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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Zolpidem tartrate , GABA A receptor alpha-1/beta-1/gamma-2 positive allosteric modulator, CAS No.13620391, GABA A receptor alpha-1/beta-1/gamma-2 positive allosteric modulator
Synonyms
Stilnox | SL 80.0750-23N | Zolpidem hemitartrate | CHEMBL3989820 | Myslee | SCHEMBL208621
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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 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
Stilnox | SL 80.0750-23N | Zolpidem hemitartrate | CHEMBL3989820 | Myslee | SCHEMBL208621
Condiciones de almacenamiento de almacenamiento
Room temperature
Tipo de acción
POSITIVE ALLOSTERIC MODULATOR
Mecanismo de acción
GABA A receptor alpha-1/beta-1/gamma-2 positive allosteric modulator
Nombres e identificadores Sonrisas canónicas CC1=CC=C(C=C1)C2=C(N3C=C(C=CC3=N2)C)CC(=O)N(C)C.CC1=CC=C(C=C1)C2=C(N3C=C(C=CC3=N2)C)CC(=O)N(C)C.C(C(C(=O)O)O)(C(=O)O)O IUPAC Name 2,3-dihydroxybutanedioic acid;N,N-dimethyl-2-[6-methyl-2-(4-methylphenyl)imidazo[1,2-a]pyridin-3-yl]acetamide InChIKey VXRDAMSNTXUHFX-UHFFFAOYSA-N INCHI 1S/2C19H21N3O.C4H6O6/c2*1-13-5-8-15(9-6-13)19-16(11-18(23)21(3)4)22-12-14(2)7-10-17(22)20-19;5-1(3(7)8)2(6)4(9)10/h2*5-10,12H,11H2,1-4H3;1-2,5-6H,(H,7,8)(H,9,10) Isómeros SMILES CC1=CC=C(C=C1)C2=C(N3C=C(C=CC3=N2)C)CC(=O)N(C)C.CC1=CC=C(C=C1)C2=C(N3C=C(C=CC3=N2)C)CC(=O)N(C)C.C(C(C(=O)O)O)(C(=O)O)O Peso molecular 764.9 Reaxy-Rn 4346450 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4346450&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 Organoheterocyclic compounds Clase Azoles Subclass Imidazoles Intermediate Tree Nodes Substituted imidazoles Direct Parent Phenylimidazoles Alternative Parents Imidazopyridines Imidazo[1,2-a]pyridines Toluenes Sugar acids and derivatives Short-chain hydroxy acids and derivatives Methylpyridines Beta hydroxy acids and derivatives Alpha hydroxy acids and derivatives N-substituted imidazoles Monosaccharides Fatty acids and conjugates Dicarboxylic acids and derivatives Tertiary carboxylic acid amides Heteroaromatic compounds Secondary alcohols 1,2-diols Azacyclic compounds Carboxylic acids Hydrocarbon derivatives Organonitrogen compounds Carbonyl compounds Organic oxides Molecular Framework Not available Substituents 5-phenylimidazole - 4-phenylimidazole - Imidazopyridine - Imidazo[1,2-a]pyridine - Beta-hydroxy acid - Methylpyridine - Short-chain hydroxy acid - Sugar acid - Toluene - Alpha-hydroxy acid - Monocyclic benzene moiety - Dicarboxylic acid or derivatives - Hydroxy acid - Monosaccharide - N-substituted imidazole - Pyridine - Fatty acid - Benzenoid - Tertiary carboxylic acid amide - Heteroaromatic compound - Carboxamide group - Secondary alcohol - 1,2-diol - Carboxylic acid derivative - Azacycle - Carboxylic acid - Organooxygen compound - Organic oxide - Hydrocarbon derivative - Carbonyl group - Organic oxygen compound - Alcohol - Organic nitrogen compound - Organonitrogen compound - Aromatic heteropolycyclic compound Descripción This compound belongs to the class of organic compounds known as phenylimidazoles. These are polycyclic aromatic compounds containing a benzene ring linked to an imidazole ring through a CC or CN bond. 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 (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Calculadoras de soluciones Molarity Calculator Determine the necessary mass, volume, or concentration for preparing a solution.
Dilution Calculator Determine the dilution needed to prepare a stock solution.
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