Isocostic acid

Isocostic acid
Product Name Isocostic acid
CAS No.: 69978-82-1
Catalog No.: CFN97186
Molecular Formula: C15H22O2
Molecular Weight: 234.3 g/mol
Purity: >=98%
Type of Compound: Sesquiterpenoids
Physical Desc.: Powder
Targets: Antifection
Source: The roots of Aucklandia lappa Decne.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
Isocostic acid may have antibacterial activity.
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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:
    The hydrodistilled essential oils of fresh aerial parts of I. viscosa (L.) Ait., collected at Ain El-Bey (Southern Constantine), was characterized by nerolidol (25.3%), Isocostic acid (10.1%), costic acid (8.0%), neo-intermedeol (6.4%) and caryophyllene oxide (5.5%), as major components. The essential oil of hydrodistilled fresh aerial parts of I. viscosa (L.) Ait., collected at Hamma-Bouziane (Northern Constantine), was mainly represented by Isocostic acid (25.1%), costic acid (15.2%), nerolidol (9.6%), linoleic acid (9.1%), neo-intermedeol (7.5%) and fokienol (7.2%). The present compositions are quite different from those reported for species growing over the world.
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    METHODS AND RESULTS:
    The acid-catalyzed rearrangement of epoxide 3a and 8a derived from sesquiterpernic Isocostic acid (1), the main component of Dittrichia viscosa, was studied using Lewis and Brönsted acids. Several new compounds were obtained with different selectivities depending on the catalyst used.
    CONCLUSIONS:
    These compounds were fully characterized by spectroscopic methods, and mechanistic explanations for their formation are proposed.
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