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Tryptamine hydrochloride

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Identification
Molecular formula
C11H15ClN2
CAS number
72-04-8
IUPAC name
3-(1,4-dimethylpyrrolidin-1-ium-2-yl)-1H-indole;chloride
State
State

The compound is typically a solid at room temperature.

Melting point (Celsius)
216.00
Melting point (Kelvin)
489.15
Boiling point (Celsius)
230.00
Boiling point (Kelvin)
503.15
General information
Molecular weight
218.71g/mol
Molar mass
218.7050g/mol
Density
1.1100g/cm3
Appearence

The compound appears as a white to off-white crystalline powder.

Comment on solubility

Solubility of 3-(1,4-dimethylpyrrolidin-1-ium-2-yl)-1H-indole;chloride

The solubility characteristics of 3-(1,4-dimethylpyrrolidin-1-ium-2-yl)-1H-indole;chloride can be intriguing due to its complex structure, which influences its interaction with solvents. Here are some key points to consider:

  • Solvent Interaction: Generally, the presence of the pyrrolidin-1-ium moiety suggests that the compound could exhibit high solubility in polar solvents, such as water or ethanol, due to its ionic nature.
  • Temperature Sensitivity: It is often observed that solubility can increase with rising temperatures. Hence, heating the solvent may enhance the solubility of this chloride compound.
  • pH Dependence: Salts like chlorides are typically sensitive to pH levels. An acidic environment may further increase solubility, while basic conditions could potentially lead to precipitation.

Understanding the solubility of this compound is essential for its potential applications. As described, favorable interactions with polar solvents are expected to facilitate its dissolution, thus making it easier to work with in research and industrial applications. Consequently, one might conclude that:

“The solubility of this compound is greatly influenced by solvent polarity, temperature, and pH, showcasing the rich interplay of chemical properties at work.”

In summary, 3-(1,4-dimethylpyrrolidin-1-ium-2-yl)-1H-indole;chloride exhibits promising solubility qualities, particularly in polar environments, fueling further exploration in various chemical techniques.

Interesting facts

Interesting Facts About 3-(1,4-Dimethylpyrrolidin-1-ium-2-yl)-1H-indole; Chloride

The compound 3-(1,4-dimethylpyrrolidin-1-ium-2-yl)-1H-indole; chloride is a fascinating example of how organic chemistry blends complexity and functionality. Here are some interesting aspects:

  • Structural Diversity: The presence of both the pyrrolidine and indole moieties enhances the structural diversity of this compound. This unique combination leads to numerous potential biological activities and applications in medicinal chemistry.
  • Biological Relevance: Indole derivatives are widely recognized for their bioactivity, including roles in neurotransmission and as building blocks for many natural products. Thus, compounds like this one may hold potential in pharmaceuticals aimed at treating neurological disorders.
  • Ionic Relationship: The chloride ion plays a crucial role in solubility and reactivity. As a counterion, it can significantly influence the molecular interactions and biological effectiveness of the compound.
  • Research Potential: There is an increasing interest in synthesizing and studying similar compounds for their potential as ion channel modulators. This could lead to advances in the development of drugs targeting specific receptors.
  • Synthesizing Challenges: The synthesis of complex organic molecules like 3-(1,4-dimethylpyrrolidin-1-ium-2-yl)-1H-indole; chloride often poses challenges, making it a compelling subject for developing new synthetic methodologies in organic chemistry.

In summary, 3-(1,4-dimethylpyrrolidin-1-ium-2-yl)-1H-indole; chloride serves as an intriguing subject for scientists looking to explore the intersections of structure, reactivity, and biological function. Its role in expanding the library of bioactive compounds only emphasizes the importance of continued research in this area.

Synonyms
3-(1,4-Dimethyl-2-pyrrolidinyl)indole hydrochloride
19134-10-2
INDOLE, 3-(1,4-DIMETHYL-2-PYRROLIDINYL)-, MONOHYDROCHLORIDE