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DEAE chloride

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Identification
Molecular formula
C17H21Cl2N
CAS number
56-34-8
IUPAC name
benzhydryl-(2-chloroethyl)-ethyl-ammonium;chloride
State
State

At room temperature, DEAE chloride is typically found in a solid state.

Melting point (Celsius)
149.00
Melting point (Kelvin)
422.15
Boiling point (Celsius)
327.00
Boiling point (Kelvin)
600.15
General information
Molecular weight
269.22g/mol
Molar mass
269.2200g/mol
Density
1.0250g/cm3
Appearence

DEAE chloride typically appears as a white crystalline solid. It can be hygroscopic, absorbing moisture from the air, which may affect its appearance and handling.

Comment on solubility

Solubility of Benzhydryl-(2-chloroethyl)-ethyl-ammonium; Chloride

The solubility of the compound benzhydryl-(2-chloroethyl)-ethyl-ammonium; chloride can be described as follows:

  • Nature of the Compound: As a quaternary ammonium salt, it typically exhibits characteristics similar to other ammonium compounds.
  • Solvent Interaction: It is generally soluble in polar solvents, particularly water, due to its ionic nature stemming from the presence of chloride ions.
  • Hydrophobic Character: The benzhydryl group contributes to hydrophobic interactions. Thus, while there's significant solubility in water, solubility may decrease in non-polar solvents.
  • Temperature Dependency: Solubility may increase with temperature, which is often the case for ionic compounds in aqueous solutions.

In summary, the solubility of benzhydryl-(2-chloroethyl)-ethyl-ammonium; chloride is generally good in polar solvents, especially water, though it may vary based on environmental factors such as temperature and the presence of other solutes. Understanding these properties is essential for applications in various chemical processes.

Interesting facts

Interesting Facts about Benzyhydryl-(2-chloroethyl)-ethyl-ammonium Chloride

Benzhydryl-(2-chloroethyl)-ethyl-ammonium chloride is a fascinating compound that can be explored through various aspects, ranging from its chemical structure to its applications in modern research. Here are some intriguing details:

Chemical Structure

  • The compound contains a benzhydryl group, which is a phenyl ring connected to another phenyl group, making it quite complex and interesting from a structural standpoint.
  • Its structure includes a 2-chloroethyl group, increasing its reactivity and potential applications, particularly in medicinal chemistry.
  • The ethyl-ammonium portion introduces basicity into the compound, which can influence how it interacts with other chemical species.

Applications

  • This compound is often studied for its potential use in drug development; specifically, it has been investigated for its pharmacological properties.
  • Due to the presence of the quaternary ammonium ion, it may act as an effective surfactant or antimicrobial agent.

Research Insights

Researchers are particularly interested in compounds such as this due to their potential applications in the following areas:

  • Medicinal Chemistry: The unique structure could lead to bioactive molecules that target specific biological pathways.
  • Biological Activity: Preliminary studies suggest that its derivatives may exhibit interesting anti-cancer properties.
  • Surface Chemistry: The quaternary ammonium nature could provide insights into novel surfactant molecules.

As a compound with diverse functionalities, benzhydryl-(2-chloroethyl)-ethyl-ammonium chloride exemplifies the creativity and complexity found in the field of organic chemistry.

To truly appreciate the significance of this compound, it's essential to consider how its unique structure can lead to innovative solutions in various scientific domains.

Synonyms
N-(2-Chloroethyl)-N-ethyl-alpha-phenylbenzylamine hydrochloride
5965-87-7
SY 2
ST 2
N-Benzohydryl-N-ethyl-beta-chloroethylamine hydrochloride
Diethylamine, 2-chloro-N-(diphenylmethyl)-, hydrochloride
Diethylamine, 2-chloro-N-(alpha-phenylbenzyl)-, hydrochloride
Benzenemethanamine, N-(2-chloroethyl)-N-ethyl-alpha-phenyl-, hydrochloride
BENZYLAMINE, N-(2-CHLOROETHYL)-N-ETHYL-alpha-PHENYL-, HYDROCHLORIDE