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224,000+ productos de investigación · Triple ISO certified · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items 2-Keto-D-Glucose - ≥95% , CAS No.1854-25-7
Synonyms
D-Arabino-2-hexosulose | D-Arabino-hexos-2-ulose | D-glucosone | Galactosone | PD053744 | Arabino-hexosulose | NSC 120040 | Q27123425 | SCHEMBL818364 | W-201665 | (3S,4R,5R)-3,4,5,6-tetrahydroxy-2-oxohexanal | aldehydo-2-keto-D-glucose | D-arabino-hexosul
Storage
Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
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Why this grade ≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -20°C,Argon charged 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.
Descripción general 2-Keto-D-Glucose is a useful synthetic intermediate.
Specifications Sinónimos
D-Arabino-2-hexosulose | D-Arabino-hexos-2-ulose | D-glucosone | Galactosone | PD053744 | Arabino-hexosulose | NSC 120040 | Q27123425 | SCHEMBL818364 | W-201665 | (3S, 4R, 5R)-3, 4, 5, 6-tetrahydroxy-2-oxohexanal | aldehydo-2-keto-D-glucose | D-arabino-hexosul
Especificaciones y pureza
≥95%
Mecanismos bioquímicos y fisiológicos
2-Keto-D-glucose is a key intermediate in the secondary metabolic pathway leading to the beta antibiotic pyrone cortalcerone. This antibiotic protects the fungus from the bacteria. Enzymatic oxidation of d-glucose by pyranose 2 oxidase produces 2-keto-D-g
Condiciones de almacenamiento de almacenamiento
Store at -20°C, Argon charged
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Propiedades del producto Nombres e identificadores Sonrisas canónicas C(C(C(C(C(=O)C=O)O)O)O)O IUPAC Name (3S,4R,5R)-3,4,5,6-tetrahydroxy-2-oxohexanal InChIKey DCNMIDLYWOTSGK-HSUXUTPPSA-N INCHI 1S/C6H10O6/c7-1-3(9)5(11)6(12)4(10)2-8/h1,4-6,8,10-12H,2H2/t4-,5-,6-/m1/s1 Isómeros SMILES C([C@H]([C@H]([C@@H](C(=O)C=O)O)O)O)O WGK Alemania 3 Peso molecular 178.14 Beilstein 1725425 Reaxy-Rn 3604769 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3604769&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 Carbohydrates and carbohydrate conjugates Intermediate Tree Nodes Monosaccharides Direct Parent Hexoses Alternative Parents Medium-chain aldehydes Beta-hydroxy ketones Beta-hydroxy aldehydes Acyloins Alpha-hydroxy ketones Alpha ketoaldehydes Secondary alcohols Polyols Primary alcohols Organic oxides Hydrocarbon derivatives Molecular Framework Aliphatic acyclic compounds Substituents Hexose monosaccharide - Medium-chain aldehyde - Acyloin - Beta-hydroxy aldehyde - Beta-hydroxy ketone - Alpha-ketoaldehyde - Alpha-hydroxy ketone - Secondary alcohol - Ketone - Polyol - Organic oxide - Primary alcohol - Hydrocarbon derivative - Aldehyde - Alcohol - Carbonyl group - Aliphatic acyclic compound Descripción This compound belongs to the class of organic compounds known as hexoses. These are monosaccharides in which the sugar unit is a is a six-carbon containing moeity. External Descriptors ketoaldohexose 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 Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Solubilidad Soluble in methanol, and water. Índice de refracción n20D1.55 (Predicted) Punto de ebullición (°C) 480.99° C at 760 mmHg (Predicted) Punto de fusión (°C) 124.69° C (Predicted) Peso molecular 178.140 g/mol XLogP3 -2.900 Hydrogen Bond Donor Count 4 Hydrogen Bond Acceptor Count 6 Rotatable Bond Count 5 Exact Mass 178.048 Da Monoisotopic Mass 178.048 Da Topological Polar Surface Area 115.000 Ų Heavy Atom Count 12 Formal Charge 0 Complexity 167.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 3 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
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