| Identification | More | [Name]
Ethyl (R)-3-hydroxybutyrate | [CAS]
24915-95-5 | [Synonyms]
ETHYL R-(-)-3-HYDROXYBUTANOATE
ETHYL (R)-(-)-3-HYDROXYBUTYRATE
ETHYL (R)-3-HYDROXYBUTYRATE
(R)-(-)-3-HYDROXYBUTYRIC ACID ETHYL ESTER
(R)-3-HYDROXYBUTYRIC ACID ETHYL ESTER
(R)-(-)-3-HYDROXY-N-BUTYRIC ACID ETHYL ESTER
(R)-(-)-ETHYL 3-HYDROXYBUTANOATE
(R)-(-)-ETHYL 3-HYDROXYBUTYRATE
ENZYME MEMBRANE REACTOR (WITHOUT SUPPLEMENTARY ACCESSORIES) EE 99+%
ETHYL (R)-3-HYDROXYBUTANOATE R-3-HYDROXYBUTYRIC ACID ETHYL ESTER | [EINECS(EC#)]
695-003-2 | [Molecular Formula]
C6H12O3 | [MDL Number]
MFCD00075386 | [Molecular Weight]
132.16 | [MOL File]
24915-95-5.mol |
| Chemical Properties | Back Directory | [Appearance]
clear colorless liquid | [alpha ]
-45.5 º (589nm, c=1, CHCl3) | [Boiling point ]
75-76 °C/12 mmHg (lit.) | [density ]
1.017 g/mL at 25 °C(lit.)
| [vapor pressure ]
17.2Pa at 20℃ | [refractive index ]
n20/D 1.42(lit.)
| [Fp ]
148 °F
| [storage temp. ]
Sealed in dry,2-8°C | [form ]
Liquid | [pka]
14.45±0.20(Predicted) | [color ]
Clear, Colorless | [Specific Gravity]
1.017 | [optical activity]
[α]20/D 46°, c = 1 in chloroform | [Water Solubility ]
soluble | [LogP]
0.341 at 20℃ | [CAS DataBase Reference]
24915-95-5(CAS DataBase Reference) |
| Safety Data | Back Directory | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S24/25:Avoid contact with skin and eyes . | [RIDADR ]
1993 | [WGK Germany ]
3
| [HS Code ]
29181990 |
| Hazard Information | Back Directory | [Description]
Ethyl (R)-(-)-3-Hydroxybutyrate is a chiral starting material for the production of numerous biologically active compounds.1 | [Chemical Properties]
clear colorless liquid | [Uses]
Ethyl (R)-(-)-3-hydroxybutyrate is a chiral building block for the preparation of bioactive compounds used in the pharmaceutical industry. It is formed during the hydrolysis of poly-3-hydroxybutyrate. | [Definition]
ChEBI: Ethyl (R)-3-hydroxybutanoate is an ethyl 3-hydroxybutyrate. It is functionally related to a (R)-3-hydroxybutyric acid. | [General Description]
Ethyl (R)-(-)-3-hydroxybutyrate is a chiral building block for the preparation of bioactive compounds used in the pharmaceutical industry. It is formed during the hydrolysis of poly-3-hydroxybutyrate. | [Synthesis]
(R)-β-Butryrolactone (20 g, 230 mmol) was dissolved in 500 mLethanol with 1.0 mL H2SO4 and stirred at room temperature. Aliquots(100 μL) were added to 1.0 mL of methanol and analyzed by GC-MS for conversion of the lactone. Upon completion (> 48 h), a small amount of solid sodium bicarbonate was added and the solvent removed by rotary evaporation. The residue was taken up in dichloromethane and washed with water. The water layer was extracted twice with ethyl acetate. The pooled organic layers were dried with magnesium sulfate, which was then filtered and the solvent removed by rotary evaporation to yield Ethyl (R)-3-hydroxybutyrate as a clear oil (20.2 g, 66%). |
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