CAS 5343-52-2
:2-Ethyl-2-methylpentanoic acid
Description:
2-Ethyl-2-methylpentanoic acid, with the CAS number 5343-52-2, is a branched-chain carboxylic acid characterized by its unique structure, which includes a five-carbon backbone with both ethyl and methyl substituents on the second carbon. This compound is typically a colorless to pale yellow liquid at room temperature and possesses a distinct, pungent odor. It is soluble in organic solvents but has limited solubility in water due to its hydrophobic alkyl chains. The acid group (-COOH) imparts acidic properties, allowing it to participate in various chemical reactions, such as esterification and neutralization. 2-Ethyl-2-methylpentanoic acid is often used in the synthesis of esters for flavoring and fragrance applications, as well as in the production of surfactants and plasticizers. Its branched structure contributes to its relatively low volatility and high boiling point compared to straight-chain carboxylic acids of similar molecular weight. Safety data indicates that it should be handled with care, as it may cause irritation upon contact with skin or eyes.
Formula:C8H16O2
InChI:InChI=1S/C8H16O2/c1-4-6-8(3,5-2)7(9)10/h4-6H2,1-3H3,(H,9,10)
InChI key:InChIKey=WUWPVNVBYOKSSZ-UHFFFAOYSA-N
SMILES:C(CCC)(C(O)=O)(CC)C
Synonyms:- 1-cyclohexyl-5-ethyl-6-hydroxy-2-thioxo-2,3-dihydropyrimidin-4(1H)-one
- 2-Ethyl-2-methylvaleric acid
- 2-Methyl-2-ethylpentanoic acid
- Nsc 466
- Pentanoic acid, 2-ethyl-2-methyl-
- Valeric acid, 2-ethyl-2-methyl-
- α-Ethyl-α-methylvaleric acid
- α-Methyl-α-ethylvaleric acid
- 2-Ethyl-2-methylpentanoic acid
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Found 10 products.
Valproic Acid Related Compound K (2-Ethyl-2-methylpentanoic acid)
CAS:Saturated acyclic monocarboxylic acids and their anhydrides, halides, peroxides etc, nesoiFormula:C8H16O2Color and Shape:Clear Yellow Oily LiquidMolecular weight:144.115032-Ethyl-2-methylpentanoic acid
CAS:Formula:C8H16O2Purity:98%Color and Shape:LiquidMolecular weight:144.21142-Ethyl-2-Methylpentanoic Acid
CAS:2-Ethyl-2-Methylpentanoic AcidPurity:98%Molecular weight:144.21g/molValproic Acid EP Impurity K (Valproic Acid USP Related Compound K)
CAS:Formula:C8H16O2Color and Shape:Yellow LiquidMolecular weight:144.212-Ethyl-2-methylpentanoic acid
CAS:Formula:C8H16O2Color and Shape:Colourless OilyMolecular weight:144.212-Ethyl-2-methylpentanoic Acid
CAS:Controlled Product<p>Applications 2-Ethyl-2-methylpentanoic Acid is a derivative of 2,5-Dimethyl-2-ethylhexanoic Acid (D461540), used in biological studies to evaluate environmental chemicals for estrogenicity.<br>References Rabinowitz, J.R., et al.: Chem. Res. Toxicol.,22, 1594 (2009); Judson, R., et al.: Environ. Health Perspect, 117, 685 (2009)<br></p>Formula:C8H16O2Color and Shape:Colourless OilyMolecular weight:144.212-ETHYL-2-METHYLPENTANOIC ACID
CAS:Formula:C8H16O2Purity:97%Color and Shape:Liquid, No data available.Molecular weight:144.2142-Ethyl-2-methylpentanoic Acid-d3
CAS:Controlled ProductFormula:C8D3H13O2Color and Shape:NeatMolecular weight:147.23(2RS)-2-Ethyl-2-methylpentanoic acid
CAS:<p>(2RS)-2-Ethyl-2-methylpentanoic acid is an organic compound that is used to synthesize the drug 2-ethylhexanoic acid. This compound can be obtained by asymmetric synthesis and it has cytosolic activity. It inhibits the growth of tumor cells by inducing necrotic cell death and hemolysis in erythrocytes. The pH of this substance is acidic and it can be used for the uptake of drugs. In addition, (2RS)-2-Ethyl-2-methylpentanoic acid has significant cytotoxicity as well as fusogenic properties. It also has endosomal excipients and can be used as a neutral or acidic buffer solution for intravenous injections.</p>Formula:C8H16O2Purity:Min. 95%Molecular weight:144.21 g/mol









