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  2. 1-Aminopentane - Wikipedia

    en.wikipedia.org/wiki/1-aminopentane

    1-Aminopentane is an organic compound with the formula CH 3 (CH 2) 4 NH 2.It is used as a solvent, as a raw material in the manufacture of a variety of other compounds, including dyes, emulsifiers, and pharmaceutical products, [1] and as a flavoring agent.

  3. Pentamine - Wikipedia

    en.wikipedia.org/wiki/Pentamine

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Help; Learn to edit; Community portal; Recent changes; Upload file

  4. Dimethylamine - Wikipedia

    en.wikipedia.org/wiki/Dimethylamine

    Dimethylamine is a weak base and the pKa of the ammonium CH 3-NH + 2-CH 3 is 10.73, a value above methylamine (10.64) and trimethylamine (9.79). Dimethylamine reacts with acids to form salts, such as dimethylamine hydrochloride, an odorless white solid with a melting point of 171.5 °C.

  5. 3-Aminopentane - Wikipedia

    en.wikipedia.org/wiki/3-Aminopentane

    3-Aminopentane is the organic compound with the formula (CH 3 CH 2) 2 CHNH 2. It is a colorless liquid. It is a colorless liquid. It is of interest for producing soluble imides and imines without introducing a chiral center.

  6. 2,3-Dimethylpentane - Wikipedia

    en.wikipedia.org/wiki/2,3-Dimethylpentane

    9 – MgBr with acetone to form 2,3-dimethyl-2-pentanol, then dehydrating this alcohol to form 2,3-dimethyl-2-pentene, and hydrogenating this product. [4] The isomer is present at about 2.4% by weight in the hydrocarbon mixture obtained by the condensation of methanol at 200 °C with a zinc iodide catalyst (the main component of the mixture ...

  7. 2,2-Dimethylpentane - Wikipedia

    en.wikipedia.org/wiki/2,2-Dimethylpentane

    2,2-Dimethylpentane can form a clathrate hydrate with helper gas molecules. The type of clathrate formed is called "clathrate H". 2,2-Dimethylpentane was the first compound for which the structure was determined. The clathrate has 34 molecules of water per molecule, and also has xenon and hydrogen sulfide as helper molecules.

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  9. Dimethylaniline - Wikipedia

    en.wikipedia.org/wiki/Dimethylaniline

    DMA was first reported in 1850 by the German chemist A. W. Hofmann, who prepared it by heating aniline and iodomethane: [3] [4] C 6 H 5 NH 2 + 2 CH 3 I → C 6 H 5 N(CH 3) 2 + 2 HI. DMA is produced industrially by alkylation of aniline with methanol in the presence of an acid catalyst: [5] C 6 H 5 NH 2 + 2 CH 3 OH → C 6 H 5 N(CH 3) 2 + 2 H 2 O

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