G7879

D-Glucose 6-phosphate sodium salt

≥98% (HPLC)

• Sinónimos: D(+)-Glucopyranose 6-phosphate sodium salt, G-6-P Na, Robison ester
• Fórmula empírica (notación de Hill): C₆H₁₂NaO₉P
• Número de CAS: 54010-71-8
• Peso molecular: 282.12
• Beilstein/REAXYS Number: 5787568
• EC Number: 258-921-0
• MDL number: MFCD00006611
• UNSPSC Code: 12352201
• PubChem Substance ID: 24895324
• NACRES: NA.25

Propiedades

• biological source: synthetic (organic)
• Quality Level: 300
• assay: ≥98% (HPLC)
• form: crystalline
• technique(s): HPLC: suitable
• color: white
• useful pH range: 4.0-5.0
• mp: 204 °C (dec.) (lit.)
• solubility: water: 50 mg/mL, clear, colorless to very faintly yellow
• cation traces: Na: 6.1-10.2% (anhydrous)
• storage temp.: room temp
• SMILES string: [Na+].O[C@@H]1O[C@H](COP(O)([O-])=O)[C@@H](O)[C@H](O)[C@H]1O
• InChI: 1S/C6H13O9P.Na/c7-3-2(1-14-16(11,12)13)15-6(10)5(9)4(3)8;/h2-10H,1H2,(H2,11,12,13);/q;+1/p-1/t2-,3-,4+,5-,6-;/m1./s1
• InChI key: ZALKNDISPIVVKC-WYRLRVFGSA-M

Descripción

Application

D-glucose-6-phosphate sodium can be used as an energy source for Mycobacterium tuberculosis.

Biochem/physiol Actions

In cells, D-glucose 6-phosphate (G6P) is generated when glucose is phosphorylated by hexokinase or glucokinase or by the conversion of glucose-1-phosphate by phosphoglucomutase during glycogenolysis. G6P lies at the beginning of both glycolysis and the pentose phosphate pathways. It also can be stored as glycogen when blood glucose levels are high.

Caution

Non-hygroscopic, and very stable to atmospheric moisture at room temperature, unlike the disodium salt.

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.

Información de seguridad

• Storage Class: 11 - Combustible Solids
• wgk_germany: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: Eyeshields, Gloves, type N95 (US)