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8-(3-oct-2-enyloxiran-2-yl)octanoic acid

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Identification
Molecular formula
C18H32O3
CAS number
79055-92-2
IUPAC name
8-(3-oct-2-enyloxiran-2-yl)octanoic acid
State
State

The compound is at a liquid state at room temperature.

Melting point (Celsius)
-25.00
Melting point (Kelvin)
248.15
Boiling point (Celsius)
305.80
Boiling point (Kelvin)
578.95
General information
Molecular weight
268.41g/mol
Molar mass
268.4090g/mol
Density
0.9885g/cm3
Appearence

The compound is a colorless to light yellow liquid.

Comment on solubility

Solubility of 8-(3-oct-2-enyloxiran-2-yl)octanoic acid (C18H32O3)

The solubility of 8-(3-oct-2-enyloxiran-2-yl)octanoic acid is influenced by its molecular structure, which features a complex hydrophobic tail and a polar functional group. Understanding its solubility characteristics is essential for applications in various fields such as pharmaceuticals and materials science.

Key Points on Solubility:

  • Hydrophobic vs. Hydrophilic balance: The long hydrocarbon chain tends to confer hydrophobic properties, while the presence of the carboxylic acid group can enhance hydrophilicity.
  • Solvent Interaction: This compound is likely to show increased solubility in organic solvents such as ethanol and acetone, but lower solubility in polar solvents like water.
  • Temperature Dependence: As with many organic compounds, solubility may increase with temperature, making it beneficial for applications requiring elevated temperatures.

In summary, the solubility of 8-(3-oct-2-enyloxiran-2-yl)octanoic acid is a product of its unique structural attributes, leading to a complex interplay between hydrophobic and hydrophilic forces. Its practical solubility can be highly dependent on the solvent used and the conditions of the environment.

Interesting facts

Interesting Facts about 8-(3-oct-2-enyloxiran-2-yl)octanoic Acid

8-(3-oct-2-enyloxiran-2-yl)octanoic acid is a fascinating compound with several intriguing characteristics that make it an interesting subject for study in the fields of organic chemistry and biochemistry.

Chemical Structure and Properties

This compound features a complex structure characterized by:

  • Oxirane ring: The presence of an epoxide (oxirane) group, which introduces significant reactivity into the compound, making it valuable for further chemical transformations.
  • Long hydrocarbon chain: With an 18-carbon backbone, this molecule has implications in studies related to fatty acids and lipid metabolism.

Applications and Uses

8-(3-oct-2-enyloxiran-2-yl)octanoic acid has potential applications in various fields:

  • Pharmaceuticals: Due to its unique structure, it could be a precursor or an intermediary in synthesizing bioactive compounds.
  • Cosmetics: Compounds involving long hydrocarbon chains are often explored for their emulsifying or moisturizing properties.
  • Biotechnology: The reactivity of the epoxide group makes it a target for modification in biochemical applications.

Fun Fact

The name "8-(3-oct-2-enyloxiran-2-yl)octanoic acid" reflects its intricate structure and emphasizes the importance of nomenclature in chemistry, which can often provide insights into the functional groups present within a compound. As the renowned chemist Linus Pauling once said, "Chemistry is the study of the properties and behavior of matter." This compound certainly embodies that essence, exhibiting both intriguing properties and diverse potential.

Synonyms
Coronarsaeure
(+)-CORONARIC ACID
8-(3-oct-2-enyloxiran-2-yl)octanoic acid
113972-57-9
65167-83-1
cis-9,10-Epoxy-12(Z)-octadecenoic acid
CBiol_001808
KBioGR_000060
KBioSS_000060
KBio2_000060
KBio2_002628
KBio2_005196
KBio3_000119
KBio3_000120
(+/-)9,10-Eode
Bio1_000094
Bio1_000583
Bio1_001072
Bio2_000060
Bio2_000540
QCA16783
(Z)-8-(3-(oct-2-enyl)oxiran-2-yl)octanoic acid