ACETYLTHIOCHOLINE CHLORIDE
ACETYLTHIOCHOLINE CHLORIDE Basic information
- Product Name:
- ACETYLTHIOCHOLINE CHLORIDE
- Synonyms:
-
- (2-acetylthio)-n,n,n-trimethylethanaminumchloride
- ammonium,(2-mercaptoethyl)trimethyl-,chloride,acetate
- N-(2-MERCAPTOETHYL)TRIMETHYLAMMONIUM CHLORIDE ACETATE
- S-ACETYLTHIOCHOLINE CHLORIDE
- THIOCHOLINE CHLORIDE ACETATE
- ACETYLTHIOCHOLINE CHLORIDE
- N-[2-(Acetylthio)ethyl]trimethylaminium·chloride
- 2-acetylsulfanylethyl(trimethyl)azanium chloride
- CAS:
- 6050-81-3
- MF:
- C7H16ClNOS
- MW:
- 197.72
- EINECS:
- 227-953-7
- Product Categories:
-
- Agonists
- Cholinergics
- Neurotransmitters
- Mol File:
- 6050-81-3.mol
ACETYLTHIOCHOLINE CHLORIDE Chemical Properties
- Melting point:
- 199-201°C
- storage temp.
- -20°C
- solubility
- DMSO (Slightly), Water (Slightly, Heated, Sonicated)
- form
- powder
- color
- White to Off-White
- CAS DataBase Reference
- 6050-81-3(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 36/37/38-41
- Safety Statements
- 26-36-39
- WGK Germany
- 3
- RTECS
- BR6954000
- HS Code
- 29309070
MSDS
- Language:English Provider:SigmaAldrich
ACETYLTHIOCHOLINE CHLORIDE Usage And Synthesis
Chemical Properties
white powder
Uses
Acetylthiocholine chloride has been used to determine the acetylcholine esterase activity of semen exosomes (SE). It has also been used as a substrate for acetylcholine esterase in microcalorimetric study of its kinetic parameters.
Biochem/physiol Actions
Acetylcholinesterase (AChE) enzyme plays an important physiological role in the neurotransmission process.
Purification Methods
The chloride can be purified in the same way as the bromide, and it can be prepared from the iodide. A few milligrams dissolved in H2O can be purified by applying onto a Dowex-1 Cl-resin column (prepared by washing with N HCl followed by CO3 -free H2O until the pH is 5.8). After equilibration for 10minutes, elution is started with CO3 -free distilled H2O, and 3mL fractions are collected and their OD values at 229nm are measured. The fractions with appreciable absorption are pooled and lyophilised at 0-5o. Note that at higher temperatures decomposition of the ester is appreciable; hydrolysis is appreciable at pH >10.5/20o. The residue is dried in vacuo over P2O5, checked for traces of iodine (add conc H2SO4 and heat, violet vapours are released), and recrystallise it from propan-1-ol. [Gal & Roth Clin Chim Acta 2 316 1957, Beilstein 4 IV 1585.]
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