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Acetylcholine iodide - 10mM in DMSO, high purity , CAS No.2260-50-6

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Acetylcholine iodide - 10mM in DMSO, high purity , CAS No.2260-50-6

5 Citations

COA

Grade & Purity:

10mM in DMSO

Cas Number: 2260-50-6
Molecular Weight: 273.11
Beilstein Registry Number: 3571339
EC Number: 218-862-3
PubChem CID: 75271

In stock

Item Number

A422713

Grouped product items
SKU	Size	Availability	Price	Qty
A422713-1ml	1ml	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$69.90

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Compound libraries (12325) Metabolite (5307)

Basic Description

Synonyms	Acetylcholine iodide \| 2260-50-6 \| Acetylcolina \| Acetylcholine (iodide) \| Choline acetate (ester), iodide \| Acetylholine iodide \| ACh (iodide) \| 2-Acetyloxyethyl(trimethyl)azanium;iodide \| Ethanaminium, 2-(acetyloxy)-N,N,N-trimethyl-, iodide \| 7ZCP12S7HQ \| Ethanaminium, 2-(
Specifications & Purity	10mM in DMSO
Storage Temp	Store at -80°C
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic nitrogen compounds
  - Class Organonitrogen compounds
    - Subclass Quaternary ammonium salts
      - Level5 Cholines
        Level6 Acyl cholines

Kingdom	Organic compounds
Superclass	Organic nitrogen compounds
Class	Organonitrogen compounds
Subclass	Quaternary ammonium salts
Intermediate Tree Nodes	Cholines
Direct Parent	Acyl cholines
Alternative Parents	Tetraalkylammonium salts Carboxylic acid esters Monocarboxylic acids and derivatives Organopnictogen compounds Organic oxides Organic iodide salts Hydrocarbon derivatives Carbonyl compounds Amines
Molecular Framework	Aliphatic acyclic compounds
Substituents	Acyl choline - Tetraalkylammonium salt - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic iodide salt - Organic salt - Organooxygen compound - Carbonyl group - Amine - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as acyl cholines. These are acylated derivatives of choline. Choline or 2-Hydroxy-N,N,N-trimethylethanaminium is a quaternary ammonium salt with the chemical formula (CH3)3N+(CH2)2OH.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Associated Targets(non-human)

Cavia porcellus (23802 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

IUPAC Name	2-acetyloxyethyl(trimethyl)azanium;iodide
INCHI	InChI=1S/C7H16NO2.HI/c1-7(9)10-6-5-8(2,3)4;/h5-6H2,1-4H3;1H/q+1;/p-1
InChIKey	SMBBQHHYSLHDHF-UHFFFAOYSA-M
Smiles	CC(=O)OCC[N+](C)(C)C.[I-]
Isomeric SMILES	CC(=O)OCC[N+](C)(C)C.[I-]
WGK Germany	3
RTECS	KH3300000
PubChem CID	75271
Molecular Weight	273.11
Beilstein	3571339
Reaxy-Rn	3571339

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Chemical and Physical Properties

Sensitivity	Light Sensitive & Hygroscopic
Melt Point(°C)	162°C
Molecular Weight	273.110 g/mol
XLogP3
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	3
Rotatable Bond Count	4
Exact Mass	273.023 Da
Monoisotopic Mass	273.023 Da
Topological Polar Surface Area	26.300 Å²
Heavy Atom Count	11
Formal Charge	0
Complexity	115.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	2

Documents & Articles

The Key Molecule in Neurotransmission—Acetylcholine

Categories: Technical articles

Tags:

Metabolites Acetylcholine Nucleosides and nucleotides Coenzymes In vitro diagnostics Metabolism Neuroscience Nerve signaling

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Wenli Shi, Wenxin Han, Yijing Liao, Jiaqi Wen, Guowen Zhang. (2024) Inhibition mechanism of fisetin on acetylcholinesterase and its synergistic effect with galantamine. SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, 305 (123452).
2. Wenli Shi, Guowen Zhang, Yijing Liao, Xiaoyun Fei, Deming Gong, Xing Hu. (2023) Anti-acetylcholinesterase mechanism of kaempferol and its synergistic effect with galanthamine hydrobromide. Food Bioscience, 56 (103174).
3. Peng Wenping, Wang Nan, Wang Shunmin, Wang Junzhen, Bian Zixiu. (2023) Effects of microwave and exogenous l-phenylalanine treatment on phenolic constituents, antioxidant capacity and enzyme inhibitory activity of Tartary buckwheat sprouts. FOOD SCIENCE AND BIOTECHNOLOGY, 32 (1): (11-19).
4. Lisiqi Xie, Xiao Huang, Bin Su. (2017) Portable Sensor for the Detection of Choline and Its Derivatives Based on Silica Isoporous Membrane and Gellified Nanointerfaces. ACS Sensors, 2 (6): (803–809).
5. Sihua Qian, Hengwei Lin. (2015) Colorimetric Sensor Array for Detection and Identification of Organophosphorus and Carbamate Pesticides. ANALYTICAL CHEMISTRY, 87 (10): (5395–5400).

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