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Butylated Hydroxytoluene

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Identification
Molecular formula
C15H24O
CAS number
128-37-0
IUPAC name
2,6-ditert-butyl-4-methoxy-phenol
State
State

At room temperature, Butylated Hydroxytoluene (BHT) is a solid.

Melting point (Celsius)
70.00
Melting point (Kelvin)
343.15
Boiling point (Celsius)
265.00
Boiling point (Kelvin)
538.15
General information
Molecular weight
220.36g/mol
Molar mass
220.3550g/mol
Density
1.0480g/cm3
Appearence

Butylated Hydroxytoluene (BHT) typically appears as a white crystalline solid.

Comment on solubility

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

The solubility of 2,6-ditert-butyl-4-methoxy-phenol, often known for its antioxidant properties, is an intriguing subject in the realm of organic compounds.

This compound exhibits a unique solubility profile influenced by its bulky tert-butyl and methoxy groups. Here are some key points regarding its solubility:

  • Non-polar Solvents: 2,6-Ditert-butyl-4-methoxy-phenol is generally more soluble in non-polar organic solvents such as hexane and toluene due to its hydrophobic nature.
  • Polar Solvents: Its solubility in polar solvents like water is considerably low, primarily because the compound lacks sufficient polar functional groups to interact with water molecules.
  • Temperature Dependency: Like many organic compounds, solubility may increase with temperature. Thus, higher temperatures can enhance its solubility in organic solvents.
  • Practical Implications: The solubility characteristics often dictate the choice of solvents in industrial processes where this compound is utilized.

In summary, while solubility in water is limited, 2,6-ditert-butyl-4-methoxy-phenol shows favorable solubility in non-polar solvents, making it versatile for various applications in the chemical industry.

Interesting facts

Exploring 2,6-Ditert-butyl-4-methoxy-phenol

2,6-Ditert-butyl-4-methoxy-phenol, often abbreviated as BHT, is a compound that captivates chemists and industry professionals alike due to its extensive applications and unique properties. This phenolic compound boasts a structured arrangement conducive to wide usage in various fields.

Applications of BHT

BHT is renowned for its role as an antioxidant, particularly in the food industry. Here are some significant applications:

  • Food Preservation: BHT is widely used to prevent oxidation in fats and oils, helping to extend the shelf life of products.
  • Cosmetic Industry: Its antioxidant properties make it an important ingredient in many cosmetic formulations, helping to stabilize products and maintain their integrity.
  • Industrial Use: BHT is found in various industrial applications, including lubricants, rubber, and plastics, where it acts as a stabilizer.

Chemical Characteristics

This compound stands out due to its distinctive structural features:

  • Phenolic Structure: The presence of both tert-butyl groups and a methoxy group enhances its activity as a free radical scavenger.
  • Stability: BHT boasts remarkable thermal stability, making it a preferred choice in formulations required to withstand high temperatures.

Health and Safety Considerations

As with many chemical compounds, it’s essential to approach BHT with caution:

  • Regulatory Status: BHT is approved for use in food products, but it is important to note that it is subject to specific regulations and limits.
  • Potential Concerns: Some studies have raised questions regarding the long-term consumption of antioxidants, including BHT, prompting ongoing research in health risk assessments.

In conclusion, 2,6-Ditert-butyl-4-methoxy-phenol is a fascinating compound with a diverse range of applications due to its stability and antioxidant properties. As research continues, the role of BHT in various industries will need to be carefully evaluated to balance its benefits against any potential risks.

Synonyms
2,6-DI-TERT-BUTYL-4-METHOXYPHENOL
3,5-Di-tert-butyl-4-hydroxyanisole
Topanol 354
2,6-ditert-butyl-4-methoxyphenol
Phenol, 2,6-bis(1,1-dimethylethyl)-4-methoxy-
CCRIS 5219
EINECS 207-693-0
NSC 14451
UNII-616072TMXY
DTXSID8041379
NSC-14451
DTXCID6021379
Phenol, 4-methoxy, 2,6-bis-(1,1-dimethylethyl)
1,3-DITERT.BUTYL,2-HYDROXY,5-METHOXY-BENZENE
3,5-DTBHA
207-693-0
inchi=1/c15h24o2/c1-14(2,3)11-8-10(17-7)9-12(13(11)16)15(4,5)6/h8-9,16h,1-7h
slukqugvtitnsy-uhfffaoysa-n
489-01-0
3,5-di-t-Butyl-4-hydroxyanisole
Phenol, 2,6-di-tert-butyl-4-methoxy-
2,6-Bis(1,1-dimethylethyl)-4-methoxyphenol
MFCD00008824
CHEMBL98253
2,6-di-t-butyl-4-methoxyphenol
616072TMXY
2,6-bis(tert-butyl)-4-methoxyphenol
2,6-di-tertbutyl-4-methoxy phenol
SCHEMBL39130
CHEBI:183868
DTXSID001263562
2,6-di-t-butyl 4-methoxy phenol
4-methoxy-2-6-di-tert-butylphenol
NSC14451
2,1-dimethylethyl)-4-methoxyphenol
Phenol,6-di-tert-butyl-4-methoxy-
Tox21_301055
4-Hydroxy-3,5-di-tert-butylanisole
BDBM50240689
GEO-01266
STL483053
2,6-Di-tert-butyl-4-methoxy-phenol
AKOS005259610
FD00075
3,5-di-tert.-butyl-4-hydroxy anisole
NCGC00248270-01
NCGC00254957-01
AS-61382
BP-31248
CAS-489-01-0
PD180191
2,6-Di-tert-butyl-4-methoxyphenol, 97%
CS-0119954
D1811
NS00015210
Phenol,6-bis(1,1-dimethylethyl)-4-methoxy-
2,6-Bis(1,1-dimethylethyl)-4-methoxyphenoxy
D89928
EN300-180510
Q27263301
2,6-Di-tert-butyl-4-methoxyphenol [Oxidation inhibitor]
Z1860333896
20137-67-1