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Acetylcholine

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Identification
Molecular formula
C7H16NO2
CAS number
51-84-3
IUPAC name
(3-acetoxyphenyl)-diethyl-methyl-ammonium
State
State

Liquid at room temperature. It is typically stored in solution due to its instability when exposed to air.

Melting point (Celsius)
-114.00
Melting point (Kelvin)
159.15
Boiling point (Celsius)
215.00
Boiling point (Kelvin)
488.15
General information
Molecular weight
181.27g/mol
Molar mass
181.2650g/mol
Density
1.1000g/cm3
Appearence

The compound typically appears as a viscous, colorless liquid. It is often handled as a chloride salt which is hygroscopic in nature.

Comment on solubility

Solubility of (3-acetoxyphenyl)-diethyl-methyl-ammonium

The solubility of (3-acetoxyphenyl)-diethyl-methyl-ammonium, due to its unique chemical structure, can be assessed by considering several factors. The presence of both organic and ammonium functional groups allows for interesting solubility characteristics:

  • Polarity: The compound contains an ammonium group, which is highly polar and enhances solubility in polar solvents such as water.
  • Hydrophobic Effects: The diethyl groups contribute hydrophobic characteristics that can limit solubility in non-polar solvents.
  • Hydrogen Bonding: The acetoxy functional group can participate in hydrogen bonding, promoting solubility in protic solvents.

It's worth noting that the solubility can also be significantly influenced by temperature and pH of the solution. In warmer conditions, solubility often increases, while in varying pH environments, the ammonium ion may undergo protonation or deprotonation, further affecting solubility. As a general statement:

"Solubility is not merely a property, but a dynamic relationship between the solute and solvent."

Understanding these interactions is crucial for applications involving (3-acetoxyphenyl)-diethyl-methyl-ammonium in various chemical processes.

Interesting facts

Interesting Facts about (3-acetoxyphenyl)-diethyl-methyl-ammonium

(3-acetoxyphenyl)-diethyl-methyl-ammonium is a fascinating compound that exemplifies the rich diversity found within organic chemistry. Here are some key points that highlight its significance:

  • Quaternary Ammonium Compound: As a quaternary ammonium salt, this compound contains a positively charged nitrogen atom surrounded by four organic groups. This unique structure contributes to its reactivity and functionality.
  • Antimicrobial Properties: Some quaternary ammonium compounds are recognized for their antimicrobial properties, making them valuable in various applications, including disinfectants and antiseptics. This raises intriguing questions about the potential antibacterial efficacy of (3-acetoxyphenyl)-diethyl-methyl-ammonium.
  • Applications in Chemistry: This compound may play a role in organic synthesis and can be a precursor for developing more complex molecules. Studying its reactivity can provide insights into the design of new compounds with desired properties.
  • Significance in Biological Studies: Compounds containing functional groups such as acetate can interact with biological systems, potentially influencing cellular processes. Researchers often explore their effects on cell membranes and receptor interactions.
  • Versatility: The structural versatility of the diethyl and methyl groups attached to the nitrogen atom allows for potential customization in synthetic chemistry, leading to targeted modifications for specific applications.
  • Historical Context: Quaternary ammonium compounds have been utilized since the mid-20th century, leading to advances in surfactants, pharmaceuticals, and other critical chemical industries. Understanding (3-acetoxyphenyl)-diethyl-methyl-ammonium could reveal additional pathways to explore.

In summary, (3-acetoxyphenyl)-diethyl-methyl-ammonium is more than just a name; it represents a blend of chemistry's historical significance, modern applications, and the exciting prospects of ongoing research in the field. Its study could potentially contribute to developing innovative solutions in medicine and industry.