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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
State
State

At room temperature, indoramin hydrochloride is a solid. Its stability under normal conditions makes it suitable for pharmaceutical uses in controlled dosages.

Melting point (Celsius)
148.00
Melting point (Kelvin)
421.15
Boiling point (Celsius)
341.30
Boiling point (Kelvin)
614.45
General information
Molecular weight
356.92g/mol
Molar mass
356.9100g/mol
Density
1.0600g/cm3
Appearence

Indoramin hydrochloride typically appears as a white to off-white crystalline powder. Its crystalline nature and consistency make it identifiable under analytical conditions.

Comment on solubility

Solubility of 2-(1H-indol-3-yl)ethyl-dipropyl-ammonium chloride

The solubility of 2-(1H-indol-3-yl)ethyl-dipropyl-ammonium chloride can be considered from various perspectives.

Aqueous Solubility

This compound typically exhibits substantial solubility in water due to the presence of the ammonium group, which creates favorable interactions with water molecules. Key points include:

  • Hydrophilic Nature: The quaternary ammonium moiety enhances its compatibility with polar solvents like water.
  • Ionization: The chloride ion contributes to greater solubility, as ionic compounds often dissolve well in polar solvents.

Solvents

In addition to water, the solubility in other organic solvents may vary:

  • Polar Organic Solvents: Moderate solubility can be expected in solvents such as methanol and ethanol.
  • Apolar Solvents: Limited solubility is likely in nonpolar solvents due to the absence of strong polar interactions.

Overall, the solubility profile of 2-(1H-indol-3-yl)ethyl-dipropyl-ammonium chloride reflects its complex structure, highlighting the influence of ionic nature and interactions with solvents. Understanding the solubility is essential for applications in chemical synthesis and pharmacology.

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.

Synonyms
N,N-Di-n-propyltryptamine hydrochloride