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Leaf Alcohol

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Identification
Molecular formula
C8H16O
CAS number
3391-86-4
IUPAC name
oct-3-en-1-ol
State
State
Liquid at room temperature (20°C to 25°C). It is generally volatile and has a noticeable scent.
Melting point (Celsius)
-76.00
Melting point (Kelvin)
197.15
Boiling point (Celsius)
194.00
Boiling point (Kelvin)
467.15
General information
Molecular weight
128.21g/mol
Molar mass
128.2120g/mol
Density
0.8476g/cm3
Appearence

Oct-3-en-1-ol, or Leaf Alcohol, appears as a clear, colorless liquid. It has a characteristic, fresh, green, and floral odor often associated with the smell of fresh cut grass or leaves and contributes to the aroma of many plants.

Comment on solubility

Solubility of Oct-3-en-1-ol

Oct-3-en-1-ol, with the chemical formula C8H16O, exhibits distinct solubility characteristics that are noteworthy. As a member of the alcohol family, oct-3-en-1-ol contains a hydroxyl group (-OH), which significantly influences its solubility in various solvents.

Generally, the solubility properties of oct-3-en-1-ol can be summarized as follows:

  • Soluble in Water: Oct-3-en-1-ol is sparingly soluble in water. Its ability to engage in hydrogen bonding due to the presence of the hydroxyl group allows it to dissolve to some extent, especially in lower concentrations.
  • Highly Soluble in Organic Solvents: The compound is more soluble in organic solvents such as ethanol, diethyl ether, and chloroform. This is primarily because of its hydrophobic hydrocarbon chain, which interacts favorably with non-polar solvent molecules.
  • Influence of Temperature: The solubility of oct-3-en-1-ol can also increase with rising temperatures. As the kinetic energy of molecules increases, the interactions that facilitate solubility can become more prevalent.

In summary, the solubility of oct-3-en-1-ol demonstrates the classic behavior of alcohols, being sparingly soluble in polar solvents like water and more soluble in non-polar organic solvents, owing to its unique molecular structure.

Interesting facts

Exploring the Chemistry of Oct-3-en-1-ol

Oct-3-en-1-ol is a fascinating organic compound that belongs to the family of alkenols, which are characterized by the presence of both a double bond and a hydroxyl (-OH) functional group. This unique structure gives it intriguing properties and applications.

Key Characteristics

  • Source: Oct-3-en-1-ol can be found naturally in several essential oils and is often associated with a variety of scents.
  • Reactivity: Its double bond makes it susceptible to various types of reactions, such as hydrogenation and oxidation, thereby participating in significant organic transformations.
  • Versatility: This compound can serve as an important intermediate in the synthesis of more complex molecules, showcasing its utility in organic chemistry.

Applications & Uses

Oct-3-en-1-ol is notable for its diverse applications:

  • Fragrance Industry: Its pleasant aroma allows it to be utilized in perfumes and flavorings, adding unique notes to various products.
  • Pharmaceuticals: Several studies have explored its potential for use in medicinal chemistry, where it can act as a building block for drug development.
  • Agricultural Chemistry: Some research has demonstrated its potential in formulations for plant protection, acting as a bioactive agent.

Quote from a Chemist

As one chemist aptly put it, "Oct-3-en-1-ol stands at the crossroads of organic synthesis and natural product chemistry, merging functionality with elegance."

In summary, Oct-3-en-1-ol is more than just an organic compound; its diverse applications and reactivity make it a noteworthy subject of study in modern chemistry.

Synonyms
3-OCTEN-1-OL
oct-3-en-1-ol
18185-81-4
SCHEMBL473592
SCHEMBL5166350
SCHEMBL8433079
DTXSID4066333
SCHEMBL15201509
SCHEMBL29101308
SB83900
DB-045101
NS00025983