01480
Acetylthiocholine iodide
≥99.0% (AT)
Synonym(s):
(2-Mercaptoethyl)trimethylammonium iodide acetate
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About This Item
Linear Formula:
CH3COSCH2CH2N(CH3)3I
CAS Number:
Molecular Weight:
289.18
NACRES:
NA.83
PubChem Substance ID:
UNSPSC Code:
12352204
EC Number:
217-474-1
MDL number:
Beilstein/REAXYS Number:
3916578
Quality Level
assay
≥99.0% (AT)
ign. residue
≤0.05%
mp
205-210 °C
solubility
H2O: 0.1 g/mL, clear, colorless
storage temp.
2-8°C
SMILES string
[I-].CC(=O)SCC[N+](C)(C)C
InChI
1S/C7H16NOS.HI/c1-7(9)10-6-5-8(2,3)4;/h5-6H2,1-4H3;1H/q+1;/p-1
InChI key
NTBLZMAMTZXLBP-UHFFFAOYSA-M
General description
Acetylcholinesterase substrate and nicotinic acetylcholine receptor agonist.
Application
Substrate for the colorimetric determination of acetylcholinesterase activity.
Acetylthiocholine iodide has been used as a substrate to determine anticholinesterase activity.
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Oral
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
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Belgin Sever et al.
International journal of biological macromolecules, 163, 1970-1988 (2020-09-16)
Alzheimer's disease (AD) is a complex, predominant, and progressive form of dementia. The treatment of AD alters depending on the cognitive and behavioral symptoms. The utility of cholinergic replacement by acetylcholinesterase (AChE) inhibitors in AD treatment has been well-documented so
Niko S Radulović et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 80, 114-129 (2015-03-15)
Herein we report on the comprehensive chemical analysis of the essential oils obtained from above- and underground parts of a previously unreported chemotype of Achillea falcata L. (Asteraceae) and, for the first time, on the biological/toxicological profile of its dominant/newly
Wei Li et al.
Fitoterapia, 98, 117-123 (2014-07-30)
Three new 2-(2-phenylethyl)chromone derivatives (1-3), together with thirteen known ones (4-16), were isolated from the EtOAc extract of Chinese agarwood induced by artificial holing, originating from Aquilaria sinensis (Lour.) Gilg (Thymelaeaceae). The chemical structures of the new compounds were identified