Agilent, 863750-906, ZORBAX StableBond 300 C8, 2.1 x 150 mm, 3.5 µm

ZORBAX StableBond 300 C8, 2.1 x 150 mm, 3.5 µm. A reversed-phase C8 HPLC column with fully porous ZORBAX particles. StableBond technology ensures stability at low pH.

Specifications:
Brand: ZORBAX 300SB-C8
Hardware: SS
Inner Diameter (ID): 2.1 mm
LC Platform: Stainless Steel
Length: 150 mm
Maximum Temperature: 80 °C
Part Number Application Domain: Biopharma
Part Number Application: Monoclonal Antibodies (mABs)PeptidesProteins
Particle Size: 3.5 µm
Particle Type: Fully Porous
Phase: 300SB-C8
Pore Size: 300 Å
Pressure Rating: 400 bar
Separation Mode: Reversed Phase
Shipping Solvent: Acetonitrile/Water
Technique: LCLC & LC/MS
UNSPSC Code: 41115709
pH Range: 1-8

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Agilent’s ZORBAX StableBond 300 C8 column is engineered for robust performance in reversed-phase high performance liquid chromatography, particularly suited for the separation of peptides, proteins, and other biomolecules. With a pore size of 300 Å and dimensions of 2.1 x 150 mm featuring 3.5 micron particle size, it provides efficient resolution and optimal peak shapes for medium to large molecular weight analytes. The C8 bonded phase offers moderate hydrophobicity, making it ideal for applications requiring reduced retention compared to traditional C18 columns, while still delivering excellent selectivity.

Common usage scenarios include LC-MS methods for protein and peptide mapping, biomolecule characterization, and quality control within pharmaceutical and biotechnological research laboratories. The column’s stable silica-based platform ensures high reproducibility and durability, even under low pH mobile phase conditions. It is fully compatible with most HPLC and UHPLC systems, including Agilent InfinityLab LC Series and comparable instruments, and works seamlessly with related ZORBAX columns for orthogonal method development or comprehensive impurity profiling. This product is a preferred choice among researchers requiring reliable analytical performance for complex biological samples and method validation processes.