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Phenylthiocarbamoylguanidine hydrochloride

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Identification
Molecular formula
C9H14ClN3S
CAS number
27887-98-1
IUPAC name
[N-phenyl-N'-(2-sulfanylethyl)carbamimidoyl]ammonium;chloride
State
State

The compound is in a solid state at room temperature, usually appearing in crystalline form.

Melting point (Celsius)
187.00
Melting point (Kelvin)
460.00
Boiling point (Celsius)
250.00
Boiling point (Kelvin)
523.00
General information
Molecular weight
243.74g/mol
Molar mass
243.7370g/mol
Density
1.2905g/cm3
Appearence

The compound is typically a white to off-white crystalline solid. It may absorb moisture from the air as some hydrates can be deliquescent, turning gelatinous upon exposure to moist air.

Comment on solubility

Solubility of N-phenyl-N'-(2-sulfanylethyl)carbamimidoyl ammonium chloride

The solubility of N-phenyl-N'-(2-sulfanylethyl)carbamimidoyl ammonium chloride can be influenced by several factors, including its molecular structure and interactions with solvents. Here are some key points to consider:

  • Solvent Types: This compound is likely to be more soluble in polar solvents due to the presence of the ammonium group, which can engage in hydrogen bonding.
  • Temperature Influence: As with many ionic compounds, increasing the temperature may enhance solubility, facilitating greater dissociation of the ions in solution.
  • pH Dependency: The solubility may also vary with pH; at extreme pH levels, the ionization state of the ammonia group could change, affecting solubility.
  • Ionic Strength: The presence of other ions in solution can alter solubility through a phenomenon known as the "common ion effect".

In summary, while exact solubility data may vary and require empirical measurement, one can expect that N-phenyl-N'-(2-sulfanylethyl)carbamimidoyl ammonium chloride demonstrates favorable solubility characteristics in polar environments. It is crucial to conduct solubility tests under controlled conditions to gather precise data.

Interesting facts

Interesting Facts about N-phenyl-N'-(2-sulfanylethyl)carbamimidoyl Ammonium Chloride

The compound N-phenyl-N'-(2-sulfanylethyl)carbamimidoyl ammonium chloride is an intriguing member of the class of compounds known as thioureas. This compound, characterized by its unique functional groups, possesses various applications in the fields of chemistry and medicinal science. Here are some interesting insights:

  • Dual Functionality: This compound features both an ammonium group and a sulfhydryl (thiol) moiety, which could allow it to participate in a variety of chemical reactions, making it a versatile building block in medicinal chemistry.
  • Biological Relevance: Compounds like this one are often explored for their potential bioactivity. Thiol groups are known to participate in redox reactions, which are critical in biological systems.
  • Potential Applications: Researchers are examining the utility of thiourea derivatives in drug development and as catalysts in organic synthesis, due to their ability to stabilize reactive intermediates and facilitate transformations.
  • Analytical Importance: Its unique structural features make it a candidate for exploration in analytical chemistry, particularly in the development of new methods for detection and quantification of biomolecules.

Furthermore, the presence of both electron-donating and electron-withdrawing elements in the structure can profoundly affect the compound's reactivity and stability. As one researcher eloquently noted, “The beauty of chemistry lies in the vastness of possibilities that each molecule can present.” This compound exemplifies that beauty, opening up numerous pathways for exploration in both academic research and practical applications.