CAS 925-57-5
:methyl 4-hydroxybutanoate
Description:
Methyl 4-hydroxybutanoate, with the CAS number 925-57-5, is an organic compound that belongs to the class of esters. It is characterized by the presence of a hydroxyl group (-OH) and a carboxylate group (-COO-) within its structure, which contributes to its solubility in polar solvents. This compound typically appears as a colorless to pale yellow liquid with a fruity odor, making it of interest in flavor and fragrance applications. Methyl 4-hydroxybutanoate is known for its potential use in the synthesis of pharmaceuticals and as an intermediate in organic synthesis. It exhibits moderate volatility and can undergo hydrolysis in the presence of water, leading to the formation of 4-hydroxybutanoic acid and methanol. Additionally, it is important to handle this compound with care, as it may pose health risks if ingested or inhaled. Overall, methyl 4-hydroxybutanoate is a versatile compound with various applications in chemical synthesis and industry.
Formula:C5H10O3
InChI:InChI=1/C5H10O3/c1-8-5(7)3-2-4-6/h6H,2-4H2,1H3
SMILES:COC(=O)CCCO
Synonyms:- Butanoic Acid, 4-Hydroxy-, Methyl Ester
- Methyl 4-hydroxybutanoate
- 4-Hydroxybutanoic acid methyl ester
- 4-Hydroxybutyric acid methyl ester
- Piracetam Impurity 10
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Found 4 products.
4-Hydroxybutyric Acid Methyl Ester
CAS:Formula:C5H10O3Purity:95%Color and Shape:LiquidMolecular weight:118.13114-Hydroxybutyric Acid Methyl Ester (>80%)
CAS:Controlled Product<p>Stability Hygroscopic<br>Applications 4-Hydroxybutyric Acid Methyl Ester is a derivative of 4-Hydroxybutyric Acid (H833015). A reactant used in the preparation of 4-aminothiazolyl analogs of natural product GE2270 A, useful against Clostridium difficile infection.<br>References LaMarche, M. et al.: J. Med. Chem., 55, 2376 (2012)<br></p>Formula:C5H10O3Purity:>80%Color and Shape:NeatMolecular weight:118.134-Hydroxybutyric acid methyl ester
CAS:Controlled Product<p>4-Hydroxybutyric acid methyl ester (4HBME) is a carbon source that can be used in the production of glycoconjugates. It has been used as a constant in analytical methods such as nucleophilic attack, antimicrobial resistance, and structural analysis. 4HBME reacts with ferrocene to form a ferrocene-4HBME complex that can be used for the synthesis of lipase and butyrolactone. It is also an organic solvent that is commonly used for mass spectrometric analysis. 4HBME has functional groups such as hydroxyl, carboxyl, and methyl ester groups. The chemical structure of 4HBME consists of one molecule of 4-hydroxybutanoic acid bound to one molecule of methanol through an ester linkage.</p>Formula:C5H10O3Purity:Min. 95%Molecular weight:118.13 g/mol



