Skip to main content

Prilocaine hydrochloride

ADVERTISEMENT
Identification
Molecular formula
C13H21ClN2O
CAS number
1786-81-8
IUPAC name
diisopropyl-methyl-[2-(N-phenylanilino)ethyl]ammonium;bromide
State
State

It is typically found in a solid state at room temperature.

Melting point (Celsius)
37.00
Melting point (Kelvin)
310.15
Boiling point (Celsius)
376.50
Boiling point (Kelvin)
649.65
General information
Molecular weight
271.82g/mol
Molar mass
271.8200g/mol
Density
1.1900g/cm3
Appearence

Off-white or pale yellow powder that may have a crystalline form. It is a hygroscopic compound.

Comment on solubility

Solubility of diisopropyl-methyl-[2-(N-phenylanilino)ethyl]ammonium bromide

When exploring the solubility of the compound diisopropyl-methyl-[2-(N-phenylanilino)ethyl]ammonium bromide, one might encounter the following considerations:

  • Polar vs Nonpolar Nature: The presence of a quaternary ammonium structure contributes to its polar characteristics, which often facilitates solubility in polar solvents.
  • Solvent Compatibility: This compound is generally soluble in polar organic solvents such as methanol and ethanol but may face challenges in nonpolar solvents like hexane.
  • Temperature Influence: Elevated temperatures often enhance solubility; thus, warming solvents can lead to increased dissolution rates.
  • Ionization Effect: The bromide ion can influence solubility by affecting the overall solvation process, making this compound more soluble in ionic form.

In summary, the solubility of diisopropyl-methyl-[2-(N-phenylanilino)ethyl]ammonium bromide can be described as generally favorable in polar solvents, making it suitable for various applications in organic reactions and synthesis.

Interesting facts

Interesting Facts about Diisopropyl-methyl-[2-(N-phenylanilino)ethyl]ammonium Bromide

Diisopropyl-methyl-[2-(N-phenylanilino)ethyl]ammonium bromide is a fascinating compound known for its unique chemical properties and utility in various scientific applications. Here are some noteworthy highlights:

  • Structural Complexity: The structure of this compound showcases intricate molecular architecture, featuring both isopropyl and phenyl substitutions that contribute to its distinctive behavior in chemical reactions.
  • Biological Relevance: Compounds like this one are often studied in the context of pharmacology and biochemistry, as they may interact with biological membranes and influence cellular processes.
  • Quaternary Ammonium Compound: Being a quaternary ammonium salt, it has applications as a surfactant and in ionic liquid technologies. Its cationic nature allows for a broad range of interactions in aqueous solutions.
  • Facilitator of Ion Exchange: Due to its unique functional groups, this compound can facilitate ion exchange in various chemical processes, enhancing its practical applications in fields such as water treatment and catalysis.
  • Research and Development: The exploration of diisopropyl-methyl-[2-(N-phenylanilino)ethyl]ammonium bromide in drug formulation and delivery systems can provide insights into new therapeutic avenues.

As an example of a compound with both industrial and academic significance, diisopropyl-methyl-[2-(N-phenylanilino)ethyl]ammonium bromide illustrates the profound connections between chemical structure and functional application, making it a subject of ongoing interest in the scientific community.

Synonyms
2933-23-5
(2-(Diphenylamino)ethyl)diisopropylmethylammonium bromide
Bromuro di metildiisopropil-beta-difenilaminoetilammonio [Italian]
AMMONIUM, (2-(DIPHENYLAMINO)ETHYL)DIISOPROPYLMETHYL-, BROMIDE
Bromuro di metildiisopropil-beta-difenilaminoetilammonio
DTXSID90951890
N-[2-(Diphenylamino)ethyl]-N-methyl-N-(propan-2-yl)propan-2-aminium bromide