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Disperse Yellow 3

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Identification
Molecular formula
C15H15Cl2N3O3
CAS number
2832-40-8
IUPAC name
2-[4-(2,6-dichloro-4-nitro-phenyl)azo-N-methyl-anilino]ethanol
State
State

The state of Disperse Yellow 3 at room temperature is solid.

Melting point (Celsius)
183.00
Melting point (Kelvin)
456.15
Boiling point (Celsius)
370.00
Boiling point (Kelvin)
643.15
General information
Molecular weight
316.20g/mol
Molar mass
316.1530g/mol
Density
1.4058g/cm3
Appearence

Disperse Yellow 3 appears as a reddish-brown powder.

Comment on solubility

Solubility of 2-[4-(2,6-Dichloro-4-nitro-phenyl)azo-N-methyl-anilino]ethanol

The solubility of the compound 2-[4-(2,6-dichloro-4-nitro-phenyl)azo-N-methyl-anilino]ethanol can be quite intriguing due to its complex structure. This compound is likely to exhibit the following characteristics when it comes to solubility:

  • Polar Solvents: Given the presence of hydroxyl (-OH) groups, this compound may have reasonable solubility in polar solvents such as water and alcohol. The hydroxyl group can form hydrogen bonds, which enhances solubility.
  • Non-Polar Solvents: Conversely, in non-polar solvents, the solubility may be limited due to the presence of large hydrophobic aromatic groups that dominate the molecular structure.
  • Temperature Impact: As with many compounds, temperature may significantly influence solubility; an increase in temperature often leads to enhanced solubility in many solvent systems.
  • pH Dependence: The solubility may also be affected by the pH of the solution, as ionizable functional groups can change their charge state, influencing interactions with the solvent.

In conclusion, the solubility of 2-[4-(2,6-dichloro-4-nitro-phenyl)azo-N-methyl-anilino]ethanol is characterized by its ability to dissolve in polar environments due to the presence of hydroxyl groups, while also presenting challenges in non-polar environments. Understanding these characteristics can be essential for practical applications and further studies.

Interesting facts

Exploring 2-[4-(2,6-Dichloro-4-nitro-phenyl)azo-N-methyl-anilino]ethanol

This fascinating compound, commonly referred to as a specific type of azo dye, stands out for its vibrant color and substantial application in various fields. Here are some compelling points to consider:

  • Azo Compounds: Azo compounds are known for their characteristic -N=N- (azo) group. This allows them to impart vivid colors, making them popular in the textile industry and other dye applications.
  • Biological Activity: The presence of the dichloro and nitro substituents on the phenyl ring contributes to the compound's unique chemical properties, which can affect its biological activity, including potential antimicrobial effects.
  • Safety Considerations: Compounds like this can pose health risks if not handled correctly. Many azo dyes are scrutinized for their potential to form carcinogenic amines upon degradation, underscoring the importance of safety protocols in chemical handling.
  • Environmental Impact: The production and disposal of dyes can have significant environmental impacts. Ongoing research focuses on developing eco-friendly alternatives and methods to degrade azo dyes, highlighting the balance between industrial use and environmental responsibility.

The synthesis of this compound typically involves complex chemical reactions that can include nucleophilic substitution and azo coupling reactions, showcasing the intricacy of organic chemistry. As scientists continue to explore the structural diversity and reactivity of azo compounds, the potential for new applications in fields such as materials science, pharmaceuticals, and environmental remediation becomes increasingly apparent.

In summary, the study of 2-[4-(2,6-dichloro-4-nitro-phenyl)azo-N-methyl-anilino]ethanol offers a glimpse into the colorful world of azo compounds, revealing their significance in both scientific research and industrial applications.

Synonyms
Ethanol, 2-((4-((2,6-dichloro-4-nitrophenyl)azo)phenyl)methylamino)-
Ethanol, 2-[[4-[(2,6-dichloro-4-nitrophenyl)azo]phenyl]methylamino]-
Ethanol, 2-((4-(2-(2,6-dichloro-4-nitrophenyl)diazenyl)phenyl)methylamino)-
Ethanol, 2-[[4-[2-(2,6-dichloro-4-nitrophenyl)diazenyl]phenyl]methylamino]-
Disperse Orange 5
6232-56-0
C.I. Disperse Orange 5
2-((4-((2,6-Dichloro-4-nitrophenyl)azo)phenyl)methylamino)ethanol
2-[4-[(2,6-dichloro-4-nitrophenyl)diazenyl]-N-methylanilino]ethanol
Artisil Brown H
Celliton Fast Brown 3R
Lenra Orange BL
Tersetile 3RL
Amacel Orange BL
Samaron Brown GR
Amacron Orange LS
Eastone Brown 2R
Nacelan Brown 2R
Palanil Brown 3R
Samaron Brown 3R
Disperse Red Brown
Disperse Brown 3R
Vonteryl Brown 6R
Cibacet Brown 4RN
Tersetile Brown 3R
Microsetile Brown 3R
Kayalon Fast Brown R
Cilla Fast Brown 3R
Amacel Fast Brown 3R
Fenacet Fast Brown 3R
Miketon Fast Brown 3R
Supracet Fast Brown 3R
Serisol Fast Brown 3RD
Diacelliton Fast Brown 3R
Celliton Discharge Brown 3RL
Celliton Fast Brown 3RA-CF
Dispersol Fast Orange Brown R
Dispersol Fast Orange Brown RN
C.I. 11100
C.I.Disperse Orange 5
EINECS 228-340-7
BRN 0763924
4-(Methyl(beta-hydroxyethyl)amino)-2',6'-dichloro-4'-nitroazobenzene
4-16-00-00458 (Beilstein Handbook Reference)
SCHEMBL11587913
DTXSID90863722
MPIGKGDPQRWZLU-UHFFFAOYSA-N
DTXSID001015434
AKOS024434703
NS00043890
2-((4-((E)-(2,6-Dichloro-4-nitrophenyl)diazenyl)phenyl)(methyl)amino)ethanol
1071691-59-2