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2,4,5-Trimethylphenol

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Identification
Molecular formula
C9H12O
CAS number
697-82-5
IUPAC name
2,4,5-trimethylphenol
State
State

At room temperature, 2,4,5-Trimethylphenol is a solid. It is generally found in crystal form and has a substantive phenolic fragrance.

Melting point (Celsius)
76.00
Melting point (Kelvin)
349.20
Boiling point (Celsius)
239.50
Boiling point (Kelvin)
512.60
General information
Molecular weight
136.19g/mol
Molar mass
136.1930g/mol
Density
0.9848g/cm3
Appearence

2,4,5-Trimethylphenol is a colorless to pale yellow crystalline solid. It may appear as white crystals, depending on the purity. It has a strong phenolic odor, which is characteristic of phenol derivatives.

Comment on solubility

Solubility of 2,4,5-trimethylphenol

2,4,5-trimethylphenol, known for its unique structure and properties, exhibits interesting solubility characteristics that can influence its application in various contexts. Here’s a breakdown of its solubility behavior:

  • Solvent Compatibility: 2,4,5-trimethylphenol is generally soluble in organic solvents such as ethanol, acetone, and chloroform, making it suitable for use in organic synthesis and formulations.
  • Water Solubility: This compound is practically insoluble in water, which can limit its usage in aqueous environments. Its hydrophobic character generally affects how it interacts with biological systems.
  • Temperature Effects: Increased temperatures tend to improve the solubility of this compound in organic solvents, allowing for more flexible application in various chemical processes.
  • pH Influence: The solubility may also be affected by the pH of the solution, as phenolic compounds can form ions in basic conditions, potentially increasing their solubility in alkaline environments.

Overall, the solubility of 2,4,5-trimethylphenol is crucial for its handling and manipulation in chemical applications. Understanding its solubility properties allows researchers and practitioners to optimize conditions for effective use.

Interesting facts

Interesting Facts about 2,4,5-Trimethylphenol

2,4,5-trimethylphenol, also known as reaction product of m-cresol and p-cresol, is a fascinating compound with a variety of applications and characteristics that intrigue scientists and chemistry students alike. Here are some noteworthy facts about this compound:

  • Structural Features: This compound features three methyl groups attached to a phenolic ring, making it a derivative of phenol. Its unique structure contributes to its phase behavior and chemical reactivity.
  • Applications: 2,4,5-trimethylphenol is used as an intermediate in the synthesis of antioxidants and antimicrobial agents. It's essential in the production of substances that prevent oxidation in various materials.
  • Chemical Reactivity: The presence of multiple methyl groups enhances the electron-donating ability of the phenol ring, making it more reactive than simple phenolic compounds. This characteristic can lead to various substitution reactions.
  • Environmental Consideration: Like many organic compounds, 2,4,5-trimethylphenol can be persistent in the environment, raising concerns about pollution and bioaccumulation. Understanding its behavior in the environment is crucial for chemists focused on sustainability.
  • Historical Context: Phenol derivatives have been studied for over a century, and their roles in various industrial applications continue to be explored, making them a significant topic in organic chemistry.

As a compound that bridges both environmental and industrial chemistry, 2,4,5-trimethylphenol serves as an excellent case study for understanding chemical interactions, reactivity, and the importance of responsible chemical management. The exploration of its properties can lead to greater innovations in how we utilize and protect our chemical resources.

Synonyms
2,4,5-TRIMETHYLPHENOL
496-78-6
Pseudocumenol
Phenol, 2,4,5-trimethyl-
5-Hydroxypseudocumene
1-Hydroxy-2,4,5-trimethylbenzene
EINECS 207-832-5
NSC 38776
BRN 2040904
3PCA9E425C
NSC-38776
DTXSID2060094
4-06-00-03247 (Beilstein Handbook Reference)
DTXCID5040706
207-832-5
UNII-3PCA9E425C
MFCD00020050
SCHEMBL395019
NSC38776
AKOS000275084
AS-76094
CS-0358957
NS00031939
F87364
2,4,5-Trimethylphenol 100 microg/mL in Acetonitrile
Q27257859