Chemistry |
Phenyl |
Separation Mode |
Reversed Phase |
Particle Substrate |
Hybrid |
pH Range Min |
1 pH |
pH Range Max |
12 pH |
Maximum Pressure |
18000 psi (1240 Bar) |
Endcapped |
Yes |
Bonding Technology |
Phenyl-Hexyl |
Silanol Activity |
Low |
Particle Shape |
Spherical |
Particle Size |
1.7 µm |
Endfitting Type |
Parker-style |
Pore Size |
130 Å |
Format |
Column |
Surface Area |
185 |
System |
UHPLC, UPLC |
Particle Technology |
BEH |
USP Classification |
L11 |
Inner Diameter |
2.1 mm |
Length |
100 mm |
Carbon Load |
15 % |
eCord |
Yes |
UNSPSC |
41115709 |
Brand |
ACQUITY UPLC |
Product Type |
Columns |
Units per Package |
1 pk |
ACQUITY UPLC BEH Phenyl Column, 130Å, 1.7 µm, 2.1 mm X 100 mm, 1/pk
Minimize the risk of method variation due to differences caused by chromatographic media batch or column inconsistency with the ACQUITY UPLC BEH Phenyl Columns. They are manufactured under the strictest ISO 9001 conditions and stringent process control using the trifunctionally-bonded phenyl-hexyl ligand.
Enjoy industry-leading pH stability, batch-to-batch reproducibility, and exceptional peak shape for all analyte types compared to other commercially available phenyl columns with the ACQUITY UPLC BEH Phenyl column.
The Waters ACQUITY UPLC BEH Phenyl Columns are specially designed to provide complementary selectivity to straight-chain-alkyl columns, particularly for analytes containing aromatic rings. This sorbent, along with the XBridge BEH Phenyl, will equip you with the most chemically stable phenyl sorbent available in the market and ensures ultra-low column bleed and long column lifetime.
The 2.1 mm I.D. Waters ACQUITY UPLC BEH Phenyl Column is suitable for the analysis of analytes with pore size 130Å, and particle size 1.7 µm, and offers a wide pH stability range (1-12).
ACQUITY UPLC BEH Phenyl Column, 130Å, 1.7 µm, 2.1 mm x 75 mm, 1/pk is also available in 2.1mm by 75 mm inner diameter for additional laboratory needs. Shop for lab equipment and learn more about our other products that are sure to be the perfect additions to your work.
How Are Cleaning And Regeneration Carried Out For ACQUITY UPLC BEH Columns?
Changes in peak shape, peak splitting, shoulders on the peak, shifts in retention, change in resolution, or increasing backpressure may indicate contamination of the column. Flushing with a neat organic solvent, taking care not to precipitate buffers, is usually sufficient to remove the contaminant. If the flushing procedure does not solve the problem, purge the column using the following cleaning and regeneration procedures. Use the cleaning routine that matches the properties of the samples and/or what you believe is contaminating the column. Flush columns with 20-column volumes of solvent. Increasing column temperature increases cleaning efficiency.