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    Natural Products
    (R)-Eriodictyol-8-C-beta-D-glucopyranoside
    (R)-Eriodictyol-8-C-beta-D-glucopyranoside
    Information
    CAS No. 1023271-51-3 Price
    Catalog No.CFN91943Purity>=98%
    Molecular Weight450.39Type of CompoundFlavonoids
    FormulaC21H22O11Physical DescriptionPowder
    Download     COA    MSDSSimilar structuralComparison (Web)  (SDF)
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    According to end customer requirements, ChemFaces provide solvent format. This solvent format of product intended use: Signaling Inhibitors, Biological activities or Pharmacological activities.
    Size /Price /Stock 10 mM * 1 mL in DMSO / Inquiry
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    (R)-Eriodictyol-8-C-beta-D-glucopyranoside

    (R)-Eriodictyol-8-C-beta-D-glucopyranoside
    Product Name (R)-Eriodictyol-8-C-beta-D-glucopyranoside
    CAS No.: 1023271-51-3
    Catalog No.: CFN91943
    Molecular Formula: C21H22O11
    Molecular Weight: 450.39 g/mol
    Purity: >=98%
    Type of Compound: Flavonoids
    Physical Desc.: Powder
    Source: The herbs of Aspalathus linearis
    Solvent: DMSO, Pyridine, Methanol, Ethanol, etc.
    Price:
    Inquire / Order: manager@chemfaces.com
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    Description: Reference standards.
    (R)-Eriodictyol-8-C-beta-D-glucopyranoside Description
    Source: The herbs of Aspalathus linearis
    Solvent: DMSO, Pyridine, Methanol, Ethanol, etc.
    Storage: 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

    After receiving: 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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    Calculate Dilution Ratios(Only for Reference)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 2.2203 mL 11.1015 mL 22.203 mL 44.406 mL 55.5074 mL
    5 mM 0.4441 mL 2.2203 mL 4.4406 mL 8.8812 mL 11.1015 mL
    10 mM 0.222 mL 1.1101 mL 2.2203 mL 4.4406 mL 5.5507 mL
    50 mM 0.0444 mL 0.222 mL 0.4441 mL 0.8881 mL 1.1101 mL
    100 mM 0.0222 mL 0.111 mL 0.222 mL 0.4441 mL 0.5551 mL
    * Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
    Protocol
    Structure Identification:
    Nat Prod Commun. 2015 Jul;10(7):1191-3.
    Chemical Constituents of Pyrrosia calvata.[Pubmed: 26411008]

    METHODS AND RESULTS:
    A novel flavanone glycoside, 3',5',5,7-tetrahydroxy-6-C-β-D-glucopyranosyl-flavanone (1), along with 16 known compounds, (R/S)-eriodictyol-8-C-β-D-glucopyranoside ((R)-Eriodictyol-8-C-beta-D-glucopyranoside,2), quercetin-3-O-α-L-rhamnosyl (1''' --> 3''')-β-D-glucopyranoside (3), hemipholin (4), 4β-carboxymethyl-(-)-epicatechin methyl ester (5), kaempferol (6), quercetin (7), mangiferin (8), chlorogenic acid (9), 1,5-O-dicaffeoylquinic acid (10), 3,5-O-dicaffeoylquinic acid (11), 3-O-caffeoylquinic acid methyl ester (12), 1-O-caffeoyl glycoside (13), 4-O-β-D-glucopyranosyl-caffeic acid (14), 3'-O-methyleplcatechin-7-O-β-D-glucopyranoside (15), hop-22(29)-en-30-ol (16) and diploptene (17), were isolated from the whole plant of Pyrrosia calvata (Backer) Ching.
    CONCLUSIONS:
    Among them, compounds 2, 3, 4, 10, 11, 13 and 14 were isolated from the family Polypodiaceae for the first time, and compound 5 has not been recorded previously from the genus Pyrrosia.
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