Sodium laureth sulfate

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Sodium laureth sulfate
Sodium laureth sulfate structure.png
Names
Other names
Sodium lauryl ether sulfate; sodium laureth sulphate; sodium lauryl ether sulphate
Identifiers
9004-82-4 YesY
Abbreviations SLES
Properties
CH3(CH2)11(OCH2CH2)nOSO3Na
Molar mass around 420 g/mol
(288.38 + 44.05n) g/mol
Vapor pressure {{{value}}}
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
YesY verify (what is YesYN ?)
Infobox references

Sodium laureth sulfate (SLES), an accepted contraction (Lauryl + Ether = Laureth) of sodium lauryl ether sulfate (SLES), is an anionic detergent and surfactant found in many personal care products (soaps, shampoos, toothpaste etc.). SLES is an inexpensive and very effective foaming agent.[1] SLES, sodium lauryl sulfate (SLS), ammonium lauryl sulfate (ALS), and sodium pareth sulfate are surfactants that are used in many cosmetic products for their cleaning and emulsifying properties. They behave similarly to soap.

Chemical structure

Its chemical formula is CH3(CH2)10CH2(OCH2CH2)nOSO3Na. Sometimes the number represented by n is specified in the name, for example laureth-2 sulfate. The product is heterogeneous in the number of ethoxyl groups, where n is the mean. It is common for commercial products for n= 3. SLES is prepared by ethoxylation of dodecyl alcohol. The resulting ethoxylate is converted to a half ester of sulfuric acid, which is neutralized by conversion to the sodium salt.[1] The related surfactant sodium lauryl sulfate (also known as sodium dodecyl sulfate or SDS) is produced similarly, but without the ethoxylation step. SLS and ammonium lauryl sulfate (ALS) are commonly used alternatives to SLES in consumer products.[1]

Toxicology

Irritation

SLES is an irritant like many other detergents, with the irritation increasing with concentration.[2] It has also been shown that SLES causes eye or skin irritation in experiments done on animals and humans.[2] The related surfactant SLS is a known irritant,[3][4] and research suggests that SLES can also cause irritation after extended exposure in some people.[5][6]

Other

It has long been speculated that the SLES would be carcinogenic, but toxicology research by the U.S. OSHA and IARC supports the conclusions of the Cosmetic, Toiletry, and Fragrance Association (CTFA) and the American Cancer Society that SLES is not a carcinogen.[citation needed] The Australian government's Department of Health and Ageing and its National Industrial Chemicals Notification and Assessment Scheme (NICNAS) have determined SLES does not react with DNA .[7]

1,4-Dioxane contamination

Some products containing SLES have been found to also contain traces (up to 279 ppm) of 1,4-dioxane; this is formed as a by-product during the ethoxylation step of its synthesis. The U.S. Food and Drug Administration recommends that these levels be monitored.[8] The U.S. Environmental Protection Agency classifies 1,4-dioxane to be a probable human carcinogen (not observed in epidemiological studies of workers using the compound, but resulting in more cancer cases in controlled animal studies), and a known irritant with a no-observed-adverse-effects level of 400 milligrams per cubic meter at concentrations significantly higher than those found in commercial products.[9] Under Proposition 65, 1,4-dioxane is classified in the U.S. state of California to cause cancer.[10][11] The FDA encourages manufacturers to remove 1,4-dioxane, though it is not required by federal law.[12]

See also

References

  1. 1.0 1.1 1.2 Kurt Kosswig,"Surfactants" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, 2005, Weinheim. doi:10.1002/14356007.a25_747
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  7. NICNAS SLES animal test
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  9. 1,4-Dioxane (1,4-Diethyleneoxide). Hazard Summary. U.S. Environmental Protection Agency. Created in April 1992; Revised in January 2000. Fact Sheet
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  12. FDA/CFSAN--Cosmetics Handbook Part 3: Cosmetic Product-Related Regulatory Requirements and Health Hazard Issues. Prohibited Ingredients and other Hazardous Substances: 9. Dioxane

External links