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Merck
CN

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:
554-91-6
Molecular Weight:
342.30
UNSPSC Code:
12352201
NACRES:
NA.25
PubChem Substance ID:
24895110
EC Number:
209-074-0
Beilstein/REAXYS Number:
93354
MDL number:
MFCD00198056

Key Documents

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Product Name

β-Gentiobiose, ≥85% (remainder primarily α-anomer)

Quality Level

200

InChI key

DLRVVLDZNNYCBX-CQUJWQHSSA-N

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

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

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

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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

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
BCCN3259
BCCM6822
BCCL8025
BCCK1104
BCCH5663

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