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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Anisotropine Methylbromide - ≥98% , Muscarinic acetylcholine receptor M1 antagonist, CAS No.80-50-2, Muscarinic acetylcholine receptor M1 antagonist
Synonyms
Lytispasm | AKOS015916559 | 8-Azoniabicyclo(3.2.1)octane, 8,8-dimethyl-3-((1-oxo-2-propylpentyl)oxy)-, bromide, endo- | Metilbromuro de octatropina | Opera_ID_1463 | ANISOTROPINE METHYLBROMIDE [VANDF] | Methyloctatropine bromide (JAN) | Valpin (TN) | Meti
Shipped In
Ice chest + Ice pads
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Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -20°C Ships Ice chest + Ice pads 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 Sinónimos
Lytispasm | AKOS015916559 | 8-Azoniabicyclo(3.2.1)octane, 8, 8-dimethyl-3-((1-oxo-2-propylpentyl)oxy)-, bromide, endo- | Metilbromuro de octatropina | Opera_ID_1463 | ANISOTROPINE METHYLBROMIDE [VANDF] | Methyloctatropine bromide (JAN) | Valpin (TN) | Meti
Especificaciones y pureza
≥98%
Mecanismos bioquímicos y fisiológicos
Anisotropine Methylbromide is an anticholinergic agent and has been used for relief of gastrointestinal spasm and for the suppression of gastric acid secretion.
Condiciones de almacenamiento de almacenamiento
Store at -20°C
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Mecanismo de acción
Muscarinic acetylcholine receptor M1 antagonist
Nombres e identificadores Pubchem Sid 504759794 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504759794 Sonrisas canónicas CCCC(CCC)C(=O)OC1CC2CCC(C1)[N+]2(C)C.[Br-] IUPAC Name [(1S,5R)-8,8-dimethyl-8-azoniabicyclo[3.2.1]octan-3-yl] 2-propylpentanoate;bromide InChIKey QSFKGMJOKUZAJM-JXMYBXCISA-M INCHI 1S/C17H32NO2.BrH/c1-5-7-13(8-6-2)17(19)20-16-11-14-9-10-15(12-16)18(14,3)4;/h13-16H,5-12H2,1-4H3;1H/q+1;/p-1/t14-,15+,16?; Isómeros SMILES CCCC(CCC)C(=O)OC1C[C@H]2CC[C@@H](C1)[N+]2(C)C.[Br-] WGK Alemania 3 RTECS YM3710000 Peso molecular 362.35 Reaxy-Rn 43598085 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=43598085&ln=
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 Alkaloids and derivatives Clase Tropane alkaloids Subclass Not available Intermediate Tree Nodes Not available Direct Parent Tropane alkaloids Alternative Parents Fatty acid esters Piperidines N-alkylpyrrolidines Tetraalkylammonium salts Carboxylic acid esters Monocarboxylic acids and derivatives Azacyclic compounds Organopnictogen compounds Organic oxides Organic bromide salts Hydrocarbon derivatives Carbonyl compounds Amines Molecular Framework Aliphatic heteropolycyclic compounds Substituents Tropane alkaloid - Fatty acid ester - Piperidine - N-alkylpyrrolidine - Fatty acyl - Pyrrolidine - Tetraalkylammonium salt - Quaternary ammonium salt - Carboxylic acid ester - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Azacycle - Organoheterocyclic compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organooxygen compound - Organonitrogen compound - Amine - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Organic bromide salt - Organic salt - Aliphatic heteropolycyclic compound Descripción This compound belongs to the class of organic compounds known as tropane alkaloids. These are organic compounds containing the nitrogenous bicyclic alkaloid parent N-Methyl-8-azabicyclo[3.2.1]octane. 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.
Estructura 3D Objetivos asociados (humanos) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Solubilidad Chloroform (Slightly), Methanol (Slightly) Punto de fusión (°C) >285°C (dec.) Peso molecular 362.300 g/mol XLogP3 Hydrogen Bond Donor Count 0 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 7 Exact Mass 361.162 Da Monoisotopic Mass 361.162 Da Topological Polar Surface Area 26.300 Ų Heavy Atom Count 21 Formal Charge 0 Complexity 318.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 2 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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