369593-42-0

Basic information

• Product Name: (R)-hesperidin
• Synonyms: (R)-hesperidin
• CAS NO: 369593-42-0
• Molecular Weight: 610.569
• Mol File: 369593-42-0.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 930.1±65.0 °C(Predicted)
• Density: 1.65±0.1 g/cm3(Predicted)
• CAS DataBase Reference: (R)-hesperidin(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-hesperidin(369593-42-0)
• EPA Substance Registry System: (R)-hesperidin(369593-42-0)

Safety Data

• Hazardous Substances Data: 369593-42-0(Hazardous Substances Data)

Usage

General Description

(R)-hesperidin is a flavonoid compound found primarily in citrus fruits such as oranges and lemons. It is known for its strong antioxidant and anti-inflammatory properties, and is often used in herbal medicine for its potential health benefits. Hesperidin has been studied for its potential to improve blood circulation, reduce inflammation, and lower the risk of heart disease. It has also been investigated for its potential to protect against neurodegenerative diseases and improve cognitive function. Additionally, (R)-hesperidin has shown potential in promoting skin health and protecting against UV radiation damage. Its diverse range of potential health benefits make it a promising natural compound for further research and development in the field of medicine and nutraceuticals.

Upstream product

• 64726-90-5 (2S)-7-[[6-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl]oxy]-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-2,3-dihydro-4H-1-benzopyran-4-one 

Relevant articles and documents

Preparation and evaluation of a triazole-bridged bis(β-cyclodextrin)–bonded chiral stationary phase for HPLC

A triazole-bridged bis(β-cyclodextrin) was synthesized via a high-yield Click Chemistry reaction between 6-azido-β-cyclodextrin and 6-propynylamino-β-cyclodextrin, and then it was bonded onto ordered silica gel SBA-15 to obtain a novel triazole-bridged bis (β-cyclodextrin)–bonded chiral stationary phase (TBCDP). The structures of the bridged cyclodextrin and TBCDP were characterized by the infrared spectroscopy, mass spectrometry, elemental analysis, and thermogravimetric analysis. The chiral performance of TBCDP was evaluated by using chiral pesticides and drugs as probes including triazoles, flavanones, dansyl amino acids and β-blockers. Some effects of the composition in mobile phase and pH value on the enantioseparations were investigated in different modes. The nine triazoles, eight flavanones, and eight dansyl amino acids were successfully resolved on TBCDP under the reversed phase with the resolutions of hexaconazole, 2′-hydroxyflavanone, and dansyl-DL-tyrosine, which were 2.49, 5.40, and 3.25 within 30 minutes, respectively. The ten β-blockers were also separated under the polar organic mode with the resolution of arotinolol reached 1.71. Some related separation mechanisms were discussed preliminary. Compared with the native cyclodextrin stationary phase (CDSP), TBCDP has higher enantioselectivity to separate more analytes, which benefited from the synergistic inclusion ability of the two adjacent cavities and bridging linker of TBCDP, thereby enabling it a promising prospect in chiral drugs and food analysis.