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Ibogaine

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Identification
Molecular formula
C20H28N2O
CAS number
83818-22-0
IUPAC name
2-(dimethylamino)-1-(1-isopropylindol-3-yl)ethanol
State
State

At room temperature, ibogaine is a solid. It is commonly encountered in a crystalline powder form, which may be slightly hygroscopic. Due to the substance's psychoactive properties, it is handled with care in controlled environments.

Melting point (Celsius)
152.00
Melting point (Kelvin)
425.15
Boiling point (Celsius)
427.10
Boiling point (Kelvin)
700.30
General information
Molecular weight
296.46g/mol
Molar mass
296.4260g/mol
Density
1.1570g/cm3
Appearence

Ibogaine appears as a slightly off-white crystalline solid. It's typically provided in a powdered form when used for research or therapeutic monitoring. The compound is known for its psychoactive properties and is derived from the root bark of the African Tabernanthe iboga shrub.

Comment on solubility

Solubility Characteristics of 2-(dimethylamino)-1-(1-isopropylindol-3-yl)ethanol

2-(dimethylamino)-1-(1-isopropylindol-3-yl)ethanol is a compound that showcases intriguing solubility properties. Several factors influence its solubility in various solvents, making it an interesting case for study:

  • Polarity: Due to the presence of the dimethylamino group, the molecule exhibits polar characteristics, which often enhance its solubility in polar solvents such as water and alcohols.
  • Hydrophobic regions: The indole structure introduces hydrophobic regions that may limit solubility in highly polar solvents, suggesting that it can display variable solubility depending on the environmental conditions.
  • pH Dependency: The protonation state of the dimethylamino group can affect solubility, making it useful to test in solutions of varying pH to see how it behaves under different conditions.

In practical applications, it is essential to note that:

  • The compound is likely to be more soluble in organic solvents due to its hydrophobic elements.
  • Its solubility might significantly change with temperature, a common phenomenon in organic compounds.

Understanding the solubility profile of this compound can provide critical insights into its behavior in biological systems and its potential applications in various chemical syntheses.

Interesting facts

Interesting Facts about 2-(dimethylamino)-1-(1-isopropylindol-3-yl)ethanol

This intriguing compound, often explored in the realm of medicinal chemistry, showcases the complex interplay of structure and biological activity. Here are some fascinating aspects to consider:

  • Structural Diversity: The presence of both a dimethylamino group and an indole moiety contributes to its unique properties and potential functionalities, making it an interesting target for research.
  • Biological Relevance: Compounds similar to 2-(dimethylamino)-1-(1-isopropylindol-3-yl)ethanol have been investigated for their pharmacological properties, particularly in the context of their actions as neurotransmitter modulators.
  • Potential Applications: Research suggests that this compound could be relevant in the development of therapies for various neurological conditions due to its structural characteristics that may interact with specific receptors in the brain.
  • Shaping the Future: As scientists delve deeper into the structure-activity relationships of such compounds, there's potential for discovering new treatments or enhancing existing medications, demonstrating the profound impact of chemical synthesis and structural analysis.

As you explore the realm of organic compounds, remember that each one, like 2-(dimethylamino)-1-(1-isopropylindol-3-yl)ethanol, holds the key to new scientific discoveries. This emphasizes how chemistry is not just about formulas but about the potential to innovate and improve human health.

Synonyms
5135-82-0
alpha-((Dimethylamino)methyl)-1-isopropylindole-3-methanol
NSC 37920
BRN 0402320
NSC37920
1H-Indole-3-methanol, alpha-((dimethylamino)methyl)-1-(1-methylethyl)-
INDOLE-3-METHANOL, alpha-((DIMETHYLAMINO)METHYL)-1-ISOPROPYL-
NSC-37920
2-(dimethylamino)-1-(1-isopropyl-1H-indol-3-yl)ethanol