Agilent, 863630-906, ZORBAX StableBond 300 C8, 1 x 150 mm, 3.5 µm

ZORBAX StableBond 300 C8, 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): 1.0 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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Designed for high-performance liquid chromatography (HPLC), this column features StableBond 300 C8 chemistry with a 1 mm internal diameter, 150 mm length, and 3.5 micron particle size. Its octylsilane bonded phase is engineered for enhanced stability under low pH conditions, making it ideal for the analysis of peptides, proteins, and other biomolecules prone to degradation. The 300 Å pore size supports optimal separation of large molecules by facilitating efficient mass transfer and reducing peak broadening, particularly beneficial in proteomics and biopharmaceutical studies.

This column is well-suited to reversed-phase separations where moderate hydrophobicity is required, permitting selective retention and excellent reproducibility in complex mixtures. Its dimensions make it compatible with capillary and micro-flow HPLC systems, offering reduced solvent consumption and increased sensitivity. The product seamlessly integrates with a range of Agilent LC instrumentation as well as other leading HPLC platforms.

Researchers in pharmaceuticals, life sciences, and analytical labs can rely on this column for consistent performance in routine analyses, method development, and detailed characterization studies. It can also be paired with complementary ZORBAX columns for well-rounded workflow solutions across various biomolecule separation requirements.