4-Formyl-3-methoxyphenyloxymethyl polystyrene resin
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4-Formyl-3-methoxyphenyloxymethyl polystyrene resin

* Please kindly note that our products are not to be used for therapeutic purposes and cannot be sold to patients.

Resins for solid phase organic synthesis

Category
Other Resins
Catalog number
BAT-000233
Synonyms
2-Methoxy-4-alkoxybenzaldehyde polystyrene resin
Appearance
Brownish powder with lumps
DVB Crosslinking
1% DVB
Mesh Size
200-400 mesh
Substitution
0.8-1.2 meq/g
Storage
Store at 2-8°C
1. Dispelling myths and misconceptions about the treatment of acute hyperkalemia
Arnav A Gupta, Michael Self, Matthew Mueller, Gabriel Wardi, Christopher Tainter Am J Emerg Med. 2022 Feb;52:85-91. doi: 10.1016/j.ajem.2021.11.030. Epub 2021 Nov 27.
Hyperkalemia represents a widespread and potentially lethal condition that affects millions of people across their lives. Despite the prevalence and severity of the condition, there are no consensus guidelines on the treatment of hyperkalemia or even a standard definition. Herein, we provide a succinct review of what we believe to be the most significant misconceptions encountered in the emergency care of hyperkalemia, examine current available literature, and discuss practical points on several modalities of hyperkalemia treatment. Additionally, we review the pathophysiology of the electrocardiographic effects of hyperkalemia and how intravenous calcium preparations can antagonize these effects. We conclude each section with recommendations to aid emergency physicians in making safe and efficacious choices for the treatment of acute hyperkalemia.
2. Surface molecular imprinting on polystyrene resin for selective adsorption of 4-hydroxybenzoic acid
Yue Sun, Weisheng Zheng Chemosphere. 2021 Apr;269:128762. doi: 10.1016/j.chemosphere.2020.128762. Epub 2020 Oct 27.
Using chloromethylated polystyrene resin, N,N-diethylaminoethyl methacrylate, and ethylene glycol dimethacrylate as support, functional monomer and cross-linker, respectively, the molecularly imprinted resin (MIR) and non-imprinted resin (NIR) were fabricated by the combination of atom transfer radical polymerization and surface imprinting technique for the selective adsorption of 4-hydroxybenzoic acid (4-HB) from aqueous solutions. The prepared adsorbents were characterized by N2 adsorption/desorption isotherms, Fourier-transform infrared spectroscopy, and X-ray photoelectron spectroscopy. The adsorption processes of the 4-HB with MIR and NIR followed pseudo-second-order kinetics, and the adsorption isotherms were appreciably described by the Langmuir model. Furthermore, the adsorption efficiencies of MIR and NIR for different compounds in single and binary solutions proved that MIR exhibited high adsorption capacity and favorable selectivity toward 4-HB over other structurally related organic compounds (i.e., benzoic acid, 2-hydroxybenzoic acid, 3-hydroxybenzoic acid, phenol, and 2-hydroxynaphthalene). In addition, MIR could effectively remove 4-HB from a simulated effluent in a dynamic adsorption experiment. This study illustrates in-depth perspectives on the adsorption mechanisms of 4-HB onto MIR; interactions between the adsorbate and adsorbent were proposed based on the adsorption behaviours and instrumental analyses. The resulting MIR is a promising material for the interference-free adsorbent in the selective adsorption of 4-HB from mixed solutions.
3. Preparation of a novel chloromethylated polystyrene-2-mercapto-1,3,4-thiadiazole chelating resin and its adsorption properties and mechanism for separation and recovery of Hg(II) from aqueous solutions
Huihua Zhou, Jianjun Zheng, Hui Wang, Jianxin Wang, Xiaoguang Song, Yanmei Cao, Lei Fang, Yuping Feng, Chunhua Xiong Water Sci Technol. 2017 Oct;76(7-8):1915-1924. doi: 10.2166/wst.2017.292.
With an efficient methodology, a novel chloromethylated polystyrene-g-2-mercapto-1,3,4-thiadiazole chelating resin (MTR resin) was prepared via a one-step reaction. The structure of MTR resin was characterized by elements analysis, Fourier transform infrared spectroscopy, thermogravimetric analysis, and scanning electron microscopy. Meanwhile, the adsorption properties of the resin for Hg(II) were investigated by batch and column experiments. The results showed that the resin possessed much better adsorption capability for Hg(II) than for other metal ions. The statically and the dynamic saturated adsorption capacities were 343.8 mg/g and 475.1 mg/g. The adsorption kinetic and equilibrium data were well fitted to the second-order model and the Langmuir isotherm model, respectively. Desorption of mercury from the resin can be achieved using 30 mL of 2 mol/L HCl-5% thiourea solution with a desorption ratio of 92.3%. Compared with other absorbents, MTR resin was greatly conserve natural resources and reduce the cost.
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