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Pralidoxime Chloride

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Identification
Molecular formula
C7H9ClN2O2
CAS number
51-15-0
IUPAC name
2-piperidin-1-ium-1-ylethyl N-(2,6-dibromophenyl)carbamate;chloride
State
State

Pralidoxime chloride exists as a solid at room temperature. It is stable under normal conditions but should be handled with care as it is intended for specific medical uses.

Melting point (Celsius)
215.00
Melting point (Kelvin)
488.15
Boiling point (Celsius)
205.00
Boiling point (Kelvin)
478.15
General information
Molecular weight
172.57g/mol
Molar mass
172.5730g/mol
Density
0.6005g/cm3
Appearence

Pralidoxime chloride typically appears as a white solid crystalline powder. It is often used in its crystal form, although it can also be processed into solutions for various applications.

Comment on solubility

Solubility of 2-piperidin-1-ium-1-ylethyl N-(2,6-dibromophenyl)carbamate;chloride

The solubility characteristics of the compound 2-piperidin-1-ium-1-ylethyl N-(2,6-dibromophenyl)carbamate;chloride are influenced by its unique structure, which incorporates both an ionic and an organic moiety. Typically, compounds containing ionic components, such as chloride ions, exhibit good solubility in polar solvents like water.

Key points to consider regarding the solubility of this compound include:

  • Polar Nature: The ionic piperidinium portion suggests enhanced solubility in polar solvents.
  • Hydrophilicity: The presence of the carbamate group may contribute to additional hydrogen bonding capabilities with water molecules.
  • Effect of Bromine: The dibromophenyl group may affect solubility due to steric hindrance and hydrophobic interactions, potentially decreasing solubility in non-polar solvents.

In general, one might expect that:

  • Water solubility: Likely high due to the ionic nature, possibly leading to complete dissolution.
  • Organic solvent solubility: Varied, potentially moderate in polar aprotic solvents.
  • Temperature dependence: Solubility often increases with temperature, allowing for better dissolution in various media.

Overall, the solubility of 2-piperidin-1-ium-1-ylethyl N-(2,6-dibromophenyl)carbamate;chloride can be described as predominantly soluble in polar solvents, which is a common trait for many ionic compounds. Researchers and chemists should consider these aspects while working with this substance in various applications.

Interesting facts

Interesting Facts about 2-piperidin-1-ium-1-ylethyl N-(2,6-dibromophenyl)carbamate;chloride

This complex compound has garnered attention in the field of chemical research due to its unique structure and potential applications. Here are some notable aspects:

  • Biological Significance: This compound could potentially serve as an important agent in medicinal chemistry, especially in developing new pharmaceutical compounds.
  • Structural Features: The presence of a piperidinium moiety contributes to its stability and ability to interact effectively with biological systems.
  • Electrophilic Versatility: The 2,6-dibromophenyl group makes this compound an interesting candidate for reactivity studies, as it can participate in electrophilic aromatic substitution.
  • Sustainability Aspect: The carbamate functional group is notable in pesticide chemistry and may have implications for agricultural science, promoting more sustainable practices.

"Understanding the nuances of such compounds allows us to harness their capabilities in real-world applications."

Due to its composition, researchers are encouraged to further explore the interactions and mechanisms this compound may exhibit, especially in the realms of medicinal and organic chemistry.


Overall, 2-piperidin-1-ium-1-ylethyl N-(2,6-dibromophenyl)carbamate;chloride presents a promising avenue for scientific exploration and could lead to developments that significantly impact various industries.

Synonyms
2-Piperidinoethyl 2,6-dibromocarbanilate hydrochloride
20229-07-6
K 502
2,6-Dibromocarbanilic acid 2-piperidinoethyl ester hydrochloride
CARBANILIC ACID, 2,6-DIBROMO-, 2-PIPERIDINOETHYL ESTER, HYDROCHLORIDE