≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
6-Deoxy-D-glucose is a structural homomorph of D-glucose, which cannot be phosphorylated by hexokinases or glucokinases, as a result of its lack of a hydroxyl group at carbon 6. Studies on|Saccharomyces cerevisiae|show that 6-Deoxy-D-glucose can be transported in and out of the cell using facilitated diffusion. The lack of its 6-hydroxyl group allows 6-Deoxy-D-glucose to be transported into cells and fully recovered in an unchanged state. It is known that glucose is an important monosaccharide which functions as an energy source for cells. Some believe that the versatility of glucose compared to other monosaccharides is due to the fact that glucose prefers its cyclic form, which reduces glycation.
| Sonrisas canónicas | CC(C(C(C(C=O)O)O)O)O |
|---|---|
| IUPAC Name | (2R,3S,4R,5R)-2,3,4,5-tetrahydroxyhexanal |
| InChIKey | PNNNRSAQSRJVSB-JGWLITMVSA-N |
| INCHI | 1S/C6H12O5/c1-3(8)5(10)6(11)4(9)2-7/h2-6,8-11H,1H3/t3-,4+,5-,6-/m1/s1 |
| Isómeros SMILES | C[C@H]([C@H]([C@@H]([C@H](C=O)O)O)O)O |
| WGK Alemania | 3 |
| Peso molecular | 164.16 |
| Beilstein | 1723317 |
| Reaxy-Rn | 3904170 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3904170&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| 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 aldehydes Alpha-hydroxyaldehydes Secondary alcohols Polyols Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Hexose monosaccharide - Medium-chain aldehyde - Beta-hydroxy aldehyde - Alpha-hydroxyaldehyde - Secondary alcohol - Polyol - Organic oxide - Hydrocarbon derivative - Carbonyl group - Aldehyde - Alcohol - 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 | quinovose |
| Solubilidad | Soluble in water (~50 mg/ml). |
|---|---|
| Índice de refracción | n20D1.59 (Predicted) |
| Rotación específica [α] | α20/D 30°±2°, c = 1.8-2.2 in water |
| Punto de ebullición (°C) | 323.91° C at 760 mmHg (Predicted) |
| Punto de fusión (°C) | 142-144° C |
| Peso molecular | 164.160 g/mol |
| XLogP3 | -2.400 |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 4 |
| Exact Mass | 164.068 Da |
| Monoisotopic Mass | 164.068 Da |
| Topological Polar Surface Area | 98.000 Ų |
| Heavy Atom Count | 11 |
| Formal Charge | 0 |
| Complexity | 126.000 |
| 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 | 1 |
L2412681