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Disperse Orange 1

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Identification
Molecular formula
C17H19N3O2
CAS number
2581-69-3
IUPAC name
N,N,2-trimethyl-4-(4-nitrophenyl)azo-aniline
State
State

At room temperature, Disperse Orange 1 is in a solid state, typically as fine powder or crystalline granules. It is not volatile and does not dissolve easily in water, which is typical for many synthetic dyes. This compound is designed to be used as a disperse dye in nonpolar media or for dyeing hydrophobic fibers such as polyester.

Melting point (Celsius)
159.00
Melting point (Kelvin)
432.15
Boiling point (Celsius)
505.00
Boiling point (Kelvin)
778.15
General information
Molecular weight
268.35g/mol
Molar mass
268.3100g/mol
Density
1.2875g/cm3
Appearence

Disperse Orange 1 is a synthetic azo dye. It typically appears as an orange to brown powder. The color can vary slightly based on the specific formulation and the matrix in which it is used. As a dye, it is often used in textile applications for coloring synthetic fibers.

Comment on solubility

Solubility of N,N,2-trimethyl-4-(4-nitrophenyl)azo-aniline

N,N,2-trimethyl-4-(4-nitrophenyl)azo-aniline, a complex azo compound, exhibits distinctive solubility characteristics influenced by its molecular structure. Its solubility can be analyzed based on several factors:

  • Polarity: The presence of the nitrophenyl group enhances the compound's polarity, potentially increasing its solubility in polar solvents.
  • Hydrophobic and Hydrophilic Regions: The trimethyl groups introduce hydrophobic regions that can limit solubility in water, while the diazo group may increase interaction with polar solvents.
  • pH Dependency: The solubility of azo compounds is often pH-sensitive; variations in pH can lead to protonation or deprotonation, affecting overall solubility.

In general:

  • This compound is more soluble in organic solvents such as ethanol and acetone.
  • It is expected to have **limited solubility in water**, primarily due to its hydrophobic diazo and trimethyl groups.

As a result, understanding the solubility profile of N,N,2-trimethyl-4-(4-nitrophenyl)azo-aniline is essential for applications in dye chemistry and materials science. The interplay between hydrophobic and hydrophilic interactions is crucial in determining the compound's behavior in various solvent systems.

Interesting facts

Interesting Facts about N,N,2-Trimethyl-4-(4-nitrophenyl)azo-aniline

N,N,2-trimethyl-4-(4-nitrophenyl)azo-aniline is a fascinating compound belonging to the azo dye family, known for its vibrant coloring properties and applications in various fields. Here are some intriguing aspects of this compound:

  • Azo Dyes: This compound contains an azo group (-N=N-), which is characteristic of azo dyes. Azo compounds are notable for their ability to produce bright and intense colors, making them widely used in textiles, food, and biological staining.
  • Applications: Aside from its use in coloring textiles and plastics, this compound can also serve in biomedical applications such as dye-ligand affinity chromatography, assisting in the separation and purification of proteins.
  • Environmental Considerations: The presence of the nitro group in this compound raises focus on its environmental impact. Many nitro-substituted azo dyes are scrutinized for their potential toxicity, leading to important discussions about sustainable practices in dye manufacturing.
  • Structure and Stability: The unique structure of N,N,2-trimethyl-4-(4-nitrophenyl)azo-aniline not only contributes to its vivid color but also affects its stability and reactivity. The configuration makes it resistant to degradation, which can be beneficial for long-lasting applications.
  • Historical Significance: Azo dyes were first synthesized in the mid-19th century, and since then, compounds like this have played a significant role in the development of the synthetic dye industry. They have been instrumental in the shift from natural to synthetic dyes, revolutionizing color use in various industries.

In conclusion, N,N,2-trimethyl-4-(4-nitrophenyl)azo-aniline stands out not only for its vibrant hues but also for its complex interactions with environmental and health concerns. Understanding this compound and others like it is crucial for advancing both chemistry and the sustainability of the dye industry.

Synonyms
4313-13-7
N,N,2-trimethyl-4-[(4-nitrophenyl)diazenyl]aniline
9GXU5C455B
3-Methyl-4'-nitro-4-N,N-dimethylaminoazobenzene
NSC-45530
o-Toluidine, N,N-dimethyl-4-((p-nitrophenyl)azo)-
N,N,2-Trimethyl-4-((4-nitrophenyl)diazenyl)aniline
NSC45530
NSC 45530
UNII-9GXU5C455B
SCHEMBL4955285
DTXSID10871905
92114-99-3
Benzenamine, N,N,2-trimethyl-4-[(4-nitrophenyl)azo]-