Acetylcholine chloride(ACh) - for cell culture, ≥99% , Muscarinic acetylcholine receptor M3 agonist, CAS No.60-31-1, Muscarinic acetylcholine receptor M3 agonist

CAS: 60-31-1 Cat. No.: A111015 Formula: C7H16ClNO2 Peso molecolare: 181.66 Beilstein Registry Number: 3571875 Numero EC: 200-468-8
Disponibile su ordine
GRADE & PURITY for Cell culture ? Cell-culture grade — low endotoxin and contaminants to support viable cell growth. Use in mammalian/other cell culture media and supplements. ≥99%
Synonyms
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-acety
Storage
Store at 2-8°C,Protected from light,Argon charged,Desiccated
Shipped In
Wet ice
★
Size
Germania (EU)
USA*
Price
Qty
25g
A111015-25g
—
3 Disponibile

198,63€

231,60€
Salva 32,97 € (14.24%)
100g
A111015-100g
—
1 Disponibile

602,12€

780,88€
Salva 178,75 € (22.89%)
Enter a quantity for the sizes you want to add.
🧪
Why this grade

for cell culture, ≥99% per la coltura cellulare for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C,Protected from light,Argon charged,Desiccated Ships Wet ice 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.

Specifications

Sinonimi
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-acety
Specifiche e purezza
for cell culture, ≥99%
Meccanismi biochimici e fisiologici
Endogenous neurotransmitter in both the central and peripheral nervous systems. Displays activity at the nicotinic and muscarinic acetylcholine receptors. Also implicated in numerous non-neuronal roles.
Condizioni di conservazione di stoccaggio
Store at 2-8°C,Protected from light,Argon charged,Desiccated
Spedito in
Wet ice
Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.
Grado
per la coltura cellulare
Tipo di azione
AGONIST
Meccanismo d'azione
Muscarinic acetylcholine receptor M3 agonist
Nota
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
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.

6 results found

Lot NumberCertificate TypeDataOggetto
F2602036Certificate of AnalysisJun 11, 2026 A111015
E2225151Certificate of AnalysisMar 11, 2026 A111015
I2312039Certificate of AnalysisSep 04, 2023 A111015
I2312040Certificate of AnalysisSep 04, 2023 A111015
E2225144Certificate of AnalysisMar 22, 2022 A111015
H2328116Certificate of AnalysisMar 22, 2022 A111015
Proprietà chimiche e fisiche
Solubilitàwater: 100 mg/mL, clear, colorless
SensibilitàLight and moisture 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
The Key Molecule in Neurotransmission—Acetylcholine
For Cell Culture
Cholinesterase Detection Systems: Reaction Principles, Method Types, and Experimental Design
Neurotransmitters, Receptors, and Transporters
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
Recensioni

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