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Alexidine dihydrochloride

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Identification
Molecular formula
(C10H7N2O)+ Cl-
CAS number
140-11-4
IUPAC name
(4-imino-1-oxo-2-naphthyl)ammonium;chloride
State
State

The compound is typically in a solid state at room temperature.

Melting point (Celsius)
190.00
Melting point (Kelvin)
463.00
Boiling point (Celsius)
350.00
Boiling point (Kelvin)
623.00
General information
Molecular weight
157.61g/mol
Molar mass
157.6100g/mol
Density
1.4500g/cm3
Appearence

This compound typically appears as a crystalline solid powder. It is often white to off-white in color.

Comment on solubility

Solubility of (4-imino-1-oxo-2-naphthyl)ammonium chloride

The solubility of (4-imino-1-oxo-2-naphthyl)ammonium chloride can be examined through various aspects that contribute to its behavior in different solvents. Typically, the following factors are influential:

  • Ionic Nature: As a salt, (4-imino-1-oxo-2-naphthyl)ammonium chloride is expected to have good solubility in polar solvents such as water due to ion-dipole interactions.
  • Hydrophilicity: The presence of the ammonium group in the compound increases its affinity for water, making it more soluble compared to non-polar compounds.
  • Temperature: Solubility can often be enhanced by increasing the temperature, allowing more particles to dissolve.
  • pH Influence: The solubility may also be influenced by the pH of the solution, which can affect the ionization state of the compound.

In conclusion, it can be stated that while (4-imino-1-oxo-2-naphthyl)ammonium chloride is expected to be soluble in water, the exact parameters of its solubility should be verified through experimental data. Understanding these factors can help predict its behavior in various environments and applications.

Interesting facts

Interesting Facts about (4-imino-1-oxo-2-naphthyl)ammonium;chloride

(4-imino-1-oxo-2-naphthyl)ammonium;chloride is a fascinating compound with unique properties and applications. Here are some intriguing aspects of this chemical:

  • Chemical Structure: The compound features a naphthalene ring, which is significant due to its ability to participate in a variety of chemical reactions and exhibit aromatic stability.
  • Potential Uses: Compounds like (4-imino-1-oxo-2-naphthyl)ammonium;chloride may be explored in fields such as organic synthesis, pharmaceuticals, and materials science. Their unique structures often lead to interesting biological activity.
  • Reactivity: The presence of the imino group contributes to the compound's reactivity. Compounds with imino functionalities are known to take part in various reactions, including nucleophilic substitutions and cycloadditions.
  • Color and Spectroscopy: Compounds containing naphthalene derivatives can result in characteristic colors, making them useful in the study of UV-Vis spectroscopy and fluorescence.
  • Historical Significance: The study of naphthalene derivatives dates back to the 19th century, contributing to the development of organic chemistry as a scientific discipline.

As a scientist or chemistry student, one might appreciate the historical context and the potential implications of this compound. As noted by chemists, "the beauty of chemistry lies not just in the reactions but in the infinite possibilities they present." Exploring (4-imino-1-oxo-2-naphthyl)ammonium;chloride could lead to exciting discoveries in fundamental and applied chemistry!