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  2. Hexamethylenediamine - Wikipedia

    en.wikipedia.org/wiki/Hexamethylenediamine

    Hexamethylenediamine or hexane-1,6-diamine, is the organic compound with the formula H 2 N(CH 2) 6 NH 2. The molecule is a diamine, consisting of a hexamethylene hydrocarbon chain terminated with amine functional groups. The colorless solid (yellowish for some commercial samples) has a strong amine odor.

  3. Diamine - Wikipedia

    en.wikipedia.org/wiki/Diamine

    [1] In terms of quantities produced, 1,6-diaminohexane (a precursor to Nylon 6-6) is most important, followed by ethylenediamine. [2] Vicinal diamines (1,2-diamines) are a structural motif in many biological compounds and are used as ligands in coordination chemistry. [3]

  4. 2-Methyleneglutaronitrile - Wikipedia

    en.wikipedia.org/wiki/2-Methyleneglutaronitrile

    2-Methylene glutaronitrile is a side-product in the production of hexanedinitrile which is used (after hydrogenation to 1,6-diaminohexane) as a key component for engineering polymers such as the polyamides (PA 66) or polyurethanes. Hexanedinitrile can be industrially produced by electrochemical hydrodimerisation or by catalytic dimerization of ...

  5. 1,6-diaminohexane - Wikipedia

    en.wikipedia.org/?title=1,6-diaminohexane&...

    From Wikipedia, the free encyclopedia. Redirect page

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  7. File:1,6-diaminohexane-2D-skeletal.svg - Wikipedia

    en.wikipedia.org/wiki/File:1,6-diaminohexane-2D...

    English: Structural formula (2D skeletal) of the chemical compound 1,6-Diaminohexane (Hexamethylenediamine) Deutsch: Strukturformel (Skelettformel) der chemischen Verbindung 1,6-Diaminohexan ( Hexamethylendiamin )

  8. Dihydrolevoglucosenone - Wikipedia

    en.wikipedia.org/wiki/Dihydrolevoglucosenone

    In a two-step hydrogenation process with a metal catalyst – first at 60 °C then at 180 °C – 1,6-hexanediol is mainly obtained via several intermediates. [ 15 ] 1,6-hexanediol can be used as a starting material for the production of polyesters , polyurethanes and diamine 1,6-diaminohexane .

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