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    Natural Products
    Indolelactic acid
    Indolelactic acid
    Information
    CAS No. 1821-52-9 Price $100 / 20mg
    Catalog No.CFN95263Purity>=98%
    Molecular Weight205.2Type of CompoundAlkaloids
    FormulaC11H11NO3Physical 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 / $29.6 / In-stock
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    Indolelactic acid

    Indolelactic acid
    Product Name Indolelactic acid
    CAS No.: 1821-52-9
    Catalog No.: CFN95263
    Molecular Formula: C11H11NO3
    Molecular Weight: 205.2 g/mol
    Purity: >=98%
    Type of Compound: Alkaloids
    Physical Desc.: Powder
    Source: The roots of Heracleum candicans.
    Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
    Price: $100 / 20mg
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  • Oncol Lett.2020, 20(4):122.
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    Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
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    Description: Indolelactic acid is a phytochormone.
    Indolelactic acid Description
    Source: The roots of Heracleum candicans.
    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 4.8733 mL 24.3665 mL 48.7329 mL 97.4659 mL 121.8324 mL
    5 mM 0.9747 mL 4.8733 mL 9.7466 mL 19.4932 mL 24.3665 mL
    10 mM 0.4873 mL 2.4366 mL 4.8733 mL 9.7466 mL 12.1832 mL
    50 mM 0.0975 mL 0.4873 mL 0.9747 mL 1.9493 mL 2.4366 mL
    100 mM 0.0487 mL 0.2437 mL 0.4873 mL 0.9747 mL 1.2183 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:
    Biologia Plantarum, 1970, 12(3):246-255.
    Pathways of IAA production from tryptophan by plants and by their epiphytic bacteria: Metabolism of indolepyruvic acid and indolelactic acid.[Reference: WebLink]

    METHODS AND RESULTS:
    Metabolites of indolepyruvic acid and Indolelactic acid were investigated using 2 systems: a bacterial (pea stem homogenates containing the epiphytic bacteria) and a plant system (pea stem sections under sterile conditions). The products of spontaneous indolepyruvic acid decomposition in aqueous solution and during chromatography were investigated, too.Biological indolepyruvic acid conversion yields, besides those substance amounts which occur spontaneously, indoleacetic acid, indoleethanol (tryptophol) and (only in the sterile plant system) indoleacetaldehyde. An inhibitor extract from pea stems decreases the indoleacetic acid and increases the indoleethanol and indoleacetaldehyde gain.
    CONCLUSIONS:
    Indolelactic acid is not metabolized in the sterile plant sections. Indolelactic acid oxidation by the bacteria-containing homogenate yields indolepyruvic acid and is inhibited by the inhibitor extract.
    Journal of Chromatography A, 2015, 205( 1):125-137.
    Identification of 3-indoleacetic acid in pinus sylvestris L. by gas chromatography-mas spectrometry, and quantitative analysis by ion-pair reversed-phase liquid chromatography wit spectrofluorimetric detection.[Reference: WebLink]

    METHODS AND RESULTS:
    The phytochormone 3-indoleacetic acid (IAA) was conclusively identified by gas chromatography-mas spetrometry of its methyl ester in purified extracts of Scots pine, Pinus sylvestris L. Preceding purification included reversed-phase ion-pair chromatography on a Nucleosil C18 column with tetrabutylammonium ion as counter ion. A number of indole acids were separated in this high-performance liquid chromatographic (HPLC) system. In particular, IAA was separated from the reported plant constituents 4-chloro-IAA, 5-hydroxy-IAA, 3-indoleacrylic acid, 3-Indolelactic acid, 3-indolepropionic acid, 3-indolebutyric acid and tytophan. In connection with a spectrofluorine detector, the HPLC system was also used for the quantitative analysis of IAA in pine samples. Systematic errors caused a constant under-estimation of the IAA content by 12% and could easily be corrected for. The random error was 14%. Eight-week-old pine seedings contained 46 ng g−1 of IAA.
    CONCLUSIONS:
    The sensitivity of the method, applied to the analysis of pine extracts, was 50 pg of IAA. Evidence is presented that the method, when applied to the analysis of pine extracts, is specific of IAA.
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