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· · COA & SDS Disponível para todos os produtos · Envio no mesmo dia em itens em estoque Rivastigmine - Moligand™, 10mM in DMSO , Cholinesterases; ACHE & BCHE inhibitor, CAS No.123441-03-2, Cholinesterases; ACHE & BCHE inhibitor
Disponível para encomenda
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. 10mM in DMSO Synonyms
AC-8250 | rivastigmine hexal | Rivastigmine impurity D | SR-05000001475 | SR-05000001475-2 | BDBM10620 | Carbamic acid, ethylmethyl-, 3-((1S)-1-(dimethylamino)ethyl)phenyl ester | DTXCID703564 | ONO-2540 | Rivastigmina | Rivastigmine sandoz | W-200966 | R
Shipped In
Dry ice packs + Cold packs
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Why this grade Moligand™, 10mM in DMSO Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -80°C Ships Dry ice packs + Cold packs 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Sinónimos
AC-8250 | rivastigmine hexal | Rivastigmine impurity D | SR-05000001475 | SR-05000001475-2 | BDBM10620 | Carbamic acid, ethylmethyl-, 3-((1S)-1-(dimethylamino)ethyl)phenyl ester | DTXCID703564 | ONO-2540 | Rivastigmina | Rivastigmine sandoz | W-200966 | R
Especificações e pureza
Moligand™, 10mM in DMSO
Condições de armazenamento de armazenamento
Store at -80°C
Enviado em
Dry ice packs + Cold packs
Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.
Mecanismo de ação
Cholinesterases; ACHE & BCHE inhibitor
Propriedades do produto Nomes e identificadores Pubchem Sid 528766958 Sorrisos canónicos CCN(C)C(=O)OC1=CC=CC(=C1)C(C)N(C)C IUPAC Name [3-[(1S)-1-(dimethylamino)ethyl]phenyl] N-ethyl-N-methylcarbamate InChIKey XSVMFMHYUFZWBK-NSHDSACASA-N INCHI 1S/C14H22N2O2/c1-6-16(5)14(17)18-13-9-7-8-12(10-13)11(2)15(3)4/h7-11H,6H2,1-5H3/t11-/m0/s1 SMILES isoméricas CCN(C)C(=O)OC1=CC=CC(=C1)[C@H](C)N(C)C PubChem CID 77991 Peso molecular 250.34
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 Benzenoids Classe Benzene and substituted derivatives Subclass Phenoxy compounds Intermediate Tree Nodes Not available Direct Parent Phenoxy compounds Alternative Parents Aralkylamines Carbamate esters Trialkylamines Organic carbonic acids and derivatives Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aromatic homomonocyclic compounds Substituents Phenoxy compound - Aralkylamine - Carbamic acid ester - Carbonic acid derivative - Tertiary amine - Tertiary aliphatic amine - Amine - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Carbonyl group - Aromatic homomonocyclic compound Descrição This compound belongs to the class of organic compounds known as phenoxy compounds. These are aromatic compounds contaning a phenoxy group. External Descriptors carbamate ester - tertiary amino compound 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.
Estrutura 3D Alvos associados (humanos) Alvos associados (não humanos) Mecanismos de ação Certificados（CoA,COO,BSE/TSE e Mapa de Análise) Propriedades químicas e físicas Sensibilidade light sensitive Ponto de inflamação (°C) 145.0 °C Ponto de ebulição (°C) 135 °C/0.26 mmHg Peso molecular 250.340 g/mol XLogP3 2.300 Hydrogen Bond Donor Count 0 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 5 Exact Mass 250.168 Da Monoisotopic Mass 250.168 Da Topological Polar Surface Area 32.800 Ų Heavy Atom Count 18 Formal Charge 0 Complexity 269.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 1 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 1
Citations of This Product Referências 1. Jieqing Feng, Qisheng Zhong, Ting Zhou. (2022) Online Pressure Change Focusing-Supercritical Fluid Selective Extraction Chromatography for Analyzing Chiral Drugs in Microliter-Scale Plasma Samples. ANALYTICAL CHEMISTRY, [PMID:36356211 ] [10.1021/acs.analchem.2c03892 ]
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