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  2. Oleylamine - Wikipedia

    en.wikipedia.org/wiki/Oleylamine

    Oleylamine is an organic compound with a molecular formula C 18 H 35 NH 2. [1] It is an unsaturated fatty amine related to the fatty acid oleic acid.The pure compound is a clear and colorless liquid.

  3. Ethoxylation - Wikipedia

    en.wikipedia.org/wiki/Ethoxylation

    In organic chemistry, ethoxylation is a chemical reaction in which ethylene oxide (C 2 H 4 O) adds to a substrate. It is the most widely practiced alkoxylation, which involves the addition of epoxides to substrates. In the usual application, alcohols and phenols are converted into R(OC 2 H 4) n OH, where n ranges from 1 to 10. Such compounds ...

  4. Fatty amine - Wikipedia

    en.wikipedia.org/wiki/Fatty_amine

    Fatty amines are commonly prepared from fatty acids; which are themselves obtained from natural sources, typically seed-oils.The overall reaction is sometimes referred to as the Nitrile Process [3] and begins with a reaction between the fatty acid and ammonia at high temperature (>250 °C) and in the presence of a metal oxide catalyst (e.g., alumina or zinc oxide) to give the fatty nitrile.

  5. Fatty alcohol - Wikipedia

    en.wikipedia.org/wiki/Fatty_alcohol

    Fatty alcohols are relatively benign materials, with LD 50 (oral, rat) ranging from 3.1–4 g/kg for hexanol to 6–8 g/kg for octadecanol. [1] For a 50 kg person, these values translate to more than 100 g. Tests of acute and repeated exposures have revealed a low level of toxicity from inhalation, oral or dermal exposure of fatty alcohols.

  6. Dectaflur - Wikipedia

    en.wikipedia.org/wiki/Dectaflur

    Dectaflur consists of oleyl amine (the amine corresponding to oleyl alcohol) and hydrofluoric acid. Oleyl amine with its long lipophilic hydrocarbon chain has surfactant properties. It forms a film layer on the surface of teeth, which facilitates incorporation of fluoride into the top layers of the enamel, reaching a depth of only a few ...

  7. Oleic acid - Wikipedia

    en.wikipedia.org/wiki/Oleic_acid

    Reduction of the carboxylic acid group yields oleyl alcohol. Ozonolysis of oleic acid is an important route to azelaic acid. The coproduct is nonanoic acid: [15] H 17 C 8 CH=CHC 7 H 14 CO 2 H + 4"O" → HO 2 CC 7 H 14 CO 2 H + H 17 C 8 CO 2 H. Esters of azelaic acid find applications in lubrication and plasticizers.

  8. How Democrats Are Faring In First Tests Of The Trump Backlash

    data.huffingtonpost.com/2017/special-elections

    In Connecticut’s 2nd Senate District, for example, Republicans decreased their loss margin by some 20 percentage points. But Democrats see promising signs in other areas. In Iowa’s 45th Senate District, where Clinton defeated Trump by about 16 percentage points, Democrat Jim Lykam defeated Mike Gonzales, the GOP candidate, by an almost 50 ...

  9. Oleyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Oleyl_alcohol

    Oleyl alcohol / ˈ oʊ l i ˌ ɪ l, ˈ oʊ l i əl /, [1] or cis-9-octadecen-1-ol, is an unsaturated fatty alcohol with the molecular formula C 18 H 36 O or the condensed structural formula CH 3 (CH 2) 7 −CH=CH−(CH 2) 8 OH. It is a colorless oil, mainly used in cosmetics.