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  2. Dibutylamine - Wikipedia

    en.wikipedia.org/wiki/Dibutylamine

    Other names (Dibutyl)amine Dibutylamine (deprecated) ... Dibutylamine is a colorless fluid with a fishy odor. It is an amine used as a corrosion inhibitor, ...

  3. Diisobutylamine - Wikipedia

    en.wikipedia.org/wiki/Diisobutylamine

    Diisobutylamine has been used in water flooding operations to control the growth of sulfate reducing bacteria. When water was treated with low concentrations of diisobutylamine, the microorganisms usually present were killed.

  4. n-Butylamine - Wikipedia

    en.wikipedia.org/wiki/N-Butylamine

    n-Butylamine is an organic compound (specifically, an amine) with the formula CH 3 (CH 2) 3 NH 2.This colourless liquid is one of the four isomeric amines of butane, the others being sec-butylamine, tert-butylamine, and isobutylamine.

  5. sec-Butylamine - Wikipedia

    en.wikipedia.org/wiki/Sec-Butylamine

    sec-Butylamine is an organic chemical compound (specifically, an amine) with the formula CH 3 CH 2 CH(NH 2)CH 3.It is a colorless liquid. sec-Butylamine is one of the four isomeric amines of butane, the others being n-butylamine, tert-butylamine, and isobutylamine.

  6. Category:Secondary amines - Wikipedia

    en.wikipedia.org/wiki/Category:Secondary_amines

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Pages for logged out editors learn more

  7. Category:Alkylamines - Wikipedia

    en.wikipedia.org/wiki/Category:Alkylamines

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Pages for logged out editors learn more

  8. Dithiobutylamine - Wikipedia

    en.wikipedia.org/wiki/Dithiobutylamine

    Dithiobutylamine (DTBA) is a reducing agent intended as an alternative for DTT in biochemical uses. It was designed to be easily synthesized in non-racemic form, to have a lower pKa (allowing more effective reduction at neutral pH), and to have a low disulfide E°′ reduction potential. [1]

  9. IUPAC nomenclature of chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    The Geneva Nomenclature of 1892 was created as a result of many other meetings in the past, the first of which was established in 1860 by August Kekulé. Another entity called the International Association of Chemical Societies (IACS) existed, and on 1911, gave vital propositions the new one should address: [ 2 ]