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Acetylcholine

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Identification
Molecular formula
C7H16NO2Cl
CAS number
51-84-3
IUPAC name
(1-acetoxy-2-carboxy-ethyl)-trimethyl-ammonium
State
State

At room temperature, acetylcholine is typically found as a solid. However, due to its hygroscopic nature, it can readily absorb moisture from the air.

Melting point (Celsius)
-114.50
Melting point (Kelvin)
158.65
Boiling point (Celsius)
206.50
Boiling point (Kelvin)
479.65
General information
Molecular weight
181.66g/mol
Molar mass
181.6640g/mol
Density
1.2110g/cm3
Appearence

Acetylcholine typically appears as a white crystalline solid or powder. It is hygroscopic and deliquescent, meaning it can absorb moisture from the air to become liquid.

Comment on solubility

Solubility of (1-acetoxy-2-carboxy-ethyl)-trimethyl-ammonium

The solubility of (1-acetoxy-2-carboxy-ethyl)-trimethyl-ammonium, with the chemical formula C7H16NO2Cl, presents intriguing characteristics owing to its unique structural composition. This compound exhibits ionic properties due to the presence of a quaternary ammonium group, which enhances its solubility in polar solvents.

Here are some key considerations regarding its solubility:

  • Polar Solvents: The compound is primarily soluble in water and other polar solvents. This is attributed to its ionic nature, which promotes interactions with the solvent molecules.
  • Non-Polar Solvents: In contrast, (1-acetoxy-2-carboxy-ethyl)-trimethyl-ammonium shows limited solubility in non-polar solvents such as hexane or benzene, due to the lack of favorable interactions.
  • Concentration Effects: The degree of solubility may vary with concentration, where higher concentrations could lead to decreased solubility due to potential ionic interactions or precipitation.

In summary, while (1-acetoxy-2-carboxy-ethyl)-trimethyl-ammonium is soluble in polar environments, it is crucial to consider the solvent type when predicting its behavior. As with many chemical compounds, "the right environment makes all the difference!"

Interesting facts

Interesting Facts about (1-acetoxy-2-carboxy-ethyl)-trimethyl-ammonium

(1-acetoxy-2-carboxy-ethyl)-trimethyl-ammonium, often referred to as a quaternary ammonium compound, presents a fascinating example of how modifications in molecular structure can enhance biological activity and effectiveness in various applications.

Key Features:

  • Quaternary Structure: The presence of a positively charged nitrogen atom allows it to interact strongly with negatively charged biological membranes, making it an effective agent for antimicrobial activity.
  • Functional Groups: This compound contains both an acetoxy group and a carboxylic acid group, which contribute to its chemical reactivity and potential uses in synthetic pathways.
  • Biological Applications: Due to its quaternary ammonium nature, it is often investigated for use in drug delivery systems and antimicrobial formulations. Its ability to disrupt microbial membranes makes it valuable in sanitation and hygiene products.
  • Synthesis Versatility: Synthetic methods often incorporate variations in the alkyl chain length or functional groups to tailor its properties for specific applications in pharmaceuticals or agriculture.

As stated by renowned chemists, "The applications of quaternary ammonium compounds are limited only by our imagination." This underscores the innovative potential of (1-acetoxy-2-carboxy-ethyl)-trimethyl-ammonium in developing effective agents for health and industry.

In summary, the diverse functional capabilities and biological impact of (1-acetoxy-2-carboxy-ethyl)-trimethyl-ammonium make it a noteworthy candidate for future research, especially within fields such as medicinal chemistry and materials science. Its ability to serve multiple roles depending on structural modifications showcases the intrinsic creativity found in chemical synthesis.

Synonyms
SPBio_000832
Spectrum_001493
Spectrum2_000926
Spectrum3_001764
Spectrum4_000330
Spectrum5_001208
BSPBio_003227
KBioGR_000679
KBioSS_001973
DivK1c_000664
CHEMBL1620807
BCBcMAP01_000171
KBio1_000664
KBio2_001973
KBio2_004541
KBio2_007109
KBio3_002727
NINDS_000664
IDI1_000664
NCGC00178197-01