QuEChERS Made Even Easier Comprehensive Solutions Simplify Sample Prep and Analysis
- New free-flowing salts in slim packs make extraction a snap.
- Complete line of easy-to-use QuEChERS products, reference standards, and accessories.
- Follow up sample prep with a wide range of analytical columns for both LC and GC.
Keep your workflow running smoothly with Q-sep extraction salts from Restek!
For years, the QuEChERS approach to sample preparation has been making the lives of food safety scientists easier. Gone are the days of time-consuming, solvent-intensive extraction techniques and multiple solid phase extraction cartridge cleanup steps! Research published by the U.S. Department of Agriculture Easter Regional Research Center in Wyndmoor, PA,  introduced to the world QuEChERS—a method that is Quick, Easy, Cheap, Effective, Rugged, and Safe.
With QuEChERS, a homogenized sample undergoes a quick extraction step where the analytes are driven into an organic solvent by the partitioning power of a blend of salts. After extraction, the sample is cleaned up through the use of a dispersive solid phase extraction (dSPE) step that is also quick and easy to perform. This simple, two-stage process offers significant savings in time, materials, and effort, making QuEChERS sample preparation faster and easier than other approaches.
Table I: Prepare samples more quickly, easily, and cost effectively with QuEChERS.
Since its introduction, the QuEChERS technique has evolved to accommodate an expanding list of pesticides in an increasingly diverse list of foodstuffs. At Restek, we offer Q-sep products to cover the four major approaches to QuEChERS, along with a host of other items to help make your QuEChERS experience simple and successful. We carry a comprehensive line of sample prep supplies, reference standards, and LC and GC columns that will help make QuEChERS even easier, whether you are new to the approach or developing a method for a new sample matrix.
Which product do I choose?
QuEChERS is primarily a two-stage process, and you’ll select Q-sep products for both stages. Your method may have specific recommendations, but in case you’re not sure what will work, here some considerations when making your selection.
Stage 1: Extraction
The choice of which extraction technique to use is made principally by considering your analytes of interest. If you’re looking for compounds that aren’t pH sensitive, the original unbuffered method  will work great. However, if your analytes of interest are pH sensitive, you will want to select one of the buffered methods—notably, the official EN 15662 method , the mini-multiresidue approach , or the official AOAC 2007.01 method .
Restek’s Q-sep products for the two European approaches, the official EN 15662 method and the mini-multiresidue approach, are the same, so it becomes essentially a choice between a European-developed method and the AOAC method. Both are buffered to lower the pH to a range where most pesticides are stable, and the methods differ only in the specific buffering salts and their ratios. Either would be a good place to start for most analyses. There are a great many studies that highlight specific instances when one buffering technique may outperform another, so a little research into your particular area of study may yield practical suggestions on which extraction method to use.
Stage 2: Dispersive Solid Phase Extraction (dSPE) Cleanup
The next big choice comes during the selection of which dSPE cleanup product to use. Where the choice of the extraction product was driven largely by the analytes of interest, the choice of cleanup is based on the sample being tested. Restek Q-sep dSPE products are formulated with different sorbents in different ratios so that your dSPE choice can be tailored to the composition of your particular sample type (e.g., fatty, highly pigmented, etc.). Use Table II to learn what each sorbent removes and to help select the best dSPE product for your particular sample.
Table II: Visit the desktop version of www.restek.com/quechers to access this table.
Table II: Select your dSPE tube based on sample type to ensure you get the best sorbent blend for removing specific matrix interferences.
|Method||Sorbent Mass (mg)
|MgSO4||PSA*||C18-EC||GCB**||Vial Volume (ml)
|Excess Water||Sugars, fatty acids, organic acids, anthocyanine pigments||Lipids, nonpolar interferences||Pigments, sterols, nonpolar interferences|
|General fruits and vegetables (e.g., celery, head lettuce, cucumber, melon)||AOAC 2007.01||150||50||-
|Original unbuffered, EN 15662, mini-multiresidue||150||25||-||-||2||26215|
|Original unbuffered, EN 15662||900||150||-||-||15||26223|
|Foods with fats and waxes (e.g., cereals, avocado, nuts, seeds, and dairy)||Mini-multiresidue||150||25||25||-||2||26216|
|Pigmented fruits and vegetables (e.g., strawberries, sweet potatoes, tomatoes)||Mini-multiresidue, EN 15662||150||25||-||2.5||2||26217|
|Highly pigmented fruits and vegetables (e.g., red peppers, spinach, blueberries)||Mini-multiresidue, EN 15662||150||25||-||7.5||2||26218|
|General purpose (wide range of commodities, including fatty and pigmented fruits and vegetables)||-||150||50||50||7.5||2||26243|
Note: No entry in the Method column refers to dSPE formulations not specifically included in one of the cited references. These products can be used to accommodate the various needs of specific matrices not directly met by the cited references.
*PSA = primary secondary amine exchange material
**GCB = graphitized carbon black
Restek is not able to provide copies of these documents.
 M. Anastassiades, S.J. Lehotay, D. Stajnbaher, F.J. Schenck, Fast and easy multiresidue method employing acetonitrile extraction/partitioning and "dispersive solid-phase extraction" for the determination of pesticide residues in produce. J. AOAC Int. 86 (2003) 412-431. http://pubag.nal.usda.gov/pubag/downloadPDF.xhtml?id=555&content=PDF
 EN 15662, Foods of Plant Origin—Determination of Pesticide Residues Using GC-MS and/or LC-MS/MS Following Acetonitrile Extraction/Partitioning and Clean-up by Dispersive SPE—QuEChERS method, 2008.
 QuEChERS-A Mini-Multiresidue Method for the Analysis of Pesticide Residues in Low-Fat Products, 2004. http://quechers.cvua-stuttgart.de/pdf/reality.pdf
 AOAC Official Method 2007.01, Pesticide Residues in Foods by Acetonitrile Extraction and Partitioning with Magnesium Sulfate, 2007.
- Ideal for high-throughput LC-MS/MS applications with minimal sample preparation.
- Well-balanced retention profile for better detection and integration of large, multiclass analyte lists.
- Sterically protected to endure low-pH mobile phases without sacrificing retention or peak quality.
- Part of Restek’s Raptor LC column line featuring 1.8, 2.7, and 5 µm SPP core-shell silica.
low-polarity phase; Crossbond 1,4-bis(dimethylsiloxy)phenylene dimethyl polysiloxane
- Engineered to be a low-bleed GC-MS column.
- Excellent inertness for active compounds.
- General-purpose columns
—ideal for GC-MS analysis of semivolatiles, polycyclic aromatic compounds, chlorinated hydrocarbons, phthalates, phenols, amines, organochlorine pesticides, organophosphorus pesticides, drugs, solvent impurities, and hydrocarbons.
- Temperature range: -60 °C to 350 °C.
- Designed for use in all QuEChERS methods for pesticides in fruits and vegetables, including the original unbuffered method, AOAC 2007.01, and EN 15662.
- Kit contains organochlorine, organonitrogen, organophosphorus, and carbamate pesticides commonly used on fruits and vegetables.
- Volatile, polar, active, base-sensitive, and nonvolatile compounds are included to allow comprehensive evaluation of QuEChERS extraction and cleanup efficiencies, and optimization of GC and LC instrumental conditions.
- Ideal for initial method evaluations and ongoing method performance validations.
- Analytes are divided into three ampuls based on compatibility for maximum stability and shelf life.*
- Precise formulations improve data quality and operational efficiency; spend more time running samples and less time sourcing and preparing standards.
- Quantitatively analyzed to confirm the composition and stability of each mixture.
*When combining compounds with different functionalities, chemical stability can be an issue. The analytes in this kit are separated into three mixes to ensure maximum long-term storage stability. For analysis, a fresh working standard should be prepared by combining the three kit mixes in a 1:1:1 ratio to prepare a 100 µg/mL working standard solution. Once blended, Restek does not recommend storing working standards or subsequent dilutions for future use.
Contains 1 mL each of these mixtures.
31153: QuEChERS Performance Standard A
31154: QuEChERS Performance Standard B
31155: QuEChERS Performance Standard C
- Single and multiple component standards as specified in EN Method 15662.
- Support for GC and HPLC with MS, MS/MS, and selective detectors.
- Ready to use for QuEChERS extractions—no dilutions necessary.
- Accurately detect and quantify pesticides of global food safety concern in a wide range of fruits, vegetables, and other commodities by LC-MS/MS.
- Full kit contains 204 compounds of interest, covering many LC-determined pesticides listed by government agencies; individual ampuls also sold separately.
- Accurately identify and quantify pesticide residues by GC-MS/MS in fruits, vegetables, botanicals, and herbals such as tea, ginseng, ginger, echinacea, and dietary supplements.
- Comprehensive 203-compound kit covers food safety lists by the FDA, USDA, and other global governmental agencies; individual ampuls also sold separately.
- Free-flowing salts transfer easily and completely.
- Easy-open packets eliminate the need for a second empty tube for salt transfer.
- Convenient slim packets fit perfectly into tubes to prevent spills.
- Ready-to-use tubes, no glassware required.
- Pre-weighed, ultra-pure extraction salts.
- Ideal for original unbuffered, AOAC (2007.01), and European (EN 15662) QuEChERS methods.
Fast, Simple Sample Prep for Multiresidue Pesticide Analysis
- Packaged in foil subpacks of 10 for enhanced protection and storage stability.
- Ready-to-use tubes, no glassware required.
- Pre-weighed, ultra-pure sorbents.
- Support original unbuffered, AOAC (2007.01), European (EN 15662), and mini-multiresidue QuEChERS methods.
- Supports 50 mL, 15 mL, and 2 mL centrifuge tubes.
- Small footprint requires less bench space.
- Safe and reliable
—UL, CSA, and CE approved; 1-year warranty.
- Adjustment knob offers 56 output volume settings from 2.5 mL to 30 mL per stroke (0.5 mL increments)
—ideal for QuEChERS methods!
- Base features 30 mm threads and includes four adaptors (25 mm, 28 mm, 38 mm, and 45 mm).
- Individually calibrated in accordance with ISO 8655 standards (certificate included) and can also be recalibrated by the user.
- PTFE, glass, and polypropylene construction for excellent chemical compatibility and 100% autoclavability.
- Integral safety discharge reduces risk of accidental dispensing, and nozzle cap prevents dripping.
- Easy to disassemble for cleaning and servicing.
Supplies & Accessories
for Agilent GCs equipped with split/splitless inlets
- Deactivation—unbelievably low breakdown for accurate and precise low-level GC analyses.
- Reproducibility—unbeatable manufacturing controls and QC testing for superior reliability across compound classes.
- Productivity—unparalleled cleanliness for maximized GC uptime and lab throughput.
- 100% Satisfaction—if a liner doesn't perform to your expectations, we will replace it or credit your account.*
Evaluation of Dispersive and Cartridge Solid Phase Extraction (SPE) Cleanups for Multiresidue Pesticides in QuEChERS Extracts of Finished Tobacco Using GCxGC-TOFMS
We compared the efficacy of dSPE and cSPE cleanup methods for multiresidue pesticide analysis of QuEChERS extracts of finished tobacco products using GCxGC-TOFMS. Cleanup with dSPE tubes containing 7.5 mg of GCB and 25 mg of PSA produced better results than other methods, with average recoveries of 92% and 91% for 500 ppb and 50 ppb fortifications respectively.
Comparing Pesticide Residues in Amish and Commercially Grown Strawberries and Spinach Using QuEChERS, Various dSPE Sorbents, and GC-TOFMS
QuEChERS extraction, dSPE cleanup, and GC-TOFMS analysis were used to assess pesticide residue levels in strawberry and spinach from both commercial and Amish growers. Various dSPE sorbent products were compared to determine which were most effective.
Determining Pesticides in Dietary Supplements with QuEChERS Extraction, Cartridge SPE, and GCxGC-TOFMS
The novel approach used here combines QuEChERS extraction, cartridge SPE cleanup, and GCxGC-TOFMS analysis, resulting in good recoveries for a wide range of pesticides in dietary supplements. Matrices include dandelion root, sage, and a multi-herb finished product. (PDF - 0MB)
Mitigating Matrix Effects: Examination of Dilution, QuEChERS, and Calibration Strategies for LC-MS/MS Analysis of Pesticide Residues in Diverse Food Types
LC-MS/MS is popular for monitoring pesticide residues in food due to its selectivity and sensitivity; however, matrix effects can cause poor data quality and difficult quantification. We evaluated the relative effectiveness of sample dilution, QuEChERS cleanup, solvent-based calibration, and matrix-matched calibration strategies to mitigate matrix effects in celery, kale, avocado, lime, and brown rice flour. (PDF - 0MB)
Learn how to use the QuEChERS approach to perform faster, easier sample preparation and cleanup for multiresidue pesticide analysis. Q-sep QuEChERS products save time, money, and materials compared to modified Luke methods. (PDF - 0MB)
QuEChERS is a simple, effective approach to sample prep that can be applied to the analysis of pesticides in dietary supplements. Here, we demonstrate a QuEChERS, cSPE, GC-TOFMS procedure that results in good recoveries for a wide range of pesticides in dandelion root. (PDF - 0MB)
QuEChERS dSPE methods simplify extract cleanup, reduce material costs, and improve sample throughput. Here we demonstrate the effectiveness of QuEChERS sample cleanup using a multiresidue analysis of pesticides on strawberries. (PDF - 0MB)
A recall of Tylenol pain reliever and other related products highlights the need for simple, quick sample preparation and a comprehensive analytical method for adulterants in consumer products. The rush to examine a multitude of samples in a short period of time is a common scenario for potential recalls, especially when a contaminant is found in a given product and rapid determinations need to be made to assess how widespread the problem may be. (PDF - 0MB)
Not all column deactivations are appropriate for analyzing basic compounds. Here, we demonstrate the effect of column inertness on peak shape and discuss its role in improving method accuracy, sensitivity, and development time. (PDF - 0MB)