Información del producto
- (S)-(-)-Ethyl lactate(-)-Ethyl (S)-2-hydroxypropionate(S)-(-)-2-Hydroxypropionic acid ethyl esterL-Lactic acid ethyl ester
- (-)-Ethyl 2-hydroxypropanoate
- (-)-Ethyl 2-hydroxypropionate
- (-)-Ethyl lactate
- (2S)-2-Hydroxypropanoic acid ethyl ester
- (2S)-2-Hydroxypropionic acid ethyl ester
- (2S)-Ethyl 2-hydroxypropanoate
- (<span class="text-smallcaps">L</span>)-(-)-Ethyl lactate
- (L)-(-)-Ethyl lactate
- (S)-(-)-Ethyl lactate
- Ver más sinónimos
- (S)-(-)-Lactic acid ethyl ester
- (S)-2-Hydroxypropanoic acid ethyl ester
- (S)-2-hidroxipropionato de etilo
- (S)-2-hydroxypropionate d'ethyle
- Ethyl (-)-(S)-lactate
- Ethyl (2S)-(-)-2-hydroxypropanoate
- Ethyl (2S)-hydroxypropanoate
- Ethyl (S)-(-)-2-hydroxypropionate
- Ethyl (S)-2-hydroxypropanoate
- Ethyl <span class="text-smallcaps">L</span>-(-)-lactate
- Ethyl-(S)-2-hydroxypropionat
- Lactate, Ethyl, L-(-)-
- Lactic acid, ethyl ester, (-)-
- Propanoic acid, 2-hydroxy-, ethyl ester, (2S)
- Propanoic acid, 2-hydroxy-, ethyl ester, (S)-
Ethyl L-lactate is a chiral compound that is an ester of benzoic acid and lactic acid. It is used in analytical chemistry as a chiral reagent to determine the optical purity of other compounds. The photochemical properties of ethyl l-lactate are ferroelectric, which means that it exhibits spontaneous electric polarization when exposed to light. This property has been exploited in the development of new materials for use in electronic devices and also for applications such as solar cells and displays. Ethyl l-lactate can also be synthesized by reacting diphenyl ether with amines or phenoxy, providing an asymmetric synthesis route with endpoints such as titration calorimetry and azobenzene.
The following product details were generated using the above information:
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Propiedades químicas
Consulta técnica sobre: 3D-FE10069 Ethyl L-lactate
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