12-Epinapelline

12-Epinapelline
Product Name 12-Epinapelline
CAS No.: 110064-71-6
Catalog No.: CFN90663
Molecular Formula: C22H33NO3
Molecular Weight: 359.5 g/mol
Purity: >=98%
Type of Compound: Alkaloids
Physical Desc.: Powder
Source: The roots of Aconitum kusnezoffii Reichb.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price: $238/20mg
12-Epinapelline is a natural product from Aconitum kusnezoffii Reichb.
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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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  • 12-Epinapelline

    Catalog No: CFN90663
    CAS No: 110064-71-6
    Price: $238/20mg
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    Chemistry of Natural Compounds, 2005,41(5):609.
    Crystal and Molecular Structure of 12-Epinapelline[Reference: WebLink]

    METHODS AND RESULTS:
    The article examines the crystal and molecular structure of 12-Epinapelline. Previous investigations showed that the conformation of ring A in crystal structures of napelline-type alkaloids depended on the presence or absence of an intramolecular H-bond between an alpha-oriented C1 hydroxyl and the N atom.
    CONCLUSIONS:
    Thus, ring A in 12-epilucidusculin had the boat conformation and in acophine it adopted the twist or chair conformation.
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