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α-Olefin sulfonates with linear alkenyl radicals from C 12 to C 18 are used as anionic surfactants in various areas of application due to their pronounced foam formation [clarification needed] and foam stability (even with high water hardness), excellent fat-dissolving power and oil dissolving power as well as a favorable ecological profile and low aquatic toxicity and human toxicity.
Alkyl (C14-C16) olefin sulfonate, sodium salt: Car wash, dog shampoo, emulsifier 9016-45-9: Alkylphenol ethoxylate surfactants: Engine cleaner, rubber sealant, emulsifier 1327-41-9: Aluminum chloride: Antiperspirant 73138-27-9: Amines, C12-14-tert-alkyl, ethoxylated: No record 71011-04-6: Amines, ditallow alkyl, ethoxylated: No record 68551-33-7
Sodium laurylsulfate tested on Uronema parduczi, a protozoan, was found to have the lowest effect value with the 20 h-EC5 being 0.75 milligrams per litre (2.7 × 10 −8 lb/cu in). Chronic exposure tests with C 12 to C 18 with the invertebrate Ceriodaphnia dubia found the highest toxicity is with C 14 ( NOEC was 0.045 mg/L).
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Sodium dodecyl sulfate; Sodium laurate; Sodium laureth sulfate; Sodium lauroyl sarcosinate; Sodium myreth sulfate; Sodium nonanoyloxybenzenesulfonate; Sodium pareth sulfate; Sodium stearate; Sodium sulfosuccinate esters; Sodium tallowate; Sodium tetradecyl sulfate; Sulfolipid
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.
The Buckeyes didn’t make this 28-14 Cotton Bowl victory easy on themselves, but Jack Sawyer removed them from harm’s way with a strip-sack of Quinn Ewers late in the fourth quarter.
An example of a linear alkylbenzene sulfonate (LAS) Linear alkylbenzene sulfonates (LAS) are prepared industrially by the sulfonation of linear alkylbenzenes (LABs), which can themselves be prepared in several ways. [2] In the most common route benzene is alkylated by long chain monoalkenes (e.g. dodecene) using hydrogen fluoride as a catalyst. [9]