CAS 26922-99-6

1,3,4,6-Tetra-O-galloylglucose

Description:

1,3,4,6-Tetra-O-galloylglucose is a polyphenolic compound derived from glucose, characterized by the presence of four galloyl groups esterified to the hydroxyl positions of the glucose molecule. This compound is known for its antioxidant properties, which are attributed to the galloyl moieties that can scavenge free radicals and chelate metal ions. It exhibits potential health benefits, including anti-inflammatory and antimicrobial activities, making it of interest in both nutritional and pharmaceutical research. The structure of 1,3,4,6-Tetra-O-galloylglucose contributes to its solubility in organic solvents, while its polar nature allows for interactions with biological systems. Additionally, it may play a role in various biochemical pathways, influencing cellular processes. Its CAS number, 26922-99-6, is a unique identifier that facilitates the tracking and study of this compound in scientific literature and databases. Overall, 1,3,4,6-Tetra-O-galloylglucose represents a significant compound in the field of natural products and medicinal chemistry.

Formula: C₃₄H₂₈O₂₂

Synonyms:

• 1,3,4,6-Tetra-O-galloyl-beta-D-glucopyranose
• 1,3,4,6-Tetragalloylglucose
• 1,3,4,6-Tetra-O-galloyl-beta-D-glucose
• 1,3,4,6-Tetra-O-galloylglucose
• β-D-Glucopyranose, 1,3,4,6-tetrakis(3,4,5-trihydroxybenzoate)

1,3,4,6-Tetragalloylglucose

CAS: 26922-99-6

1,3,4,6-Tetragalloylglucose is a useful organic compound for research related to life sciences. The catalog number is T125150 and the CAS number is 26922-99-6.

Formula: C₃₄H₂₈O₂₂

Color and Shape: Solid

Molecular weight: 788.576

Ref: TM-T125150

1,3,4,6-Tetra-O-galloylglucose

CAS: 26922-99-6

Formula: C₃₄H₂₈O₂₂

Purity: 95%~99%

Molecular weight: 788.576

Ref: BP-BP5406

1,3,4,6-Tetra-O-galloyl glucose

CAS: 26922-99-6

Tetra-O-galloyl glucose is a pentagalloyl glucose that is found in the Chinese herb Paeonia lactiflora. It has been shown to inhibit the replication of hepatitis B virus, and can be used for the treatment of hepatitis B infection. Tetra-O-galloyl glucose also has anti-inflammatory activities, which may be due to its ability to inhibit prostaglandin synthesis.

Formula: C₃₄H₂₈O₂₂

Purity: Min. 95%

Molecular weight: 788.57 g/mol

Ref: 3D-MT46233