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Bufotenin acetate

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Identification
Molecular formula
C16H22N2O3
CAS number
17542-21-4
IUPAC name
2-(5-butanoyloxy-1H-indol-3-yl)ethylammonium;acetate
State
State

At room temperature, bufotenin acetate exists in a solid state. It is usually found as a crystalline powder and is usually handled as a chemical reagent in laboratories for various studies.

Melting point (Celsius)
122.00
Melting point (Kelvin)
395.15
Boiling point (Celsius)
305.00
Boiling point (Kelvin)
578.15
General information
Molecular weight
290.35g/mol
Molar mass
290.3490g/mol
Density
1.2600g/cm3
Appearence

Bufotenin acetate typically appears as a crystalline solid. The color of the crystals can vary from off-white to pale yellow based on purity and exposure to light and air. It can also be somewhat hygroscopic, meaning it may absorb moisture from the surroundings.

Comment on solubility

Solubility of 2-(5-butanoyloxy-1H-indol-3-yl)ethylammonium Acetate

The solubility of 2-(5-butanoyloxy-1H-indol-3-yl)ethylammonium acetate is influenced by several factors including its molecular structure and the functional groups present. Here are some key points regarding its solubility:

  • Ammonium Group: The presence of the ammonium group generally contributes to a higher solubility in polar solvents. This is due to its ability to form hydrogen bonds with water molecules.
  • Acetate Ion: The acetate component can also enhance solubility, as it is a small and polar ion that interacts favorably with water.
  • Hydrophobic Portions: However, the butanoyloxy moiety introduces a hydrophobic region which may pose challenges in solubility when transitioning into non-polar solvents.

In summary, while 2-(5-butanoyloxy-1H-indol-3-yl)ethylammonium acetate exhibits good solubility in aqueous solutions due to the presence of the polar ammonium and acetate groups, the overall solubility may be moderated by the larger hydrophobic regions, affecting its behavior in mixed solvent systems. Therefore, it is crucial to consider the solvent used when predicting the solubility outcomes of this compound.

Interesting facts

Exploring 2-(5-butanoyloxy-1H-indol-3-yl)ethylammonium;acetate

This intriguing compound, 2-(5-butanoyloxy-1H-indol-3-yl)ethylammonium;acetate, is a part of the indole derivatives family, known for their diverse biological activities and applications in medicinal chemistry. Here are some fascinating aspects:

  • Indole Framework: The compound features the indole structure, which is pivotal in numerous natural products and pharmaceuticals, providing a robust scaffold for drug development.
  • Potential Biological Activity: Compounds with similar structures have been studied for their potential in anti-inflammatory and antitumor activities, highlighting the therapeutic importance of this class of compounds.
  • Structure-Activity Relationship: The presence of the butanoyloxy group might influence biological properties, making it an interesting subject for structure-activity relationship studies.
  • Ammonium Ion: The ethylammonium component suggests potential for ionic interactions, which can enhance solubility and bioavailability, critical aspects in drug formulation.

As we delve deeper into the world of chemical compounds like this one, it's crucial to explore their synthesis, mechanisms of action, and broader implications in the fields of pharmacology and biotechnology. Understanding the nuances of such compounds not only broadens our scientific knowledge but also paves the way for innovations in drug design and therapy.

"Chemistry is the science of matter, and matter is anything that has mass and takes up space." This quote emphasizes the significance of studying compounds like 2-(5-butanoyloxy-1H-indol-3-yl)ethylammonium;acetate, as they contribute to a larger understanding of chemical interactions and biological functions.

Synonyms
19615-96-4
BUTYRIC ACID, 3-(2-AMINOETHYL)INDOL-5-YL ESTER, MONOACETATE
3-(2-Aminoethyl)indol-5-yl ester of butyric acid acetate
DTXSID10173279
DTXCID8095770
RefChem:331278