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· · COA & SDS available for every product · Same-day shipping on in-stock items Scopolamine Methyl Nitrate - ≥98%(HPLC)(T) , CAS No.6106-46-3
Synonyms
HYOSCINE METHONITRATE [MART.] | N-Methylscopolaminium-nitrat | REGID_for_CID_657297 | 3-Oxa-9-azoniatricyclo(3.3.1.02,4)nonane, 7-((2S)-3-hydroxy-1-oxo-2-phenylpropoxy)-9,9-dimethyl-, (1alpha,2beta,4beta,5alpha,7beta)-, nitrate (1:1) | Methylscopolaminnit
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Why this grade ≥98%(HPLC)(T) 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 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonyms
HYOSCINE METHONITRATE [MART.] | N-Methylscopolaminium-nitrat | REGID_for_CID_657297 | 3-Oxa-9-azoniatricyclo(3.3.1.02, 4)nonane, 7-((2S)-3-hydroxy-1-oxo-2-phenylpropoxy)-9, 9-dimethyl-, (1alpha, 2beta, 4beta, 5alpha, 7beta)-, nitrate (1:1) | Methylscopolaminnit
Specifications & Purity
≥98%(HPLC)(T)
Names and Identifiers Canonical Smiles C[N+]1(C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4)C.[N+](=O)([O-])[O-] IUPAC Name [(1R,2R,4S,5S)-9,9-dimethyl-3-oxa-9-azoniatricyclo[3.3.1.02,4]nonan-7-yl] (2S)-3-hydroxy-2-phenylpropanoate;nitrate InChIKey BSQIVYOSLFLSGE-OZVSTBQFSA-N INCHI 1S/C18H24NO4.NO3/c1-19(2)14-8-12(9-15(19)17-16(14)23-17)22-18(21)13(10-20)11-6-4-3-5-7-11;2-1(3)4/h3-7,12-17,20H,8-10H2,1-2H3;/q+1;-1/t12?,13-,14-,15+,16-,17+;/m1./s1 Isomeric SMILES C[N+]1([C@@H]2CC(C[C@H]1[C@H]3[C@@H]2O3)OC(=O)[C@H](CO)C4=CC=CC=C4)C.[N+](=O)([O-])[O-] RTECS YM3675150 PubChem CID 657297 Molecular Weight 380.4 Reaxy-Rn 11258389
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 Organic acids and derivatives Class Hydroxy acids and derivatives Subclass Beta hydroxy acids and derivatives Intermediate Tree Nodes Not available Direct Parent Beta hydroxy acids and derivatives Alternative Parents Benzene and substituted derivatives Piperidines Morpholines N-alkylpyrrolidines Tetraalkylammonium salts Organic nitrates Carboxylic acid esters Organic nitric acids Organic nitro compounds Azacyclic compounds Oxacyclic compounds Dialkyl ethers Epoxides Monocarboxylic acids and derivatives Hydrocarbon derivatives Carbonyl compounds Primary alcohols Amines Organopnictogen compounds Organic zwitterions Organic salts Organic oxides Molecular Framework Aromatic heteropolycyclic compounds Substituents Beta-hydroxy acid - Monocyclic benzene moiety - Morpholine - Oxazinane - Piperidine - Benzenoid - N-alkylpyrrolidine - Tetraalkylammonium salt - Organic nitrate - Pyrrolidine - Quaternary ammonium salt - Carboxylic acid ester - Organic nitric acid - Organic nitric acid or derivatives - Organic nitro compound - Carboxylic acid derivative - Dialkyl ether - Oxirane - Ether - Monocarboxylic acid or derivatives - Oxacycle - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Allyl-type 1,3-dipolar organic compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Alcohol - Organonitrogen compound - Organooxygen compound - Organopnictogen compound - Organic salt - Primary alcohol - Amine - Organic zwitterion - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as beta hydroxy acids and derivatives. These are compounds containing a carboxylic acid substituted with a hydroxyl group on the C3 carbon atom. 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) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Specific Rotation[α] -25° (C=1,H2O) Melt Point(°C) 199 °C Molecular Weight 380.400 g/mol XLogP3 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 7 Rotatable Bond Count 5 Exact Mass 380.158 Da Monoisotopic Mass 380.158 Da Topological Polar Surface Area 122.000 Ų Heavy Atom Count 27 Formal Charge 0 Complexity 472.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 5 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
Citations of This Product References 1. Kewei Liu, Juan Zhu, Yuan Chang, Zhenzhou Lin, Zhu Shi, Xing Li, Xing Chen, Chuman Lin, Suyue Pan, Kaibin Huang. (2021) Attenuation of cerebral edema facilitates recovery of glymphatic system function after status epilepticus. JCI Insight, [PMID:34494549 ] [10.1172/jci.insight.151835 ] 2. Tingting Yang, Zhenzhou Lin, Mingjia Yu, Yongchuan Li, Jiancong Chen, Yuanchi Liu, Kaibin Huang, Suyue Pan. (2025) SUR1-TRPM4 Regulates Aquaporin-4 Subcellular Localization by Astrocytic Endfeet Calcium Signals Following Status Epilepticus. GLIA, [PMID:40631759 ] [10.1002/glia.70056 ]
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