Product Description
PLRP-S 300Å, 4.6 x 50 mm, 3 µm. Reversed-phase HPLC column with fully porous PS/DVB particle support stable at elevated temperatures and a wide pH range(1-14). Available in range of particle and pore sizes for targeted applications
Specifications:
Brand: PLRP-S
Hardware: SS
Inner Diameter (ID): 4.6 mm
LC Platform: Stainless Steel
Length: 50 mm
Maximum Temperature: 200 °C
Part Number Application Domain: Biopharma
Part Number Application: Intact & Subunit AnalysisMonoclonal Antibodies (mABs)PeptidesProteins
Particle Size: 3 µm
Particle Type: Fully Porous
Phase: DVB
Pore Size: 300 Å
Pressure Rating: 275 bar
Separation Mode: Reversed Phase
Shipping Solvent: Acetonitrile/Water
Technique: LCLC & LC/MS
UNSPSC Code: 41115711
pH Range: 1-14
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This reverse-phase HPLC column features a highly stable, polymeric polystyrene-divinylbenzene (PS-DVB) media with a 300 angstrom pore size, 3 micron particle size, and dimensions of 4.6 x 50 mm. Engineered for robust performance, it delivers excellent resolution and batch-to-batch reproducibility, making it ideal for the analysis of peptides, small proteins, and other biomolecules. The wide pore structure enables efficient separation of larger analytes while minimizing secondary interactions, supporting applications in proteomics, pharmaceutical research, and quality control environments.
Designed for compatibility with all standard HPLC and UHPLC systems, this column is particularly suitable for high-throughput screening, method development, and sample characterization workflows. Its chemically inert stationary phase ensures resilience against extreme pH conditions and provides extended column longevity for demanding analytical tasks. Commonly integrated with mass spectrometry and UV detection platforms, it also aligns seamlessly with Agilent instrumentation and related liquid chromatography systems.
The advanced construction supports rapid analysis without compromising on sensitivity or reproducibility. This column is a preferred choice for professionals seeking high performance in biomolecule separation, and its robust design ensures reliable operation across diverse laboratory settings.
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Collaboration
Tony Tang
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