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Phenylguanidinium chloride

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Identification
Molecular formula
C7H10ClN3
CAS number
139-91-3
IUPAC name
(N'-phenylcarbamimidoyl)ammonium;chloride
State
State

At room temperature, phenylguanidinium chloride is in a solid state, commonly found as a crystalline powder.

Melting point (Celsius)
205.00
Melting point (Kelvin)
478.15
Boiling point (Celsius)
85.00
Boiling point (Kelvin)
358.15
General information
Molecular weight
171.63g/mol
Molar mass
171.6300g/mol
Density
1.2200g/cm3
Appearence

Phenylguanidinium chloride typically appears as a white to off-white crystalline powder. It is known for its hygroscopic nature, meaning it can absorb moisture from the air.

Comment on solubility

Solubility of (N'-phenylcarbamimidoyl)ammonium;chloride

The solubility of (N'-phenylcarbamimidoyl)ammonium;chloride is influenced by its ionic nature and the presence of functional groups. Here are some key points regarding its solubility:

  • Water Solubility: As an ammonium salt, (N'-phenylcarbamimidoyl)ammonium;chloride is expected to be soluble in water due to the ionic interaction between the positively charged ammonium ion and the negatively charged chloride ion.
  • Polar Solvents: This compound is likely to exhibit good solubility in polar solvents, which can stabilize its ionic form.
  • Non-Polar Solvents: In contrast, solubility in non-polar solvents may be very low, as these do not adequately solvate the ionic species.
  • Temperature Effects: The solubility might increase with temperature, which is a common characteristic of many salts.
  • pH Sensitivity: The solubility could also be influenced by the pH of the solution, as changes in pH may impact ionization and interaction with water.

In conclusion, while (N'-phenylcarbamimidoyl)ammonium;chloride is expected to exhibit significant water solubility due to its ionic nature, the actual solubility will depend on other factors like solvent polarity, temperature, and pH, making it essential to consider these influences during practical applications.

Interesting facts

Introduction to N'-phenylcarbamimidoyl)ammonium;chloride

N'-phenylcarbamimidoyl)ammonium;chloride, often referred to in shorthand as a specialized organic compound, presents a fascinating area of study within the realm of chemistry. Its unique structure and properties open the door to an array of applications and theoretical research, making it a worthy subject of exploration.

Key Features and Interesting Facts

  • Chemical Structure: This compound contains a phenyl group attached to a carbamimidoyl moiety, leading to intriguing interactions and reactivity profiles that can be utilized in synthetic organic chemistry.
  • Applications in Synthesis: As an ammonium salt, it has potential uses in synthetic pathways, particularly in the preparation of various nitrogen-containing compounds, which are pivotal in pharmaceuticals and agrochemicals.
  • Role in Catalysis: Compounds like N'-phenylcarbamimidoyl)ammonium;chloride may act as intermediates or catalysts in organic reactions, facilitating transformations that would be challenging under standard conditions.
  • Surprisingly Versatile: Despite its niche status, this compound's ability to form hydrogen bonds and its proton-donating properties make it a subject of interest in supramolecular chemistry and materials science.
  • Theoretical Implications: Researchers often study such compounds to understand better the role of ammonium salts in chemistry, particularly how their interactions can influence reaction kinetics and mechanisms.

In summary, N'-phenylcarbamimidoyl)ammonium;chloride is an intriguing compound that not only contributes to the vast landscape of organic chemistry but also propels forward our understanding of nitrogen-containing compounds. Its varied applications and theoretical aspects underscore the significance of further investigation in this field!