Suvarna Garge (Editor)

2 Ethylhexanoic acid

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Formula  C8H16O2
Appearance  Colorless liquid
Density  903 kg/m³
2-Ethylhexanoic acid httpsuploadwikimediaorgwikipediacommonsbb
Related compounds  2-Methylhexane 3-Methylhexane Valnoctamide 2-Methylheptane 3-Methylheptane 2-Ethylhexanol Valpromide Propylheptyl alcohol

2015 deep research report on global 2 ethylhexanoic acid industry


2-Ethylhexanoic 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.

Contents

2-Ethylhexanoic acid is produced industrially in two steps from butyraldehyde. Aldol condensation of the aldehyde gives 2-ethylhexanal. Oxidation of the latter gives the carboxylic acid.

Metal ethylhexanoates

These lipophilic metal-containing derivatives are used in many ways as catalysts in polymerizations, oxidation (drying agents), and organic synthesis. The high solubility of these metal complexes is attributable to the long hydrocarbon chain and the presence of a chiral center which leads to mixtures of enantiomeric complexes. These metal complexes, which exist as mixtures of several diastereoisomer, 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)
  • References

    2-Ethylhexanoic acid Wikipedia


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