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  2. 1-Ethynylcyclohexanol - Wikipedia

    en.wikipedia.org/wiki/1-Ethynylcyclohexanol

    1-Ethynylcyclohexanol (ECX) is an alkynyl alcohol derivative which is both a synthetic precursor to, and an active metabolite of the tranquilizer ethinamate, and has similar sedative, anticonvulsant and muscle relaxant effects. It has been sold as a designer drug, first being identified in the UK in March 2012. [1] [2] [3] [4]

  3. Ethinamate - Wikipedia

    en.wikipedia.org/wiki/Ethinamate

    Ethinamate (1-ethynylcyclohexanone carbamate) is synthesized by combining acetylene with cyclohexanone to make 1-ethynylcyclohexanol, and then transforming this into a carbamate by the subsequent reaction with phosgene, and later with ammonia. Some lithium metal or similar is used to make the acetylene react with the cyclohexanone in the first ...

  4. Triton X-100 - Wikipedia

    en.wikipedia.org/wiki/Triton_X-100

    The hydrocarbon group is a 4-(1,1,3,3-tetramethylbutyl)-phenyl group. Triton X-100 is closely related to IGEPAL CA-630, which might differ from it mainly in having slightly shorter ethylene oxide chains. As a result, Triton X-100 is slightly more hydrophilic than Igepal CA-630 thus these two detergents may not be considered functionally ...

  5. Cyclohexanol - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanol

    Cyclohexanol is produced by the oxidation of cyclohexane in air, typically using cobalt catalysts: [5]. 2 C 6 H 12 + O 2 → 2 C 6 H 11 OH. This process coforms cyclohexanone, and this mixture ("KA oil" for ketone-alcohol oil) is the main feedstock for the production of adipic acid.

  6. 2-Ethylhexyl acrylate - Wikipedia

    en.wikipedia.org/wiki/2-Ethylhexyl_acrylate

    2-Ethylhexyl acrylate polymerizes easily. The polymerization can be initiated by light, peroxides, heat, or contaminants.It can react violently when combined with strong oxidants and can form explosive mixtures with air at temperatures above 82 °C (180 °F). [2]

  7. Cyclohexylmethanol - Wikipedia

    en.wikipedia.org/wiki/Cyclohexylmethanol

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  8. Benzyl group - Wikipedia

    en.wikipedia.org/wiki/Benzyl_group

    Bond-dissociation energy [2] [3] Comment (kcal/mol) (kJ/mol) C 6 H 5 CH 2 −H: benzylic C−H bond 90 377 akin to allylic C−H bonds such bonds show enhanced reactivity H 3 C−H: methyl C−H bond 105 439 one of the strongest aliphatic C−H bonds C 2 H 5 −H: ethyl C−H bond 101 423 slightly weaker than H 3 C−H: C 6 H 5 −H: phenyl C ...

  9. Propargyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Propargyl_alcohol

    Propargyl alcohol, or 2-propyn-1-ol, is an organic compound with the formula C 3 H 4 O. It is the simplest stable alcohol containing an alkyne functional group. [ 3 ] Propargyl alcohol is a colorless viscous liquid that is miscible with water and most polar organic solvents.