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    1-Methoxycarbonyl-beta-carboline-N-oxide
    1-Methoxycarbonyl-beta-carboline-N-oxide
    Information
    CAS No. 74690-74-7 Price $318 / 5mg
    Catalog No.CFN95023Purity>=98%
    Molecular Weight242.2Type of CompoundAlkaloids
    FormulaC13H10N2O3Physical DescriptionYellow powder
    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 / $222.6 / In-stock
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    1-Methoxycarbonyl-beta-carboline-N-oxide

    1-Methoxycarbonyl-beta-carboline-N-oxide
    Product Name 1-Methoxycarbonyl-beta-carboline-N-oxide
    CAS No.: 74690-74-7
    Catalog No.: CFN95023
    Molecular Formula: C13H10N2O3
    Molecular Weight: 242.2 g/mol
    Purity: >=98%
    Type of Compound: Alkaloids
    Physical Desc.: Yellow powder
    Source: The barks of Picrasma quassioides
    Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
    Price: $318 / 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
  • Alkaloids Compound Library
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    Description: Reference standards.
    1-Methoxycarbonyl-beta-carboline-N-oxide Description
    Source: The barks of Picrasma quassioides
    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 4.1288 mL 20.6441 mL 41.2882 mL 82.5764 mL 103.2205 mL
    5 mM 0.8258 mL 4.1288 mL 8.2576 mL 16.5153 mL 20.6441 mL
    10 mM 0.4129 mL 2.0644 mL 4.1288 mL 8.2576 mL 10.322 mL
    50 mM 0.0826 mL 0.4129 mL 0.8258 mL 1.6515 mL 2.0644 mL
    100 mM 0.0413 mL 0.2064 mL 0.4129 mL 0.8258 mL 1.0322 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:
    Journal of Liquid Chromatography & Related Technologies, 2012, 35(11):1597-1606.
    PREPARATIVE ISOLATION AND PURIFICATION OF ALKALOIDS FROM PICRASMA QUASSIODES (D. DON) BENN. BY HIGH-SPEED COUNTERCURRENT CHROMATOGRAPHY.[Reference: WebLink]

    METHODS AND RESULTS:
    By using a two-phase solvent system composed of n-hexane-ethyl acetate-methanol-water (2:2:2:2, v/v/v/v), a high-speed counter-current chromatography technique was successfully used for isolation and purification of three alkaloids from Picrasma quassiodes (D. Don) Benn. for the first time. A total of 22.1 mg of 3-methylcanthin-2,6-dione, 4.9 mg of 4-methoxy-5-hydroxycanthin-6-one and 1.2 mg of 1-methoxycarbonyl-β-carboline were obtained from 100 mg of crude extract of Picrasma quassiodes (D. Don) Benn. in less than 5 hr, with purities of 89.30%, 98.32%, and 98.19%, respectively.
    CONCLUSIONS:
    The target compounds were identified by ESI-MS, 1H NMR, and 13C NMR.
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