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  2. Trimethylolethane triglycidyl ether - Wikipedia

    en.wikipedia.org/wiki/Trimethylolethane...

    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 ...

  3. Bisphenol A diglycidyl ether - Wikipedia

    en.wikipedia.org/wiki/Bisphenol_A_diglycidyl_ether

    [12] [13] From the 1990s onward, concern has been raised over the use of BADGE-based epoxy resins in the lining of some cans for foodstuffs, with the chemical being found to leach into foods. [ 12 ] [ 14 ] Bisphenol A Diglycidyl ether-based epoxy coatings are extensively used for coating the inside of cans which come into contact with food and ...

  4. Glycidyl methacrylate - Wikipedia

    en.wikipedia.org/wiki/Glycidyl_methacrylate

    It is a common monomer used in the production of epoxy resins. While typical home epoxies contain diglycidyl ether of bisphenol A (DGEBA), glycidyl methacrylate is instead used to provide epoxy functionalization to polyolefins and other acrylate resins. Glycidyl methacrylate is produced by several companies worldwide, including Dow Chemical. [2]

  5. Castor oil glycidyl ether - Wikipedia

    en.wikipedia.org/wiki/Castor_oil_glycidyl_ether

    A 2018 study concluded that its use as a flexiblizing agent as well as an epoxy diluent has application in the aviation field. [7] Poly(propylene glycol) diglycidyl ether may also be used for the same application but has the perceived disadvantage that it is petroleum based rather than renewable plant based like the castor oil glycidyl ether.

  6. Sodium bis (2-methoxyethoxy)aluminium hydride - Wikipedia

    en.wikipedia.org/wiki/Sodium_bis(2-methoxyethoxy...

    The reagent can be modified to effect partial reductions. [ 1 ] SMEAH in toluene under reflux has been used to reduce aliphatic p- toluenesulfonamides (TsNR 2 ) to the corresponding free amines and is one of the few reagents that can carry out this challenging reduction in general settings.

  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 ...