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Etomidate hydrochloride

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Identification
Molecular formula
C15H24ClN2O2
CAS number
33125-97-2
IUPAC name
(1-ethylpiperidin-1-ium-3-yl)methyl N-(o-tolyl)carbamate;chloride
State
State

At room temperature, etomidate hydrochloride is in the form of a solid crystalline powder.

Melting point (Celsius)
60.00
Melting point (Kelvin)
333.15
Boiling point (Celsius)
80.00
Boiling point (Kelvin)
353.15
General information
Molecular weight
344.86g/mol
Molar mass
344.8630g/mol
Density
1.1000g/cm3
Appearence

The compound typically appears as a white to off-white crystalline powder.

Comment on solubility

Solubility of (1-ethylpiperidin-1-ium-3-yl)methyl N-(o-tolyl)carbamate;chloride

The solubility of (1-ethylpiperidin-1-ium-3-yl)methyl N-(o-tolyl)carbamate;chloride is influenced by several key factors that can dictate its behavior in various solvents. Here are some observations:

  • Polarity of Solvent: Because this compound contains both ionic and polar covalent characteristics, it is likely to exhibit solubility in polar solvents such as water, while being less soluble in non-polar solvents.
  • Hydrogen Bonding: The amine and carbamate functional groups can participate in hydrogen bonding, enhancing solubility in polar solvents.
  • Concentration Gradient: Increased temperature often leads to increased solubility as it enhances the kinetic energy of molecules, allowing for better interactions.
  • pH Influence: The solubility may vary depending on the pH of the solution, as deprotonation of certain groups can lead to increased solubility.

As a result of these factors, one might expect a varied solubility profile that is sensitive to the environment. When testing solubility, it is always important to consider the specific solvent conditions and the potential interactions that may affect dissolution.

Interesting facts

Interesting Facts about (1-ethylpiperidin-1-ium-3-yl)methyl N-(o-tolyl)carbamate;chloride

The compound (1-ethylpiperidin-1-ium-3-yl)methyl N-(o-tolyl)carbamate;chloride is a fascinating example of a charged organic compound that showcases the diversity of chemical interactions and applications in the pharmaceutical and agrochemical fields.

Key Features

  • Quaternary Ammonium Structure: The presence of the quaternary ammonium group gives this compound unique properties, as it is likely to exhibit both cationic behavior and increased solubility in polar solvents, making it of high interest in various chemical applications.
  • Biological Activity: Many compounds with structures similar to this one are known for their biological activities, potentially serving as intermediates in drug synthesis or as active ingredients in pesticides. The interaction of the piperidine ring with biological systems can lead to significant medicinal effects.
  • Application Potential: Due to its structure, this compound might be extensively studied for its potential in drug delivery systems or as a catalyst in organic reactions due to its ionic nature.

Scientific Significance

This compound underscores the importance of studying not just individual molecules but also the effects of their interactions in larger systems. As chemists explore the properties of such ammonium salts, they can optimize the design of new materials for specific needs in medicinal chemistry and agriculture. Understanding the reactivity and stability of this compound can also contribute to a wider array of applications, including:

  • Development of targeted therapies in medicine.
  • Enhanced formulation methods in agrochemicals.
  • Investigation as a potential ionic liquid, given its charged nature.

As we continue to explore compounds like (1-ethylpiperidin-1-ium-3-yl)methyl N-(o-tolyl)carbamate;chloride, we may uncover even more innovative applications that could revolutionize our approach to chemistry and its practical uses.

Synonyms
o-Methylcarbanilic acid (1-ethyl-3-piperidyl)methyl ester hydrochloride
20930-84-1
CARBANILIC ACID, o-METHYL-, (1-ETHYL-3-PIPERIDYL)METHYL ESTER, MONOHYDROCHLORIDE