2425-84-5

Basic information

• Product Name: sucrose octabenzoic acid
• Synonyms: sucrose octabenzoic acid;1-O-(1-O,3-O,4-O,6-O-Tetrabenzoyl-β-D-fructofuranosyl)-2-O,3-O,4-O,6-O-tetrabenzoyl-α-D-glucopyranose;1-O,3-O,4-O,6-O-Tetrabenzoyl-2-O-(2-O,3-O,4-O,6-O-tetrabenzoyl-α-D-glucopyranosyl)-β-D-fructofuranose;1-O,3-O,4-O,6-O-Tetrabenzoyl-β-D-fructofuranosyl 2-O,3-O,4-O,6-O-tetrabenzoyl-α-D-glucopyranoside;1-O,3-O,4-O,6-O-Tetrabenzoyl-β-D-fructofuranosyl α-D-glucopyranoside tetrabenzoate;2-O-(2-O,3-O,4-O,6-O-Tetrabenzoyl-α-D-glucopyranosyl)-β-D-fructofuranose tetrabenzoate;2-O,3-O,4-O,6-O-Tetrabenzoyl-1-O-(1-O,3-O,4-O,6-O-tetrabenzoyl-β-D-fructofuranosyl)-α-D-glucopyranose
• CAS NO: 2425-84-5
• Molecular Formula: C₆₈H₅₄O₁₉
• Molecular Weight: 1175.15
• Mol File: 2425-84-5.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• Density: 1.42±0.1 g/cm3(Predicted)
• CAS DataBase Reference: sucrose octabenzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: sucrose octabenzoic acid(2425-84-5)
• EPA Substance Registry System: sucrose octabenzoic acid(2425-84-5)

Safety Data

• Hazardous Substances Data: 2425-84-5(Hazardous Substances Data)

Upstream product

• 1434596-35-6 1'-O-trifluoromethanesulfonyl-2,3,4,6,3',4',6'-,hepta-O-benzoylsucrose 
• 98-88-4 benzoyl chloride 
• 57-50-1 Sucrose 

Downstream Products

• 131267-69-1 2,3,4,6,1',3',6'-hepta-O-benzoylsucrose 
• 131267-70-4 C₅₄H₄₆O₁₇ 

Relevant articles and documents

DISSACHARIDE FORMULATIONS FOR CONTROLLED DRUG RELEASE

The present invention relates to a composition comprising non-water soluble dissacharides and oil, a solvent and at least one pharmaceutical ingredient, wherein the composition contains at least two compounds selected from saccharides and lipid oils such

Chemical synthesis of 1′-deoxy-1′-fluorosucrose

The first chemical synthesis of 1′-deoxy-1′-fluorosucrose has been accomplished in eight steps from sucrose by an unlikely, but ultimately successful, SN2 displacement reaction.

Sucrose octabenzoate: assignment of 13C and 1H resonances of the sucrose moiety and the 13C resonances of the carbonyl carbons. Use of 13C-n.m.r. spectroscopy for the study of selective deacylation

Assignment of the 1H and 13C signals arising from the carbohydrate portion of sucrose octabenzoate has been achieved using homonuclear shift correlation experiments (COSY) and one-bond 1H-13C heteronuclear shift correlation measurements, respectively.The