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    Natural Products
    Taxifolin 3'-O-glucoside
    Taxifolin 3'-O-glucoside
    Information
    CAS No. 31106-05-5 Price
    Catalog No.CFN96494Purity>95%
    Molecular Weight342.29Type of CompoundFlavonoids
    FormulaC21H22O12Physical 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
    Other Packaging *Packaging according to customer requirements(100uL/well, 200uL/well and more), and Container use Storage Tube With Screw Cap
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    Taxifolin 3'-O-glucoside

    Taxifolin 3'-O-glucoside
    Product Name Taxifolin 3'-O-glucoside
    CAS No.: 31106-05-5
    Catalog No.: CFN96494
    Molecular Formula: C21H22O12
    Molecular Weight: 342.29 g/mol
    Purity: >95%
    Type of Compound: Flavonoids
    Physical Desc.: Powder
    Source: The leaves of Chamaecyparis obtuse
    Solvent: DMSO, Pyridine, Methanol, Ethanol, etc.
    Price:
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    Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
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    Description: Taxifolin 3'-O-glucoside is a natural product from Chamaecyparis obtuse.
    Taxifolin 3'-O-glucoside Description
    Source: The leaves of Chamaecyparis obtuse
    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 2.9215 mL 14.6075 mL 29.215 mL 58.43 mL 73.0375 mL
    5 mM 0.5843 mL 2.9215 mL 5.843 mL 11.686 mL 14.6075 mL
    10 mM 0.2921 mL 1.4607 mL 2.9215 mL 5.843 mL 7.3037 mL
    50 mM 0.0584 mL 0.2921 mL 0.5843 mL 1.1686 mL 1.4607 mL
    100 mM 0.0292 mL 0.1461 mL 0.2921 mL 0.5843 mL 0.7304 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:
    Biochemical Systematics & Ecology, 2002, 30(11):1011-1022.
    Flavonoids from Pinus sylvestris needles and their variation in trees of different origin grown for nearly a century at the same area[Reference: WebLink]

    METHODS AND RESULTS:
    Flavonoids in needles of Scots pine planted in 1912–1914 in Poland from seeds originating from different parts of Europe, were isolated, chemically characterised and analysed by HPLC. It was shown that flavonoid profiles were similar in all tested populations and were different from those previously reported for Scots pine seedlings. They included taxifolin, Taxifolin 3'-O-glucoside, quercetin as well as quercetin 3-O-glucoside and 3′-O-glucoside. The quercetin 3-O-glucoside could be found only in a trace amount in all samples and quercetin 3′-O-glucoside appeared in all samples regardless their origin. The relative concentration of taxifolin 3′-O-glucoside, quercetin, taxifolin and total flavonoids showed dependence on the origin of seeds; needles from high latitude populations contained smaller amounts of these compounds.
    CONCLUSIONS:
    Presented data clearly indicate that Scots pine contain glycosidases specific for glycosylation at C-3′ rather than at C-3. Besides, they indicate that long lasting influence of similar environmental factors is not able to change genetic regulatory systems responsible for flavonoid biosynthesis.
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