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Na ion exchange resin, strongly acidic, 20-50 mesh

CAS Number:
MDL number:

Quality Level




~45% loss on drying, 110°C

particle size

20-50 mesh


AMBERLITE® HPR1100 is a cation-exchange resin and can be used:
  • For grafting polyethylene glycols for catalyzing regioselective azidolysis of epoxides.
  • For the immobilization of β-cyclodextrin to be used as a phase transfer catalyst for the reduction of epoxides to alcohols.
  • As an adsorbent for the removal of arsenic and copper from aqueous solutions.


250 g in poly bottle
1 kg in poly bottle

Legal Information

Amberlite is a registered trademark of The Dow Chemical Company or an affiliated company of Dow


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Hazard Statements

Precautionary Statements

Hazard Classifications

Eye Irrit. 2

Storage Class Code

11 - Combustible Solids



Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificate of Analysis

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Certificate of Origin

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Wei Zhang et al.
Chemosphere, 227, 247-255 (2019-04-17)
Previous studies have demonstrated that anaerobic digestion (AD) enhances sludge dewaterability. However, the mechanism of AD influence on digested sludge dewaterability is still not well understood. In this study, moisture distribution and bond energy were used to evaluate the influence
Poly (ethylene glycol) grafted onto dowex resin: an efficient, recyclable, and mild polymer-supported phase transfer catalyst for the regioselective azidolysis of epoxides in water.
Kiasat AR, et al.
The Journal of Organic Chemistry, 73(21), 8382-8385 (2008)
Arsenite and arsenate sorption by hydrous ferric oxide/polymeric material.
Habuda-Stanic M, et al.
Desalination, 229(1-3), 1-9 (2008)
Removal of copper from aqueous solution by ion exchange resins.
Veli S and Pekey B
Fresenius Environmental Bulletin, 13(3), 244-250 (2004)
Han-Quan Wen et al.
Environment international, 139, 105683-105683 (2020-04-04)
Photo-fermentative hydrogen production, the new energy production alternative, was greatly enhanced by formed biofilm. To understand the mechanism of enhancement, the intracellular proteome and extracellular polymeric substance (EPS)i during biofilm formation were investigated in this work. Experimental results indicated that

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