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6-(3-Decyloxiran-2-yl)hexanoic acid

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Identification
Molecular formula
C16H30O3
CAS number
94288-06-7
IUPAC name
6-(3-decyloxiran-2-yl)hexanoic acid
State
State

This compound is generally in a liquid state at room temperature, characterized by its viscosity and potential to form emulsions or mixtures with other organic solvents.

Melting point (Celsius)
-10.00
Melting point (Kelvin)
263.15
Boiling point (Celsius)
180.00
Boiling point (Kelvin)
453.15
General information
Molecular weight
270.41g/mol
Molar mass
270.4090g/mol
Density
1.0200g/cm3
Appearence

This compound is typically a viscous liquid that may range from colorless to pale yellow, depending on its purity and the presence of impurities or oxidation products.

Comment on solubility

Solubility of 6-(3-decyloxiran-2-yl)hexanoic acid

When it comes to the solubility of 6-(3-decyloxiran-2-yl)hexanoic acid, several key factors come into play, primarily due to its molecular structure and functional groups. This compound is likely to exhibit interesting solubility characteristics:

  • Hydrophobic Characteristics: The presence of the long decyl chain (from the decyloxirane group) suggests that the compound may have a significant hydrophobic character.
  • Hydrophilic Group: The carboxylic acid group (-COOH) is polar and can interact favorably with water, potentially aiding in solubility in polar solvents.
  • Solvent Interaction: It is likely to be soluble in organic solvents such as ethanol, methanol, and acetone, while having limited solubility in water due to the competing hydrophobic effects of the alkyl chains.
  • Temperature Influence: As with many organic acids, an increase in temperature may enhance solubility, facilitating better interaction between solute and solvent molecules.

Overall, the solubility profile of 6-(3-decyloxiran-2-yl)hexanoic acid can be summarized as follows:

  1. High solubility in non-polar and moderately polar organic solvents.
  2. Moderate to low solubility in water, dependent on pH and temperature conditions.

Understanding these solubility aspects is crucial for applications in synthesis, formulation, and various industrial processes involving this compound.

Interesting facts

Interesting Facts about 6-(3-decyloxiran-2-yl)hexanoic Acid

6-(3-decyloxiran-2-yl)hexanoic acid is a fascinating compound that holds significance in various fields of chemistry, especially in organic synthesis and material science. Here are some engaging facts about this unique substance:

  • Epoxide Chemistry: The presence of the epoxide functional group (the oxirane ring) in its structure endows this compound with intriguing reactivity. Epoxides are known for their ability to undergo ring-opening reactions, which makes them valuable intermediates in the synthesis of various pharmaceuticals and agrochemicals.
  • Role in Polymer Science: This compound can serve as a precursor for creating novel polymeric materials. Thanks to its unique structure, it can be incorporated into copolymers that exhibit tailored properties, including increased strength and flexibility.
  • Biological Significance: The hexanoic acid chain contributes to the compound's biological activities. In various studies, fatty acids have been shown to influence cellular functions, making this compound worthy of further exploration for potential health benefits.
  • Applications: Compounds with such structures have potential applications in various industries, including:
    • Chemical synthesis
    • Surface coatings
    • Adhesive technologies
    • Agricultural formulations
  • Synthetic Challenges: The synthesis of 6-(3-decyloxiran-2-yl)hexanoic acid presents interesting challenges due to the precise control required in forming the epoxide group and the desired functional groups. The chemistry employed often requires advanced techniques such as catalysis and protected group strategies.

The study of 6-(3-decyloxiran-2-yl)hexanoic acid not only highlights its unique chemical properties but also exemplifies the diverse applications that can arise from the intricate interplay of organic chemistry and industrial needs. Its multifaceted nature invites ongoing research, making it a compound of interest in both academic and industrial laboratories.

Synonyms
trans-7,8-epoxystearic acid