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Mesityl alcohol

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Identification
Molecular formula
C10H14O
CAS number
2835-89-8
IUPAC name
(2,4,6-trimethylphenyl)methanol
State
State

At room temperature, mesityl alcohol is typically a liquid. It retains its liquid state under normal atmospheric conditions, characterized by its clear color and aromatic odor.

Melting point (Celsius)
24.00
Melting point (Kelvin)
297.15
Boiling point (Celsius)
223.00
Boiling point (Kelvin)
496.15
General information
Molecular weight
150.22g/mol
Molar mass
150.2170g/mol
Density
0.9460g/cm3
Appearence

Mesityl alcohol is a colorless to light yellow liquid with a pleasant aromatic odor. It can be found in the form of a slightly viscous solution and it may have a yellow appearance if impurities are present.

Comment on solubility

Solubility of (2,4,6-trimethylphenyl)methanol

(2,4,6-trimethylphenyl)methanol, known for its unique structural attributes, exhibits interesting solubility characteristics that are important in various applications. As a member of the alcohol family, this compound displays some distinct behaviors when interacting with solvents.

Key Points on Solubility:

  • In Water: (2,4,6-trimethylphenyl)methanol is likely to have low solubility in water. This can be attributed to its bulky hydrophobic aromatic group that hinders favorable interactions with water molecules.
  • In Organic Solvents: Conversely, it demonstrates good solubility in organic solvents such as ethanol, acetone, and chloroform. This solubility is primarily due to its non-polar characteristics, which enhance compatibility with non-polar solvents.
  • Temperature Dependency: The solubility of (2,4,6-trimethylphenyl)methanol may vary with temperature, often increasing at higher temperatures due to heightened molecular motion that overcomes intermolecular forces.

Given these factors, it is critical to consider the context of use for (2,4,6-trimethylphenyl)methanol, as its solubility influences its reactivity and role in chemical processes. Understanding its solubility profile can help in designing experiments and applications where this compound is relevant.

Interesting facts

Interesting Facts about (2,4,6-Trimethylphenyl)methanol

(2,4,6-Trimethylphenyl)methanol, often referred to in the scientific community as a substituted phenolic compound, showcases fascinating applications and properties that intrigue chemists and industry professionals alike. This compound is particularly notable for its structural features and potential uses.

Unique Structural Attributes

One of the most interesting aspects of (2,4,6-trimethylphenyl)methanol is its *bulky aromatic structure*. The presence of three methyl groups attached to the benzene ring contributes to steric hindrance, influencing its reactivity and interactions. Key points include:

  • Substitution Patterns: The specific locations of the methyl groups (at the 2-, 4-, and 6-positions) can significantly affect the compound's stability and reactivity.
  • Hydroxyl Group: The alcohol functional group (-OH) provides opportunities for various chemical reactions, including esterification and oxidation.

Applications and Uses

This compound is not merely of theoretical interest; it has practical applications that highlight its significance:

  • Synthesis: It serves as an important intermediate in organic synthesis, allowing the production of more complex molecules.
  • Flavor and Fragrance Industry: Due to its aromatic nature, it is often utilized in creating specific scent profiles in perfumes and flavorings.

Research and Fun Facts

Within research settings, (2,4,6-trimethylphenyl)methanol has been an interesting subject for studies in organic chemistry:

  • Reactivity Studies: Its ability to undergo various chemical transformations makes it a valuable model for studying reaction mechanisms.
  • Comparative Analysis: Its properties can be compared with other phenolic compounds, allowing scientists to discern the effects of different substituents on chemical behavior.

In conclusion, (2,4,6-trimethylphenyl)methanol is a compound that embodies the interplay between structure and function in chemistry, sparking curiosity and inspiring innovative research. As one delves deeper into its chemistry, the myriad possibilities associated with its application and study become increasingly evident.

Synonyms
2,4,6-TRIMETHYLBENZYL ALCOHOL
4170-90-5
Mesitylmethanol
(2,4,6-trimethylphenyl)methanol
Mesitylcarbinol
Benzenemethanol, 2,4,6-trimethyl-
MFCD00014422
REV3KVT84N
(2,4,6-Trimethyl-phenyl)-methanol
BRN 1862608
2,4,6-Trimethylbenzylic alcohol
Benzyl alcohol, 2,4,6-trimethyl-
EINECS 224-032-1
UNII-REV3KVT84N
2,4,6-Trimethylbenzenemethanol
2,4,6-Trimethyl-benzenemethanol
SCHEMBL95192
4-06-00-03362 (Beilstein Handbook Reference)
TRIMETHYLBENZENEMETHANOL
DTXSID70194506
AKOS000249582
benzyl, 2,4,6-trimethyl- alcohol-
2,4,6-Trimethylbenzyl alcohol, 99%
FT34610
DS-11387
SY049612
DB-050796
CS-0153274
NS00031039
T1905
EN300-55811
Q27288082
Z335244802
InChI=1/C10H14O/c1-7-4-8(2)10(6-11)9(3)5-7/h4-5,11H,6H2,1-3H