Serotonin Hydroxycinnamate | Solubility of Things

Identification

Molecular formula

C₁₄H₁₆N₂O₄

CAS number

71610-00-9

IUPAC name

2-(5-hydroxy-1H-indol-3-yl)ethylammonium;4-hydroxy-4-oxo-but-2-enoate

State

At room temperature, this compound is typically found in a solid state.

Melting point (Celsius)

180.00

Melting point (Kelvin)

453.15

Boiling point (Celsius)

378.00

Boiling point (Kelvin)

651.15

General information

Molecular weight

319.34g/mol

Molar mass

319.3360g/mol

Density

1.7000g/cm³

Appearence

A crystalline solid that is typically off-white to slightly yellow in color.

Comment on solubility

Solubility of 2-(5-hydroxy-1H-indol-3-yl)ethylammonium; 4-hydroxy-4-oxo-but-2-enoate

The solubility of the compound 2-(5-hydroxy-1H-indol-3-yl)ethylammonium; 4-hydroxy-4-oxo-but-2-enoate can be quite multifaceted due to its complex structure. Here are some key aspects:

Polar Characteristics: The presence of hydroxyl (-OH) groups in both the indole and the butenoate contributes to increased polarity, suggesting a tendency for higher solubility in polar solvents, such as water or alcohols.
Ammonium Group: The ammonium part of the compound adds a positive charge, which further enhances its solubility in aqueous environments.
Hydrogen Bonding: The potential for hydrogen bonding due to the hydroxyl groups means this compound could interact effectively with solvent molecules, leading to greater solubility in suitable solvents.

However, it's important to note:

The overall solubility may be influenced by factors such as pH, temperature, and the presence of other ionic species in solution.
Solubility in non-polar solvents is likely to be minimal due to the compound's polar nature.
Experimental determination of solubility under various conditions would provide more accurate insights into practical applications.

In summary, you can anticipate that 2-(5-hydroxy-1H-indol-3-yl)ethylammonium; 4-hydroxy-4-oxo-but-2-enoate will demonstrate appreciable solubility in polar solvents, but specific conditions will play a crucial role in defining the extent of its solubility.

Interesting facts

Interesting Facts about 2-(5-hydroxy-1H-indol-3-yl)ethylammonium; 4-hydroxy-4-oxo-but-2-enoate

This compound is an intriguing example of a bi-functional molecule that interacts with both biological systems and synthetic processes. Here are some fascinating insights:

Biosynthetic Role: This compound is involved in various biosynthetic pathways, linking it to important metabolic processes in living organisms. The indole moiety is especially notable, as indole derivatives are common in many natural products and pharmaceuticals.
Interaction with Receptors: Due to its indole structure, this compound can potentially interact with serotonin receptors, making it a topic of interest in psychopharmacology. Researchers are investigating its implications in mood regulation and neurological functions.
Antioxidant Properties: The presence of hydroxy groups in its structure is often indicative of antioxidant activity. Compounds with phenolic structures can scavenge free radicals, which are damaging to biological tissues.
Potential Therapeutic Uses: Ongoing studies might reveal its utility in developing therapeutic agents for various conditions, including cancer and neurodegenerative diseases. The compound's unique structural features contribute to its potential efficacy.
Versatile Synthesis: The synthetic pathways to access this compound can include various methods of organic synthesis, highlighting its versatility and relevance in organic chemistry education.

As scientists continue to explore the complexity of such compounds, the potential applications in areas ranging from medicine to materials science remain vast. The study of 2-(5-hydroxy-1H-indol-3-yl)ethylammonium; 4-hydroxy-4-oxo-but-2-enoate exemplifies the intersection of chemistry, biology, and pharmacology.