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2-Ethylhexanoic acid (2-EHA), commonly known as octoic acid, [2] is the organic compound with the formula CH 3 (CH 2) 3 CH(C 2 H 5)CO 2 H. 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 ...
The systematic IUPAC name is not always the preferred IUPAC name, for example, lactic acid is a common, and also the preferred, name for what systematic rules call 2-hydroxypropanoic acid. This list is ordered by the number of carbon atoms in a carboxylic acid.
65% Solution of cobalt(II) bis(2-ethylhexanoate) in mineral spirits, tilted vial to illustrate color and viscosity. Like naphthenic acid, 2-ethylhexanoic acid forms lipophilic complexes that are used in organic and industrial chemical synthesis. They function as catalysts in polymerizations as well as for oxidation reactions as oil drying ...
Resin acids are tacky, yellowish gums that are water-insoluble. They are used to produce soaps for diverse applications, but their use is being displaced increasingly by synthetic acids such as 2-ethylhexanoic acid or petroleum-derived naphthenic acids.
2-EHA may refer to: 2-Ethylhexanoic acid; 2-Ethylhexyl acrylate This page was last edited on 4 November 2023, at 17:13 (UTC). Text is available under the Creative ...
One of the anti-corrosion components presented as sodium or potassium 2-ethylhexanoate and ethylhexanoic acid is incompatible with nylon 6,6 and silicone rubber, and is a known plasticizer. Class action lawsuits were registered in several states of the US, and in Canada, [27] to address some of these claims.
The molecular formula C 8 H 16 O 2 may refer to: ... 2-Ethylhexanoic acid; Hexyl acetate; Manzanate; Pentyl propanoate; 2,2,4,4-Tetramethyl-1,3-cyclobutanediol ...
An example of an ester formation is the substitution reaction between a carboxylic acid (R−C(=O)−OH) and an alcohol (R'OH), forming an ester (R−C(=O)−O−R'), where R and R′ are organyl groups, or H in the case of esters of formic acid.