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· · COA & SDS available for every product · Same-day shipping on in-stock items Home Applications Enzymes Hydrolases Rivastigmine - Moligand™, ≥99% , Cholinesterases; ACHE & BCHE inhibitor, CAS No.123441-03-2, Cholinesterases; ACHE & BCHE inhibitor Rivastigmine - Moligand™, ≥99% , Cholinesterases; ACHE & BCHE inhibitor, CAS No.123441-03-2, Cholinesterases; ACHE & BCHE inhibitor
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. ≥99% 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
Storage
Store at 2-8°C,Argon charged
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Why this grade Moligand™, ≥99% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at 2-8°C,Argon charged Ships Wet ice 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 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
Specifications & Purity
Moligand™, ≥99%
Storage
Store at 2-8°C, Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Mechanism of action
Cholinesterases; ACHE & BCHE inhibitor
Product Properties Names and Identifiers Pubchem Sid 504755231 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504755231 Canonical Smiles 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 Isomeric SMILES CCN(C)C(=O)OC1=CC=CC(=C1)[C@H](C)N(C)C PubChem CID 77991 Molecular Weight 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 Class 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 Description 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.
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 Soluble in methanol and ethanol Sensitivity light sensitive Flash Point(°C) 145.0 °C Boil Point(°C) 135 °C/0.26 mmHg Molecular Weight 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 References 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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