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2,3-Diethylphenol

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Identification
Molecular formula
C10H14O
CAS number
29247-30-5
IUPAC name
2,3-diethylphenol;2,5-diethylphenol;3,5-diethylphenol
State
State

At room temperature, 2,3-diethylphenol is usually found as a liquid, given its melting point is slightly above room temperature. However, its state may vary around this point, sometimes appearing solid but easily liquefies upon slight warming.

Melting point (Celsius)
20.00
Melting point (Kelvin)
293.15
Boiling point (Celsius)
232.00
Boiling point (Kelvin)
505.15
General information
Molecular weight
150.22g/mol
Molar mass
150.2210g/mol
Density
0.9615g/cm3
Appearence

2,3-Diethylphenol is typically a colorless to yellow solid or liquid, depending on the temperature. It may appear as crystals when solid, and has an aromatic odor characteristic of phenolic compounds. The appearance can vary slightly based on the diethyl position isomerization, but generally they maintain similar physical properties across the isomers.

Comment on solubility

Solubility of 2,3-Diethylphenol, 2,5-Diethylphenol, and 3,5-Diethylphenol

The compounds 2,3-diethylphenol, 2,5-diethylphenol, and 3,5-diethylphenol present interesting challenges regarding their solubility due to their molecular structures.

General Trends in Solubility:

These compounds are organic compounds featuring ethyl groups attached to a phenolic structure. Their solubility properties can be summarized as follows:

  • Polar vs Nonpolar: The introduction of ethyl groups increases the nonpolar character of the molecule, which can lead to decreased solubility in water.
  • Hydrogen Bonding: The phenol functional group can engage in hydrogen bonding, enhancing solubility in polar solvents like alcohols and ethers.
  • Solvent Interaction: Solubility in nonpolar solvents is generally higher due to the affinity of the ethyl groups for similar nonpolar environments.

Specific Solubility Insights:

For these specific diethylphenols:

  • 2,3-Diethylphenol: It shows relatively low solubility in water but is more soluble in alcohols.
  • 2,5-Diethylphenol: Similar to 2,3-diethylphenol, it demonstrates limited water solubility and favorable solubility in organic solvents.
  • 3,5-Diethylphenol: This compound may exhibit similar solubility characteristics, with a preference for nonpolar solvents.

In summary, while these diethylphenols will show low solubility in water due to their increased nonpolar character, their hydrogen bonding capabilities allow for enhanced solubility in more polar organic solvents. This dual behavior is what makes them particularly interesting for applications in organic chemistry and related fields.

Interesting facts

Exploring Diethylphenols: Insights into 2,3-Diethylphenol, 2,5-Diethylphenol, and 3,5-Diethylphenol

Diethylphenols are intriguing compounds that belong to the family of phenolic compounds, characterized by their unique *chemical structure* and various applications in different fields. Below are some interesting facts about 2,3-diethylphenol, 2,5-diethylphenol, and 3,5-diethylphenol:

Key Characteristics

  • Structural Variants: Each diethylphenol compound features ethyl groups substituted at different positions on the phenolic ring, which significantly influences their *chemical properties* and *reactivity*.
  • Versatile Applications: These compounds are used as intermediates in the production of various chemicals, including synthetic dyes and agrochemicals.
  • Analytical Importance: Their presence can be a focus in analytical chemistry, particularly in environmental monitoring where they may appear as pollutants.

Health and Safety Considerations

As with many chemical compounds, it is essential to handle diethylphenols with care:

  • Toxicity: These compounds may pose health risks if ingested or inhaled in significant amounts, necessitating appropriate safety measures during usage.
  • Environmental Impact: Understanding their fate and transport in the environment is crucial for assessing ecological risks associated with industrial discharge.

Conclusion

In summary, diethylphenols are more than just chemical entities; they represent significant topics of study in *organic chemistry* and *industrial applications*. Their diverse structural forms not only impact their functionality but also their behavior in various environments, making them a fascinating subject for future research and exploration.

Synonyms
UNII-O7TO8QV9YC
26967-65-7
O7TO8QV9YC