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Dichlorophenyltrichloroethylbenzene

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Identification
Molecular formula
C14H11Cl3N2
CAS number
5465-92-7
IUPAC name
4-[1-(4-aminophenyl)-2,2,2-trichloro-ethyl]aniline
State
State

Solid at room temperature, usually appearing as a fine powder or crystalline material.

Melting point (Celsius)
215.00
Melting point (Kelvin)
488.15
Boiling point (Celsius)
413.00
Boiling point (Kelvin)
686.15
General information
Molecular weight
315.60g/mol
Molar mass
315.0990g/mol
Density
1.4600g/cm3
Appearence

This compound typically appears as an off-white powder or crystalline solid. It may be fine granulated with a slight odor dependent on purity and other factors.

Comment on solubility

Solubility of 4-[1-(4-aminophenyl)-2,2,2-trichloro-ethyl]aniline

The solubility characteristics of 4-[1-(4-aminophenyl)-2,2,2-trichloro-ethyl]aniline can be intriguing due to its structural complexity. This compound contains both hydrophilic (amine) and hydrophobic (trichloroethyl) functional groups, which can influence its solubility in various solvents. Here are some key points to consider:

  • Aqueous Solubility: Generally, compounds with amine groups tend to demonstrate better solubility in water; however, the presence of three chlorine atoms may hinder this solubility due to increased hydrophobic interactions.
  • Organic Solubility: This compound may exhibit higher solubility in organic solvents such as ethanol or acetone, where its hydrophobic regions can interact more favorably with the solvent molecules.
  • Temperature Effect: Solubility can be temperature-dependent. Increasing the temperature often enhances solubility, which could be particularly relevant for this compound due to its structural profile.

As with many chemical compounds, the overall solubility is a balance of both hydrophilic and hydrophobic interactions. It is crucial to determine the specific solvent environment to predict the solubility behavior accurately. In practical applications, understanding the solubility not only aids in formulation but also impacts the compound's biological and chemical reactivity.


Interesting facts

Interesting Facts about 4-[1-(4-Aminophenyl)-2,2,2-trichloro-ethyl]aniline

4-[1-(4-aminophenyl)-2,2,2-trichloro-ethyl]aniline, often referred to in scientific literature as a potent compound, boasts a variety of interesting aspects that make it a focus of considerable attention in chemical research.

Applications in Research and Industry

This compound finds utility in numerous fields due to its chemical structure, which allows for:

  • Pesticide development: Its chlorinated ethyl group contributes to its effectiveness in creating agrochemicals that tackle pests.
  • Dye manufacturing: The aniline portion is crucial for synthesizing various dyes, imparting color properties essential in textiles and materials.
  • Pharmaceutical exploration: Ongoing studies investigate its potential therapeutic properties, inspired by its structural resemblance to known medicinal compounds.

Structural Insights

Examining the structure of this compound can reveal much about its reactivity and interactions:

  • Amino group: The -NH2 functional group provides the compound with basic properties, making it a good candidate for nucleophilic reactions.
  • Chlorinated groups: The presence of three chlorine atoms can significantly affect the compound’s hydrophobicity, volatility, and biological activity.
  • Phenyl rings: These contribute to the aromatic character of the compound, influencing its stability and reactivity patterns.

Environmental and Safety Considerations

With great potential comes great responsibility. Researchers emphasize the need to:

  • Assess the environmental impact of chlorinated compounds, particularly their degradation pathways and bioaccumulation potential.
  • Implement safety measures when handling such compounds, due to their toxicity and possible carcinogenic effects.

In summary, 4-[1-(4-aminophenyl)-2,2,2-trichloro-ethyl]aniline serves as a prime example of how chemical compounds can impact both industry and research. As investigations into its properties continue, this compound exemplifies the intricate interplay between molecular structure and application.

Synonyms
p,p'-Amino-DDT
DADT
4485-25-0
p,p'-NH2-DDT
p,p'-Diaminodiphenyltrichloroethane
2,2-Bis(p-aminophenyl)-1,1,1-trichloroethane
Aniline, 4,4'-(2,2,2-trichloroethylidene)di-
Benzenamine, 4,4'-(2,2,2-trichloroethylidene)bis-
ETHANE, 2,2-BIS(p-AMINOPHENYL)-1,1,1-TRICHLORO-
NSC-15802
4-[1-(4-aminophenyl)-2,2,2-trichloroethyl]aniline
NSC 15802
BRN 2980482
2,2-Bis(p-aniline)-1,1,1-trichloroethane
WLN: ZR DYR DZ&XGGG
3-13-00-00478 (Beilstein Handbook Reference)
4X45W8W8HZ
2,2-BIS(p-AMINOPHENYL)-1,1,1-TRICHLORO ETHANE
Aniline, 4,4'-(2,2,2-trichloroethylidene)di- (8CI)
DTXSID10196322
NSC15802
DS-003458
p,p'-(2,2,2-Trichloroethylidene)dianiline
Aniline,4'-(2,2,2-trichloroethylidene)di-
Ethane,2-bis(p-aminophenyl)-1,1,1-trichloro-
Benzenamine,4'-(2,2,2-trichloroethylidene)bis-
4,4'-(2,2,2-Trichloroethylidene)bis[benzenamine]
4-[1-(4-aminophenyl)-2,2,2-trichloro-ethyl]aniline