UHPLC and HPLC Columns



Product Listing

  • Product Part
    Description:

    Shim-pack Scepter Claris features a column body with a newly-developed bioinert coating packed with Scepter series stationary phases. Bioinert coating is applied to the column body and stainless steel frit Ideal for analysis of metal-coordinating and hydrophobically adsorbing compounds such as nucleic acids, proteins, and lipids Outstanding pH and lifetime stability due to Scepter organic silica hybrid packing   Superior Sensitivity and Separation Performance in Nucleic Acid Analysis Shim-pack Scepter Claris C18-120 with the bioinert coating and Scepter C18-120 with traditional stainless steel hardware were compared in this example of an analysis of a synthetic oligonucleotide. Results from Claris were highly sensitive and reproducible from the rst injection, with no loss of sample signal. Scepter C18-120 in a stainless steel column body produced low-sensitivity results and showed adsorption from the first sample injection. Outstanding Performance in Oligonucleic Acid Analysis Shim-pack Scepter Claris C18-120 (bioinert coating) and Scepter C18-20 (stainless steel body) were compared in this analysis of Oligodeoxythymidylic acid [d(T)20]. Results from Scepter C18-120 show low peak intensity, suggesting adsorption on metal surfaces. In contrast, Scepter Claris C18-120 produced a sharper and high-intensity peak. Improved Sensitivity and Separation of Phospholipids Shim-pack Scepter Claris C18-120 minimizes metal-mediated adsorption and hydrophobic absorption on the column surfaces, resulting in high-resolution separations. In this example of structurally complex phosphatidylcholine isomers, Scepter Claris C18-120 achieved increased baseline resolution between isomers with higher sensitivity.  

    OUT OF STOCK

    Shim-pack Scepter Claris features a column body with a newly-developed bioinert coating packed with Scepter series stationary phases. Bioinert coating is applied to the column body and stainless steel frit Ideal for analysis of metal-coordinating and hydrophobically adsorbing compounds such as nucleic acids, proteins, and lipids Outstanding pH and lifetime stability due to Scepter organic silica hybrid packing   Superior Sensitivity and Separation Performance in Nucleic Acid Analysis Shim-pack Scepter Claris C18-120 with the bioinert coating and Scepter C18-120 with traditional stainless steel hardware were compared in this example of an analysis of a synthetic oligonucleotide. Results from Claris were highly sensitive and reproducible from the rst injection, with no loss of sample signal. Scepter C18-120 in a stainless steel column body produced low-sensitivity results and showed adsorption from the first sample injection. Outstanding Performance in Oligonucleic Acid Analysis Shim-pack Scepter Claris C18-120 (bioinert coating) and Scepter C18-20 (stainless steel body) were compared in this analysis of Oligodeoxythymidylic acid [d(T)20]. Results from Scepter C18-120 show low peak intensity, suggesting adsorption on metal surfaces. In contrast, Scepter Claris C18-120 produced a sharper and high-intensity peak. Improved Sensitivity and Separation of Phospholipids Shim-pack Scepter Claris C18-120 minimizes metal-mediated adsorption and hydrophobic absorption on the column surfaces, resulting in high-resolution separations. In this example of structurally complex phosphatidylcholine isomers, Scepter Claris C18-120 achieved increased baseline resolution between isomers with higher sensitivity.  

  • Product Part
    Description:

    Shim-pack Scepter Claris features a column body with a newly-developed bioinert coating packed with Scepter series stationary phases. Bioinert coating is applied to the column body and stainless steel frit Ideal for analysis of metal-coordinating and hydrophobically adsorbing compounds such as nucleic acids, proteins, and lipids Outstanding pH and lifetime stability due to Scepter organic silica hybrid packing   Superior Sensitivity and Separation Performance in Nucleic Acid Analysis Shim-pack Scepter Claris C18-120 with the bioinert coating and Scepter C18-120 with traditional stainless steel hardware were compared in this example of an analysis of a synthetic oligonucleotide. Results from Claris were highly sensitive and reproducible from the rst injection, with no loss of sample signal. Scepter C18-120 in a stainless steel column body produced low-sensitivity results and showed adsorption from the first sample injection. Outstanding Performance in Oligonucleic Acid Analysis Shim-pack Scepter Claris C18-120 (bioinert coating) and Scepter C18-20 (stainless steel body) were compared in this analysis of Oligodeoxythymidylic acid [d(T)20]. Results from Scepter C18-120 show low peak intensity, suggesting adsorption on metal surfaces. In contrast, Scepter Claris C18-120 produced a sharper and high-intensity peak. Improved Sensitivity and Separation of Phospholipids Shim-pack Scepter Claris C18-120 minimizes metal-mediated adsorption and hydrophobic absorption on the column surfaces, resulting in high-resolution separations. In this example of structurally complex phosphatidylcholine isomers, Scepter Claris C18-120 achieved increased baseline resolution between isomers with higher sensitivity.  

    OUT OF STOCK

    Shim-pack Scepter Claris features a column body with a newly-developed bioinert coating packed with Scepter series stationary phases. Bioinert coating is applied to the column body and stainless steel frit Ideal for analysis of metal-coordinating and hydrophobically adsorbing compounds such as nucleic acids, proteins, and lipids Outstanding pH and lifetime stability due to Scepter organic silica hybrid packing   Superior Sensitivity and Separation Performance in Nucleic Acid Analysis Shim-pack Scepter Claris C18-120 with the bioinert coating and Scepter C18-120 with traditional stainless steel hardware were compared in this example of an analysis of a synthetic oligonucleotide. Results from Claris were highly sensitive and reproducible from the rst injection, with no loss of sample signal. Scepter C18-120 in a stainless steel column body produced low-sensitivity results and showed adsorption from the first sample injection. Outstanding Performance in Oligonucleic Acid Analysis Shim-pack Scepter Claris C18-120 (bioinert coating) and Scepter C18-20 (stainless steel body) were compared in this analysis of Oligodeoxythymidylic acid [d(T)20]. Results from Scepter C18-120 show low peak intensity, suggesting adsorption on metal surfaces. In contrast, Scepter Claris C18-120 produced a sharper and high-intensity peak. Improved Sensitivity and Separation of Phospholipids Shim-pack Scepter Claris C18-120 minimizes metal-mediated adsorption and hydrophobic absorption on the column surfaces, resulting in high-resolution separations. In this example of structurally complex phosphatidylcholine isomers, Scepter Claris C18-120 achieved increased baseline resolution between isomers with higher sensitivity.  

  • Product Part
    Description:

    Shim-pack Scepter Claris features a column body with a newly-developed bioinert coating packed with Scepter series stationary phases. Bioinert coating is applied to the column body and stainless steel frit Ideal for analysis of metal-coordinating and hydrophobically adsorbing compounds such as nucleic acids, proteins, and lipids Outstanding pH and lifetime stability due to Scepter organic silica hybrid packing   Superior Sensitivity and Separation Performance in Nucleic Acid Analysis Shim-pack Scepter Claris C18-120 with the bioinert coating and Scepter C18-120 with traditional stainless steel hardware were compared in this example of an analysis of a synthetic oligonucleotide. Results from Claris were highly sensitive and reproducible from the rst injection, with no loss of sample signal. Scepter C18-120 in a stainless steel column body produced low-sensitivity results and showed adsorption from the first sample injection. Outstanding Performance in Oligonucleic Acid Analysis Shim-pack Scepter Claris C18-120 (bioinert coating) and Scepter C18-20 (stainless steel body) were compared in this analysis of Oligodeoxythymidylic acid [d(T)20]. Results from Scepter C18-120 show low peak intensity, suggesting adsorption on metal surfaces. In contrast, Scepter Claris C18-120 produced a sharper and high-intensity peak. Improved Sensitivity and Separation of Phospholipids Shim-pack Scepter Claris C18-120 minimizes metal-mediated adsorption and hydrophobic absorption on the column surfaces, resulting in high-resolution separations. In this example of structurally complex phosphatidylcholine isomers, Scepter Claris C18-120 achieved increased baseline resolution between isomers with higher sensitivity.  

    OUT OF STOCK

    Shim-pack Scepter Claris features a column body with a newly-developed bioinert coating packed with Scepter series stationary phases. Bioinert coating is applied to the column body and stainless steel frit Ideal for analysis of metal-coordinating and hydrophobically adsorbing compounds such as nucleic acids, proteins, and lipids Outstanding pH and lifetime stability due to Scepter organic silica hybrid packing   Superior Sensitivity and Separation Performance in Nucleic Acid Analysis Shim-pack Scepter Claris C18-120 with the bioinert coating and Scepter C18-120 with traditional stainless steel hardware were compared in this example of an analysis of a synthetic oligonucleotide. Results from Claris were highly sensitive and reproducible from the rst injection, with no loss of sample signal. Scepter C18-120 in a stainless steel column body produced low-sensitivity results and showed adsorption from the first sample injection. Outstanding Performance in Oligonucleic Acid Analysis Shim-pack Scepter Claris C18-120 (bioinert coating) and Scepter C18-20 (stainless steel body) were compared in this analysis of Oligodeoxythymidylic acid [d(T)20]. Results from Scepter C18-120 show low peak intensity, suggesting adsorption on metal surfaces. In contrast, Scepter Claris C18-120 produced a sharper and high-intensity peak. Improved Sensitivity and Separation of Phospholipids Shim-pack Scepter Claris C18-120 minimizes metal-mediated adsorption and hydrophobic absorption on the column surfaces, resulting in high-resolution separations. In this example of structurally complex phosphatidylcholine isomers, Scepter Claris C18-120 achieved increased baseline resolution between isomers with higher sensitivity.  

  • Product Part
    Description:

    Shim-pack Scepter Claris features a column body with a newly-developed bioinert coating packed with Scepter series stationary phases. Bioinert coating is applied to the column body and stainless steel frit Ideal for analysis of metal-coordinating and hydrophobically adsorbing compounds such as nucleic acids, proteins, and lipids Outstanding pH and lifetime stability due to Scepter organic silica hybrid packing   Superior Sensitivity and Separation Performance in Nucleic Acid Analysis Shim-pack Scepter Claris C18-120 with the bioinert coating and Scepter C18-120 with traditional stainless steel hardware were compared in this example of an analysis of a synthetic oligonucleotide. Results from Claris were highly sensitive and reproducible from the rst injection, with no loss of sample signal. Scepter C18-120 in a stainless steel column body produced low-sensitivity results and showed adsorption from the first sample injection. Outstanding Performance in Oligonucleic Acid Analysis Shim-pack Scepter Claris C18-120 (bioinert coating) and Scepter C18-20 (stainless steel body) were compared in this analysis of Oligodeoxythymidylic acid [d(T)20]. Results from Scepter C18-120 show low peak intensity, suggesting adsorption on metal surfaces. In contrast, Scepter Claris C18-120 produced a sharper and high-intensity peak. Improved Sensitivity and Separation of Phospholipids Shim-pack Scepter Claris C18-120 minimizes metal-mediated adsorption and hydrophobic absorption on the column surfaces, resulting in high-resolution separations. In this example of structurally complex phosphatidylcholine isomers, Scepter Claris C18-120 achieved increased baseline resolution between isomers with higher sensitivity.

    OUT OF STOCK

    Shim-pack Scepter Claris features a column body with a newly-developed bioinert coating packed with Scepter series stationary phases. Bioinert coating is applied to the column body and stainless steel frit Ideal for analysis of metal-coordinating and hydrophobically adsorbing compounds such as nucleic acids, proteins, and lipids Outstanding pH and lifetime stability due to Scepter organic silica hybrid packing   Superior Sensitivity and Separation Performance in Nucleic Acid Analysis Shim-pack Scepter Claris C18-120 with the bioinert coating and Scepter C18-120 with traditional stainless steel hardware were compared in this example of an analysis of a synthetic oligonucleotide. Results from Claris were highly sensitive and reproducible from the rst injection, with no loss of sample signal. Scepter C18-120 in a stainless steel column body produced low-sensitivity results and showed adsorption from the first sample injection. Outstanding Performance in Oligonucleic Acid Analysis Shim-pack Scepter Claris C18-120 (bioinert coating) and Scepter C18-20 (stainless steel body) were compared in this analysis of Oligodeoxythymidylic acid [d(T)20]. Results from Scepter C18-120 show low peak intensity, suggesting adsorption on metal surfaces. In contrast, Scepter Claris C18-120 produced a sharper and high-intensity peak. Improved Sensitivity and Separation of Phospholipids Shim-pack Scepter Claris C18-120 minimizes metal-mediated adsorption and hydrophobic absorption on the column surfaces, resulting in high-resolution separations. In this example of structurally complex phosphatidylcholine isomers, Scepter Claris C18-120 achieved increased baseline resolution between isomers with higher sensitivity.

  • Product Part
    Description:

    Shim-pack Scepter Claris features a column body with a newly-developed bioinert coating packed with Scepter series stationary phases. Bioinert coating is applied to the column body and stainless steel frit Ideal for analysis of metal-coordinating and hydrophobically adsorbing compounds such as nucleic acids, proteins, and lipids Outstanding pH and lifetime stability due to Scepter organic silica hybrid packing   Superior Sensitivity and Separation Performance in Nucleic Acid Analysis Shim-pack Scepter Claris C18-120 with the bioinert coating and Scepter C18-120 with traditional stainless steel hardware were compared in this example of an analysis of a synthetic oligonucleotide. Results from Claris were highly sensitive and reproducible from the rst injection, with no loss of sample signal. Scepter C18-120 in a stainless steel column body produced low-sensitivity results and showed adsorption from the first sample injection. Outstanding Performance in Oligonucleic Acid Analysis Shim-pack Scepter Claris C18-120 (bioinert coating) and Scepter C18-20 (stainless steel body) were compared in this analysis of Oligodeoxythymidylic acid [d(T)20]. Results from Scepter C18-120 show low peak intensity, suggesting adsorption on metal surfaces. In contrast, Scepter Claris C18-120 produced a sharper and high-intensity peak. Improved Sensitivity and Separation of Phospholipids Shim-pack Scepter Claris C18-120 minimizes metal-mediated adsorption and hydrophobic absorption on the column surfaces, resulting in high-resolution separations. In this example of structurally complex phosphatidylcholine isomers, Scepter Claris C18-120 achieved increased baseline resolution between isomers with higher sensitivity.  

    OUT OF STOCK

    Shim-pack Scepter Claris features a column body with a newly-developed bioinert coating packed with Scepter series stationary phases. Bioinert coating is applied to the column body and stainless steel frit Ideal for analysis of metal-coordinating and hydrophobically adsorbing compounds such as nucleic acids, proteins, and lipids Outstanding pH and lifetime stability due to Scepter organic silica hybrid packing   Superior Sensitivity and Separation Performance in Nucleic Acid Analysis Shim-pack Scepter Claris C18-120 with the bioinert coating and Scepter C18-120 with traditional stainless steel hardware were compared in this example of an analysis of a synthetic oligonucleotide. Results from Claris were highly sensitive and reproducible from the rst injection, with no loss of sample signal. Scepter C18-120 in a stainless steel column body produced low-sensitivity results and showed adsorption from the first sample injection. Outstanding Performance in Oligonucleic Acid Analysis Shim-pack Scepter Claris C18-120 (bioinert coating) and Scepter C18-20 (stainless steel body) were compared in this analysis of Oligodeoxythymidylic acid [d(T)20]. Results from Scepter C18-120 show low peak intensity, suggesting adsorption on metal surfaces. In contrast, Scepter Claris C18-120 produced a sharper and high-intensity peak. Improved Sensitivity and Separation of Phospholipids Shim-pack Scepter Claris C18-120 minimizes metal-mediated adsorption and hydrophobic absorption on the column surfaces, resulting in high-resolution separations. In this example of structurally complex phosphatidylcholine isomers, Scepter Claris C18-120 achieved increased baseline resolution between isomers with higher sensitivity.  

  • Product Part
    Description:

    With different pore sizes, Shim-pack Bio Diol LC columns are effective for analysis of aggregates and fragments of mAb, oligonucleotides and carbohydrates. By reducing the particle size from 5μm to 2μm, the resolution between aggregates and monomers was greatly improved. Furthermore, by reducing the column length from 300mm to 150mm using a 2μm particle, 50% less run time was achieved, while maintaining resolution as compared to the original method that used a 5μm, 4.6 × 300mm column.

    OUT OF STOCK

    With different pore sizes, Shim-pack Bio Diol LC columns are effective for analysis of aggregates and fragments of mAb, oligonucleotides and carbohydrates. By reducing the particle size from 5μm to 2μm, the resolution between aggregates and monomers was greatly improved. Furthermore, by reducing the column length from 300mm to 150mm using a 2μm particle, 50% less run time was achieved, while maintaining resolution as compared to the original method that used a 5μm, 4.6 × 300mm column.

  • Product Part
    Description:

    With different pore sizes, Shim-pack Bio Diol LC columns are effective for analysis of aggregates and fragments of mAb, oligonucleotides and carbohydrates. By reducing the particle size from 5μm to 2μm, the resolution between aggregates and monomers was greatly improved. Furthermore, by reducing the column length from 300mm to 150mm using a 2μm particle, 50% less run time was achieved, while maintaining resolution as compared to the original method that used a 5μm, 4.6 × 300mm column.

    OUT OF STOCK

    With different pore sizes, Shim-pack Bio Diol LC columns are effective for analysis of aggregates and fragments of mAb, oligonucleotides and carbohydrates. By reducing the particle size from 5μm to 2μm, the resolution between aggregates and monomers was greatly improved. Furthermore, by reducing the column length from 300mm to 150mm using a 2μm particle, 50% less run time was achieved, while maintaining resolution as compared to the original method that used a 5μm, 4.6 × 300mm column.

  • Product Part
    Description:

    High Isomer Separation Capability The long C30 chains of the SR-C30 provide hydrophobic retention capacity and responsiveness to structure, enabling clear separation of isomer peaks that have insufficient resolution when run on C18 columns. That makes it the perfect column for analyzing isomers of retinoic acid or aldehydes regulated by U.S. Environmental Protection Agency (EPA) 8315A or the Japanese Offensive Odor Control Law.   Analyzing Retinoic Acid Isomers   Although geometric isomers of retinoic acid, such as all-trans, 9-cis, and 13-cis, can be separated using a typical C18 column, sufficient resolution is not always achieved due to their similar hydrophobic and structural properties. Here, a baseline separation of all-trans and 13-cis-retinoic acid isomers using a Shim-pack SR-C30 column is shown.         Simultaneous Analysis of Six Aldehydes Specified in the Offensive Odor Control Law The Offensive Odor Control Law*1 specifically designates 22 substances as offensive odors. Here, results from an analysis of six DNPH-derivatized aldehydes specified as offensive odor substances (Table 1) are shown Table 1: Six Aldehydes Specified in the Offensive Odor Control Law Acetaldehyde n-butyraldehyde n-valeraldehyde Propionaldehyde Isobutyraldehyde Isovaleraldehyde   *1) Ministry of the Environment Methods for Measuring Specific Offensive Odor Substances—Attached Table 4 (Described in only Japanese, April 1, 2026)    

    OUT OF STOCK

    High Isomer Separation Capability The long C30 chains of the SR-C30 provide hydrophobic retention capacity and responsiveness to structure, enabling clear separation of isomer peaks that have insufficient resolution when run on C18 columns. That makes it the perfect column for analyzing isomers of retinoic acid or aldehydes regulated by U.S. Environmental Protection Agency (EPA) 8315A or the Japanese Offensive Odor Control Law.   Analyzing Retinoic Acid Isomers   Although geometric isomers of retinoic acid, such as all-trans, 9-cis, and 13-cis, can be separated using a typical C18 column, sufficient resolution is not always achieved due to their similar hydrophobic and structural properties. Here, a baseline separation of all-trans and 13-cis-retinoic acid isomers using a Shim-pack SR-C30 column is shown.         Simultaneous Analysis of Six Aldehydes Specified in the Offensive Odor Control Law The Offensive Odor Control Law*1 specifically designates 22 substances as offensive odors. Here, results from an analysis of six DNPH-derivatized aldehydes specified as offensive odor substances (Table 1) are shown Table 1: Six Aldehydes Specified in the Offensive Odor Control Law Acetaldehyde n-butyraldehyde n-valeraldehyde Propionaldehyde Isobutyraldehyde Isovaleraldehyde   *1) Ministry of the Environment Methods for Measuring Specific Offensive Odor Substances—Attached Table 4 (Described in only Japanese, April 1, 2026)    

  • Product Part
    Description:

    High Isomer Separation Capability The long C30 chains of the SR-C30 provide hydrophobic retention capacity and responsiveness to structure, enabling clear separation of isomer peaks that have insufficient resolution when run on C18 columns. That makes it the perfect column for analyzing isomers of retinoic acid or aldehydes regulated by U.S. Environmental Protection Agency (EPA) 8315A or the Japanese Offensive Odor Control Law.   Analyzing Retinoic Acid Isomers   Although geometric isomers of retinoic acid, such as all-trans, 9-cis, and 13-cis, can be separated using a typical C18 column, sufficient resolution is not always achieved due to their similar hydrophobic and structural properties. Here, a baseline separation of all-trans and 13-cis-retinoic acid isomers using a Shim-pack SR-C30 column is shown.         Simultaneous Analysis of Six Aldehydes Specified in the Offensive Odor Control Law The Offensive Odor Control Law*1 specifically designates 22 substances as offensive odors. Here, results from an analysis of six DNPH-derivatized aldehydes specified as offensive odor substances (Table 1) are shown Table 1: Six Aldehydes Specified in the Offensive Odor Control Law Acetaldehyde n-butyraldehyde n-valeraldehyde Propionaldehyde Isobutyraldehyde Isovaleraldehyde   *1) Ministry of the Environment Methods for Measuring Specific Offensive Odor Substances—Attached Table 4 (Described in only Japanese, April 1, 2026)    

    OUT OF STOCK

    High Isomer Separation Capability The long C30 chains of the SR-C30 provide hydrophobic retention capacity and responsiveness to structure, enabling clear separation of isomer peaks that have insufficient resolution when run on C18 columns. That makes it the perfect column for analyzing isomers of retinoic acid or aldehydes regulated by U.S. Environmental Protection Agency (EPA) 8315A or the Japanese Offensive Odor Control Law.   Analyzing Retinoic Acid Isomers   Although geometric isomers of retinoic acid, such as all-trans, 9-cis, and 13-cis, can be separated using a typical C18 column, sufficient resolution is not always achieved due to their similar hydrophobic and structural properties. Here, a baseline separation of all-trans and 13-cis-retinoic acid isomers using a Shim-pack SR-C30 column is shown.         Simultaneous Analysis of Six Aldehydes Specified in the Offensive Odor Control Law The Offensive Odor Control Law*1 specifically designates 22 substances as offensive odors. Here, results from an analysis of six DNPH-derivatized aldehydes specified as offensive odor substances (Table 1) are shown Table 1: Six Aldehydes Specified in the Offensive Odor Control Law Acetaldehyde n-butyraldehyde n-valeraldehyde Propionaldehyde Isobutyraldehyde Isovaleraldehyde   *1) Ministry of the Environment Methods for Measuring Specific Offensive Odor Substances—Attached Table 4 (Described in only Japanese, April 1, 2026)