2alpha-Hydroxyeupatolide 8-O-angelate

2alpha-Hydroxyeupatolide 8-O-angelate
Product Name 2alpha-Hydroxyeupatolide 8-O-angelate
CAS No.: 72229-39-1
Catalog No.: CFN89039
Molecular Formula: C20H26O5
Molecular Weight: 346.42 g/mol
Purity: >=98%
Type of Compound: Sesquiterpenoids
Physical Desc.: Powder
Source: The herbs of Eupatorium chinense var. tozanense.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
2alpha-Hydroxyeupatolide 8-O-angelate is a natural product from Eupatorium chinense var. tozanense.
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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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    Helvetica Chimica Acta, 2010, 91(11):2115-2121.
    Eupatozansins A-C, Sesquiterpene Lactones from Eupatorium chinense var. tozanense[Reference: WebLink]

    METHODS AND RESULTS:
    Phytochemical investigation of Eupatorium chinense var. tozanense has resulted in the isolation of three new germacranolides, designated as eupatozansins A–C (1–3), along with five known compounds, (5S,6R,7R,8R)-8-angeloyloxy-2-oxoguaia-1(10),3,11(13)-trien-12,6-olide (4), costunolide (5), leptocarpin (6), 2alpha-Hydroxyeupatolide 8-O-angelate (7), and quercetin (8).
    CONCLUSIONS:
    The structures of the new compounds were identified by 1D and 2D NMR experiments, as well as high-resolution mass spectrometry. The in vitro cytotoxic activities of compounds 1–8 were evaluated.
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