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  2. Epoxy - Wikipedia

    en.wikipedia.org/wiki/Epoxy

    Epoxy is the family of basic components or cured end products of epoxy resins. Epoxy resins, also known as polyepoxides, are a class of reactive prepolymers and polymers which contain epoxide groups. The epoxide functional group is also collectively called epoxy. [1] The IUPAC name for an epoxide group is an oxirane.

  3. 4,4'-Diaminodicyclohexylmethane - Wikipedia

    en.wikipedia.org/wiki/4,4...

    4,4'-Diaminodicyclohexylmethane is the name for organic compounds with the formula CH 2 (C 6 H 10 NH 2) 2.It is classified as a diamine.In the epoxy industry it is often referred to as PACM, short for para-diamino­dicyclohexyl­methane.

  4. Tetraethylenepentamine - Wikipedia

    en.wikipedia.org/wiki/Tetraethylenepentamine

    It is primarily used as a curing agent or hardener in epoxy chemistry. This can be on its own or reacted with tall oil fatty acid (TOFA) and its dimer to make an amidoamine. [2] This amidoamine is then used as the curing agent for epoxy resin systems. TEPA is a pentadentate ligand in coordination chemistry.

  5. Pentaerythritol tetraacrylate - Wikipedia

    en.wikipedia.org/wiki/Pentaerythritol_tetraacrylate

    PETA is part of a family of acrylates used in epoxy resin chemistry and ultraviolet cure of coatings. 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.

  6. C12–C14 alcohol glycidyl ether - Wikipedia

    en.wikipedia.org/wiki/C12–C14_alcohol_glycidyl...

    C12-C14 alcohol glycidyl ether (AGE) is an organic chemical in the glycidyl ether family. [2] It is a mixture of mainly 12 and 14 carbon chain alcohols, also called fatty alcohols that have been glycidated.

  7. Sharpless epoxidation - Wikipedia

    en.wikipedia.org/wiki/Sharpless_epoxidation

    The Sharpless epoxidation is viable with a large range of primary and secondary alkenic alcohols. Furthermore, with the exception noted above, a given dialkyl tartrate will preferentially add to the same face independent of the substitution on the alkene.To demonstrate the synthetic utility of the Sharpless epoxidation, the Sharpless group created synthetic intermediates of various natural ...

  8. Johnson–Corey–Chaykovsky reaction - Wikipedia

    en.wikipedia.org/wiki/Johnson–Corey...

    The vast majority of reagents are monosubstituted at the ylide carbon (either R 1 or R 2 as hydrogen). Disubstituted reagents are much rarer but have been described: [1] If the ylide carbon is substituted with an electron-withdrawing group (EWG), the reagent is referred to as a stabilized ylide. These, similarly to sulfoxonium reagents, react ...

  9. Epoxide - Wikipedia

    en.wikipedia.org/wiki/Epoxide

    A generic epoxide. In organic chemistry, an epoxide is a cyclic ether, where the ether forms a three-atom ring: two atoms of carbon and one atom of oxygen.This triangular structure has substantial ring strain, making epoxides highly reactive, more so than other ethers.