Search results
Results From The WOW.Com Content Network
Dodecanol / ˈ d oʊ ˈ d ɛ k ɑː n ɒ l /, or lauryl alcohol, is an organic compound produced industrially from palm kernel oil or coconut oil. It is a fatty alcohol . Sulfate esters of lauryl alcohol, especially sodium lauryl sulfate , are very widely used as surfactants .
1-Decanol is a straight chain fatty alcohol with ten carbon atoms and the molecular formula C 10 H 21 OH. It is a colorless to light yellow viscous liquid that is insoluble in water and has an aromatic odor. [3] The interfacial tension against water at 20 °C is 8.97 mN/m.
184.323 g·mol −1 Appearance Colorless liquid [1] Density: 0.83 g cm −3 [1] ... but commercial samples are usually produced from dodecanol by dehydrogenation. [2]
Lauryl acetate, Dodecan-1-yl acetate, 1-Dodecanol acetate, n-Dodecyl ethanoate, Dodecanol acetate, Dodecanyl acetate, n-Dodecyl acetate ... Solubility in ethanol: 80% ...
Arachidyl alcohol (1-eicosanol) 20 carbon atoms: C 20 H 42 O Heneicosyl alcohol (1-heneicosanol) 21 carbon atoms: C 21 H 44 O Behenyl alcohol (1-docosanol) 22 carbon atoms: C 22 H 46 O Erucyl alcohol (cis-13-docosen-1-ol) 22 carbon atoms: unsaturated: C 22 H 44 O Lignoceryl alcohol (1-tetracosanol) 24 carbon atoms: C 24 H 50 O Ceryl alcohol (1 ...
Octyldodecanol is a branched-chain primary alcohol used as the isomer 2-octyl-1-dodecanol in cosmetics such as lipstick, [2] or as an anti-blooming agent in facepowder. [3] It is a medium spreading emollient, with equilibrium spreading pressure of 17.0 dyne/cm. [4] Octyldodecanol is in the class of Guerbet alcohols, because it has the branch at the β position. [5]
Hume-Rothery rules, named after William Hume-Rothery, are a set of basic rules that describe the conditions under which an element could dissolve in a metal, forming a solid solution. There are two sets of rules; one refers to substitutional solid solutions, and the other refers to interstitial solid solutions.
Most 1-bromoalkanes are prepared by free-radical addition of hydrogen bromide to the 1-alkene, which is 1-dodecene in the case of 1-bromododecane. These conditions lead to anti-Markovnikov addition, giving the 1-bromo derivative. [2] 1-Bromododecane can also be prepared by treating dodecanol with hydrobromic acid and sulfuric acid. [3]