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Benzyl(2-chloroethyl)ammonium chloride

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Identification
Molecular formula
C9H13Cl2N
CAS number
6336-51-2
IUPAC name
benzyl(2-chloroethyl)ammonium;chloride
State
State

At room temperature, Benzyl(2-chloroethyl)ammonium chloride is in a solid state.

Melting point (Celsius)
111.00
Melting point (Kelvin)
384.20
Boiling point (Celsius)
305.50
Boiling point (Kelvin)
578.70
General information
Molecular weight
204.12g/mol
Molar mass
204.1230g/mol
Density
1.1480g/cm3
Appearence

Benzyl(2-chloroethyl)ammonium chloride typically appears as a crystalline solid. Its color can range from white to off-white.

Comment on solubility

Solubility of benzyl(2-chloroethyl)ammonium;chloride

The solubility of benzyl(2-chloroethyl)ammonium;chloride can be an intriguing subject due to the presence of both organic and ionic components within its structure. Here are some key points regarding its solubility:

  • Polar Nature: The compound is polar due to the ammonium group and the chlorine atom, which enhances its interaction with polar solvents.
  • Water Solubility: It is expected to be soluble in water as ionic compounds tend to dissociate in solution, allowing the ions to interact effectively with water molecules.
  • Organic Solvents: It may have limited solubility in non-polar organic solvents due to the presence of hydrophilic groups, which do not favorably interact with non-polar environments.
  • Temperature Effects: The solubility may also depend on temperature; generally, solubility increases with temperature in many salt-like compounds.

In summary, while benzyl(2-chloroethyl)ammonium;chloride demonstrates considerable solubility in polar solvents like water, its solubility in non-polar solvents is likely minimal. This dual solubility behavior makes it a compound of interest for various applications in chemistry and biochemistry.

Interesting facts

Interesting Facts about Benzyl(2-chloroethyl)ammonium Chloride

Benzyl(2-chloroethyl)ammonium chloride is a fascinating compound with a variety of intriguing uses and properties. Here are some key points that highlight its significance:

  • Quaternary Ammonium Compound: This compound belongs to the class of quaternary ammonium salts, which are notable for their surfactant properties and disinfecting capabilities.
  • Applications in Chemistry: It serves as a versatile reagent in organic synthesis, where its unique structure aids in the formation of other important compounds.
  • Use in Biological Research: Benzyl(2-chloroethyl)ammonium chloride has been studied for its effects on biological systems, particularly in understanding cell signaling pathways and mechanisms of action in various cellular processes.
  • Industrial Significance: This compound is frequently employed in the manufacturing of coatings, textiles, and personal care products due to its ability to enhance surface activities.
  • Safety Considerations: As with many chemical compounds, proper handling and usage guidelines are essential. It’s important to observe safety protocols to mitigate any potential risks associated with its use.

In the realm of chemistry, the exploration of compounds such as benzyl(2-chloroethyl)ammonium chloride exemplifies the interplay between structure and function, revealing how minor changes in chemical makeup can lead to significant differences in behavior and application.

As one chemist once said, "The beauty of chemistry lies in the connections we draw between different compounds and their roles in our world."


Synonyms
N-(2-Chloroethyl)benzylamine hydrochloride
NSC 11462
EINECS 228-525-2
Benzenemethanamine, N-(2-chloroethyl)-, hydrochloride
BENZYLAMINE, N-(2-CHLOROETHYL)-, HYDROCHLORIDE
benzyl(2-chloroethyl)azanium;chloride