enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  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. 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.

  5. 3-Mercaptopropionitrile - Wikipedia

    en.wikipedia.org/wiki/3-Mercaptopropionitrile

    3-Mercaptopropionitrile is the organosulfur compound with the formula HSCH 2 CH 2 CN. [1] Containing both thiol and nitrile functional groups , it is a bifunctional compound . A colorless liquid, the compound has found some use as a masked form of thiolate.

  6. Pentaerythritol tetraacrylate - Wikipedia

    en.wikipedia.org/wiki/Pentaerythritol_tetraacrylate

    It is a tetrafunctional acrylate ester used as a monomer in the manufacture of polymers. [1] As it is a polymerizable acrylate monomer, it is nearly always supplied with an added polymerisation inhibitor , such as MEHQ (monomethyl ether hydroquinone).

  7. -oate - Wikipedia

    en.wikipedia.org/wiki/-oate

    The suffix-oate is the IUPAC nomenclature used in organic chemistry to form names of compounds formed with ester. They are of two types: They are of two types: Formed by replacing the hydrogen atom in the –COOH by some other radical , usually an alkyl or aryl radical forming an ester .

  8. Sodium propionate - Wikipedia

    en.wikipedia.org/wiki/Sodium_propionate

    Structure of sodium propionate, with methyl groups and H atoms omitted. [5] Color code: red = O, blue = Na. Anhydrous sodium propionate is a polymeric structure, featuring trigonal prismatic Na + centers bonded to six oxygen ligands provided by the carboxylates.

  9. Dibasic ester - Wikipedia

    en.wikipedia.org/wiki/Dibasic_ester

    Dibasic ester or DBE is an ester of a dicarboxylic acid.Depending on the application, the alcohol may be methanol or higher molecular weight monoalcohols. Mixtures of different methyl dibasic esters are commercially produced from short-chain acids such as adipic acid, glutaric acid, and succinic acid. [1]