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Name: 2-Ethylcaproic acid   

CAS NO: 149-57-5

EINECS:205-743-6

MF: C8H16O2

MW: 144.211

MP: -59 °C

BP:228.0±0.0 °C at 760 mmHg

Density:0.9±0.1 g/cm3

Appearance: colorless liquid

Purity: 99% min

Package: 25g, 100g, 500g, bulk package

Application:pharmaceutical industry

DESCRIPTION OF 2-Ethylhexanoic acid (2-EHA) CAS NO: 149-57-5

2-Ethylhexanoic acid (2-EHA) CAS NO: 149-57-5 is an industrial chemical with a medium-sized carbon chain, commonly used as an active ingredient in wood preservatives. It is also a known metabolite of important phthalates and has applications in materials science, such as serving as a metal-organic precursor in the synthesis of various materials, and in the painting industry as a drying agent.

2-Ethylhexanoic acid CAS NO: 149-57-5 is an organic acid that is synthesized in the liver from 2-ethylhexanol and can be found in the blood, urine, and cerebrospinal fluid of humans. It has been shown that 2-ethylhexanoic acid is metabolized by cytochrome P450 enzymes to produce a number of products, including alpha-, beta-, and gamma-hydroxyacids. The hydrolysis of 2-ethylhexanoic acid by esterases or glucuronidases leads to the formation of corresponding carboxylic acids. This process can also be catalyzed by glutathione reductase or cytochrome P450 enzymes. Dimethyl fumarate is one example of a product formed from 2-ethylhexanoic acid metabolism. Dimethyl fumarate inhibits two enzymes, fatty acid synthase and acyl CoA oxidase, which are involved in fatty acid synthesis.

Other name:

Octanoic Acid;

2-ethyl-1-hexanoic acid;

Hexanoic acid, 2-ethyl-;

Ethylhexanoic acid;

CARBOXYLIC ACID C8;

Neodymoctic acid;

Ethylhexanoic acid CAS NO: 149-57-5 is the organic compound with the formula CH3(CH2)3CH(C2H5)CO2H. This carboxylic acid is widely used to prepare metal derivatives that are soluble in nonpolar organic solvents. These lipophilic metal-containing derivatives are used as catalysts in polymerizations. For example, tin 2-ethylhexanoate CAS NO: 149-57-5  is used in the production of poly(lactic-co-glycolic acid). 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 are often described as salts, when in fact they are not ionic but charge-neutral coordination complexes akin to the better defined, more crystalline acetates.

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