Handbook of Detergents, Part E: Applications. CRC Press. ISBN   9781574447576.
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