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Shim-pack Scepter
Shim-pack Scepter columns are made of fully porous hybrid particles. Due to the different particle sizes and different columns dimensions, Shim-pack Scepter columns can be used in UHPLC, HPLC and preparative LC.
Product Line
Technical Data
| Phase | Modification | Particle size | Pore size | Endcapping | pH range | USP |
| Shim-pack Scepter C18 | C18 (trifunctional) | 1.9, 3, 5 μm | 120 Å | proprietary | 1.0-12 | L1 |
| Shim-pack Scepter HD-C18 | C18 (trifunctional) | 1.9, 3, 5 μm | 80 Å | proprietary | 1.0-12 | L1 |
| Shim-pack Scepter C8 | C8 (trifunctional) | 1.9, 3, 5 μm | 120 Å | proprietary | 1.0-12 | L7 |
| Shim-pack Scepter C4 | C4 (trifunctional) | 1.9, 3, 5 μm | 300 Å | proprietary | 1.0-10 | L26 |
| Shim-pack Scepter Phenyl | Ph (trifunctional) | 1.9, 3, 5 μm | 120 Å | proprietary | 1.0-10 | L11 |
| Shim-pack Scepter PFPP | PFP (trifunctional) | 1.9, 3, 5 μm | 120 Å | - | 1.0-8.0 | L43 |
| Shim-pack Scepter Diol-HILIC | Diol (trifunctional) | 1.9, 3, 5 μm | 120 Å | - | 2.0-10 | L20 |
Downloads
Brochures
Shimdazu Shim-pack HPLC Column Guidebook
Applications
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Shimadzu High-Sensitivity Quantitative Analysis of Nitrosamines on Shim-pack Scepter C18-120
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Shimadzu Shim-pack Scepter Claris C18 Simple Analysis of Impurities in Oligonucleotide Therapeutics
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Shimadzu Shim-pack Scepter C4-300 Analysis of Protein and Peptide Standards
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Shimadzu Shim-pack Scepter C18 Rapid UHPLC Analysis of DNA (12mer) and its Impurities
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Shimadzu Shim-pack Scepter C18 Achieving Improved Sensitivity and Reliable Analytical Performances in Nucleotides Analysis
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Shimadzu Shim-pack Scepter Claris C18 Analysis of mRNA 5'Cap Structure
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Shimadzu Shim-pack Scepter Claris C18 Analysis of Synthetic DNA
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Shimadzu Shim-pack Scepter Claris C18 Oligonucleotide Characterization for Quality Control
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Shimadzu Shim-pack Scepter Claris C18 An Oligonucleotide Impurity Analysis Workflow
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Shimadzu Shim-pack Scepter Claris C18 Qualitative Analysis of Synthetic DNA
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Shimadzu Shim-pack Scepter HD-C18 In-Pair Reversed Phase Separation and Identification of Oligonucleotides
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