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4-(o-tolyl)butan-1-ol

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Identification
Molecular formula
C11H16O
CAS number
7512-17-6
IUPAC name
4-(o-tolyl)butan-1-ol
State
State

At room temperature, 4-(o-tolyl)butan-1-ol is typically found in a liquid state. Its low melting point ensures that it remains a liquid in most ambient conditions.

Melting point (Celsius)
-10.00
Melting point (Kelvin)
263.15
Boiling point (Celsius)
270.00
Boiling point (Kelvin)
543.15
General information
Molecular weight
164.26g/mol
Molar mass
164.2590g/mol
Density
0.9445g/cm3
Appearence

4-(o-Tolyl)butan-1-ol is generally a clear or pale yellow liquid with a slightly oily consistency. It may emit a mild aromatic odor, characteristic of similar alcohols with an aromatic hydrocarbon group.

Comment on solubility

Solubility of 4-(o-tolyl)butan-1-ol

4-(o-tolyl)butan-1-ol, with its unique structure, exhibits several noteworthy characteristics when it comes to its solubility.

This compound is primarily characterized as:

  • Moderately soluble in polar solvents such as water due to its hydroxyl (-OH) group, which can form hydrogen bonds, thereby enhancing its interaction with polar molecules.
  • Soluble in organic solvents like ethanol and acetone, given its hydrophobic aromatic tolyl group which allows good solubility in less polar environments.
  • Poorly soluble in non-polar solvents, as the hydrophilic nature of the alcohol functional group is diminished, limiting its ability to interact with non-polar molecules.

It's essential to consider the following factors which affect solubility:

  • Temperature: Increased temperature typically enhances solubility in most solvents.
  • pH Levels: The acidity or basicity of the solution can significantly influence the ionization of the compound, impacting its solubility characteristics.
  • Concentration: The concentration of the solvent and the solute can lead to variations in solubility; higher concentrations could lead to saturation and precipitation.

In summary, the solubility behavior of 4-(o-tolyl)butan-1-ol intricately reflects its chemical structure, exhibiting versatility across various solvents, attributed largely to its hydroxyl functional group and aromatic nature.

Interesting facts

Interesting Facts about 4-(o-Tolyl)butan-1-ol

4-(o-Tolyl)butan-1-ol is an intriguing compound that captures the interest of chemists and students alike due to its unique structure and potential applications. Here are some fascinating aspects of this compound:

  • Functional Group Diversity: This compound features a primary alcohol functional group, which makes it a valuable precursor in organic synthesis, allowing for versatile derivatization.
  • Substitution Effects: The presence of the o-tolyl group introduces interesting steric and electronic effects that can influence the reactivity and properties of the compound compared to its alkyl counterparts.
  • Applications in Synthesis: 4-(o-Tolyl)butan-1-ol can be utilized in various synthetic pathways, particularly in the manufacture of pharmaceuticals and agrochemicals, where the alcohol moiety plays a critical role.
  • Chiral Characteristics: Depending on the synthesis route, this compound can also exhibit chirality, potentially leading to enantiomers with distinct biological activities, which is a significant consideration in drug design.
  • Sustainable Chemistry: The exploration of such compounds is increasingly important as scientists strive towards developing greener and more sustainable synthetic methodologies, contributing to the broader field of green chemistry.

As we delve deeper into the world of organic compounds, compounds like 4-(o-tolyl)butan-1-ol illustrate the intricate dance between structure and function in chemistry. It serves as a reminder of the boundless creativity available in the realm of organic synthesis.

Synonyms
O-methylphenylbutanol
Benzenebutanol, 2-methyl-
UNII-990FMK80X8
990FMK80X8
2-METHYL BENZENEBUTANOL
4-(2-methylphenyl)butan-1-ol
2-Methyl-benzenebutanol
196409-31-1
TOLYLBUTANOL
toluene-butanol
4-(O-tolyl)butan-1-ol
SCHEMBL285786
CHEBI:230159
AKOS013840846
CS-0449535
Q27272155