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Vortioxetine hydrobromide

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Identification
Molecular formula
C18H23BrN2O5
CAS number
146234-92-4
IUPAC name
5-[4-(2-propylsulfanylphenyl)piperazin-1-ium-1-yl]pentyl N-ethylcarbamate;chloride
State
State

At room temperature, Vortioxetine hydrobromide is found in a solid state, appearing primarily as a stable crystalline powder suitable for formulation into pharmaceutical preparations.

Melting point (Celsius)
234.00
Melting point (Kelvin)
507.00
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
298.46g/mol
Molar mass
298.4590g/mol
Density
1.3600g/cm3
Appearence

Vortioxetine hydrobromide is generally available as a white to very slightly beige powder. It may change color slightly depending on its purity and the methods used during its synthesis and isolation.

Comment on solubility

Solubility Characteristics

The solubility of 5-[4-(2-propylsulfanylphenyl)piperazin-1-ium-1-yl]pentyl N-ethylcarbamate; chloride is influenced by several important factors:

  • Polarity: This compound contains both polar and non-polar functional groups, which can lead to variable solubility in different solvents.
  • Ionization: As a quaternary ammonium salt, the chloride component indicates good solubility in polar solvents like water due to its ionic nature.
  • Hydrophilicity and Hydrophobicity: The presence of the piperazine and carbamate groups may enhance hydrophilicity while the alkyl chains introduce hydrophobic characteristics, suggesting possible solubility in organic solvents.
  • Temperature Effects: Solubility may increase with higher temperatures, making it essential to consider temperature when evaluating its solubility in various solvents.

Overall, the solubility of this compound is likely to be favorable in polar solvents, while its behavior in non-polar solvents would need to be assessed experimentally.

Interesting facts

Interesting Facts about 5-[4-(2-Propylsulfanylphenyl)piperazin-1-ium-1-yl]pentyl N-ethylcarbamate;chloride

This intriguing compound, often referred to in scientific literature, showcases the dynamic interplay between organic synthesis and pharmacological applications. Here are some key points that capture the fascination of this chemical:

  • Applications in Medicine: Compounds like this one are often investigated for their potential therapeutic effects, particularly in the field of psychopharmacology, where modifications can lead to substances that act on neurotransmitter systems.
  • Structural Diversity: The molecule features a piperazine ring, a common motif in many pharmaceuticals, which allows for versatile interactions with biological receptors and can enhance bioactivity.
  • Sulfanyl Group Influence: The presence of the propylsulfanyl moiety plays a significant role in the compound's properties, influencing both its solubility and interaction with other biological molecules.
  • Carbamate Functionality: The N-ethylcarbamate portion suggests potential utility in agricultural applications or as a precursor in further synthetic endeavors, highlighting the compound's versatility beyond medicinal chemistry.
  • Stability and Reactivity: The incorporation of chloride ion implies an ionic nature that can contribute to the overall stability of the compound, making it suitable for various applications, from laboratory research to practical use in drug development.
  • Potential Discoveries: Researchers are actively exploring the effects of structurally related compounds on biological systems, which can lead to significant advances in understanding and treating complex diseases.

As we delve deeper into the complex world of chemical compounds like 5-[4-(2-propylsulfanylphenyl)piperazin-1-ium-1-yl]pentyl N-ethylcarbamate;chloride, we unlock new possibilities in science and medicine. Such compounds are essential not just for their individual properties but also for their contributions to broader scientific knowledge and discoveries.

Synonyms
CI 384 hydrochloride
CI 384 HCl
4-(o-Propylthiophenyl)-1-piperazinepentanol N-ethyl carbamate hydrochloride
5697-50-7
Carbamic acid, ethyl-, 5-(4(o-(propylthio)phenyl)-1-piperazinyl)pentyl ester, hydrochloride