Beta-Rotunol
Standard reference
Inquire / Order:
manager@chemfaces.com
Technical Inquiries:
service@chemfaces.com
Tel:
+86-27-84237783
Fax:
+86-27-84254680
Address:
1 Building, No. 83, CheCheng Rd., Wuhan Economic and Technological Development Zone, Wuhan, Hubei 430056, PRC
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.
Pharmacognosy Magazine2018, 14(56):418-424
Plant Physiol.2024, 194(4):2580-2599.
J. Soc. Cosmet. Sci. Korea2016, 163-171
Food Hydrocolloids2024, 152:109898
Exp Biol Med (Maywood).2019, 244(16):1463-1474
Int J Mol Sci.2022, 23(24):16000.
J. Traditional Thai Medical Res. 2022,8(1):1-14.
Biomed Chromatogr.2020, e5021.
Front Pharmacol.2021, 12:770667.
Toxicol In Vitro.2023, 86:105521.
Related and Featured Products
Tetrahedron,1971, 27(19):4831-6.
Structure and absolute configuration of α-rotunol and β-rotunol, sesquiterpenoids of Cyperus rotundus.[Reference:
WebLink]
METHODS AND RESULTS:
Two novel sesquiterpenic keto-alcohols, α-rotunol and β-rotunol(Beta-Rotunol), have been isolated from nutgrass, Cyperus rotundus ;Cyperaceae). The stereostructure II of β-rotunol is based on spectral properties and by transformation to the dienone (V) which has also been derived from hinesol (VI). α-Rotunol has been given the stereostructure I based on its physico-chemical properties.
