2 ethylhexanoic acid

    2-Ethylhexanoic acid GudangMovies21 Rebahinxxi LK21

    2-Ethylhexanoic acid (2-EHA), commonly known as octoic acid, is the organic compound with the formula CH3(CH2)3CH(C2H5)CO2H. It is a carboxylic acid that is widely used to prepare lipophilic metal derivatives that are soluble in nonpolar organic solvents. 2-Ethylhexanoic acid is a colorless viscous oil. It is supplied as a racemic mixture.


    Production


    2-Ethylhexanoic acid is produced industrially from propylene, which is hydroformylated to give butyraldehyde. Aldol condensation of the aldehyde gives 2-ethylhexenal, which is hydrogenated to give 2-ethylhexanal. Oxidation of this aldehyde gives the carboxylic acid.


    Metal ethylhexanoates



    2-Ethylhexanoic acid forms compounds with metal cations that have stoichiometry as metal acetates. These ethylhexanoate complexes are used in organic and industrial chemical synthesis. They function as catalysts in polymerizations as well as for oxidation reactions as "oil drying agents." They are highly soluble in nonpolar solvents. These metal complexes are often described as salts. They are, however, not ionic but charge-neutral coordination complexes. Their structures are akin to the corresponding acetates.


    = Examples of metal ethylhexanoates

    =
    Hydroxyl aluminium bis(2-ethylhexanoate), used as a thickener
    Tin(II) ethylhexanoate (CAS# 301-10-0), a catalyst for polylactide and poly(lactic-co-glycolic acid).
    Cobalt(II) ethylhexanoate (CAS# 136-52-7), a drier for alkyd resins
    Nickel(II) ethylhexanoate (CAS# 4454-16-4)


    Regulations


    2-Ethylhexanoic acid is banned in the EU for use in cosmetics.


    See also


    2-Ethylhexanol


    References

Kata Kunci Pencarian: 2 ethylhexanoic acid

2 ethylhexanoic acid2 ethylhexanoic acid uses2 ethylhexanoic acid boiling point2-ethylhexanoic acid msds2 ethylhexanoic acid molecular weight2 ethylhexanoic acid cas no2 ethylhexanoic acid density2 ethylhexanoic acid manufacturers in india2 ethylhexanoic acid and its salts2 ethylhexanoic acid synthesis