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Propamidine isethionate

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Identification
Molecular formula
C17H20Cl2N4
CAS number
370-81-0
IUPAC name
[N'-[N'-(3,4-dichlorophenyl)carbamimidoyl]carbamimidoyl]-isopropyl-ammonium;chloride
State
State

At room temperature, propamidine isethionate is in a solid state, forming a crystalline powder.

Melting point (Celsius)
158.00
Melting point (Kelvin)
431.15
Boiling point (Celsius)
275.00
Boiling point (Kelvin)
548.15
General information
Molecular weight
364.68g/mol
Molar mass
364.6760g/mol
Density
1.3400g/cm3
Appearence

Propamidine isethionate typically appears as a white to off-white crystalline powder. It is known to be odorless.

Comment on solubility

Solubility of [N'-[N'-(3,4-dichlorophenyl)carbamimidoyl]carbamimidoyl]-isopropyl-ammonium;chloride

The solubility of the compound [N'-[N'-(3,4-dichlorophenyl)carbamimidoyl]carbamimidoyl]-isopropyl-ammonium;chloride can be discussed from several angles:

  • Type of Solvent: This compound is likely to exhibit higher solubility in polar solvents, such as water or alcohols, due to the presence of the ammonium group, which enhances its interaction with polar molecules.
  • Ionic Character: Given that it is a chloride salt, the ionic character suggests that it may dissociate readily in solution, leading to increased compatibility with solvent systems.
  • Temperature Influence: The solubility may vary significantly with temperature; typically, increasing temperature can enhance solubility for many compounds, including ionic salts.
  • Effect of pH: The pH of the solution can also influence its solubility. The ionization state of the compound may change with pH adjustments, affecting solubility and stability.

In summary, while specific solubility data for [N'-[N'-(3,4-dichlorophenyl)carbamimidoyl]carbamimidoyl]-isopropyl-ammonium;chloride may be limited, attention to the solvent type, temperature, and pH can help predict its solubility behavior. As always, experimental confirmation is essential for accurate solubility measurements.

Interesting facts

Interesting Facts about N'-[N'-(3,4-dichlorophenyl)carbamimidoyl]carbamimidoyl]-isopropyl-ammonium;chloride

This compound, often referred to in the context of its unique structure and potential applications, has garnered attention for several compelling reasons:

  • Biological Relevance: The *3,4-dichlorophenyl* moiety is known for its biological activity, making this compound a subject of interest in medicinal chemistry. Its potential therapeutic properties could be explored in the realm of pharmaceuticals, especially in drug design and development.
  • Structural Complexity: The presence of multiple functional groups such as the carbamimidoyl constitutes a fascinating aspect of its chemistry. This complex structure not only influences its reactivity but also its interaction with biological targets, paving the way for innovative uses in various chemical applications.
  • Potential Applications: Compounds with ammonium groups are often employed as catalysts and intermediates in organic synthesis. This compound could potentially be used to facilitate reactions thanks to its ability to act as a proton donor, thereby playing a significant role in acid-base chemistry.
  • Environmental Considerations: With the increasing focus on sustainability, exploring the environmental impacts and biodegradability of such compounds is crucial. Understanding how *isopropyl-ammonium* compounds behave in ecological systems can lead to more eco-friendly practices in chemistry.
  • Research Opportunities: This compound presents a wide range of research opportunities, from exploring its synthesis and characterization to investigating its interactions in pharmacological contexts. Its unique properties may inspire new studies in various scientific fields.

As we continue to innovate and discover new applications for such compounds, it becomes clear that the intersection of chemistry and biology holds promising potential. In the words of chemist Linus Pauling, "The best way to have a good idea is to have a lot of ideas." This compound exemplifies that spirit of exploration in the scientific community.