6-O-Vanilloylajugol

6-O-Vanilloylajugol
Product Name 6-O-Vanilloylajugol
CAS No.: 124168-04-3
Catalog No.: CFN99354
Molecular Formula: C23H30O12
Molecular Weight: 498.5 g/mol
Purity: >=98%
Type of Compound: Iridoids
Physical Desc.: Powder
Source: The herbs of Rehmannia glutinosa (Gaert.) Libosch. ex Fisch. et Mey.
Solvent: DMSO, Pyridine, Methanol, Ethanol, etc.
Price:
6-O-Vanilloylajugol demonstrates scavenging properties toward the 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical.
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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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    Turk. J.Chem., 2004, 28(2):227-34.
    Iridoid and phenylethanoid glycosides from Verbascum lasianthum[Reference: WebLink]

    METHODS AND RESULTS:
    Three iridoid glucosides, 8-O-acethylharpagide (1), harpagoside (2), and 6-O-Vanilloylajugol (3), were isolated from the roots of Verbascum lasianthum Boiss. ex Bentham. In addition, 2 phenylethanoid glycosides, verbascoside {=acteoside, [β-(3,4-dihydroxyphenyl)-ethyl]-(3′-O-α-L- rhamnopyranosyl)-(4′-O-caffeoyl)-β-D-glucopyranoside} (4) and poliumoside {= [β-(3,4-dihydroxyphenyl)-ethyl]-(3′,6′-O- α-L-dirhamnopyranosyl)-(4′-O-caffeoyl)-β-D-glucopyranoside} (5), were also isolated. The structures of all compounds were established by spectroscopic evidence (UV, IR, 1D and 2D NMR, LC-ESIMS).
    CONCLUSIONS:
    Compounds 2-5 demonstrated scavenging properties toward the 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical in TLC autographic assays.
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