Interesting facts
Interesting Facts about 4-(1H-indol-3-yl)butylammonium chloride
4-(1H-indol-3-yl)butylammonium chloride, often referred to in the scientific community as a derivative of indole, presents a fascinating profile due to its structure and potential applications. Here are some engaging insights about this compound:
- Indole Backbone: This compound contains an indole moiety, which is a bicyclic structure that plays a crucial role in biochemistry. Indole is known for appearing in many natural products, including the amino acid tryptophan and various alkaloids.
- Biological Significance: Compounds derived from indole are often biologically active, leading to significant research in areas such as pharmacology and medicinal chemistry. They are studied for their potential anticancer, antimicrobial, and anti-inflammatory properties.
- Ion Exchange Properties: The presence of the ammonium group in this compound suggests that it may possess interesting ion exchange capabilities. This characteristic can be useful in drug delivery systems and other applications in material science.
- Research Applications: One of the fascinating aspects of this compound is its potential utility in neuroscience research. Indole derivatives have been shown to interact with neurotransmitter systems, which could provide insights into brain function and disorders.
- Unique Synthesis: The synthesis of 4-(1H-indol-3-yl)butylammonium chloride is an exciting area of study, often involving various organic synthesis techniques that demonstrate principles of green chemistry and alternative synthesis methods.
With these attributes, 4-(1H-indol-3-yl)butylammonium chloride not only enhances our understanding of chemical structures but also opens doors for innovative applications in science and technology.
Synonyms
delta-Indolylbutylamine hydrochloride
3-(4-Aminobutyl)indole hydrochloride
INDOLE, 3-(4-AMINOBUTYL)-, MONOHYDROCHLORIDE
Solubility of 4-(1H-indol-3-yl)butylammonium Chloride
The solubility of 4-(1H-indol-3-yl)butylammonium chloride is influenced by various factors including temperature, pH, and the presence of other solvents. Generally, this compound is considered to be soluble in water due to the presence of the ammonium group, which enhances its ability to engage in hydrogen bonding and ionic interactions with polar solvents.
Key Points on Solubility:
Investigating such solubility characteristics is vital for applications in biological systems where 4-(1H-indol-3-yl)butylammonium chloride might be utilized. As quote "solubility is the key to bioavailability," understanding its solubility profile can lead to better insights in drug formulation and therapeutic effectiveness.