Agilent, PL1512-5802, PLRP-S 1000Å, 4.6 x 250 mm, 8 µm

PLRP-S 1000Å, 4.6 x 250 mm, 8 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: 250 mm
Maximum Temperature: 200 °C
Part Number Application Domain: Biopharma
Part Number Application: Intact & Subunit AnalysisMonoclonal Antibodies (mABs)PeptidesProteins
Particle Size: 8 µm
Particle Type: Fully Porous
Phase: DVB
Pore Size: 1000 Å
Pressure Rating: 207 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 preparative HPLC column features a 1000-angstrom pore size and 8-micron particle size, making it ideal for the analysis and purification of large biomolecules such as peptides, oligonucleotides, proteins, and synthetic polymers. Utilizing rigid polymeric reverse phase (PLRP-S) media, the column delivers exceptional chemical and pH stability across a wide pH range, supporting robust separations under diverse laboratory conditions. Its 4.6 x 250 mm dimensions are well suited for high-resolution purification in both method development and routine analysis.

Designed for compatibility with a broad range of liquid chromatography systems, including Agilent and third-party HPLC instruments, this column integrates seamlessly into biopharmaceutical, proteomics, and life science research workflows. It supports applications in protein purity analysis, peptide mapping, and polymer research, delivering consistent results even after repeated exposure to harsh solvents or high temperatures. The durable construction ensures prolonged column life, reducing maintenance and replacement costs in busy laboratory environments. Pairing with other columns in the PLRP-S family allows researchers to streamline method scaling, from analytical screening through to semi-preparative and preparative workflows, ensuring reproducible performance throughout the purification process.