PRODUCTS

2-ETHYL-1-HEXANOIC ACID

2-Ethyl-1-hexanoic acid is the organic compound with the formula CH3(CH2)3CH(C2H5)CO2H.
2-Ethyl-1-hexanoic acid is a carboxylic acid that is widely used to prepare lipophilic metal derivatives that are soluble in nonpolar organic solvents.
2-Ethyl-1-hexanoic acid is a colorless viscous oil.

CAS Number: 149-57-5
Molecular Formula: C8H16O2
Molecular Weight: 144.21
EINECS Number: 205-743-6

2-Ethyl-1-hexanoic acid , 149-57-5, 2-Ethylcaproic acid, Hexanoic acid, 2-ethyl-, Ethylhexanoic acid, Ethylhexoic acid, 2-Ethylhexoic acid, Butylethylacetic acid, 2-Butylbutanoic acid, 3-Heptanecarboxylic acid, Ethyl hexanoic acid, 2-ethyl-hexoic acid, 2-Ethyl-1-hexanoic acid , alpha-Ethylcaproic acid, 2-ethyl-hexanoic acid, Ethyl hexanoic acid, 2-, alpha-ethyl caproic acid, .alpha.-Ethylcaproic acid, 2-Ethyl-1-hexanoic acid, 61788-37-2, 01MU2J7VVZ, 2-EHA, 2-ETHYL HEXOIC ACID, AR, DTXSID9025293, CHEBI:89058, NSC-8881, MFCD00002675, 2-ethylhexanoicacid, 2-Ethylhexansaeure, DTXCID805293, 2-Ethyl-1-hexanoic acid , >=99%, 2-Ethyl-1-hexanoic acid , analytical standard, CAS-149-57-5, 2 ETHYL HEXANOIC ACID, CCRIS 3348, HSDB 5649, Kyselina 2-ethylkapronova [Czech], NSC 8881, Kyselina 2-ethylkapronova, EINECS 205-743-6, (+/-)-2-Ethyl-1-hexanoic acid , UNII-01MU2J7VVZ, Kyselina heptan-3-karboxylova [Czech], BRN 1750468, Kyselina heptan-3-karboxylova, AI3-01371, Hexanoic acid, 2-ethyl-, (-)-, EINECS 262-971-9, 2-Ethylcapronic acid, 2-Ethyl-Hexonic acid, alpha-Ethylhexanoic acid, .alpha.-Ethylhexanoic acid, EC 205-743-6, SCHEMBL25800, 2-Ethyl-1-hexanoic acid , 99%, MLS002415695, CHEMBL1162485, WLN: QVY4 & 2, NSC8881, HMS2267F21, STR05759, 2-Ethyl-1-hexanoic acid [HSDB], Tox21_201406, Tox21_300108, LMFA01020087, AKOS009031416, AT29893, CS-W016381, SB44987, SB44994, Hexanoic acid,2-ethyl-, tridecyl ester, NCGC00091324-01, NCGC00091324-02, NCGC00091324-03, NCGC00253985-01, NCGC00258957-01, SMR001252268, E0120, FT-0612273, FT-0654390, EN300-20410, Q209384, W-109079, F0001-0703, Z104478072, 18FEB650-7573-4EA0-B0CD-9D8BED766547, 2-Ethyl-1-hexanoic acid , Pharmaceutical Secondary Standard; Certified Reference Material.

2-Ethyl-1-hexanoic acid is supplied as a racemic mixture.
2-Ethyl-1-hexanoic 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.

2-Ethyl-1-hexanoic acid is a colorless to light yellow liquid with a mild odor.
2-Ethyl-1-hexanoic acid is a very hydrophobic molecule, practically insoluble in water, and relatively neutral.
2-Ethyl-1-hexanoic acid is a potentially toxic compound.

2-Ethyl-1-hexanoic acid is colourless viscous oil.
2-Ethyl-1-hexanoic acid is supplied as a racemic mixture.
2-Ethyl-1-hexanoic 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.
2-Ethyl-1-hexanoic acid , also known as 2-EHA or 2-Ethylcaproic acid, is a saturated fatty acid with the chemical formula C8H16O2.
2-Ethyl-1-hexanoic acid is a colorless liquid with a characteristic odor.

2-Ethyl-1-hexanoic acid is widely used in various industries, including the production of plasticizers, lubricants, and coatings.
2-Ethyl-1-hexanoic acid is used in the preparation of metal derivatives, which act as a catalyst in polymerization reactions.
2-Ethyl-1-hexanoic acid is used in the manufacturing of poly(lactic-co-glycolic acid).

2-Ethyl-1-hexanoic acid is also used as a stabilizer for polyvinyl chlorides.
In addition to this, 2-Ethyl-1-hexanoic acid serves as a catalyst for polyurethane foaming.
2-Ethyl-1-hexanoic acid is an industrially important aliphatic carboxylic acid.

2-Ethyl-1-hexanoic acid is widely employed as a stabilizer and a wood preservative.
2-Ethyl-1-hexanoic acid has various industrial applications, such as:coolant in automotivessynthetic lubricantwetting agent co-solventdrying of paintsdefoaming agent in pesticides
2-Ethyl-1-hexanoic acid , also known as 2-ethylhexanoate or sinesto b, belongs to the class of organic compounds known as medium-chain fatty acids.

2-Ethyl-1-hexanoic acid is supplied as a racemic mixture.
2-Ethyl-1-hexanoic acid is produced industrially from propylene, which is hydroformylated to give butyraldehyde.
Aldol condensation of the aldehyde gives 2-Ethyl-1-hexanoic acid , which is hydrogenated to 2-ethylhexanal.

Oxidation of this aldehyde gives the carboxylic acid.
2-Ethyl-1-hexanoic 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.
2-Ethyl-1-hexanoic acid is a colorless to light yellow, liquid organic compound.

2-Ethyl-1-hexanoic acid is widely used in the preparation of metal derivatives that are soluble in nonpolar organic solvents.
The highly toxic, combustible carboxylic acid is used to make paint dryers and plasticizers.
2-Ethyl-1-hexanoic acid is a colorless, transparent liquid with a faint odor.

2-Ethyl-1-hexanoic acid is slightly soluble in water.
2-Ethyl-1-hexanoic acid can be industrially produced from propylene which can be renewably produced.
2-Ethyl-1-hexanoic acid is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.

2-Ethyl-1-hexanoic acid is a potentially toxic compound.
2-Ethyl-1-hexanoic acid (2-EHA) is one of the flagship products within Perstorp Group which has the largest production capacity in the world.
2-Ethyl-1-hexanoic acid is a colorless liquid with one carboxylic group based on a C8 carbon chain.

2-Ethyl-1-hexanoic acid is widely used in esters for PVB film plasticizers and synthetic lubricants, in production of metal soaps for paint driers, in automotive coolants and PVC stabilizers.
Other application areas include wood preservatives, catalyst for polyurethane and in pharmaceuticals.
2-Ethyl-1-hexanoic acid is used by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.

2-Ethyl-1-hexanoic acid (EHXA, 2-EHA) is an industrially important aliphatic carboxylic acid.
2-Ethyl-1-hexanoic acid is widely employed as a stabilizer and a wood preservative.
2-Ethyl-1-hexanoic acid is a colorless to light yellow liquid with a mild odor.

2-Ethyl-1-hexanoic acid will burn though it may take some effort to ignite.
2-Ethyl-1-hexanoic acid is slightly soluble in water.
2-Ethyl-1-hexanoic acid is corrosive to metals and tissue.

2-Ethyl-1-hexanoic acid is also involved in solvent extraction and dye granulation.
Further, 2-Ethyl-1-hexanoic acid is used to prepare plasticizers, lubricants, detergents, flotation aids, corrosion inhibitors and alkyd resins.
2-Ethyl-1-hexanoic 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.
2-Ethyl-1-hexanoic acid is the organic compound with the formula CH3(CH2)3CH(C2H5)CO2H.
2-Ethyl-1-hexanoic acid is used to make paint dryers and plasticizers.

2-Ethyl-1-hexanoic acid is produced industrially from propylene, which is hydroformylated to give butyraldehyde.
Aldol condensation of the aldehyde gives 2-Ethyl-1-hexanoic acid , which is hydrogenated to 2-ethylhexanal.
Oxidation of this aldehyde gives the carboxylic acid.

2-Ethyl-1-hexanoic 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.

2-Ethyl-1-hexanoic acid is a carboxylic acid primarily used to prepare metal derivatives that are soluble in nonpolar organic solvents.
Ungraded products supplied by Spectrum are indicative of a grade suitable for general industrial use or research purposes and typically are not suitable for human consumption or therapeutic use.
2-Ethyl-1-hexanoic acid can be used as an intermediate for paint and coating driers, as an alkyd resin modifier, as a catalyst for the production of peroxides and as a stabilizer for lubricating oil esters and
PVC, etc., and has a wide range of market applications.

2-Ethyl-1-hexanoic acid is a chiral compound that is synthesized by the asymmetric synthesis of (R)-2-hydroxyacetic acid.
The enantiomers of 2-Ethyl-1-hexanoic acid are separated by an injection column, which can be used to determine the enantiomeric purity of racemic mixtures.
2-Ethyl-1-hexanoic acid is also a natural substrate for human enzymes and has been shown to have stereoselective activity in assays.

Enzymes that metabolize 2-Ethyl-1-hexanoic acid include carboxylic acid synthase, which converts it into crotonic acid, and acyl coenzyme A dehydrogenase, which converts it into 3-methylcrotonyl-CoA.
The stereoselectivity of these enzymes has been investigated using crystallographic techniques.
2-Ethyl-1-hexanoic acid is also a regioselective inhibitor of branched-chain amino acid aminot

2-Ethyl-1-hexanoic acid 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.
2-Ethyl-1-hexanoic acid is a synthetic mixture of isomers of tertiary carboxylic acids with ten carbon atoms.

It can be used to replace 2-Ethyl-1-hexanoic acid and most of its salts, which have been reclassified as Reprotoxic Category 1B by the Risk Assessment Committee of ECHA, taking effect November 2023.
2-Ethyl-1-hexanoic acid , also known as 2-EH Acid, is a colorless to slightly yellow liquid substance with a mildly sweet odor.
2-Ethyl-1-hexanoic acid is slightly soluble in water and it is flammable, though will not self-ignite.

2-Ethyl-1-hexanoic acid is considered corrosive to most metals.
2-Ethyl-1-hexanoic acid is most commonly used in the paint and coatings industry as well as in the manufacturing of various plasticizers.
2-Ethyl-1-hexanoic acid is widely used in the production of paint dryers and plasticizers.

2-Ethyl-1-hexanoic acid is most often used in esters for PVB film plasticizers and in synthetic lubricants.
Other common applications are in automobile coolants as a corrosion inhibitor, in PVC stabilizers and in the production of metal soaps for paint driers.
2-Ethyl-1-hexanoic acid is also a common catalyst in pharmaceuticals and for polyurethane.

2-Ethyl-1-hexanoic acid is often found as an ingredient in wood preservatives.
2-Ethyl-1-hexanoic acid is often used as a chemical intermediate in the production of various chemicals and materials.
2-Ethyl-1-hexanoic acid has applications in the synthesis of esters, plasticizers, and metal derivatives.

2-Ethyl-1-hexanoic acid is commonly employed as a raw material in the production of metal carboxylates, which are used as catalysts in various chemical processes.
Additionally, 2-Ethyl-1-hexanoic acid is utilized as a component in the formulation of certain coatings, adhesives, and sealants.
2-Ethyl-1-hexanoic acid is unique properties make it suitable for use in these applications, contributing to properties such as adhesion and flexibility.

2-Ethyl-1-hexanoic acid can be synthesized through various methods, including the oxidation of 2-ethylhexanol or the esterification of 2-ethylhexanol with acetic acid, followed by hydrolysis.
2-Ethyl-1-hexanoic acid is commonly used in the production of plasticizers, which are additives that improve the flexibility and durability of plastics.
2-Ethyl-1-hexanoic acid serves as a precursor in the preparation of metal carboxylates, which are used as catalysts in reactions such as the production of polyurethanes.

2-Ethyl-1-hexanoic acid is utilized in the formulation of coatings, resins, and inks, contributing to the performance and application properties of these materials.
2-Ethyl-1-hexanoic acid acts as a versatile intermediate in the synthesis of various chemicals.
2-Ethyl-1-hexanoic acid is a valuable industrial chemical with applications in diverse fields such as the production of adhesives, sealants, lubricants, and certain pharmaceuticals.

Like any chemical, proper safety precautions should be taken when handling 2-Ethyl-1-hexanoic acid .
2-Ethyl-1-hexanoic acid is important to follow recommended safety guidelines, use appropriate personal protective equipment, and store the compound in accordance with safety regulations.
2-Ethyl-1-hexanoic acid , also known as 2-Ethyl-1-hexanoic acid or 2-EHA, is a carboxylic acid with the molecular formula C8H16O2.

2-Ethyl-1-hexanoic acid is a branched-chain, eight-carbon organic acid with a carboxyl group (COOH) at one end.
The chemical structure of 2-Ethyl-1-hexanoic acid is derived from hexanoic acid by adding an ethyl group (C2H5) to the second carbon atom of the chain.
2-Ethyl-1-hexanoic acid (EHXA, 2-EHA) is an industrially important aliphatic carboxylic acid.

2-Ethyl-1-hexanoic acid is widely employed as a stabilizer and a wood preservative.
2-Ethyl-1-hexanoic acid , also called 2-EHA, is a commonly used organic compound, mainly to make lipophilic metal by-products that can dissolve in nonionic organic solvents.
2-Ethyl-1-hexanoic acid is a carboxylic acid with the formula C8H16O2 with a generally high boiling point and mild odor.

2-Ethyl-1-hexanoic acid is a viscous and colorless oil with one carboxylic class found on a C8 carbon chain and is immiscible in water.
2-Ethyl-1-hexanoic acid can be used as a substitute for naphthenic acid in some applications.
Industrially, 2-Ethyl-1-hexanoic acid is manufactured using propylene, often generated from fossil fuels and other sources which are renewable.

In other words, 2-Ethyl-1-hexanoic acid can be more effectively manufactured than naphthenic acid.
2-Ethyl-1-hexanoic acid produces metallic compounds that undergo stoichiometry in the form of metal acetates.
In most cases, 2-Ethyl-1-hexanoic acid derivatives are used in industrial and organic chemical applications.

The ethyl hexanoate complexes also serve as catalysts in oxidation reactions and polymerizations (as oil drying agents).
As a versatile chemical intermediate, 2-Ethyl-1-hexanoic acid has multiple applications, including the following.
2-Ethyl-1-hexanoic acid is the organic compound with the formula CH3(CH2)3CH(C2H5)CO2H.

2-Ethyl-1-hexanoic acid is a carboxylic acid that is widely used to prepare lipophilic metal derivatives that are soluble in nonpolar organic solvents.
2-Ethyl-1-hexanoic acid is a colorless viscous oil.
2-Ethyl-1-hexanoic acid is supplied as a racemic mixture.

2-Ethyl-1-hexanoic acid is a colorless, high boiling liquid having a mild odor.
The metallic salts of Eastman™ 2-Ethyl-1-hexanoic acid are used as driers for odorless paints, inks, varnishes, and enamels.
Cobalt and manganese are the most important driers.

2-Ethyl-1-hexanoic acid , also known as 2-ethylhexanoate or alpha-ethylcaproic acid, belongs to the class of organic compounds known as medium-chain fatty acids.
2-Ethyl-1-hexanoic acid will burn though 2-Ethyl-1-hexanoic acid may take some effort to ignite.
2-Ethyl-1-hexanoic acid is slightly soluble in water.

2-Ethyl-1-hexanoic acid is a carboxylic acid that is widely used to prepare lipophilic metal derivatives that are soluble in nonpolar organic solvents.
2-Ethyl-1-hexanoic acid is corrosive to metals and tissue.
2-Ethyl-1-hexanoic acid is used to make paint dryers and plasticizers.

Melting point: -59 °C
Boiling point: 228 °C(lit.)
Density: 0.906
vapor density: 4.98 (vs air)
vapor pressure: <0.01 mm Hg ( 20 °C)
refractive index: n20/D 1.425(lit.)
Flash point: 230 °F
storage temp.: Store below +30°C.
solubility: 1.4g/l
form: Liquid
pka: pK1:4.895 (25°C)
color: Clear
PH: 3 (1.4g/l, H2O, 20℃)
Odor: Mild odour
PH Range: 3 at 1.4 g/l at 20 °C
Viscosity: 7.73 cps
explosive limit: 1.04%, 135°F
Water Solubility: 2 g/L (20 ºC)
BRN: 1750468
Exposure limits ACGIH: TWA 5 mg/m3
Stability: Stable. Combustible. Incompatible with strong oxidizing agents, reducing agents, bases.
InChIKey: OBETXYAYXDNJHR-UHFFFAOYSA-N
LogP: 2.7 at 25℃

In consumer products, 2-Ethyl-1-hexanoic acid is found in de-icers, car care products, paints, greases and lubricants to name a few.
Industrially, this chemical has applications in stabilisers, preservatives, coolants, wetting agents, pesticides and lubricants.
2-Ethyl-1-hexanoic acid is a chemical intermediate used as a compound for example in the production of synthetic lubricants as well oil additives.

BASF operates a 2-Ethyl-1-hexanoic acid production plant at its Verbund site in Ludwigshafen, Germany.
The first of its kind in the ASEAN region and is expected to be commissioned in Q4 2016, with a total annual capacity of 30,000 metric tons.
The term “backward integration” explains the benefits of BASF’s Verbund concept.

By linking one plant with another, products and by-products from one plant could serve as a precursor in other plants.
2-Ethyl-1-hexanoic acid is a carboxylic acid.
Carboxylic acids donate hydrogen ions if a base is present to accept them.

They react in this way with all bases, both organic (for example, the amines) and inorganic.
Their reactions with bases, called "neutralizations", are accompanied by the evolution of substantial amounts of heat.
Neutralization between an acid and a base produces water plus a salt.

Carboxylic acids with six or fewer carbon atoms are freely or moderately soluble in water; those with more than six carbons are slightly soluble in water.
Soluble carboxylic acid dissociate to an extent in water to yield hydrogen ions.
Many insoluble 2-Ethyl-1-hexanoic acid s react rapidly with aqueous solutions containing a chemical base and dissolve as the neutralization generates a soluble salt.

2-Ethyl-1-hexanoic acid s in aqueous solution and liquid or molten carboxylic acids can react with active metals to form gaseous hydrogen and a metal salt.
Such reactions occur in principle for solid 2-Ethyl-1-hexanoic acid s as well, but are slow if the solid acid remains dry.
Even "insoluble" carboxylic acids may absorb enough water from the air and dissolve sufficiently in 2-Ethyl-1-hexanoic acid to corrode or dissolve iron, steel, and aluminum parts and containers.

2-Ethyl-1-hexanoic acid s, like other acids, react with cyanide salts to generate gaseous hydrogen cyanide.
The reaction is slower for dry, solid carboxylic acids.
Insoluble carboxylic acids react with solutions of cyanides to cause the release of gaseous hydrogen cyanide.

Flammable and/or toxic gases and heat are generated by the reaction of carboxylic acids with diazo compounds, dithiocarbamates, isocyanates, mercaptans, nitrides, and sulfides.
2-Ethyl-1-hexanoic acid s, especially in aqueous solution, also react with sulfites, nitrites, thiosulfates (to give H2S and SO3), dithionites (SO2), to generate flammable and/or toxic gases and heat.
Their reaction with carbonates and bicarbonates generates a harmless gas (carbon dioxide) but still heat.

Like other organic compounds, 2-Ethyl-1-hexanoic acid s can be oxidized by strong oxidizing agents and reduced by strong reducing agents.
2-Ethyl-1-hexanoic acid can undergo various chemical reactions to form derivatives.
2-Ethyl-1-hexanoic acid contributes to the adhesive's ability to bond to various surfaces.

Analytical techniques, such as gas chromatography, mass spectrometry, and nuclear magnetic resonance (NMR), are often employed to identify and quantify 2-Ethyl-1-hexanoic acid in different samples.
While 2-Ethyl-1-hexanoic acid is not known for extreme toxicity, appropriate precautions should be taken when handling it.
For example, 2-Ethyl-1-hexanoic acid can be esterified to produce esters that are used as plasticizers in the manufacturing of flexible plastics.

When used in the synthesis of polymers, 2-Ethyl-1-hexanoic acid can influence the properties of the resulting materials.
2-Ethyl-1-hexanoic acid is incorporation can affect factors such as flexibility, adhesion, and thermal stability in the final product.
Due to its ability to enhance adhesion properties, 2-Ethyl-1-hexanoic acid is sometimes incorporated into adhesive formulations.

As with any chemical, its impact on biological systems and the environment should be considered in industrial applications.
The production and market demand for 2-Ethyl-1-hexanoic acid can vary across regions and industries.
2-Ethyl-1-hexanoic acid is produced on a commercial scale and is an important chemical in the manufacturing sector.

Ongoing research may focus on optimizing the synthesis of 2-Ethyl-1-hexanoic acid , exploring new applications, or developing more environmentally friendly production methods.
The chemical compatibility of 2-Ethyl-1-hexanoic acid with other compounds is an important consideration in various applications, such as in the formulation of complex mixtures like coatings, inks, and adhesives.
2-Ethyl-1-hexanoic acid is known for forming stable metal complexes.

Metal salts and complexes of 2-Ethyl-1-hexanoic acid find applications in various industries, such as in the production of heat stabilizers for PVC (polyvinyl chloride).
2-Ethyl-1-hexanoic acid is used in the production of polymeric materials.
For instance, 2-Ethyl-1-hexanoic acid can be involved in the synthesis of polymers through processes like polycondensation reactions.

Certain metal carboxylates derived from 2-Ethyl-1-hexanoic acid can act as catalysts in various chemical reactions, including esterification and transesterification reactions.
2-Ethyl-1-hexanoic acid is sometimes used as an additive in lubricants to enhance their performance.
2-Ethyl-1-hexanoic acid can contribute to improving the lubricating properties and thermal stability of oils.

2-Ethyl-1-hexanoic acid has a characteristic, somewhat unpleasant odor.
This property can be relevant in applications where odor may be a consideration, such as in the formulation of consumer products.
As with any chemical, regulatory standards and guidelines may apply to the production, handling, and use of 2-Ethyl-1-hexanoic acid .

Users should be aware of and adhere to relevant safety and environmental regulations.
Ongoing research explores new applications and processes involving 2-Ethyl-1-hexanoic acid .
Researchers may investigate 2-Ethyl-1-hexanoic acid is properties for potential advancements in materials science, catalysis, or other fields.

2-Ethyl-1-hexanoic acid , Europe is a colorless, high boiling liquid having a mild odor.
The metallic salts of 2-Ethyl-1-hexanoic acid are used as driers for odorless paints, inks, varnishes, and enamels. Cobalt and manganese are the most important driers.
2-Ethyl-1-hexanoic acid is a clear liquid with a mild odour. An organic compound, this chemical is an aliphatic carboxylic acid with uses in both industrial and consumer products.

Uses Of 2-Ethyl-1-hexanoic acid:
2-Ethyl-1-hexanoic acid helps enhance the bonding characteristics of these products.
In the lubricant industry, 2-Ethyl-1-hexanoic acid is sometimes used as an additive to improve the lubricating properties and thermal stability of oils.
2-Ethyl-1-hexanoic acid is involved in the synthesis of various polymers.

The chemical can be used as a monomer or a reactant in polycondensation reactions, contributing to the formation of polymeric materials with specific properties.
2-Ethyl-1-hexanoic acid is used in the extraction of certain metals from ores.
2-Ethyl-1-hexanoic acid is ability to form stable metal complexes is utilized in processes related to metal extraction and purification.

Metal carboxylates derived from 2-Ethyl-1-hexanoic acid act as catalysts in chemical reactions, facilitating processes such as esterification and transesterification.
2-Ethyl-1-hexanoic acid is used in the preparation of metal derivatives, which act as a catalyst in polymerization reactions.
For example, tin 2-ethylhexanoate is used in the manufacturing of poly(lactic-co-glycolic acid).

2-Ethyl-1-hexanoic acid is also used as a stabilizer for polyvinyl chlorides.
2-Ethyl-1-hexanoic acid is also involved in solvent extraction and dye granulation.
Further, 2-Ethyl-1-hexanoic acid is used to prepare plasticizers, lubricants, detergents, flotation aids, corrosion inhibitors and alkyd resins.

In addition to this, 2-Ethyl-1-hexanoic acid serves as a catalyst for polyurethane foaming.
As a reactant in esterification , decarboxylative alkynylation , and preparation of alkyl coumarins via decarboxylative coupling reactions.
In the organocatalytic medium for the preparation of various 2-Ethyl-1-hexanoic acid by Biginelli reaction.

2-Ethyl-1-hexanoic acid s of light metals are used to convert some mineral oils to greases.
2-Ethyl-1-hexanoic acid is esters are used as plasticizers.
2-Ethyl-1-hexanoic acid is used to produce corrosion inhibitors for lubricants and automotive coolants.

2-Ethyl-1-hexanoic acid also serves as wood preservatives and makes lubricant additives as well as synthetic lubricants.
2-Ethyl-1-hexanoic acid is also used in the production of PVC heat stabilizers, PVB film plasticizers, metal soaps for paint driers, and other chemicals.
2-Ethyl-1-hexanoic acid is commonly used in esters in Polyvinyl butyral (PVB) film plasticizers and as a raw material for polyesters applied in synthetic oils.

2-Ethyl-1-hexanoic acid ’s metal salts are used to prepare synthetic lubricant additives used in various industrial lubricant applications.
2-Ethyl-1-hexanoic acid is widely used in coating applications to enhance performance and resistance.
2-Ethyl-1-hexanoic acid produces alkyd resins that help improve yellowing resistance better than ordinary fatty acids.

This monomer is ideal for stoving enamels and 2-component coatings.
2-Ethyl-1-hexanoic acid can also be used in other applications, including the catalyst for polyurethane, wood preservatives, and pharmaceuticals.
2-Ethyl-1-hexanoic acid is sometimes used in the formulation of inks, particularly in the production of printing inks.

2-Ethyl-1-hexanoic acid is properties contribute to the ink's adhesion and printability on various surfaces.
2-Ethyl-1-hexanoic acid can be involved in the production of certain detergents, where its surfactant properties may be advantageous in enhancing cleaning performance.
In the textile industry, 2-Ethyl-1-hexanoic acid may be used as an auxiliary agent in processes like dyeing or finishing to achieve specific textile properties.

2-Ethyl-1-hexanoic acid is utilized as a flotation agent in mineral processing, helping to separate minerals from ores during the flotation process.
Some derivatives of 2-Ethyl-1-hexanoic acid may find applications in the formulation of herbicides and pesticides in agriculture.
In the construction industry, 2-Ethyl-1-hexanoic acid may be used in the formulation of certain construction materials, including sealants and caulks.

2-Ethyl-1-hexanoic acid can be found in certain cleaning products, contributing to their formulation for effective removal of dirt, grease, or other contaminants.
Certain food-grade derivatives of 2-Ethyl-1-hexanoic acid may be used in the production of food contact materials, such as coatings for packaging materials.
In the cosmetic industry, 2-Ethyl-1-hexanoic acid or its derivatives may be used in the formulation of cosmetic and personal care products such as lotions, creams, and hair care products.

In the production of solar panels, 2-Ethyl-1-hexanoic acid can be used in certain processes related to the fabrication of photovoltaic cells.
2-Ethyl-1-hexanoic acid may find application in the oil and gas industry as a component in certain oilfield chemicals used for drilling, production, or enhanced oil recovery processes.
In biomedical research, 2-Ethyl-1-hexanoic acid or its derivatives may be explored for potential applications, such as in drug delivery systems or biomaterials.

The chemicals in 2-Ethyl-1-hexanoic acid are reported to have cosmetic use to produce emollients and skin conditioners.
2-Ethyl-1-hexanoic acid is widely used in hair care products, hand creams, face creams, body lotions, and make-up products like foundation, concealer, and hair care products.
2-Ethyl-1-hexanoic acid is also used in manufacturing polyvinyl chloride (PVC) stabilizers and Polyvinyl butyral (PVB) plasticizers in the form of metal salts.

2-Ethyl-1-hexanoic acid reacts with metallic components like manganese and cobalt to produce metallic salt derivatives.
Bisley International has been the leading chemical raw material supplier in the United States and worldwide for over half a century.
2-Ethyl-1-hexanoic acid contains metal salts that serve as corrosion inhibitors in coolants.

2-Ethyl-1-hexanoic acid is also used to make polyol ester which acts as a lubricant for refrigerant appliances.
In the rubber industry, 2-Ethyl-1-hexanoic acid is sometimes used as a vulcanization aid.
2-Ethyl-1-hexanoic acid can contribute to the cross-linking of rubber polymers, enhancing the strength and elasticity of rubber products.

2-Ethyl-1-hexanoic acid is employed as an additive in certain paint formulations to improve characteristics such as flow properties, drying time, and adhesion to surfaces.
2-Ethyl-1-hexanoic acid is used as an additive in fuel formulations to improve combustion properties and reduce engine deposits.
2-Ethyl-1-hexanoic acid finds application in the textile industry, where it may be used in the processing of fibers and fabrics, contributing to certain desirable properties.

Due to its lubricating properties, 2-Ethyl-1-hexanoic acid can be incorporated into metalworking fluids to enhance their performance in cutting, grinding, and machining operations.
In the pharmaceutical industry, 2-Ethyl-1-hexanoic acid can serve as an intermediate in the synthesis of certain pharmaceutical compounds.
2-Ethyl-1-hexanoic acid can be involved in the production of surfactants, which are compounds that lower the surface tension between two phases (such as between a liquid and a solid).

In laboratories, researchers may use 2-Ethyl-1-hexanoic acid as a building block in the development of new materials, catalysts, or processes.
Some derivatives of 2-Ethyl-1-hexanoic acid may find application in the flavor and fragrance industry.

In electroplating processes, 2-Ethyl-1-hexanoic acid can be used in the formulation of certain electrolyte solutions.
2-Ethyl-1-hexanoic acid can be used: As a reactant in esterification , decarboxylative alkynylation , and preparation of alkyl coumarins via decarboxylative coupling reactions.

2-Ethyl-1-hexanoic acid is a versatile carboxylic acid that is commonly used in a variety of industrial applications.
2-Ethyl-1-hexanoic acid and its metal salts are used to produce a variety of functional fluids including polymer production catalysts, plasticizers in PVC production, corrosion inhibitors in coolants stabilizers, wood preservatives and to produce lubricant additives.
The zinc salt of 2-Ethyl-1-hexanoic acid is used as a corrosion inhibitor in lubricants and hydrogen sulfide scavenger.

One of the primary uses of 2-Ethyl-1-hexanoic acid is in the production of plasticizers.
Plasticizers are additives that increase the flexibility and durability of plastics.
Esters derived from 2-Ethyl-1-hexanoic acid , such as dioctyl phthalate (DOP) and dioctyl adipate (DOA), are commonly used in the production of flexible PVC (polyvinyl chloride) products, including cables, flooring, and synthetic leather.

When reacted with certain metals, it forms salts that are widely used as additives in paint and plasticizer formulations, as well as in the production of paint and lacquer dryers and PVC stabilizers.
The esters of 2-Ethyl-1-hexanoic acid , particularly those obtained by glycols, tri glycols, and polyethylene glycols, are known for their lubricant properties.
They are excellent plasticizers for PVC, nitrocellulose, chlorinated rubber, and polypropylene.

These properties make 2-Ethyl-1-hexanoic acid a popular choice in producing various chemicals and materials in the industry.
2-Ethyl-1-hexanoic acid is used in the preparation of metal derivatives, which act as a catalyst in polymerization reactions.
For example, 2-Ethyl-1-hexanoic acid is used in the manufacturing of poly(lactic-co-glycolic acid).

In addition to this, 2-Ethyl-1-hexanoic acid serves as a catalyst for polyurethane foaming.
2-Ethyl-1-hexanoic acid is used as a chemical intermediate and for manufacture of resins used for baking enamels, lubricants, detergents, flotation aids, and corrosion inhibitors; also used as a catalyst for polyurethane foaming, for solvent extraction, and for dye granulation.

2-Ethyl-1-hexanoic acid is used as a chemical intermediate for many products; Approximately 400 workers in US manufacturing are potentially exposed; Used in alkyd resins; Used in the mid-1980s as a wood preservative to replace chlorophenols; [ACGIH] Used to make plasticizers, lubricants, detergents, flotation aids, corrosion inhibitors, and alkyd resins; Also used as a co-solvent and defoamer in pesticides, as the active ingredient in the wood preservative Sinesto B (not used in the US), in paint dryers, heat stabilizers for PVC, and as a catalyst for polyurethane foaming, solvent extraction, and dye granulation; [HSDB] Not found in any pesticide products registered in the US.
2-Ethyl-1-hexanoic acid is used as a starting material to produce polyol ester oil which is mainly used as a synthetic lubricant in refrigerant systems.

2-Ethyl-1-hexanoic acid is utilized in the synthesis of metal carboxylates, which serve as catalysts in various chemical processes.
These catalysts find applications in the production of polyurethanes, coatings, and other polymerization reactions.
2-Ethyl-1-hexanoic acid is employed in the formulation of coatings, resins, and inks.

Safety Profile Of 2-Ethyl-1-hexanoic acid:
2-Ethyl-1-hexanoic acid can be irritating to the skin, eyes, and respiratory system.
Prolonged or repeated exposure to 2-Ethyl-1-hexanoic acid may lead to sensitization in some individuals, resulting in allergic reactions upon subsequent exposure.
There is a potential aspiration hazard if the substance is swallowed.

Aspiration into the lungs during ingestion can lead to chemical pneumonia, which can be serious.
Improper disposal or release of 2-Ethyl-1-hexanoic acid into the environment can have adverse effects.
2-Ethyl-1-hexanoic acid may be harmful to aquatic life and can contribute to pollution if not handled and disposed of responsibly.

Moderately toxic by ingestion and skin contact.
Direct contact with the skin or eyes may cause irritation, and inhalation of vapors or mists may irritate the respiratory tract.
Swallowing 2-Ethyl-1-hexanoic acid can cause irritation to the digestive tract.

Ingestion is not a common route of exposure in industrial settings, but accidental ingestion should be avoided.
An experimental teratogen.
A skin and severe eye irritant.

Combustible when exposed to heat or flame.
When heated to decomposition, it emits acrid and irritating fumes.