M5500
Melibiose
≥98% (HPLC)
Synonym(s):
α-D-Melibiose hydrate, 6-α-D-Galactopyranosyl-D-glucopyranose, 6-O-α-D-Galactopyranosyl-D-glucose
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About This Item
Empirical Formula (Hill Notation):
C12H22O11
CAS Number:
Molecular Weight:
342.30
NACRES:
NA.25
PubChem Substance ID:
UNSPSC Code:
12352201
EC Number:
209-568-6
MDL number:
Quality Level
assay
≥98% (HPLC)
form
powder
technique(s)
HPLC: suitable
color
white to off-white
mp
182 °C (dec.) (lit.)
solubility
water: 50 mg/mL, clear to very slightly hazy, colorless
SMILES string
O.OC[C@H]1O[C@H](OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O)[C@H](O)[C@@H](O)[C@H]1O
InChI
1S/C12H22O11.H2O/c13-1-4(15)7(17)8(18)5(16)3-22-12-11(21)10(20)9(19)6(2-14)23-12;/h1,4-12,14-21H,2-3H2;1H2/t4-,5+,6+,7+,8+,9-,10-,11+,12-;/m0./s1
InChI key
CHIDEFLSUMQFBY-CQIZOMOZSA-N
General description
Melibiose is a carbon substrate.
Application
Melibiose has been used in a study to improve the preparation of benzoylated ethyl 1-thioglycosides. It has also been used in a study to investigate the effect of water plasticization on the molecular mobility and crystallization tendency of amorphous disaccharides.
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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Activity of MUC1 cancer antigen-binding plasma anti-α-galactoside antibody correlates inversely with size of autologous lipoprotein(a).
Jessy John et al.
Experimental biology and medicine (Maywood, N.J.), 244(11), 893-900 (2019-08-10)
Parameswaran Hariharan et al.
BMC biology, 16(1), 85-85 (2018-08-05)
Membrane lipids play critical roles in the structure and function of membrane-embedded transporters. Salmonella typhimurium MelB (MelBSt) is a symporter coupling melibiose translocation with a cation (Na+, Li+, or H+). We present an extensive study on the effects of specific
Ville Aumala et al.
ChemSusChem, 12(4), 848-857 (2018-12-28)
Plant-derived carbohydrates are an abundant renewable resource. Transformation of carbohydrates into new products, including amine-functionalized building blocks for biomaterials applications, can lower reliance on fossil resources. Herein, biocatalytic production routes to amino carbohydrates, including oligosaccharides, are demonstrated. In each case