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Vortioxetine acetate

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Identification
Molecular formula
C18H22N2O.C2H4O2
CAS number
508233-74-7
IUPAC name
3-[2-(1H-indol-5-yloxy)-2-oxo-ethyl]hexylammonium;acetate
State
State

Vortioxetine acetate is a solid at room temperature. The compound is typically used in powdered form.

Melting point (Celsius)
158.50
Melting point (Kelvin)
431.65
Boiling point (Celsius)
220.00
Boiling point (Kelvin)
493.15
General information
Molecular weight
441.56g/mol
Molar mass
379.5070g/mol
Density
1.2700g/cm3
Appearence

Vortioxetine acetate appears as a white to slightly off-white powder. It is typically solid at room temperature.

Comment on solubility

Solubility of 3-[2-(1H-indol-5-yloxy)-2-oxo-ethyl]hexylammonium;acetate

The solubility of 3-[2-(1H-indol-5-yloxy)-2-oxo-ethyl]hexylammonium;acetate can be quite intricate due to its unique molecular structure. Understanding its solubility characteristics is essential when considering its applications in various chemical environments. Here are several key points to note:

  • Polar Nature: The ammonium group in this compound typically imparts a significant degree of polarity, which often leads to solubility in polar solvents such as water.
  • Influence of Acetate: The acetate moiety is known for enhancing solubility due to its ability to form hydrogen bonds with water molecules.
  • Hydrophobic Interactions: The hexylammonium chain could limit solubility in highly polar solvents due to hydrophobic interactions, suggesting a dichotomy in solubility depending on solvent type.
  • Temperature Dependence: It's also worth noting that the solubility may vary with temperature, generally increasing as temperature rises, owing to greater molecular motion.

Despite these points, specific solubility data in various solvents may be scarce, making empirical testing essential for precise applications. In summary, the solubility of this compound reflects a balance between its polar and non-polar characteristics, fostering interesting behavior in diverse chemical contexts.

Interesting facts

Interesting Facts about 3-[2-(1H-indol-5-yloxy)-2-oxo-ethyl]hexylammonium;acetate

This unique compound, 3-[2-(1H-indol-5-yloxy)-2-oxo-ethyl]hexylammonium;acetate, presents a fascinating intersection of organic chemistry and pharmacology. Here are some intriguing facts:

  • Indole Derivative: This compound contains an indole structure, which is a significant motif in many biological systems, especially in neurotransmitters. Indoles play an essential role in the functioning of serotonin, impacting mood regulation.
  • Involvement in Drug Design: The indole moiety has been extensively studied for its biological activity, making compounds like this an interesting subject in the field of drug discovery.
  • Ammonium Ion: The ammonium component adds a positive charge at physiological pH, which can influence its interaction with biological membranes, thereby altering its bioavailability and transport across cell membranes.
  • Biological Applications: Compounds with similar structures have been investigated for their potential therapeutic roles, including as anti-cancer agents and anti-inflammatory drugs.
  • Acetic Acid Component: The acetate part of the compound can enhance solubility and bioactivity, allowing it to be an effective building block in various synthetic pathways or as a final pharmaceutical product.

Research surrounding this compound is ongoing, and scientists are continually uncovering new applications and mechanisms of action. The synergy between the indole structure and ammonium can lead to novel properties that are not found in simpler compounds.

Thus, 3-[2-(1H-indol-5-yloxy)-2-oxo-ethyl]hexylammonium;acetate stands as a testament to the complexity and beauty of chemical compounds, providing endless opportunities for exploration and discovery in the world of chemistry.

Synonyms
19716-83-7
HEXANOIC ACID, 3-(2-AMINOETHYL)INDOL-5-YL ESTER, MONOACETATE
3-(2-Aminoethyl)indol-5-yl ester of hexanoic acid acetate