G3000

β-Gentiobiose

≥85% (remainder primarily α-anomer)

• Synonyme(s) : 6-O-β-D-Glucopyranosyl-D-glucose, Amygdalose
• Formule empirique (notation de Hill) : C₁₂H₂₂O₁₁
• Numéro CAS: 554-91-6
• Poids moléculaire : 342.30
• UNSPSC Code: 12352201
• NACRES: NA.25
• PubChem Substance ID: 24895110
• EC Number: 209-074-0
• Beilstein/REAXYS Number: 93354
• MDL number: MFCD00198056

Propriétés

• biological source: synthetic
• Quality Segment: 200
• assay: ≥85% (remainder primarily α-anomer)
• form: powder
• optical activity: [α]20/D 8.5 to 10.5, c = 2% (w/v) in water
• color: beige
• solubility: water: 100 mg/mL, clear to slightly hazy, colorless to light yellow (; ; )
• storage temp.: room temp
• SMILES string: OC[C@H]1O[C@@H](OC[C@H]2OC(O)[C@H](O)[C@@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@@H]1O
• InChI: 1S/C12H22O11/c13-1-3-5(14)8(17)10(19)12(23-3)21-2-4-6(15)7(16)9(18)11(20)22-4/h3-20H,1-2H2/t3-,4-,5-,6-,7+,8+,9-,10-,11?,12-/m1/s1
• InChI key: DLRVVLDZNNYCBX-CQUJWQHSSA-N

Description

Application

Gentiobiose was used in binding aβays to determine if coelomic cytolytic factor 1 (CCF-1) binds to β-1,3-glucans to stimulate the pro-PO-activating system.

Other Notes

To gain a comprehensive understanding of our extensive range of Disaccharides 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)