3',4'-dihydro-3'-hydroxy-Xanthyletin

3',4'-dihydro-3'-hydroxy-Xanthyletin
Product Name 3',4'-dihydro-3'-hydroxy-Xanthyletin
CAS No.: 5993-18-0
Catalog No.: CFN92775
Molecular Formula: C14H14O4
Molecular Weight: 246.3 g/mol
Purity: >=98%
Type of Compound: Coumarins
Physical Desc.: Powder
Source: The roots of Angelica gigas
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
3',4'-dihydro-3'-hydroxy-Xanthyletin is a natural product from Angelica gigas.
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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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    Natural Product Communications, 2008 , 3 (5) :785-790.
    Isolation of pyranocoumarins from Angelica gigas.[Reference: WebLink]

    METHODS AND RESULTS:
    A mixture of diastereomers of the coumarin glycoside 3′-O-a-D- glucopyranosyl-3′,4′-dihydroxanthyletin (1), along with six known pyranocoumarins, columbianoside (4), marmesin (5), 3′-hydroxy-3′, 4′-dihydroxanthyletin (3',4'-dihydro-3'-hydroxy-Xanthyletin,6), decursin (7), decursinol angelate (8), and isoimperatorin (9), were isolated from the roots of Angelica gigas Nakai.
    CONCLUSIONS:
    The racemic compound 1 was successfully separated by preparative HPLC to obtain a new isomer 3′(S)-O-β-D-glucopyranosyl-3′,4′- dihydroxanthyletin (2), and a known isomer 3′(R)-O-β-D- glucopyranosyl-3′,4′-dihydroxanthyletin (3). The absolute configuration of compounds 2 and 3 was determined by comparison of optical rotation and NMR data of their acid hydrolysis products.
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