Atlantis T3 OBD Prep Column, 100Å, 10 µm, 30 mm X 150 mm, 1/pk
The Waters Atlantis T3 HPLC lab equipment uses reversed-phase C18 sorbents that are entirely porous and have high retention and loading for highly polar substances. The capacity to inject large amounts of polar compounds results in fewer preparative runs, as well as faster library screening and purification. Use the universal, silica-based, reversed-phase C18 Atlantis T3 OBD Prep Column to provide balanced retention of polar and hydrophobic molecules and should be your first choice when developing separations of polar and non-polar compounds. These attributes make the lab equipment a much sought-after instrument by scientists the world over.
The Atlantis T3 OBD Prep Column contains a sorbent that has intermediate ligand density and strikes the perfect balance between ligand coverage and a low concentration of residual surface silanols. With polar alkaline species, traditional end-capping, for example, is insufficient to decrease unwanted silanol activity. When compared to trimethyl silane (TMS) end-capping, the patented T3 end-capping technique used in the lab equipment provides more surface coverage, resulting in higher analyte retention while preserving superior peak form.
Depend on the Atlantis T3 OBD Prep Column when you need increased polar compound retention for applications with high mass loading. In addition to this, at pH 7, the lab equipment also supports basic polar compounds to have better peak forms than other compounds. You can also rely on the Atlantis T3 OBD Prep Column to give you low pH stability and retention without the use of ion-pairing reagents.
The Atlantis T3 OBD Prep Column is manufactured using high purity packing materials and undergoes strict quality control during the process.
Store your analytes and samples in a safe and inert storage unit by investing in the LCGC Certified Clear Glass 12 x 32 mm Screw Neck Vial, with Cap and Preslit PTFE/Silicone Septum, 2 mL Volume, 100/pk. These vials are designed to account for all aspects of use, including needle design, tray design, and volatility, as well as meet LC/GC certification standards. All vials are subjected to an HPLC test to detect trace quantities of substances introduced during processing and manufacturing.
