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N-Ethylthiourea

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Identification
Molecular formula
C3H8N2S2
CAS number
539-31-9
IUPAC name
N-ethyl-5-ethylimino-dithiol-3-amine
State
State

At room temperature, N-Ethylthiourea is a solid.

Melting point (Celsius)
75.00
Melting point (Kelvin)
348.15
Boiling point (Celsius)
224.70
Boiling point (Kelvin)
497.85
General information
Molecular weight
118.20g/mol
Molar mass
118.2020g/mol
Density
1.1700g/cm3
Appearence

N-Ethylthiourea is typically a crystalline solid with a slightly yellow tint. It is often found in powder form and may exhibit a mild odor characteristic of organic sulfur compounds.

Comment on solubility

Solubility of N-ethyl-5-ethylimino-dithiol-3-amine

N-ethyl-5-ethylimino-dithiol-3-amine presents an intriguing profile regarding its solubility, influenced by its structural characteristics and functional groups. Here are some key aspects to consider:

  • Polarity: The presence of dithiol and amine groups suggests that the compound may exhibit significant polarity, likely enhancing its solubility in polar solvents such as water.
  • Hydrogen Bonding: The amino groups can engage in hydrogen bonding, potentially leading to increased solubility in polar solvents.
  • Solvent Interaction: The solubility could vary widely depending on the solvent. While it may dissolve well in alcohols or water, solubility in non-polar solvents is likely to be limited.
  • Concentration Effects: As with many compounds, increased concentration may lead to a saturation point which should be noted in systematic studies.

Overall, understanding the solubility behavior of N-ethyl-5-ethylimino-dithiol-3-amine requires a comprehensive examination of its interactions with various solvents. By focusing on polarity, hydrogen bonding, and solvent compatibility, we can better predict its solubility profile.

Interesting facts

Interesting Facts about N-ethyl-5-ethylimino-dithiol-3-amine

N-ethyl-5-ethylimino-dithiol-3-amine is a fascinating compound that belongs to a category rich in biological and chemical significance. Here are some intriguing insights:

  • Redox Properties: The presence of dithiol groups in this compound makes it an excellent candidate for various redox reactions. These reactive sulfhydryl groups can undergo oxidation and reduction, which is crucial in many biochemical pathways.
  • Potential Biological Activity: Compounds like N-ethyl-5-ethylimino-dithiol-3-amine are often studied for their biological activities. They may exhibit pharmacological properties that can influence enzyme activities or act as antioxidants in biological systems.
  • Chemical Versatility: The unique structure of this compound allows it to participate in diverse chemical reactions, including nucleophilic additions and coordination with metal ions, which can be valuable in fields like coordination chemistry and catalysis.
  • Structure-Activity Relationship: The substitution on the nitrogen and the presence of dithiol moieties make it intriguing to explore the impacts of structural changes on the biological activity and reactivity of similar compounds.
  • Applications in Research: It is often utilized as a useful intermediate in synthetic organic chemistry, particularly in the development of more complex chemical entities or as a probe in molecular biology due to its distinct functional groups.

In summary, N-ethyl-5-ethylimino-dithiol-3-amine exemplifies the intricate intersections of structure, reactivity, and biological relevance in the realm of chemical compounds. As scientists explore its various aspects, it continues to unveil potential applications that could span from medicinal chemistry to synthetic applications.