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· · COA & SDS available for every product · Same-day shipping on in-stock items Propantheline bromide - ≥97% , Muscarinic acetylcholine receptor M1 antagonist, CAS No.50-34-0, Muscarinic acetylcholine receptor M1 antagonist
Synonyms
NCGC00015854-10 | Propantelina bromuro | PROPANTHELINE BROMIDE [WHO-DD] | propanthelinii bromidum | SCHEMBL40291 | A03AB05 | Bromure de propantheline [INN-French] | Prodixamon | PROPANTHELINE BROMIDE (USP IMPURITY) | CAS-50-34-0 | Neopepulsan | MFCD000502
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Why this grade ≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature Ships Normal Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonyms
NCGC00015854-10 | Propantelina bromuro | PROPANTHELINE BROMIDE [WHO-DD] | propanthelinii bromidum | SCHEMBL40291 | A03AB05 | Bromure de propantheline [INN-French] | Prodixamon | PROPANTHELINE BROMIDE (USP IMPURITY) | CAS-50-34-0 | Neopepulsan | MFCD000502
Specifications & Purity
≥97%
Biochemical and Physiological Mechanisms
Inhibits action of acetylcholine at post-ganglionic synapses; muscarinic acetylcholine receptor antagonist; antispasmodic; reduces gastric acid secretion.
Mechanism of action
Muscarinic acetylcholine receptor M1 antagonist
Names and Identifiers Pubchem Sid 488180962 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488180962 Canonical Smiles CC(C)[N+](C)(CCOC(=O)C1C2=CC=CC=C2OC3=CC=CC=C13)C(C)C.[Br-] IUPAC Name methyl-di(propan-2-yl)-[2-(9H-xanthene-9-carbonyloxy)ethyl]azanium;bromide InChIKey XLBIBBZXLMYSFF-UHFFFAOYSA-M INCHI 1S/C23H30NO3.BrH/c1-16(2)24(5,17(3)4)14-15-26-23(25)22-18-10-6-8-12-20(18)27-21-13-9-7-11-19(21)22;/h6-13,16-17,22H,14-15H2,1-5H3;1H/q+1;/p-1 Isomeric SMILES CC(C)[N+](C)(CCOC(=O)C1C2=CC=CC=C2OC3=CC=CC=C13)C(C)C.[Br-] WGK Germany 3 RTECS BP8249200 PubChem CID 9279 Molecular Weight 448.39
Documentation 📋 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 Kingdom Organic compounds Superclass Organoheterocyclic compounds Class Benzopyrans Subclass 1-benzopyrans Intermediate Tree Nodes Dibenzopyrans Direct Parent Xanthenes Alternative Parents Diarylethers Benzenoids Tetraalkylammonium salts Carboxylic acid esters Oxacyclic compounds Monocarboxylic acids and derivatives Organopnictogen compounds Organic zwitterions Organic oxides Organic bromide salts Hydrocarbon derivatives Carbonyl compounds Amines Molecular Framework Aromatic heteropolycyclic compounds Substituents Xanthene - Diaryl ether - Benzenoid - Tetraalkylammonium salt - Quaternary ammonium salt - Carboxylic acid ester - Carboxylic acid derivative - Ether - Oxacycle - Monocarboxylic acid or derivatives - Organic oxygen compound - Organic zwitterion - Organic nitrogen compound - Organic salt - Organooxygen compound - Organonitrogen compound - Organic bromide salt - Hydrocarbon derivative - Amine - Organic oxide - Organopnictogen compound - Carbonyl group - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as xanthenes. These are polycyclic aromatic compounds containing a xanthene moiety, which consists of two benzene rings joined to each other by a pyran ring. External Descriptors Not available Data sources 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.
3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Solubility H2O: 50 mg/mL Molecular Weight 448.400 g/mol XLogP3 Hydrogen Bond Donor Count 0 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 7 Exact Mass 447.141 Da Monoisotopic Mass 447.141 Da Topological Polar Surface Area 35.500 Ų Heavy Atom Count 28 Formal Charge 0 Complexity 474.000 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
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