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  2. 1,4-Dioxane - Wikipedia

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

    1,4-Dioxane (/ d aɪ ˈ ɒ k s eɪ n /) is a heterocyclic organic compound, classified as an ether. It is a colorless liquid with a faint sweet odor similar to that of diethyl ether . The compound is often called simply dioxane because the other dioxane isomers ( 1,2- and 1,3- ) are rarely encountered.

  3. File:Binary phase diagram dioxane-water.svg - Wikipedia

    en.wikipedia.org/wiki/File:Binary_phase_diagram...

    Printable version; Page information; ... Binary vapor-liquid diagram for the system 1,4-dioxane/water ... Version 1.2 or any later version published by the Free ...

  4. File:1-4-Dioxane.svg - Wikipedia

    en.wikipedia.org/wiki/File:1-4-Dioxane.svg

    The following other wikis use this file: Usage on ar.wikipedia.org 4،1-ديوكسان; Usage on be.wikipedia.org Дыаксан; Простыя эфіры

  5. Dioxane (compounds) - Wikipedia

    en.wikipedia.org/wiki/Dioxane_(compounds)

    Printable version; In other projects Wikidata item; Appearance. move to sidebar hide ... Dioxane may refer to the following chemical compounds: 1,2-dioxane; 1,3-dioxane;

  6. 1,2-Dioxane - Wikipedia

    en.wikipedia.org/wiki/1,2-dioxane

    Print/export Download as PDF; Printable version; In other projects Wikidata item; ... 1,2-Dioxane or o-dioxane is an organic compound with the molecular formula ...

  7. 1,3-Dioxane - Wikipedia

    en.wikipedia.org/wiki/1,3-dioxane

    1,3-Dioxane or m-dioxane is an organic compound with the molecular formula (CH 2) 4 O 2. It is a saturated six-membered heterocycle with two oxygen atoms in place of carbon atoms at the 1- and 3- positions. 1,4-Dioxane, which is of greater commercial value, is an isomer. Both dioxanes are colorless liquids. [1]

  8. Poly (3,4-ethylenedioxythiophene) - Wikipedia

    en.wikipedia.org/wiki/Poly(3,4-ethylenedioxythio...

    PEDOT possesses many advantageous properties compared to earlier conducting polythiophenes like 3-alkylthiophenes.For example, the polymer is optically transparent in its conducting state and has high stability, moderate band gap, and low redox potential.

  9. 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone - Wikipedia

    en.wikipedia.org/wiki/2,3-Dichloro-5,6-dicyano-1...

    The resulting hydroquinone is poorly soluble in typical reaction solvents (dioxane, benzene, alkanes), which facilitates workup. Solutions of DDQ in benzene are red, due to the formation of a charge-transfer complex. [9]