Acetylcholine chloride(ACh) - ≥99% , CAS No.60-31-1

CAS: 60-31-1 Cat. No.: A111014 Formula: C7H16ClNO2 Peso molecolare: 181.66 Beilstein Registry Number: 3571875 Numero EC: 200-468-8
Disponibile su ordine
GRADE & PURITY ≥99%
Synonyms
ACh | MLS000028640 | NCGC00018123-07 | SCHEMBL40885 | Acetylcholine chloride (USP:INN:BAN:JAN) | Acetylcholine hydrochloride | AI3-51676 | REGID_for_CID_6060 | 2-acetyloxy-N,N,N-trimethylethanaminium chloride | AKOS005111031 | O-Acetylcholine chloride | 2
Storage
Argon charged,Room temperature
Shipped In
Normal
★
Size
Germania (EU)
USA*
Price
Qty
5g
A111014-5g
—
Disponibile ≥10
21,61€
25g
A111014-25g
—
2 Disponibile
69,33€
100g
A111014-100g
—
1 Disponibile
196,02€
Enter a quantity for the sizes you want to add.
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Why this grade

≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Argon charged,Room temperature Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 25 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Panoramica

Acetylcholine chloride, more commonly referred to as just acetylcholine, is a cholinergic neurotransmitter that can induce the opening of calcium channels, as well as act on nicotinic and muscarinic acetylcholine receptors. Acetylcholine plays an important role at many sites in the central nervous system. The compound has been shown to have ophthalmological uses and can be broken down quickly by choliesterases. Studies show that non-neuronal acetylcholine influences many basic cells functions, such as mitosis, cells differentiation, cytoskeletal organization, and cell to cell contact, among other functions.
A cholinergic neurotransmitter that can induce the opening of calcium channels

Specifications

Sinonimi
ACh | MLS000028640 | NCGC00018123-07 | SCHEMBL40885 | Acetylcholine chloride (USP:INN:BAN:JAN) | Acetylcholine hydrochloride | AI3-51676 | REGID_for_CID_6060 | 2-acetyloxy-N,N,N-trimethylethanaminium chloride | AKOS005111031 | O-Acetylcholine chloride | 2
Specifiche e purezza
≥99%
Meccanismi biochimici e fisiologici
Endogenous neurotransmitter. Acts at nicotinic and muscarinic acetylcholine receptors.
Condizioni di conservazione di stoccaggio
Argon charged,Room temperature
Spedito in
Normal
Purezza
≥99%
Nomi e identificatori
Pubchem Sid
Sorrisi canonici
CC(=O)OCC[N+](C)(C)C.[Cl-]
IUPAC Name
2-acetyloxyethyl(trimethyl)azanium;chloride
InChIKey
JUGOREOARAHOCO-UHFFFAOYSA-M
INCHI
1S/C7H16NO2.ClH/c1-7(9)10-6-5-8(2,3)4;/h5-6H2,1-4H3;1H/q+1;/p-1
Isomeri SMILES
CC(=O)OCC[N+](C)(C)C.[Cl-]
WGK Germania
2
RTECS
FZ9800000
Peso molecolare
181.66
Beilstein
3571875
Reaxy-Rn
3571875
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3571875&ln=

Documentazione

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic nitrogen compounds
ClasseOrganonitrogen compounds
SubclassQuaternary ammonium salts
Intermediate Tree Nodes Cholines
Direct ParentAcyl cholines
Alternative Parents Tetraalkylammonium salts  Carboxylic acid esters  Monocarboxylic acids and derivatives  Organopnictogen compounds  Organic oxides  Organic chloride salts  Hydrocarbon derivatives  Carbonyl compounds  Amines  
Molecular FrameworkAliphatic 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 chloride salt - Organic salt - Organooxygen compound - Carbonyl group - Amine - Aliphatic acyclic compound
DescrizioneThis 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 quaternary ammonium salt
Struttura 3D
Modello di struttura chimica interattiva





Obiettivi associati (umani)
CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRM5 Tclin Muscarinic acetylcholine receptor M5 (4677 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRM3 Tclin Muscarinic acetylcholine receptor M3 (7750 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GLP1R Tclin Glucagon-like peptide 1 receptor (111429 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Homo sapiens (32628 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC5A7 Tchem High-affinity choline transporter (1462 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (38016 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TNNC1 Tclin Troponin, cardiac muscle (276 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Obiettivi associati (non umani)
ampC Beta-lactamase AmpC (62480 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pseudomonas aeruginosa (123386 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Klebsiella pneumoniae (43867 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Acinetobacter baumannii (41033 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Escherichia coli (133304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cryptococcus neoformans (21258 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Candida albicans (78123 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Trpc4 Short transient receptor potential channel 4 (1615 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
vpr Aberrant vpr protein (14595 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Meccanismi d'azione
Certificati (CoA, COO, BSE/TSE e tabella di analisi)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

42 results found

Lot NumberCertificate TypeDataOggetto
H2620189Certificate of AnalysisAug 13, 2026 A111014
H2620129Certificate of AnalysisAug 13, 2026 A111014
H2620128Certificate of AnalysisAug 13, 2026 A111014
G2616273Certificate of AnalysisJul 09, 2026 A111014
G2616272Certificate of AnalysisJul 09, 2026 A111014
D2628151Certificate of AnalysisApr 16, 2026 A111014
D2628148Certificate of AnalysisApr 16, 2026 A111014
D2628146Certificate of AnalysisApr 16, 2026 A111014
A2609144Certificate of AnalysisDec 31, 2025 A111014
A2609143Certificate of AnalysisDec 31, 2025 A111014
A2619161Certificate of AnalysisDec 31, 2025 A111014
C2414105Certificate of AnalysisDec 10, 2025 A111014
L2305120Certificate of AnalysisSep 09, 2025 A111014
I2502219Certificate of AnalysisAug 08, 2025 A111014
I2502218Certificate of AnalysisAug 08, 2025 A111014
I2502217Certificate of AnalysisAug 08, 2025 A111014
F2519223Certificate of AnalysisJun 27, 2025 A111014
F2519224Certificate of AnalysisJun 27, 2025 A111014
F2519250Certificate of AnalysisJun 27, 2025 A111014
L2425228Certificate of AnalysisNov 23, 2024 A111014
K2413158Certificate of AnalysisNov 23, 2024 A111014
K2413157Certificate of AnalysisNov 23, 2024 A111014
K2413154Certificate of AnalysisNov 23, 2024 A111014
D2429095Certificate of AnalysisMar 18, 2024 A111014
D2429096Certificate of AnalysisMar 18, 2024 A111014
D2429097Certificate of AnalysisMar 18, 2024 A111014
D2429098Certificate of AnalysisMar 18, 2024 A111014
D2407105Certificate of AnalysisMar 08, 2024 A111014
D2407107Certificate of AnalysisMar 08, 2024 A111014
D2407106Certificate of AnalysisMar 08, 2024 A111014
C2414106Certificate of AnalysisFeb 26, 2024 A111014
C2414107Certificate of AnalysisFeb 26, 2024 A111014
C2414104Certificate of AnalysisFeb 26, 2024 A111014
H2330068Certificate of AnalysisAug 21, 2023 A111014
H2330067Certificate of AnalysisAug 21, 2023 A111014
H2330066Certificate of AnalysisAug 21, 2023 A111014
H2330061Certificate of AnalysisAug 15, 2023 A111014
H2330064Certificate of AnalysisAug 15, 2023 A111014
H2330063Certificate of AnalysisAug 15, 2023 A111014
J2209009Certificate of AnalysisSep 08, 2022 A111014
J2209012Certificate of AnalysisSep 08, 2022 A111014
J2209013Certificate of AnalysisSep 08, 2022 A111014
Proprietà chimiche e fisiche
SolubilitàSolvent:water, Max Conc. mg/mL: 18.17, Max Conc. mM: 100; Solvent:DMSO, Max Conc. mg/mL: 18.17, Max Conc. mM: 100
SensibilitàLight, Moisture and Heat Sensitive
Punto di fusione (°C)149-152°C
Peso molecolare181.660 g/mol
XLogP3
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count3
Rotatable Bond Count4
Exact Mass181.087 Da
Monoisotopic Mass181.087 Da
Topological Polar Surface Area26.300 Ų
Heavy Atom Count11
Formal Charge0
Complexity115.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count2
Domande frequenti e articoli
Metabolic signaling pathway
The Key Molecule in Neurotransmission—Acetylcholine
Cholinesterase Detection Systems: Reaction Principles, Method Types, and Experimental Design
GPCR/G Protein Signal Transduction Mechanisms and Disease Research
Neuronal Signal Transduction Mechanisms and Disease Research
Choline Metabolism and Detection Methods: Pathway Analysis of Choline, Phosphatidylcholine, Betaine, Acetylcholine, and TMAO
Mechanistic Basis of Acetyl Hexapeptide-8 in the Management of Expression Lines: SNARE Complex Interference, Constraints on Percutaneous Delivery, and Combination Strategies
Citations of This Product
Calcolatori di soluzioni
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