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    1-Methyl-2,8-dihydroxy-3-carboxy-9,10-anthraquinone
    1-Methyl-2,8-dihydroxy-3-carboxy-9,10-anthraquinone
    Information
    CAS No. 1401414-53-6 Price $338 / 5mg
    Catalog No.CFN95101Purity>=98%
    Molecular Weight298.3Type of CompoundAnthraquinones
    FormulaC16H10O6Physical DescriptionPowder
    Download     COA    MSDSSimilar structuralComparison (Web)  (SDF)
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    Size /Price /Stock 10 mM * 1 mL in DMSO / $236.6 / In-stock
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    1-Methyl-2,8-dihydroxy-3-carboxy-9,10-anthraquinone

    1-Methyl-2,8-dihydroxy-3-carboxy-9,10-anthraquinone
    Product Name 1-Methyl-2,8-dihydroxy-3-carboxy-9,10-anthraquinone
    CAS No.: 1401414-53-6
    Catalog No.: CFN95101
    Molecular Formula: C16H10O6
    Molecular Weight: 298.3 g/mol
    Purity: >=98%
    Type of Compound: Anthraquinones
    Physical Desc.: Powder
    Source: The roots of Rheum palmatum L.
    Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
    Price: $338 / 5mg
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  • Related Screening Libraries
    Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
    10 mM * 1 mL in DMSO / Inquiry / In-stock
    Related Libraries
  • Anthraquinones Compound Library
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    Description: Reference standards.
    1-Methyl-2,8-dihydroxy-3-carboxy-9,10-anthraquinone Description
    Source: The roots of Rheum palmatum L.
    Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, 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 3.3523 mL 16.7616 mL 33.5233 mL 67.0466 mL 83.8082 mL
    5 mM 0.6705 mL 3.3523 mL 6.7047 mL 13.4093 mL 16.7616 mL
    10 mM 0.3352 mL 1.6762 mL 3.3523 mL 6.7047 mL 8.3808 mL
    50 mM 0.067 mL 0.3352 mL 0.6705 mL 1.3409 mL 1.6762 mL
    100 mM 0.0335 mL 0.1676 mL 0.3352 mL 0.6705 mL 0.8381 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:
    Chinese Journal of Natural Medicines, 2011, 9(6):410-413.
    Two New Compounds from the Roots of Rheum palmatum.[Reference: WebLink]
    To study the constituents of Rheum palmatum.
    METHODS AND RESULTS:
    Chromatographic separations of silica gel and polyamide were used. All the structures were elucidated on the basis of chemical and spectroscopic analysis. Nine compounds were isolated and their structure were identified as 2, 5-dimethyl-6, 8-dihydroxy-chromone (1), 1-methyl-2, 8-dihydroxy- 3-carboxy −9, 10-anthraquinone (2), citreorosein (3), 4-(4-hydroxyphenyl)-2-butanone (4), 4-(4-hydroxyphenyl)-2-butanone-4′-O-β-D- (2″-galloyl-6″-O-p-coumaroyl)-glucopyranoside (5), trans-3, 5, 4′-trihydroxystilbene-4′-O-β-D-(6″-galloyl)-glucopyranoside (6), 4-(4- hydroxyphenyl)-2-butanone-4′-O-β-D-(6″-O-cinnamoyl)-glucopyranoside (7), 4-(4-hydroxyphenyl)-2-butanone-4′-O-β-D-(6″-O-p-coumaroyl)-glucopyranoside (8), trans-3, 5, 4′-trihydroxystilbene-4′-O-β-D-glucopyranoside (9).
    CONCLUSIONS:
    Compounds 1 and 2 were newly isolated from Rheum palmatum.
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