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  2. Ethylene oxide - Wikipedia

    en.wikipedia.org/wiki/Ethylene_oxide

    Ethylene oxide is an organic compound with the formula C 2 H 4 O. It is a cyclic ether and the simplest epoxide: a three-membered ring consisting of one oxygen atom and two carbon atoms. Ethylene oxide is a colorless and flammable gas with a faintly sweet odor.

  3. Epoxide - Wikipedia

    en.wikipedia.org/wiki/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. They are produced on a large scale for many applications.

  4. Cationic polymerization - Wikipedia

    en.wikipedia.org/wiki/Cationic_polymerization

    Upon addition of an initiator, cyclic monomers go on to form linear polymers. The reactivity of heterocyclic monomers depends on their ring strain. Monomers with large ring strain, such as oxirane, are more reactive than 1,3-dioxepane which has considerably less ring strain. Rings that are six-membered and larger are less likely to polymerize ...

  5. 1,4-Cyclohexanedimethanol diglycidyl ether - Wikipedia

    en.wikipedia.org/wiki/1,4-Cyclohexanedimethanol...

    1,4-Cyclohexanedimethanol diglycidyl ether is an organic chemical in the glycidyl ether family. [2] Its formula is C 14 H 24 O 4 and the IUPAC name is 2-[[4-(oxiran-2-ylmethoxymethyl)cyclohexyl]methoxymethyl]oxirane.

  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. It is an industrial chemical used as a surfactant but primarily for epoxy resin viscosity reduction. [3]

  7. Ring-opening polymerization - Wikipedia

    en.wikipedia.org/wiki/Ring-opening_polymerization

    A polymerization in which a cyclic monomer yields a monomeric unit which is acyclic or contains fewer cycles than the monomer. Note: If monomer is polycyclic, the opening of a single ring is sufficient to classify the reaction as ring-opening polymerization. Modified from the earlier definition. [1] [2]

  8. Tetrahydropyran - Wikipedia

    en.wikipedia.org/wiki/Tetrahydropyran

    Oxanes are the class of hexic cyclic ether rings with tetrahydropyran as the root chemical. Oxanes have one or more carbon atoms replaced with an oxygen atom. [8] The IUPAC preferred name for tetrahydropyran is now oxane. [9] Oxane is also the brand name for cis-2-methyl-4-propyl-1,3-oxathiane, a commercial fragrance. [10]

  9. C3H4O - Wikipedia

    en.wikipedia.org/wiki/C3H4O

    C 3 H 4 O is a chemical formula that represents each of several actual and hypothetical compounds that differ in structure, but each consist of three atoms of carbon, four of hydrogen, and one of oxygen. The following compounds are among them: