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Ethyl sorbate

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Identification
Molecular formula
C8H12O2
CAS number
2396-84-1
IUPAC name
ethyl hexa-2,4-dienoate
State
State

Ethyl sorbate is typically a liquid at room temperature.

Melting point (Celsius)
-60.00
Melting point (Kelvin)
213.15
Boiling point (Celsius)
206.00
Boiling point (Kelvin)
479.15
General information
Molecular weight
140.19g/mol
Molar mass
140.1860g/mol
Density
0.9076g/cm3
Appearence

Ethyl sorbate is generally a colorless to pale yellow liquid. It has a characteristic fruity odor and is clear in appearance.

Comment on solubility

Solubility of Ethyl Hexa-2,4-dienoate

Ethyl hexa-2,4-dienoate, a compound with the chemical formula C8H12O2, demonstrates interesting solubility characteristics that are worth noting:

  • Solvent Compatibility: Ethyl hexa-2,4-dienoate is mainly soluble in organic solvents due to its non-polar characteristics. Common solvents include:
    • Alcohols (e.g., ethanol)
    • Acetone
    • Ether
  • Limited Water Solubility: This compound exhibits poor solubility in water, as is typical for many organic compounds with similar structures. The presence of hydrophobic alkyl groups hinders interaction with polar water molecules.
  • Temperature Influence: The solubility can be affected by temperature; generally, higher temperatures can lead to an increased solubility in organic solvents.

To summarize, it's essential to keep in mind that the solubility of ethyl hexa-2,4-dienoate is significantly influenced by the solvent environment, showcasing its preference for organic solutions over aqueous ones. Understanding these solubility properties can help in applications involving this compound in synthesis and formulation processes.

Interesting facts

Interesting Facts About Ethyl hexa-2,4-dienoate

Ethyl hexa-2,4-dienoate is a fascinating compound that plays a significant role in organic chemistry and related applications. It belongs to a broader class of compounds known as esters, which are crucial in both synthetic and natural processes.

Key Characteristics:

  • Structure and Function: Ethyl hexa-2,4-dienoate contains a unique conjugated system that contributes to its reactivity and properties. The double bonds offer sites for various chemical reactions, making it an interesting subject for synthetic chemists.
  • Applications: This compound is utilized in the production of plastics, resins, and coatings due to its ability to polymerize effectively. Its derivatives are also found in flavoring agents and fragrances, highlighting its versatility.
  • Reactivity: The presence of double bonds in ethyl hexa-2,4-dienoate allows for various addition reactions, which chemists often exploit to create more complex molecules. For instance, it can undergo Diels-Alder reactions, making it valuable in synthetic organic chemistry.

Cultural and Practical Significance:

Ethyl hexa-2,4-dienoate's significance extends beyond the lab. In the world of cosmetics and personal care, its derivatives can be found in products aimed at enhancing sensory experience through fragrance. Additionally, it serves as an important precursor in the synthesis of bioactive compounds, drawing interest in the pharmaceutical field.

Quote from a Chemist:

"The beauty of compounds like ethyl hexa-2,4-dienoate lies in their complexity and potential. They are the building blocks of innovation in chemical synthesis." - A Leading Organic Chemist

In summary, ethyl hexa-2,4-dienoate exemplifies the intersection of chemistry and practical applications, making it a compound of interest for students and professionals alike. Its unique characteristics and reactivity not only offer opportunities for research but also contribute to industries that impact our everyday lives.

Synonyms
DTXSID20862920
DTXCID60811619
nocas_862920
ETHYL HEXADIENOATE
Hexa-2,4-dienoic acid ethyl ester
MFCD00009296
5941-48-0
BCP21819
AKOS017265621
SY048320
DB-046306
NS00018671
Ethyl 2,4-hexadienoate pound>>Ethyl hexa-2,4-dienoate