1-(4-Hydroxyphenyl)propan-1-one
Paroxypropione(1-(4-Hydroxyphenyl)propan-1-one) is a manufactured, nonsteroidal estrogen which has been used medically as an antigonadotropin.
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.
Chem Pharm Bull (Tokyo).2017, 65(9):826-832
Phys Chem Chem Phys.2018, 20(23):15986-15994
Cell Prolif.2021, 54(8):e13083.
Research Square2022, rs.3.rs-1948239
J Pharmacopuncture.2023, 26(4):357-365.
J Korean Med Ophthalmol Otolaryngol Dermatol2023, 36(1):1-20.
Food Analytical Methods2020, 13,1603-1612(2020)
Molecules.2020, 25(15):3353.
LWT2020, 126:109313
South African Journal of Botany2024, 168:209-220.
Related and Featured Products
Modern Chinese Medicine, 2008,10(11):13-5.
Studies on the Chemical Constituents of Alpinia Calanga Willd.[Reference:
WebLink]
To study the chemical constituents of Alpinia galanga Willd.
METHODS AND RESULTS:
The chem- ical constituents were isolated by various column chromatographic methods,and the structures were elucidated on the basis of UV,IR,MS,~1H-NMR,~(13)C-NMR spectral analysis. Eleven compounds were isolated and their structures were elucidated as 4-[(E)-3-hydroxyprop-1-enyl]phenyl acetate(1),trans-p-hydroxylcinnamaldehyde acetate(2),5-hydroxy-7-(4″-hydroxy-3″-methoxyphenyl)-1-phenyl-3-heptanone(3),7-(4″-hydroxy-3″-me- thoxyphenyl)-1-phenylhep-4-en-3-one(4),[1′S]-1′-acetoxyeugenol acetate(5),trans-p-hydroxylcinnamalde- hyde(6),p-hydroxybenzaldehyde(7),1-(4-Hydroxyphenyl)propan-1-one(8),galangin(9),trans-p-coumaryl diacetate(10),β-sitosterol(11).
CONCLUSIONS:
Compound 1 was obtained from nature for the first time,com- pound 2 was obtained from this genus for the first time,and compounds 3 and 4 were obtained from this plant for the first time.
