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Sulforaphene

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Origin: China

Cas No: 592-95-0

Specification: 99%min

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  • Products Specification
  • Product Description

  • Property

    CAS No.: 592-95-0 Formula: C6H9NOS2 Molecular Weight: 175.27200

    Description

    Raphanin is the main sulfur component found in radish seeds of Raphanus sativus and is also found in broccoli and red cabbage. It was first described by G. Ivanovics and S. Horvath in 1947. Raphanin inhibits activity of viruses, some fungi and various bacteria including Staphylococus, Streptococus, Pneumococcus and Escherichia coli (see table). The effect is stronger against Gram-positive than Gram-negative bacteria and against DNA than RNA viruses; it is suppressed by serum and by sulfur compounds such as hydrogen sulfide, mercaptoacetic acid, cystine and glutathione. The antibacterial, antifungal and antiviral effects from consuming radishes were recognized in traditional Chinese medicine. Given that Raphanin can be chiefly responsible for keeping the production of thyroxine and calcitonin in normal balance, in Russia, radishes have long been used for treating both types of thyroid problems. However, in the abstract to his 1947 paper, Ivanovics noted that because raphanin is highly toxic, it did not "hold the promise of a useful therapeutic agent".; Minimum inhibitory concentration of raphanin Bacteria MIC (mg/mL) Staphylococus 0.04 Shigella dysenteriae 0.125 Salmonella typhi 0.125 Escherichia coli 0.2

    Basic Info

    Chemical Name Sulforaphene
    Synonyms

    4-isothiocyanato-1-(methylsulfinyl)-1-buten;
    S-SULFORAPHENE;
    SULFORAPHENE,L;
    4-methylsulfinyl-3-butenyl isothiocyanate;
    RAPHANIN;
    L-SULFORAPHENE;
    L-SULPHORAPHENE;
    4-Methylsulfinyl-3-butenyl-isothiocyanat (Sulphoraphen);
    SULFORAPHANE,DL-(SH);
    sativin;

    CAS No. 592-95-0
    Molecular Formula C6H9NOS2
    Molecular Weight 175.27200
    PSA 80.73000
    LogP 2.23720

    Properties

    Appearance & Physical State Slightly yellowish liquid.
    Density 1.16 g/cm3
    Boiling Point 362.2ºC at 760 mmHg
    Flash Point 172.8ºC
    Refractive Index 1.566

    Synthesis Route

    4-isothiocyanato-1-(methylthio)-1-Butene→Sulforaphene
    glucoraphenin→Sulforaphene

    Toxicity

    Exposure Route Type of Test Species Observed Dose/Duration Toxic Effects
    Intravenous LD50 - Lethal dose, 50 percent kill Rodent - mouse 10 mg/kg 1.Details of toxic effects not reported other than lethal dose value

    Precursor

    4-isothiocyanato-1-(methylthio)-1-Butene
    glucoraphenin

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