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Automated Purification Systems for Flash and Prep Chromatography

 

Automated purification systems integrate gradient solvent pumping, UV/Vis detection, automated fraction collection, and chromatography column management into a single instrument, replacing manual flash chromatography and preparative HPLC column work with a reproducible, hands-free workflow. They are used in drug discovery and synthesis laboratories to isolate and purify reaction products from complex mixtures at milligram to multi-gram scale using normal-phase silica, reversed-phase C18, or chiral stationary phases.

MBP provides quote-based procurement and purchase order support for automated purification systems for US and Canadian research and pharmaceutical laboratories. Request a quote for automated purification systems for flash chromatography, preparative purification, and compound isolation by contacting customerservice@mbpinc.net.

Automated Purification Systems

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6-well reagent vessel for IsoPure Mini, cs 100
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USD183.10
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USD130.79
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8-place magnetic tip comb for IsoPure Mini, cs 50
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USD102.62
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USD73.30
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96 deep well plates for IsoPure™, cs 50
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USD365.01
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USD260.72
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96 well elution plates for IsoPure™, cs 100
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USD695.26
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USD496.61
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Accuris IsoPure Automated Purification Systems
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USD68,625.58 - USD68,651.85
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USD49,018.27 - USD49,037.04
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Aluminum Sample Rack for AP1016-6W reagent vessels
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USD701.50
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USD501.07
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IsoPURE Mini Demo Case
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USD708.82
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USD506.30
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IsoPURE™ 24 14.6mL Deep Well Plate, 24/pack
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USD319.99
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USD228.57
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IsoPURE™ 24 Tip Combs, 24/pack
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USD306.21
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USD218.72
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IsoPure™ 96, Automated Purification System
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USD65,670.41 - USD65,670.41
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USD46,907.44 - USD46,907.44
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IsoPure™ Mini, Automated Purification System
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USD14,665.66 - USD14,665.66
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USD10,475.47 - USD10,475.47
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Nucleic Acid Purifier 16 (1 Unit)
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USD14,787.19
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USD10,562.28
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What Are Automated Purification Systems?

 

Automated purification systems are integrated chromatography instruments that combine a multi-channel solvent delivery pump, a sample injection module, a chromatography column holder (accepting prepacked cartridges or reusable columns), a UV/Vis (and optionally ELSD or mass detector) detection system, and an automated fraction collector into a single controlled platform. The system runs gradient elution programs that change solvent composition over time, separating sample components by their differential affinity for the stationary phase. UV signal peaks trigger fraction collection into numbered tubes or microplates, eliminating the need for the operator to monitor the separation and manually collect fractions. Mass-directed systems add an inline mass spectrometer to trigger fraction collection on a specific molecular mass rather than UV absorbance, enabling selective collection of the target compound even when it co-elutes with impurities of similar UV absorption. Specify an automated purification system when your lab runs more than 3 to 5 flash chromatography purifications per day; the time saved on each run compounds rapidly and improves fraction quality through consistent, reproducible gradient programming.

 

What You Will Find:

 

  • Compact and high-throughput magnetic bead-based instruments, including IsoPure™ Mini, IsoPure™ 24, IsoPure™ 96, and Nucleic Acid Purifier 16 systems for automated nucleic acid purification.
  • Compatible 24-well and 96-well deep-well plates and elution plates for automated purification workflows.
  • Replacement magnetic tip combs for IsoPure™ Mini, IsoPure™ 24, and IsoPure™ 96 automated purification systems.
  • Reagent vessels and aluminum sample racks designed for efficient sample loading and workflow organization.
  • System Accessories, including Tablets, demo cases, and other compatible accessories to support the setup, operation, and maintenance of automated purification systems.

 

How to Choose an Automated Purification System

 

Flash chromatography vs. preparative HPLC

Automated flash chromatography systems (operating at 5 to 30 bar with spherical 25 to 100 micron silica or C18 cartridges) are optimized for fast, cost-effective purification of 0.1 to 10 g samples with throughputs of 3 to 10 runs per day. Preparative HPLC systems (operating at 50 to 300 bar with 5 to 25 micron particle columns) provide higher resolution for complex mixtures, smaller sample loads (mg to g scale), and are required when flash chromatography cannot resolve closely similar compounds. Some systems integrate both flash and prep HPLC capability in one instrument.

Sample load and column capacity

Match the column loading to your typical sample mass. Standard flash cartridges in 4 g, 12 g, 25 g, 40 g, 80 g, and 120 g silica sizes handle sample loads of roughly 0.04 to 1.2 g on normal-phase silica. Reversed-phase C18 cartridges handle lower loads per gram of silica. For larger sample loads (5 to 100 g), large-diameter columns or multi-injection protocols are used. Confirm the system's maximum column size and flow rate capacity against your typical sample mass.

Detection: UV/Vis vs. ELSD vs. mass directed

UV/Vis detection (monitoring at 254 nm and 280 nm) is standard and sufficient for compounds with a chromophore (most synthetic products). Evaporative light scattering detection (ELSD) is added for compounds with poor UV absorption (lipids, carbohydrates, alkyl chains). Mass-directed purification adds an inline single-quadrupole mass spectrometer that triggers fraction collection only when the target mass is detected; this is the highest-selectivity option for purifying one compound from a complex mixture, but at significantly higher instrument cost.

Number of solvent lines

Entry-level systems use two solvent lines (binary gradient). Advanced systems provide four solvent lines (quaternary gradient), enabling more complex separation strategies, modifier additions (e.g., acetic acid or ammonium formate in reversed-phase), and reduced operator setup time for multi-method labs. For most flash chromatography in synthetic chemistry, a binary gradient (organic/non-polar + polar modifier) is sufficient.

Software and workflow integration

Automated systems vary widely in software capability: basic systems provide gradient programming and peak detection; advanced platforms add automatic injection, queue management for multiple samples, solvent level monitoring, LIMS connectivity, and 21 CFR Part 11 compliance for regulated pharmaceutical environments. For open-access use in multi-chemist departments, queue-based software allowing each user to submit samples independently increases throughput.

 

Specifications Context

 

Column and cartridge consumables are a significant ongoing cost for automated purification systems; prepacked silica cartridges for flash systems are single-use or limited-use. Confirm cartridge availability and pricing for the specific system before purchase, as some systems lock users to proprietary cartridges at premium pricing while others accept standard-thread cartridges from multiple suppliers. Solvent consumption (L/run) scales with column size and flow rate; larger cartridges and longer gradients use more solvent. For high-throughput labs, solvent waste management (evaporation, recycling, or disposal) is a practical operational consideration. UV detection wavelength settings (254 nm for aromatic compounds, 210 to 220 nm for carbonyl-containing compounds) should be confirmed for your compound class to avoid missing low-UV-absorbing peaks. 

 

Complete your purification setup today—browse our accessories collection and contact the MBP team for a quote.

FAQ

An automated purification system integrates a gradient solvent pump, sample injector, chromatography column holder, UV/Vis (and optionally mass or ELSD) detector, and automated fraction collector into one instrument. The system runs a preprogrammed gradient elution that changes solvent polarity over time, separating sample components by their affinity for the stationary phase (silica for normal phase, C18 for reversed phase). When the detector identifies a compound peak, it triggers fraction collection into a numbered tube or plate -- eliminating the manual column monitoring and fraction collection steps of traditional flash chromatography.
Automated flash chromatography operates at 5 to 30 bar with larger stationary phase particles (25 to 100 micron) and higher flow rates (10 to 300 mL/min), making it fast and cost-effective for purifying 0.1 to 10+ g samples per run in drug discovery and synthetic chemistry workflows. Preparative HPLC uses smaller particles (5 to 25 micron) at higher pressure (50 to 300 bar), providing higher chromatographic resolution for complex or closely similar compound mixtures at mg to low-g scale. For most synthetic chemistry purification, automated flash chromatography is the practical choice; use prep HPLC when flash resolution is insufficient.
Sample loading on normal-phase silica flash cartridges is roughly 1 to 5% of the silica mass for well-separated compounds and 0.5 to 1% for difficult separations. A 12 g silica cartridge handles approximately 0.06 to 0.6 g of sample; a 40 g cartridge handles 0.2 to 2 g; a 120 g cartridge handles 0.6 to 6 g. For larger loads (above 5 g), use 100 g to 300 g large-bed cartridges or multi-injection protocols. Overloading reduces resolution and peak sharpness -- confirm the recommended loading ratio for your specific separation before injection.
Standard automated purification systems include UV/Vis detection at fixed wavelengths (254 nm, 280 nm) or variable wavelength for compounds with a chromophore. Evaporative light scattering detection (ELSD) is added for compounds with poor UV absorbance, such as lipids, saturated alkyl chains, and carbohydrates. Mass-directed purification integrates an inline single-quadrupole mass spectrometer that triggers fraction collection only when the target molecular mass is detected, providing the highest selectivity for complex mixture purification. Confirm that the detection option matches your compound class before specifying a system.
Yes. Most modern automated purification systems support both normal-phase silica columns (for separation by polarity in organic solvent gradients such as hexane-ethyl acetate) and reversed-phase C18 columns (for separation by hydrophobicity in aqueous-organic gradients such as water-acetonitrile or water-methanol). Some systems automate column switching between normal and reversed-phase workflows in the same queue. Confirm that the system's solvent pump wetted materials, flow rate range, and detection wavelengths are appropriate for aqueous reversed-phase solvents if both modes are required.
Most automated flash purification systems are designed for use with prepacked cartridges (single-use or limited-use silica or C18 cartridges in standardized sizes). Prepacked cartridges provide consistent bed packing, eliminate the user-to-user variability of hand-packed columns, and reduce setup time. Some systems also accept refillable column housings packed with bulk silica for higher-throughput labs seeking to reduce cartridge costs. Confirm cartridge supplier compatibility -- some systems use proprietary cartridge connectors that restrict users to the manufacturer's own cartridges.
Mass-directed purification adds an inline mass spectrometer (typically single-quadrupole) to an automated prep HPLC or flash system, triggering fraction collection only when the target compound's molecular mass is detected in the eluate. This eliminates collection of impurities that co-elute with the target compound but have different masses -- useful when the target has similar UV absorbance to impurities, when the crude mixture is complex, or when maximum selectivity and purity in a single pass are required. Mass-directed systems are most common in drug discovery and natural product isolation workflows.
Yes. MBP provides quote-based procurement and purchase order support for automated purification systems for research and pharmaceutical laboratories in the USA and Canada. MBP is a registered vendor for Howard Hughes Medical Institute, Vanderbilt University, and MD Anderson Cancer Center. Contact MBP via the contact page or Quick Order portal with your purification scale, sample load, detection requirements, and column mode (normal phase, reversed phase, or both) for a prompt quote.
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