2-Keto-D-Glucose - ≥95% , CAS No.1854-25-7

CAS: 1854-25-7 Cat. No.: K353157 Peso molecular: 178.14 Beilstein Registry Number: 1725425
Disponible para pedir
GRADE & PURITY ≥95%
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
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
100mg
K353157-100mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
399,90US$
250mg
K353157-250mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
897,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -20°C,Argon charged Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

📋

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.
Pureza
≥95%
Propiedades del producto
pKapKa: 8.62 (Predicted)
Nombres e identificadores
Sonrisas canónicasC(C(C(C(C(=O)C=O)O)O)O)O
IUPAC Name(3S,4R,5R)-3,4,5,6-tetrahydroxy-2-oxohexanal
InChIKeyDCNMIDLYWOTSGK-HSUXUTPPSA-N
INCHI1S/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

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic oxygen compounds
ClaseOrganooxygen compounds
SubclassCarbohydrates and carbohydrate conjugates
Intermediate Tree Nodes Monosaccharides
Direct ParentHexoses
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 FrameworkAliphatic 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
DescripciónThis 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
Estructura 3D
Modelo de Estructura Química Interactiva





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propiedades químicas y físicas
SolubilidadSoluble in methanol, and water.
Índice de refracciónn20D1.55 (Predicted)
Punto de ebullición (°C)480.99° C at 760 mmHg (Predicted)
Punto de fusión (°C)124.69° C (Predicted)
Peso molecular178.140 g/mol
XLogP3-2.900
Hydrogen Bond Donor Count4
Hydrogen Bond Acceptor Count6
Rotatable Bond Count5
Exact Mass178.048 Da
Monoisotopic Mass178.048 Da
Topological Polar Surface Area115.000 Ų
Heavy Atom Count12
Formal Charge0
Complexity167.000
Isotope Atom Count0
Defined Atom Stereocenter Count3
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Calculadoras de soluciones
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