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Anilinoformamidine Hydrochloride

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Identification
Molecular formula
C13H14ClN3
CAS number
21436-97-5
IUPAC name
[amino(anilino)methylene]-phenyl-ammonium;chloride
State
State

At room temperature, anilinoformamidine hydrochloride is typically a solid. It is usually handled in its solid crystalline form for chemical purposes and research.

Melting point (Celsius)
205.00
Melting point (Kelvin)
478.15
Boiling point (Celsius)
261.00
Boiling point (Kelvin)
534.15
General information
Molecular weight
212.68g/mol
Molar mass
212.6770g/mol
Density
1.2300g/cm3
Appearence

Anilinoformamidine hydrochloride typically appears as a white to off-white crystalline powder. It may form clear, colorless crystals when highly purified.

Comment on solubility

Solubility of [amino(anilino)methylene]-phenyl-ammonium;chloride

The solubility of [amino(anilino)methylene]-phenyl-ammonium; chloride can be influenced by various factors, including temperature, pH, and solvent polarity. Generally speaking, ionic compounds tend to exhibit high solubility in polar solvents, particularly water, due to the strong interactions between the charged ions and water molecules. In the case of this specific compound, its ammonium component suggests that it may display significant solubility in aqueous solutions.

Key points to consider regarding its solubility include:

  • Nature of the Ions: The presence of ammonium ions typically enhances solubility.
  • Polarity: The polar character of the compound likely supports its solubility in polar solvents.
  • Temperature Effects: Higher temperatures may increase solubility, as solvation processes often become more favorable.
  • pH Sensitivity: The solubility may vary with changes in pH, particularly if any of the constituents can protonate or deprotonate.

In conclusion, while predicting exact solubility without experimental data can be challenging, it is reasonable to expect [amino(anilino)methylene]-phenyl-ammonium; chloride to demonstrate good solubility characteristics, especially in polar solvents like water.

Interesting facts

Interesting Facts about [amino(anilino)methylene]-phenyl-ammonium;chloride

[amino(anilino)methylene]-phenyl-ammonium;chloride is a fascinating compound that showcases the intricate interplay of organic chemistry and biological systems. This compound, often referred to in scientific literature, serves as an intriguing example of how various functional groups can be integrated into a single molecular structure.

Key Features

  • Structurally Diverse: The incorporation of amino and anilino groups lends this compound unique properties, making it a subject of interest in both research and applications.
  • Biological Relevance: Compounds of this nature may find biological applications, potentially acting as drug candidates or biological probes due to their ability to interact with various biological molecules.
  • Versatile Application: As a salt, its behavior in solution can be manipulated for various applications, including catalysis and materials science.

One notable aspect is the potential for this compound to act as a cationic surfactant, which means it can affect both the solubility of substances and the surface tension of liquids. This property is especially important in fields like pharmaceuticals and cosmetics, where solubility plays a critical role in effectiveness.

Moreover, its ability to form hydrogen bonds and ionic interactions can influence its reactivity and the way it engages with other compounds. Future research may uncover further applications or adaptations of [amino(anilino)methylene]-phenyl-ammonium;chloride, particularly in drug design or material sciences.

As students and researchers delve into the world of organic chemistry, understanding compounds like this one opens the door to a broader comprehension of molecular interactions, paving the way for innovations in a myriad of scientific fields.

Synonyms
N,N'-Diphenylguanidine monohydrochloride
24245-27-0
[amino(anilino)methylidene]-phenylazanium;chloride
Guanidine, N,N'-diphenyl-, monohydrochloride
EINECS 246-107-8
GUANIDINE, 1,3-DIPHENYL-, MONOHYDROCHLORIDE
Guanidine, N,N'-diphenyl-, hydrochloride (1:1)