CAMAG TLC-MS InterfaceRapid extraction of compounds for online transfer into APCI-MS, APPI-MS or ESI-MS The versatile instrument to extract compounds from a TLC/HPTLC plate and feed into a mass spectrometer for substance identification or structure elucidation. CAMAG TLC-MS Interface can be connected to any brand of LC-coupled mass spectrometer.  | - Compatible with all common HPLC-MS systems
- Rapid and convenient extraction directly into your MS
- Identification of unknown substances
- Confirmation of target compounds
- Semi-automatic performance
- Reproducible results and detectability similar to HPLC-MS
- Compatible with most common TLC/HPTLC layers
- Extraction into vials for NMR or (ATR-)FTIR [12], static nanospray, direct
inlet EI-MS and MALDI - No more scraping off the plate
Brochure as pdfExamples, Applications |
Why a TLC-MS Interface? Surveys have shown that not all samples may be processed by HPLC-MS or HPLC-DAD systems due to no or low detectability of the compounds or impurities in the UV range, a heavy matrix load or a lack of MS compatible solvents. On the other hand HPTLC is another very fast and convenient method to separate samples. In the past unknown substances were scraped off from the TLC/HPTLC plate, eluted into a tube and transferred into the MS. Now a very convenient and universal TLC-MS Interface is available which can semi-automatically extract zones of interest and direct them online into any brand of HPLC-MS system. The interface is quickly and easily connected (by two fittings) to any LC-coupled mass spectrometer without adjustments or mass spectrometer modifications. Questioned substances are directly extracted from a TLC/HPTLC plate and sensitive mass spectrometric signals are obtained within a minute per substance zone. The interface extracts the complete substance zone with its depth profile and thus allows detections comparable to HPLC down to the pg/zone range. The interface has been proven to be one of the most reliable and versatile interfaces for TLC/HPTLC-MS coupling [1-13]. Principle The versatile instrument is used to isolate unknown compounds from a TLC/HPTLC plate and transfer them into a mass spectrometer for identification or structure elucidation. CAMAG TLC-MS Interface can be connected to any brand of LC-coupled mass spectrometer. - Plug & play installation by two HPLC fittings at a given HPLC-MS system
- Semi-automatic instrument involving automatic piston movement for pressure seal of the TLC/HPTLC zone on both glass plates and aluminum foils
- Extraction directly from the plate using a suitable solvent delivered by the HPLC pump
- Online transfer into the mass spectrometer
- Automatic cleaning of the piston between the extractions
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Technical functionality and requirements: The instrument extracts circular zones of 4 mm diameter from a TLC/HPTLC plate, e.g. with methanol or any other appropriate solvent, using the standard flow speed of the HPLC-MS system (e.g. 0.1 mL/min). Additional extraction head geometries for a reduced or an enlarged layer thickness [5, 12] or oval geometry [11] will be available. Materials: Plates or aluminum foils up to 20 x 20 cm can be positioned accurately and analyzed zone by zone. Automation: Semi-automatic instrument involving automatic piston movement, automatic cleaning of the piston, manual positioning and switching - Weight: approx. 11 kg
- Size: approx. 23 x 50 x 25 cm; size with optional
- large table is 40 x 50 x 25 cm (w x d x h)
- Requirements: 5 bar compressed air or N2,HPLC pump or HPLC-MS system
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Scheme: Extraction head (principle of Dr. Luftmann) |
Application example: Identification of a substance in a mixture (caffeine, paracetamol, acetylsalicylic acid)  | | Chromatogram with 4 mm bands | Same plate after extraction of spot RF 0.15 | Extracted spot identified as caffeine with MS (APCI ionisation); extraction and MS-measurement of this spot was achieved within 40 s |
Literature [1] H. Luftmann, M. Aranda, G. Morlock, Rapid Commun Mass Spectrom 21 (2007) 3772 [2] M. Aranda, G. Morlock, Rapid Commun Mass Spectrom 21 (2007) 1297 [3] M. Aranda, G. Morlock, J Chromatogr A 1131 (2006) 253 [4] M. Aranda, G. Morlock, J Chromatogr Sci 45 (2007) 251 [5] U. Jautz, G. Morlock, Anal Bioanal Chem 387 (2007) 1083 [6] U. Jautz, G. Morlock, J Chromatogr A 1128 (2006) 244 [7] G. Morlock, Y. Ueda, J Chromatogr A 1143 (2007) 243 | 8] A. Alpmann, G. Morlock, J Sep Sci 31 (2008) 71 [9] G. Morlock, W. Schwack, Anal Bioanal Chem 385 (2006) 586 [10] A. Alpmann, G. Morlock, Anal Bioanal Chem 386 (2006) 1543 [11] G. Morlock, U. Jautz, J Planar Chromatogr 21 (2008) 367 [12] G. Morlock, E. Dytkiewitz, J. AOAC Int. 91 (2008) 1237 [13 G. Morlock, F. BrŸmmer, A. Kloeppel, A. Kolm, CBS 102 (2009) 2-5 |
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