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Lobeline hydrochloride

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Identification
Molecular formula
C22H27NO2Cl
CAS number
90-70-4
IUPAC name
(2-oxo-1,2-diphenyl-ethyl)-(2-phenylethyl)ammonium;chloride
State
State

At room temperature, lobeline hydrochloride is typically in a solid state, possessing a stable crystalline form.

Melting point (Celsius)
110.00
Melting point (Kelvin)
383.00
Boiling point (Celsius)
260.00
Boiling point (Kelvin)
533.00
General information
Molecular weight
371.87g/mol
Molar mass
371.8730g/mol
Density
1.1910g/cm3
Appearence

Lobeline hydrochloride appears as a white to off-white crystalline powder. It is often utilized in a laboratory setting and is known for its distinct appearance which may also be described as fibrous.

Comment on solubility

Solubility of (2-oxo-1,2-diphenyl-ethyl)-(2-phenylethyl)ammonium;chloride

The solubility of this compound, (2-oxo-1,2-diphenyl-ethyl)-(2-phenylethyl)ammonium;chloride, can be influenced by several factors including polarity, temperature, and the solvent used. Here are some key points to consider:

  • Solvent Effects: Typically, this compound may be more soluble in polar solvents such as water or alcohols due to the presence of the ammonium group, which can engage in hydrogen bonding.
  • Temperature Dependence: Solubility can increase with temperature; thus, dissolution in higher temperatures can improve solubility for many ionic compounds.
  • Ionic Nature: As it contains a chloride ion, it suggests the compound may dissociate in solution, enhancing its solubility.
  • Concentration Variability: At higher concentrations, the solubility might limit due to precipitation, forming a saturated solution.

In summary, while it is anticipated that this compound exhibits fair solubility in polar solvents due to its ionic character, experimental determination is key for precise values. The behavior of such a compound in solution can often be summed up with the phrase: “Like dissolves like”, emphasizing the role of polarity in solubility.

Interesting facts

Interesting Facts about (2-oxo-1,2-diphenyl-ethyl)(2-phenylethyl)ammonium;chloride

This intriguing compound, known as (2-oxo-1,2-diphenyl-ethyl)(2-phenylethyl)ammonium chloride, has piqued the interest of chemists due to its unique structure and potential applications. Here are some fascinating insights into this compound:

  • Complex Structure: The compound features an ammonium group, which is essential in organic chemistry for forming ionic bonds. Its dual phenyl groups contribute to significant steric hindrance, affecting its reactivity and interactions with other molecules.
  • Biological Implications: Compounds with ammonium groups are often studied for their biological activities. Many ionic compounds have been found to exhibit antimicrobial properties or act as medication precursors in drug development.
  • Potential Applications: This compound might be relevant in areas such as pharmaceutical chemistry, material science, or catalysis, where ionic interactions can play a crucial role in the efficacy of drug formulations or the efficiency of chemical reactions.
  • Research Interest: The unique combination of the 2-oxo group and the diphenyl moiety makes this compound a exciting subject for ongoing research. It's essential in developing new methodologies for synthesizing complex organic molecules.
  • Intermolecular Interactions: The ionic nature of the compound allows it to engage in a range of intermolecular interactions, making it useful in studies related to solubility and ionic strength in various solvents.

In conclusion, the study of (2-oxo-1,2-diphenyl-ethyl)(2-phenylethyl)ammonium chloride encapsulates a blend of organic chemistry concepts, highlighting the significance of molecular structure in determining functional properties. With further research, this compound could unlock valuable advancements within multiple scientific fields.

Synonyms
2-(Phenethylamino)-2-phenyl-acetophenone hydrochloride
6312-35-2
NSC 40323
ACETOPHENONE, 2-(PHENETHYLAMINO)-2-PHENYL-, HYDROCHLORIDE