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Epichlorohydrin fatty acid ester

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Identification
Molecular formula
C16H21ClO4
CAS number
18829-55-5
IUPAC name
2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate
State
State

At room temperature, this compound is in a liquid state. Its oily nature can be attributed to its fatty acid ester linkage, contributing to its viscosity and colorless to pale yellow appearance.

Melting point (Celsius)
-20.00
Melting point (Kelvin)
253.15
Boiling point (Celsius)
262.00
Boiling point (Kelvin)
535.15
General information
Molecular weight
338.80g/mol
Molar mass
338.8120g/mol
Density
1.0805g/cm3
Appearence

The compound appears as a clear colorless oily liquid. Due to the presence of oxirane and carboxylate groups, it can demonstrate slight yellow hues depending on the purity and exposure to environmental conditions.

Comment on solubility

Solubility of 2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate

The solubility of 2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate (C16H21ClO4) exhibits some intriguing characteristics, primarily influenced by its chemical structure.

Factors Influencing Solubility

  • Polarity: This compound contains both hydrophobic (the long carbon chain) and hydrophilic (the carboxylate group) regions. As a result, its solubility may vary significantly between polar and non-polar solvents.
  • Solvent Interaction: It is more likely to dissolve in organic solvents such as acetone or ethanol rather than in water, owing to its overall hydrophobic character.
  • Temperature: Generally, the solubility of organic compounds tends to increase with temperature; thus, heating the solvent might enhance the solubility of this compound.

To summarize, while the solubility characteristics of 2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate are largely dependent on the solvent used, this compound shows a penchant for dissolving in non-polar organic solvents, making it versatile for various applications. As a guideline: limit exposure to highly polar mediums.

Interesting facts

Interesting Facts About 2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate

2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate is a fascinating compound that embodies several intriguing aspects of organic chemistry. Here are some key points to consider:

  • Structure and Functionality: This compound features an oxirane ring, a type of epoxide that is known for its reactivity. The presence of the oxirane ring contributes to its potential applications in various chemical reactions, particularly in the formation of larger and more complex molecules.
  • Chlorophenoxy Group: The 4-chlorophenoxy substituent is noteworthy as chlorinated aromatic systems are often essential in pharmaceuticals and agrochemicals. This functional group can influence the compound's biological activity and physical properties.
  • Biological Relevance: Compounds like 2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate may exhibit interesting pharmacological properties. Researchers often explore such compounds for their potential use in drug development or as agrochemical agents.
  • Applications in Synthesis: The unique structure allows for utilization in organic synthesis, especially in the preparation of new materials. Its versatility can facilitate reactions such as nucleophilic substitutions and ring-opening polymerizations.
  • Environmental Considerations: Compounds with chlorinated components raise environmental and safety questions. Understanding their stability and reactivity is crucial as it can affect their persistence in ecosystems.

In summary, 2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate not only showcases the elegance of organic chemistry with its intricate structure but also highlights the cross-section between chemistry and environmental science. It's a compound that invites further exploration and could unlock new avenues in both industrial and medicinal chemistry.