Skip to main content

1-Octen-3-ol

ADVERTISEMENT
Identification
Molecular formula
C8H16O
CAS number
3391-86-4
IUPAC name
oct-2-en-1-ol
State
State

At room temperature, 1-Octen-3-ol is a liquid that is slightly soluble in water but miscible with most organic solvents.

Melting point (Celsius)
-40.00
Melting point (Kelvin)
233.15
Boiling point (Celsius)
177.00
Boiling point (Kelvin)
450.15
General information
Molecular weight
128.21g/mol
Molar mass
128.2120g/mol
Density
0.8325g/cm3
Appearence

1-Octen-3-ol is a colorless to pale yellow liquid with a characteristic mushroom-like odor. It is commonly used as a flavoring agent and possesses a strong earthy and herbal scent.

Comment on solubility

Solubility of Oct-2-en-1-ol

Oct-2-en-1-ol, with the chemical formula C8H16O, is a type of alcohol characterized by its unique linear structure and the presence of a double bond. The solubility of this compound is influenced by several factors:

  • Polarity: As an alcohol, oct-2-en-1-ol possesses a polar hydroxyl group (-OH) that can interact favorably with polar solvents like water.
  • Hydrophobic Chain: The long hydrocarbon chain contributes significantly to its hydrophobic characteristics, which can reduce its overall solubility in water.
  • Solvent Compatibility: While oct-2-en-1-ol is moderately soluble in water, it tends to be more soluble in organic solvents such as ethanol, acetone, and ether.

In practical terms, this means that:

  • It can be used in various organic reactions where a soluble alcohol is necessary.
  • Its solubility may be affected by temperature; typically, increased temperatures can enhance its solubility in both water and organic solvents.

In summary, oct-2-en-1-ol exhibits moderate solubility in water, but its solubility profile becomes more favorable when interacting with non-polar organic solvents. This dual affinity makes it a versatile compound in chemical applications.

Interesting facts

Interesting Facts about Oct-2-en-1-ol

Oct-2-en-1-ol, a member of the alcohol family, is a fascinating compound that showcases the beauty of organic chemistry. Here are some remarkable insights about this compound:

  • Structure and Isomerism: Oct-2-en-1-ol features a double bond in its carbon chain, contributing to its classification as an alkene alcohol. Its structural formula reveals interesting stereochemical variations, allowing for both cis and trans isomers, each with distinct physical and chemical properties.
  • Natural Occurrence: This compound is not merely synthetic; it can be found in nature, particularly in various essential oils. It plays a role in the aroma and flavor profiles of certain fruits and plants, making it a compound of interest in agribusiness and the food industry.
  • Applications: Oct-2-en-1-ol serves several purposes in industrial applications, such as in the manufacture of surfactants, and it is utilized in the production of various polymers. Its unique chemical properties facilitate reactions that lead to useful compounds in warping and dye industries.
  • Biochemical Significance: Research has indicated that similar compounds might have implications in biological systems, such as mediating biochemical pathways or serving as precursors to important biomolecules.
  • Potential in Research: Scientists are continuously exploring the potential of oct-2-en-1-ol and its derivatives for development in pharmaceuticals and environmentally friendly green chemistry processes.

The study of oct-2-en-1-ol illustrates the interconnectedness of chemistry with both nature and industry. Its diverse applications and the complex chemistry behind its structure make it a noteworthy subject among organic compounds.

Synonyms
Oct-2-en-1-ol
2-aOcten-a1-aol
SCHEMBL294233
SCHEMBL329457
SCHEMBL8437430
SCHEMBL8437433
SCHEMBL15201511
DB-044516
DB-115692
D91843
Q209454