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    Natural Products
    Sesamoside
    Sesamoside
    Information
    CAS No. 117479-87-5 Price $100 / 20mg
    Catalog No.CFN99274Purity>=98%
    Molecular Weight420.4 Type of CompoundIridoids
    FormulaC17H24O12Physical DescriptionPowder
    Download Manual    COA    MSDS    SDFSimilar 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 / $33.8 / In-stock
    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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    Sesamoside

    Sesamoside
    Product Name Sesamoside
    CAS No.: 117479-87-5
    Catalog No.: CFN99274
    Molecular Formula: C17H24O12
    Molecular Weight: 420.4 g/mol
    Purity: >=98%
    Type of Compound: Iridoids
    Physical Desc.: Powder
    Source: The herbs of Sesamum angolense.
    Solvent: DMSO, Pyridine, Methanol, Ethanol, etc.
    Price: $100 / 20mg
    Inquire / Order: manager@chemfaces.com
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  • Nutr Res Pract.2020, 14(5):478-489.
  • Nutrients2022, 14(3),695.
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    Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
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    Description: Sesamoside has antinociceptive and anti-inflammatory activities.
    Sesamoside Description
    Source: The herbs of Sesamum angolense.
    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 2.3787 mL 11.8934 mL 23.7869 mL 47.5737 mL 59.4672 mL
    5 mM 0.4757 mL 2.3787 mL 4.7574 mL 9.5147 mL 11.8934 mL
    10 mM 0.2379 mL 1.1893 mL 2.3787 mL 4.7574 mL 5.9467 mL
    50 mM 0.0476 mL 0.2379 mL 0.4757 mL 0.9515 mL 1.1893 mL
    100 mM 0.0238 mL 0.1189 mL 0.2379 mL 0.4757 mL 0.5947 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:
    Zhong Yao Cai. 2014 Mar;37(3):439-42.
    Isolation and identification of nine iridoid glycosides from Lamiophlomis rotata by HPLC combining PDA and MS.[Pubmed: 25174110]
    To establish a rapid chromatographic method to separate the iridoid glycosides from Lamioplomis rotata, and to identify the target compounds with PDA and MS.
    METHODS AND RESULTS:
    Methanol-water gradient elution was used to separate and analyze the target compounds. The fluid fractions were gathered according to the chromatogram and dried with the nitrogen airflow. The mass fractions of the target compounds were determined with RP-HPLC and the structures were identified with PDA and MS. The purity of some compounds exceeded 90% and these 9 compounds were identified as iridoid glycosides, which were Phlorigidoside C (1), Schismoside (2), Sesamoside (3), Shanzhiside methylester (4), 6-O-Acetyl shanzhiside methylester (5), Phloyoside II (6), Penstemoside (7), Loganin (8) and 8-O-Acetyl shanzhiside methylester (9).
    CONCLUSIONS:
    The method is simple and practicable with high efficiency. It can be used to qualitative and quantitative analysis of the 9 iridoid glycosides in Lamiphlomis rotata and its preparations.
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