Isosativenediol

Isosativenediol
Product Name Isosativenediol
CAS No.: 57079-92-2
Catalog No.: CFN89167
Molecular Formula: C15H24O2
Molecular Weight: 236.35 g/mol
Purity: >=98%
Type of Compound: Sesquiterpenoids
Physical Desc.: Powder
Source: The culture filtrates of a Bipolaris species pathogenic to Johnson grass.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
Isosativenediol is a natural product from the culture filtrates of a Bipolaris species pathogenic to Johnson grass.
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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

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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    Journal of Natural Products, 1988, 51(5):821-8.
    Toxins from Weed Pathogens, I. Phytotoxins from a Bipolaris Pathogen of Johnson Grass.[Reference: WebLink]

    METHODS AND RESULTS:
    Two strongly phytotoxic metabolites, prehelminthosporol [1] and dihydroprehelminthosporol [4], have been isolated from culture filtrates of a Bipolaris species pathogenic to Johnson grass. Prehelminthosporol [1] occurs naturally as a mixture of epimers. The isomers have been separated as the corresponding acetyl derivatives, and the stereochemistry at the hemiacetal carbon has been determined by nOe experiments.
    CONCLUSIONS:
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