AChE Substrates
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
S-Butyrylthiocholine Iodide | 1866-16-6 | sc-286740 sc-286740A sc-286740B sc-286740C | 5 g 50 g 100 g 500 g | $59.00 $587.00 $959.00 $3927.00 | ||
S-Butyrylthiocholine Iodide acts as a potent substrate for cholinesterases, exhibiting rapid hydrolysis due to its electrophilic carbonyl group. The presence of the thioether moiety enhances nucleophilic attack, facilitating swift enzymatic interactions. Its iodide component contributes to unique solubility characteristics, influencing reaction kinetics and stability in various environments. This compound's structural features promote specific binding affinities, impacting its reactivity in biochemical pathways. | ||||||
Butyrylcholine chloride | 2963-78-2 | sc-255007 sc-255007A | 10 g 25 g | $54.00 $138.00 | ||
Butyrylcholine chloride is characterized by its reactive acyl chloride functionality, which readily engages in nucleophilic acyl substitution reactions. The chloride ion enhances its electrophilicity, making it a prime target for nucleophiles. This compound exhibits unique solubility properties in polar solvents, influencing its reactivity profile. Its ability to form stable intermediates during hydrolysis contributes to distinct reaction kinetics, allowing for selective interactions in various chemical environments. | ||||||
Acetylthiocholine iodide | 1866-15-5 | sc-208323 sc-208323A sc-208323B sc-208323C sc-208323D | 1 g 5 g 25 g 100 g 250 g | $36.00 $85.00 $362.00 $1153.00 $2657.00 | ||
Acetylthiocholine iodide features a thioester linkage that enhances its reactivity through the formation of thiol derivatives upon nucleophilic attack. The iodide moiety increases electrophilic character, facilitating rapid interactions with nucleophiles. This compound demonstrates unique solubility in organic solvents, which can influence its reactivity and stability. Its propensity to undergo hydrolysis leads to distinct reaction pathways, allowing for diverse chemical transformations. | ||||||
Acetylthiocholine chloride | 6050-81-3 | sc-257066 sc-257066A | 1 g 5 g | $95.00 $356.00 | ||
Acetylthiocholine chloride exhibits a unique reactivity profile due to its quaternary ammonium structure, which enhances its interaction with nucleophiles. The chloride ion contributes to its electrophilic nature, promoting swift reaction kinetics. This compound is highly soluble in polar solvents, affecting its stability and reactivity. Its ability to form stable complexes with various ligands opens pathways for diverse synthetic applications, showcasing its versatility in chemical reactions. | ||||||