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Identification
Molecular formula
C15H16N2O2
CAS number
31482-56-1
IUPAC name
(4-methoxy-2-methyl-phenyl)-(4-methoxyphenyl)diazene
State
State

The compound is typically found in a solid state at room temperature due to its high melting point.

Melting point (Celsius)
100.00
Melting point (Kelvin)
373.15
Boiling point (Celsius)
355.50
Boiling point (Kelvin)
628.65
General information
Molecular weight
270.31g/mol
Molar mass
270.3130g/mol
Density
0.7930g/cm3
Appearence

The compound appears as an orange to red powdery solid, making it identifiable by its distinct coloration often used in dyes.

Comment on solubility

Solubility of (4-methoxy-2-methyl-phenyl)-(4-methoxyphenyl)diazene

The solubility of (4-methoxy-2-methyl-phenyl)-(4-methoxyphenyl)diazene is a subject of interest when considering its practical applications in various chemical processes. Here are some important points regarding its solubility:

  • Solvent Interaction: This compound features polar functional groups, such as methoxy (-OCH3), which can enhance its interaction with polar solvents like ethanol and methanol.
  • Limited Solubility: Due to its relatively large aromatic structure, (4-methoxy-2-methyl-phenyl)-(4-methoxyphenyl)diazene may exhibit limited solubility in non-polar solvents such as hexane or toluene.
  • Temperature Dependence: The solubility is often temperature-dependent, where an increase in temperature may lead to enhanced solubility in specific solvents.
  • pH Influence: The solubility can also be affected by the pH of the solution, particularly if the compound undergoes protonation or deprotonation in certain pH ranges.

In summary, while (4-methoxy-2-methyl-phenyl)-(4-methoxyphenyl)diazene demonstrates increased solubility in polar solvents due to its functional groups, its overall solubility profile is shaped by factors like temperature, solvent choice, and solution pH. As always, it is essential to conduct empirical studies to better understand the solubility characteristics of this compound in various conditions.

Interesting facts

Interesting Facts about (4-methoxy-2-methyl-phenyl)-(4-methoxyphenyl)diazene

(4-methoxy-2-methyl-phenyl)-(4-methoxyphenyl)diazene, also known in some circles as a substituted azo compound, has intrigued chemists due to its unique structural attributes and potential applications. Here are some engaging highlights:

  • Diverse Applications: This compound is notable for its applications in the fields of dye chemistry and organic synthesis. Azo compounds are widely used in the production of vibrant dyes and pigments, showcasing their prominence in textile manufacturing.
  • Unique Binding Properties: The diazene group in this compound can participate in various chemical reactions, making it a valuable compound in the development of new materials and intermediates in organic chemistry.
  • Stability Factors: Understanding the stability of such compounds under different conditions is crucial. Azo linkages can be sensitive to light and heat, leading to potential applications in photochemical reactions.
  • Biological Significance: Some studies have suggested that substituted azo compounds may exhibit biological activity, which leads researchers to explore their potential roles in pharmaceuticals or as indicators of biological processes.
  • Synthetic Versatility: The synthesis of such compounds often involves multistep reactions, giving chemists the opportunity to tailor properties by varying substituents, such as the methoxy groups present in this compound.

In summary, (4-methoxy-2-methyl-phenyl)-(4-methoxyphenyl)diazene exemplifies the intricate interplay between structure and function in organic chemistry. By harnessing its unique characteristics, chemists can push the boundaries of material science and organic chemistry, opening pathways for innovative research and applications.

Synonyms
4,4'-DIMETHOXY-2-METHYLAZOBENZENE
29418-53-9
Diazene, (4-methoxy-2-methylphenyl)(4-methoxyphenyl)-
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(E)-1-(4-Methoxy-2-methylphenyl)-2-(4-methoxyphenyl)diazene #