G3000
β-Gentiobiose
≥85% (remainder primarily α-anomer)
Synonym(s):
6-O-β-D-Glucopyranosyl-D-glucose, Amygdalose
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About This Item
Empirical Formula (Hill Notation):
C12H22O11
CAS Number:
Molecular Weight:
342.30
UNSPSC Code:
12352201
NACRES:
NA.25
PubChem Substance ID:
EC Number:
209-074-0
Beilstein/REAXYS Number:
93354
MDL number:
Quality Segment
biological source
synthetic
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
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.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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