Cloruro di betanecolo - ≥98%(T) , Muscarinic acetylcholine receptor M2 agonist, CAS No.590-63-6, Muscarinic acetylcholine receptor M2 agonist

CAS: 590-63-6 Cat. No.: B153105 Formula: C7H17ClN2O2 Peso molecolare: 196.68 Numero EC: 209-686-8
Disponibile su ordine
GRADE & PURITY ≥98%(T)
Synonyms
Mictrol | Pharmakon1600-01500146 | 2-carbamoyloxypropyltrimethylammonium chloride | Betanecolo cloruro [USP:BAN:JAN] | DTXSID2022676 | Betanecolo cloruro 10 mg | Betanecolo cloruro 50 mg | Mechothane | NC00660 | 1-Propanaminium, 2-((aminocarbonyl)ox
Storage
Conservare a 2-8°C, con carica di argon
Shipped In
Ghiaccio umido
★
Size
Germania (EU)
USA*
Price
Qty
1g
B153105-1g
—
3 Disponibile

8,59€

12,93€
Salva 4,34 € (33.56%)
5g
B153105-5g
—
3 Disponibile

26,81€

40,70€
Salva 13,88 € (34.12%)
25g
B153105-25g
—
3 Disponibile

85,82€

129,21€
Salva 43,39 € (33.58%)
100g
B153105-100g
—
2 Disponibile

240,28€

360,89€
Salva 120,62 € (33.42%)
Enter a quantity for the sizes you want to add.
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Why this grade

≥98%(T) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Conservare a 2-8°C, con carica di argon Ships Ghiaccio umido 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Panoramica

Il betanecolo cloruro è un agonista selettivo dei recettori muscarinici senza alcun effetto sui recettori nicotinici. Bersaglio: mAChR Il betanecolo è un carbammato di colina parasimpaticomimetico che stimola selettivamente i recettori muscarinici senza alcun effetto sui recettori nicotinici. A differenza dell'acetilcolina, il betanecolo non viene idrolizzato dalla colinesterasi e ha quindi una lunga durata d'azione. Il betanecolo orale migliora significativamente la pressione di contrazione e il transito del bolo nella porzione muscolare liscia dell'esofago nei pazienti con IEM grave. Il betanecolo ha un potenziale beneficio nel trattamento della paralisi cerebrale.

Specifications

Sinonimi
Mictrol | Pharmakon1600-01500146 | 2-carbamoyloxypropyltrimethylammonium chloride | Betanecolo cloruro [USP:BAN:JAN] | DTXSID2022676 | Betanecolo cloruro 10 mg | Betanecolo cloruro 50 mg | Mechothane | NC00660 | 1-Propanaminium, 2-((aminocarbonyl)ox
Specifiche e purezza
≥98%(T)
Meccanismi biochimici e fisiologici
Agonista dei recettori muscarinici (i valori di EC 50 sono 7 (M 4 ), 14,5 (M 3 ), 35 (M 1 ) e 32 μM (M 5 )). Attività agonista M 2 in vitro . Capacità limitata di attraversare la barriera emato-encefalica.
Condizioni di conservazione di stoccaggio
Conservare a 2-8°C, con carica di argon
Spedito in
Ghiaccio umido
Tipo di azione
AGONIST
Meccanismo d'azione
Muscarinic acetylcholine receptor M2 agonist
Nota
Per quanto possibile, si consiglia di preparare e utilizzare le soluzioni lo stesso giorno. Tuttavia, se è necessario preparare in anticipo le soluzioni di riserva, si consiglia di conservarle in aliquote in fiale ben chiuse a -20°C. In genere, queste possono essere utilizzate per un mese. In genere, queste soluzioni sono utilizzabili fino a un mese. Prima dell'uso e dell'apertura della fiala, si consiglia di lasciare che il prodotto si equilibri a temperatura ambiente per almeno 1 ora. Avete bisogno di ulteriori consigli su solubilità, uso e manipolazione? Per ulteriori informazioni, visitare la pagina delle domande frequenti (FAQ).
Purezza
≥98%(T)
Nomi e identificatori
Pubchem Sid
Sorrisi canonici
CC(C[N+](C)(C)C)OC(=O)N.[Cl-]
IUPAC Name
2-carbamoyloxypropyl(trimethyl)azanium;chloride
InChIKey
XXRMYXBSBOVVBH-UHFFFAOYSA-N
INCHI
1S/C7H16N2O2.ClH/c1-6(11-7(8)10)5-9(2,3)4;/h6H,5H2,1-4H3,(H-,8,10);1H
Isomeri SMILES
CC(C[N+](C)(C)C)OC(=O)N.[Cl-]
Peso molecolare
196.68
Reaxy-Rn
3731819
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3731819&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 acids and derivatives
ClasseCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives - Carbamic acids and derivatives
Direct ParentCarbamate esters
Alternative Parents Tetraalkylammonium salts  Organic carbonic acids and derivatives  Organopnictogen compounds  Organic oxides  Organic chloride salts  Hydrocarbon derivatives  Carbonyl compounds  Amines  
Molecular FrameworkAliphatic acyclic compounds
Substituents Quaternary ammonium salt - Carbamic acid ester - Tetraalkylammonium salt - Carbonic acid derivative - Amine - Organic oxide - Hydrocarbon derivative - Organic chloride salt - Organic salt - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Carbonyl group - Aliphatic acyclic compound
DescrizioneThis compound belongs to the class of organic compounds known as carbamate esters. These are compounds containing an ester of carbamic acid with the general structure R2NC(=O)OR' (R' not H). They are esters of carbamic acids.
External Descriptors chloride salt - carbamate ester - quaternary ammonium salt
Struttura 3D
Modello di struttura chimica interattiva





Obiettivi associati (umani)
CHRM3 Tclin Muscarinic acetylcholine receptor M3 (7750 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ERG Tbio Transcriptional regulator ERG (5589 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
LMNA Tbio Prelamin-A/C (36751 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GMNN Tbio Geminin (128009 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MPHOSPH8 Tbio M-phase phosphoprotein 8 (656 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 (2517 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Obiettivi associati (non umani)
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
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mapt Microtubule-associated protein tau (6 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.

5 results found

Lot NumberCertificate TypeDataOggetto
D2621066Certificate of AnalysisApr 28, 2026 B153105
L2503188Certificate of AnalysisJul 13, 2024 B153105
L2503189Certificate of AnalysisJul 13, 2024 B153105
E2427408Certificate of AnalysisMay 29, 2024 B153105
F1912154Certificate of AnalysisMar 09, 2023 B153105
Proprietà chimiche e fisiche
SolubilitàSolubility in water: Completely soluble; Slightly soluble in Ethanol
SensibilitàHygroscopic,Heat Sensitive
Punto di fusione (°C)216 °C
Peso molecolare196.670 g/mol
XLogP3
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count4
Exact Mass196.098 Da
Monoisotopic Mass196.098 Da
Topological Polar Surface Area52.300 Ų
Heavy Atom Count12
Formal Charge0
Complexity140.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count1
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count2
Calcolatori di soluzioni
Recensioni

Recensioni dei clienti

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