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Tiapride

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Identification
Molecular formula
C20H23NOS
CAS number
5001-32-1
IUPAC name
2-[(4-butylsulfanylphenyl)-(p-tolyl)methyl]sulfanyl-N,N-dimethyl-ethanamine
State
State

Tiapride is usually in solid form at room temperature, appearing as a crystalline powder. In medical applications, it may be provided in prepared solutions or as tablets.

Melting point (Celsius)
153.00
Melting point (Kelvin)
426.20
Boiling point (Celsius)
469.60
Boiling point (Kelvin)
742.80
General information
Molecular weight
317.48g/mol
Molar mass
317.4870g/mol
Density
1.1844g/cm3
Appearence

Tiapride is typically found as a white to off-white crystalline powder. It is often sold as a hydrochloride salt, which enhances its solubility in water. When prepared in pharmaceutical formulations, it is usually in the form of tablets or injectable solutions.

Comment on solubility

Solubility of 2-[(4-butylsulfanylphenyl)-(p-tolyl)methyl]sulfanyl-N,N-dimethyl-ethanamine

The solubility of 2-[(4-butylsulfanylphenyl)-(p-tolyl)methyl]sulfanyl-N,N-dimethyl-ethanamine can be influenced by various factors, making it quite complex. This particular compound, due to its diverse functional groups, may exhibit unique solubility characteristics in different solvents. Here are some key points to consider:

  • Polarity: The presence of sulfanyl (–SH) groups can enhance solubility in polar solvents, while the butyl and tolyl groups lend considerable hydrophobic character.
  • Solvent Interaction: It may be more soluble in solvents like dimethyl sulfoxide (DMSO) or methanol, which can help stabilize the molecule through hydrogen bonding and dipole interactions.
  • Temperature Dependency: Like many organic compounds, its solubility may increase with temperature, suggesting that temperature control in applications could be beneficial.
  • pH Influence: The ionization state of the amine group can also play a role in solubility, potentially becoming more soluble in acidic conditions where protonation occurs.

In summary, understanding the solubility of this compound requires consideration of its structural complexities and the solvent environment. As the saying goes, "like dissolves like," so finding the right solvent is key to optimizing solubility.

Interesting facts

Interesting Facts about 2-[(4-butylsulfanylphenyl)-(p-tolyl)methyl]sulfanyl-N,N-dimethyl-ethanamine

This fascinating compound, known for its complex structure, falls under the category of organosulfur compounds. Organosulfur chemistry is a significant sub-field due to the unique properties that sulfur introduces to molecular interactions.

Key Features:

  • Molecular Complexity: The presence of both butyl and tolyl groups indicates a degree of steric hindrance, which can greatly influence the compound's reactivity and physical properties.
  • Biological Activity: Organosulfur compounds are known for their diverse biological activities. Many such compounds possess antibacterial, antifungal, and anticancer properties. This particular structure may have potential applications in medicinal chemistry.
  • Synthetic Pathways: The synthesis of this compound may involve various methods like nucleophilic substitution reactions or reductive amination, showcasing the versatility of modern synthetic techniques.
  • Applications in Material Science: The sulfanyl groups can contribute to enhanced electrical conductivity, making such compounds suitable for applications in electronic materials and sensors.

As scientists delve deeper into the properties and applications of complex compounds like this one, it is vital to investigate how modifications in its structure can lead to novel functionalities. In the words of renowned chemist Linus Pauling, “The best way to have a good idea is to have a lot of ideas.” This statement resonates well in the realm of organic synthesis, where creativity drives exploration.

In summary, 2-[(4-butylsulfanylphenyl)-(p-tolyl)methyl]sulfanyl-N,N-dimethyl-ethanamine represents a rich field for further investigation, promising intriguing possibilities in both chemical research and practical applications.

Synonyms
VUFB2360
BRN 2298725
7799-35-1
ETHYLAMINE, 2-((p-(BUTYLTHIO)-alpha-(p-TOLYL)BENZYL)THIO)-N,N-DIMETHYL-
2-((p-(Butylthio)-alpha-(p-tolyl)benzyl)thio)-N,N-dimethylethylamine
DTXSID60999244
2-({[4-(Butylsulfanyl)phenyl](4-methylphenyl)methyl}sulfanyl)-N,N-dimethylethan-1-amine