A7000
Acetylcholine iodide
≥97%
Synonym(s):
ACh
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About This Item
Linear Formula:
(CH3)3N(I)CH2CH2OCOCH3
CAS Number:
Molecular Weight:
273.11
UNSPSC Code:
12352107
NACRES:
NA.25
PubChem Substance ID:
EC Number:
218-862-3
Beilstein/REAXYS Number:
3571339
MDL number:
Assay:
≥97%
Form:
powder
Quality Level
assay
≥97%
form
powder
storage temp.
−20°C
SMILES string
[I-].CC(=O)OCC[N+](C)(C)C
InChI
1S/C7H16NO2.HI/c1-7(9)10-6-5-8(2,3)4;/h5-6H2,1-4H3;1H/q+1;/p-1
InChI key
SMBBQHHYSLHDHF-UHFFFAOYSA-M
Gene Information
human ... CHRM3(1131)
Application
Acetylcholine is an endogenous neurotransmitter at cholinergic synapses that amplifies action potential of the sarcolemma thereby inducing muscle contractions. Acetylcholine iodide is used as an acetylcholine receptor agonist to identify, characterize and differentiate among types of cholinergic receptors. Acetylcholine iodide is used as a substrate to identify and characterize natural and mutated acetylcholinesterase(s).
Biochem/physiol Actions
Endogenous neurotransmitter at cholinergic synapses; amplifies action potential of the sarcolemma thereby inducing muscle contractions.
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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Iryna Andrusenko et al.
Angewandte Chemie (International ed. in English), 58(32), 10919-10922 (2019-06-19)
Orthocetamol is a regioisomer of the well-known pain medication paracetamol and a promising analgesic and an anti-arthritic medicament itself. However, orthocetamol cannot be grown as single crystals suitable for X-ray diffraction, so its crystal structure has remained a mystery for
Marie Briet et al.
Journal of the American Heart Association, 2(2), e000128-e000128 (2013-04-16)
Recent studies have raised concern about the safety of erythropoiesis-stimulating agents because of evidence of increased risk of hypertension and cardiovascular morbidity and mortality in chronic kidney disease (CKD) patients. In the present study, we investigated the effects of recombinant
Yingchuan B Qi et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 33(12), 5319-5325 (2013-03-22)
Excitatory acetylcholine motor neurons drive Caenorhabditis elegans locomotion. Coordinating the activation states of the backward-driving A and forward-driving B class motor neurons is critical for generating sinusoidal and directional locomotion. Here, we show by in vivo calcium imaging that expression
Global Trade Item Number
| SKU | GTIN |
|---|---|
| A7000-100G-A | 04061832281445 |
| A7000-5G | 04061833383179 |
| A7000-25G | 04061833383162 |
| A7000-25G-A | 04061835176922 |