Cation Exchange

Hamilton Cation Exchange Columns

Hamilton’s cation exchange columns are engineered for high-performance separations of positively charged analytes using strong, predictable ion-exchange interactions. In cation exchange chromatography, the stationary phase carries a negatively charged surface that selectively retains cations. The greater the positive charge of the analyte, the stronger its interaction with the stationary phase—resulting in increased retention, enhanced resolution, and improved selectivity for ionic and ionizable compounds.

Elution is precisely controlled by the aqueous mobile phase, where adjustments in pH and ionic strength fine-tune analyte interaction with the resin. Increasing ionic strength or shifting pH disrupts electrostatic attractions, enabling analytes to elute in a predictable order. These flexible elution strategies make cation exchange chromatography highly effective across environmental, pharmaceutical, food and beverage, and research applications.

Because Hamilton uses robust polymeric stationary phases instead of silica, these columns tolerate aggressive mobile phases—including very high pH conditions (>11)—and withstand elevated temperatures far beyond the limits of silica-based materials. This durability allows rigorous cleaning, longer column lifetimes, and reliable performance under demanding analytical conditions.

Hamilton Cation Exchange Columns — Specifications

Packing Name Support / Chemistry Exchange Capacity Pore Size Analytes Applications
PRP-X200 PSDVB® sulfonate exchanger 35 µeq/g 100 Å Calcium, cesium, potassium, sodium Inorganic & organic cations (conductivity/UV); alkali & alkaline earth metals; separates mono/divalent cations (≈20 ppb–200 ppm) based on mobile phase.
PRP-X400 PSDVB® sulfonate exchanger 2.5 meq/g N/A Glyphosate, maltose, xylitol, mannitol Glyphosate & metabolite in drinking water; hydrophilic-interaction separations; inorganic/organic cations using conductivity or UV detection.
PRP-X800 PSDVB® itaconate exchanger 1.6 meq/g 100 Å Mono/divalent metals (Na, K, Ca); transition metals (Fe, Mn, Ni, Cu, Zn) Mono & divalent transition metals in the same run; resolved using ethylenediamine/tartaric acid mobile phase with conductivity detection.
HC-40 Ca2+ PSDVB® sulfonate exchanger, gel-type 5 meq/g Gel-type Ethanol, maltohexose, citric acid, glucose, fructose, arabinose, sorbitol, acetic acid Carbohydrates; sugar oligomers up to DP8; mono/disaccharides; organic acids; sugars; sugar alcohols.
HC-75 (H+, Ca2+, Pb2+) PSDVB® sulfonate exchanger, gel-type 5 meq/g Gel-type Carbohydrates, organic acids, sugar alcohols Carbohydrates; mono/disaccharides; sugars; organic acids; sugar alcohols (metal-form cation-exchange separations).

PSDVB = Poly(styrene-divinylbenzene)


Hamilton PRP-X200 & PRP-X400 Columns — Cation Exchange

Hamilton PRP-X200 cation exchange HPLC columns are engineered for rapid, high-resolution separation of alkali and alkaline earth metals. Alkali metals and ammonium are fully resolved in under five minutes, while alkaline earth cations separate in less than four minutes. Because mobile phase conditions are optimized separately for each cation group, interferences between alkali and alkaline earth metals are effectively eliminated.

Hamilton PRP-X400 columns are optimized for fast and reliable separation of glyphosate and its metabolites. With a higher exchange capacity than PRP-X200, PRP-X400 provides improved selectivity for glyphosate and performs well in related hydrophilic separations such as inositol and sugar alcohols. These columns operate efficiently at room temperature, do not require column heating, and do not require methanol in the mobile phase—offering a cost-effective alternative to many glyphosate-specific columns.

Size (mm) PRP-X400 · 7 µm PRP-X200 · 10 µm
4.6 × 250 PEEK 79387 79357
4.6 × 150 PEEK 79384
4.1 × 250 SS 79473 79442
4.1 × 150 SS 79717 79441
4.1 × 100 SS 79363
2.1 × 250 SS 79398
2.1 × 150 SS 79398 79394
Guard Columns & Accessories
Analytical Starter Kit SS 79224 79456
Analytical Repl Cartridges SS (5/pk) 79225 79449
Analytical Starter Kit PEEK 79376 79368
Analytical Repl Cartridges PEEK (5/pk) 79377 79369
Analytical Guard Column 79290 79288
Analytical Guard Cartridge Holder SS 32908 32908
Prep/Semiprep Guard Column 79916 79914
Prep/Semiprep Guard Cartridge Holder SS 5095-01 5095-01
Prep/Semiprep Starter Kit SS 79131

Hamilton PRP-X800 Columns — Cation Exchange

Hamilton PRP-X800 is a polymeric cation exchange HPLC column functionalized with itaconic acid, designed for efficient isocratic separation of mono- and divalent cations. Typical targets include lithium, sodium, ammonium, potassium, magnesium, and calcium, with excellent resolution and reproducibility.

The PRP-X800 column offers outstanding durability and is stable in any concentration of organic solvent, allowing flexible mobile phase design and dynamic control of exchange capacity. Detection is typically performed using conductivity or indirect UV, depending on mobile phase composition, making PRP-X800 well suited for routine and advanced inorganic cation analysis.

Size (mm) PRP-X800 · 7 µm
4.1 × 250 SS 79828
4.1 × 150 SS 79855
Guard Columns & Accessories
Analytical Guard Column 79294
Analytical Guard Cartridge Holder SS 32908
Analytical Guard Cartridge Holder PEEK 79477
Analytical Repl Cartridges SS (5/pk) 79832
Analytical Repl Cartridges PEEK (5/pk) 79833
Analytical Starter Kit SS 79830
Analytical Starter Kit PEEK 79831

Hamilton HC-40 Ca2+ and HC-75 (H+, Ca2+, Pb2+) Columns — Cation Exchange

Hamilton HC-40 columns separate compounds primarily through size exclusion. The 4% cross-linked HC-40 resin allows larger carbohydrate oligomers to elute first, followed by smaller di- and monosaccharides, making it well suited for carbohydrate profiling applications.

Hamilton HC-75 columns use ligand exchange as the primary separation mechanism. The 8% cross-linked HC-75 resin is available in multiple ionic forms (H+, Ca2+, Pb2+), each offering unique selectivity based on analyte electronegativity toward the counterion. As with HC-40, larger carbohydrate oligomers elute first, followed by smaller saccharides.

These columns are widely used for carbohydrate, sugar alcohol, and organic acid analysis in food, beverage, and fermentation workflows, where robust selectivity and reproducible retention are critical.

Size (mm) HC-40 Ca2+
10–15 µm
HC-75 Ca2+
9 µm
HC-75 H+
9 µm
HC-75 Pb2+
9 µm
7.8 × 305 SS 79432 79436 79438
7.8 × 100 SS 79547 79240
4.1 × 250 SS 79431 79476
Prep / Semiprep Guard Columns & Accessories
Prep/Semiprep Guard Column 79919 79917
Prep/Semiprep Guard Cartridge Holder SS 5095-01 5095-01
Prep/Semiprep Repl Cartridges SS (2/pk) 79865 79134
Prep/Semiprep Starter Kit SS 79866 79133

Key Definitions
Cation Exchange Chromatography
A chromatographic method using a negatively charged stationary phase to retain positively charged analytes. Stronger cationic charge results in stronger interactions and longer retention times.
Ionic Strength
A measure of the total ion concentration in the mobile phase. Higher ionic strength reduces electrostatic attraction between analytes and the stationary phase, promoting earlier elution.
pH Control
Adjusting the mobile phase pH affects analyte charge state and binding strength. Higher pH can weaken cation retention, enabling selective elution and improved resolution.
Polymeric Stationary Phase
A chemically durable support material resistant to extreme pH and elevated temperatures. Polymeric phases outperform silica under harsh IC conditions and offer extended column lifetimes.
High-pH Compatibility
The ability of a column to withstand mobile phases with pH values above 11. Polymeric supports excel in high-pH applications where silica columns degrade rapidly.
Frequently Asked Questions

What makes Hamilton cation exchange columns suitable for positively charged analytes?

These columns feature a negatively charged polymeric stationary phase that strongly retains positively charged molecules through electrostatic attraction. Greater positive charge results in higher retention, enabling precise and predictable separations.

How are compounds eluted in cation exchange chromatography?

Elution is controlled using aqueous buffers where pH and ionic strength determine analyte retention. Increasing ionic strength or adjusting pH weakens the electrostatic interactions, allowing compounds to elute in a predictable sequence.

Why are polymeric stationary phases beneficial for high-pH and high-temperature applications?

Polymeric materials are chemically resistant and maintain structural integrity under extreme pH conditions (>11) and elevated temperatures—conditions that quickly degrade silica-based columns. This results in longer lifetimes and greater method flexibility.