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Betel nut base

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Identification
Molecular formula
C8H18NO2
CAS number
78-00-2
IUPAC name
trimethyl-[2-(methylcarbamoyloxy)ethyl]ammonium
State
State

At room temperature, this compound is typically found in a liquid state.

Melting point (Celsius)
-20.00
Melting point (Kelvin)
253.15
Boiling point (Celsius)
189.50
Boiling point (Kelvin)
462.65
General information
Molecular weight
161.23g/mol
Molar mass
161.2300g/mol
Density
1.0100g/cm3
Appearence

The compound is typically a colorless to pale yellow liquid.

Comment on solubility

Solubility of Trimethyl-[2-(methylcarbamoyloxy)ethyl]ammonium (C8H18NO2)

The solubility of Trimethyl-[2-(methylcarbamoyloxy)ethyl]ammonium, with the formula C8H18NO2, primarily depends on its ionic characteristics and the presence of polar functional groups in its structure. Notable aspects of its solubility include:

  • Polarity: The molecule contains functional groups such as the methylcarbamoyloxy group that enhances polarity, potentially increasing solubility in polar solvents like water.
  • Ionic Behavior: Being an ammonium compound, it is likely to dissociate in solution, aiding in solubility due to the attraction between the ions and the solvent molecules.
  • Hydrophilicity: The presence of oxygen atoms contributes to the hydrophilic nature of the compound, making it more favorable for dissolution in aqueous environments.
  • Alkyl Chain Influence: The trimethyl group can create some degree of hydrophobic character, which might reduce solubility but is often offset by the polar functionalities present.

Overall, while specific solubility data may vary and require empirical determination, Trimethyl-[2-(methylcarbamoyloxy)ethyl]ammonium is anticipated to have moderate solubility in water while exhibiting varied solubility in organic solvents, emphasizing the significance of environmental conditions and solvent interactions.

Interesting facts

Interesting Facts about Trimethyl-[2-(methylcarbamoyloxy)ethyl]ammonium

Trimethyl-[2-(methylcarbamoyloxy)ethyl]ammonium is a fascinating compound with a variety of intriguing characteristics and applications. Here are some key points to consider:

  • Quaternary Ammonium Compound: As a quaternary ammonium salt, it includes a positively charged nitrogen atom surrounded by three methyl groups and a hydroxyethyl group. This structure contributes to its unique properties and broad utility.
  • Biological Significance: Compounds with quaternary ammonium groups often demonstrate antimicrobial properties, making them valuable in various applications, including disinfectants and antiseptics. They can disrupt microbial cell membranes, which enhances their effectiveness.
  • Versatile Applications: Trimethyl-[2-(methylcarbamoyloxy)ethyl]ammonium finds usage not just in the field of microbiology, but also in pharmaceutical formulations. The compound can serve as a surfactant, helping to stabilize and improve the solubility of drugs.
  • Research Importance: Its structure allows researchers to modify it for specific functions, making it a topic of interest in organic synthesis and medicinal chemistry. It can be utilized as a precursor for synthesizing more complex molecules.
  • Synthesis Potential: The synthesis of this compound can be achieved through various chemical reactions, such as alkylation of nitrogen compounds. This process provides a creative opportunity for chemists to explore reaction mechanisms and improve yields.
  • Environmental Considerations: Given the increasing environmental awareness, studying such compounds also prompts the evaluation of their biodegradability and the impact they may have when used in consumer products or pharmaceuticals.

Overall, trimethyl-[2-(methylcarbamoyloxy)ethyl]ammonium is not just a compound, but a gateway to exploring facets of chemistry that intersects with biology, pharmaceuticals, and environmental science. It stands as an example of how dissecting the structure can lead to a more comprehensive understanding of functional applications in real-world scenarios.

Synonyms
N-methylcarbamylcholine
Methylcarbachol
Methylcarbamylcholine
14721-69-8
DTXSID2048450
Ethanaminium, N,N,N-trimethyl-2-(((methylamino)carbonyl)oxy)-
NMCC
Lopac-M-140
trimethyl-[2-(methylcarbamoyloxy)ethyl]azanium
Lopac0_000873
SCHEMBL155237
CHEMBL1472561
DTXCID8028424
BDBM82546
CCG-204955
NCGC00015633-01
NCGC00015633-02
NCGC00162285-01
CAS_14721-69-8