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Strychnine hydrochloride

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Identification
Molecular formula
C20H25N2 . 2Cl-
CAS number
130-10-7
IUPAC name
diethyl-[2-[3-(1-methylpyrrolidin-1-ium-2-yl)indol-1-yl]ethyl]ammonium;dichloride
State
State

This compound is typically solid at room temperature.

Melting point (Celsius)
199.00
Melting point (Kelvin)
472.15
Boiling point (Celsius)
235.00
Boiling point (Kelvin)
508.15
General information
Molecular weight
443.46g/mol
Molar mass
443.4600g/mol
Density
1.1400g/cm3
Appearence

Diethyl-[2-[3-(1-methylpyrrolidin-1-ium-2-yl)indol-1-yl]ethyl]ammonium dichloride appears as a white to off-white crystalline powder. It is typically used in its salt form, which enhances its solubility in water.

Comment on solubility

Solubility of Diethyl-[2-[3-(1-methylpyrrolidin-1-ium-2-yl)indol-1-yl]ethyl]ammonium Dichloride

The solubility of diethyl-[2-[3-(1-methylpyrrolidin-1-ium-2-yl)indol-1-yl]ethyl]ammonium dichloride can be influenced by several factors:

  • Polarity: Given the presence of the quaternary ammonium ion, this compound is likely to exhibit significant polarity, which can enhance its solubility in polar solvents such as water.
  • Ionic Interaction: The dichloride component introduces ionic interactions, typically favoring solubility in aqueous environments, as these ions can dissociate and interact effectively with solvent molecules.
  • Hydrogen Bonding: The compound might also form hydrogen bonds due to functional groups present, which can further increase its affinity for water.
  • Solubility Limitations: However, the overall solubility can be affected by temperature, concentration, and the presence of other solutes in the solution.

In summary, one might say, "The behavior of diethyl-[2-[3-(1-methylpyrrolidin-1-ium-2-yl)indol-1-yl]ethyl]ammonium dichloride in solution is governed by its ionic and polar characteristics." Thus, while it is expected to be soluble in polar solvents like water, variations may occur based on specific environmental conditions.

Interesting facts

Interesting Facts about diethyl-[2-[3-(1-methylpyrrolidin-1-ium-2-yl)indol-1-yl]ethyl]ammonium;dichloride

This fascinating compound, often utilized in the realm of organic and medicinal chemistry, displays remarkable characteristics that pique the interest of scientists and researchers alike. Here are some compelling aspects:

  • Structural Complexity: The compound has a distinct structure that includes both a pyrrolidine moiety and an indole ring system, known for their significance in various biological activities.
  • Interactions: The presence of quaternary ammonium denotes that this compound is cationic, giving it unique interaction properties, particularly with biological membranes and other macromolecules.
  • Biological Activity: Compounds possessing indole derivatives are often linked to pharmacological activities, making this compound a candidate for further exploration in drug discovery and development.
  • Electrochemical Properties: The quaternary ammonium group enhances the compound’s solubility and ionic strength in solution, contributing to its utility in various electrochemical applications.
  • Research Potential: Studies may focus on its role in cellular processes as well as its potential as a therapeutic agent, particularly in neuropharmacology due to the presence of the pyrrolidine ring.

As you delve into the chemical landscape of diethyl-[2-[3-(1-methylpyrrolidin-1-ium-2-yl)indol-1-yl]ethyl]ammonium;dichloride, keep in mind its intricate connections to both synthetic and biological domains. This compound not only exemplifies the beauty of chemical synthesis but also holds promise in advancing our understanding of molecular interactions in living systems.

In the words of a renowned chemist, "Every molecule has a story to tell." This compound surely offers a tale worth telling.

Synonyms
1-(2-Diethylaminoethyl)-3-(1-methyl-2-pyrrolidinyl)indole dihydrochloride
4802-61-3
INDOLE, 1-(2-DIETHYLAMINOETHYL)-3-(1-METHYL-2-PYRROLIDINYL)-, DIHYDROCHLORIDE