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N-ethyl-N'-phenyl-ethane-1,2-diamine

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Identification
Molecular formula
C10H16N2
CAS number
92-45-5
IUPAC name
N-ethyl-N'-phenyl-ethane-1,2-diamine
State
State

The compound is a liquid at room temperature.

Melting point (Celsius)
-12.00
Melting point (Kelvin)
261.00
Boiling point (Celsius)
273.00
Boiling point (Kelvin)
546.00
General information
Molecular weight
178.28g/mol
Molar mass
178.2820g/mol
Density
0.9800g/cm3
Appearence

The compound is typically a colorless to pale yellow liquid.

Comment on solubility

Solubility of N-ethyl-N'-phenyl-ethane-1,2-diamine

N-ethyl-N'-phenyl-ethane-1,2-diamine, with the molecular formula C10H16N2, presents interesting characteristics regarding its solubility. This compound, often referred to as a diamine due to its two amine functional groups, exhibits varying degrees of solubility in different solvents:

  • Polar solvents: Given the presence of amine groups, N-ethyl-N'-phenyl-ethane-1,2-diamine tends to be soluble in polar solvents, such as water and alcohols. The ability to form hydrogen bonds significantly enhances its interactions with polar molecules.
  • Non-polar solvents: Conversely, its solubility in non-polar solvents may be limited. The large phenyl group can decrease the overall polarity of the molecule, making it less favorable for dissolution in non-polar environments.
  • Temperature dependence: As with many organic compounds, the solubility can be affected by temperature. An increase in temperature often enhances solubility in most solvents due to increased molecular motion.

In conclusion, while N-ethyl-N'-phenyl-ethane-1,2-diamine shows good solubility in polar solvents due to its amine functionality, it may struggle to dissolve in non-polar solvents, making its application in various fields particularly intriguing and dependent on the solvent system used.

Interesting facts

Interesting Facts about N-ethyl-N'-phenyl-ethane-1,2-diamine

N-ethyl-N'-phenyl-ethane-1,2-diamine is a fascinating compound that finds its significance in both industrial applications and academic research. Here are some intriguing aspects of this compound:

  • Composition: This compound belongs to the class of diamines, possessing two amine functional groups. Its structural complexity allows for various interactions and potential applications in different fields.
  • Biological Relevance: Due to its amine groups, N-ethyl-N'-phenyl-ethane-1,2-diamine has been studied for its biological activities, which may include the potential to act as a substrate or inhibitor for various enzymes and receptors.
  • Versatility in Synthesis: This compound can be synthesized through various methods, making it a candidate for research in synthetic organic chemistry, often showcasing the importance of functional group transformations.
  • Applications: It has potential uses in the manufacture of polymers, pharmaceuticals, and dyes. This versatility is attributed to its ability to participate in nucleophilic attacks and coupling reactions.
  • Research Tool: N-ethyl-N'-phenyl-ethane-1,2-diamine serves as an important reference material in the development of new chemical assays and methodologies, providing a basis for studying reaction mechanisms.

In summary, N-ethyl-N'-phenyl-ethane-1,2-diamine is not just a chemical compound; it represents a bridge between fundamental chemistry and practical applications. Whether in the lab or in industry, its properties and behaviors are valuable for continued exploration and innovation.

Synonyms
ETHYLENEDIAMINE, N-ETHYL-N-PHENYL-
RefChem:1085223
N-Ethyl-N-phenylethylenediamine
N-ethyl-N'-phenylethane-1,2-diamine
1551 F
BRN 2803418
SCHEMBL8346697
SCHEMBL11485745
DTXSID10946526
N~1~-Ethyl-N~2~-phenylethane-1,2-diamine