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    Natural Products
    (3E,5E,11E)-tridecatriene-7,9-diyne-1,2-diacetate
    (3E,5E,11E)-tridecatriene-7,9-diyne-1,2-diacetate
    Information
    CAS No. N/A Price $318 / 5mg
    Catalog No.CFN95191Purity>95%
    Molecular Weight286.3Type of CompoundMiscellaneous
    FormulaC17H18O4Physical DescriptionOil
    Download     COA    MSDSSimilar structuralComparison (Web)  (SDF)
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    * Packaging according to customer requirements(5mg, 10mg, 20mg and more). We shipped via FedEx, DHL, UPS, EMS and others courier.
    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 / $222.6 / 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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    (3E,5E,11E)-tridecatriene-7,9-diyne-1,2-diacetate

    (3E,5E,11E)-tridecatriene-7,9-diyne-1,2-diacetate
    Product Name (3E,5E,11E)-tridecatriene-7,9-diyne-1,2-diacetate
    CAS No.: N/A
    Catalog No.: CFN95191
    Molecular Formula: C17H18O4
    Molecular Weight: 286.3 g/mol
    Purity: >95%
    Type of Compound: Miscellaneous
    Physical Desc.: Oil
    Source: The roots of Atractylodes chinensis
    Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
    Price: $318 / 5mg
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    Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
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    Description: Reference standards.
    (3E,5E,11E)-tridecatriene-7,9-diyne-1,2-diacetate Description
    Source: The roots of Atractylodes chinensis
    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 3.4928 mL 17.4642 mL 34.9284 mL 69.8568 mL 87.321 mL
    5 mM 0.6986 mL 3.4928 mL 6.9857 mL 13.9714 mL 17.4642 mL
    10 mM 0.3493 mL 1.7464 mL 3.4928 mL 6.9857 mL 8.7321 mL
    50 mM 0.0699 mL 0.3493 mL 0.6986 mL 1.3971 mL 1.7464 mL
    100 mM 0.0349 mL 0.1746 mL 0.3493 mL 0.6986 mL 0.8732 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:
    Phytochemistry (Oxford), 1997, 46(6):1023-1028.
    Diacetoxy-substituted polyacetylenes from Atractylodes lancea.[Reference: WebLink]

    METHODS AND RESULTS:
    Six new polyacetylenes have been isolated from the rhizomes of Atractylodes lancea. Besides 1-(2-furyl)-(7E)-nonene-3,5-diyne-1,2-diacetate, a new natural compound, two further vicinal diacetoxyalkenynes were postulated as erythro- and threo-forms of (1,5E, 11E)-tridecatriene-7,9-diyne-3,4-diacetate in comparison with similar structures in the literature. Three other constituents turned out to be (3E,5E,11E)-tridecatriene-7,9-diyne-1,2-diacetate together with its (3Z)- and (5Z)-isomers.
    CONCLUSIONS:
    All structures were established by UV, EI-mass spectrometry, 1D and 2D NMR experiments.
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