G5500

L-(−)-Glucose

≥99%

• Synonyme(s) : Aldehydo-L-glucose
• Formule empirique (notation de Hill) : C₆H₁₂O₆
• Numéro CAS: 921-60-8
• Poids moléculaire : 180.16
• UNSPSC Code: 12352201
• NACRES: NA.25
• PubChem Substance ID: 24895211
• EC Number: 213-068-3
• Beilstein/REAXYS Number: 1724626
• MDL number: MFCD00148913

Propriétés

• Quality Segment: 200
• assay: ≥99%
• form: powder
• technique(s): gas chromatography (GC): suitable
• color: white
• mp: 153-156 °C (lit.)
• solubility: water: 50 mg/mL, clear, colorless
• storage temp.: 2-8°C
• SMILES string: [H]C(=O)[C@@H](O)[C@H](O)[C@@H](O)[C@@H](O)CO
• InChI: 1S/C6H12O6/c7-1-3(9)5(11)6(12)4(10)2-8/h1,3-6,8-12H,2H2/t3-,4+,5+,6+/m1/s1
• InChI key: GZCGUPFRVQAUEE-VANKVMQKSA-N

Description

General description

L-(−)-Glucose is an enantiomer of the more common D-glucose. L-Glucose cannot be used by cells as an energy source because it cannot be phosphorylated by hexokinase.

Application

L-(-)-Glucose has been used in phospho-buffered saline (PBS) solution to induce metabolic responses in Saccharomyces cerevisiae. It has also been used to study the substrate competition pattern of IICB glucose transporter.

Other Notes

To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.

Informations sur la sécurité

• Classe de stockage: 11 - Combustible Solids
• wgk: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: Eyeshields, Gloves, type N95 (US)