Skip to main content

Disperse Orange 3

ADVERTISEMENT
Identification
Molecular formula
C16H13ClN2O2
CAS number
730-40-5
IUPAC name
2-(3-chlorophenyl)azo-1-phenyl-butane-1,3-dione
State
State

At room temperature, Disperse Orange 3 is in a solid state in the form of a powder.

Melting point (Celsius)
155.00
Melting point (Kelvin)
428.15
Boiling point (Celsius)
400.00
Boiling point (Kelvin)
673.15
General information
Molecular weight
274.69g/mol
Molar mass
274.6910g/mol
Density
1.3710g/cm3
Appearence

Disperse Orange 3 appears as an orange crystalline powder. It is commonly used as a dye and has a bright, orange hue.

Comment on solubility

Solubility of 2-(3-chlorophenyl)azo-1-phenyl-butane-1,3-dione

The solubility of 2-(3-chlorophenyl)azo-1-phenyl-butane-1,3-dione can be influenced by several factors, primarily its structural integrity and the presence of functional groups. Let's explore its solubility characteristics:

  • Polar vs. Nonpolar: This compound exhibits a balance of polar and nonpolar characteristics due to its azo group and aromatic rings. As a result, its solubility can vary significantly in different solvents.
  • Solvent Interaction: In polar solvents like ethanol or methanol, the compound might have limited solubility due to its hydrophobic regions, while in nonpolar solvents such as hexane, it could dissolve more readily.
  • Temperature Effects: Generally, increasing temperature can increase solubility for many organic compounds, so experimenting with higher temperatures in suitable solvents may yield better results.
  • Hydrogen Bonding: The potential for hydrogen bonding with solvent molecules may also affect solubility, highlighting the role of intermolecular forces.

In summary, while 2-(3-chlorophenyl)azo-1-phenyl-butane-1,3-dione exhibits unique solubility behaviors, understanding the influence of solvent polarity and temperature is crucial for predicting its solubility in various environments. As always, experimental validation is recommended to determine exact solubility parameters.

Interesting facts

Interesting Facts about 2-(3-Chlorophenyl)azo-1-phenyl-butane-1,3-dione

2-(3-Chlorophenyl)azo-1-phenyl-butane-1,3-dione is a fascinating compound that belongs to the class of azo compounds, which are known for their vibrant colors and applications in various fields. Here are some noteworthy aspects of this compound:

  • Azo Linkage: The presence of the azo functional group (-N=N-) in this compound contributes to its unique chemical properties. Azo compounds are widely recognized for their ability to form colorful dyes, which are utilized in textiles and inks.
  • Utilization in Dye Chemistry: Compounds like 2-(3-chlorophenyl)azo-1-phenyl-butane-1,3-dione are often explored in dye chemistry due to their vivid hues. The manipulation of the functional groups can lead to a variety of colors, making them popular in the dye industry.
  • Biological Implications: Some azo compounds have been studied for their potential biological activity, including anti-cancer properties. The interactions of this compound within biological systems can be a topic of interest for research into medicinal applications.
  • Research Applications: This compound might be investigated in fields such as material science and environmental chemistry, where azo-based compounds are evaluated for their stability and degradation under various conditions.

Overall, 2-(3-Chlorophenyl)azo-1-phenyl-butane-1,3-dione exemplifies the complex interplay between chemical structure and functionality, showcasing its importance in both industrial and scientific realms. As one delves deeper into the world of azo compounds, the exploration of innovative applications and the underlying chemistry is both engaging and essential for advancements in various fields.

Synonyms
2-((m-Chlorophenyl)azo)-1-phenyl-1,3-butanedione
3701-23-3
F 2311
BRN 0665924
3-Chlor-phenyl-azo-benzoyl-aceton [German]
3-Chlor-phenyl-azo-benzoyl-aceton
1,3-Butanedione, 2-((3-chlorophenyl)azo)-1-phenyl-
1,3-BUTANEDIONE, 2-((m-CHLOROPHENYL)AZO)-1-PHENYL-