Indoramin hydrochloride

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Identification

Molecular formula
C22H27ClN2
CAS Number
38821-53-3
IUPAC Name
2-(1H-indol-3-yl)ethyl-dipropyl-ammonium;chloride
Molecular Weight
356.92g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.0600g/cm3
Synonyms
N, N-Di-n-propyltryptamine hydrochloride
Interesting facts

Exploring 2-(1H-indol-3-yl)ethyl-dipropyl-ammonium;chloride

2-(1H-indol-3-yl)ethyl-dipropyl-ammonium;chloride is a fascinating compound that excels in several areas of scientific study and application. Here are some interesting facts:

  • Biological Significance: This compound is often associated with indole derivatives, which are known for their roles in various biological processes, including neurotransmission, due to their structural similarity to neurotransmitters.
  • Pharmacological Interest: Compounds with ammonium groups like this one are frequently investigated for their potential as pharmaceutical agents, particularly in areas such as neurology and psychiatry.
  • Structural Diversity: The unique combination of the indole ring and the dipropylammonium moiety provides interesting properties, enabling unprecedented interactions with biological systems.
  • Research Applications: Scientists are exploring the use of this compound in drug design and development, focusing on how its structure can be modified for enhanced efficacy.
  • Cationic Nature: As a quaternary ammonium compound, it can exhibit interesting surface activity, making it a candidate for applications in antibacterial and antiviral agents.

In summary, 2-(1H-indol-3-yl)ethyl-dipropyl-ammonium;chloride is not just another chemical entity; it's a bridge between organic chemistry, pharmacology, and biochemistry. Its potential applications could lead to significant advancements in medical science. As we continue to uncover its mechanisms and effects, we realize the intricate ways in which chemistry can influence health and well-being.

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