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  2. Pentaerythritol tetrakis(3-mercaptopropionate) - Wikipedia

    en.wikipedia.org/wiki/Pentaerythritol_tetrakis(3...

    Pentaerythritol tetrakis(3-mercaptopropionate) is a common thiol monomer reacted with alkenes in the thiol-ene reaction to form polymeric networks. [3] Being functionalized with four thiol groups, it can react with multifunctional alkenes to form thiol-ene networks.

  3. 3-Mercaptopropionic acid - Wikipedia

    en.wikipedia.org/wiki/3-Mercaptopropionic_acid

    3-Mercaptopropionic acid (3-MPA) is an organosulfur compound with the formula HSCH 2 CH 2 CO 2 H. It is a bifunctional molecule, containing both carboxylic acid and thiol groups. It is a colorless oil. It is derived from the addition of hydrogen sulfide to acrylic acid.

  4. List of unsaturated fatty acids - Wikipedia

    en.wikipedia.org/.../List_of_unsaturated_fatty_acids

    Cervonic acid (or docosahexaenoic acid) has 22 carbons, is found in fish oil, is a 4,7,10,13,16,19-hexa unsaturated fatty acid. In the human body its generation depends on consumption of omega 3 essential fatty acids (e.g., ALA or EPA), but the conversion process is inefficient. [ 22 ]

  5. Ester - Wikipedia

    en.wikipedia.org/wiki/Ester

    An ester of a carboxylic acid.R stands for any group (typically hydrogen or organyl) and R ′ stands for any organyl group.. In chemistry, an ester is a compound derived from an acid (organic or inorganic) in which the hydrogen atom (H) of at least one acidic hydroxyl group (−OH) of that acid is replaced by an organyl group (R ′). [1]

  6. List of esters - Wikipedia

    en.wikipedia.org/wiki/List_of_esters

    An ester of carboxylic acid. R stands for any group (organic or inorganic) and R′ stands for organyl group. In chemistry, an ester is a compound derived from an acid (organic or inorganic) in which the hydrogen atom (H) of at least one acidic hydroxyl group (−OH) of that acid is replaced by an organyl group (−R).

  7. Pentaerythritol - Wikipedia

    en.wikipedia.org/wiki/Pentaerythritol

    Pentaerythritol was first reported in 1891 by German chemist Bernhard Tollens and his student P. Wigand. [5] It may be prepared via a base-catalyzed multiple-addition reaction between acetaldehyde and 3 equivalents of formaldehyde to give pentaerythrose (CAS: 3818-32-4), followed by a Cannizzaro reaction with a fourth equivalent of formaldehyde to give the final product plus formate ion.

  8. Pentaerythritol tetraacrylate - Wikipedia

    en.wikipedia.org/wiki/Pentaerythritol_tetraacrylate

    Similar monomers used are 1,6-hexanediol diacrylate and trimethylol propane triacrylate. It is a derivative of pentaerythritol [2] One of the key uses of the material is in polymeric synthesis where it can form micelles and block copolymers. [3] [4] The molecule's acrylate group functionality enables the molecule to do the Michael reaction with ...

  9. Category:Propionate esters - Wikipedia

    en.wikipedia.org/wiki/Category:Propionate_esters

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