Sodium laureth sulfate
α-Sulfo-ω-(dodecyloxy)-poly(oxyethane-1,2-diyl), sodium salt
Sodium lauryl ether sulfate
Sodium laureth sulphate
Sodium lauryl ether sulphate
|Molar mass||Variable; typically around 420 g/mol
(288.38 + 44.05n) g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|what is ?)(|
Sodium laureth sulfate (SLES), an accepted contraction 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. 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.
Its chemical formula is CH3(CH2)11(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. 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.
Tests in the US indicate that it is safe for consumer use. 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.
Like many other detergents, SLES is an irritant. It has also been shown that SLES causes eye or skin irritation in experiments conducted on animals and humans. The related surfactant SLS is a known irritant.
Some products containing SLES contain traces (up to 300 ppm) of 1,4-dioxane, which is formed as a by-product during the ethoxylation step of its production. 1,4-Dioxane is classified by the International Agency for Research on Cancer as a Group 2B carcinogen: possibly carcinogenic to humans. The United States Food and Drug Administration (FDA) recommends that these levels be monitored, and encourages manufacturers to remove 1,4-dioxane, though it is not required by federal law.
- Sodium lauroyl sarcosinate
- Sodium dodecyl sulfate
- Sodium myreth sulfate
- Sodium pareth sulfate
- Magnesium laureth sulfate
- Sodium dodecylbenzenesulfonate
- 1,4-Dioxane, a common impurity of SLES
- Kurt Kosswig,"Surfactants" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, 2005, Weinheim. doi:10.1002/14356007.a25_747
- Cara, A.M. Bondi, Julia L. Marks, Lauren B. Wroblewski, Heidi S. Raatikainen, Shannon R Lenox, Kay E Gebhardt (2015). "Human and Environmental Toxicity of Sodium Lauryl Sulfate (SLS): Evidence for Safe Use in Household Cleaning Products". Environ Health Insights. 9: 27–32. doi:10.4137/EHI.S31765. PMC . PMID 26617461. .
- NICNAS SLES animal test
- "Final report on the safety assessment of sodium laureth sulfate and ammonium laureth sulfate". Journal of the American College of Toxicology. 2 (5): 1–34. 1983. doi:10.3109/10915818309140713.
- Agner T (1991). "Susceptibility of atopic dermatitis patients to irritant dermatitis caused by sodium lauryl sulphate". Acta Dermato-venereologica. 71 (4): 296–300. PMID 1681644.
- Nassif A, Chan SC, Storrs FJ, Hanifin JM (November 1994). "Abnormal skin irritancy in atopic dermatitis and in atopy without dermatitis". Archives of Dermatology. 130 (11): 1402–7. doi:10.1001/archderm.130.11.1402. PMID 7979441.
- Magnusson B, Gilje O (1973). "Allergic contact dermatitis from a dish-washing liquid containing lauryl ether sulphate". Acta Dermato-venereologica. 53 (2): 136–40. PMID 4120956.
- Van Haute N, Dooms-Goossens A (March 1983). "Shampoo dermatitis due to cocobetaine and sodium lauryl ether sulphate". Contact Dermatitis. 9 (2): 169. doi:10.1111/j.1600-0536.1983.tb04348.x. PMID 6851541.
- Black RE, Hurley FJ, Havery DC (2001). "Occurrence of 1,4-dioxane in cosmetic raw materials and finished cosmetic products". Journal of AOAC International. 84 (3): 666–70. PMID 11417628.
- FDA/CFSAN--Cosmetics Handbook Part 3: Cosmetic Product-Related Regulatory Requirements and Health Hazard Issues. Prohibited Ingredients and other Hazardous Substances: 9. Dioxane