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Our Carbohydrate Analysis HPLC Columns are designed for the high-resolution separation of sugars, organic acids, peptides, and nucleic acids. Utilizing a core-shell technology, these columns are packed with spherical polystyrene/divinylbenzene (PS/DVB) particles. The stationary phase undergoes a specialized dual-modification process: surface sulfonation followed by chelation with specific metal ions. This design leverages ligand exchange and ion exclusion mechanisms to deliver exceptional select

AY-Ca-NP HPLC Column for Carbohydrates & Organic Acids

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Product Detail

Key Features:

1. Advanced Dual-Modification Technology

Sulfonic Acid Modification: The PS/DVB surface is first modified with sulfonic acid groups (-SO3H), creating a stable hydrophilic layer.
Metal Ion Chelation: The phase is further chelated with Calcium (Ca²⁺), Lead (Pb²⁺), Sodium (Na⁺), or Potassium (K⁺). This allows users to select the optimal column based on specific separation requirements for different sugar types (e.g., mono- vs. disaccharides).
2. Superior Matrix Structure

Low Cross-Linking PS/DVB: The support material features a low cross-linking degree (5%, 8%, and 10%), optimized for the separation of small organic molecules.
Spherical Geometry: The uniform spherical particle shape ensures excellent packing density and column bed stability.
3. High Separation Efficiency

Tight Particle Distribution: Available in 5 µm and 10 µm particle sizes with uniform distribution, minimizing eddy diffusion and maximizing theoretical plate numbers for sharp peak shapes.


Technical Specifications:

ItemSpecification
Matrix MaterialSpherical Polystyrene/Divinylbenzene (PS/DVB)
Surface ChemistrySulfonic Acid (-SO3H) + Metal Ion Chelation
Available Ion FormsCa-NP, Pb-NP, Na-NP, K-NP
Cross-Linking Degree5%, 8%, 10%
Particle Sizes5 µm, 10 µm
Separation ModeLigand Exchange / Ion Exclusion
Target AnalytesCarbohydrates, Organic Acids, Peptides, Nucleic Acids

Application:

  • Food & Beverage Industry: Analysis of sugar content (glucose, fructose, sucrose) in juices, wine, honey, and dairy products.
  • Biochemical Research: Separation of oligosaccharides and peptides.
  • Pharmaceuticals: Purity analysis of organic acids and nucleic acid components.

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Product Detail
Key Features:

1. Advanced Dual-Modification Technology

Sulfonic Acid Modification: The PS/DVB surface is first modified with sulfonic acid groups (-SO3H), creating a stable hydrophilic layer.
Metal Ion Chelation: The phase is further chelated with Calcium (Ca²⁺), Lead (Pb²⁺), Sodium (Na⁺), or Potassium (K⁺). This allows users to select the optimal column based on specific separation requirements for different sugar types (e.g., mono- vs. disaccharides).
2. Superior Matrix Structure

Low Cross-Linking PS/DVB: The support material features a low cross-linking degree (5%, 8%, and 10%), optimized for the separation of small organic molecules.
Spherical Geometry: The uniform spherical particle shape ensures excellent packing density and column bed stability.
3. High Separation Efficiency

Tight Particle Distribution: Available in 5 µm and 10 µm particle sizes with uniform distribution, minimizing eddy diffusion and maximizing theoretical plate numbers for sharp peak shapes.


Technical Specifications:

ItemSpecification
Matrix MaterialSpherical Polystyrene/Divinylbenzene (PS/DVB)
Surface ChemistrySulfonic Acid (-SO3H) + Metal Ion Chelation
Available Ion FormsCa-NP, Pb-NP, Na-NP, K-NP
Cross-Linking Degree5%, 8%, 10%
Particle Sizes5 µm, 10 µm
Separation ModeLigand Exchange / Ion Exclusion
Target AnalytesCarbohydrates, Organic Acids, Peptides, Nucleic Acids

Application:

  • Food & Beverage Industry: Analysis of sugar content (glucose, fructose, sucrose) in juices, wine, honey, and dairy products.
  • Biochemical Research: Separation of oligosaccharides and peptides.
  • Pharmaceuticals: Purity analysis of organic acids and nucleic acid components.
AY-Ca-NP HPLC Column for Carbohydrates & Organic Acids
Our Carbohydrate Analysis HPLC Columns are designed for the high-resolution separation of sugars, organic acids, peptides, and nucleic acids. Utilizing a core-shell technology, these columns are packed with spherical polystyrene/divinylbenzene (PS/DVB) particles. The stationary phase undergoes a specialized dual-modification process: surface sulfonation followed by chelation with specific metal ions. This design leverages ligand exchange and ion exclusion mechanisms to deliver exceptional select
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