D-(+)-Glucose, anhydrous, 99%
D-(+)-Glucose, anhydrous, 99%
D-(+)-Glucose, anhydrous, 99%
Thermo Scientific Chemicals

D-(+)-Glucose, anhydrous, 99%

CAS: 50-99-7 | C6H12O6 | 180.156 g/mol
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產品號碼 A16828.0C
亦稱為 A16828-0C
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化學識別
CAS50-99-7
IUPAC Name6-(hydroxymethyl)oxane-2,3,4,5-tetrol
Molecular FormulaC6H12O6
InChI KeyWQZGKKKJIJFFOK-UHFFFAOYNA-N
SMILESOCC1OC(O)C(O)C(O)C1O
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規格Specification Sheet規格表
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Assay from Supplier's CofA≥98.5% (US-sourced material)
Melting Point (clear melt)141-153°C (UK-sourced material)
CommentMaterial sourced in UK and US
Optical Rotation+53° ± 1° (c=10 in Water, 3h)
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D-Glucose is used in various metabolic processes including enzymic synthesis of cyclohexyl-alpha and beta -D-glucosides. It is involved in the detection of type 2 diabetes mellitus and the most widely used aldohexose in living organisms. Its availability influences psychological processes since it is a primary energy source for the brain.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
D-Glucose is used in various metabolic processes including enzymic synthesis of cyclohexyl-alpha and beta -D-glucosides. It is involved in the detection of type 2 diabetes mellitus and the most widely used aldohexose in living organisms. Its availability influences psychological processes since it is a primary energy source for the brain.

Solubility
Soluble in water, hot glacial acetic acid, pyridine, aniline and dimethyl sulfoxide. Slightly soluble in methanol, ethanol and acetone.

Notes
Store in cool place. Hygroscopic. Incompatible with strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Wlodarczyk, P.; Paluch, M.; Wlodarczyk, A.; Hyra, M. A mutarotation mechanism based on dual proton exchange in the amorphous D-glucose. Phys. Chem. Chem. Phys. 2014, 16 (10), 4694-4698.
  2. Chelouan, A.; Recio, R.; Alcudia, A.; Khiar, N.; Fernández, I. DMAP-Catalysed Sulfinylation of Diacetone-D-Glucose: Improved Method for the Synthesis of Enantiopure tert-Butyl Sulfoxides and tert-Butanesulfinamides. Eur. J. Org. Chem. 2014, 2014 (31), 6935-6944.