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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Miglustat hydrochloride - ≥98% , CAS No.210110-90-0
Synonyms
SMR000058560 | Miglustat HCl | Miglustat hydrochloride | (2R,3R,4R,5S)-1-butyl-2-(hydroxymethyl)piperidine-3,4,5-triol hydrochloride | AKOS024457437 | (2R,3R,4R,5S)-1-Butyl-2-(hydroxymethyl)-,3,4,5-Piperidinetriol Hydrochloride | AKOS000269030 | E73460 |
Storage
Store at -20°C,Desiccated
Shipped In
Ice chest + Ice pads
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Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -20°C,Desiccated Ships Ice chest + Ice pads 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
SMR000058560 | Miglustat HCl | Miglustat hydrochloride | (2R, 3R, 4R, 5S)-1-butyl-2-(hydroxymethyl)piperidine-3, 4, 5-triol hydrochloride | AKOS024457437 | (2R, 3R, 4R, 5S)-1-Butyl-2-(hydroxymethyl)-, 3, 4, 5-Piperidinetriol Hydrochloride | AKOS000269030 | E73460 |
Especificaciones y pureza
≥98%
Mecanismos bioquímicos y fisiológicos
Orally activeα-glucosidase I and II and ceramide-specific glycosyltransferase inhibitor. Rescues trafficking-deficient F508del-CFTR in human airway epithelial cells via inhibition of ERα-glucosidases I and II. Also has broad spectrum antiviral activity.De
Condiciones de almacenamiento de almacenamiento
Store at -20°C, Desiccated
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nombres e identificadores Sonrisas canónicas CCCCN1CC(C(C(C1CO)O)O)O.Cl IUPAC Name (2R,3R,4R,5S)-1-butyl-2-(hydroxymethyl)piperidine-3,4,5-triol;hydrochloride InChIKey QPAFAUYWVZMWPR-ZSOUGHPYSA-N INCHI 1S/C10H21NO4.ClH/c1-2-3-4-11-5-8(13)10(15)9(14)7(11)6-12;/h7-10,12-15H,2-6H2,1H3;1H/t7-,8+,9-,10-;/m1./s1 Isómeros SMILES CCCCN1C[C@@H]([C@H]([C@@H]([C@H]1CO)O)O)O.Cl Peso molecular 255.74 Reaxy-Rn 59683538 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=59683538&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 Piperidines Subclass Not available Intermediate Tree Nodes Not available Direct Parent Piperidines Alternative Parents Trialkylamines Secondary alcohols 1,2-aminoalcohols Polyols Azacyclic compounds Primary alcohols Organopnictogen compounds Organic zwitterions Organic chloride salts Hydrochlorides Hydrocarbon derivatives Molecular Framework Aliphatic heteromonocyclic compounds Substituents Piperidine - 1,2-aminoalcohol - Secondary alcohol - Tertiary amine - Tertiary aliphatic amine - Polyol - Azacycle - Organic nitrogen compound - Organic salt - Organic zwitterion - Hydrochloride - Organic chloride salt - Hydrocarbon derivative - Primary alcohol - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Amine - Alcohol - Aliphatic heteromonocyclic compound Descripción This compound belongs to the class of organic compounds known as piperidines. These are compounds containing a piperidine ring, which is a saturated aliphatic six-member ring with one nitrogen atom and five carbon atoms. 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) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Solubilidad Solvent:water, Max Conc. mg/mL: 19.18, Max Conc. mM: 75; Solvent:DMSO, Max Conc. mg/mL: 19.18, Max Conc. mM: 75 Peso molecular 255.740 g/mol XLogP3 Hydrogen Bond Donor Count 5 Hydrogen Bond Acceptor Count 5 Rotatable Bond Count 4 Exact Mass 255.124 Da Monoisotopic Mass 255.124 Da Topological Polar Surface Area 84.200 Ų Heavy Atom Count 16 Formal Charge 0 Complexity 190.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 4 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
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