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G3000

Sigma-Aldrich

β-Gentiobiose

≥85% (remainder primarily α-anomer)

Sinónimos:

6-O-β-D-Glucopyranosyl-D-glucose, Amygdalose

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About This Item

Fórmula empírica (notación de Hill):
C12H22O11
Número de CAS:
554-91-6
Peso molecular:
342.30
Beilstein/REAXYS Number:
93354
EC Number:
209-074-0
MDL number:
MFCD00198056
UNSPSC Code:
12352201
PubChem Substance ID:
24895110
NACRES:
NA.25

biological source

synthetic

Quality Level

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

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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_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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