Optimization of reactions between reducing sugars and 1-phenyl-3-methyl-5-pyrazolone (PMP) by response surface methodology☆
-
Add time:09/24/2019 Source:sciencedirect.com
Reducing sugars have strong reactivity with 1-phenyl-3-methyl-5-pyrazolone (PMP) to form the sugar-PMP derivatives, which can be more accurately analyzed by HPLC-UV at 248 nm. Glucose and glucosamine reacted with the PMP based on the response surface methodology within a range of temperature between 60 °C and 80 °C, and time between 60 and 180 min. The optimal conditions for the glucose-PMP and glucosamine-PMP reactions were obtained at 71 °C for 129 min, and 73 °C for 96 min, respectively. Subsequently, other sugars and their derivatives, including xylose, ribose, fructose, galactose, mannose, lactose, maltose, sucrose, glucuronic acid, sorbitol, mannitol, xylitol, and cyclodextrins were investigated and compared under the optimized condition for glucose. All of the above compounds, except the fructose, sugar alcohols and non-reducing sugars, could form the sugar-PMP derivatives. This study demonstrated that different chemical structures of sugars and their derivatives could significantly influence the rate and yield of the PMP derivatization.
We also recommend Trading Suppliers and Manufacturers of [methyl(phenyl)amino]acetonitrile (cas 16728-83-9). Pls Click Website Link as below: cas 16728-83-9 suppliers
Prev:Selectivity evaluation of phenyl based stationary phases for the analysis of amino acid diastereomers by liquid chromatography coupled with mass spectrometry
Next:Synthesis and spectral properties of Methyl-Phenyl pyrazoloquinoxaline fluorescence emitters: Experiment and DFT/TDDFT calculations) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Synthesis of α-aminophosphonate functionalized chitosan sorbents: Effect of methyl vs phenyl group on uranium sorption09/26/2019
- Synthesis and spectral properties of Methyl-Phenyl pyrazoloquinoxaline fluorescence emitters: Experiment and DFT/TDDFT calculations09/25/2019
- Selectivity evaluation of phenyl based stationary phases for the analysis of amino acid diastereomers by liquid chromatography coupled with mass spectrometry09/10/2019
- Data ArticleFacile one pot synthesis of 3-{[(1, 3-benzoxazol-2-yl) sulfanyl] (phenyl) methyl}-4‑hydroxy-2H-1-benzopyran-2-one derivatives and evaluation of their biological activities09/09/2019
- Chemical and electrochemical synthesis, structure and magnetic properties of mono- and binuclear 3d-metal complexes of N-[2-[(hydroxyalkylimino)methyl]phenyl]-4-methylbenzenesulfonamides09/08/2019
- A facile and efficient reaction of α,β-unsaturated ketones and 3-amino-1-phenyl-1H-pyrazol-5(4H)-one in aqueous and acetonitrile medium09/07/2019


