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Sebacic acid is also found in other lipids that coat the skin surface. Human neutrophils can convert sebacic acid to its 5-oxo analog, i.e., 5-oxo-6E,8Z-octadecenoic acid, a structural analog of 5-oxo-eicosatetraenoic acid and like this oxo-eicosatetraenoic acid is an exceptionally potent activator of eosinophils, monocytes, and other pro ...
Sebacic acid, named from sebum . Thenard isolated this compound from distillation products of beef tallow in 1802. It is produced industrially by alkali fission of castor oil. [3] Sebacic acid and its derivatives have a variety of industrial uses as plasticizers, lubricants, diffusion pump oils, cosmetics, candles, etc. It is also used in the ...
The systematic IUPAC name is not always the preferred IUPAC name, for example, lactic acid is a common, and also the preferred, name for what systematic rules call 2-hydroxypropanoic acid. This list is ordered by the number of carbon atoms in a carboxylic acid.
Dibutyl sebacate (DBS) is an organic chemical, a dibutyl ester of sebacic acid. Its main use is as a plasticizer in production of plastics , namely cellulose acetate butyrate , cellulose acetate propionate , ethyl cellulose , polyvinyl butyral , polyvinyl chloride , polystyrene , and many synthetic rubbers (especially nitrile rubber and ...
Dioctyl sebacate (also di(2-ethylhexyl) sebacate, commonly abbreviated as DOS, DEHS, and BEHS) is an organic compound which is the diester of sebacic acid and 2-ethylhexanol. It is an oily colorless liquid and is used as a plasticizer, including in the explosive C4. [1]
Sebacoyl chloride (or sebacoyl dichloride) is a di-acyl chloride, with formula (CH 2) 8 (COCl) 2.A colorless oily liquid with a pungent odor, it is soluble in hydrocarbons and ethers.
2-Octanol is produced commercially by base-cleavage of ricinoleic acid. [8] The coproduct is a mixture of sebacic acid ((C 8 H 16 CO 2 H) 2). Castor oil, which consists mainly of triglycerides of ricinoleic acid, is the main feedstock. [9] [10]
Sebacic acid; 1,4-Butanediol diglycidyl ether This page was last edited on 21 February 2024, at 16:29 (UTC). Text is available under the Creative Commons Attribution ...