CAS 3976-69-0

Methyl (-)-3-hydroxybutyrate

Description:

Methyl (-)-3-hydroxybutyrate is an organic compound characterized by its ester functional group, derived from the hydroxybutyric acid. It is a chiral molecule, with the (-) designation indicating its specific stereochemistry, which can influence its biological activity and interactions. This compound is typically a colorless to pale yellow liquid with a fruity odor, and it is soluble in water and organic solvents, making it versatile in various applications. Methyl (-)-3-hydroxybutyrate is often studied for its role in metabolic processes, particularly in the context of ketogenesis and energy metabolism. It is also of interest in the fields of nutrition and biochemistry, as it may have implications in athletic performance and weight management. Additionally, due to its ester nature, it can participate in various chemical reactions, including hydrolysis and transesterification. Safety data indicates that, while it should be handled with care, it is generally considered to have low toxicity.

Formula: C₅H₁₀O₃

InChI: InChI=1S/C5H10O3/c1-4(6)3-5(7)8-2/h4,6H,3H2,1-2H3/t4-/m1/s1

InChI key: InChIKey=LDLDJEAVRNAEBW-SCSAIBSYSA-N

SMILES: C(C[C@@H](C)O)(OC)=O

Synonyms:

• (-)-(3R)-3-Hydroxybutanoic acid methyl ester
• (R)-(-)-3-Hydroxy-N-Butyric Acid Methyl Ester
• (R)-(-)-3-Hydroxy-n-butyrate methyl ester
• (R)-(-)-3-Hydroxybutyric Acid Methyl Ester
• (R)-(-)-methyl 3-hydroxybutyrate
• (R)-Methyl 3-Hydroxybutanoate
• (R)-β-Hydroxybutyric acid methyl ester
• <span class="text-smallcaps">D</span>-3-Hydroxybutyric acid methyl ester
• Butanoic acid, 3-hydroxy-, methyl ester, (3R)-
• Butanoic acid, 3-hydroxy-, methyl ester, (R)-
• Butyric acid, 3-hydroxy-, methyl ester
• Butyric acid, 3-hydroxy-, methyl ester, <span class="text-smallcaps">D</span>-(-)-
• Methyl (3R)-hydroxybutanoate
• Methyl (R)-3-hydroxybutanoate
• Methyl 3-Hydroxybutanoate
• Methyl 3-Hydroxybutyrate
• Methyl 3R-hydroxybutyrate
• Methyl D-(R)-3-Hydroxybutyrate
• methyl (3R)-3-hydroxybutanoate
• Butyric acid, 3-hydroxy-, methyl ester, D-(-)-
• methyl (r)-(-)-3-hydroxybutyrate

(R)-Methyl 3-hydroxybutanoate

CAS: 3976-69-0

Formula: C₅H₁₀O₃

Purity: 98%

Color and Shape: Liquid

Molecular weight: 118.1311

Ref: IN-DA003RIU

Methyl (R)-(-)-3-Hydroxybutyrate

CAS: 3976-69-0

Formula: C₅H₁₀O₃

Purity: >98.0%(GC)

Color and Shape: Colorless to Almost colorless clear liquid

Molecular weight: 118.13

Ref: 3B-H0705

Methyl (R)-(-)-3-hydroxybutyrate, 98%

CAS: 3976-69-0

Can undergo aldol-type reactions with aldehydes with either syn- or anti-selectivity according to the conditions, for use in the synthesis of chiral -lactams. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label informat

Formula: C₅H₁₀O₃

Purity: 98%

Color and Shape: Clear colorless, Liquid

Molecular weight: 118.13

Ref: 02-L14151

Methyl (R)-3-hydroxybutanoate

CAS: 3976-69-0

Methyl (R)-3-hydroxybutanoate

Formula: C₅H₁₀O₃

Purity: 97%

Color and Shape: clear. colourless liquid

Molecular weight: 118.13g/mol

Ref: 54-OR28835

(R)-(-)-Methyl 3-hydroxybutyrate

CAS: 3976-69-0

Formula: C₅H₁₀O₃

Purity: ≥ 98.5%

Color and Shape: Colourless liquid

Molecular weight: 118.13

Ref: 7W-GK4856

(R)-Methyl 3-hydroxybutanoate

CAS: 3976-69-0

Formula: C₅H₁₀O₃

Purity: 97%

Color and Shape: Liquid, Clear

Molecular weight: 118.132

Ref: 10-F079225

Methyl (R)-3-Hydroxybutyrate

Controlled Product

CAS: 3976-69-0

Applications Methyl (R)-3-Hydroxybutyrate, a derivative of 3-hydroxybutyric acid, has inhibitory effects on cell apoptosis which is mediated by signaling pathways related to the elevation of cytosolic Ca2+ concentration. Also a potential effective neutral protective agent.
References Xiao, X.Q., et al.: Biomaterials, 28, 3608 (2007)

Formula: C₅H₁₀O₃

Color and Shape: Neat

Molecular weight: 118.131

Ref: TR-M312580

(R)-(-)-3-Hydroxybutyric acid methyl ester

CAS: 3976-69-0

(R)-(-)-3-Hydroxybutyric acid methyl ester is a monocarboxylic acid that is metabolized by phosphofructokinase and other enzymes to produce the corresponding 3-hydroxybutyrate. This compound is synthesized from tiglic acid, which can be obtained from corynebacterium. The production of (R)-(-)-3-Hydroxybutyric acid methyl ester can be optimized by using a biotransformation process. This process includes enzymatic reactions and chemical transformations, such as hydroxylation, carbonylation, and stereoselective synthesis. The metabolic pathway for this compound has been studied using a DNA microarray analysis.

Formula: C₅H₁₀O₃

Purity: Min. 95%

Molecular weight: 118.13 g/mol

Ref: 3D-FM12107