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Serotonin Oxalate

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Identification
Molecular formula
C10H12N2O · C2H4O4
CAS number
153-98-0
IUPAC name
2-(5-hydroxy-1H-indol-3-yl)ethyl-dimethyl-ammonium;2-hydroxy-2-oxo-acetate
State
State

In room temperature conditions, serotonin oxalate is typically a solid.

Melting point (Celsius)
148.00
Melting point (Kelvin)
421.15
Boiling point (Celsius)
196.85
Boiling point (Kelvin)
470.00
General information
Molecular weight
344.36g/mol
Molar mass
344.3590g/mol
Density
1.4000g/cm3
Appearence

Serotonin oxalate appears as a white to off-white crystalline powder.

Comment on solubility

Solubility of 2-(5-hydroxy-1H-indol-3-yl)ethyl-dimethyl-ammonium; 2-hydroxy-2-oxo-acetate

The solubility of the compound 2-(5-hydroxy-1H-indol-3-yl)ethyl-dimethyl-ammonium; 2-hydroxy-2-oxo-acetate can be influenced by several factors due to its complex chemical structure. Here are some important points to consider:

  • Polarity: The presence of hydroxyl groups in the structure usually enhances solubility in polar solvents, such as water. This is due to the ability of these groups to form hydrogen bonds.
  • Ionization: As a quaternary ammonium compound, the dimethylammonium part could impart positive charge, enhancing solubility in aqueous solutions.
  • Solvent Compatibility: This compound may exhibit good solubility in common solvents such as ethanol, methanol, and dimethyl sulfoxide (DMSO), while being less soluble in non-polar solvents like hexane.
  • pH Influence: The solubility could also vary with pH level. An increase in acidity will likely facilitate the protonation of functional groups, impacting solubility.

In summary, while the solubility of 2-(5-hydroxy-1H-indol-3-yl)ethyl-dimethyl-ammonium; 2-hydroxy-2-oxo-acetate is expected to be relatively high in polar solvents due to the nature of its functional groups, factors such as temperature, ionic strength, and environmental conditions can also significantly affect its overall solubility profile.

Interesting facts

Interesting Facts about 2-(5-hydroxy-1H-indol-3-yl)ethyl-dimethyl-ammonium; 2-hydroxy-2-oxo-acetate

This intriguing compound, often associated with the study of biological systems, stands out due to its unique structure and diverse applications. Here are some fascinating aspects to consider:

  • Biological Significance: Compounds similar to this one are frequently explored for their roles in neurotransmission and hormonal regulation, particularly because they share features with neurotransmitters.
  • Pharmacological Potential: The presence of the indole moiety in this compound hints at potential uses in pharmacology, given that many indole derivatives are recognized for their medicinal properties.
  • Research Focus: Ongoing studies are investigating the potential of such compounds in neurodegenerative diseases, where their unique chemical properties could influence therapeutic pathways.
  • Synthetic Relevance: The synthesis of this compound may involve innovative reaction pathways that are of interest to synthetic chemists aiming to design new molecules with specific biological activities.
  • Complex Interactions: Due to its ammonium group, this compound might form various interactions with biomolecules, influencing its behavior in biological systems and enhancing its study in molecular biology.

In summary, the compound 2-(5-hydroxy-1H-indol-3-yl)ethyl-dimethyl-ammonium; 2-hydroxy-2-oxo-acetate provides a rich field for exploration due to its potential implications in health sciences and its unique chemical properties. As a field of study, the interactions and effects of such compounds could broaden our understanding of how small molecules can affect biological functions.

Synonyms
4382-50-7
1H-INDOL-5-OL, 3-(2-(DIMETHYLAMINO)ETHYL)-, BIOXALATE
Mappine bioxalate
Bufotenine bioxalate
N,N-Dimethylserotonin bioxalate
5-Hydroxy-N-dimethyltryptamine bioxalate
3-(2-Dimethylaminoethyl)-5-indolol bioxalate
3-(beta-Dimethylaminoethyl)-5-hydroxyindole bioxalate
N,N-Dimethyltryptamine oxalate
DTXSID20195942
EAA38250