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2-Benzylsulfanylethylammonium chloride

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Identification
Molecular formula
C9H14ClNS
CAS number
69495-26-7
IUPAC name
2-benzylsulfanylethylammonium;chloride
State
State
Solid at room temperature, typically found as a crystalline or powdered form.
Melting point (Celsius)
156.00
Melting point (Kelvin)
429.15
Boiling point (Celsius)
287.00
Boiling point (Kelvin)
560.15
General information
Molecular weight
215.73g/mol
Molar mass
215.7270g/mol
Density
1.0000g/cm3
Appearence

2-Benzylsulfanylethylammonium chloride typically appears as a white to off-white crystalline solid. The powder is often fine and may have a slight odor.

Comment on solubility

Solubility of 2-benzylsulfanylethylammonium chloride

2-benzylsulfanylethylammonium chloride is an intriguing compound that showcases unique solubility characteristics. This compound's solubility can be influenced by various factors, which include:

  • Polarity: The presence of the ammonium group makes the compound relatively polar, which generally enhances solubility in polar solvents.
  • Hydrogen Bonding: The ammonium ion can participate in hydrogen bonding, which may lead to increased solubility in water and similar solvents.
  • Counterion Effects: The chloride ion serves as a counterion, which is known for good solubility in various solvent systems.
  • Hydrophobic Interactions: The benzyl group introduces hydrophobic characteristics, potentially limiting solubility in very polar solvents.

Generally, “Like dissolves like” is a rule of thumb in chemistry. Thus:

  • This compound is expected to dissolve well in water and other polar solvents.
  • However, it may exhibit reduced solubility in nonpolar solvents due to the hydrophobic nature of the benzyl group.

Understanding these factors can provide insight into the practical applications and behavior of 2-benzylsulfanylethylammonium chloride in various chemical environments.

Interesting facts

Exploring 2-benzylsulfanylethylammonium Chloride

2-benzylsulfanylethylammonium chloride is a fascinating compound that belongs to the class of ammonium salts. This compound showcases a variety of intriguing properties and potential applications that are of great interest to chemists and researchers alike.

Key Features:

  • Structure: The structure of 2-benzylsulfanylethylammonium chloride consists of a positively charged ammonium ion that is attached to a benzylsulfanyl group, providing unique reactivity and interaction potential.
  • Potential Applications: Due to its unique properties, this compound may have applications in medicinal chemistry, especially in the development of drug delivery systems.
  • Ion Interaction: As a quaternary ammonium compound, it exhibits interesting behavior in ionic interactions, which could lead to the development of new materials or catalysts.
  • Biological Activity: Research indicates that similar structures can exhibit biological activity, paving the way for further studies in pharmacology and biochemistry.

In the words of the renowned chemist Linus Pauling, "The best way to have a good idea is to have lots of ideas." This sentiment rings true in the study of compounds like 2-benzylsulfanylethylammonium chloride, where understanding one compound can lead to discoveries about many others.

Furthermore, the exploration of this ammonium salt could inspire future investigations into:

  • Novel synthesis techniques that can lead to variations of this compound.
  • New applications in the field of nanotechnology.
  • Understanding the solubility behavior in different environments, which is crucial for both industrial applications and biological systems.

With ongoing research and innovations, the potential of 2-benzylsulfanylethylammonium chloride to contribute to scientific advancements remains an exciting area of study!

Synonyms
beta-(Benzylthio)ethylamine hydrochloride
2-benzylsulfanylethylazanium;chloride
USAF A-2341
ETHYLAMINE, 2-(BENZYLTHIO)-, HYDROCHLORIDE
Ethanamine, 2-((phenylmethyl)thio)-, hydrochloride