2-Ethylhexanoic acid
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Names | |
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Preferred IUPAC name 2-Ethylhexanoic acid[1] | |
Identifiers | |
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3D model (JSmol) |
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Beilstein Reference | 1750468 |
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ChemSpider |
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ECHA InfoCard | 100.005.222 ![]() |
EC Number |
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MeSH | 2-ethylhexanoic+acid |
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UNII |
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CompTox Dashboard (EPA) |
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InChI
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Properties | |
Chemical formula | C8H16O2 |
Molar mass | 144.214 g·mol−1 |
Appearance | Colorless liquid |
Density | 903 mg mL−1 |
Melting point | −59.00 °C; −74.20 °F; 214.15 K |
Boiling point | 228.1 °C; 442.5 °F; 501.2 K |
log P | 2.579 |
Vapor pressure | <1 Pa (at 25 °C) |
Acidity (pKa) | 4.819 |
Basicity (pKb) | 9.178 |
Refractive index (nD) | 1.425 |
Thermochemistry | |
Std enthalpy of formation (ΔfH⦵298) | −635.1 kJ mol−1 |
Std enthalpy of combustion (ΔcH⦵298) | -4.8013–4.7979 MJ mol−1 |
Hazards | |
GHS labelling: | |
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Danger | |
H312, H318, H361 | |
P280, P305+P351+P338 | |
Flash point | 114 °C (237 °F; 387 K) |
Autoignition temperature | 371 °C (700 °F; 644 K) |
Explosive limits | 0.9–6.7% |
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). ![]() ![]() ![]() Infobox references |
2-Ethylhexanoic acid (2-EHA), commonly known as octoic acid,[2] 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 2-ethylhexanal. Oxidation of this aldehyde gives the carboxylic acid.[3]
Metal ethylhexanoates
![](http://upload.wikimedia.org/wikipedia/commons/thumb/3/36/Co%28Ethexanoate%292.jpg/220px-Co%28Ethexanoate%292.jpg)
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.[4] They function as catalysts in polymerizations as well as for oxidation reactions as "oil drying agents."[5] 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).[6]
- Cobalt(II) ethylhexanoate (CAS# 136-52-7), a drier for alkyd resins
- Nickel(II) ethylhexanoate (CAS# 4454-16-4)[7]
See also
References
- ^ "2-ethylhexanoic acid - Compound Summary". PubChem Compound. USA: National Center for Biotechnology Information. 26 March 2005. Identification and Related Records. Retrieved 21 February 2012.
- ^ Economic Impact Analysis of Proposed Test Rule for 2-ethylhexanoic Acid (final) (epa Contract No. 68-01-6630) (Report). Environmental Protection Agency, Washington, DC. Office of Toxic. 2000.
- ^ Riemenschneider, Wilhelm (2002). "Carboxylic Acids, Aliphatic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a05_235. ISBN 978-3527306732.
- ^ Mishra, Shashank; Daniele, Stéphane; Hubert-Pfalzgraf, Liliane G. (2007). "Metal 2-Ethylhexanoates and Related Compounds as Useful Precursors in Materials Science". Chemical Society Reviews. 36 (11): 1770–1787. doi:10.1039/B614334M. PMID 18213985.
- ^ Raju, Ravinder; Prasad, Kapa (2012). "Synthetic applications of 2-ethylhexanoic acid derived reagents". Tetrahedron. 68 (5): 1341–1349. doi:10.1016/j.tet.2011.10.078.
- ^ Coulembier, O.; Degee, P.; Hedrick, J. L.; Dubois, P. (2006). "Controlled Ring-Opening Polymerization to Biodegradable Aliphatic Polyester: Especially Poly(Β-Malic Acid) Derivatives". Prog. Polym. Sci. 31: 723–747. doi:10.1016/j.progpolymsci.2006.08.004.
- ^ Burrows, Cynthia J.; Wey, Shiow-Jyi (2001). "Nickel(II) 2-Ethylhexanoate". Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.rn014m. ISBN 0-471-93623-5.