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    3,4-Dihydrocoumarin
    3,4-Dihydrocoumarin
    Information
    CAS No. 119-84-6 Price $50 / 20mg
    Catalog No.CFN90890Purity>=98%
    Molecular Weight148.2Type of CompoundCoumarins
    FormulaC9H8O2Physical DescriptionPowder
    Download     COA    MSDSSimilar structuralComparison (Web)
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    3,4-Dihydrocoumarin Description
    Source: The leaves of Southern sweet-grass.
    Biological Activity or Inhibitors: 1. 3,4-Dihydrocoumarin is widespread used as a flavoring agent in beverages, gelatins, puddings, candy, and other food items; as a fragrance in perfumes, creams, and cosmetics.
    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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    Recently, ChemFaces products have been cited in many studies from excellent and top scientific journals

    Cell. 2018 Jan 11;172(1-2):249-261.e12.
    doi: 10.1016/j.cell.2017.12.019.

    PMID: 29328914

    Mol Cell. 2017 Nov 16;68(4):673-685.e6.
    doi: 10.1016/j.molcel.2017.10.022.

    PMID: 29149595

    Scientific Reports 2017 Dec 11;7(1):17332.
    doi: 10.1038/s41598-017-17427-6.

    PMID: 29230013

    Molecules. 2017 Oct 27;22(11). pii: E1829.
    doi: 10.3390/molecules22111829.

    PMID: 29077044

    J Cell Biochem. 2018 Feb;119(2):2231-2239.
    doi: 10.1002/jcb.26385.

    PMID: 28857247

    Phytomedicine. 2018 Feb 1;40:37-47.
    doi:10.1016/j.phymed.2017.12.030

    PMID: 29496173
    Calculate Dilution Ratios(Only for Reference)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 6.7476 mL 33.7382 mL 67.4764 mL 134.9528 mL 168.691 mL
    5 mM 1.3495 mL 6.7476 mL 13.4953 mL 26.9906 mL 33.7382 mL
    10 mM 0.6748 mL 3.3738 mL 6.7476 mL 13.4953 mL 16.8691 mL
    50 mM 0.135 mL 0.6748 mL 1.3495 mL 2.6991 mL 3.3738 mL
    100 mM 0.0675 mL 0.3374 mL 0.6748 mL 1.3495 mL 1.6869 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.
    3,4-Dihydrocoumarin References Information
    Citation [1]

    Natl Toxicol Program Tech Rep Ser. 1993 Sep;423:1-336.

    NTP Toxicology and Carcinogenesis Studies of 3,4-Dihydrocoumarin (CAS No. 119-84-6) in F344/N Rats and B6C3F1 Mice (Gavage Studies).[Pubmed: 12616288]
    3,4-Dihydrocoumarin was nominated by the Food and Drug Administration and the National Cancer Institute for study because of its widespread use as a flavoring agent in beverages, gelatins, puddings, candy, and other food items; as a fragrance in perfumes, creams, and cosmetics; and because of interest in the structure-activity relationships of the coumarin derivatives. Toxicity and carcinogenicity studies were conducted by administering 3,4-Dihydrocoumarin (99% pure) in corn oil by gavage to groups of male and female F344/N rats and B6C3F1 mice for 16 days, 13 weeks, and 2 years. Genetic toxicology studies were conducted in Salmonella typhimurium, cultured Chinese hamster ovary cells, and peripheral blood cells of mice.
    Citation [2]

    Herba Polonica, 2010 , 56 (4) :14-9.

    The influence of shading on the yield and quality of southern sweet-grass (Hierochloë australis (Schrad.) Roem. & Schult.) raw material[Reference: WebLink]
    Southern sweet-grass (Poaceae) rarely occurs in Polish coniferous or mixed forests. Leaves of this plant, rich in coumarin compounds, are mainly used as a flavouring raw material in alcohol, tobacco and cosmetic industry. The aim of the study was to investigate the influence of shading on the yield and quality of southern sweet-grass. The experiment was established at the certificated organic field of Department of Vegetable and Medicinal Plants. The sunlight was reduced up to 50 and 70% by using shading nets. The object of experiment was two-year-old plants grown on the alluvial soil. Leaves were harvested two times: in mid-May and in the last week of August (regrowth). The highest yield of leaves was observed at 50% of shading. The shaded plants were characterized by higher content of coumarin and 3,4-Dihydrocoumarin and lower content of bergapten in comparison to non-shaded ones. In the leaves five phenolic acids and two flavonoids were identified.