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Ethnchlorvynol

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Identification
Molecular formula
C15H20ClN
CAS number
5577-95-9
IUPAC name
2-chloroethyl-ethyl-(2-naphthylmethyl)ammonium;chloride
State
State

It is generally found in a solid crystalline state at room temperature.

Melting point (Celsius)
177.00
Melting point (Kelvin)
450.00
Boiling point (Celsius)
320.00
Boiling point (Kelvin)
593.00
General information
Molecular weight
310.83g/mol
Molar mass
310.8320g/mol
Density
1.0800g/cm3
Appearence

This compound typically appears as a white crystalline powder.

Comment on solubility

Solubility of 2-chloroethyl-ethyl-(2-naphthylmethyl)ammonium chloride

The solubility of 2-chloroethyl-ethyl-(2-naphthylmethyl)ammonium chloride is influenced by several factors, primarily its polar characteristics due to the presence of the quaternary ammonium group. This compound generally exhibits moderate solubility in polar solvents, particularly in water and alcohols, while showing significantly lower solubility in non-polar solvents such as hexane.

Key Points on Solubility:

  • Water Solubility: As a quaternary ammonium salt, it is expected to be soluble in water due to ion-dipole interactions.
  • Alcohol Solubility: It can dissolve in alcohols, which can help to stabilize the ionic nature of the compound.
  • Non-Polar Solvents: The presence of hydrophobic naphthalene moieties results in lower solubility in non-polar environments.

This duality in solubility highlights the importance of considering solvent polarity when evaluating ionic compounds like this. Overall, while 2-chloroethyl-ethyl-(2-naphthylmethyl)ammonium chloride is not freely soluble in all solvents, its solubility profile can be effectively exploited in various chemical contexts, particularly in formulations where both polar and non-polar properties are desired.

Interesting facts

Interesting Facts about 2-Chloroethyl-ethyl-(2-naphthylmethyl)ammonium Chloride

2-Chloroethyl-ethyl-(2-naphthylmethyl)ammonium chloride is a fascinating compound that falls into the category of quaternary ammonium salts, which have a variety of applications in both the industrial and medical fields.

Key Characteristics

  • Quaternary Ammonium Salt: This compound features a positively charged nitrogen atom bonded to four organic groups, characteristic of quaternary ammonium compounds.
  • Potential Biological Activity: These types of compounds are often evaluated for their antibacterial and antifungal activities, making them of interest in drug development and hygiene products.
  • Versatile Applications: Quaternary ammonium salts are used in various applications such as surfactants, disinfectants, and phase transfer catalysts.

Historical Perspective

The study of ammonium salts dates back to the 19th century, where they were initially explored for their utility in various chemical reactions. The introduction of complex structures, like that of 2-chloroethyl-ethyl-(2-naphthylmethyl)ammonium chloride, showcases the advancements in organic synthesis and modification. As scientists aimed to synthesize more complex structures, compounds like this became important for both theoretical studies and practical applications.

Notable Reactions

  • Reactivity: The presence of a chlorine atom in the 2-chloroethyl group can facilitate nucleophilic substitution reactions, making this compound a useful intermediate in various synthesis pathways.
  • Biochemical Interactions: This compound can interact with biological membranes, raising questions about its interactions at the cellular level and its potential utility as a drug delivery system.

This compound exemplifies the complexity and potential of modern chemistry, emphasizing how quaternary ammonium compounds can bridge the gap between synthetic chemistry and practical applications. As research evolves, so does the understanding and utility of compounds like 2-chloroethyl-ethyl-(2-naphthylmethyl)ammonium chloride in addressing contemporary challenges in fields such as pharmacology and materials science.

Synonyms
2-NAPHTHALENEMETHYLAMINE, N-(2-CHLOROETHYL)-N-ETHYL-, HYDROCHLORIDE
2-Chloro-N-(2-naphthalenemethyl)diethylamine hydrochloride
N-(2-Chloroethyl)-N-ethyl-2-naphthaleneamine hydrochloride
1215-34-5
NSC 11487
Diethylamine, 2-chloro-N-(2-naphthalenemethyl)-, hydrochloride