Agilent, PL1412-6801, PLRP-S 300Å, 8 µm, bulk media, 1 kg

PLRP-S 300Å, 8 µm, bulk media, 1 kg. Fully porous PS/DVB reversed-phase particle support that is stable at elevated temperatures and a wide pH range(1-14). Available in wide range of particle and pore sizes for targeted applications

Specifications:
Brand: PLRP-S
Hardware: Bulk Media
LC Platform: Bulk Media
Maximum Temperature: 200 °C
Part Number Application Domain: Biopharma
Part Number Application: PeptidesPreparative HPLC Columns & Bulk MediaProteins
Particle Size: 8 µm
Particle Type: Fully Porous
Phase: DVB
Pore Size: 300 Å
Separation Mode: Reversed Phase
Technique: LCLC & LC/MS
UNSPSC Code: 41115711
Weight: 1 kg
pH Range: 1-14

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This bulk media is designed for reversed-phase liquid chromatography separations, offering a pore size of 300 angstroms and particle size of 8 microns. Engineered from highly cross-linked polystyrene-divinylbenzene, it provides chemical and mechanical durability, making it suitable for the purification and analysis of large biomolecules such as proteins, peptides, and oligonucleotides. Its non-porous, rigid structure ensures stable performance under a wide range of pH and temperature conditions, providing reliable and reproducible retention characteristics.

Typical applications include the isolation and fractionation of biological macromolecules in pharmaceutical, biotechnological, and research laboratories. The high pore volume facilitates efficient mass transfer and recovery rates for large molecular weight analytes. Compatible with most preparative and analytical HPLC systems as well as automated purification platforms, the media can be packed into custom columns or used in large-scale preparative chromatography.

Related products include pre-packed columns and laboratory consumables designed for biomolecule purification. Researchers value this media for its longevity, ease of use, and versatility in method development or scale-up processes. Its high loading capacity and consistent performance make it a trusted choice in demanding workflows where protein or oligonucleotide purification efficiency is critical.