Asarylaldehyde
Reference standards.
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.
Int J Mol Sci.2023, 24(3):2102.
J. Traditional Thai Medical Res. 2022,8(1):1-14.
Viruses2023, 15(6), 1377
Int J Mol Sci.2020, 21(19):7209.
Research Square2024, 4805471.
Phytochem Anal.2022, doi: 10.1002
Food Chem.2021, 337:128023.
J Nat Prod.2018, 81(4):966-975
Front Pharmacol.2022, 13:870553.
Molecules.2019, 24(24):E4536
Related and Featured Products
Zhongguo Zhong Yao Za Zhi. 2013 Feb;38(4):569-73.
Chemical constituents from rhizomes of Acorus tatarinowii[Pubmed:
23713285]
METHODS AND RESULTS:
Fifteen compounds were isolated from the rhizomes of Acorus tatarinowii by means of various chromatographic techniques such as silica gel, ODS, Sephadex LH-20 and preparative HPLC, and their structures were elucidated as tatanone A (1), calamusenone (2), acoronene (3), 2-acetyloxyacoronene (4), acorenone (5), alpha-asarone (6), beta-asarone (7), 1,2-dimethoxy-4-(1'Z-propenyl) benzene (8), methyleugenol (9), Asarylaldehyde (10), acoramone (11), gamma-asarone (12), 5-hydroxymethyl-2-furaldehyde (13), galgravin (14) and eudesmin (15) on the basis of spectroscopic data analysis.
CONCLUSIONS:
Compound 1 was a new compound, and compounds 3-5 were separated from Acorus species for the first time.
