5,7-Dihydroxychromone 7-rutinoside

5,7-Dihydroxychromone 7-rutinoside
Product Name 5,7-Dihydroxychromone 7-rutinoside
CAS No.: 52538-46-2
Catalog No.: CFN92369
Molecular Formula: C21H26O13
Molecular Weight: 486.4 g/mol
Purity: >=98%
Type of Compound: Flavonoids
Physical Desc.: Powder
Source: The herbs of Drynaria roosii Nakaike
Solvent: DMSO, Pyridine, Methanol, Ethanol, etc.
Price:
Reference standards.
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Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com

The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
  • Nat Prod Communications2018, 10.1177
  • Toxicol In Vitro.2018, 52:94-105
  • EXCLI J.2023, 22:482-498.
  • Phytomedicine.2023, 116:154841.
  • Theoretical and Experimental Plant Physiology 2022, 34,53-62
  • Food Funct.2024, 15(4):1852-1866.
  • Metabolites2023, 13(1), 3.
  • ACS Omega.2023, 9(1):1278-1286.
  • Plant Physiol Biochem.2023, 201:107795.
  • Preprints2022, 202211.0388.v1.
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    Postmortale bildung von 5,7-dihydroxychromon-7-rutinosid in Mentha longifolia.[Reference: WebLink]

    METHODS AND RESULTS:
    5,7-Dihydroxychromone 7-rutinoside isolated from Mentha longifolia must be considered to be a product of postmortem processes. It is only formed after heating fresh plant material and its production is connected with the degradation of flavonoids, and particularly of eriodictyol 7-rutinoside.
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    Investigations with four other Mentha species confirm these results. Eriodictyol 7-rutinoside and eriodictyol are degraded up to 50%, by horseradish peroxidase but 5,7-dihydroxychromone-7-rutinoside cannot be detected.
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