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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Tetrandrini dimethiodidum , Muscle-type nicotinic acetylcholine receptor antagonist, CAS No.7601-55-0, Muscle-type nicotinic acetylcholine receptor antagonist
Synonyms
D00761 | DIMETHYLTUBOCURARINIUM IODIDE [WHO-DD] | NCGC00263444-01 | CHEBI:6901 | Q20817012 | UNII-O0U0E87X7F | METOCURINE IODIDE [VANDF] | Dimethyl tubocurarine iodide | 13H-4,6:21,24-DIETHENO-8,12-METHENO-1H-PYRIDO(3',2':14,15)(1,11)DIOXACYCLOEICOSINO(2,
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Why this grade 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 Sinónimos
D00761 | DIMETHYLTUBOCURARINIUM IODIDE [WHO-DD] | NCGC00263444-01 | CHEBI:6901 | Q20817012 | UNII-O0U0E87X7F | METOCURINE IODIDE [VANDF] | Dimethyl tubocurarine iodide | 13H-4, 6:21, 24-DIETHENO-8, 12-METHENO-1H-PYRIDO(3', 2':14, 15)(1, 11)DIOXACYCLOEICOSINO(2,
Condiciones de almacenamiento de almacenamiento
Room temperature
Mecanismo de acción
Muscle-type nicotinic acetylcholine receptor antagonist
Nombres e identificadores Sonrisas canónicas C[N+]1(CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C6C(CC7=CC(=C(C=C7)OC)O3)[N+](CCC6=CC(=C5OC)OC)(C)C)OC)C.[I-].[I-] IUPAC Name (1S,16R)-9,10,21,25-tetramethoxy-15,15,30,30-tetramethyl-7,23-dioxa-15,30-diazoniaheptacyclo[22.6.2.23,6.18,12.118,22.027,31.016,34]hexatriaconta-3(36),4,6(35),8(34),9,11,18(33),19,21,24,26,31-dodecaene;diiodide InChIKey DIGFQJFCDPKEPF-OIUSMDOTSA-L INCHI 1S/C40H48N2O6.2HI/c1-41(2)17-15-27-22-34(44-6)36-24-30(27)31(41)19-25-9-12-29(13-10-25)47-40-38-28(23-37(45-7)39(40)46-8)16-18-42(3,4)32(38)20-26-11-14-33(43-5)35(21-26)48-36;;/h9-14,21-24,31-32H,15-20H2,1-8H3;2*1H/q+2;;/p-2/t31-,32+;;/m0../s1 Isómeros SMILES C[N+]1(CCC2=CC(=C3C=C2[C@@H]1CC4=CC=C(C=C4)OC5=C6[C@@H](CC7=CC(=C(C=C7)OC)O3)[N+](CCC6=CC(=C5OC)OC)(C)C)OC)C.[I-].[I-] Peso molecular 906.63 Reaxy-Rn 4651705 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4651705&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 Organic oxygen compounds Clase Organooxygen compounds Subclass Ethers Intermediate Tree Nodes Not available Direct Parent Diarylethers Alternative Parents Tetrahydroisoquinolines Anisoles Aralkylamines Alkyl aryl ethers Tetraalkylammonium salts Oxacyclic compounds Azacyclic compounds Organopnictogen compounds Organic zwitterions Organic iodide salts Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents Diaryl ether - Tetrahydroisoquinoline - Anisole - Alkyl aryl ether - Aralkylamine - Benzenoid - Tetraalkylammonium salt - Quaternary ammonium salt - Oxacycle - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Organic zwitterion - Organic salt - Organic iodide salt - Organonitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Amine - Aromatic heteropolycyclic compound Descripción This compound belongs to the class of organic compounds known as diarylethers. These are organic compounds containing the dialkyl ether functional group, with the formula ROR', where R and R' are aryl groups. 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) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Peso molecular 906.600 g/mol XLogP3 Hydrogen Bond Donor Count 0 Hydrogen Bond Acceptor Count 8 Rotatable Bond Count 4 Exact Mass 906.16 Da Monoisotopic Mass 906.16 Da Topological Polar Surface Area 55.400 Ų Heavy Atom Count 50 Formal Charge 0 Complexity 1060.000 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 3
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