Skip to main content

p-Tolyl (2,4,6-trimethylphenyl)diazene

ADVERTISEMENT
Identification
Molecular formula
C16H18N2
CAS number
1611-10-3
IUPAC name
p-tolyl-(2,4,6-trimethylphenyl)diazene
State
State

Solid at room temperature.

Melting point (Celsius)
37.00
Melting point (Kelvin)
310.15
Boiling point (Celsius)
344.00
Boiling point (Kelvin)
617.15
General information
Molecular weight
238.35g/mol
Molar mass
238.3460g/mol
Density
1.0020g/cm3
Appearence

Red or orange crystalline solid.

Comment on solubility

Solubility of p-tolyl-(2,4,6-trimethylphenyl)diazene

When considering the solubility of p-tolyl-(2,4,6-trimethylphenyl)diazene, it is essential to note several key factors that influence its behavior in various solvents:

  • Polarity: Since this compound possesses a significant nonpolar character due to its aromatic structures, it is likely to have limited solubility in polar solvents such as water.
  • Solvent Selection: It may dissolve more readily in nonpolar solvents, including hydrocarbons like hexane or toluene. As with many organic compounds, "like dissolves like" is a guiding principle.
  • Temperature Effect: Temperature variations can also impact solubility; typically, higher temperatures can enhance solubility in most organic solvents.

In summary, while p-tolyl-(2,4,6-trimethylphenyl)diazene may show solubility in specific organic solvents, its solubility in water is expected to be minimal. It is essential to carefully consider the solvent environment when working with this diazene to achieve desired outcomes.

Interesting facts

Interesting Facts About p-tolyl-(2,4,6-trimethylphenyl)diazene

p-tolyl-(2,4,6-trimethylphenyl)diazene, often classified as an azo compound, is a fascinating substance with various applications and intriguing properties. Here are some noteworthy aspects of this compound:

  • Structure and Composition: This compound features the azo functional group, characterized by a nitrogen-nitrogen double bond. The arrangement of methyl groups enhances its stability and reactivity.
  • Dyes and Pigments: Azo compounds, like p-tolyl-(2,4,6-trimethylphenyl)diazene, have significant roles in the dye industry. They can be used to create a wide range of vibrant colors due to their ability to absorb specific wavelengths of light.
  • Biological Activity: Some azo compounds exhibit interesting biological properties, including antimicrobial and antioxidant activities. Research in this area is ongoing, exploring potential therapeutic applications.
  • Synthetic Versatility: p-tolyl-(2,4,6-trimethylphenyl)diazene showcases the versatility of synthetic methods in organic chemistry, allowing chemists to create various derivatives by modifying its structure.
  • Reaction Mechanisms: Understanding the reaction mechanisms involving azo compounds can be crucial for fields such as material science and pharmaceuticals, as they can lead to new materials with desirable properties.

As you delve into the world of p-tolyl-(2,4,6-trimethylphenyl)diazene, remember that compounds like these play a significant role not only in academic chemistry but also in practical applications that affect our daily lives. The potential for discovery in this area is vast, with exciting challenges ahead for future chemists.

Synonyms
2,4,4',6-TETRAMETHYLAZOBENZENE
29418-29-9