Skip to main content

Serotonin Hydrogen Succinate

ADVERTISEMENT
Identification
Molecular formula
C14H18N2O5
CAS number
65004-53-5
IUPAC name
2-(5-hydroxy-1H-indol-3-yl)ethylammonium;4-hydroxy-4-oxo-butanoate
State
State
At room temperature, serotonin hydrogen succinate exists as a solid, typically handled in a powder form suitable for laboratory use and research applications.
Melting point (Celsius)
213.00
Melting point (Kelvin)
486.15
Boiling point (Celsius)
-1.00
Boiling point (Kelvin)
-1.00
General information
Molecular weight
309.34g/mol
Molar mass
309.3400g/mol
Density
1.2400g/cm3
Appearence

Serotonin Hydrogen Succinate typically appears as a white to off-white powder. It may have crystalline characteristics, though its exact appearance can vary depending on the purity and form of the sample. It is often used in research settings relating to neurotransmitter function and studies.

Comment on solubility

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

The solubility of 2-(5-hydroxy-1H-indol-3-yl)ethylammonium;4-hydroxy-4-oxo-butanoate can be influenced by various factors including its structural features and the presence of functional groups. This compound contains both an amine and a carboxylate group, which generally enhance solubility in polar solvents.

Key Factors Affecting Solubility:

  • Functional Groups: The presence of hydroxyl groups can provide hydrogen bonding opportunities with water, increasing solubility.
  • Ionic Nature: As an ammonium salt, the ionic character may facilitate solubility in aqueous environments.
  • Temperature: Like many compounds, solubility may increase with temperature, allowing for a greater degree of dissolution.
  • pH: The solubility may also vary with pH changes, as the ionization of the amine and carboxylic acid groups can alter the overall charge and solubility properties.

In general, one could expect that at physiological pH, this compound may exhibit decent solubility due to the balance of hydrophilic and hydrophobic characteristics presented by its structure. It’s important to also consider experimental data for precise solubility measurements, as the theoretical predictions may differ based on specific environmental conditions.

Interesting facts

Interesting Facts About 2-(5-Hydroxy-1H-Indol-3-yl)ethylammonium; 4-Hydroxy-4-oxo-butanoate

The compound 2-(5-hydroxy-1H-indol-3-yl)ethylammonium; 4-hydroxy-4-oxo-butanoate is a fascinating chemical that combines elements from biochemistry and medicinal chemistry. Here are some noteworthy aspects:

  • Biological Relevance: This compound exhibits connections to indole metabolism, which is crucial as indoles occur naturally in many biological processes, including the synthesis of neurotransmitters.

  • Structure and Stability: The bipartite structure of this compound demonstrates the interaction between an indole derivative and an α-keto acid, enriching its potential functionality in biochemical pathways.

  • Potential Applications: Due to its organization, this compound might show promise in drug development, particularly in targeting metabolic pathways related to neurotransmission and hormonal regulation.

  • Research Insights: The 5-hydroxy substitution on the indole ring enhances its ability to engage in various biochemical activities, possibly affecting enzyme kinetics.

  • Historical Significance: Indole compounds have long been researched for their biological effects, emphasizing their role in nature as \emph{plant hormones} and \emph{neurotransmitter precursors}.

As scientists continue to explore this compound’s applications, the intersection of its structural properties and biological significance offers exciting opportunities for novel discoveries in the field of medicinal chemistry.

Synonyms
Serotonin succinate
21716-89-2
3-(2-Aminoethyl)indol-5-ol, succinate
DTXSID90176107
INDOL-5-OL, 3-(2-AMINOETHYL)-, SUCCINATE
RefChem:380148
DTXCID6098598
Butanedioic acid, compd. with 3-(2-aminoethyl)-1H-indol-5-ol (1:1) (8CI)