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Dimethyl-[3-(1-methyl-3-phenyl-indolin-1-ium-3-yl)propyl]ammonium dichloride

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Identification
Molecular formula
C23H30Cl2N2
CAS number
63867-89-8
IUPAC name
dimethyl-[3-(1-methyl-3-phenyl-indolin-1-ium-3-yl)propyl]ammonium;dichloride
State
State

At room temperature, dimethyl-[3-(1-methyl-3-phenyl-indolin-1-ium-3-yl)propyl]ammonium dichloride is in a solid state.

Melting point (Celsius)
166.00
Melting point (Kelvin)
439.15
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
273.15
General information
Molecular weight
424.62g/mol
Molar mass
424.6200g/mol
Density
0.9000g/cm3
Appearence

Dimethyl-[3-(1-methyl-3-phenyl-indolin-1-ium-3-yl)propyl]ammonium dichloride typically appears as a crystalline solid. The specific appearance can vary, but it is generally a white or off-white powder.

Comment on solubility

Solubility of Dimethyl-[3-(1-methyl-3-phenyl-indolin-1-ium-3-yl)propyl]ammonium Dichloride

The solubility of dimethyl-[3-(1-methyl-3-phenyl-indolin-1-ium-3-yl)propyl]ammonium dichloride (C23H30Cl2N2) can be quite intriguing due to its unique structural composition. This compound is characterized by the presence of both polar and non-polar groups, affecting its solubility behavior in various solvents.

Factors Influencing Solubility:

  • Ionization: The dichloride salt form suggests it is likely ionizable in solution, which can enhance solubility in polar solvents like water.
  • Hydrophobic Characteristics: The bulky organic groups in its structure may discourage solubility in water, making dimethyl-[3-(1-methyl-3-phenyl-indolin-1-ium-3-yl)propyl]ammonium preferentially soluble in organic solvents such as ethanol or dimethyl sulfoxide (DMSO).
  • Hydrogen Bonding: The possible formation of hydrogen bonds between the solvent molecules and the functional groups can significantly affect solubility, particularly in polar environments.

In summary, when considering dimethyl-[3-(1-methyl-3-phenyl-indolin-1-ium-3-yl)propyl]ammonium dichloride's solubility, it is essential to note that its behavior will greatly depend on the solvent environment, and further experimental data would be beneficial to assess its practical applications.

Interesting facts

Interesting Facts about Dimethyl-[3-(1-methyl-3-phenyl-indolin-1-ium-3-yl)propyl]ammonium Dichloride

Dimethyl-[3-(1-methyl-3-phenyl-indolin-1-ium-3-yl)propyl]ammonium dichloride is a fascinating compound with a rich backdrop in organic chemistry. Here are some intriguing insights:

  • Structure and Function: This compound comprises a unique indolin-1-ium structure which contributes to its broad range of biological and chemical activities. The presence of the methyl and phenyl groups enhances its stability and reactivity.
  • Applications: Thanks to its intriguing chemical properties, this compound finds applications in pharmaceutical sciences, particularly in the development of new medications and therapies requiring targeted delivery systems.
  • Charge Properties: The quaternary ammonium structure of the compound introduces a positive charge, making it effective in various biochemical interactions, such as acting as a cationic surfactant.
  • Research Focus: Researchers are particularly interested in exploring its role as a potential agent in antimicrobial formulations, where its ability to penetrate microbial cell walls can be beneficial.
  • Metabolic Pathways: Its structural complexity means that its interactions within metabolic pathways can lead to unique insights in biochemical processes, sparking further research in the field of medicinal chemistry.

Given its combination of both aromatic and aliphatic properties, Dimethyl-[3-(1-methyl-3-phenyl-indolin-1-ium-3-yl)propyl]ammonium dichloride serves as an excellent example of how intricate structures can yield multifunctional applications. As researchers continue to probe its capabilities, we may uncover even more striking uses for this compound in future advancements.

Synonyms
Propylamine, N,N-dimethyl-3-(3-phenylindolin-3-yl)-, dihydrochloride
10565-88-5
LU 3-024
INDOLINE, 3-(3-DIMETHYLAMINOPROPYL)-1-METHYL-3-PHENYL-, DIHYDROCHLORIDE