Skip to main content

Benzoin

ADVERTISEMENT
Identification
Molecular formula
C14H14O
CAS number
119-53-9
IUPAC name
3-(1-methyl-1-phenyl-ethyl)phenol
State
State

At room temperature, benzoin exists as a solid.

Melting point (Celsius)
134.50
Melting point (Kelvin)
407.65
Boiling point (Celsius)
344.00
Boiling point (Kelvin)
617.15
General information
Molecular weight
212.26g/mol
Molar mass
212.2580g/mol
Density
1.0678g/cm3
Appearence

Benzoin is a colourless crystalline compound that may appear as white crystals or powder. It is often used as a precursor for perfumes and dyes and has a distinct, pleasant aromatic odor.

Comment on solubility

Solubility of 3-(1-methyl-1-phenyl-ethyl)phenol

The solubility of 3-(1-methyl-1-phenyl-ethyl)phenol is an intriguing aspect of its chemical behavior, influenced by both its molecular structure and various environmental factors. This compound exhibits the following notable solubility characteristics:

  • Solvent Dependence: 3-(1-methyl-1-phenyl-ethyl)phenol is primarily soluble in organic solvents such as ethanol, acetone, and chloroform, but shows limited solubility in polar solvents like water.
  • Hydrophobic Interactions: Due to its hydrophobic aromatic structure, the compound demonstrates a lower affinity for aqueous solutions, often leading to a precipitation in polar solvents.
  • Temperature Effects: An increase in temperature can enhance solubility in organic solvents, making it essential to conduct solubility assessments at defined temperatures.

In summary, the solubility of 3-(1-methyl-1-phenyl-ethyl)phenol is characterized by its compatibility with non-polar and moderately polar solvents, with limited interactions in water. This behavior is crucial for understanding its applications in various chemical processes and formulations.

Interesting facts

Interesting Facts about 3-(1-methyl-1-phenyl-ethyl)phenol

3-(1-methyl-1-phenyl-ethyl)phenol, often referred to in scientific literature, is a fascinating organic compound with a range of interesting properties and applications. Here are some noteworthy facts:

  • Structural Diversity: This compound is an example of a substituted phenol, which means that it has a phenolic ring with an additional alkyl side chain. The presence of the bulky 1-methyl-1-phenyl-ethyl group significantly influences its chemical behavior.
  • Biological Activity: Compounds like 3-(1-methyl-1-phenyl-ethyl)phenol are often studied for their potential biological applications. Some derivatives have been found to exhibit antioxidant properties, which could be beneficial in various pharmaceutical contexts.
  • Applications in Industry: Due to the functionality provided by the phenolic group, this compound (and its derivatives) may find applications in the production of polymers, resins, and coatings. Phenols are known for their ability to form strong bonds, enhancing durability.
  • Research Significance: This compound is of interest in organic synthesis and medicinal chemistry. Researchers utilize it to explore modifications that could enhance functionality or reduce toxicity in drug formulations.
  • Environmental Impact: Understanding the environmental behavior of compounds like 3-(1-methyl-1-phenyl-ethyl)phenol is vital as it allows scientists to evaluate their persistence, bioaccumulation potential, and effects on ecosystems.

In conclusion, 3-(1-methyl-1-phenyl-ethyl)phenol is not just a simple chemical entity; it embodies a wealth of possibilities in both scientific research and industrial applications. Its unique structure and properties make it a compound of considerable interest within the field of chemistry.

Synonyms
m-cumylphenol
3-Cumylphenol
3-(2-phenylpropan-2-yl)phenol
UNII-0DDA9N8D2J
27576-86-9
0DDA9N8D2J
Phenol, 3-(1-methyl-1-phenylethyl)-
Phenol, (1-methyl-1-phenylethyl)-
87852-47-9
UNII-E76192MWPA
SCHEMBL50818
E76192MWPA
SCHEMBL9577058
SCHEMBL27427898
SCHEMBL29459449
DTXSID30883141
PARGHORKDQHVPM-UHFFFAOYSA-N
3-(1-Methyl-1-phenylethyl)phenol
EINECS 248-539-2
NS00051224
Q27236643