CAS 3976-69-0
:Metil (-)-3-hidroxibutirato
Descripción:
Metil (-)-3-hidroxibutirato es un compuesto orgánico caracterizado por su grupo funcional éster, derivado del ácido hidroxibutírico. Es una molécula quiral, con la designación (-) que indica su estereoequilibrio específico, lo que puede influir en su actividad biológica e interacciones. Este compuesto es típicamente un líquido incoloro a amarillo pálido con un olor afrutado, y es soluble en agua y disolventes orgánicos, lo que lo hace versátil en diversas aplicaciones. Metil (-)-3-hidroxibutirato se estudia a menudo por su papel en los procesos metabólicos, particularmente en el contexto de la cetogénesis y el metabolismo energético. También es de interés en los campos de la nutrición y la bioquímica, ya que puede tener implicaciones en el rendimiento atlético y el control del peso. Además, debido a su naturaleza de éster, puede participar en diversas reacciones químicas, incluyendo la hidrólisis y la transesterificación. Los datos de seguridad indican que, aunque debe manejarse con cuidado, generalmente se considera que tiene baja toxicidad.
Fórmula:C5H10O3
InChI:InChI=1S/C5H10O3/c1-4(6)3-5(7)8-2/h4,6H,3H2,1-2H3/t4-/m1/s1
Clave InChI:InChIKey=LDLDJEAVRNAEBW-SCSAIBSYSA-N
SMILES:C(C[C@@H](C)O)(OC)=O
Sinónimos:- (-)-(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
- Ver más sinónimos
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Encontrado 8 productos.
(R)-Methyl 3-hydroxybutanoate
CAS:Fórmula:C5H10O3Pureza:98%Forma y color:LiquidPeso molecular:118.1311Methyl (R)-(-)-3-Hydroxybutyrate
CAS:Fórmula:C5H10O3Pureza:>98.0%(GC)Forma y color:Colorless to Almost colorless clear liquidPeso molecular:118.13Methyl (R)-(-)-3-hydroxybutyrate, 98%
CAS:<p>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</p>Fórmula:C5H10O3Pureza:98%Forma y color:Clear colorless, LiquidPeso molecular:118.13Methyl (R)-3-hydroxybutanoate
CAS:Methyl (R)-3-hydroxybutanoateFórmula:C5H10O3Pureza:97%Forma y color: clear. colourless liquidPeso molecular:118.13g/mol(R)-(-)-Methyl 3-hydroxybutyrate
CAS:Fórmula:C5H10O3Pureza:≥ 98.5%Forma y color:Colourless liquidPeso molecular:118.13(R)-Methyl 3-hydroxybutanoate
CAS:Fórmula:C5H10O3Pureza:97%Forma y color:Liquid, ClearPeso molecular:118.132Methyl (R)-3-Hydroxybutyrate
CAS:Producto controlado<p>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.<br>References Xiao, X.Q., et al.: Biomaterials, 28, 3608 (2007)<br></p>Fórmula:C5H10O3Forma y color:NeatPeso molecular:118.131(R)-(-)-3-Hydroxybutyric acid methyl ester
CAS:<p>(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.</p>Fórmula:C5H10O3Pureza:Min. 95%Peso molecular:118.13 g/mol







