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Parabensox

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Identification
Molecular formula
C22H22O
CAS number
27955-94-8
IUPAC name
4-methyl-2,6-bis(1-phenylethyl)phenol
State
State

At room temperature, 4-methyl-2,6-bis(1-phenylethyl)phenol is typically found in its solid-state.

Melting point (Celsius)
147.50
Melting point (Kelvin)
420.65
Boiling point (Celsius)
442.00
Boiling point (Kelvin)
715.15
General information
Molecular weight
320.44g/mol
Molar mass
320.4440g/mol
Density
1.0200g/cm3
Appearence

4-Methyl-2,6-bis(1-phenylethyl)phenol is a white crystalline solid. It may appear as a fine powder or as glossy crystals depending on its preparation.

Comment on solubility

Solubility of 4-methyl-2,6-bis(1-phenylethyl)phenol

4-methyl-2,6-bis(1-phenylethyl)phenol exhibits interesting solubility characteristics that reflect its unique molecular structure. The solubility of this compound can be influenced by several factors:

  • Polarity: The presence of hydroxyl (-OH) groups in the phenolic structure generally enhances solubility in polar solvents, such as water. However, the hydrocarbon chains can hinder solubility in highly polar environments.
  • Solvent Interaction: This compound is more likely to dissolve in organic solvents, such as ethanol, acetone, and chloroform, where it can effectively engage in van der Waals interactions.
  • Temperature Effects: Increased temperatures can often increase solubility for many organic compounds. Due to its larger, more complex structure, solubility may significantly rise with temperature adjustments.
  • Functional Groups: The presence of multiple phenyl groups may also affect solubility, as they can lead to increased hydrophobic interactions which may limit solubility in polar solvents.

Overall, while 4-methyl-2,6-bis(1-phenylethyl)phenol shows some solubility in various solvents, understanding these interactions is crucial for predicting its behavior in different environments. As with many organic compounds, the balance of polarity and hydrophobicity plays a central role in determining solubility.

Interesting facts

Interesting Facts about 4-methyl-2,6-bis(1-phenylethyl)phenol

4-methyl-2,6-bis(1-phenylethyl)phenol is a fascinating compound that intrigues both chemists and industry professionals for its unique structure and properties. Here are some noteworthy points about it:

  • Chemical Structure: This compound features two phenyl groups attached to a central phenol ring, making it a derivative of bisphenol. The presence of alkyl groups adds to its steric bulk and affects its reactivity.
  • Applications: Due to its phenolic nature, this compound can serve as an important reagent in organic synthesis. It may also have applications in polymers or materials science, specifically where high-temperature stability is required.
  • Biological Activity: Research indicates that compounds similar to this one can exhibit interesting biological properties, including potential antioxidant activities. This opens the door for further exploration in medicinal chemistry.
  • Environmental Impact: As with many phenolic compounds, its environmental persistence and bioaccumulation potential should not be overlooked. Understanding its behavior in natural systems is crucial for assessing its ecological impact.
  • Research Potential: Ongoing investigations into the structure-activity relationship (SAR) of such compounds may yield new insights into their functionalities and could lead to the development of novel materials or pharmaceuticals.

In summary, 4-methyl-2,6-bis(1-phenylethyl)phenol stands out not just for its chemical composition, but also for its versatility and potential applications across various fields. As we continue to unlock its mysteries, we hold the key to innovative achievements in both chemistry and industry.

Synonyms
4-Methyl-2,6-bis(1-phenylethyl)phenol
1817-68-1
2,6-Bis(1-phenylethyl)-p-cresol
Ionol 6
Alkofen MBP
EINECS 217-328-7
UNII-65T4T73YKT
2,6-Bis(1-phenylethyl)-4-methylphenol
Phenol, 4-methyl-2,6-bis(1-phenylethyl)-
2,6-Bis(alpha-methylbenzyl)-p-cresol
2,6-Bis(.alpha.-methylbenzyl)-p-cresol
p-CRESOL, 2,6-BIS(alpha-METHYLBENZYL)-
SCHEMBL224197
65T4T73YKT
DTXSID0051813
QFCGHEBLSUPGPF-UHFFFAOYSA-N
2,6-bis(methylbenzyl)-4-methylphenol
NS00021777