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A compound containing the epoxide functional group can be called an epoxy, epoxide, oxirane, and ethoxyline. Simple epoxides are often referred to as oxides. Thus, the epoxide of ethylene (C 2 H 4) is ethylene oxide (C 2 H 4 O). Many compounds have trivial names; for instance, ethylene oxide is called "oxirane".
Propylene oxide is an acutely toxic and carcinogenic organic compound with the molecular formula C 3 H 6 O. This colourless volatile liquid with an odour similar to ether, is produced on a large scale industrially.
As oxygen transfer occurs, the plane of the oxirane is perpendicular to and bisects the plane of the alkene pi system. The configuration of the alkene is maintained in the product, ruling out long-lived radical intermediates.
In chemistry, dioxirane (systematically named dioxacyclopropane, also known as methylene peroxide or peroxymethane) is an organic compound with formula CH 2 O 2.The molecule consists of a ring with one methylene and two oxygen atoms.
As the molecule has 3 oxirane functionalities, a key use is modifying and reducing the viscosity of epoxy resins but giving higher functionality. [7] These reactive diluent modified epoxy resins may then be further formulated into CASE applications: Coatings, Adhesives, Sealants, and Elastomers. The use of the diluent does effect mechanical ...
Allyl glycidyl ether is an organic compound used in adhesives and sealants and as a monomer for polymerization reactions. It is formally the condensation product of allyl alcohol and glycidol via an ether linkage.
Trimethylolpropane triglycidyl ether (TMPTGE) is an organic chemical in the glycidyl ether family. [2] [3] It has the formula C 15 H 26 O 6 and the IUPAC name is 2-[2,2-bis(oxiran-2-ylmethoxymethyl)butoxymethyl]oxirane, and the CAS number 3454-29-3.
Methyldioxirane is an organic chemical consisting of a methyl group as substituent on a dioxirane ring. It is a highly unstable structure that has been proposed as part of a decomposition reaction of acetaldehyde oxide, the Criegee intermediate during some ozonolysis reactions.