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  2. Ethanethiol - Wikipedia

    en.wikipedia.org/wiki/Ethanethiol

    Ethanethiol was originally reported by Zeise in 1834. [7] Zeise treated calcium ethyl sulfate with a suspension of barium sulfide saturated with hydrogen sulfide. He is credited with naming the C 2 H 5 S- group as mercaptum. Ethanethiol can also be prepared by a halide displacement reaction, where ethyl halide is treated with aqueous sodium ...

  3. Thiol - Wikipedia

    en.wikipedia.org/wiki/Thiol

    Thiol with a blue highlighted sulfhydryl group.. In organic chemistry, a thiol (/ ˈ θ aɪ ɒ l /; [1] from Ancient Greek θεῖον (theion) 'sulfur' [2]), or thiol derivative, is any organosulfur compound of the form R−SH, where R represents an alkyl or other organic substituent.

  4. Piranha solution - Wikipedia

    en.wikipedia.org/wiki/Piranha_solution

    A closely related mixture, sometimes called "base piranha", is a 5:1:1 mixture of water, ammonia solution (NH 4 OH, or NH 3 (aq)), and 30% hydrogen peroxide. [2] [3] As hydrogen peroxide is less stable at high pH than under acidic conditions, NH 4 OH (pH c. 11.6) also accelerates its decomposition.

  5. Hydroperoxyl - Wikipedia

    en.wikipedia.org/wiki/Hydroperoxyl

    The molecule has a bent structure. [3] The superoxide anion, • O − 2, and the hydroperoxyl radical exist in equilibrium in aqueous solution: • O − 2 + H 2 O ⇌ HO • 2 + HO −. The pK a of HO 2 is 4.88. Therefore, about 0.3% of any superoxide present in the cytosol of a typical cell is in the protonated form. [4] It oxidizes nitric ...

  6. Organic peroxides - Wikipedia

    en.wikipedia.org/wiki/Organic_peroxides

    The general structure of an organic peroxide. In organic chemistry, organic peroxides are organic compounds containing the peroxide functional group (R−O−O−R′).If the R′ is hydrogen, the compounds are called hydroperoxides, which are discussed in that article.

  7. Dakin oxidation - Wikipedia

    en.wikipedia.org/wiki/Dakin_oxidation

    The Dakin oxidation. The Dakin oxidation (or Dakin reaction) is an organic redox reaction in which an ortho- or para-hydroxylated phenyl aldehyde (2-hydroxybenzaldehyde or 4-hydroxybenzaldehyde) or ketone reacts with hydrogen peroxide (H 2 O 2) in base to form a benzenediol and a carboxylate.

  8. tert-Butyl hydroperoxide - Wikipedia

    en.wikipedia.org/wiki/Tert-Butyl_hydroperoxide

    It is one of the most widely used hydroperoxides in a variety of oxidation processes, like the Halcon process. [3] It is normally supplied as a 69–70% aqueous solution. Compared to hydrogen peroxide and organic peracids, tert-butyl hydroperoxide is less reactive and more soluble in organic solvents. Overall, it is renowned for the convenient ...

  9. Methanethiol - Wikipedia

    en.wikipedia.org/wiki/Methanethiol

    Methanethiol is mainly used to produce the essential amino acid methionine, which is used as a dietary component in poultry and animal feed. [10] Methanethiol is also used in the plastic industry as a moderator for free-radical polymerizations [10] and as a precursor in the manufacture of pesticides.