Skip to main content

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

ADVERTISEMENT
Identification
Molecular formula
C16H26O
CAS number
4130-42-1
IUPAC name
2,6-ditert-butyl-4-ethyl-phenol
State
State

At room temperature, 2,6-Di-tert-butyl-4-ethylphenol is a solid. It remains stable under normal conditions and is used for its antioxidant properties.

Melting point (Celsius)
45.00
Melting point (Kelvin)
318.15
Boiling point (Celsius)
258.00
Boiling point (Kelvin)
531.15
General information
Molecular weight
234.38g/mol
Molar mass
234.3720g/mol
Density
0.9497g/cm3
Appearence

2,6-Di-tert-butyl-4-ethylphenol appears as a white to off-white crystalline solid. It is known for its stability and resistance to oxidation, which makes it widely used as an antioxidant.

Comment on solubility

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

2,6-Ditert-butyl-4-ethyl-phenol, also known by its common name, is a phenolic compound that exhibits interesting solubility characteristics. Understanding its solubility behavior is vital for applications in various fields, including pharmaceuticals and material science.

Key Points about Solubility:

  • Solvent Compatibility: This compound is generally soluble in organic solvents such as ethanol, acetone, and chloroform, but it shows limited solubility in water due to its bulky tert-butyl groups.
  • Hydrophobic Nature: The hydrophobic nature of the bulky groups makes it less favorable for interactions with polar solvents like water, leading to its low aqueous solubility.
  • Influence of Temperature: Solubility can often increase with temperature, so exploring solubility at elevated temperatures may yield different results.

In summary, 2,6-ditert-butyl-4-ethyl-phenol predominantly dissolves in non-polar or weakly polar solvents while presenting notable limitations in polar conditions. Such properties are essential for its effective usage in various chemical applications.

Interesting facts

Interesting Facts About 2,6-Ditert-butyl-4-ethyl-phenol

2,6-Ditert-butyl-4-ethyl-phenol, often abbreviated as DBE, is a noteworthy compound widely used in various industries. Here are some fascinating insights about this compound:

  • Antioxidant Properties: This compound is primarily recognized for its effectiveness as an antioxidant, which helps prevent oxidative degradation of materials. It's commonly integrated into plastics, rubber, and lubricants to enhance their longevity.
  • Chemical Structure: The presence of bulky tert-butyl groups in the structure contributes to its stability and resistance to heat, making it favorable for high-temperature applications.
  • Versatile Applications: Aside from being utilized in material preservation, DBE is also employed in the formulation of cosmetics and personal care products, serving to protect formulations from oxidative damage.
  • Environmental Considerations: While the use of this compound is widespread, it is crucial for industries to consider its environmental impact. Researchers are continually studying alternatives that offer similar protective qualities with reduced ecological footprints.
  • Regulatory Status: Due to its extensive use, DBE is subject to regulatory scrutiny in various jurisdictions, requiring manufacturers to maintain compliance with safety and environmental standards.

In summary, 2,6-ditert-butyl-4-ethyl-phenol is a compound with significant importance in material science, offering stability and protection in various formulations. As a chemistry student or a scientist, understanding its properties and applications not only enhances your knowledge but also equips you to contribute to advancements in sustainable chemical practices.

Synonyms
2,6-Di-tert-butyl-4-ethylphenol
4130-42-1
Ionol 2
4-Ethyl-2,6-di-tert-butylphenol
Yoshinox 250
Phenol, 2,6-bis(1,1-dimethylethyl)-4-ethyl-
Sandant 425
Phenol, 2,6-di-tert-butyl-4-ethyl-
Nocrac M 17
2,6-Bis(1,1-dimethylethyl)-4-ethylphenol
1-Hydroxy-4-ethyl-2,6-di-tert-butylbenzene
NSC 14453
2,6-di-t-Butyl-4-ethylphenol
EINECS 223-945-2
SV7OZ6J97M
Nocrac M17
CCRIS 8263
DTXSID0029262
NSC-14453
NOCLIZER M 17
DTXCID909262
2,6-di-tert-butyl-4-ethyl-phenol
2,6-Bis(1,1-dimethylethyl)-4-ethyl-Phenol
1-Hydroxy-4-ethyl-2, 6-di-tert-butylbenzene
Phenol, 2,6-bis-(1.1-dimethylethyl)-4-ethyl
2,6-Bis(1,1-dimethylethyl)-4-ethylphenol, 9CI
Phenol, 2,6-di-tert-butyl-4-ethyl-(8CI)
223-945-2
2,6-ditert-butyl-4-ethylphenol
2,?6-?Di-?tert-?butyl-?4-?ethylphenol
CAS-4130-42-1
4-ethyl-2,6-ditert-butyl-phenol
UNII-SV7OZ6J97M
MFCD00017366
SCHEMBL39434
2,6-ditert.butyl4-ethylphenol
CHEMBL225620
SCHEMBL10865531
2,6-di-tertbutyl-4-ethylphenol
BVUXDWXKPROUDO-UHFFFAOYSA-
CHEBI:177477
2,1-dimethylethyl)-4-ethylphenol
Phenol,6-di-tert-butyl-4-ethyl-
2,6-di-tert-butyl-4-ethyl phenol
NSC14453
Tox21_201584
Tox21_303397
AKOS015837918
FD70708
NCGC00249077-01
NCGC00257348-01
NCGC00259133-01
2,6-Di-tert-butyl-4-ethylphenol, 99%
AS-14442
Phenol,6-bis(1,1-dimethylethyl)-4-ethyl-
CS-0152544
D1667
NS00020303
Phenol, 2,6-di-tert-butyl-4-ethyl- (8CI)
E76076
Q26841169
2,6-Bis(1,1-dimethylethyl)-4-ethylphenol;1-Hydroxy-4-ethyl-2,6-di-tert-butylbenzene
InChI=1/C16H26O/c1-8-11-9-12(15(2,3)4)14(17)13(10-11)16(5,6)7/h9-10,17H,8H2,1-7H3