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Sodium tetradecyl sulfate. CCCCC (CC)CCC (CC (C)C)OS (=O) (=O) [O-]. [Na+] Sodium tetradecyl sulfate (STS) is a common anionic surfactant. The compound consists of the sodium salt of the micelle -forming sulfate ester of tetradecanol. It is a white, water-soluble solid of low toxicity with many practical uses. [1]
Straight-chain terminal alkenes, also called linear alpha olefins (LAO) or normal alpha olefins (NAO), are alkenes (olefins) having a chemical formula C n H 2n, distinguished from other alkenes with a similar molecular formula by being terminal alkenes, in which the double bond occurs at the alpha (α-, 1-or primary) position, and by having a linear (unbranched) hydrocarbon chain.
The sulfonate ion. In organosulfur chemistry, a sulfonate is a salt, anion or ester of a sulfonic acid. Its formula is R−S (=O)2−O−, containing the functional group − S (= O)2−O−, where R is typically an organyl group, amino group or a halogen atom. Sulfonates are the conjugate bases of sulfonic acids.
2-propenoic acid, homopolymer, ammonium salt. Moisturizer, Sunscreen, Friction reducer. 25987-30-8. 2-Propenoic acid, polymer with 2 p-propenamide, sodium salt / Copolymer of acrylamide and sodium acrylate. Friction Reducer. 71050-62-9. 2-Propenoic acid, polymer with sodium phosphinate (1:1) No record. 66019-18-9.
Alkylbenzene sulfonates are a class of anionic surfactants, consisting of a hydrophilic sulfonate head-group and a hydrophobic alkylbenzene tail-group. Along with sodium laureth sulfate, they are one of the oldest and most widely used synthetic detergents and may be found in numerous personal-care products (soaps, shampoos, toothpaste etc.) and ...
Tetradecane. Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is YN ?) Tetradecane is an alkane hydrocarbon with the chemical formula CH 3 (CH 2) 12 CH 3. Tetradecane has 1858 structural isomers.
Aromatic sulfonation. In organic chemistry, aromatic sulfonation is an organic reaction in which a hydrogen atom on an arene is replaced by a sulfonic acid (−SO2OH) functional group in an electrophilic aromatic substitution. [ 1 ] Aryl sulfonic acids are used as detergents, dye, and drugs.
Desulfonylation reactionsare chemical reactions leading to the removal of a sulfonylgroup from organic compounds. As the sulfonyl functional group is electron-withdrawing,[1]methods for cleaving the sulfur–carbon bonds of sulfones are typically reductive in nature. Olefination or replacement with hydrogenmay be accomplished using reductive ...