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2-(3,4-dimethylphenyl)ethanol

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Identification
Molecular formula
C10H14O
CAS number
2440-21-3
IUPAC name
2-(3,4-dimethylphenyl)ethanol
State
State

At room temperature, 2-(3,4-dimethylphenyl)ethanol is a liquid. It is typically found in this state under normal atmospheric conditions.

Melting point (Celsius)
18.00
Melting point (Kelvin)
291.15
Boiling point (Celsius)
244.00
Boiling point (Kelvin)
517.15
General information
Molecular weight
150.22g/mol
Molar mass
150.2170g/mol
Density
0.9781g/cm3
Appearence

2-(3,4-dimethylphenyl)ethanol typically appears as a colorless liquid. It is an aromatic alcohol and may have a mild fragrant odor characteristic of phenyl ethanols.

Comment on solubility

Solubility of 2-(3,4-dimethylphenyl)ethanol

2-(3,4-dimethylphenyl)ethanol, a compound with intriguing properties, exhibits notable solubility characteristics that can affect its applications in various fields.

The solubility of this organic compound can be influenced by several factors:

  • Polarity: Due to the presence of a hydroxyl group (–OH), it is generally more soluble in polar solvents like water.
  • Hydrophobic Interactions: The dimethylphenyl group contributes hydrophobic properties, which can limit solubility in polar environments.
  • Temperature Dependence: As with many organic compounds, solubility may increase with temperature, allowing for greater dissolution in organic solvents.

In assessing its solubility, one might quote that "like dissolves like," which means the polar –OH group allows it to engage effectively in hydrogen bonding with water, yet the bulky aromatic ring can create challenges.

Overall, the solubility of 2-(3,4-dimethylphenyl)ethanol is a balance of its polar and non-polar characteristics, leading to varying degrees of solubility in different solvents:

  1. High solubility in polar solvents (e.g., water, alcohols)
  2. Moderate solubility in non-polar solvents (e.g., hexane, benzene)

Understanding these solubility dynamics is crucial for optimizing its usage in chemical applications and formulations.

Interesting facts

Interesting Facts about 2-(3,4-Dimethylphenyl)ethanol

2-(3,4-Dimethylphenyl)ethanol is a fascinating compound that has intrigued chemists due to its unique structure and properties. This compound features a benzene ring substituted with two methyl groups and a hydroxyl group, making it a versatile part of various chemical and biochemical processes.

Key Characteristics:

  • Structural Versatility: The presence of methyl groups on the phenyl ring not only influences the compound's physical properties but also its reactivity, allowing it to participate in numerous substitution reactions.
  • Biological Relevance: Compounds similar to 2-(3,4-dimethylphenyl)ethanol are often studied for their potential effects in medicinal chemistry, offering insights into novel drug designs.
  • Taste and Aroma: Alcohols typically have distinct sensory properties, and 2-(3,4-dimethylphenyl)ethanol could contribute to specific flavor profiles or scents in food and fragrance industries.

Applications in Research:

This compound serves as a valuable intermediate in organic synthesis, often utilized for creating more complex molecular architectures. Its ability to act as a building block in reactions such as:

  • Catalytic hydrogenation
  • Grignard reactions
  • Aldol condensations

makes it a staple in the toolbox of chemists engaged in synthetic organic chemistry. Additionally, studying the dynamics of such compounds aids in understanding their hydrophobic interactions, a critical element in pharmaceutical formulations.

In Conclusion:

With its rich potential for industrial and academic applications, 2-(3,4-dimethylphenyl)ethanol showcases the synergy between chemistry and practical innovation. As a compound that bridges organic and medicinal chemistry, it continues to be a subject of interest for ongoing and future research.

Synonyms
2-(3,4-dimethylphenyl)ethanol
87776-80-5
2-(3,4-dimethylphenyl)ethan-1-ol
3,4-dimethylphenethyl alcohol
Benzeneethanol,3,4-dimethyl-
MFCD09926178
SCHEMBL6301819
SCHEMBL9025862
DTXSID30275087
WJOJFYXMOJHANU-UHFFFAOYSA-N
AKOS011827996
SB84879
CS-0281604
EN300-103103