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Colterol hydrochloride

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Identification
Molecular formula
C14H23ClNO
CAS number
79660-73-6
IUPAC name
(4-allyloxy-3,5-dipropyl-phenyl)methyl-dimethyl-ammonium;chloride
State
State

At room temperature, Colterol hydrochloride is a solid. It is stable under normal conditions and should be stored in a dry environment.

Melting point (Celsius)
170.00
Melting point (Kelvin)
443.00
Boiling point (Celsius)
285.00
Boiling point (Kelvin)
558.00
General information
Molecular weight
313.89g/mol
Molar mass
313.8870g/mol
Density
1.0183g/cm3
Appearence

Colterol hydrochloride appears as a white to off-white crystalline powder. It is typically odorless and has a bitter taste.

Comment on solubility

Solubility of (4-allyloxy-3,5-dipropyl-phenyl)methyl-dimethyl-ammonium;chloride

The solubility of the compound (4-allyloxy-3,5-dipropyl-phenyl)methyl-dimethyl-ammonium;chloride can be influenced by multiple factors, including its structural characteristics and the properties of the solvent used. Here are some key points to consider:

  • Solvent Compatibility: This compound tends to be soluble in polar solvents due to its ammonium group, which can interact favorably with polar molecules.
  • Ionic Nature: As a quaternary ammonium salt, its chloride counterpart contributes to its solubility, particularly in aqueous solutions.
  • Hydrophobic Interactions: The presence of the dipropyl and allyloxy groups can create hydrophobic regions that might limit solubility in purely non-polar solvents.

In general, it is expected that the solubility will be higher in water and organic solvents that exhibit polar characteristics. However, due to the bulky groups attached to the ammonium, solubility might not be absolute, and concentration limits can play a significant role:

  • Higher concentrations: May lead to decreased solubility as saturation can be reached.
  • Temperature Effects: Elevated temperatures commonly increase the solubility of many compounds, and this may hold true for this quaternary ammonium salt.

Thus, if experimenting with (4-allyloxy-3,5-dipropyl-phenyl)methyl-dimethyl-ammonium;chloride, it is advisable to consider both the solvent choice and the conditions to optimize its solubility.

Interesting facts

Interesting Facts about (4-allyloxy-3,5-dipropyl-phenyl)methyl-dimethyl-ammonium;chloride

(4-allyloxy-3,5-dipropyl-phenyl)methyl-dimethyl-ammonium;chloride is a fascinating compound that showcases the versatility and complexity of organic chemistry. Here are some intriguing aspects:

  • Quaternary Ammonium Compound: This compound features a quaternary ammonium structure, which plays a significant role in various applications, particularly as surfactants and disinfectants.
  • Biological Activity: Compounds like this one often exhibit biocidal properties, making them valuable in pharmaceutical and agricultural settings by helping to combat pathogens.
  • Electrophilic Behavior: The presence of the allyloxy group can enhance the electrophilicity of the compound, potentially allowing for interesting reactivity in synthetic chemistry.
  • Potential Uses: Quaternary ammonium compounds are often used in hair conditioners, antiseptics, and even as ionic liquids, showcasing their adaptability in different fields.
  • Color and Charge: The behavior of this ionic compound provides insights into how different groups contribute to overall charge distribution and polarization.

As science continues to explore the intricacies of chemical compounds, studying (4-allyloxy-3,5-dipropyl-phenyl)methyl-dimethyl-ammonium;chloride allows researchers to further understand their properties and potential for innovation in various fields, including medicine and materials science.

In the words of a famous chemist, "Chemistry is the magic that transforms the ordinary into the extraordinary!" This compound is a perfect example of that transformative power.

Synonyms
NSC 37930
4-Allyloxy-N,N-dimethyl-3,5-dipropylbenzylamine hydrochloride
BENZYLAMINE, 4-(ALLYLOXY)-N,N-DIMETHYL-3,5-DIPROPYL-, HYDROCHLORIDE
7229-44-9