Sodium laureth sulfate

Chemical compound From Wikipedia, the free encyclopedia

Sodium laureth sulfate (SLES), an accepted contraction of sodium lauryl ether sulfate, also called sodium alkylethersulfate, is an anionic detergent and surfactant found in many personal care products (soaps, shampoos, toothpaste, etc.) and for industrial uses. 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. It is derived from palm kernel oil or coconut oil. In herbicides, it is used as a surfactant to improve absorption of the herbicidal chemicals[2] and reduces time the product takes to be rainfast, when enough of the herbicidal agent will be absorbed.

Quick Facts Names, Identifiers ...
Sodium laureth sulfate
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Names
IUPAC name
α-Sulfo-ω-(dodecyloxy)-poly(oxyethane-1,2-diyl), sodium salt
Other names
Sodium lauryl ether sulfate
Sodium laureth sulphate
Sodium dodecyl polyoxyethylene sulfate
Sodium lauryl polyoxyethylene sulfate
Sodium lauryl dioxyethylene sulfate
Sodium lauryl trioxyethylene sulfate
Sodium laureth-2 sulfate
Sodium laureth-3 sulfate
Identifiers
Abbreviations SLES
ChemSpider
  • sodium laureth-2 sulfate: none
ECHA InfoCard 100.036.281
  • 23665884 (sodium 2-dodecoxyethyl sulfate)
UNII
Properties
CH3(CH2)11(OCH2CH2)nOSO3Na
Molar mass Variable; typically around 421 g/mol
(288.38 + 44.05n) g/mol
Hazards
NFPA 704 (fire diamond)
ThumbHealth 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g. chloroformFlammability 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g. canola oilInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
2
1
0
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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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. Laureth-3 sulfate is the most common one in commercial products.

Production

SLES is prepared by ethoxylation of dodecyl alcohol, which is produced industrially from palm kernel oil or coconut oil. 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 or SLS (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]

Safety

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 that SLES does not react with DNA.[3]

Irritation

Like many other detergents, SLES is an irritant.[4] It has been shown that SLES causes eye or skin irritation in experiments conducted on animals and humans.[4] The related surfactant SLS is also a known irritant.[5][6][7][8]

1,4-Dioxane contamination

Products containing SLES can be contaminated with up to 300 ppm of 1,4-dioxane, a by-product of SLES 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,[9] and encourages manufacturers to remove 1,4-dioxane, though it is not required by federal law.[10]

See also

References

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