PHL89346

Quercitrin

phyproof^® Reference Substance

• Synonym(s): 3,3′,4′,5,7-Pentahydroxyflavone 3-rhamnoside, 3-O-Rhamnosylquercetin, Quercetin 3-rhamnoside, Quercimelin, Quercitroside
• Empirical Formula (Hill Notation): C₂₁H₂₀O₁₁
• CAS Number: 522-12-3
• Molecular Weight: 448.38
• Beilstein: 68135
• MDL number: MFCD00016932
• UNSPSC Code: 41116107
• NACRES: NA.24

Properties

• grade: primary reference standard
• product line: phyproof^® Reference Substance
• Assay: ≥95.0% (HPLC)
• manufacturer/tradename: PhytoLab
• application(s): food and beverages
• format: neat
• SMILES string: C[C@@H]1O[C@@H](OC2=C(Oc3cc(O)cc(O)c3C2=O)c4ccc(O)c(O)c4)[C@H](O)[C@H](O)[C@H]1O
• InChI: 1S/C21H20O11/c1-7-15(26)17(28)18(29)21(30-7)32-20-16(27)14-12(25)5-9(22)6-13(14)31-19(20)8-2-3-10(23)11(24)4-8/h2-7,15,17-18,21-26,28-29H,1H3/t7-,15-,17+,18+,21-/m0/s1
• InChI key: OXGUCUVFOIWWQJ-HQBVPOQASA-N

Description

General description

This substance is a primary reference substance with assigned absolute purity (considering chromatographic purity, water, residual solvents, inorganic impurities). The exact value can be found on the certificate. Produced by PhytoLab GmbH & Co. KG

Application

• Quercitrin in anti-inflammatory and analgesic applications: Quercitrin has been evaluated for its potential antioxidant, anti-inflammatory, and analgesic properties. The study conducted on Cistus albidus L. highlights the role of Quercitrin in modulating inflammatory responses, suggesting its utility in pharmacological research and development of anti-inflammatory agents (Zouhri et al., 2024).


• Quercitrin in flavonoid research for oxidative stress management: Research on various blackberry cultivars, incorporating Quercitrin, employed metabolomics and network pharmacology to explore its antioxidant effects. This study underscores the flavonoid′s role in mitigating oxidative stress, relevant in cellular health and chronic disease management (Lee et al., 2024).


• Quercitrin for laboratory studies in enzymatic extraction processes: A study on the enzymatic-assisted ultrasonic extraction of flavonoids highlights the use of Quercitrin in improving the yield of bioactive compounds from plant materials. This application is crucial for the pharmaceutical and nutraceutical industries, where high-purity extracts are essential (Chu et al., 2024).

Other Notes

This compound is commonly found in plants of the genus: eucalyptus ginkgo hypericum mentha

Legal Information

phyproof is a registered trademark of PhytoLab GmbH & Co. KG

Safety Information

• Storage Class Code: 11 - Combustible Solids
• WGK: WGK 3
• Flash Point(F): Not applicable
• Flash Point(C): Not applicable