79886-49-0

Basic information

• Product Name: (1R)-3,5-bis-O-(3,4,5-trihydroxybenzoyl)-2-C-{[(3,4,5-trihydroxybenzoyl)oxy]methyl}pentofuranose
• Synonyms: 1,2,6-Tri-O-galloylglucose;1,2,6-Tri-galloyl-beta-D-glucose;1,2,6-TRI-O-GALLOYL-BETA-D-GLUCOSE;1,2,6-tris-O-galloyl-beta-D-glucose;1,2,6-tri-O-galloyl β-D-glucopyranoside;1,2,6-Tri-O-galloyl-beta-D-glucopyranose;β-D-Glucopyranose, 1,2,6-tris(3,4,5-trihydroxybenzoate)
• CAS NO: 79886-49-0
• Molecular Formula: C₂₇H₂₄O₁₈
• Molecular Weight: 636.4687
• Mol File: 79886-49-0.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 1096.6°C at 760 mmHg
• Flash Point: 360.8°C
• Density: 1.99g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.826
• CAS DataBase Reference: (1R)-3,5-bis-O-(3,4,5-trihydroxybenzoyl)-2-C-{[(3,4,5-trihydroxybenzoyl)oxy]methyl}pentofuranose(CAS DataBase Reference)
• NIST Chemistry Reference: (1R)-3,5-bis-O-(3,4,5-trihydroxybenzoyl)-2-C-{[(3,4,5-trihydroxybenzoyl)oxy]methyl}pentofuranose(79886-49-0)
• EPA Substance Registry System: (1R)-3,5-bis-O-(3,4,5-trihydroxybenzoyl)-2-C-{[(3,4,5-trihydroxybenzoyl)oxy]methyl}pentofuranose(79886-49-0)

Safety Data

• Hazardous Substances Data: 79886-49-0(Hazardous Substances Data)

Usage

Description

(1R)-3,5-bis-O-(3,4,5-trihydroxybenzoyl)-2-C-[(3,4,5-trihydroxybenzoyl)oxy]methylpentofuranose is a complex organic compound that features a pentofuranose core with multiple galloyl and trihydroxybenzoyl groups attached at various positions. This molecule is characterized by its unique structure, which includes a 1R configuration and a 2-C-[(3,4,5-trihydroxybenzoyl)oxy]methylpentofuranose moiety, along with 3,5-bis-O-(3,4,5-trihydroxybenzoyl) substitutions. The presence of multiple hydroxyl groups in its structure suggests potential interactions with other molecules and applications in various fields.

Uses

Used in Pharmaceutical Industry:
(1R)-3,5-bis-O-(3,4,5-trihydroxybenzoyl)-2-C-[(3,4,5-trihydroxybenzoyl)oxy]methylpentofuranose is used as a pharmaceutical candidate for its potential therapeutic properties. The presence of multiple hydroxyl and carboxylic acid groups allows for interactions with biopolymers and macromolecules, which can be harnessed for the development of new drugs or drug delivery systems.
Used in Cosmetic Industry:
In the cosmetic industry, (1R)-3,5-bis-O-(3,4,5-trihydroxybenzoyl)-2-C-[(3,4,5-trihydroxybenzoyl)oxy]methylpentofuranose may be used as an active ingredient in skincare products due to its potential antioxidant and anti-inflammatory properties. The hydroxyl groups in its structure can help protect the skin from oxidative stress and inflammation, contributing to healthier and more youthful-looking skin.
Used in Food Industry:
(1R)-3,5-bis-O-(3,4,5-trihydroxybenzoyl)-2-C-[(3,4,5-trihydroxybenzoyl)oxy]methylpentofuranose could be utilized in the food industry as a natural preservative or flavor enhancer. Its complex structure and multiple hydroxyl groups may provide antioxidant properties that can help extend the shelf life of food products and enhance their taste and aroma.
Used in Research and Development:
(1R)-3,5-bis-O-(3,4,5-trihydroxybenzoyl)-2-C-[(3,4,5-trihydroxybenzoyl)oxy]methylpentofuranose can also be used in research and development settings to study its chemical properties, interactions with other molecules, and potential applications in various fields. Understanding the structure and function of (1R)-3,5-bis-O-(3,4,5-trihydroxybenzoyl)-2-C-[(3,4,5-trihydroxybenzoyl)oxy]methylpentofuranose can lead to the discovery of new uses and applications in different industries.

Upstream product

• 23363-08-8 1,6-di-O-galloyl-(α/β)-glucopyranose 
• 13405-60-2 β-glucogallin 

Relevant articles and documents

BIOSYNTHESIS OF 1,2,3,6-TETRA-O-GALLOYL-β-D-GLUCOSE

An enzyme that catalysed the β-glucogallin (1-O-galloyl-β-D-glucose)-dependent galloylation of 1,2,6-tri-O-galloyl-β-D-glucose to 1,2,3,6-tetra-O-galloyl-β-D-glucose was partially purified from leaves of the oak (Quercus robur).This acyltransferase had a Mr of ca 380000, and pH and temperature optima of 6.0 and 55 deg, respectively, and was most stable between pH 4.0 and 6.5.In addition to the natural substrates β-glucogallin (donor) and 1,2,6-trigalloylglucose (acceptor), 1,3,6-trigalloylglucose (which is not an intermediate in the biosynthesis of hydrolysable tannins in oak and sumac) was an equally efficient acceptor molecule; in both cases, 1,2,3,6-tetragalloylglucose was the reaction product.Based on the physiological role of this new enzyme, the systematic name "β-glucogallin: 1,2,6-tri-O-galloyl-β-D-glucose 3-O-galloyltransferase" (EC.2.3.1.-) is proposed. Key Word Index - Quercus robur (Q. pedunculata); Fagaceae; pedunculate oak; Rhus typhina; Anacardiaceae; staghorn sumac; biosynthesis; hydrolysable tannins; galloyltransferase; β-glucogallin; 1,2,6-tri-O-galloyl-β-D-glucose; 1,2,3,6-tetra-O-galloyl-β-D-glucose.