Methyl isovanillate

Methyl isovanillate
Product Name Methyl isovanillate
CAS No.: 6702-50-7
Catalog No.: CFN92984
Molecular Formula: C9H10O4
Molecular Weight: 182.17 g/mol
Purity: >=98%
Type of Compound: Phenylpropanoids
Physical Desc.: Powder
Source: The herbs of Sarcandra glabra.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price: $30/20mg
Methyl isovanillate is a natural product from Vitex agnus-castus.
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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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    METHODS AND RESULTS:
    Nine secondary metabolites-artemetin (1), casticin (2), 3-hydroxy-5,6,7,4'-tetramethoxy flavone U(3), penduletin (4), p-hydroxybenzoic acid (5), methyl 3,4-dihydroxybenzoate (6), Methyl isovanillate (7), vanillic acid (8), and 3,4-dihydroxybenzoic acid (9)-were isolated from a folkloric medicinal plant, Vitex agnus-castus. The structures of compounds 1-9 were identified using spectroscopic techniques. Compound 7 was isolated for the first time from this plant. These compounds were screened for their antioxidant activity.
    CONCLUSIONS:
    Compounds 6 and 9 exhibited significant activity against the DPPH free radical.
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