HPLC, LC/MS Columns InertSustain C18
Brochures and specifications | 2024 | Watrex PragueInstrumentation
The selection of a reliable reversed phase column with high inertness and broad pH tolerance is pivotal in analytical chemistry. InertSustain C18 addresses common challenges of silica based phases by combining mechanical stability with minimal secondary interactions across acid, base and chelating analytes. Robust performance over a wide pH range enhances method flexibility, data quality and reduces downtime and column replacement costs.
This document evaluates the chromatographic properties of InertSustain C18. Key objectives include demonstration of lot to lot reproducibility, assessment of inertness against strongly interacting compounds, evaluation of column lifetime under alkaline conditions and performance benchmarking against competitive wide pH phases.
Reproducibility tests involved injections of basic, acidic and chelating compounds across multiple lots and particle sizes under standardized mobile phase, flow rate and temperature settings. Long term stability was measured by monitoring retention over 300 hours of continuous purging at pH 10. Representative analytes included dextromethorphan and berberine chloride for basic compounds, phenol and brilliant blue FCF for acidic compounds, and hinokitiol for chelating compounds.
InertSustain C18 exhibited highly reproducible retention times and sharp peak shapes for strong basic analytes across different lots and particle sizes, indicating superior surface inertness. Under acidic and chelating conditions the column maintained clear, reproducible chromatograms even after multiple injections. In long term tests at pH 10, InertSustain C18 retained over eighty percent of initial efficiency after 300 hours, outperforming competing wide pH columns such as Xterra MS C18 and Gemini-NX.
Further advances in surface modification technologies are expected to reduce residual silanol activity even more, enabling direct analysis of polar and ionizable compounds without derivatization. Integration with ultra-high pressure and microflow LC systems will increase throughput and reduce solvent use. Coupling with mass spectrometry and adoption in green analytical protocols will expand the utility of these columns in pharmaceutical, bioanalytical and environmental laboratories.
InertSustain C18 combines high inertness, broad pH stability and outstanding reproducibility, making it a versatile and cost-effective choice for challenging separations in modern analytical workflows.
No literature references were provided in the original document.
HPLC, Consumables, LC columns, LC/MS
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Summary
Importance of Topic
The selection of a reliable reversed phase column with high inertness and broad pH tolerance is pivotal in analytical chemistry. InertSustain C18 addresses common challenges of silica based phases by combining mechanical stability with minimal secondary interactions across acid, base and chelating analytes. Robust performance over a wide pH range enhances method flexibility, data quality and reduces downtime and column replacement costs.
Aims and Overview of the Study
This document evaluates the chromatographic properties of InertSustain C18. Key objectives include demonstration of lot to lot reproducibility, assessment of inertness against strongly interacting compounds, evaluation of column lifetime under alkaline conditions and performance benchmarking against competitive wide pH phases.
Methodology
Reproducibility tests involved injections of basic, acidic and chelating compounds across multiple lots and particle sizes under standardized mobile phase, flow rate and temperature settings. Long term stability was measured by monitoring retention over 300 hours of continuous purging at pH 10. Representative analytes included dextromethorphan and berberine chloride for basic compounds, phenol and brilliant blue FCF for acidic compounds, and hinokitiol for chelating compounds.
Used Instrumentation
- HPLC system with UV detection at 220, 230 and 254 nm
- InertSustain C18 columns: 150×4.6 mm I.D. and 150×2.1 mm I.D.
- Base material: high purity ES silica gel with octadecyl functional groups, end-capped for silanol suppression
- Particle sizes: 2, 3, 3.5, 4, 5, 7 and 10 μm; surface area 350 m2/g; pore size 100 Å; pore volume 0.85 mL/g; carbon load 14%
- Mobile phases: mixtures of acetonitrile or methanol with phosphate or triethylamine buffers at pH 7.0 to 10.0
Main Results and Discussion
InertSustain C18 exhibited highly reproducible retention times and sharp peak shapes for strong basic analytes across different lots and particle sizes, indicating superior surface inertness. Under acidic and chelating conditions the column maintained clear, reproducible chromatograms even after multiple injections. In long term tests at pH 10, InertSustain C18 retained over eighty percent of initial efficiency after 300 hours, outperforming competing wide pH columns such as Xterra MS C18 and Gemini-NX.
Benefits and Practical Applications
- High inertness enables accurate analysis of strongly basic, acidic and chelating compounds without carryover or tailing
- Wide pH compatibility (1–10) supports versatile method development and robustness
- Excellent lot to lot reproducibility ensures consistent results in QA/QC, pharmaceutical and environmental analyses
- Extended column lifetime reduces operational costs and maintenance intervals
Future Trends and Potential Applications
Further advances in surface modification technologies are expected to reduce residual silanol activity even more, enabling direct analysis of polar and ionizable compounds without derivatization. Integration with ultra-high pressure and microflow LC systems will increase throughput and reduce solvent use. Coupling with mass spectrometry and adoption in green analytical protocols will expand the utility of these columns in pharmaceutical, bioanalytical and environmental laboratories.
Conclusion
InertSustain C18 combines high inertness, broad pH stability and outstanding reproducibility, making it a versatile and cost-effective choice for challenging separations in modern analytical workflows.
References
No literature references were provided in the original document.
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