trans-Stilbene
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.
Evid Based Complement Alternat Med.2020, 2020:2584783.
Molecules.2019, 24(16):E3003
Front Nutr.2021, 8: 687851.
Chemistry of Natural Compounds2019, 55(1):127-130
Int J Mol Sci.2017, 18(5)
Biotechnol Bioeng.2020, 117(7):2198-2208.
Sci Rep.2019, 9(1):18080
The Journal of Internal Korean Medicine2015, 36(4):486-497
Antioxidants (Basel).2023, 12(7):1324.
Front Endocrinol (Lausanne).2020, 11:568436.
Related and Featured Products
Macromolecular Chemistry & Physics, 1995, 196(6):1999-2009.
Complex‐radical alternating terpolymerization of maleic anhydride, trans-stilbene and N-phenylmaleimide.[Reference:
WebLink]
METHODS AND RESULTS:
Radical terpolymerizations of maleci anhydride (MA), trans-Stilbene (Stb) and N-phenylmale-imide (PhMI) were carried out in methyl ethyl ketone (MEK) at 60-80 C in the presence of 2,2'-azoisobutyronitrile (AIBN) as initiator. The terpolymerization was evaluated by using either the free monomer or complex participation models. The relative of MA toward poly(Stb) radical was found to be about 10,6 times lower than that of PhMl. The initial rate of copolymerization, the participation of the charge transfer complex (CTC) monomers and free monomers was quantitatively estimated. It was established that, even with a considerable change in the ratio of electron-acceptor monomers (MA and PhMI) in the initial reaction mixture, terpolymers possessed always a composition ratio close to 1:2:1. Constants for copolymerization of MA-Stb (M1) and PhMI-Stb (M3) were determined by using the Kelen-Tudos equation, and r1 . K1/K3 = 0,03 and r2 . K3/1 =0,08, where K1 and K3 are complex-formation constants of MA-Stb and PhMl-Stb complexes, respectively, were obtained.
CONCLUSIONS:
The result of kinetic studies of terpolymerization was interpreted as involving mainly alternating copolymerization of two complexomers with predominant participation in chain growth. Thermogravimetric analyses indicated the high thermal stabilities of terpolymers obtained.
Journal of Photochemistry & Photobiology A Chemistry, 1995, 85(3):225-229.
Solid state photoaddition reactions in polycrystalline mixtures of NH heteroaromatic compounds and trans-stilbene.[Reference:
WebLink]
METHODS AND RESULTS:
Photoaddition reactions of indole ( 1a ), carbazole ( 1b ) and phenothiazine ( 1c ) to trans -stilbene ( 2 ) occurred in the mixed crystal state to give the corresponding adducts 3a , 3b and 3c with an N C bond. Photoadduct 4a with a C C bond was also obtained by the solid state photoreaction of 1a with 2 . The mixed crystals prepared by the melting and resolidifying method were simple polycrystalline mixtures of the two components, and the photoreactions proceeded at the interface of the two crystallites.
CONCLUSIONS:
The selectivity of the photoaddition reaction was higher in the solid state than in solution.
