CAS 3976-69-0
:Metile (-)-3-idrossibutirrato
Descrizione:
Metile (-)-3-idrossibutirrato è un composto organico caratterizzato dal suo gruppo funzionale estere, derivato dall'acido idrossibutirrico. È una molecola chirale, con la designazione (-) che indica la sua stereochimica specifica, che può influenzare la sua attività biologica e le interazioni. Questo composto è tipicamente un liquido incolore o giallo pallido con un odore fruttato, ed è solubile in acqua e solventi organici, rendendolo versatile in varie applicazioni. Metile (-)-3-idrossibutirrato è spesso studiato per il suo ruolo nei processi metabolici, in particolare nel contesto della chetogenesi e del metabolismo energetico. È anche di interesse nei campi della nutrizione e della biochimica, poiché può avere implicazioni nelle prestazioni atletiche e nella gestione del peso. Inoltre, a causa della sua natura di estere, può partecipare a varie reazioni chimiche, inclusa l'idrolisi e la transesterificazione. I dati di sicurezza indicano che, sebbene debba essere maneggiato con cura, è generalmente considerato a bassa tossicità.
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
Sinonimi:- (-)-(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
- Vedi altri sinonimi
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8 prodotti.
(R)-Methyl 3-hydroxybutanoate
CAS:Formula:C5H10O3Purezza:98%Colore e forma:LiquidPeso molecolare:118.1311Methyl (R)-(-)-3-Hydroxybutyrate
CAS:Formula:C5H10O3Purezza:>98.0%(GC)Colore e forma:Colorless to Almost colorless clear liquidPeso molecolare: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>Formula:C5H10O3Purezza:98%Colore e forma:Clear colorless, LiquidPeso molecolare:118.13Methyl (R)-3-hydroxybutanoate
CAS:Methyl (R)-3-hydroxybutanoateFormula:C5H10O3Purezza:97%Colore e forma: clear. colourless liquidPeso molecolare:118.13g/mol(R)-(-)-Methyl 3-hydroxybutyrate
CAS:Formula:C5H10O3Purezza:≥ 98.5%Colore e forma:Colourless liquidPeso molecolare:118.13(R)-Methyl 3-hydroxybutanoate
CAS:Formula:C5H10O3Purezza:97%Colore e forma:Liquid, ClearPeso molecolare:118.132Methyl (R)-3-Hydroxybutyrate
CAS:Prodotto controllato<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>Formula:C5H10O3Colore e forma:NeatPeso molecolare: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>Formula:C5H10O3Purezza:Min. 95%Peso molecolare:118.13 g/mol







