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2-ETHYLHEXANOIC ACID (CAS 149-57-5)

 

2-Ethylhexanoic acid (CAS 149-57-5) is used in the manufacture of adhesive and sealant chemicals, corrosion inhibitors and scale inhibitors, intermediates, lubricant and lubricant additives, paint and coating additives, and process conditioners.
2-Ethylhexanoic acid (CAS 149-57-5) is widely used to prepare metal derivatives that are soluble in nonpolar organic solvents. 
2-Ethylhexanoic acid (CAS 149-57-5) is used in the following products: coating products.


CAS Number: 149-57-5 
72377-05-0 S enantiomer 
56006-48-5 R enantiomer 
EC Number: 205-743-6
MDL number: MFCD00002675
Molecular Formula: C8H16O2 / CH3(CH2)3CH(C2H5)COOH
Chemical formula: C8H16O2

SYNONYMS:
α-Ethylcaproic acid, α-Ethylhexanoic acid, Butylethylacetic acid, Ethylhexanoic acid, Ethylhexoic acid, 2-Butylbutanoic acid, 2-Ethylcaproic acid, 2-Ethylhexanoic acid, 2-Ethylhexoic acid, 3-Heptanecarboxylic acid, Kyselina 2-ethylkapronova, Kyselina heptan-3-karboxylova, 2-Ethyl-1-hexanoic acid, 2-Ethylcapronic acid, NSC 8881, α-ethylhexanoic acid, 2-ethylcaproic acid, (RS)-2-ethylcaproic acid, 2-EHA, ⍺-ethylcaproic acid, ⍺-ethylhexanoic acid, 2-bubylbutanoic acid, butylethylacetic acid, 2-ethyl-1-hexanoic acid, 2-ethylcaproic acid, ethylhexanoic acid, ethylhexoic acid, 2-ETHYLHEXANOIC 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 hexanoic acid, alpha-Ethylcaproic acid, 2-ethyl-hexanoic acid, Ethyl hexanoic acid, 2-, alpha-ethyl caproic acid, MFCD00002675, .alpha.-Ethylcaproic acid, 2-Ethyl-1-hexanoic acid, 61788-37-2, 01MU2J7VVZ, 2-EHA, 2-ETHYL HEXOIC ACID,AR, DTXSID9025293, CHEBI:89058, NSC-8881, 2-Ethylhexansaeure, 2-ethylhexanoicacid, DTXCID805293, 2-Ethylhexanoic acid, >=99%, 2-Ethylhexanoic 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-ETHYLHEXANOIC 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-Ethylhexanoic acid, 99%, MLS002415695, CHEMBL1162485, WLN: QVY4 & 2, NSC8881, HMS2267F21, STR05759, 2-ETHYLHEXANOIC ACID [HSDB], Tox21_201406, Tox21_300108, LMFA01020087, AKOS009031416, AT29893, CS-W016381, SB44987, SB44994, NCGC00091324-01, NCGC00091324-02, NCGC00091324-03, NCGC00253985-01, NCGC00258957-01, SMR001252268, 1ST157439, E0120, NS00010660, EN300-20410, 1ST157439-1000, Q209384, W-109079, F0001-0703, Z104478072, 18FEB650-7573-4EA0-B0CD-9D8BED766547, 2-Ethylhexanoic acid Solution in Acetonitrile, 1000mug/mL, 2-Ethylhexanoic acid, Pharmaceutical Secondary Standard; Certified Reference Material, α-Ethylcaproic acid, α-Ethylhexanoic acid, Butylethylacetic acid, Ethylhexanoic acid, Ethylhexoic acid, 2-Butylbutanoic acid, 2-Ethylcaproic acid, 2-Ethylhexanoic acid, 2-Ethylhexoic acid, 3-Heptanecarboxylic acid, Kyselina 2-ethylkapronova, Kyselina heptan-3-karboxylova, 2-Ethyl-1-hexanoic acid, 2-Ethylcapronic acid, NSC 8881, α-ethylhexanoic acid, 2-ethylcaproic acid, (RS)-2-ethylcaproic acid, 2-EHA, ⍺-ethylcaproic acid, ⍺-ethylhexanoic acid, 2-bubylbutanoic acid, butylethylacetic acid, 2-ethyl-1-hexanoic acid, 2-ethylcaproic acid, ethylhexanoic acid, ethylhexoic acid, 2-butyl butanoic acid, butyl ethyl acetic acid, 2-butylbutanoic acid, butylethylacetic acid, 2-ethyl caproic acid, alpha-ethyl caproic acid, 2-ethyl hexoic acid, 2-ethyl-hexanoic acid, 2-ethyl-hexoic acid, 2-ethylcaproic acid, a-ethylcaproic acid, alpha-ethylcaproic acid, 2-ethylcapronic acid, 2-ethylhexanoic acid, a-ethylhexanoic acid, 2-ethylhexanoicacid, 2-ethylhexoic acid, 3-heptane carboxylic acid, 3-heptanecarboxylic acid, hexanoic acid, 2-ethyl-, sinesto B, Hexanoic acid, 2-ethyl-, Caproic acid, α-ethyl-, 2-Ethylhexanoic acid, Butylethylacetic acid, α-Ethylcaproic acid, 2-Ethylhexoic acid, 3-Heptanecarboxylic acid, 2-Ethylcaproic acid, Ethylhexanoic acid, α-Ethylhexanoic acid, 2-Butylbutanoic acid, 2-Ethyl-1-hexanoic acid, (±)-2-Ethylhexanoic acid, NSC 8881, Octylic acid

2-Ethylhexanoic acid (CAS 149-57-5) is a branched-chain fatty acid.
2-Ethylhexanoic acid (CAS 149-57-5) is a colorless to light yellow liquid with a mild odor. 
2-Ethylhexanoic acid (CAS 149-57-5) will burn though 2-Ethylhexanoic acid may take some effort to ignite. 


2-Ethylhexanoic acid (CAS 149-57-5) is a versatile carboxylic acid that is commonly used in a variety of industrial applications. 
When reacted with certain metals, 2-Ethylhexanoic acid (CAS 149-57-5) 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-Ethylhexanoic acid (CAS 149-57-5), 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-Ethylhexanoic acid (CAS 149-57-5) a popular choice in producing various chemicals and materials in the industry.
2-Ethylhexanoic acid (CAS 149-57-5) is an acid used to prepare metal derivatives.
2-Ethylhexanoic acid (CAS 149-57-5) is a colourless liquid


2-Ethylhexanoic acid (CAS 149-57-5) is slightly soluble in water. 
2-Ethylhexanoic acid (CAS 149-57-5) is corrosive to metals and tissue. 
2-Ethylhexanoic acid (CAS 149-57-5) is the organic compound with the formula CH3(CH2)3CH(C2H5)CO2H. 


2-Ethylhexanoic acid (2-EHA) is an industrially important aliphatic carboxylic acid which is widely employed as a stabilizer and a wood preservative.
2-Ethylhexanoic acid (CAS 149-57-5) has various industrial applications, such as: coolant in automotive, synthetic lubricant, wetting agent, co-solvent, drying of paints, and defoaming agent in pesticides.


2-Ethylhexanoic acid (CAS 149-57-5) is a clear liquid with a mild odour. 
An organic compound, 2-Ethylhexanoic acid (CAS 149-57-5) is an aliphatic carboxylic acid with uses in both industrial and consumer products.
As a carboxylic acid, 2-Ethylhexanoic acid (CAS 149-57-5) has a carboxy group that gives it its reactive profile. 


The carboxylic acid group enables, among other things, a conversion of 2-Ethylhexanoic acid (CAS 149-57-5) by dehydration or by esterification together with an alcohol. 
2-Ethylhexanoic acid (CAS 149-57-5) has eight carbon atoms, six of which are arranged to form a regular molecule of hexanoic acid with a terminal functional group.


An ethyl group is also attached to the carbon atom adjacent to the carboxy group. 
The possible spatial arrangement of the bonds on this atom results in two stereoisomers of 2-Ethylhexanoic acid (CAS 149-57-5). 
These are referred to as (S)-enantiomer and as (R)-enantiomer. 


Technically used and commercially traded 2-Ethylhexanoic acid (CAS 149-57-5) consists of a mixture of these two variants.
2-Ethylhexanoic acid (CAS 149-57-5), also known as 2-EHA or 2-Ethylcaproic acid, is a saturated fatty acid with the chemical formula C8H16O2. 
2-Ethylhexanoic acid (CAS 149-57-5) is a colorless liquid with a characteristic odor. 


2-Ethylhexanoic acid (CAS 149-57-5) is a colourless, transparent liquid that is slightly miscible in water, and can be renewably produced from propylene.
2-Ethylhexanoic acid (CAS 149-57-5) is a substance from the group of carboxylic acids. 
2-Ethylhexanoic acid (CAS 149-57-5) can be manufactured in different ways. 


Production by oxidation of 2-ethylhexanal or 2-ethyl-1-hexanol and production in a multi-stage process of hydroformulation, condensation, hydrogenation and oxidation of propylene via the intermediates butanal, 2-ethylhexenal and 2-ethylhexanal are common.
2-Ethylhexanoic acid (CAS 149-57-5) is an important starting material for the production of metal salts, heavy metal soaps for paints and varnishes, thickeners for petrol and mineral oils, as well as stabilizers, plasticizers, emulsifiers and corrosion inhibitors. 


2-Ethylhexanoic acid (CAS 149-57-5) is a versatile monocarboxylic acid chemical intermediate.
2-Ethylhexanoic acid (CAS 149-57-5) is an industrial chemical.
2-Ethylhexanoic acid (CAS 149-57-5) is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 10 000 to < 100 000 tonnes per annum.


2-Ethylhexanoic acid (CAS 149-57-5) is a carboxylic acid with the formula C8H16O2 with a generally high boiling point and mild odor.
2-Ethylhexanoic acid (CAS 149-57-5) is a viscous and colorless oil with one carboxylic class found on a C8 carbon chain and is immiscible in water. 
2-Ethylhexanoic acid (CAS 149-57-5) produces metallic compounds that undergo stoichiometry in the form of metal acetates. 


In most cases, 2-Ethylhexanoic acid (CAS 149-57-5) 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-Ethylhexanoic acid (CAS 149-57-5) has multiple applications, including the following.


2-Ethylhexanoic acid (CAS 149-57-5) is a building block for alkyd resins and for production of organic metal salts. 
Alkyd resins modified with 2-Ethylhexanoic acid (CAS 149-57-5) are used in stoving enamels and two-component paints (primers and topcoats). 
2-Ethylhexanoic acid (CAS 149-57-5) is a versatile monocarboxylic acid chemical intermediate. 


2-Ethylhexanoic acid (CAS 149-57-5) is a colorless to light yellow liquid with a mild odor. 
2-Ethylhexanoic acid (CAS 149-57-5) will burn though it may take some effort to ignite. 
2-Ethylhexanoic acid (CAS 149-57-5) is slightly soluble in water. 


2-Ethylhexanoic acid (CAS 149-57-5) is corrosive to metals and tissue. 
2-Ethylhexanoic acid (CAS 149-57-5) is a branched-chain fatty acid.
2-Ethylhexanoic acid (CAS 149-57-5) has been reported in Vitis vinifera and Artemisia arborescens with data available.


2-Ethylhexanoic acid (CAS 149-57-5) is found in fruits. 
2-Ethylhexanoic acid (CAS 149-57-5) is found in grapes. 
2-Ethylhexanoic acid (CAS 149-57-5) belongs to the family of Branched Fatty Acids. 


These are fatty acids containing a branched chain.
2-Ethylhexanoic acid (CAS 149-57-5), commonly known as octoic acid, is the organic compound with the formula CH3(CH2)3CH(C2H5)CO2H. 
2-Ethylhexanoic acid (CAS 149-57-5) is a carboxylic acid that is widely used to prepare lipophilic metal derivatives that are soluble in nonpolar organic solvents. 


2-Ethylhexanoic acid (CAS 149-57-5) is a colorless viscous oil. 
2-Ethylhexanoic acid (CAS 149-57-5) is supplied as a racemic mixture.

USES and APPLICATIONS of 2-ETHYLHEXANOIC ACID (CAS 149-57-5):
2-Ethylhexanoic acid (CAS 149-57-5) is used in the manufacture of adhesive and sealant chemicals, corrosion inhibitors and scale inhibitors, intermediates, lubricant and lubricant additives, paint and coating additives, and process conditioners.


2-Ethylhexanoic acid (CAS 149-57-5) is widely used in the market as an intermediate for paint and paint dryers, as an alkyd resin modifier, as a catalyst for the production of peroxides as polymerization reactions, and as a lubricant ester and PVC stabilizer.


2-Ethylhexanoic acid (CAS 149-57-5) 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-Ethylhexanoic acid (CAS 149-57-5) 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-Ethylhexanoic acid (CAS 149-57-5) is also used as a stabilizer for polyvinyl chlorides. 
2-Ethylhexanoic acid (CAS 149-57-5) is also involved in solvent extraction and dye granulation. 


Further, 2-Ethylhexanoic acid (CAS 149-57-5) is used to prepare plasticizers, lubricants, detergents, flotation aids, corrosion inhibitors and alkyd resins. 
In addition to this, 2-Ethylhexanoic acid (CAS 149-57-5) serves as a catalyst for polyurethane foaming.
2-Ethylhexanoic acid (CAS 149-57-5) is used as a reactant in esterification , decarboxylative alkynylation , and preparation of alkyl coumarins via decarboxylative coupling reactions.


2-Ethylhexanoic acid (CAS 149-57-5) is used in the organocatalytic medium for the preparation of various 3,4-dihydropyrimidin-2(1H)-ones/thiones by Biginelli reaction.
2-Ethylhexanoic acid (CAS 149-57-5) is used paint and varnish driers (metallic salts). 


Ethylhexoates of light metals are used to convert some mineral oils to greases. 
2-Ethylhexanoic acid (CAS 149-57-5)'s esters are used as plasticizers.
2-Ethylhexanoic acid (CAS 149-57-5) is used to make paint dryers and plasticizers.


This carboxylic acid, 2-Ethylhexanoic acid (CAS 149-57-5), is widely used to prepare metal derivatives that are soluble in nonpolar organic solvents.
2-Ethylhexanoic acid (CAS 149-57-5) is used to prepare plasticizers, lubricants, detergents, flotation aids, corrosion inhibitors and alkyd resins.
2-Ethylhexanoic acid (CAS 149-57-5) is used Antifreeze & Coolant, Chemical Synthesis, Corrosion Inhibitors, Industrial Chemicals, Lubricant & Grease, Personal Care & Cosmetics, Thickening Agents, Catalysts, Esters, Plasticizers


In consumer products, 2-Ethylhexanoic acid (CAS 149-57-5) is found in de-icers, car care products, paints, greases and lubricants to name a few. 
Industrially, 2-Ethylhexanoic acid (CAS 149-57-5) has applications in stabilisers, preservatives, coolants, wetting agents, pesticides and lubricants.
2-Ethylhexanoic acid (CAS 149-57-5) is widely used in various industries, including the production of plasticizers, lubricants, and coatings.


2-Ethylhexanoic acid (CAS 149-57-5) is an industrially important aliphatic carboxylic acid which is widely employed as a stabilizer and a wood preservative.
2-Ethylhexanoic acid (CAS 149-57-5) has various industrial applications, such as: coolant in automotive, synthetic lubricant, wetting agent, co-solvent, drying of paints, and defoaming agent in pesticides.


2-Ethylhexanoic acid (CAS 149-57-5) is also used to modify acrylic resins.
Areas of application of 2-Ethylhexanoic acid (CAS 149-57-5): Manufacture of metal salts, heavy metal soaps, thickeners, plasticizers, stabilizers, emulsifiers and corrosion inhibitors


2-Ethylhexanoic acid (CAS 149-57-5) is used as a plasticizer in PVC production, as a corrosion inhibitor in coolants, as a stabilizer, in wood preservatives and to produce lubricant additives. 
The zinc salt of 2-Ethylhexanoic acid (CAS 149-57-5) is used as a corrosion inhibitor in lubricants and as a hydrogen sulfide scavenger.


When it comes to maintaining your vehicle’s performance and longevity, the importance of coolant can’t be overstated. 
However, few are aware of the critical role played by a seemingly obscure compound: 2-Ethylhexanoic acid (CAS 149-57-5). 
This carboxylic acid, 2-Ethylhexanoic acid (CAS 149-57-5), is a game changer in automotive coolants, ensuring engines run smoothly under various conditions. 


2-Ethylhexanoic acid (CAS 149-57-5) is used by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.
2-Ethylhexanoic acid (CAS 149-57-5) is used in the following products: anti-freeze products, laboratory chemicals and metal working fluids. 
2-Ethylhexanoic acid (CAS 149-57-5) is used in the following areas: scientific research and development. 


Other release to the environment of 2-Ethylhexanoic acid (CAS 149-57-5) is likely to occur from: indoor use as processing aid, indoor use in close systems with minimal release (e.g. cooling liquids in refrigerators, oil-based electric heaters) and outdoor use in close systems with minimal release (e.g. hydraulic liquids in automotive suspension, lubricants in motor oil and break fluids).


2-Ethylhexanoic acid (CAS 149-57-5) is used in the following products: coating products.
Release to the environment of 2-Ethylhexanoic acid (CAS 149-57-5) can occur from industrial use: formulation of mixtures.
2-Ethylhexanoic acid (CAS 149-57-5) is used in the following products: coating products, laboratory chemicals, lubricants and greases and metal working fluids.


2-Ethylhexanoic acid (CAS 149-57-5) has an industrial use resulting in manufacture of another substance (use of intermediates).
Release to the environment of 2-Ethylhexanoic acid (CAS 149-57-5) can occur from industrial use: in processing aids at industrial sites, as an intermediate step in further manufacturing of another substance (use of intermediates) and of substances in closed systems with minimal release.


Release to the environment of 2-Ethylhexanoic acid (CAS 149-57-5) can occur from industrial use: manufacturing of the substance.
Automotive,  2-Ethylhexanoic acid (CAS 149-57-5) is used in the production of corrosion inhibitors for automotive coolants.
Lubricants: 2-Ethylhexanoic acid (CAS 149-57-5) is a major raw material for polyolesters used in synthetic lubricants.


Personal Care: In cosmetics, 2-Ethylhexanoic acid (CAS 149-57-5) is used to produce emollients.
2-Ethylhexanoic acid (CAS 149-57-5) is a commonly used organic compound, mainly to make lipophilic metal by-products that can dissolve in nonionic organic solvents. 


2-Ethylhexanoic acid (CAS 149-57-5) can be used as a substitute for naphthenic acid in some applications. 
Industrially, 2-Ethylhexanoic acid (CAS 149-57-5) is manufactured using propylene, often generated from fossil fuels and other sources which are renewable. 
In other words, 2-Ethylhexanoic acid (CAS 149-57-5) can be more effectively manufactured than naphthenic acid.


2-Ethylhexanoic acid (CAS 149-57-5) is also used to make polyol ester which acts as a lubricant for refrigerant appliances.
Automotive: 2-Ethylhexanoic acid (CAS 149-57-5) is used in the production of corrosion inhibitors for automotive coolants.
Lubricants: 2-Ethylhexanoic acid (CAS 149-57-5) is a major raw material for polyolesters used in synthetic lubricants. 


Personal Care: In cosmetics, 2-Ethylhexanoic acid (CAS 149-57-5) is used to produce emollients.
The production of polyvinylbutyral (PVB) plasticizers and polyvinylchloride (PVC) stabilizers in the form of metal salts. Other applications of 2-Ethylhexanoic acid (CAS 149-57-5) include, catalyst for polymer production, raw material for acid chloride and fragrances.


2-Ethylhexanoic acid (CAS 149-57-5) is used to make paint dryers and plasticizers.
Metal salts of 2-Ethylhexanoic acid (CAS 149-57-5) are used for siccatives in oxidative drying paints and printing inks.


-Coatings uses of 2-Ethylhexanoic acid (CAS 149-57-5):
2-Ethylhexanoic acid (CAS 149-57-5) is used in the synthesis of alkyd resins provides improved yellowing resistanct than the standard fatty acids. 
2-Ethylhexanoic acid (CAS 149-57-5) is particularly suitable for stoving enamels and two-component coatings.
2-Ethylhexanoic acid (CAS 149-57-5) is also used as a raw material for metal based paint driers.


-Lubricants uses of 2-Ethylhexanoic acid (CAS 149-57-5):
2-Ethylhexanoic acid (CAS 149-57-5) is commonly used in esters in Polyvinyl butyral (PVB) film plasticizers and as a raw material for polyesters applied in synthetic oils. 
2-Ethylhexanoic acid (CAS 149-57-5)’s metal salts are used to prepare synthetic lubricant additives used in various industrial lubricant applications.


-Coatings uses of 2-Ethylhexanoic acid (CAS 149-57-5):
2-Ethylhexanoic acid (CAS 149-57-5) is widely used in coating applications to enhance performance and resistance. 

2-Ethylhexanoic acid (CAS 149-57-5) produces alkyd resins that help improve yellowing resistance better than ordinary fatty acids. 2-Ethylhexanoic acid (CAS 149-57-5) is ideal for stoving enamels and 2-component coatings. 
2-Ethylhexanoic acid (CAS 149-57-5) can also be used in other applications, including the catalyst for polyurethane, wood preservatives, and pharmaceuticals.


-Cosmetics uses of 2-Ethylhexanoic acid (CAS 149-57-5):
The chemicals in 2-Ethylhexanoic acid (CAS 149-57-5) are reported to have cosmetic use to produce emollients and skin conditioners. 
2-Ethylhexanoic acid (CAS 149-57-5) is widely used in hair care products, hand creams, face creams, body lotions, and make-up products like foundation, concealer, and hair care products.


-Plastics uses of 2-Ethylhexanoic acid (CAS 149-57-5):
2-Ethylhexanoic acid (CAS 149-57-5) is also used in manufacturing polyvinyl chloride (PVC) stabilizers and Polyvinyl butyral (PVB) plasticizers in the form of metal salts. 
2-Ethylhexanoic acid (CAS 149-57-5) reacts with metallic components like manganese and cobalt to produce metallic salt derivatives.


-Automotive uses of 2-Ethylhexanoic acid (CAS 149-57-5):
2-Ethylhexanoic acid (CAS 149-57-5) is used to produce corrosion inhibitors for lubricants and automotive coolants. 
2-Ethylhexanoic acid (CAS 149-57-5) also serves as wood preservatives and makes lubricant additives as well as synthetic lubricants. 

2-Ethylhexanoic acid (CAS 149-57-5) is also used in the production of PVC heat stabilizers, PVB film plasticizers, metal soaps for paint driers, and other chemicals.


-Coatings uses of 2-Ethylhexanoic acid (CAS 149-57-5):
2-Ethylhexanoic acid (CAS 149-57-5) is used in the synthesis of alkyd resins provides improved yellowing resistanct than the standard fatty acids. 
2-Ethylhexanoic acid (CAS 149-57-5) is particularly suitable for stoving enamels and two-component coatings.  
2-Ethylhexanoic acid (CAS 149-57-5) is also used as a raw material for metal based paint driers.

PREPARATION OF 2-Ethylhexanoic acid (CAS 149-57-5):
In a dry 1L three-neck bottle, Add isooctyl aldehyde (80g, 0.62mol) And the solvent 2-ethylhexanoic acid (240g, 1.66mol), ligand L8 (5.24mg, 0.007mmol), cesium carbonate (18.24mg, 0.056mmol), potassium acetate 160mg, placed in a water bath, mechanical under nitrogen atmosphere Stir, after the temperature rises to 30 ° C, Air flow was started at a flow rate of 11.9 g/h, and the reaction temperature was maintained at 30-35 ° C by adding cooling water to the water bath. 

After 6 hours of reaction, the conversion of isooctyl aldehyde was calculated to be 99.6%. 
The selectivity of 2-Ethylhexanoic acid (CAS 149-57-5) was 99.5%, and the yield was 99.10%.

HOW IS 2-Ethylhexanoic acid (CAS 149-57-5) USED?
A major use of 2-Ethylhexanoic acid (CAS 149-57-5) is in the preparation of metal salts and soaps used as drying agents in paint and inks, and as thermal stabilizers in polyvinyl chloride (PVC).
2-Ethylhexanoic acid (CAS 149-57-5) is also used in the manufacture of resins used in automobile windshields and vinyl flooring.
2-Ethylhexanoic acid (CAS 149-57-5) is not manufactured in Canada, but it is imported into Canada.

OCCURRENCE AND USE OF 2-Ethylhexanoic acid (CAS 149-57-5):
2-Ethylhexanoic acid (CAS 149-57-5) 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

WHAT IS 2-Ethylhexanoic acid (CAS 149-57-5) AND 2-Ethylhexanoic acid (CAS 149-57-5)'S ROLE IN COOLANTS?
2-Ethylhexanoic acid (CAS 149-57-5) is a fatty acid that has made significant strides in the automotive industry. 
2-Ethylhexanoic acid (CAS 149-57-5)’s a key ingredient in producing polyesters for lubricants and serves as an essential component in coolants. 
In simple terms, 2-Ethylhexanoic acid (CAS 149-57-5) helps prevent rust and corrosion in your vehicle’s engine. 

WHY CHOOSE 2-Ethylhexanoic acid (CAS 149-57-5) COOLANTS?
Opting for coolants with 2-EHA offers multiple benefits:
*Enhanced Corrosion Resistance: 
2-Ethylhexanoic acid (CAS 149-57-5) creates a protective layer on metal surfaces, shielding them from corrosive elements.

*Stability Under Heat: 
2-Ethylhexanoic acid (CAS 149-57-5) ensures the coolant remains effective even under high temperatures, a common scenario in engine operations.

*Compatibility: 
2-Ethylhexanoic acid (CAS 149-57-5) works well with various materials used in engines, making it a versatile choice.

PHYSICAL AND CHEMICAL PROPERTIES OF 2-Ethylhexanoic acid (CAS 149-57-5):
2-Ethylhexanoic acid (CAS 149-57-5) is a slightly volatile liquid. 
2-Ethylhexanoic acid (CAS 149-57-5) is colorless to slightly yellowish and almost odorless. 
In aqueous solution, 2-Ethylhexanoic acid (CAS 149-57-5) is acidic. 
2-Ethylhexanoic acid (CAS 149-57-5) is only sparingly soluble in water, but readily soluble in diethyl ether and carbon tetrachloride and other polar solvents.

PRODUCTION OF 2-Ethylhexanoic acid (CAS 149-57-5):
2-Ethylhexanoic acid (CAS 149-57-5) is produced industrially from propylene, which is hydroformylated to give butyraldehyde. 
Aldol condensation of the aldehyde gives 2-ethylhexenal, which is hydrogenated to give 2-ethylhexanal. 
Oxidation of this aldehyde gives the carboxylic acid.


Metal ethylhexanoates
2-Ethylhexanoic acid (CAS 149-57-5) 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.


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]

REACTIVITY PROFILE OF 2-Ethylhexanoic acid (CAS 149-57-5):
2-Ethylhexanoic acid (CAS 149-57-5) 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. 
The pH of solutions of carboxylic acids is therefore less than 7.0. 
Many insoluble carboxylic acids react rapidly with aqueous solutions containing a chemical base and dissolve as the neutralization generates a soluble salt. 

Carboxylic acids 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 carboxylic acids 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-Ethylhexanoic acid (CAS 149-57-5) to corrode or dissolve iron, steel, and aluminum parts and containers. 

Carboxylic acids, 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. 
Carboxylic acids, 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, carboxylic acids can be oxidized by strong oxidizing agents and reduced by strong reducing agents. 
These reactions generate heat. 

A wide variety of products is possible. 
Like other acids, carboxylic acids may initiate polymerization reactions; like other acids, they often catalyze (increase the rate of) chemical reactions.

STABILITY AND REACTIVITY OF 2-Ethylhexanoic acid (CAS 149-57-5):
Under normal conditions, 2-Ethylhexanoic acid (CAS 149-57-5) is chemically stable. 
2-Ethylhexanoic acid (CAS 149-57-5) is flammable, but very difficult to ignite. 
However, the vapors of 2-Ethylhexanoic acid (CAS 149-57-5)  combine with the ambient air to form explosive mixtures.

Because they are denser, the vapors are heavier than air.
They gather on the ground and can spread unnoticed. 
Remote ignition of the vapor-air mixture is therefore possible. 

2-Ethylhexanoic acid (CAS 149-57-5) must therefore be kept away from all types of ignition sources and in particular from open flames, sparks and electrical discharges. 
The decomposition and combustion of 2-Ethylhexanoic acid (CAS 149-57-5) produces irritating and acrid gases. 

PHYSICAL and CHEMICAL PROPERTIES of 2-ETHYLHEXANOIC ACID (CAS 149-57-5):
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
Molecular Weight: 144.21 g/mol
XLogP3: 2.6
Hydrogen Bond Donor Count: 1
Hydrogen Bond Acceptor Count: 2
Rotatable Bond Count: 5
Exact Mass: 144.115029749 g/mol
Monoisotopic Mass: 144.115029749 g/mol
Topological Polar Surface Area: 37.3Ų
Heavy Atom Count: 10

Formal Charge: 0
Complexity: 99.4
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 1
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
CAS Number: 149-57-5
Molecular Formula: C8H16O2

Appearance: Colorless liquid
Odor: Characteristic
Purity: 99% min
Melting Point: -78°C
Boiling Point: 227-228°C
Density (20°C): 0.894 g/cm³
Flash Point: 112°C
Solubility in Water: Negligible
Solubility in Organic Solvents: Miscible
Physical description: A colorless to light yellow liquid with a mild odor.
Boiling point: 442°F

Molecular weight: 144.21
Freezing point/melting point: -117°F
Vapor pressure:
Flash point: 260°F
Vapor density:
Specific gravity: 0.903
Ionization potential:
Lower explosive limit (LEL): 1.04% at 275°F
Upper explosive limit (UEL): 8.64% at 370.4°F
CAS number: 149-57-5
EC index number: 607-230-00-6
EC number: 205-743-6

Hill Formula: C₈H₁₆O₂
Molar Mass: 144.21 g/mol
HS Code: 2915 90 21
Boiling point: 226 - 229 °C (1013 hPa)
Density: 0.906 g/cm³ (20 °C)
Explosion limit: 0.9 - 6.7 %(V)
Flash point: 114 °C
Ignition temperature: 310 °C
Melting Point: -59 °C
pH value: 3 (1.4 g/l, H₂O, 20 °C)
Vapor pressure: <0.01 hPa (20 °C)

Solubility: 1.4 g/l
Appearance: Colorless clear liquid (est)
Assay: 99.00 to 100.00
Food Chemicals Codex Listed: No
Specific Gravity: 0.89300 to 0.91300 @ 25.00 °C
Pounds per Gallon - (est.): 7.431 to 7.597
Refractive Index: 1.42000 to 1.42600 @ 20.00 °C
Melting Point: -59.00 °C @ 760.00 mm Hg
Boiling Point: 220.00 to 223.00 °C @ 760.00 mm Hg
Vapor Pressure: 0.030000 mmHg @ 20.00 °C
Vapor Density: 4.98 (Air = 1)
Flash Point: 244.00 °F TCC (117.78 °C)

logP (o/w): 2.640
Soluble in:
alcohol, water, 2000 mg/L @ 20 °C (exp)
Insoluble in: water
CBNumber: CB5425330
Molecular Formula: C8H16O2
Molecular Weight: 144.21
MDL Number: MFCD00002675
MOL File: 149-57-5.mol
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: 1.4 g/l
Form: Liquid
pKa: pK1: 4.895 (25°C)
Color: Clear
pH: 3 (1.4 g/l, H2O, 20℃)
Odor: Mild odor
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℃
CAS DataBase Reference: 149-57-5 (CAS DataBase Reference)
EWG's Food Scores: 2
FDA UNII: 01MU2J7VVZ
NIST Chemistry Reference: Hexanoic acid, 2-ethyl- (149-57-5)
EPA Substance Registry System: 2-Ethylhexanoic acid (149-57-5)

FIRST AID MEASURES of 2-ETHYLHEXANOIC ACID (CAS 149-57-5):
-Description of first-aid measures
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation: 
Fresh air.
*In case of skin contact: 
Take off immediately all contaminated clothing. 
Rinse skin with
water/ shower.
*In case of eye contact:
After eye contact: 
Rinse out with plenty of water. 
Call in ophthalmologist. 
Remove contact lenses.
*If swallowed:
After swallowing: 
Immediately make victim drink water (two glasses at most). 
Consult a physician.
-Indication of any immediate medical attention and special treatment needed.
No data available

ACCIDENTAL RELEASE MEASURES of 2-ETHYLHEXANOIC ACID (CAS 149-57-5):
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains. 
Collect, bind, and pump off spills. 
Observe possible material restrictions. 
Take up dry. 
Dispose of properly. 
Clean up affected area.

FIRE FIGHTING MEASURES of 2-ETHYLHEXANOIC ACID (CAS 149-57-5):
-Extinguishing media:
*Suitable extinguishing media:
Carbon dioxide (CO2) 
Foam 
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.

EXPOSURE CONTROLS/PERSONAL PROTECTION of 2-ETHYLHEXANOIC ACID (CAS 149-57-5):
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection. 
Safety glasses
*Body Protection:
protective clothing
*Respiratory protection:
Recommended Filter type: Filter A 
-Control of environmental exposure:
Do not let product enter drains.

HANDLING and STORAGE of 2-ETHYLHEXANOIC ACID (CAS 149-57-5):
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed. 
Dry.

STABILITY and REACTIVITY of 2-ETHYLHEXANOIC ACID (CAS 149-57-5):
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Possibility of hazardous reactions:
No data available

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