2,4-Dihydroxy-6-methoxy-3-formylacetophenone
2,4-Dihydroxy-6-methoxy-3-formylacetophenone is a natural product from Euphorbia pekinensis Rupr.
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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.
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Analytical Letters.2020, doi 10.1008
Chung Shan Medical University2020, US20200323790A1
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Food Chemistry: X2023, 101032.
Applied Biological Chemistry2021, 64(4)
Drug Dev Res.2022, 83(7):1673-1682.
J Lipid Res.2024, 65(10):100640.
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Archiv Der Pharmazie, 2010 , 306 (11) :857-865.
Einige Inhaltsstoffe der Rinde von Cedrelopsis grevei Baillon[Reference:
WebLink]
METHODS AND RESULTS:
Some Constituents of the Bark of Cedrelopsis Grevei Baillon2,4-Dihydroxy-6-methoxy-3-formylacetophenone (1) as well as an α,ß-unsaturated ketone of unknown structure were isolated from the bark of Cedrelopsis grevei Baillon (Meliaceae or Ptaeroxylaceae).
Alloevodionol (3), a dialkoxy-derivative of Aesculetin (4), the 2,6-dihydroxy-4-methoxy-acetophenone (5) and the 2-(2′-hydroxyisopropyl)-6-hydroxy-4-methoxy-7-acetylcoumaran (6) were separated by sodium hydroxide extraction from the petroleum ether extract.
CONCLUSIONS:
β-Amyrin, lupeol and ß-sitosterol could be isolated from the neutral fraction of the petroleum ether extract. Quercetin could be separated by ethanol extraction. No evidence was found for the presence of alkaloids in the drug.
