<h4>Continuing the conversation on toxicology innovation</h4>In our ongoing toxicology blog series, we’ve explored sample preparation strategies, cutting-edge HRAM methods, innovative PaperSpray MS techniques, and productivity boosters for toxicology labs. Now, let’s take a deep dive into one of the most commonly requested yet technically challenging areas of forensic toxicology—accurate, efficient detection of THC and its metabolites.<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Thermo_Fisher_Scientific_Behind_the_Bench_Tips_to_Simultaneously_Analyze_THC_Its_Metabolites_and_Other_Drugs_of_Abuse_Using_LC_MS_84c59fe1e6.jpg" alt="Thermo Fisher Scientific: Behind the Bench - Tips to Simultaneously Analyze THC, Its Metabolites, and Other Drugs of Abuse Using LC-MS" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Thermo_Fisher_Scientific_Behind_the_Bench_Tips_to_Simultaneously_Analyze_THC_Its_Metabolites_and_Other_Drugs_of_Abuse_Using_LC_MS_84c59fe1e6.jpg 245w," sizes="100vw" width="1024" height="512"><h3>The challenge: THC’s lipophilic nature and matrix effects</h3>Tetrahydrocannabinol (THC) remains one of the most frequently detected drugs in forensic testing after alcohol. Yet, its strong lipophilic properties make reliable measurement by LC-MS particularly challenging. THC and its metabolites tend to adhere to nonpolar surfaces of consumables and biological matrices, often leading to signal loss or inconsistent recovery.The latest Thermo Fisher Scientific smart note demonstrates how strategic sample handling and consumable selection can mitigate these challenges. By maintaining methanol (MeOH) in every step of the extraction process—from collection through elution—analysts can prevent THC adsorption and improve recovery. For example, increasing MeOH content during sample prep and using a 30% MeOH wash step helped boost signal strength dramatically.<h3>Extraction optimization: simple tweaks, big gains</h3>The study’s workflow employed DPX XTR tips with mixed-mode SCX/WAX chemistry, analyzed on the Thermo Scientific <a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/products/744">Vanquish Horizon UHPLC system </a>and Thermo Scientific <a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/products/1149">Stellar mass spectrometer</a>. Four small but impactful changes—raising MeOH concentration, adjusting the SPE wash, switching to a biphenyl column, and altering the solvent reconstitution order—resulted in a sevenfold increase in THC signal intensity (Figure 1).<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Thermo_Fisher_Scientific_Behind_the_Bench_Tips_to_Simultaneously_Analyze_THC_Its_Metabolites_and_Other_Drugs_of_Abuse_Using_LC_MS_2_ae1c729642.jpg" alt="Thermo Fisher Scientific: Behind the Bench: Tips to Simultaneously Analyze THC, Its Metabolites, and Other Drugs of Abuse Using LC-MS: Figure 1. THC signal in extracted oral fluid sample before and after changes were made to increase signal by 7x." srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Thermo_Fisher_Scientific_Behind_the_Bench_Tips_to_Simultaneously_Analyze_THC_Its_Metabolites_and_Other_Drugs_of_Abuse_Using_LC_MS_2_ae1c729642.jpg 245w," sizes="100vw" width="800" height="334">These incremental adjustments underscore how critical it is to balance organic composition and consumable materials for each matrix type. For oral fluid assays, using silanized glass vials and incorporating Quantisal™ collection buffers can also prevent degradation and significantly improve stability—up to 150× higher THC signal compared to common buffers (Figure 2).<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Thermo_Fisher_Scientific_Behind_the_Bench_Tips_to_Simultaneously_Analyze_THC_Its_Metabolites_and_Other_Drugs_of_Abuse_Using_LC_MS_3_7fc8699115.jpg" alt="Thermo Fisher Scientific: Behind the Bench: Tips to Simultaneously Analyze THC, Its Metabolites, and Other Drugs of Abuse Using LC-MS: Figure 2. Extracted ion chromatogram of THC using common oral fluid buffer compared to Quantisal extraction buffer." srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Thermo_Fisher_Scientific_Behind_the_Bench_Tips_to_Simultaneously_Analyze_THC_Its_Metabolites_and_Other_Drugs_of_Abuse_Using_LC_MS_3_7fc8699115.jpg 245w," sizes="100vw" width="800" height="276"><h3>Ensuring stability and recovery</h3>Beyond extraction, analyte stability is another make-or-break factor. THC degrades quickly in standard plastic vials or at room temperature but can remain stable 6–12 months when stored at –20°C in sodium heparin tubes. The Smart Note also provides practical recovery assessments for extraction development, including dry down tests and sequential elution testing, to ensure that each analyte is retained through every stage of the workflow.By quantifying pre- and post-extraction spikes, analysts achieved high percent drug recovery and low LOQ’s across a 31-drug oral fluid panel, meeting or exceeding clinical cutoff requirements.<h3>Isomer separation: Δ⁸-THC vs. Δ⁹-THC</h3>With emerging cannabinoids on the market, separating Δ⁸-THC and Δ⁹-THC is increasingly important. The note highlights that <a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/products?category=346&amp;manufacturerItems=3&amp;search=pfp">Pentafluorophenyl (PFP) columns</a>—paired with a water/methanol mobile phase containing 0.1% formic acid—can efficiently resolve these isomers. Using a Vanquish Horizon UHPLC coupled to a <a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/products/403">Thermo Scientific™ Orbitrap Exploris™ 120 MS</a>, researchers achieved clear chromatographic separation (Figure 3).<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Thermo_Fisher_Scientific_Behind_the_Bench_Tips_to_Simultaneously_Analyze_THC_Its_Metabolites_and_Other_Drugs_of_Abuse_Using_LC_MS_4_cf9379f345.jpg" alt="Thermo Fisher Scientific: Behind the Bench: Tips to Simultaneously Analyze THC, Its Metabolites, and Other Drugs of Abuse Using LC-MS: Figure 3. Extracted ion chromatogram of Δ8-THC-COOH and Δ9-THC-COOH separation." srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Thermo_Fisher_Scientific_Behind_the_Bench_Tips_to_Simultaneously_Analyze_THC_Its_Metabolites_and_Other_Drugs_of_Abuse_Using_LC_MS_4_cf9379f345.jpg 245w," sizes="100vw" width="800" height="328"><h3>The takeaway: Building a robust, reliable THC assay</h3>The bottom line? Including THC and its metabolites within a broader LC-MS drug panel is not only cost-effective but also critical to modern toxicology workflows. With deliberate choices in solvent composition, consumables, column chemistry, and buffer systems, laboratories can dramatically enhance recovery and detection reliability.These “behind the bench” optimizations, rooted in real-world forensic workflows, illustrate how small procedural changes can deliver big performance improvements.<h3>Continue your toxicology journey</h3>Stay tuned for the next post in our Analyte Guru series and learn more on our website: <a target="_blank" rel="noopener noreferrer" href="https://www.thermofisher.com/content/lifetech/global/en/home/industrial/forensics/forensic-toxicology.html">Forensic Toxicology</a>.<h3>Resources</h3><ul><li><a target="_blank" rel="noopener noreferrer" href="https://www.thermofisher.com/content/lifetech/global/en/home/industrial/forensics/forensic-toxicology/drug-screening-confirmation/workflows.html">Drug screening and confirmation workflows</a></li><li><a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/products/1149">Stellar Mass Spectrometer</a> &amp; <a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/products/403">Orbitrap Exploris 120 MS</a> webpages</li><li>Promotions<ul><li><a target="_blank" rel="noopener noreferrer" href="https://www.thermofisher.com/content/lifetech/global/en/home/o/b/clinical-lcms-discounts.html">Save up to 40% on complete LC-MS toxicology configurations</a></li><li><a target="_blank" rel="noopener noreferrer" href="https://www.thermofisher.com/content/lifetech/global/en/home/industrial/mass-spectrometry/mass-spectrometer-price-affordability-programs.html">Mass spectrometer affordability programs</a><ul><li>Refurbished MS</li><li>Trade-in</li><li>Financing/ leasing</li></ul></li></ul></li><li>Past blogs in this series<ul><li>Sample prep – <a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/article/6189">Sample Preparation Strategies Demystified: Choosing the Right Fit for Your Toxicology Workflow</a></li><li>Tox Explorer – <a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/article/6587">Beyond Blood: Sheffield Teaching Hospitals NHS Foundation Trust Develops HRAM-Powered Method for Post-Mortem Toxicology Analysis</a></li><li>VeriSpray – <a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/article/6860">Advancing Drug Analysis with PaperSpray MS</a></li><li><a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/article/6953">Boosting Productivity in Toxicology Labs</a></li></ul></li><li>On-demand workshop – <a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/webinar/4735">Next-Generation Workflows for Small Molecule Quantitation Using the Thermo Scientific Stellar Mass Spectrometer</a></li><li>Featured content: <a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/labrulez-bucket-strapi-h3hsga3/sn_004171_cl_lsms_stellar_thc_sn004171_na_en_62724465f8.pdf">Tips and tricks smartnote</a></li></ul><blockquote>Visit us on&nbsp;<a target="_blank" rel="noopener noreferrer" href="https://www.linkedin.com/showcase/72003132/admin/dashboard/">LinkedIn:</a>&nbsp;#THC #LCMS #DrugsOfAbuse #DoA</blockquote>

Behind the Bench: Tips to Simultaneously Analyze THC, Its Metabolites, and Other Drugs of Abuse Using LC-MS

<h3>Eluent Preheating in Preparative HPLC: Why It Matters and What It Improves</h3>In preparative high-performance liquid chromatography (HPLC), where large-format columns and elevated flow rates are routinely used, temperature control becomes a decisive factor for achieving reliable separation performance. Although many HPLC systems are equipped with column ovens to regulate column temperature, heating the mobile phase before it reaches the column is often just as important. If the incoming eluent is significantly cooler than the column, thermal imbalance can occur, leading to temperature gradients, lower separation efficiency, and compromised peak shapes.This article explains why eluent preheating is important in preparative HPLC and summarizes the practical advantages it offers. It also presents the role of KNAUER Heating Sleeves and the KNAUER High Flow Eluent Heater, both of which are designed to provide stable and controlled thermal conditions in preparative LC workflows.<h3>Why Eluent Preheating Is Important in Preparative HPLC</h3><h4>Larger column dimensions and thermal gradients</h4>Preparative HPLC columns usually have much larger inner diameters than analytical columns. As the column diameter increases, it becomes more difficult for a conventional column oven, which heats the column from the outside, to heat the full column cross-section evenly. This challenge becomes even more pronounced when room-temperature solvent continuously enters the column and cools its internal core.When a cold mobile phase enters a heated column, it can create a radial temperature gradient: the outer part of the column remains warmer, while the center stays cooler. As a result, different parts of the column operate under different temperature conditions. This affects solvent viscosity, retention behavior, and mass transfer, causing analytes to migrate unevenly through the column bed. The practical consequence is often peak broadening, distortion, or loss of resolution.<h4>Effects on peak shape and chromatographic efficiency</h4>If the eluent temperature does not match the column temperature, column performance can deteriorate substantially. In one reported example using a 4 mm ID column under fast UHPLC conditions, a radial thermal gradient reduced the effective plate count by more than 50%, severely affecting the separation.In preparative HPLC, the risk is even greater because columns often have inner diameters of 20 mm, 50 mm, or even 100 mm. Experiments with a 20 mm ID preparative column showed that running at 40 °C without mobile phase preheating resulted in poor peak shapes. Only when the mobile phase was preconditioned to the same temperature as the column did the peaks become sharp and symmetric again.This clearly shows that temperature mismatches can cause severe band broadening or even peak splitting, while proper preheating helps preserve peak integrity.<h4>Frictional heating at high flow rates</h4>Preparative HPLC also operates at much higher flow rates than analytical methods, which can generate significant frictional heat inside the column. The amount of heat generated is related to the product of pressure and flow rate. In practical terms, 800 bar at 1 mL/min can generate a similar heating effect as 400 bar at 2 mL/min.In preparative chromatography, pressures may be lower, for example 100–200 bar, but flow rates can reach 10–50 mL/min or more. This means that frictional heating can still be considerable. If the incoming solvent is much cooler than the column, the internally generated heat may intensify temperature differences both along the column and across its radius. Therefore, even at moderate pressure, very high flow rates require careful thermal management.Without eluent preheating, a preparative column operated at elevated temperature may suffer from:<ul><li>Radial temperature differences between the column core and the column wall, resulting in non-uniform separation conditions</li><li>Lower efficiency and resolution due to thermally induced band broadening</li><li>Poor peak shapes, including tailing, fronting, or peak splitting caused by uneven temperature distribution</li><li>Variable retention times, because different regions of the column effectively operate at different temperatures</li><li>Potentially increased backpressure, since colder solvent entering a heated column has higher viscosity until it reaches thermal equilibrium</li></ul>These issues demonstrate why mobile phase preheating is often necessary in preparative HPLC. It ensures that the solvent enters the column at, or close to, the target column temperature, reducing thermal shock and minimizing temperature gradients.<h3>Benefits of Eluent Preheating</h3>Preheating the eluent helps establish stable and uniform thermal conditions throughout the chromatographic system. This provides several important advantages.<h5>Sharper peaks and improved efficiency</h5>When the mobile phase is heated to match the column temperature, the column operates under near-isothermal conditions. This minimizes radial thermal gradients and allows the entire sample band to travel through a consistent separation environment. As a result, peak shape improves, band broadening is reduced, and separation efficiency increases. This is especially important for large-diameter preparative columns.<h5>Reproducible retention times</h5>Retention times are sensitive to temperature. Preheating the mobile phase helps keep the entire column, from inlet to outlet, at a stable and defined temperature. This improves run-to-run reproducibility and supports reliable method transfer and scale-up.<h5>Avoidance of thermal mismatch effects</h5>A controlled thermal environment prevents problems that occur when cold solvent enters a hot column. These include distorted peak shapes, irregular peak profiles, and peak splitting. Optimal results require not only heating the column itself, but also equilibrating the complete flow path. A preheated eluent ensures that the conditions at the column inlet match the conditions inside the column.<h5>Lower solvent viscosity and reduced backpressure</h5>Heating the mobile phase reduces solvent viscosity. A warmer solvent flows more easily through the column, which can lower system backpressure. This is particularly useful in preparative HPLC, where high flow rates and viscous solvent mixtures may otherwise approach pump pressure limits. Reduced viscosity can also improve mass transfer kinetics and may support faster, more efficient separations.<h5>Better performance and higher throughput</h5>With improved peak shape, better resolution, and potentially higher flow rates, preparative productivity can increase. Larger sample amounts can be processed more efficiently without sacrificing separation quality. Stable temperature control also improves method robustness, which is especially valuable in regulated environments and scale-up workflows.In short, eluent preheating is not only a convenient enhancement. In many preparative HPLC applications, it is essential for achieving stable, reproducible, and high-quality separations.<h4>Preparative HPLC With and Without Eluent Preheating</h4><h5>Column temperature profile</h5><ul><li>Without preheating: Significant radial and axial temperature gradients may form. The center of the column can remain cooler than the outer region.</li><li>With eluent preheating: Temperature is more uniform throughout the column, with minimal radial gradients.</li></ul><h5>Peak shape and efficiency</h5><ul><li>Without preheating: Peaks may become broadened, tailing, fronting, or split due to thermal mismatch and uneven analyte migration. Efficiency can be strongly reduced.</li><li>With eluent preheating: Peaks remain sharper and more symmetric. Band broadening is minimized and the column can deliver its full efficiency potential.</li></ul><h5>Retention time stability</h5><ul><li>Without preheating: Retention times can become less predictable because the solvent warms inside the column during the run.</li><li>With eluent preheating: Retention times are highly reproducible due to stable isothermal conditions.</li></ul><h5>Backpressure</h5><ul><li>Without preheating: Backpressure may initially be higher because cold solvent has greater viscosity when it enters the heated column.</li><li>With eluent preheating: Backpressure is lower and more consistent because solvent viscosity is reduced before column entry.</li></ul><h5>Throughput and sample load</h5><ul><li>Without preheating: Operating conditions may need to be more conservative to avoid thermal effects, limiting flow rate or loading.</li><li>With eluent preheating: Higher flow rates and larger loads can often be used while maintaining chromatographic performance.</li></ul>By solving these thermal challenges, eluent preheating helps protect separation quality and allows users to fully exploit the capabilities of preparative columns.<h4>KNAUER Heating Sleeves for Uniform Column Temperature</h4>KNAUER Heating Sleeves are designed to maintain stable column temperature across the full column body, particularly for large preparative columns that may not fit into standard column ovens. These flexible heaters wrap directly around the column and provide uniform heat along its length.<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/KNAUER_column_heating_sleeves_94659add66.jpg" alt="KNAUER: Column heating sleeves" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_KNAUER_column_heating_sleeves_94659add66.jpg 245w," sizes="100vw" width="1306" height="657">They can thermostatically control column temperature up to 100 °C and are suitable for very large columns, up to 1000 mm in length and 100 mm ID. This makes them highly suitable for preparative applications, where column dimensions are often customized and difficult to accommodate in conventional thermostatted compartments.<h5>Key features and advantages include:</h5><ul><li>Direct and uniform heating for large columns: Heating sleeves transfer heat directly to the column wall, unlike air-based ovens that may struggle with larger column diameters. This helps eliminate cold spots and improves temperature consistency.</li><li>Custom fit and broad compatibility: KNAUER Heating Sleeves are available in standard sizes and can also be manufactured for specific column dimensions. They can accommodate preparative columns up to 100 cm in length and 10 cm in diameter.</li><li>Temperature range up to 100 °C: This covers the typical temperature range used in HPLC method development and preparative purification. Elevated temperatures, such as 50–80 °C, can improve separation behavior and reduce solvent viscosity.</li><li>Improved chromatographic performance: By maintaining the column at the desired temperature, the sleeves help reduce solvent viscosity, lower backpressure, and improve mass transfer. This can support more efficient preparative separations.</li><li>Easy installation and flexible setup: Heating sleeves are compact and easy to mount. They do not require bulky oven hardware and can be used in flexible system configurations.</li></ul>When combined with an eluent preheater, a column heating sleeve helps ensure that both the mobile phase and column remain thermally equilibrated throughout the separation.<h4>KNAUER High Flow Eluent Heater for Pre-Column Temperature Control</h4>While the heating sleeve controls the temperature of the column itself, the KNAUER High Flow Eluent Heater heats the mobile phase before it reaches the column inlet. Devices such as the AZURA® ELH 2.1L Eluent Heater are specifically designed for the high flow rates used in preparative LC.<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Knauer_AZURA_ELH_2_1_L_High_Flow_Eluent_Heater_Single_Channel_with_One_Column_Heating_Plug_2_508f4955cd.jpg" alt="Knauer: AZURA® ELH 2.1L High-Flow Eluent Heater Single Channel, with One Column Heating Plug" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Knauer_AZURA_ELH_2_1_L_High_Flow_Eluent_Heater_Single_Channel_with_One_Column_Heating_Plug_2_508f4955cd.jpg 237w," sizes="100vw" width="1015" height="669">The eluent heater is typically installed after the pump and injector. As the mobile phase passes through the heating coil, it is brought to the target temperature before entering the column. This prevents a cold solvent front from disturbing the thermal equilibrium of the column.<h5>Important features and advantages include:</h5><ul><li>Support for high flow rates: The device is designed for preparative-scale flow rates up to 300 mL/min, covering a wide range of semi-preparative and preparative applications.</li><li>Wide temperature range: The heater can bring eluents up to 100 °C, providing flexibility for method optimization and viscosity reduction.</li><li>Dual eluent channels: Depending on the configuration, the system can heat two solvent streams in parallel, which is useful for binary solvent systems or dual-column setups.</li><li>Column sleeve integration: The AZURA ELH 2.1L can control the temperature of up to two eluents and support two column heating sleeves, allowing coordinated thermal management of both solvent and column.</li><li>Precise temperature control with low dead volume: The device uses efficient heating coil cartridges designed to minimize dispersion. External PT100 sensors can monitor temperatures at key points, such as the column inlet and outlet.</li><li>Software and touchscreen control: The heater integrates with KNAUER AZURA preparative HPLC systems and can be controlled via PurityChrom® software or through an integrated 5.7” color touchscreen.</li><li>Cleanroom-compatible version: KNAUER also offers versions suitable for cleanroom environments, supporting eluent preheating and column sleeve control in one device.</li></ul>By heating the mobile phase before it reaches the column, the High Flow Eluent Heater prevents sudden temperature drops at the column inlet and reduces the formation of thermal profiles inside the column.<h4>Conclusion</h4>Eluent preheating is a critical factor in preparative HPLC, where large column dimensions and high flow rates make temperature control more challenging than in analytical-scale separations. By reducing temperature differences between the mobile phase and the column, preheating helps preserve efficiency, resolution, and reproducibility.In practice, this means sharper peaks, more stable retention times, lower and more consistent backpressure, and improved high-throughput purification performance.KNAUER offers dedicated temperature-control solutions for preparative HPLC, including Heating Sleeves for large columns and the High Flow Eluent Heater for pre-column mobile phase conditioning. Together, these tools address common thermal problems such as radial gradients, cold solvent effects, and frictional heating.For laboratories working with preparative HPLC, eluent preheating and column heating are straightforward but highly effective steps toward more reproducible, efficient, and high-performing separations.<blockquote>For further information on this topic, please contact our author: losch@knauer.net</blockquote>

The importance of temperature control in preparative liquid chromatography.

News from LabRulezLCMS Library - Week 18, 2026

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Toxicology

A unique company dedicated to serving science helping our customers drive productivity and accelerate results. Through our premier brands – Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific and Unity Lab Services.

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Based in Berlin, KNAUER is a medium-sized, owner-managed company that has been serving the sciences since 1962. We develop and manufacture scientific instruments of superior quality for liquid chromatography, including: Analytical HPLC/UHPLC, Preparative HPLC, Fast protein liquid chromatography (FPLC), Multi-column chromatography/Simulated moving bed (SMB) chromatography. High pressure dosing, in-line detection systems, and osmometry are additional business areas.

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Waters XBridge BEH Protein C4 HPLC Columns

Waters XBridge Protein BEH C4 column is QC tested and optimized to separate proteins based on size, hydrophobicity and isoelectric point. 

The XBridge Protein BEH C4 column is QC tested and optimized to separate proteins based on size, hydrophobicity and isoelectric point. If you compare to traditional C18 phases, the C4 ligand is less retentive and will minimize protein carryover, increase protein recovery, and improve peak capacity.<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Waters_X_Bridge_BEH_Protein_C4_HPLC_Columns_0aa4f56918.jpeg" alt="Waters: XBridge BEH Protein C4 HPLC Columns" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Waters_X_Bridge_BEH_Protein_C4_HPLC_Columns_0aa4f56918.jpeg 234w," sizes="100vw" width="660" height="440"><h4>Specifications</h4><ul><li>Chemistry: C4</li><li>Separation Mode: Reversed Phase</li><li>Particle Substrate: Hybrid</li><li>pH Range Min: 2 pH</li><li>pH Range Max: 10 pH</li><li>Maximum Pressure: 6000 psi (415 Bar)</li><li>Endcapped: No</li><li>Silanol Activity: Low</li><li>Molecular Weight Range Max: 150000</li><li>Particle Shape: Spherical</li><li>System: HPLC</li><li>Particle Technology: BEH</li><li>USP Classification: L26</li><li>Carbon Load: 8 %</li></ul><h3>XBridge Columns</h3><h4>Particle stability and performance for methods development</h4>Withstanding extreme operating conditions like high pH and high temperatures is essential for methods development. XBridge HPLC and UHPLC Columns utilize Ethylene Bridged Hybrid (BEH) Particle Technology and are built to withstand high pH, high temperatures, and other extreme operating conditions like volatile eluents, for a wide range of small molecule and biomolecule LC-MS analysis.XBridge HPLC and UHPLC Columns are available in a broad range of sorbent particles and sizes: XBridge eXtended Perfomance (XP) 2.5 µm Columns for rapid analytical UHPLC separations; 3.5 and 5 µm HPLC columns for reliable analytical method development; and 5 and 10 µm optimum bed density (OBD) preparative columns for purification chromatography.<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Waters_X_Bridge_Columns_b0b55de501/Waters-XBridge-Columns.jpg" alt="Waters: XBridge Columns" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Waters_X_Bridge_Columns_b0b55de501/thumbnail_Waters-XBridge-Columns.jpg 203w," sizes="100vw" width="900" height="691">

Waters Symmetry C4 HPLC Columns

With Waters Symmetry C4 Column, you get the sharpest peaks for biomolecules and more peak capacity for complex tryptic maps. 

Primarily supports legacy methods. Symmetry columns give you confidence in the long-term compliance of your HPLC methods. No need to compromise on peak shape, selectivity, column-to-column and batch-to-batch reproducibility, or other critical performance characteristics. Available in a variety of particle sizes, chemistries and dimensions.<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Waters_Atlantis_d_C18_HPLC_Columns_d7a741df9f.jpg" alt="Waters: Symmetry C4 HPLC Columns" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Waters_Atlantis_d_C18_HPLC_Columns_d7a741df9f.jpg 234w," sizes="100vw" width="660" height="440"><h4>Specifications</h4><ul><li>Chemistry: C4</li><li>Separation Mode: Reversed Phase</li><li>Particle Substrate: Silica</li><li>pH Range Min: 2 pH</li><li>pH Range Max: 8 pH</li><li>Maximum Pressure: 6000 psi (415 Bar)</li><li>Endcapped: Yes</li><li>Silanol Activity: Low</li><li>Particle Shape: Spherical</li><li>Pore Size: 300 Å</li><li>System: HPLC</li><li>USP Classification: L26</li><li>Carbon Load: 2.8 %</li><li>Application: Protein</li></ul><h3>Symmetry HPLC Columns</h3><h4>Silica-based columns that exceed HPLC column performance expectations</h4>Reproducible HPLC columns are essential when developing analytical methods for pharmaceutical and biopharmaceutical products. Achieving the same chromatographic results over the lifetime of a new drug product is critical, and no other silica-based LC column brand can match the column-to-column and batch-to-batch reproducibility of the Symmetry family.Available in column and guard formats, Symmetry Columns are manufactured using high purity silica and tightly controlled manufacturing processes to ensure that you receive a column that exceeds the standards for HPLC column performance.<h4>Overview</h4><ul><li>Deliver maximum reproducibility batch-to-batch and column-to-column</li><li>Provide superior peak shape</li><li>Achieve high recoveries of peptides and proteins</li><li>Manufactured using high purity silica and tightly controlled manufacturing processes</li><li>Recommended Use: For rugged and reproducible HPLC column performance.</li></ul><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Waters_Symmetry_Columns_a2367d8095/Waters-Symmetry-Columns.jpg" alt="Waters: Symmetry Columns" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Waters_Symmetry_Columns_a2367d8095/thumbnail_Waters-Symmetry-Columns.jpg 223w," sizes="100vw" width="700" height="490">

Waters ACQUITY UPLC Protein BEH C4 Column

The Waters ACQUITY UPLC Protein BEH C4 column is QC tested and optimized to separate proteins based on size, hydrophobicity and isoelectric point. 

The ACQUITY UPLC Protein BEH C4 column is QC tested and optimized to separate proteins based on size, hydrophobicity and isoelectric point. If you compare to traditional C18 phases, the C4 ligand is less retentive and will minimize protein carryover, increase protein recovery, and improve peak capacity.<h5>Specifications</h5><ul><li>Chemistry: C4</li><li>Separation Mode: Reversed Phase</li><li>Particle Substrate: Hybrid</li><li>pH Range Min: 2 pH</li><li>pH Range Max: 10 pH</li><li>Endcapped: No</li><li>Silanol Activity: Low</li><li>Particle Shape: Spherical</li><li>Pore Size: 300 Å</li><li>System: UHPLC, UPLC</li><li>Particle Technology: BEH</li><li>USP Classification: L26</li><li>Carbon Load: 8 %</li></ul><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Waters_ACQUITY_UPLC_BEH_C8_Column_9c78ca994d.jpg" alt="Waters: Kolona ACQUITY UPLC BEH C8" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Waters_ACQUITY_UPLC_BEH_C8_Column_9c78ca994d.jpg 234w," sizes="100vw" width="660" height="440"><h3>ACQUITY UPLC Columns</h3><h5>Increase speed, sensitivity, and resolution, without compromising data integrity</h5>Increasing sample throughput, achieving unmatched resolution, and improving analyte sensitivity are priorities for your separation goals. With Waters ACQUITY UPLC Columns, you can meet all your method requirements and substantially reduce your analysis time and cost-per-sample.Waters ACQUITY UPLC Columns’ sub-2-µm particle chemistries enable chromatographers to harness the separation efficiency improvements at increased flow rates of ultra-performance liquid chromatography (UPLC) technology, thereby improving analyte resolution and sensitivity as well as business productivity and profitability. &nbsp;<h4>Overview</h4><ul><li>Best-in-class column efficiency for superior separation speed, sensitivity, and resolution</li><li>8 UPLC particles of various substrate technologies, including Ethylene Bridged Hybrid (BEH), High Strength Silica (HSS), and Charged Surface Hybrid (CSH)</li><li>22 stationary phases, including C18, Phenyl-Hexyl, C8, Embedded-Polar, C4, HILIC, Amide, Diol, Cyano, and PFP</li><li>7 application-specific UPLC Column chemistries for SEC, proteins, peptides, oligonucleotides, glycan, and amino acid analysis</li><li>More than 50 different column dimensions and configurations, with internal column diameters ranging from 1.0–4.6 mm and column lengths ranging from 30–300 mm</li><li>Prolonged column lifetimes with optional VanGuard Cartridges specifically designed using ACQUITY stationary phases</li><li>Recommended Use: For improved speed, sensitivity, and resolution in methods development.</li></ul><h4>Particle technology</h4><h5>BEH - Ethylene Bridged Hybrid Particle Technology</h5>ACQUITY UPLC BEH 1.7 µm fully porous columns provide superior analyte peak shape, efficiency, and chemical stability to any separation. ACQUITY UPLC BEH Columns are available in both reversed-phase and HILIC separation modes, with chemistries that provide selectivities for a wide range of compounds. With the ruggedness to operate at extreme pH conditions, ACQUITY UPLC BEH Columns enable the separation scientist to use a wide pH range to influence retention, selectivity, and sensitivity for ionizable compounds.<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Waters_BEH_technology_c07876b8a3.jpg" alt="Waters: BEH particle technology" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Waters_BEH_technology_c07876b8a3.jpg 170w," sizes="100vw" width="1050" height="964"><h5>CSH - Charged Surface Hybrid Particle Technology</h5>ACQUITY UPLC CSH™ 1.7 µm fully porous columns provide superior peak shape for basic analytes when using low ionic strength acidic mobile phases (e.g. 0.1% formic acid). With CSH Technology, the controlled low-level positive surface charge provides exceptional peak shape for basic analytes which can be achieved without the use of ion pairing reagents. Typically reversed-phase bonded phases have poor peak shape for basic compounds in formic acid even at analytical mass loads. Built on the rugged Ethylene Bridged Hybrid (BEH) particle, ACQUITY UPLC CSH phases can withstand the toughest operating conditions.<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Waters_CSH_technology_ff4ddc1708.jpg" alt="Waters: CSH particle technology" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Waters_CSH_technology_ff4ddc1708.jpg 169w," sizes="100vw" width="1049" height="968"><h5>HSS - High Strength Silica (HSS) Particle Technology</h5>ACQUITY UPLC HSS 1.8 µm fully porous columns provide expected silica particle-like performance to the UPLC family. The HSS particles’ high surface area, and lower pore volume provide increased retentivity over the hybrid particles. This robust particle technology is available in five uniquely different bonded phases, which truly maximize the selectivity space. The wide array of bonded phases associated with ACQUITY UPLC HSS Columns enable traditional hydrophobic reversed-phase interactions along with dipole-dipole interactions, aromatic interactions, and hydrogen bonding interactions.<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Waters_HSS_technology_b12d3ddfab.jpg" alt="Waters: HSS particle technology" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Waters_HSS_technology_b12d3ddfab.jpg 162w," sizes="100vw" width="975" height="936"><h4>Get superior peak shape for basic analytes</h4>Reversed-phase bonded phases typically have poor peak shape for basic compounds when using formic acid, even at analytical mass loads. However, ACQUITY UPLC CSH Columns are the exception. These rugged UPLC Columns provide superior peak shape for basic analytes with formic acid or other low ionic-strength, acidic mobile phases. The controlled, low-level, positive surface charge bonded to the ethylene-bridged hybrid (BEH) particles provides excellent peak shape for bases—without the need for the use of ion-pairing reagents.<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Waters_Analysis_of_ziprasidone_peroxide_degradation_on_an_ACQUITY_UPLC_CSH_C18_Column_56909f1dc8.jpeg" alt="Waters: Analysis of ziprasidone peroxide degradation on an ACQUITY UPLC CSH C18 Column" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Waters_Analysis_of_ziprasidone_peroxide_degradation_on_an_ACQUITY_UPLC_CSH_C18_Column_56909f1dc8.jpeg 245w," sizes="100vw" width="1024" height="485"><h4>The ruggedness you want, the repeatability you need</h4>ACQUITY UPLC BEH 1.7 µm fully porous columns provide superior analyte peak shape, efficiency, and chemical stability to any separation. ACQUITY UPLC BEH Columns are available in both reversed-phase and HILIC separation modes, with chemistries that provide selectivities for a wide range of compounds. With the ruggedness to operate at extreme pH conditions, ACQUITY UPLC BEH Columns enable separation scientists to use a wide pH range to influence retention, selectivity, and sensitivity for ionizable compounds.<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Waters_ACQUITY_UPLC_BEH_Columns_can_be_used_at_the_extremes_of_mobile_phase_p_H_1_12_to_enhance_retention_and_specificity_for_complex_samples_that_include_mixtures_of_acidic_basic_and_neutral_analytes_5104d9a155.jpeg" alt="Waters: ACQUITY UPLC BEH Columns can be used at the extremes of mobile phase pH (1-12) to enhance retention and specificity for complex samples that include mixtures of acidic, basic, and neutral analytes." srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Waters_ACQUITY_UPLC_BEH_Columns_can_be_used_at_the_extremes_of_mobile_phase_p_H_1_12_to_enhance_retention_and_specificity_for_complex_samples_that_include_mixtures_of_acidic_basic_and_neutral_analytes_5104d9a155.jpeg 195w," sizes="100vw" width="1024" height="823"><h4>Achieve flexibility in method development</h4>Chromatographic laboratories need to quickly and easily develop robust methods that are compatible with all modern chromatographic detection modes and transferrable to laboratories and sites that operate different LC system platforms. With ACQUITY UPLC CSH and XSelect Columns, method development scientists in all application areas can achieve a wide range of selectivities without compromising performance across attributes, including superior peak shape for basic compounds, low column bleeds, excellent batch-to-batch reproducibility, and high efficiency.<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Waters_CSH_Columns_offer_a_wide_range_of_selectivity_differences_large_S_values_733305abf8.jpeg" alt="Waters: CSH Columns offer a wide range of selectivity differences (large S-values)." srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Waters_CSH_Columns_offer_a_wide_range_of_selectivity_differences_large_S_values_733305abf8.jpeg 136w," sizes="100vw" width="1024" height="1173">

Products from category C4 HPLC columns focused on Consumables from Waters - page 1

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