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4,4'-Bipyridinium chloride

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Identification
Molecular formula
C10H10ClN2
CAS number
5124-97-4
IUPAC name
4-pyridin-1-ium-1-ylpyridine;chloride
State
State

At room temperature, 4,4'-Bipyridinium chloride is generally in a solid state.

Melting point (Celsius)
235.00
Melting point (Kelvin)
508.15
Boiling point (Celsius)
290.10
Boiling point (Kelvin)
563.25
General information
Molecular weight
162.57g/mol
Molar mass
162.5690g/mol
Density
1.1600g/cm3
Appearence

The compound in question typically appears as a white or pale yellow crystalline powder.

Comment on solubility

Solubility of 4-pyridin-1-ium-1-ylpyridine;chloride

The solubility of 4-pyridin-1-ium-1-ylpyridine;chloride is a significant attribute that impacts its applications in various chemical and biological contexts. Understanding its solubility can help predict its behavior in different solvents.

Key Points on Solubility:

  • Polarity: As a quaternary ammonium compound, its positive charge tends to enhance solubility in polar solvents such as water.
  • Hydrogen Bonding: The presence of nitrogen atoms can participate in hydrogen bonding, which further increases solubility in polar environments.
  • Solvent Compatibility: It is generally less soluble in non-polar solvents due to its ionic character. Polar protic solvents like methanol and ethanol can provide better solvation.

In summary, the solubility of this compound can be highlighted as follows:

  1. Highly soluble in polar solvents.
  2. Moderate solubility in some organic solvents.
  3. Minimal solubility in non-polar solvents.

As we consider the various applications for 4-pyridin-1-ium-1-ylpyridine;chloride, understanding its solubility characteristics is crucial. Its ability to dissolve in specific environments means it can successfully engage with target molecules, which is particularly important in pharmaceutical and biochemical applications.

Interesting facts

Interesting Facts about 4-pyridin-1-ium-1-ylpyridine;chloride

4-pyridin-1-ium-1-ylpyridine;chloride, often characterized by its unique nitrogen-containing aromatic structure, has garnered the attention of chemists for a variety of intriguing reasons:

  • Versatile Applications: This compound plays a significant role in both organic synthesis and medicinal chemistry. Its structure allows it to act as a building block for more complex molecules.
  • Biological Activity: Pyridine derivatives are known to exhibit various biological properties, including anti-inflammatory and anti-cancer effects, making them essential in drug design.
  • Coordination Chemistry: Due to the presence of nitrogen atoms, 4-pyridin-1-ium-1-ylpyridine can coordinate with metals, leading to the formation of various metal complexes that have applications in catalysis.
  • Electrochemical Properties: This compound demonstrates interesting electrochemical behavior. Its ability to accept and donate electrons can be crucial in the development of sensors and energy storage devices.
  • Solvatochromism: Some derivatives of pyridine show solvatochromic properties, meaning their color changes depending on the solvent used, which can be a tool for studying solvent interactions.

In conclusion, 4-pyridin-1-ium-1-ylpyridine;chloride serves as a prime example of how a single compound can have multifaceted roles in both academia and industry, providing exciting opportunities for research and application.

Synonyms
22752-98-3
4-pyridylpyridinium chloride
[1,4'-Bipyridin]-1-ium chloride
4-pyridin-1-ium-1-ylpyridine;chloride
1,4'-Bipyridinium, chloride
EINECS 245-197-6
AI3-61629
SCHEMBL1882973
DTXSID30945435
AKOS016373555
SB54025
1-(Pyridin-4-yl)pyridin-1-ium chloride
NS00085331