P/N: 0001-01037

Advanchrom HIC-Butyl, 3μm, 4.6×50mm

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Advanchrom HIC-Butyl is a high-performance column designed for protein separation based on hydrophobic interaction chromatography (HIC). It is built on advanced wide-pore silica microspheres and employ a proprietary surface bonding technology, making it especially suitable for the separation and characterization of antibodies and antibody-drug conjugates (ADCs).

Pairs well with

Powerful HIC Columns for ADC Characterizartion

Welch Advanchrom HIC-Butyl Column is a high-performance hydrophobic interaction column (HIC), designed for antibody and ADC characterization.

ADC Structure Diagram

Features:

  • Unique chemical design offering excellent selectivity for ADC molecules.
  • Ultra-high purity large-pore silica microsphere matrix for superior
    column efficiency.
  • Low non-specific adsorption ensuring high recovery rates.
  • Excellent pressure tolerance and durability.
  • Outstanding batch-to-batch reproducibility.
  • Effective retention and separation using lower salt concentrations.

Product Information:

Product Name Advanchrom HIC-Butyl Column Column Material Stainless Steel
Bonded Phase Butyl Dimensions 4.6×50 mm; 4.6×35 mm
Matrix Ultra-high purity large-pore silica Max Pressure 6000 psi
Particle Size 3 μm Max Temperature 60°C
Pore Size 1000 Å pH Range 2 – 8

Applications:

DAR Analysis of Bispecific ADC

DAR Distribution of Bispecific ADCChromatographic Conditions of Bispecific ADC Analysis

Under ammonium sulfate conditions, ADC molecules with different DAR values show effective retention and separation on HIC columns.

Analysis of Monoclonal ADC & Intact Antibody (Rituximab)

Chromatograms of Monoclonal ADC and RituximabChromatographic Conditions of Monoclonal ADC and Rituximab Analysis

Although ammonium sulfate is widely used for DAR determination, it is non-volatile and incompatible with mass spectrometry (MS). A volatile ammonium acetate system was tested, achieving excellent retention and peak shape for both DAR2 ADC and rituximab, providing an MS-compatible solution for future DAR characterization.

Separation of Standard Proteins

Chromatogram of Standard ProteinsChromatographic Conditions of Standard Proteins Separation

Both Welch HIC columns provided excellent retention and separation of the three standard proteins, delivering superior peak shape and theoretical plates compared to competitor columns.

Mobile Phase Recommendation:

Due to the non-volatile nature of conventional ammonium sulfate mobile phase, it is incompatible with mass spectrometry and thus can only be used in HIC-UV systems. For HIC-MS applications, ammonium acetate should be used instead.

Brand: Advanchrom

Phase: Butyl

Particle Size: 3μm

Pore Size: 1000Å

USP Classification:

Separation Mode: HIC

pH Range: 2.0-8.0

Surface Area:

Carbon Load:

Max.Pressure: 6000psi

Endcapped:

Max.Temp.: 60°C

Particle Shape: Spherical

Product Description

Powerful HIC Columns for ADC Characterizartion

Welch Advanchrom HIC-Butyl Column is a high-performance hydrophobic interaction column (HIC), designed for antibody and ADC characterization.

ADC Structure Diagram

Features:

  • Unique chemical design offering excellent selectivity for ADC molecules.
  • Ultra-high purity large-pore silica microsphere matrix for superior
    column efficiency.
  • Low non-specific adsorption ensuring high recovery rates.
  • Excellent pressure tolerance and durability.
  • Outstanding batch-to-batch reproducibility.
  • Effective retention and separation using lower salt concentrations.

Product Information:

Product Name Advanchrom HIC-Butyl Column Column Material Stainless Steel
Bonded Phase Butyl Dimensions 4.6×50 mm; 4.6×35 mm
Matrix Ultra-high purity large-pore silica Max Pressure 6000 psi
Particle Size 3 μm Max Temperature 60°C
Pore Size 1000 Å pH Range 2 – 8

Applications:

DAR Analysis of Bispecific ADC

DAR Distribution of Bispecific ADCChromatographic Conditions of Bispecific ADC Analysis

Under ammonium sulfate conditions, ADC molecules with different DAR values show effective retention and separation on HIC columns.

Analysis of Monoclonal ADC & Intact Antibody (Rituximab)

Chromatograms of Monoclonal ADC and RituximabChromatographic Conditions of Monoclonal ADC and Rituximab Analysis

Although ammonium sulfate is widely used for DAR determination, it is non-volatile and incompatible with mass spectrometry (MS). A volatile ammonium acetate system was tested, achieving excellent retention and peak shape for both DAR2 ADC and rituximab, providing an MS-compatible solution for future DAR characterization.

Separation of Standard Proteins

Chromatogram of Standard ProteinsChromatographic Conditions of Standard Proteins Separation

Both Welch HIC columns provided excellent retention and separation of the three standard proteins, delivering superior peak shape and theoretical plates compared to competitor columns.

Mobile Phase Recommendation:

Due to the non-volatile nature of conventional ammonium sulfate mobile phase, it is incompatible with mass spectrometry and thus can only be used in HIC-UV systems. For HIC-MS applications, ammonium acetate should be used instead.

Specifications

Brand: Advanchrom

Phase: Butyl

Particle Size: 3μm

Pore Size: 1000Å

USP Classification:

Separation Mode: HIC

pH Range: 2.0-8.0

Surface Area:

Carbon Load:

Max.Pressure: 6000psi

Endcapped:

Max.Temp.: 60°C

Particle Shape: Spherical

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