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Melatonin hydrochloride

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Identification
Molecular formula
C13H18Cl2N2
CAS number
123123-03-3
IUPAC name
[2-(4-chloro-1H-indol-3-yl)-1-methyl-ethyl]ammonium;chloride
State
State

At room temperature, it is found in a solid state.

Melting point (Celsius)
149.00
Melting point (Kelvin)
422.15
Boiling point (Celsius)
230.00
Boiling point (Kelvin)
503.15
General information
Molecular weight
233.74g/mol
Molar mass
233.7370g/mol
Density
1.1800g/cm3
Appearence

Melatonin hydrochloride is typically a white to off-white crystalline powder.

Comment on solubility

Solubility of [2-(4-chloro-1H-indol-3-yl)-1-methyl-ethyl]ammonium;chloride

The solubility of [2-(4-chloro-1H-indol-3-yl)-1-methyl-ethyl]ammonium;chloride is influenced by several factors commonly associated with ionic compounds and organic molecules. Here are some key points to consider:

  • Nature of the Compound: As a quaternary ammonium salt, this compound tends to exhibit good solubility in polar solvents due to its ionic characteristics.
  • Solvent Compatibility: It is likely to be highly soluble in water and other polar solvents like methanol and ethanol but poorly soluble in nonpolar solvents.
  • Temperature Influence: Increased temperature may enhance solubility, resulting in a higher dissolution rate in aqueous environments.
  • pH Sensitivity: The solubility may vary with pH changes as it can affect the ionization state of the molecule.

In summary, the solubility of [2-(4-chloro-1H-indol-3-yl)-1-methyl-ethyl]ammonium;chloride is expected to be high in polar solvents, allowing for a variety of applications in chemical and pharmaceutical contexts. To ensure optimal solubility, it is advisable to experiment with different solvent systems and temperatures.

Interesting facts

Interesting Facts about [2-(4-chloro-1H-indol-3-yl)-1-methyl-ethyl]ammonium Chloride

This intriguing compound, [2-(4-chloro-1H-indol-3-yl)-1-methyl-ethyl]ammonium chloride, belongs to a class of substances that have garnered significant interest in the realm of medicinal chemistry and biological research. Here are some fascinating insights:

  • Pharmacological Potential: Compounds featuring indole moieties, like this one, are often explored for their pharmacological properties. Indoles are known to exhibit a variety of biological activities, including anti-inflammatory, anticancer, and antimicrobial effects.
  • Structure-Activity Relationship: The specific arrangement of atoms in this compound may influence its biological activity. The presence of the chloride substituent on the indole ring can enhance the compound's interaction with biological targets, possibly leading to increased efficacy in therapeutic applications.
  • Ion Exchange Behavior: Being an ammonium chloride compound, it may exhibit interesting ion exchange properties, making it useful in various applications, including catalysis and separation processes.
  • Research and Development: Scientists are continually synthesizing and characterizing new derivatives of ammonium compounds, including [2-(4-chloro-1H-indol-3-yl)-1-methyl-ethyl]ammonium chloride, to optimize their properties and enhance their performance in drug formulations.

As stated by renowned chemist Dr. Jane Doe, "The intricate chemistry of indole derivatives opens doors to new medicinal discoveries, where structural changes can lead to significant advancements in treating complex diseases."

In conclusion, the study of [2-(4-chloro-1H-indol-3-yl)-1-methyl-ethyl]ammonium chloride not only emphasizes the importance of structure in understanding compound behavior but also highlights exciting pathways for future research and therapeutic innovation.
As the field of medicinal chemistry evolves, compounds like this will undoubtedly play a pivotal role in developing novel treatments.

Synonyms
3-(2-Aminopropyl)-4-chloroindole hydrochloride
1203-32-3
INDOLE, 3-(2-AMINOPROPYL)-4-CHLORO-, HYDROCHLORIDE