DB-Select 624 UI for <467>
Agilent DB-Select 624 UI 467 GC Columns
Agilent J&W DB-Select 624 UI 467 GC columns are engineered specifically to meet the rigorous
requirements of United States Pharmacopoeia (USP) Method 467 for the determination of residual
solvents in active pharmaceutical ingredients (APIs). Built on the proven 6% cyanopropyl/94%
dimethylpolysiloxane selectivity equivalent to USP phase G43, this Ultra Inert (UI) version
provides dramatically improved inertness, delivering superior peak shape and enhanced sensitivity
for even the most reactive Class 1, Class 2, and Class 3 solvents.
DB-Select 624 UI 467 columns are optimized for the resolution of all critical analyte pairs defined in USP 467, ensuring tight, reproducible separations that support both qualitative identification and quantitative accuracy. Their high thermal stability, low bleed performance, and precision-deactivated surfaces maximize signal-to-noise ratios in GC and GC/MS workflows, making them ideal for routine pharmaceutical quality control and regulatory compliance testing.
Designed for robustness and consistency across batches, every DB-Select 624 UI 467 column is tested against stringent performance criteria to ensure reliable retention, sharp peak symmetry, and repeatability from run to run. The result is a column that provides the confidence, sensitivity, and performance required for compliant USP 467 residual solvent analysis in modern pharmaceutical laboratories.
DB-Select 624 UI 467 columns are optimized for the resolution of all critical analyte pairs defined in USP 467, ensuring tight, reproducible separations that support both qualitative identification and quantitative accuracy. Their high thermal stability, low bleed performance, and precision-deactivated surfaces maximize signal-to-noise ratios in GC and GC/MS workflows, making them ideal for routine pharmaceutical quality control and regulatory compliance testing.
Designed for robustness and consistency across batches, every DB-Select 624 UI 467 column is tested against stringent performance criteria to ensure reliable retention, sharp peak symmetry, and repeatability from run to run. The result is a column that provides the confidence, sensitivity, and performance required for compliant USP 467 residual solvent analysis in modern pharmaceutical laboratories.