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Disperse Orange 3

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Identification
Molecular formula
C13H12N2O
CAS number
730-40-5
IUPAC name
(2-methoxy-6-methyl-phenyl)-phenyl-diazene
State
State

At room temperature, Disperse Orange 3 is generally in a solid state, as a crystalline powder.

Melting point (Celsius)
130.00
Melting point (Kelvin)
403.00
Boiling point (Celsius)
373.00
Boiling point (Kelvin)
646.00
General information
Molecular weight
240.28g/mol
Molar mass
240.2820g/mol
Density
1.1600g/cm3
Appearence

Disperse Orange 3 appears as an orange-brown crystalline powder. It is commonly used as a dye, and its powder form may vary from light orange to brown in color based on its processing and impurities present.

Comment on solubility

Solubility of (2-methoxy-6-methyl-phenyl)-phenyl-diazene

The solubility of (2-methoxy-6-methyl-phenyl)-phenyl-diazene in various solvents is pivotal for understanding its chemical behavior and potential applications. Here are some key points to consider:

  • Polar Solvents: This compound exhibits limited solubility in polar solvents such as water and alcohols due to its largely non-polar character.
  • Non-Polar Solvents: It shows better solubility in non-polar organic solvents like hexane or toluene, where the interactions between solvent and solute are more favorable.
  • Temperature Effects: As with many organic compounds, solubility may increase with temperature; thus, heating the solvent can enhance the dissolution process.
  • Influence of Functional Groups: The presence of the methoxy group can contribute to some solubility in moderately polar solvents, but the overall effect is modest.

In summary, understanding the solubility traits of (2-methoxy-6-methyl-phenyl)-phenyl-diazene is essential for its practical applications in organic synthesis and material science. "Choosing the right solvent is key!" as solubility determines the ease of use in various chemical processes.

Interesting facts

Interesting Facts About (2-Methoxy-6-methyl-phenyl)-phenyl-diazene

(2-Methoxy-6-methyl-phenyl)-phenyl-diazene, commonly referred to in the scientific community by its IUPAC name, is an intriguing organic compound that falls under the category of azo compounds. Here are some fascinating insights about this compound:

1. Chemical Structure and Properties

  • Azo Compound: This compound contains a distinctive azo group (-N=N-), which is a characteristic feature of azo compounds. The presence of this group contributes to its unique chemical and physical properties.
  • Substitution Patterns: The presence of the methoxy and methyl groups in the aromatic ring influences the reactivity and stability of the compound, making it an interesting subject of study in both synthetic and theoretical chemistry.

2. Applications in the Scientific Community

  • Dyes and Pigments: Azo compounds are widely known for their applications as dyes and pigments in textiles and other materials. Research on this compound could lead to innovations in color chemistry.
  • Biological Activity: Some azo compounds have exhibited biological activities, which opens avenues for research into their potential as pharmaceutical agents. Understanding the biological behavior of (2-methoxy-6-methyl-phenyl)-phenyl-diazene could lead to significant findings.

3. Synthesis and Research

The synthesis of this compound often involves diazotization reactions, a fundamental transformation in organic chemistry. This process allows for the formation of various diazene derivatives, showcasing the versatility of azobenzenes. As chemists continue to explore the reactivity of such compounds, they may discover new uses in photochemistry and material science.

4. Environmental Considerations

With the increasing awareness of environmental impacts, the study of azo compounds includes a focus on their degradation pathways and potential toxicity. Understanding how compounds like (2-methoxy-6-methyl-phenyl)-phenyl-diazene can be managed is critical for sustainable chemistry.

In summary, (2-methoxy-6-methyl-phenyl)-phenyl-diazene represents more than just a chemical formula; it is a gateway into a broader realm of research possibilities that marry chemistry with innovation and environmental responsibility.

Synonyms
2-METHOXY-6-METHYLAZOBENZENE
29268-77-7