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Tropisetron Hydrochloride

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Identification
Molecular formula
C17H20ClNS
CAS number
105826-92-4
IUPAC name
dimethyl-[1-methyl-3,3-bis(2-thienyl)allyl]ammonium;chloride
State
State

At room temperature, Tropisetron Hydrochloride is in a solid state.

Melting point (Celsius)
180.00
Melting point (Kelvin)
453.15
Boiling point (Celsius)
293.00
Boiling point (Kelvin)
566.15
General information
Molecular weight
290.86g/mol
Molar mass
290.8570g/mol
Density
1.2330g/cm3
Appearence

Tropisetron Hydrochloride appears as a white to off-white crystalline powder.

Comment on solubility

Solubility of Dimethyl-[1-methyl-3,3-bis(2-thienyl)allyl]ammonium Chloride

Dimethyl-[1-methyl-3,3-bis(2-thienyl)allyl]ammonium chloride is an ionic compound and its solubility is influenced by several factors. Known for exhibiting interesting solvation properties, its solubility in water can be characterized by the following points:

  • Ionic Nature: The presence of the ammonium cation and the chloride anion contributes to its general solubility in polar solvents, particularly water.
  • Hydrophilicity: The structure includes polar functional groups which enhance its interaction with water molecules, promoting solubility.
  • Concentration Dependency: Like many salts, the solubility can vary depending on the temperature and the concentration of the solution.
  • Complex Formation: The ability of the compound to form complexes with solvents can also impact how readily it dissolves.

Overall, while specific solubility data may vary, one can expect that dimethyl-[1-methyl-3,3-bis(2-thienyl)allyl]ammonium chloride will exhibit moderate to high solubility in aqueous environments. As a general rule, the solubility profiles of such compounds should always be confirmed through experimental data for precise applications.

Interesting facts

Interesting Facts About Dimethyl-[1-methyl-3,3-bis(2-thienyl)allyl]ammonium Chloride

This remarkable compound, known as dimethyl-[1-methyl-3,3-bis(2-thienyl)allyl]ammonium chloride, is part of the broader family of quaternary ammonium salts, which exhibit unique properties making them valuable in various applications.

Key Characteristics

  • Versatile Applications: This compound showcases potential in medicinal chemistry and material science, serving as a precursor for synthesizing more complex structures.
  • Chirality: The presence of specific alkyl groups in its structure introduces chirality, which may have implications for its biological activity.
  • Electrochemical Properties: Compounds like this may exhibit interesting electrochemical characteristics, opening avenues for research in sensors and batteries.

Chemical Family and Synthesis

Dimethyl-[1-methyl-3,3-bis(2-thienyl)allyl]ammonium chloride is synthesized through a straightforward reaction involving the appropriate precursors, typically requiring the following:

  1. Amine precursors
  2. Allyl halides
  3. Thienyl compounds for the bis substituents

This synthesis highlights a common strategy in organic chemistry where various functionalities are incorporated systematically to fine-tune the final product's properties.

Biological Relevance

Research has suggested that quaternary ammonium compounds can possess antimicrobial properties, making them potential candidates for disinfectants or antiseptics. Given the increasing concern over antibiotic resistance, this compound's structure may warrant further investigation for its viability as a safe and effective substitute.

In summary, dimethyl-[1-methyl-3,3-bis(2-thienyl)allyl]ammonium chloride presents exciting opportunities not only within the laboratory but also in real-world applications. As we continue to explore its properties and potential, it stands as a testament to the innovative spirit of modern chemistry.

Synonyms
Dimethylthiambutene hydrochloride
Ohton hydrochloride
5786-77-6
3-Buten-2-amine, N,N-dimethyl-4,4-di-2-thienyl-, hydrochloride
ZI2995I73Y
Dimethylthiambutene HCl
UNII-ZI2995I73Y
3,3-Di-2-thienyl-N,N,1-trimethylallylamine hydrochloride
ALLYLAMINE, 3,3-DI-2-THIENYL-N,N,1-TRIMETHYL-, HYDROCHLORIDE
FD22411
N,N-Dimethyl-4,4-di-2-thienyl-3-buten-2-amine hydrochloride;Aminobutene hydrochloride;Dimethibutin hydrochloride