Perillen

Perillen
Product Name Perillen
CAS No.: 539-52-6
Catalog No.: CFN90862
Molecular Formula: C10H14O
Molecular Weight: 150.2 g/mol
Purity: >=98%
Type of Compound: Alkaloids
Physical Desc.: Oil
Source: The herbs of Perilla frutescens.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price: $168/20mg
Perillen is a nartural product from Perilla frutescens.
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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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    Insect Biochemistry, 1980 , 10 (1) :107-12.
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    Chemical analysis of the mandibular gland secretion of seven ant species in the tribe Tetramoriini showed that 3-octanone was the major component in Tetramorium sericeiventre (70%), T. caespitum (71%) and T. guineense (87%), and 3-octanol in Decamorium uelense (96%). 2-Undecanol, was the major component in T. termitobium (80%), but in two members of the subgenus Xiphomyrmex, T. angulinode and an unidentified species (D), the sesquiterpene furan, Perillen, was predominant (91% and 98% respectively). Ants in this subgenus also contained 2-nonanol, 2-undecanol and 2-undecanone in their mandibular glands.
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