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Benzydamine Hydrochloride

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Identification
Molecular formula
C19H24ClNO3
CAS number
132-69-4
IUPAC name
(4-allyloxy-3,5-diethyl-phenyl)methyl-diethyl-ammonium;chloride
State
State

At room temperature, Benzydamine hydrochloride is typically in a solid state. It is usually encountered as a crystalline powder used in the formulation of medications.

Melting point (Celsius)
167.40
Melting point (Kelvin)
440.60
Boiling point (Celsius)
338.95
Boiling point (Kelvin)
612.10
General information
Molecular weight
309.87g/mol
Molar mass
309.8840g/mol
Density
0.8917g/cm3
Appearence

Benzydamine hydrochloride typically appears as a white to off-white crystalline powder. It is highly soluble in water, which is why it is often found dissolved in various pharmaceutical formulations for ease of use.

Comment on solubility

Solubility of (4-allyloxy-3,5-diethyl-phenyl)methyl-diethyl-ammonium;chloride

The solubility of (4-allyloxy-3,5-diethyl-phenyl)methyl-diethyl-ammonium chloride can provide insight into its behavior in various solvents and its potential applications.

Key Factors Affecting Solubility:

  • Ionic Nature: Being a quaternary ammonium compound, it contains a positively charged ammonium ion which generally enhances solubility in polar solvents.
  • Hydrophobic Effects: The presence of alkyl chains (in this case, the diethyl groups) may contribute to a hydrophobic character, which can affect solubility in non-polar solvents.
  • Temperature: Solubility often increases with temperature; thus, heating may improve its ability to dissolve.

Typically, ionic compounds like this chloride are more soluble in water and other polar solvents compared to non-polar solvents. However, it’s important to note:

  • While ionic species typically have high solubility in polar environments due to strong ion-dipole interactions, the bulky diethyl groups may introduce steric hindrance, potentially reducing solubility.
  • In practical applications, testing in different solvents is essential to obtain specific solubility data.

In summary, the solubility of (4-allyloxy-3,5-diethyl-phenyl)methyl-diethyl-ammonium;chloride is influenced by its ionic nature and hydrophobic components, making it particularly interesting for further studies and potential uses.

Interesting facts

Interesting Facts about (4-allyloxy-3,5-diethyl-phenyl)methyl-diethyl-ammonium;chloride

(4-allyloxy-3,5-diethyl-phenyl)methyl-diethyl-ammonium;chloride is a fascinating compound that bridges the gap between organic chemistry and applications in various fields. Here are some intriguing insights:

  • Ammonium ion significance: This compound features a quaternary ammonium structure, which is essential due to its role in biological systems and its applications in antimicrobial agents.
  • Versatile reactivity: The allyloxy group contributes to the reactivity of this compound, making it a valuable intermediate in organic synthesis for creating more complex molecules.
  • Pharmaceutical potential: Its unique structure hints at possible pharmaceutical applications, particularly in the development of new drugs targeting specific biological receptors.
  • Industrial use: Compounds like this can function as surfactants, aiding in emulsification and dispersion in various industrial processes.
  • Environmental considerations: The applications of quaternary ammonium compounds must consider their environmental impact, particularly in terms of their biodegradable properties and effects on aquatic ecosystems.

As scientists continue to explore the properties and applications of such compounds, the potential for new discoveries remains significant. The integration of organic groups allows researchers to modify and enhance the characteristics of the compound, leading to innovative solutions in chemistry and related fields.

Overall, (4-allyloxy-3,5-diethyl-phenyl)methyl-diethyl-ammonium;chloride exemplifies how chemical structures can unlock a wide range of functionalities, paving the way for further research and practical applications.

Synonyms
4-Allyloxy-N,N,3,5-tetraethylbenzylamine hydrochloride
7192-70-3
BENZYLAMINE, 4-(ALLYLOXY)-N,N,3,5-TETRAETHYL-, HYDROCHLORIDE