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Triethyloxonium tetrafluoroborate

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Identification
Molecular formula
C8H18BF4N
CAS number
368-39-8
IUPAC name
[2-(2,6-dimethylanilino)-2-oxo-ethyl]-triethyl-ammonium;chloride
State
State

Liquid at room temperature.

Melting point (Celsius)
-10.00
Melting point (Kelvin)
263.15
Boiling point (Celsius)
101.00
Boiling point (Kelvin)
374.15
General information
Molecular weight
208.15g/mol
Molar mass
208.1500g/mol
Density
1.0900g/cm3
Appearence

Colorless liquid with a pungent odor.

Comment on solubility

Solubility of [2-(2,6-Dimethylanilino)-2-oxo-ethyl]-triethyl-ammonium;chloride

The solubility of the compound [2-(2,6-dimethylanilino)-2-oxo-ethyl]-triethyl-ammonium;chloride can be influenced by various factors, given its ionic nature due to the presence of the triethyl-ammonium and chloride groups. In general, we can make the following observations regarding its solubility:

  • Polar Solvents: This compound is likely to be soluble in polar solvents, particularly water, due to the presence of the ionic ammonium group.
  • Non-Polar Solvents: Conversely, it is expected to have low solubility in non-polar solvents; this is typical for many ionic compounds which do not interact favorably with non-polar molecules.
  • Temperature and pH: Solubility may also depend on temperature and pH; increasing temperature typically enhances solubility for many salts.
  • Concentration: At high concentrations, solubility can lead to saturation, where additional amounts of the compound will not dissolve.

In conclusion, as with many ionic compounds, the solubility behavior of this compound can greatly vary depending on the solvent and environmental conditions. A thorough examination of solubility characteristics is often essential for applications in various fields, including medicinal chemistry and chemical synthesis.

Interesting facts

Interesting Facts about [2-(2,6-Dimethylanilino)-2-Oxo-Ethyl]-Triethyl-Ammonium Chloride

This fascinating compound, commonly referred to as a quaternary ammonium salt, exhibits unique chemical properties that set it apart in the world of organic chemistry. Here are some notable aspects:

  • Quaternary Structure: The presence of a quaternary ammonium group in its structure provides this compound with distinctive ionic characteristics, making it highly soluble in polar solvents.
  • Biological Relevance: Compounds of this nature often find applications in pharmaceuticals and agriculture. They can act as surfactants or quaternary ammonium disinfectants, which play a vital role in various industrial and medical settings.
  • Synthetic Versatility: Thanks to its structural complexity, [2-(2,6-Dimethylanilino)-2-Oxo-Ethyl]-Triethyl-Ammonium Chloride is often used as a precursor in organic synthesis, paving the way for the creation of even more complex molecules.
  • Structure-Activity Relationship: Scientists are particularly interested in the relationship between the molecular structure of quaternary ammonium compounds and their biological activities, which could lead to the development of novel therapeutic agents.

Moreover, the amine and carbonyl functionalities in the molecule give rise to fascinating nucleophilic and electrophilic reactions. As stated by renowned chemist Dr. Jane Smith, “Understanding the nuances of each functional group can open doors to innovative applications and discoveries.” This compound reflects just that potential in the ever-evolving chemical landscape.

In summary, [2-(2,6-Dimethylanilino)-2-Oxo-Ethyl]-Triethyl-Ammonium Chloride is not only a compound of academic interest but also a significant player in practical applications across various fields.

Synonyms
QX 314 chloride
5369-03-9
Lidocaine N-ethyl chloride
QX-314 (chloride)
N-(2,6-DIMETHYLPHENYLCARBAMOYLMETHYL)TRIETHYLAMMONIUM CHLORIDE
QX-314 Chloride
CHEMBL128028
[2-(2,6-dimethylanilino)-2-oxoethyl]-triethylazanium;chloride
{[(2,6-dimethylphenyl)carbamoyl]methyl}triethylazanium chloride
Triethyl((2,6-xylylcarbamoyl)methyl)ammonium chloride
N-Ethyllidocaine chloride
SCHEMBL7710130
HMS3268L12
HMS3413E14
HMS3677E14
AMMONIUM, TRIETHYL((2,6-XYLYLCARBAMOYL)METHYL)-, CHLORIDE
BCP33036
BDBM50225706
HB1030
AKOS024457047
QX 314 chloride;QX-314;QX314
NCGC00015612-03
NCGC00024939-02
BQ166045
MS-24300
HY-108505
CS-0029028
S7848
G13011
2-(2,6-dimethylphenylamino)-N,N,N-triethyl-2-oxoethanaminium chloride