CAS No.: | 141-97-9 |
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Formula: | C6h10o3 |
EINECS: | 205-516-1 |
Classification: | Phosphoric Acid |
Appearance: | Liquid |
Grade Standard: | Agriculture Grade |
Customization: |
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Common Name | Ethyl acetoacetate | ||
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CAS Number | 141-97-9 | Molecular Weight | 130.142 |
Density | 1.0±0.1 g/cm3 | Boiling Point | 180.6±8.0 °C at 760 mmHg |
Molecular Formula | C6H10O3 | Melting Point | −43 °C(lit.) |
MSDS | ChineseUSA | Flash Point | 67.0±18.5 °C |
Density | 1.0±0.1 g/cm3 |
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Boiling Point | 180.6±8.0 °C at 760 mmHg |
Melting Point | −43 °C(lit.) |
Molecular Formula | C6H10O3 |
Molecular Weight | 130.142 |
Flash Point | 67.0±18.5 °C |
Exact Mass | 130.062988 |
PSA | 43.37000 |
LogP | 0.72 |
Vapour density | 4.48 (vs air) |
Vapour Pressure | 0.9±0.3 mmHg at 25°C |
Index of Refraction | 1.408 |
Stability | Stable. Incompatible with acids, bases, oxidizing agents, reducing agents, alkali metals. Combustible. |
Water Solubility | 116 g/L (20 ºC) |
Ethyl acetoacetate is an organic compound with the chemical formula C6H10O3. It is an ester derived from acetoacetic acid and ethanol. Ethyl acetoacetate is a clear, colorless liquid with a fruity odor.
Chemical Properties: Ethyl acetoacetate consists of an acetoacetate group (-CH2COCH2COOCH2CH3) attached to an ethyl group (-CH2CH3). It has a molecular weight of approximately 130.14 g/mol and a boiling point of around 180-183 °C. It is soluble in water to a limited extent and miscible with many organic solvents.
Synthesis: Ethyl acetoacetate can be synthesized through the reaction of acetoacetic acid with ethanol in the presence of an acid catalyst, typically sulfuric acid. The reaction involves the esterification of the carboxylic acid group of acetoacetic acid with ethanol, resulting in the formation of ethyl acetoacetate.
Applications: Ethyl acetoacetate is widely used as a versatile intermediate in various chemical syntheses. It serves as a building block in the synthesis of many pharmaceuticals, agrochemicals, dyes, and perfumes. It is also used as a starting material for the production of other compounds, such as pyrazoles, pyrazolones, and beta-diketones.
Chemical Reactivity: Ethyl acetoacetate contains both a carbonyl group and an acidic hydrogen atom, making it susceptible to various chemical reactions. It can undergo nucleophilic addition reactions, condensation reactions, and undergo enolization, where the carbonyl group forms an enol tautomer.
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