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6-Methoxytryptamine hydrochloride

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Identification
Molecular formula
C11H15ClN2O
CAS number
4033-51-2
IUPAC name
2-(6-methoxy-1H-indol-3-yl)ethylammonium;chloride
State
State

At room temperature, 6-Methoxytryptamine hydrochloride is a solid. It is typically shipped and stored as a powder or in crystalline form.

Melting point (Celsius)
158.00
Melting point (Kelvin)
431.15
Boiling point (Celsius)
278.00
Boiling point (Kelvin)
551.15
General information
Molecular weight
218.70g/mol
Molar mass
202.7060g/mol
Density
1.2650g/cm3
Appearence

6-Methoxytryptamine hydrochloride appears as a solid crystalline powder. Its color can range from white to off-white, depending on the degree of purity and the preparation method. The compound is typically odorless and hygroscopic, meaning it can absorb moisture from the environment.

Comment on solubility

Solubility of 2-(6-methoxy-1H-indol-3-yl)ethylammonium chloride

The solubility of 2-(6-methoxy-1H-indol-3-yl)ethylammonium chloride in various solvents can be characterized by several key factors:

  • Water Solubility: This compound is expected to be soluble in water due to the presence of the ammonium group, which can form hydrogen bonds with water molecules.
  • Solubility in Organic Solvents: The methoxy group present in the structure may influence its solubility in organic solvents. It could potentially be soluble in polar aprotic solvents, given the molecule's polar characteristics.
  • Aqueous Solutions: When dissolved in aqueous solutions, the compound may dissociate into its ammonium and chloride ions, further enhancing its solubility due to ion-dipole interactions.
  • Temperature Dependency: As with many chemical compounds, the solubility of this compound could also be temperature-dependent, often increasing with higher temperatures.

In summary, the solubility of 2-(6-methoxy-1H-indol-3-yl)ethylammonium chloride is influenced by its polar functional groups, making it more likely to dissolve in aqueous and some polar organic solvents. Scientists often note that “the nature of the solvent plays a pivotal role in solubility,” which rings true for this compound as well.

Interesting facts

Interesting Facts about 2-(6-Methoxy-1H-indol-3-yl)ethylammonium Chloride

2-(6-Methoxy-1H-indol-3-yl)ethylammonium chloride is a fascinating compound with a range of intriguing characteristics and applications.

Chemical Structure and Properties

  • Indole Derivative: This compound features an indole ring, a fundamental structure in many biologically active molecules, which plays a vital role in various biological processes.
  • Methoxy Group: The presence of a methoxy group on the indole ring can influence the compound's solubility, reactivity, and biological interactions, making it an interesting subject of study.

Biological Significance

  • Potential Pharmaceutical Applications: Many compounds containing indole structures are known for their therapeutic properties, including anti-cancer, anti-inflammatory, and anti-depressant effects.
  • Neurotransmitter Research: Given the compound's ammonium group, it may interact with neurotransmitter systems, making it valuable in neurological studies.

Research and Development

This compound is not just a theoretical construct; ongoing research is vital to uncover its full potential:

  • Drug Development: Researchers are investigating how alterations to its structure can enhance efficacy and reduce side effects.
  • Analytical Chemistry: This compound serves as a model for studying the interaction of ions in biological systems, highlighting its relevance in the field.

In summary, 2-(6-methoxy-1H-indol-3-yl)ethylammonium chloride offers a rich avenue for exploration within medicinal chemistry and biochemical research. Its unique structural components and potential biological relevance make it a valuable compound in scientific study, encouraging further investigation into its applications and effects.

Synonyms
2-(6-methoxy-1H-indol-3-yl)ethylazanium;chloride
3-(2-Aminoethyl)-6-methoxyindole hydrochloride
INDOLE, 3-(2-AMINOETHYL)-6-METHOXY-, HYDROCHLORIDE