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2,6-Di-tert-butyl-4-phenylphenol

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Identification
Molecular formula
C22H30O
CAS number
6807-17-6
IUPAC name
2,6-ditert-butyl-4-phenyl-phenol
State
State

The compound is in a solid state at room temperature (around 20°C or 68°F). Due to its bulky tert-butyl groups, it is relatively solid compared to other phenolic derivatives and resistant to decomposition under normal conditions.

Melting point (Celsius)
158.00
Melting point (Kelvin)
431.15
Boiling point (Celsius)
373.00
Boiling point (Kelvin)
646.15
General information
Molecular weight
282.42g/mol
Molar mass
282.4220g/mol
Density
1.0200g/cm3
Appearence

2,6-Di-tert-butyl-4-phenylphenol typically appears as an off-white crystalline solid. It is solid at room temperature and exhibits a slight aromatic smell typical of phenolic compounds. The compound is relatively stable and insoluble in water but may dissolve in organic solvents such as ethanol or methanol.

Comment on solubility

Solubility of 2,6-Ditert-butyl-4-phenyl-phenol

The solubility of 2,6-ditert-butyl-4-phenyl-phenol, a complex organic compound, can be quite intriguing. This compound exhibits unique characteristics that influence its solubility behavior:

  • Non-polar Nature: With its bulky tert-butyl groups, the compound is largely non-polar, leading to its low solubility in polar solvents like water.
  • Solvent Preference: It tends to dissolve better in non-polar organic solvents such as hexane, chloroform, or ethyl acetate.
  • Temperature Impact: As with many organic compounds, solubility can increase with temperature, allowing for better dissolution in suitable solvents.
  • Hydrogen Bonding: The presence of the hydroxyl (-OH) group allows for some degree of hydrogen bonding, which can marginally enhance solubility in polar solvents compared to purely hydrophobic compounds.

Overall, the solubility attributes of 2,6-ditert-butyl-4-phenyl-phenol highlight the intricate balance between its structural features and its interactions with various solvents. As one expert noted, "The solubility of organic compounds often reveals the underlying molecular interactions at play." The understanding of these interactions can guide effective applications and usage in various chemical processes.

Interesting facts

Exploring 2,6-Di-tert-butyl-4-phenyl-phenol

2,6-Di-tert-butyl-4-phenyl-phenol is a fascinating compound that showcases the interplay of organic chemistry and industrial applications. This compound is primarily recognized for its role as an effective antioxidant in various materials. Here are some interesting aspects:

  • Industrial Importance: It is commonly used in the formulation of plastics, lubricants, and rubber products to prevent oxidative degradation. This property highlights its critical role in enhancing the longevity and durability of materials.
  • Mechanism of Action: Acting as a free radical scavenger, this compound helps to neutralize harmful radicals before they can cause significant damage to molecular structures. This mechanism is vital in protecting sensitive materials from deterioration.
  • Structure and Stability: The unique structural elements, including the bulky tert-butyl groups, provide steric hindrance that contributes to its stability and effectiveness as a stabilizer in various formulations.
  • Research Opportunities: The compound is a subject of interest for scientists focused on improving antioxidant systems and exploring potential applications in food preservation and biomedical fields.
  • Environmental Considerations: As with many chemical compounds, understanding its environmental impact is crucial. Research into its biodegradability and toxicity is ongoing to ensure safe usage in industrial applications.

In conclusion, 2,6-di-tert-butyl-4-phenyl-phenol is not just an ordinary chemical compound. Its significance extends into various fields, making it a subject worth studying for its numerous applications and the ecological implications it entails. As a student of chemistry or a professional scientist, you might find this compound's balance of stability, functionality, and industrial relevance very intriguing.

Synonyms
2668-47-5
2,6-Di-tert-butyl-4-phenylphenol
[1,1'-Biphenyl]-4-ol, 3,5-bis(1,1-dimethylethyl)-
2,6-DI-TERT-BUTYL-P-PHENYLPHENOL
4-Biphenylol, 3,5-di-tert-butyl-
EINECS 220-207-1
93V393Y48W
(1,1'-Biphenyl)-4-ol, 3,5-bis(1,1-dimethylethyl)-
DTXSID7062582
3,5-DI-TERT-BUTYL-4-BIPHENYLOL
4-PHENYL-2,6-DI-TERT-BUTYLPHENOL
3,5-DI-TERT-BUTYL-4-HYDROXYBIPHENYL
PHENOL, 2,6-DI-TERT-BUTYL-4-PHENYL-
DTXCID8037544
220-207-1
3,5-DI-TERT-BUTYL-[1,1'-BIPHENYL]-4-OL
2,6-Bis(1,1-dimethylethyl)-4-phenylphenol
UNII-93V393Y48W
2,6-ditert-butyl-4-phenylphenol
SCHEMBL426214
CHEMBL1795388
4-phenyl-2,6-di-t-butylphenol
3,5-di-tert-butylbiphenyl-4-ol
STK670834
AKOS005592272
NCGC00340724-01
2,6-DI(TERT-BUTYL)-4-PHENYLPHENOL
DB-278521
3,5-Ditert-butyl[1,1'-biphenyl]-4-ol #
NS00014254
G66857
AB01333120-02
SR-01000511056
SR-01000511056-1
Q27271613
[1,1-BIPHENYL]-4-OL, 3,5-BIS(1,1-DIMETHYLETHYL)-