Skip to main content

Trimetaphan camsilate

ADVERTISEMENT
Identification
Molecular formula
C17H25Cl2N2
CAS number
7142-64-9
IUPAC name
(2-chlorophenyl)methyl-[[4-[[(2-chlorophenyl)methylammonio]methyl]-1-bicyclo[2.2.2]octanyl]methyl]ammonium;dichloride
State
State

At room temperature, Trimetaphan camsilate is typically in a solid-state, provided as a crystalline powder. It is intended for medicinal use, usually after being dissolved in solution for intravenous administration.

Melting point (Celsius)
210.00
Melting point (Kelvin)
483.15
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.15
General information
Molecular weight
431.39g/mol
Molar mass
431.3870g/mol
Density
1.8000g/cm3
Appearence

Trimetaphan camsilate is typically available as a white or slightly off-white crystalline powder. It is hygroscopic, meaning it can absorb moisture from the air, and is often supplied in solid form for reconstitution before use.

Comment on solubility

Solubility of (2-chlorophenyl)methyl-[[4-[[(2-chlorophenyl)methylammonio]methyl]-1-bicyclo[2.2.2]octanyl]methyl]ammonium;dichloride

The solubility of the compound (2-chlorophenyl)methyl-[[4-[[(2-chlorophenyl)methylammonio]methyl]-1-bicyclo[2.2.2]octanyl]methyl]ammonium;dichloride is influenced by various factors given its complex structure. Understanding the solubility is crucial, as it affects the compound's behavior in different environments.

Factors Affecting Solubility:

  • Polarity: Due to the presence of polar functional groups, this compound may exhibit increased solubility in polar solvents such as water.
  • Ionic Nature: The dichloride component implies ionic character, which typically enhances solubility in aqueous media.
  • Temperature: Higher temperatures can increase solubility for many compounds, leading to increased molecular movement.
  • pH of the Solution: The pH can significantly affect the ionization of the ammonium groups, further influencing solubility.

Overall, while predicting the exact solubility is challenging without empirical data, we can infer that this compound may show a moderate to high solubility in water and other polar solvents, primarily due to its ionic and polar characteristics. Thus, it becomes essential to test various conditions to attain comprehensive solubility data.

Interesting facts

Interesting Facts about (2-chlorophenyl)methyl-[[4-[[(2-chlorophenyl)methylammonio]methyl]-1-bicyclo[2.2.2]octanyl]methyl]ammonium;dichloride

This compound, with its complex name reflecting its intricate structure, is a fascinating example of modern synthetic chemistry. Here are some engaging aspects of this compound:

  • Structure Complexity: The presence of bicyclo[2.2.2]octanyl units alongside multiple ammonium groups contributes to its unique three-dimensional architecture, which can influence its biological activity and interactions.
  • Chlorophenyl Groups: The inclusion of 2-chlorophenyl moieties not only adds to the compound's structural diversity but could also play a significant role in its pharmacological properties, as chlorinated aromatic systems often exhibit interesting reactivity and biological effects.
  • Quaternary Ammonium Compounds: Being a quaternary ammonium compound, it can have unique surfactant properties that make it useful in various applications including antimicrobial activity. Compounds in this class are known for their use in pharmaceuticals and as disinfectants.
  • Potential Applications: Due to its molecular characteristics, this compound may hold promise in drug design, particularly in the development of neuromodulators or antitumor agents, making it a subject of interest in medicinal chemistry.
  • Emerging Research: Current studies are focusing on how the structural features of such complex molecules can enhance selectivity and reduce side effects in therapeutic contexts, emphasizing the importance of chemical structure in drug efficacy.

In summary, the multifaceted nature of this compound opens doors to numerous research avenues, making it an exciting topic for both chemists and pharmacologists alike.

Synonyms
1,4-Bicyclo(2.2.2)octanebis(methylamine), N,N'-bis(2-chlorobenzyl)-, dihydrochloride
1877-12-9
Benzylamine, N,N'-(1,4-bicyclo(2.2.2)octylenedimethylene)bis(2-chloro-, dihydrochloride
N,N'-(1,4-Bicyclo(2.2.2)octylenedimethylene)bis(2-chlorobenzylamine) dihydrochloride
N,N'-Bis(2-chlorobenzyl)-1,4-bicyclo(2.2.2)octanebis(methylamine) dihydrochloride