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Benproperine Hydrochloride

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Identification
Molecular formula
C23H30ClNO3
CAS number
1235-07-0
IUPAC name
(1-ethylpiperidin-1-ium-4-yl)methyl 2-ethoxy-2,2-diphenyl-acetate;chloride
State
State

At room temperature, Benproperine Hydrochloride is in a solid state.

Melting point (Celsius)
164.50
Melting point (Kelvin)
437.70
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
429.00g/mol
Molar mass
429.0000g/mol
Density
1.1500g/cm3
Appearence

Benproperine Hydrochloride typically appears as a white to off-white crystalline powder.

Comment on solubility

Solubility of (1-ethylpiperidin-1-ium-4-yl)methyl 2-ethoxy-2,2-diphenyl-acetate;chloride

The solubility profile of the compound (1-ethylpiperidin-1-ium-4-yl)methyl 2-ethoxy-2,2-diphenyl-acetate; chloride is intriguing and multifaceted. Solubility is influenced by several key factors, which can be categorized as follows:

  • Polarity: The presence of both ionic and non-polar groups suggests ionic character may enhance solubility in polar solvents, while the diphenyl acetyl group could promote solubility in organic solvents.
  • Solvent Interaction: The solubility will vary significantly between aqueous and organic solvents. In water, as an ionic compound, it is likely to have moderate solubility due to the presence of the chloride ion, which can dissociate.
  • Functional Groups: The ethoxy and diphenyl groups may provide sites for hydrophobic interactions, enhancing solubility in non-polar solvents.
  • Temperature Effect: Generally, as temperature increases, solubility of the compound in most solvents also tends to increase; thus, understanding how temperature can impact solubility is essential.

In summary, the solubility of (1-ethylpiperidin-1-ium-4-yl)methyl 2-ethoxy-2,2-diphenyl-acetate; chloride will be subject to a balance of its ionic and hydrophobic characteristics, providing unique opportunities for interaction in various solvent systems.

Interesting facts

Interesting Facts about (1-ethylpiperidin-1-ium-4-yl)methyl 2-ethoxy-2,2-diphenyl-acetate;chloride

In the realm of organic chemistry, compounds like (1-ethylpiperidin-1-ium-4-yl)methyl 2-ethoxy-2,2-diphenyl-acetate;chloride showcase the fascinating interplay of functional groups and structural diversity. Here are some intriguing aspects of this compound:

  • Quaternary Ammonium Ion: The presence of a quaternary ammonium structure adds significant complexity to this compound. Such structures often exhibit unique properties, including enhanced solubility in water and biological systems.
  • Potential Applications: Compounds of this nature have promising applications in drug design and pharmaceutical chemistry. The ethylpiperidinium moiety has been studied for its potential in targeting various biological pathways.
  • Reactivity: The unique arrangement of the substituents in this compound might influence its reactivity, making it an interesting subject of study for synthetic organic chemists.
  • Biological Importance: Compounds with similar structures are often examined for their biological activity, including antimicrobial and neuroprotective effects. This aspect makes them critical in the development of new therapeutic agents.
  • Historical Context: The study of quaternary ammonium compounds dates back to the early 20th century, where their diverse functionalities were first explored. This highlights the evolving nature of chemistry as more applications are discovered over time.

With its intricate structure and potential for diverse applications, (1-ethylpiperidin-1-ium-4-yl)methyl 2-ethoxy-2,2-diphenyl-acetate;chloride serves as a reminder of the vast array of possibilities within the world of chemical compounds. As we continue to investigate such compounds, we may uncover new pathways for innovation in various fields, from medicine to materials science.

Synonyms
2893-42-7
Acetic acid, 2,2-diphenyl-2-ethoxy-, (1-ethyl-4-piperidyl)methyl ester, hydrochloride
2,2-Diphenyl-2-ethoxyacetic acid (1-ethyl-4-piperidyl)methyl ester hydrochloride