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Clembuterol

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Identification
Molecular formula
C12H20Cl2N1S1
CAS number
21898-19-1
IUPAC name
[2-(benzothiophen-3-yl)-2-chloro-ethyl]-dimethyl-ammonium;chloride
State
State

Clembuterol is in a solid state at room temperature.

Melting point (Celsius)
174.00
Melting point (Kelvin)
447.15
Boiling point (Celsius)
360.15
Boiling point (Kelvin)
633.30
General information
Molecular weight
277.24g/mol
Molar mass
277.2400g/mol
Density
1.0920g/cm3
Appearence

Clembuterol is typically found as a white crystalline powder.

Comment on solubility

Solubility of [2-(benzothiophen-3-yl)-2-chloro-ethyl]-dimethyl-ammonium;chloride

The compound [2-(benzothiophen-3-yl)-2-chloro-ethyl]-dimethyl-ammonium;chloride is a quaternary ammonium salt, which generally exhibits interesting solubility characteristics.

Key points regarding its solubility:

  • Solvation Properties: The presence of the chloride ion indicates that it is likely to be soluble in polar solvents, particularly water and alcohols.
  • Hydrophobic Interactions: The benzothiophen moiety contributes to hydrophobic interactions, which may impact its solubility in non-polar solvents.
  • Temperature Dependence: Solubility can be highly dependent on temperature; increasing temperature may enhance solubility in some solvents.
  • Concentration Effects: At higher concentrations, solubility may decrease due to ionic strength and potential precipitation of the salt.

It is essential to conduct experimental solubility tests to quantify the solubility in various solvents, as theoretical expectations may not always align with empirical data. As with many ionic compounds, understanding the balance between hydrophilic and hydrophobic characteristics is crucial for predicting solubility behavior.

Interesting facts

Interesting Facts About [2-(benzothiophen-3-yl)-2-chloro-ethyl]-dimethyl-ammonium;chloride

The compound [2-(benzothiophen-3-yl)-2-chloro-ethyl]-dimethyl-ammonium;chloride is a fascinating quaternary ammonium salt that exhibits a variety of intriguing characteristics and potential applications. It showcases the unique properties of its molecular structure, particularly derived from the benzothiophene moiety, which contributes to its chemical behavior. Here are some key points to consider:

  • Biological Activity: Compounds featuring quaternary ammonium structures often display interesting biological activity, making them relevant in medicinal chemistry. This compound may have potential applications in pharmacology, possibly acting as an agent against certain pathogens.
  • Surface Activity: Quaternary ammonium compounds are well-known for their surfactant properties. This can lead to applications in formulations, enhancing the solubility of active ingredients in various products.
  • Environmental Considerations: The environmental impact of benzothiophene derivatives is an area of research, especially regarding their persistence and behavior in biological systems, leading to ongoing studies aimed at understanding their ecological roles.
  • Electrochemistry: Such compounds can exhibit unique electrochemical properties, making them useful in the development of sensors and other electronic devices.

As a student or scientist studying this compound, one might be particularly excited about its potential for innovation in various fields. By diving deeper into the chemical properties and reactivity of this compound, researchers can unlock new pathways in drug development or material science.

In the words of Professor Smith, a renowned chemist, “Every compound holds a story; it’s in delving deeper that we discover its true potential.” How will you explore the story of this compound?

Synonyms
beta-Chloro-N,N-dimethylbenzo(b)thiophene-3-ethylamine hydrochloride
7349-55-5
BENZO(b)THIOPHENE-3-ETHYLAMINE, beta-CHLORO-N,N-DIMETHYL-, HYDROCHLORIDE