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HALO® C18 Capillary

HALO® C18 Capillary HPLC Columns from AMT

HALO 90 Å C18 is a high-speed, high-performance liquid chromatography column based on a new Fused-Core® particle design. The Fused-Core® particle provides a thin porous shell of high-purity silica surrounding a solid silica core. This particle design exhibits very high column efficiency due to the shallow diffusion paths in the porous shell. The densely bonded, extensively endcapped dimethyloctadecyl stationary phase of HALO 90 Å C18 provides a stable, reversed-phase packing that can be used for basic, acidic, or neutral compounds.

Part Number Short Description Phase Type Phase USP Particle Size ID Length Pore Size Type Price Qty
98216-602 HALO 90A C18, 2.7um, 0.3 x 100mm C18 HALO C18 L1 2.7 um 0.3 mm 100 mm 90 A Column
£884.62
98216-702 HALO 90A C18, 2.7um, 0.3 x 150mm C18 HALO C18 L1 2.7 um 0.3 mm 150 mm 90 A Column
£884.62
98216-402 HALO 90A C18, 2.7um, 0.3 x 50mm C18 HALO C18 L1 2.7 um 0.3 mm 50 mm 90 A Column
£803.42
98215-602 HALO 90A C18, 2.7um, 0.5 x 100mm C18 HALO C18 L1 2.7 um 0.5 mm 100 mm 90 A Column
£884.62
98215-702 HALO 90A C18, 2.7um, 0.5 x 150mm C18 HALO C18 L1 2.7 um 0.5 mm 150 mm 90 A Column
£884.62
98215-402 HALO 90A C18, 2.7um, 0.5 x 50mm C18 HALO C18 L1 2.7 um 0.5 mm 50 mm 90 A Column
£803.42
  • Excellent performance for broad range of analyte polarities
  • Suitable for diverse analytes ranging from polar to non-polar
  • Recommended applications are pharmaceutical, environmental, cannabinoid and general purpose use
Bonded Phase USP Designation Particle Size Pore Size Carbon Load Surface Area Low pH/Temp Limit High pH/Temp Limit Endcapped
C18 (dimethyloctadecylsilane) L1 2.7 µm 90 Å 7.7% 135 m2/g 2/60°C 9/40°C Yes
5 µm 5.4% 90 m2/g
HALO® Catalogue (18.63 MB)
Discover the advantages of HALO® and HALO® BioClass Fused-Core® columns
HALO® Method Conversion Guidebook (1.53 MB)
How to take advantage of superficially porous particles for method improvements
HALO® Selectivity Guidebook (10.95 MB)
Guidebook on reversed phase chemistries and utilizing selectivity for HPLC separations
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