Skip to main content

Ethyl 4-oxopentanoate

ADVERTISEMENT
Identification
Molecular formula
C7H12O3
CAS number
6703-52-8
IUPAC name
ethyl 4-oxopentanoate
State
State

At room temperature, ethyl 4-oxopentanoate is in a liquid state.

Melting point (Celsius)
-60.00
Melting point (Kelvin)
213.15
Boiling point (Celsius)
190.00
Boiling point (Kelvin)
463.15
General information
Molecular weight
144.17g/mol
Molar mass
144.1740g/mol
Density
0.9632g/cm3
Appearence

Ethyl 4-oxopentanoate is typically a colorless liquid. It may have a faint, sweet odor, characteristic of esters.

Comment on solubility

Solubility of Ethyl 4-Oxopentanoate

Ethyl 4-oxopentanoate, represented by the chemical formula C7H12O3, exhibits intriguing solubility characteristics that are influenced by its molecular structure. Understanding its solubility is crucial for various applications in organic synthesis and chemical analysis.

Solubility Properties

  • Polar vs. Nonpolar Solvents: Ethyl 4-oxopentanoate is moderately polar due to the presence of the carbonyl group (C=O) and the ester functional group. Therefore, it is expected to be more soluble in polar solvents such as ethanol and acetone, while showing reduced solubility in nonpolar solvents like hexane.
  • Temperature Influence: Like many organic compounds, the solubility of ethyl 4-oxopentanoate can increase with temperature. As the temperature rises, the kinetic energy of the molecules increases, leading to better dispersion and interaction with the solvent.
  • Hydrogen Bonding: The capability of ethyl 4-oxopentanoate to form hydrogen bonds with solvents can significantly enhance its solubility in water, although it may remain limited compared to highly polar compounds.

In summary, the solubility of ethyl 4-oxopentanoate is governed by a complex interplay of its chemical structure and the nature of the solvent. Thus, for practical applications, it is advised to consider solvent polarity and temperature as key factors for achieving optimal solubility.

Interesting facts

Interesting Facts about Ethyl 4-Oxopentanoate

Ethyl 4-oxopentanoate, a fascinating compound in the realm of organic chemistry, offers a plethora of intriguing characteristics that make it significant in various fields, including pharmaceuticals and flavor chemistry.

Key Characteristics

  • Synthetic Utility: This compound serves as a key intermediate in the synthesis of various bioactive molecules and complex organic compounds.
  • Flavor and Fragrance: Ethyl 4-oxopentanoate is often studied for its potential use in the flavor and fragrance industry, where it can contribute to fruity and sweet profiles.
  • Ketone Chemistry: Its ketone functional group plays a crucial role in reactivity, allowing it to participate in various chemical reactions such as condensation and reduction.

Applications in Research

This compound has garnered interest in research settings for its applications, such as:

  • Development of enantioselective synthesis methodologies.
  • Investigating its behavior in biological systems for understanding metabolic pathways.
  • Utilization in the fabrication of materials with specific properties.

Noteworthy Facts

Here are some noteworthy facts that highlight the significance of ethyl 4-oxopentanoate:

  • Exploration in Drug Development: Its derivatives have been explored in the development of new pharmaceuticals due to their biological activities.
  • Environmental Studies: Researchers are also studying its environmental impact as it breaks down in soil and water systems.
  • Patents and Innovations: Numerous patents have emerged around novel uses and synthesis routes of ethyl 4-oxopentanoate, emphasizing its importance in innovation.

Overall, ethyl 4-oxopentanoate is more than just a simple ester; it embodies the complexities and creativity inherent in organic chemistry, offering vast opportunities for exploration and application.

Synonyms
ETHYL LEVULINATE
Ethyl 4-oxopentanoate
Ethyl levulate
Ethyl laevulinate
Ethyl 4-ketovalerate
Ethyl 4-oxovalerate
Ethyl 3-acetylpropionate
Levulinic acid, ethyl ester
Pentanoic acid, 4-oxo-, ethyl ester
Ethyl ketovalerate
Ethyl acetylpropanoate
4-oxopentanoic acid ethyl ester
FEMA No. 2442
Ethyl levulinate (natural)
NSC 24876
UNII-7BU24CSS2G
EINECS 208-728-2
7BU24CSS2G
BRN 0507641
DTXSID8047058
AI3-00677
NSC-24876
ETHYL LEVULINATE [MI]
ETHYL LEVULINATE [FCC]
ETHYL LEVULINATE [FHFI]
DTXCID6027058
GMEONFUTDYJSNV-UHFFFAOYSA-
4-03-00-01562 (Beilstein Handbook Reference)
Ethyl laevulate
gmeonfutdyjsnv-uhfffaoysa-n
inchi=1/c7h12o3/c1-3-10-7(9)5-4-6(2)8/h3-5h2,1-2h3
539-88-8
MFCD00009209
4-oxo-pentanoic acid ethyl ester
ethyllevulinate
4-Ketovaleric Acid Ethyl Ester
3-Acetylpropionic Acid Ethyl Ester
Ethyl4-oxopentanoate
Ethyl levulinate, 99%
Levulinic Acid Ethyl Ester
SCHEMBL92709
ethyl 4-oxidanylidenepentanoate
4-Oxovaleric Acid Ethyl Ester
CHEMBL3182933
FEMA 2442
NSC8863
CHEBI:169371
AAA53988
BCP30245
NSC-8863
NSC24876
Tox21_302292
BBL009708
STL141073
AKOS005716867
CS-W011009
DS-4184
Ethyl levulinate, >=98%, FCC, FG
Ethyl levulinate, natural, >=98%, FG
NCGC00256288-01
CAS-539-88-8
DB-052448
CS-0204023
L0120
NS00012425
EN300-59517
D77713
A829891
doi:10.14272/GMEONFUTDYJSNV-UHFFFAOYSA-N.1
Q27268032
F0001-1401
BKQ
Levulinic acid ethyl ester 4-oxopentanoate; 4-Oxopentanoic acid ethyl ester; Ethyl laevulinate;Ethyl 4-oxovalerate; Ethyl 4-ketovalerate; Ethyl 3-acetylpropionate