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Acetylthiocholine

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Identification
Molecular formula
C9H20NO2S
CAS number
1866-15-5
IUPAC name
2-acetylsulfanylethyl(trimethyl)ammonium
State
State

Acetylthiocholine is generally found in a solid state at room temperature.

Melting point (Celsius)
119.00
Melting point (Kelvin)
392.15
Boiling point (Celsius)
216.00
Boiling point (Kelvin)
489.15
General information
Molecular weight
213.33g/mol
Molar mass
213.7500g/mol
Density
1.0730g/cm3
Appearence

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

Comment on solubility

Solubility of 2-acetylsulfanylethyl(trimethyl)ammonium

The solubility of 2-acetylsulfanylethyl(trimethyl)ammonium can be influenced by several factors due to its unique structure. As an ammonium compound, it generally exhibits behavior typical of quaternary ammonium salts, which often have a diverse range of solubilities. Here are some key points regarding its solubility:

  • Polar Nature: The presence of the polar ammonium group tends to enhance solubility in polar solvents like water.
  • Hydrophobic Character: The acetyl group introduces some hydrophobic characteristics that may limit solubility in very polar media.
  • pH Dependence: The solubility can also vary with pH, as changes in protonation could affect the overall charge and solubility of the compound.

In summary, while 2-acetylsulfanylethyl(trimethyl)ammonium is likely to be soluble in aqueous solutions due to its ionic nature, its solubility can be context-dependent, varying with solvent polarity and environmental conditions. Understanding these solubility characteristics is crucial in applications where this compound is utilized.

Interesting facts

Exploring 2-acetylsulfanylethyl(trimethyl)ammonium

2-acetylsulfanylethyl(trimethyl)ammonium is a fascinating compound with unique properties and applications in various scientific fields. Here are some engaging facts that highlight its significance:

  • Unique Structure: The presence of both sulfur and nitrogen within the structure creates intriguing chemical behavior. The sulfonium ion, characterized by its electron-withdrawing properties, plays a crucial role in its reactivity.
  • Biological Relevance: Compounds similar to 2-acetylsulfanylethyl(trimethyl)ammonium are often studied for their potential biological activity. They can act as intermediates in the synthesis of biologically active molecules, showcasing their importance in pharmaceutical research.
  • Versatile Applications: This compound finds utility in various fields, including:
    • Synthesis of other organic compounds
    • As an ionic liquid, showcasing properties such as high stability and low volatility
    • Potential use in electrochemical applications due to its ionic nature
  • Stability Factors: The trimethylammonium group contributes to the compound's stability, allowing it to withstand various chemical environments and making it a valuable building block in organic synthesis.

In conclusion, 2-acetylsulfanylethyl(trimethyl)ammonium stands out not only for its intriguing chemical structure but also for its diverse applications and biological relevance. As scientists continue to explore its properties, this compound may hold the key to new discoveries in chemistry and related fields.

Synonyms
ACETYLTHIOCHOLINE
4468-05-7
2-acetylsulfanylethyl(trimethyl)azanium
4V9VG6MX6E
Ethanaminium, 2-(acetylthio)-N,N,N-trimethyl-
2-(acetylsulfanyl)-N,N,N-trimethylethanaminium
S-Acetylthiocholine
2ha5
(2-Mercaptoethyl)trimethylammonium Acetate
Lopac-A-5626
UNII-4V9VG6MX6E
Lopac0_000058
SCHEMBL77666
BDBM8959
CHEMBL1231076
DTXSID90196269
GFFIJCYHQYHUHB-UHFFFAOYSA-N
PDSP1_000368
PDSP2_000366
STL257106
AKOS022097766
CCG-204153
NCGC00015069-01
NCGC00015069-02
NCGC00015069-03
NCGC00015069-04
NCGC00162055-01
2-(ACETYLTHIO)-N,N,N-TRIMETHYLETHANAMINIUM
(2-ACETYLSULFANYL-ETHYL)-TRIMETHYL-AMMONIUM
AMMONIUM, (2-MERCAPTOETHYL)TRIMETHYL-, ACETATE
Q27458037
AMMONIUM, (2-MERCAPTOETHYL)TRIMETHYL-, ACETATE (ESTER)
2-{[(1S)-1-HYDROXYETHYL]THIO}-N,N,N-TRIMETHYLETHANAMINIUM
ACETIC ACID, THIO-, S-ESTER WITH (2-MERCAPTOETHYL)TRIMETHYL AMMONIUM
InChI=1/C7H16NOS/c1-7(9)10-6-5-8(2,3)4/h5-6H2,1-4H3/q+