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4-(2-amino-1-phenylethyl)aniline

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Identification
Molecular formula
C14H16N2
CAS number
1234-65-7
IUPAC name
4-(2-amino-1-phenyl-ethyl)aniline
State
State

4-(2-amino-1-phenylethyl)aniline is a solid at room temperature.

Melting point (Celsius)
125.00
Melting point (Kelvin)
398.15
Boiling point (Celsius)
362.70
Boiling point (Kelvin)
635.85
General information
Molecular weight
198.30g/mol
Molar mass
198.2700g/mol
Density
1.1070g/cm3
Appearence

The compound 4-(2-amino-1-phenylethyl)aniline typically appears as a solid crystalline substance which can be white or have a slight tint depending on its purity and form.

Comment on solubility

Solubility of 4-(2-amino-1-phenyl-ethyl)aniline

4-(2-amino-1-phenyl-ethyl)aniline, commonly recognized for its intriguing structure, exhibits specific solubility properties that are essential to understanding its behavior in various environments. This compound is primarily known to be sparingly soluble in water, indicative of the influence of its non-polar aromatic groups which limit hydrophilicity.

In exploring its solubility characteristics, several key points emerge:

  • Polar Solvents: 4-(2-amino-1-phenyl-ethyl)aniline tends to dissolve better in polar organic solvents, such as ethanol, methanol, and acetone.
  • Hydrogen Bonding: The presence of the amino group (-NH2) provides opportunities for hydrogen bonding, which enhances solubility in polar solvents.
  • Temperature Dependence: Solubility can increase with temperature, a common phenomenon observed in many organic compounds.
  • pH Influence: Adjusting the pH can also have an effect on solubility. In alkaline conditions, the amino group may become protonated, which can either increase or decrease solubility in water, depending on the overall structure and environment.

In summary, while 4-(2-amino-1-phenyl-ethyl)aniline may not be readily soluble in water, it demonstrates a propensity for solubility in polar organic solvents and is affected by factors such as temperature and pH. Understanding these nuances is crucial for applications where solubility plays a vital role.

Interesting facts

Exploring 4-(2-amino-1-phenyl-ethyl)aniline

4-(2-amino-1-phenyl-ethyl)aniline, often abbreviated as 4-AEP, is a fascinating compound with a rich background in organic chemistry. Here are some interesting facts that highlight its significance:

  • Synthetic Versatility: 4-AEP is widely used in the synthesis of various organic compounds and serves as a crucial intermediate in the production of dyes and pigments.
  • Biological Relevance: The compound's structure, featuring an amino group, suggests potential biological activity, making it a candidate for pharmacological studies.
  • Color Chemistry: Due to its aniline base, 4-AEP can participate in diazotization reactions, leading to the formation of vibrant azo compounds, which are essential in textile and ink industries.
  • Research Potential: Scientists are exploring the compound's application in materials science, particularly in the development of organic semiconductors and electronic devices.
  • Foundation in Aromatic Chemistry: As an aromatic amine, 4-AEP exemplifies the properties of aromatic compounds, such as stability and reactivity, making it a subject of study for those interested in organic reactions.

In summary, 4-(2-amino-1-phenyl-ethyl)aniline is not just a simple organic compound; it plays a pivotal role in various fields ranging from dye synthesis to potential medicinal applications. Its multifaceted nature continues to intrigue chemists and researchers alike.

Synonyms
Skf 12185
6578-31-0
SK&F 12185
RefChem:931837
p-Amino-beta-phenylphenethylamine
2-(p-Aminophenyl)-2-phenylethylamine
Benzeneethanamine, 4-amino-.beta.-phenyl-
42SFY71DC8
p-Amino-.beta.-phenylphenethylamine
Phenethylamine, p-amino-beta-phenyl-
NSC-405163
4-(2-amino-1-phenylethyl)aniline
2-(4-Aminophenyl)-2-phenethylamine
NSC 405163
Phenethylamine, p-amino-.beta.-phenyl-
UNII-42SFY71DC8
SCHEMBL757855
2-p-aminophenyl-2-phenylethylamine
NSC405163
SKF-12185
Benzeneethanamine, 4-amino-beta-phenyl-
DS-016698
Q26841343