| Identification | Back Directory | [Name]
Benzylhepta-O-acetyl-b-D-lactoside4%CaCO3 | [CAS]
67310-53-6 | [Synonyms]
Benzyl β-Lactoside Heptaacetate
Benzyl hepta-O-acetyl-b-D-lactoside
Benzyl hepta-O-acetyl beta-D-lactose
Benzylhepta-O-acetyl-b-D-lactoside4%CaCO3
Benzylhepta-O-acetyl-b-D-lactoside4%CaCO3 USP/EP/BP
PhenylMethyl 4-O-(2,3,4,6-Tetra-O-acetyl-β-D-galactopyranosyl)-β-D-glucopyranoside Triacetate
Benzyl 4-O-(2,3,4,6-tetra-O-acetyl-β-O-galactopyranosyl)- 2,3,6-tri-O-acetyl-β-D-glucopyranoside
β-D-Glucopyranoside, phenylmethyl 4-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-, 2,3,6-triacetate | [Molecular Formula]
C33H42O18 | [MDL Number]
MFCD02094217 | [MOL File]
67310-53-6.mol | [Molecular Weight]
726.68 |
| Hazard Information | Back Directory | [Chemical Properties]
Oil | [Uses]
Benzyl β-D-Lactoside Heptaacetate is a class of biochemical reagents used in glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It involves carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the role of glycans in biological systems. This field is closely related to basic research, biomedicine, and biotechnology[1]. | [References]
[1] Varki A, et al editors. Essentials of Glycobiology [Internet]. 4th ed. Cold Spring Harbor (NY): Cold Spring Harbor Laboratory Press; 2022. PMID:35536922 |
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