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Sodium Lauryl Sulfate (SLS ) | Effects of sodium lauryl sulfate natural-health-informatio... | Buy Quinine Sulphate Online | Order Cheap Quinine Sulphate | Generic... 24x7pharmacy.com | Sodium Lauryl Sulfate Free | Therapeutic body wash kopecnaturals.com |
Not to be confused with sodium laureth sulfate.
Sodium lauryl sulfate (SLS), sodium laurilsulfate or sodium dodecyl sulfate (SDS or NaDS) (C12H25SO4Na) is an anionic surfactant used in many cleaning and hygiene products. The molecule has a tail of 12 carbon atoms, attached to a sulfate group, giving the molecule the amphiphilic properties required of a detergent.
[edit] ApplicationsSLS is a highly effective surfactant used in any task requiring the removal of oily stains and residues. As such the compound is found in high concentrations in industrial products including engine degreasers, floor cleaners, and car wash soaps. In household products, SLS is used in lower concentrations with toothpastes, shampoos, and shaving foams. It is an important component in bubble bath formulations for its thickening effect and its ability to create a lather. It has recently found application as a surfactant in gas hydrate or methane hydrate formation reactions, increasing the rate of formation as much as 700 times.[1] The product can also be used to aid in lysing cells during DNA extraction and for unraveling proteins in SDS-PAGE (see below). [edit] In medicineIn medicine, sodium laurilsulfate is used rectally as a laxative in enemas, and as an excipient on some dissolvable aspirins and other fiber therapy caplets. [edit] SDS-PAGEMain article: SDS-PAGE Sodium lauryl sulfate, in science referred to as sodium dodecyl sulfate (SDS), is commonly used in preparing proteins for electrophoresis in the SDS-PAGE technique.[2] This compound works by disrupting non-covalent bonds in the proteins, denaturing them, and causing the molecules to lose their native shape (conformation). Also, anions of SDS bind to the main peptide chain at a ratio of one SDS anion for every two amino acid residues. This effectively imparts a negative charge on the protein that is proportional to the mass of that protein (about 1.4 g SDS/g protein). This new negative charge is significantly greater than the original charge of that protein. The electrostatic repulsion that is created by binding of SDS causes proteins to unfold into a rod-like shape thereby eliminating differences in shape as a factor for separation in the gel. Sodium lauryl sulfate is probably the most researched anionic surfactant compound. Like all detergent surfactants (including soaps), sodium lauryl sulfate removes oils from the skin, and can cause skin and eye irritation. The critical micelle concentration (CMC) in pure water at 25°C is 0.0082 M[3], and the aggregation number at this concentration is usually considered to be about 62[4]. The micelle ionization fraction (α) is around 0.3 (or 30%).[5] [edit] SynthesisSLS is synthesized by reacting lauryl alcohol with sulfuric acid to produce hydrogen lauryl sulfate which is then neutralized through the addition of sodium carbonate[6]. Lauryl alcohol is in turn usually derived from either coconut or palm kernel oil by esterification of their fatty acids followed by reduction of the acid group to an alcohol. Due to this synthesis method, SLS is actually not pure dodecyl sulfate but a mixture of alkyl sulfates with dodecyl sulfate as the main component.[7] [edit] Health and safetySLS has not been proven to be carcinogenic when either applied directly to skin or consumed.[8] SLS however is a strong surfactant and a number of health concerns have been raised in published reports.[9]
Research suggests that SLS could represent a potential effective microbicide, which can also inhibit and possibly prevent infection by various enveloped and non-enveloped viruses such as the Herpes simplex viruses, HIV, and the Semliki Forest Virus.[18][19] [edit] See also[edit] References
[edit] External links
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