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Acetylthiocholine chloride

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Identification
Molecular formula
C9H20ClNO2S
CAS number
1866-15-5
IUPAC name
2-acetylsulfanylethyl(trimethyl)ammonium;chloride
State
State
At room temperature, it is usually found in the form of a crystalline solid.
Melting point (Celsius)
145.00
Melting point (Kelvin)
418.15
Boiling point (Celsius)
330.00
Boiling point (Kelvin)
603.15
General information
Molecular weight
227.77g/mol
Molar mass
227.7680g/mol
Density
1.1600g/cm3
Appearence

Acetylthiocholine chloride typically appears as a white or off-white crystalline powder or solid.

Comment on solubility

Solubility of 2-acetylsulfanylethyl(trimethyl)ammonium chloride

The solubility of 2-acetylsulfanylethyl(trimethyl)ammonium chloride can be understood through various factors that influence how this compound interacts with solvents, particularly water. Here are some key points to consider:

  • Ionic Nature: As a quaternary ammonium salt, 2-acetylsulfanylethyl(trimethyl)ammonium ions may dissociate in solution, enhancing solubility due to the favorable interactions with solvent molecules.
  • Polarity: This compound’s structure, which includes both hydrophilic and hydrophobic regions, suggests that it is likely to exhibit variable solubility depending on the medium. The ammonium group is polar and often aids in solubility in polar solvents.
  • Temperature Dependency: The solubility could increase with temperature, as is common with many salts, allowing for greater ion dissociation.

In summary, the solubility of this compound is expected to be relatively significant in polar solvents like water while exhibiting lesser solubility in non-polar solvents. However, specific solubility data should be consulted for exact values in practical applications. As always, when dealing with chemical compounds, it's prudent to conduct empirical testing to ascertain solubility behavior.

Interesting facts

Exploring 2-Acetylsulfanylethyl(trimethyl)ammonium Chloride

2-Acetylsulfanylethyl(trimethyl)ammonium chloride is a fascinating compound that belongs to the class of quaternary ammonium compounds. Here are some interesting insights about this compound:

  • Chemical Family: It is part of the quaternary ammonium salts, which are recognized for their cationic nature. This allows them to interact well with various anions, making them highly versatile.
  • Applications: Compounds like 2-acetylsulfanylethyl(trimethyl)ammonium chloride are often utilized in various fields, including pharmaceuticals, where they can serve as antibacterial agents or react as quaternary ammonium surfactants.
  • Mechanism of Action: The cationic part of the molecule helps to disrupt microbial cell membranes, which is a common mechanism among many antimicrobial compounds.
  • Environmental Considerations: As with many quaternary ammonium compounds, understanding their environmental impact and degradation pathways is vital for sustainable use in industry and agriculture.

Interesting Properties

Some additional properties that make this compound noteworthy include:

  • Stability: The quaternary ammonium structure contributes to enhanced stability, allowing it to remain effective under a variety of conditions.
  • Ion Exchange Capacity: The presence of the trimethylammonium moiety allows for significant interactions with other ionic species, enhancing the compound's utility in various applications.

Scientists are continually exploring the potential uses of 2-acetylsulfanylethyl(trimethyl)ammonium chloride in innovative applications, ranging from antimicrobial surfaces to advanced drug delivery systems. Its unique structure makes it a prime candidate for further research in both theoretical and applied chemistry.

As noted by researchers, "The versatility of quaternary ammonium compounds like 2-acetylsulfanylethyl(trimethyl)ammonium chloride provides a rich avenue for exploration in both synthetic and applied chemistry."

Synonyms
Acetylthiocholine chloride
6050-81-3
EINECS 227-953-7
AMMONIUM, (2-MERCAPTOETHYL)TRIMETHYL-, CHLORIDE, ACETATE
s-Acetylthiocholine chloride
gzyvlkkmmdfckr-uhfffaoysa-m
2-(Acetylthio)-N,N,N-trimethylethanaminium chloride
2-Acetylthioethyltrimethylammonium chloride
[2-(acetylsulfanyl)ethyl]trimethylazanium chloride
Ethanaminium, 2-(acetylthio)-N,N,N-trimethyl-, chloride
2-acetylsulfanylethyl(trimethyl)azanium;chloride
(2-Mercaptoethyl)trimethylammonium chloride acetate
(2-Acetylthio)-N,N,N-trimethylethanaminum chloride
MFCD00038727
2-acetylsulfanylethyl(trimethyl)azanium chloride
2-acetylsulfanylethyl(trimethyl)azanium,chloride
MLS001056723
SCHEMBL1276372
CHEMBL1256181
DTXSID90975910
HMS2233H15
HMS3260K17
HMS3371D04
Tox21_500058
AKOS006230681
CCG-221362
LP00058
NCGC00093572-01
NCGC00260743-01
AS-58773
SMR000326680
DB-053634
CS-0199449
EU-0100058
NS00044890
A 5626
E78561
SR-01000075669
2-(Acetylthio)-N,N,N-trimethylethanaminiumchloride
SR-01000075669-1
2-(Acetylthio)-N,N,N-trimethyl-ethanaminium Chloride; (2-Mercaptoethyl)trimethylammonium Chloride Acetate