Emodin-8-O-beta-gentiobioside

Emodin-8-O-beta-gentiobioside
Product Name Emodin-8-O-beta-gentiobioside
CAS No.: 66466-22-6
Catalog No.: CFN95132
Molecular Formula: C27H30O15
Molecular Weight: 594.5 g/mol
Purity: >=98%
Type of Compound: Anthraquinones
Physical Desc.: Powder
Source: The roots and rhizomes of Rheum palmatum L.
Solvent: DMSO, Pyridine, Methanol, Ethanol, etc.
Price: $368/5mg
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.
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  • Industrial Crops and Products2022, 188:115638
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  • Universitat Stuttgart2022, opus-12200.
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    Demuth G , Hinz H , Seligmann O , et al. Planta Medica, 1978, 33(1):53-56.
    Investigations on anthrachinonglycosides of Rhamnus species, V Emodin-8-O-beta-gentiobiosid,e a new O-glycoside from Rhamnus frangula[Reference: WebLink]

    METHODS AND RESULTS:
    From the bark of Rhamnus frangula a new glycoside has been isolated and its structure elucidated as Emodin-8-O-beta-gentiobioside. The structure was confirmed by glycosidation of 6–O–benzoyl–emodin with α–acetobromgentiobiose in a Koenigs–Knorr reaction followed by saponification.
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