Agilent, 883750-906, ZORBAX StableBond 300 C8, 2.1 x 150 mm, 5 µm

ZORBAX StableBond 300 C8, 2.1 x 150 mm, 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: 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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The ZORBAX StableBond 300 C8 column features a 2.1 mm inner diameter, 150 mm length, and 5 µm particle size, making it a robust solution for reversed-phase high performance liquid chromatography. Engineered with a wide pore size of 300 Å, this column is ideal for the analysis of peptides, proteins, and other biomolecules, providing enhanced retention and resolution for moderately hydrophobic compounds. The StableBond C8 chemistry offers high stability under low pH conditions, making it suitable for use with trifluoroacetic acid or formic acid mobile phases commonly employed in proteomics, pharmaceutical development, and quality control laboratories.

This column integrates seamlessly with Agilent 1100, 1200, and 1260 Series HPLC systems, as well as other conventional liquid chromatography instruments. It is particularly valuable in applications requiring reproducible peptide mapping, intact protein characterization, and hydrophobic interaction studies. The reliable silica-based C8 bonded phase ensures long column life and consistent performance, even under rigorous analysis conditions. Related products include the wider range of ZORBAX StableBond columns with various chemistries and dimensions for method development flexibility. This column is a trusted choice for researchers and analysts demanding reliable, high-efficiency separations of biomolecules with medium hydrophobicity.