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G3000

Sigma-Aldrich

β-Gentiobiose

≥85% (remainder primarily α-anomer)

Sinônimo(s):

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

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About This Item

Fórmula empírica (Notação de Hill):
C12H22O11
Número CAS:
554-91-6
Peso molecular:
342.30
Beilstein:
93354
Número CE:
209-074-0
Número MDL:
MFCD00198056
Código UNSPSC:
12352201
ID de substância PubChem:
24895110
NACRES:
NA.25

fonte biológica

synthetic

Ensaio

≥85% (remainder primarily α-anomer)

forma

powder

atividade óptica

[α]20/D 8.5 to 10.5, c = 2% (w/v) in water

cor

beige

solubilidade

water: 100 mg/mL, clear to slightly hazy, colorless to light yellow (

)

temperatura de armazenamento

room temp

cadeia de caracteres SMILES

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

chave InChI

DLRVVLDZNNYCBX-CQUJWQHSSA-N

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Categorias relacionadas

Aplicação

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.

Outras notas

To gain a comprehensive understanding of our extensive range of Disaccharides for your research, we encourage you to visit our Carbohydrates Category page.

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)

Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

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