Apigenin 7-O-(6''-O-malonylglucoside)
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.
Separations2023, 10(7), 411.
Pharm Biol.2022, 60(1):2040-2048.
Plants.2024, 13(10):1348;
Phytomedicine.2019, 67:153159
Plant Physiol.2023, 193(3):1758-1771.
Nutrients2022, 14(3),695.
Nat Prod Sci.2014, 20(3):182-190
Arch Biochem Biophys.2024, 759:110111.
Environ Toxicol.2019, 34(4):513-520.
J Pharm Biomed Anal.2024, 247:116257.
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Phytochemistry. 2004 Aug;65(16):2323-32.
Isolation, identification and stability of acylated derivatives of apigenin 7-O-glucoside from chamomile (Chamomilla recutita [L.] Rauschert).[Pubmed:
15381003 ]
METHODS AND RESULTS:
The major flavonoids in the white florets of chamomile (Chamomilla recutita [L.] Rauschert) were rapidly purified using a combination of polyamide solid-phase extraction and preparative HPLC. From the combined LC/MS, LC/MS/MS, and NMR data the apigenin glucosides were identified as apigenin 7-O-glucoside (Ap-7-Glc), Ap-7-(6"-malonyl-Glc)(Apigenin 7-O-(6''-O-malonylglucoside)
), Ap-7-(6"-acetyl-Glc), Ap-7-(6"-caffeoyl-Glc), Ap-7-(4"-acetyl-Glc), Ap-7-(4"-acetyl,6"-malonyl-Glc), and a partially characterised apigenin-7-(mono-acetyl/mono-malonylglucoside) isomer. Malonyl and caffeoyl derivatives of Ap-7-Glc have not previously been identified in chamomile.
CONCLUSIONS:
The two mono-acetyl/mono-malonyl flavonoids have not previously been reported in any plant species. These acylated glucosides are unstable and degrade to form acetylated compounds or Ap-7-Glc.
The degradation products formed are dependent on the extraction and storage conditions, i.e. temperature, pH and solvent.
