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%
solubility
H2O: 0.1 g/mL, clear, colorless
storage temp.
2-8°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
Acetylthiocholine iodide has been used as a substrate to determine anticholinesterase activity.
Substrate for the colorimetric determination of acetylcholinesterase 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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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
J Blohberger et al.
Cell death & disease, 6, e1685-e1685 (2015-03-15)
Proliferation, differentiation and death of ovarian cells ensure orderly functioning of the female gonad during the reproductive phase, which ultimately ends with menopause in women. These processes are regulated by several mechanisms, including local signaling via neurotransmitters. Previous studies showed
Thiazolyl-pyrazoline derivatives: In vitro and in silico evaluation as potential acetylcholinesterase and carbonic anhydrase inhibitors.
Sever, et al.
International Journal of Biological Macromolecules, 163, 1970-1988 (2021)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| I21904-5ML | 04061833848333 |
| 01480-1G | 04061838609380 |
| 01480-25G | 04061838609397 |
| 01480-5G | 04061838609403 |