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Hex-3-enyl acetate

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Identification
Molecular formula
C8H14O2
CAS number
638-72-2
IUPAC name
hex-3-enyl acetate
State
State
Hex-3-enyl acetate is a liquid at room temperature.
Melting point (Celsius)
-90.00
Melting point (Kelvin)
183.00
Boiling point (Celsius)
184.00
Boiling point (Kelvin)
457.00
General information
Molecular weight
142.20g/mol
Molar mass
142.1960g/mol
Density
0.8770g/cm3
Appearence

Hex-3-enyl acetate is a colorless liquid with a pleasant, fruity aroma reminiscent of apples or bananas. Its scent is often described as fresh and green, making it a popular choice in perfumery and flavoring industries.

Comment on solubility

Solubility of Hex-3-enyl Acetate

Hex-3-enyl acetate, with its chemical formula C7H12O2, exhibits interesting solubility characteristics that can be summarized as follows:

  • Solvent Compatibility: This compound is known to be soluble in organic solvents such as ethanol, ether, and acetone.
  • Water Solubility: Hex-3-enyl acetate has limited solubility in water, making it more compatible with non-polar or slightly polar environments.
  • Effect of Temperature: As with many organic compounds, solubility can increase with temperature, facilitating its use in various applications.

In general, the solubility of hex-3-enyl acetate in different solvents is a crucial factor in its applications in fragrance, flavor, and chemical synthesis. As quoted by chemists, "Understanding solubility helps unlock the potential of many compounds," and hex-3-enyl acetate is no exception to this principle.

Interesting facts

Hex-3-enyl Acetate: An Aromatic Exploration

Hex-3-enyl acetate is an intriguing compound that falls within the category of esters. Known for its pleasant fruity aroma, it plays a significant role in both the culinary and fragrance industries. Here are some fascinating aspects of this compound:

  • Aromatic Qualities: Hex-3-enyl acetate is often associated with notes reminiscent of juicy fruits, making it a coveted ingredient in flavoring and perfumery.
  • Synthesis and Production: This compound can be synthesized through esterification, a process where a carboxylic acid reacts with an alcohol. Its production showcases the principles of organic chemistry, making it a popular subject in educational settings.
  • Versatile Applications: Beyond its use in scents and flavors, hex-3-enyl acetate can serve in the formulation of solvents and plasticizers, demonstrating its versatility across various industries.
  • Natural Occurrence: Interestingly, this compound can be found in some fruits and flowers, highlighting its importance in nature and its potential use in natural product synthesis.
  • Research and Study: Scientists are continually exploring the properties and applications of hex-3-enyl acetate, as it may offer insights into new materials and fragrances that enhance our sensory experiences.

In summary, hex-3-enyl acetate not only rounds out our understanding of organic compounds but also enriches our experiences through its delightful aroma. It serves as a reminder of the intersection between chemistry and the world around us.

Synonyms
Hex-3-enyl acetate
1708-82-3
DTXSID6047234
DTXCID4027234
216-965-8
3-hexen-1-yl acetate
3-hexen-1-ol acetate
NPFVOOAXDOBMCE-UHFFFAOYSA-N
AKOS025243684
NS00077432