Agilent, 693975-349, AdvanceBio Peptide Plus 3.0 x 150 mm, 2.7 µm

AdvanceBio Peptide Plus 3.0 x 150 mm, 2.7 µm. Reversed-phase HPLC column with superficially porous particle support functionalized with a charged surface C18 column chemistry designed and optimized for challenging peptide separations.

Specifications:
Brand: AdvanceBio Peptide Plus
Guard Column: No
Hardware: SS
Inner Diameter (ID): 3 mm
LC Platform: Stainless Steel
Length: 150 mm
Maximum Temperature: 90 °C
Molecular Weight Lower Limit: 0 Da
Molecular Weight Upper Limit: 3000 Da
Particle Size: 2.7 µm
Particle Type: Superficially Porous
Phase: Peptide Plus
Pore Size: 100 Å
Pressure Rating: 600 bar
Separation Mode: Reversed Phase
Shipping Solvent: Acetonitrile
Technique: LC
pH Range: 1-11

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Agilent’s AdvanceBio Peptide Plus column provides high-performance separation for complex peptide mapping and characterization workflows. With a 3.0 x 150 mm format and 2.7 µm particle size, this column is engineered for optimal efficiency, enabling sharp peak resolution and enhanced sensitivity in LC and LC-MS applications. Its innovative stationary phase chemistry is specifically designed for robust peptide analysis, ensuring high recovery and reproducibility across a wide range of peptide sizes and hydrophobicities.

Ideal for proteomics, biopharmaceutical development, and quality control laboratories, this column supports critical tasks such as peptide mapping, quantitation, and impurity profiling. It delivers reliable performance under varying pH and a wide range of mobile phases, making it suitable for both standard and complex peptide mixtures. The column seamlessly integrates with Agilent’s 1290 Infinity II and 1260 Infinity II LC systems and is compatible with major third-party LC instruments that accept 3.0 mm ID columns. It also complements other AdvanceBio consumables, providing a complete solution for peptide and protein characterization. This column offers exceptional lot-to-lot consistency, ensuring reproducible results essential for regulated environments and demanding research or QC workflows in pharmaceuticals and biotechnology.