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Acetylthiocholine iodide

Acetylthiocholine iodide Structure
CAS No.
1866-15-5
Chemical Name:
Acetylthiocholine iodide
Synonyms
Acetylthiocholine io;Acetylthiocholinjodid;acetylthiocholine iodie;Kamovsky-roots solution;ACETYLTHIOCHOLINE IODIDE;Iodine thioacetylcholine;s-acetylthio-choliniodide;acetylthiocholinediiodide;acethylthiocholine iodide;S-ACETYLTHIOCHOLINE IODIDE
CBNumber:
CB5248470
Molecular Formula:
C7H16INOS
Molecular Weight:
289.18
MOL File:
1866-15-5.mol
MSDS File:
SDS
Modify Date:
2024/3/20 8:48:31

Acetylthiocholine iodide Properties

Melting point 205-210 °C(lit.)
Density 1.4885 (estimate)
storage temp. 2-8°C
solubility H2O: 100 mg/mL
form powder
color white
Sensitive Light Sensitive & Hygroscopic
BRN 3916578
InChI InChI=1S/C7H16NOS.HI/c1-7(9)10-6-5-8(2,3)4;/h5-6H2,1-4H3;1H/q+1;/p-1
InChIKey NTBLZMAMTZXLBP-UHFFFAOYSA-M
SMILES [N+](C)(C)(C)CCSC(=O)C.[I-]
CAS DataBase Reference 1866-15-5(CAS DataBase Reference)
EPA Substance Registry System Ethanaminium, 2-(acetylthio)-N,N,N-trimethyl-, iodide (1866-15-5)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS06
Signal word  Danger
Hazard statements  H301+H311
Precautionary statements  P264-P270-P280-P301+P310-P302+P352+P312-P361+P364
Hazard Codes  T,Xi
Risk Statements  21-25-36/37/38
Safety Statements  26-36
RIDADR  UN 2811 6.1/PG 3
WGK Germany  3
RTECS  FZ9865000
3-8-10
TSCA  Yes
HazardClass  6.1
PackingGroup  III
HS Code  29309099
NFPA 704
1
3 0

Acetylthiocholine iodide price More Price(18)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) A5751 Acetylthiocholine iodide ≥98% (TLC), powder or crystals 1866-15-5 1G ₹2024.28 2022-06-14 Buy
Sigma-Aldrich(India) A5751 Acetylthiocholine iodide ≥98% (TLC), powder or crystals 1866-15-5 250MG ₹2868.63 2022-06-14 Buy
Sigma-Aldrich(India) A5751 Acetylthiocholine iodide ≥98% (TLC), powder or crystals 1866-15-5 5G ₹6419.23 2022-06-14 Buy
Sigma-Aldrich(India) A5751 Acetylthiocholine iodide ≥98% (TLC), powder or crystals 1866-15-5 25G ₹44988.7 2022-06-14 Buy
Sigma-Aldrich(India) 01480 Acetylthiocholine iodide ≥99.0% (AT) 1866-15-5 1G ₹3723.8 2022-06-14 Buy
Product number Packaging Price Buy
A5751 1G ₹2024.28 Buy
A5751 250MG ₹2868.63 Buy
A5751 5G ₹6419.23 Buy
A5751 25G ₹44988.7 Buy
01480 1G ₹3723.8 Buy

Acetylthiocholine iodide Chemical Properties,Uses,Production

Description

Acetylthiocholine iodide, also known as ATCI, serves as both an acetylcholinesterase (AChE) substrate and a nicotinic acetylcholine receptor (AChR) agonist. ATCI itself is a colorless and odorless compound. It exhibits solubility in both water and ethanol. It is a synthetic compound extensively employed in laboratory experiments to measure the activity of AChE, a vital enzyme responsible for the breakdown of the neurotransmitter acetylcholine (ACh) in the central and peripheral nervous systems. Additionally, it enables the evaluation of drug effects on AChE activity and facilitates investigations into the impact of toxins on the nervous system. Acetylthiocholine iodide functions as an inhibitor of AChE. By binding to the enzyme′s active site, it prevents AChE from catalyzing the breakdown of ACh. Consequently, ACh accumulates in the synaptic cleft, leading to increased neuron excitability. This inhibition of AChE by ATCI ultimately results in a higher ACh concentration within the synaptic cleft, yielding a range of physiological effects. These effects encompass heightened muscle contraction, increased heart rate and blood pressure, elevated salivation, intensified bronchial secretions, and augmented gastrointestinal activity[1].

Chemical Properties

white crystalline powder

Uses

Acetylthiocholine iodide has been used as a substrate in the preparation of acetylcholine esterase (AChE) assay working solution for AChE activity assay. It has also been used as a component in phosphate buffer (PB) for cholinesterase assay.

Purification Methods

Recrystallise the iodide from propan-1-ol (or iso-PrOH, or EtOH/Et2O) until almost colourless and dry it in a vacuum desiccator over P2O5. Its solubility in H2O is 1% w/v. A 0.075M (21.7mg/mL) solution in 0.1M phosphate buffer pH 8.0 is stable for 10-15 days if kept refrigerated. Store it away from light. It is commercially available as a 1% solution in H2O. [Ellman et al. Biochemical Pharmacology 7, 88 1961, IR: Hansen Acta Chem Scand 13 151 1959, 11 537 1957, Clin Chim Acta 2 316 1957, Ivin Zh Obshch Khim 22 267 1952, Beilstein 4 III 726, 4 IV 1585.]

References

[1] Madalina-Petruta Bucur, Gabriel-Lucian Radu, Bogdan Bucur. “Critical evaluation of acetylthiocholine iodide and acetylthiocholine chloride as substrates for amperometric biosensors based on acetylcholinesterase.” Sensors 13 2 (2013): 1603–13.

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Acetylthiocholinjodid S-ACETYLTHIOCHOLINE IODIDE extrapure AR substrate for acetylcholinesterase S-Acetylthiocholine iodide,98% acetylthiocholinediiodide Ethanaminium,2-(acetylthio)-N,N,N-trimethyl-,iodide S-[2-(trimethyl-lambda5-azanyl)ethyl] ethanethioate hydroiodide s-acetylthio-choliniodide (2-MERCAPTOETHYL)TRIMETHYLAMMONIMUM IODIDE ACETATE (2-MERCAPTOETHYL)TRIMETHYLAMMONIUM IODIDE ACETATE 2-ACETOTHIOETHYLTRIMETHYLAMMONIUM IODIDE [2-(ACETYLTHIO)ETHYL](TRIMETHYL)AMMONIUM IODIDE 2-(THIOACETYLOXY)-N,N,N-TRIMETHYLETHANAMINIUM IODIDE Acetylthiocholine iodide ,98% Acetylthiocholine iodide,(2-Mercaptoethyl)trimethylammonium iodide acetate Acetylthiocholine io S-Acetylthiocholine iodide, 98% 1GR S-Acetylthiocholine iodide, 98% 5GR acetylthiocholine iodie acethylthiocholine iodide 2-acetylsulfanylethyl(trimethyl)azanium,iodide INDICATOR PAPER PH 4,5-10 100 STRIPS (2-mercaptoethyl)trimethyl-ammoniuiodideacetate 2-(acetylthio)-n,n,n-trimethyl-ethanaminiuiodide 2-(acetylthio)-n,n,n-trimethylethanaminiumiodide S-ACETYLTHIOCHOLINE IODIDE N-(2-MERCAPTOETHYL)TRIMETHYLAMMONIUM IODIDE ACETATE THIOCHOLINE IODIDE ACETATE Acetylthiocholine iodide≥ 98% (HPLC) ACETYLTHIOCHOLINE IODIDE 2-(acetylsulfanyl)-N,N,N-trimethylethanaminium iodide AcetylthiocholineIodide> S-Acetylthiocholine Iodide extrapure AR, 99% 2-acetylsulfanylethyl(trimethyl)azanium Iodine thioacetylcholine 2-(Acetylthio)-N,N,N-trimethylethan-1-aminium iodide Kamovsky-roots solution 1866-15-5 CH3COSCH2CH2NCH33I C7H16SNOI C7H16NOSI C7H16INOS Substrates by Enzyme Acetylcholinesterase Enzyme Substrates Enzymes, Inhibitors, and Substrates Ligand-Gated Ion Channels Ion Channels Nicotinic Acetylcholine Receptor Modulators Cell Biology Cell Signaling and Neuroscience Ammonium Iodides (Quaternary) Quaternary Ammonium Compounds BioChemical Biochemicals and Reagents susbtrate Substrates Ammonium Iodides (Quaternary) Quaternary Ammonium Compounds