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Diethyl-(2-(2-nitrobenzamido)ethyl)ammonium chloride

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Identification
Molecular formula
C13H20ClN3O3
CAS number
134660-89-4
IUPAC name
diethyl-[2-[(2-nitrobenzoyl)amino]ethyl]ammonium;chloride
State
State

Diethyl-(2-(2-nitrobenzamido)ethyl)ammonium chloride is typically found as a solid at room temperature.

Melting point (Celsius)
205.00
Melting point (Kelvin)
478.15
Boiling point (Celsius)
-1.00
Boiling point (Kelvin)
-1.00
General information
Molecular weight
284.77g/mol
Molar mass
284.7320g/mol
Density
1.1940g/cm3
Appearence

This compound typically appears as a powdery solid. The color, due to the nitrobenzoyl group, can range from light yellow to off-white, depending on the purity and specific batch. It is often crystalline in nature.

Comment on solubility

Solubility of Diethyl-[2-[(2-nitrobenzoyl)amino]ethyl]ammonium Chloride

Diethyl-[2-[(2-nitrobenzoyl)amino]ethyl]ammonium chloride, with its unique molecular structure, exhibits fascinating solubility characteristics. Here are some key points regarding its solubility:

  • In general, compounds with quaternary ammonium moieties tend to show high solubility in polar solvents due to their ionic nature.
  • The presence of the nitrobenzoyl group can enhance solubility in organic solvents, making this compound more versatile in different environments.
  • Being a salt, it is expected to be readily soluble in water, particularly at elevated temperatures.
  • Compatibility with various solvents can be evaluated by observing its behavior in ethanol, methanol, and other polar solvents.

As with many chemical compounds, the solubility may be influenced by factors such as temperature, pH, and the presence of other solutes. Thus, understanding these variables is crucial in predicting solubility behavior. As we explore the solubility of this compound, one must keep in mind that "solubility is not just a trait; it is a complex interaction of molecular forces."
These interactions make it an enticing subject for further study in various chemical applications.

Interesting facts

Interesting Facts about Diethyl-[2-[(2-nitrobenzoyl)amino]ethyl]ammonium Chloride

This unique compound, known as diethyl-[2-[(2-nitrobenzoyl)amino]ethyl]ammonium chloride, belongs to a broader class of quaternary ammonium compounds that are widely studied due to their diverse applications in various fields. As a chemically rich structure, it includes both an amine functionality and a nitro group, which contribute to its distinctive behavior and potential uses.

1. Applications in Medicine

The versatility of this compound makes it a subject of interest in pharmaceutical research. Its ability to interact with biological systems can lead to developments in:

  • Drug Delivery: Its ammonium group can enhance the solubility and permeability of drug molecules, potentially improving therapeutic outcomes.
  • Antibacterial Activity: Alterations in the structure can reflect its efficacy against pathogenic bacteria, making it valuable in the development of new antibiotics.

2. Synthetic Importance

From a synthetic chemistry perspective, this compound serves as an important intermediate in various reactions. The presence of both the nitro and ethyl groups provides a rich environment for:

  • Nucleophilic Substitution Reactions: The amine group can facilitate further chemical transformations, allowing for the synthesis of more complex molecules.
  • Functionalized Derivatives: Scientists can modify this compound to create derivatives with tailored properties for specific applications, such as enhancing selectivity in biological interactions.

3. Research Potential

Ongoing studies involving diethyl-[2-[(2-nitrobenzoyl)amino]ethyl]ammonium chloride focus on:

  • Environmental Science: Understanding its stability and degradation products in various ecosystems can help assess its environmental impact.
  • Material Science: There is potential for developing novel materials that incorporate this compound, which can exhibit unique electronic or optical properties.

This compound is not just a simple formulation; it symbolizes the intricate relationship between chemical structure and function. As with many compounds in chemistry, its future applications hinge on further research and exploration in academic and industrial laboratories, echoing the sentiment that “the most profound discoveries are often hidden within the complexities of simple compounds.”

Synonyms
BENZAMIDE, N-(2-(DIETHYLAMINO)ETHYL)-o-NITRO-, HYDROCHLORIDE
1910-60-7
N-(2-(Diethylamino)ethyl)-o-nitrobenzamide hydrochloride
Benzamide, N-(2-(diethylamino)ethyl)-2-nitro-, monohydrochloride