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Oxethazaine hydrochloride

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Identification
Molecular formula
C22H34ClNO2
CAS number
972-02-1
IUPAC name
2-[2-(1-hydroxybutyl)phenoxy]ethyl-diisopropyl-ammonium;chloride
State
State

At room temperature, Oxethazaine hydrochloride is found in a solid state, specifically as a powder form that allows for easy handling and formulation.

Melting point (Celsius)
189.00
Melting point (Kelvin)
462.15
Boiling point (Celsius)
220.00
Boiling point (Kelvin)
493.15
General information
Molecular weight
358.97g/mol
Molar mass
358.9400g/mol
Density
1.0455g/cm3
Appearence

Oxethazaine hydrochloride typically appears as a white to off-white powder. It is generally odorless and used in formulations that require dissolution in solutions.

Comment on solubility

Solubility of 2-[2-(1-hydroxybutyl)phenoxy]ethyl-diisopropyl-ammonium;chloride

The compound 2-[2-(1-hydroxybutyl)phenoxy]ethyl-diisopropyl-ammonium;chloride is known for its unique solubility characteristics influenced by several factors. Generally, the solubility of ammonium compounds, especially those containing quaternary ammonium groups, tends to be favorable in polar solvents.

  • Solvent Compatibility: This compound exhibits good solubility in water and other polar solvents due to its ionic nature attributed to the chloride ion.
  • Hydrophobic and Hydrophilic Dynamics: The presence of a hydrophobic hydrocarbon chain (from the diisopropyl groups) alongside hydrophilic sites (the hydroxyl and ionic portions) creates a complex interaction with solvents, balancing solubility in both aqueous and organic phases.
  • Temperature Influence: Solubility may increase with temperature, making warm solutions more accommodating for dissolution.

It’s essential to note that:

  • The formation of micelles and solubilization phenomena can enhance its effective solubility in non-polar environments.
  • The presence of substituents can significantly impact solubility, as different groups can either stabilize or destabilize the compound in solution.

Therefore, when considering 2-[2-(1-hydroxybutyl)phenoxy]ethyl-diisopropyl-ammonium;chloride, one might say, "The interplay between its ionic structure and organic components offers a fascinating insight into solubility dynamics."

Interesting facts

Interesting Facts about 2-[2-(1-hydroxybutyl)phenoxy]ethyl-diisopropyl-ammonium;chloride

This compound, also known as a quaternary ammonium salt, exhibits properties that make it intriguing in both pharmaceutical and material science applications. It is characterized by a positively charged nitrogen atom surrounded by alkyl groups, which enhances its chemical stability and reactivity.

Key Features:

  • Versatile Applications: Quaternary ammonium compounds, like this one, are used as surfactants, antimicrobial agents, and even in drug delivery systems.
  • Biocompatibility: The presence of hydroxybutyl groups may contribute to its compatibility with biological systems, making it a candidate for biomedical research.
  • Charge Characteristics: The quaternary ammonium center provides unique cationic properties, allowing for interactions with anionic species, which can be useful in formulation chemistry.

Researchers have observed that compounds similar to this one exhibit antibacterial and antifungal properties, making them valuable in developing new therapeutics and disinfectants. Furthermore, the unique structure of this compound suggests that it could be tailored to enhance specific interactions with cell membranes, potentially improving the efficacy of drugs.

In summary, 2-[2-(1-hydroxybutyl)phenoxy]ethyl-diisopropyl-ammonium;chloride is not only a fascinating subject of study due to its chemical features but also holds promise for real-world applications across various scientific fields.

Synonyms
Ketocainol hydrochloride
UNII-0QK6O7A30O
Benzyl alcohol, 6-(2-(diisopropylamino)ethoxy)-alpha-propyl-, hydrochloride
0QK6O7A30O
1-Butanol, 1-(o-(2-(diisopropylamino)ethoxy)phenyl)-, hydrochloride
2-(2-(Diisopropylamino)ethoxy)-alpha-propylbenzyl alcohol hydrochloride
2-(alpha-Hydroxybutyl)-beta-(N,N-diisopropyl)phenoxyethylamine, hydrochloride
Benzenemethanol, 2-(2-(diisopropylamino)ethoxy)-alpha-propyl-, hydrochloride
Benzenemethanol, 6-(2-(diisopropylamino)ethoxy)-alpha-propyl-, hydrochloride
BENZYL ALCOHOL, 2-(2-(DIISOPROPYLAMINO)ETHOXY)-alpha-PROPYL-, HYDROCHLORIDE
7241-38-5
BENZYL ALCOHOL, O-(2-(DIISOPROPYLAMINO)ETHOXY)-.ALPHA.-PROPYL-, HYDROCHLORIDE
BENZENEMETHANOL, 2-(2-(BIS(1-METHYLETHYL)AMINO)ETHOXY)-.ALPHA.-PROPYL-, HYDROCHLORIDE
BENZENEMETHANOL, 2-(2-(BIS(1-METHYLETHYL)AMINO)ETHOXY)-.ALPHA.-PROPYL-, HYDROCHLORIDE (1:1)
BENZENEMETHANOL, 2-(2-(BIS(1-METHYLETHYL)AMINO)ETHOXY)-ALPHA-PROPYL-, HYDROCHLORIDE
BENZYL ALCOHOL, O-(2-(DIISOPROPYLAMINO)ETHOXY)-ALPHA-PROPYL-, HYDROCHLORIDE
BENZENEMETHANOL, 2-(2-(BIS(1-METHYLETHYL)AMINO)ETHOXY)-ALPHA-PROPYL-, HYDROCHLORIDE (1:1)