Cumulative CAMAG Bibliography Service CCBS
Our CCBS database includes more than 11,000 abstracts of publications. Perform your own detailed search of TLC/HPTLC literature and find relevant information.
The Cumulative CAMAG Bibliography Service CCBS contains all abstracts of CBS issues beginning with CBS 51. The database is updated after the publication of every other CBS edition. Currently the Cumulative CAMAG Bibliography Service includes more than 11'000 abstracts of publications between 1983 and today. With the online version you can perform your own detailed TLC/HPTLC literature search:
- Full text search: Enter a keyword, e.g. an author's name, a substance, a technique, a reagent or a term and see all related publications
- Browse and search by CBS classification: Select one of the 38 CBS classification categories where you want to search by a keyword
- Keyword register: select an initial character and browse associated keywords
- Search by CBS edition: Select a CBS edition and find all related publications
Registered users can create a tailor made PDF of selected articles throughout CCBS search – simply use the cart icon on the right hand of each abstract to create your individual selection of abstracts. You can export your saved items to PDF by clicking the download icon.
J. Planar Chromatogr. 2, 297-303 (1989). HPTLC of 10 fungicides (captafol, captan, cymoxanil, dichlofuanid, dithianon, folpet, iprodione, procymidone, vinclozolin, triadimefon) on prewashed silica (100 µm) with toluene - hexane - diisopropyl ether - ethyl acetate 667:20:8:5. Detection and quantitative determination by densitometry.
J. Hygienic Chem. (Eisei Kagaku) 37, 1-5 (1991). TLC detection of octyltin compounds from diper covers using 0.1% pyrocatechol violet solution as spray reagent. Identification as tri- and di-n-octyltin by GC-MS after derivatization to tetrasubstituted organotins with PrMgBr.
J. Planar Chromatogr. 7, 461-463 (1994). TLC on silica with benzene - ethyl acetate 10:1. Detection under daylight and UV 254 nm.
Dünnschicht-Chromatographie InCom Sonderband 1996, 157-165. HPTLC of benzo[g,h,i]perylene, indeno[1,2,3]pyrene, benzo[a]pyrene, benzo[b]fluoroanthene, benzo[k]fluoroanthene and fluoroanthene on caffeine-impregnated silica prewashed with dichloromethane, precooled for 30 min at -20 °C, with dichloromethane at -20 °C. After removal of the eluent the plates are dipped for 2 s into a solution of paraffin (low viscosity)/n-hexane 1:2 and dried again (for stabilization and intensification of the inherent fluorescence of the PAH). Quantification by densitometry.
CBS 88, 12-13 (2002). TLC of waste water samples or spinach extract on silica gel. Selective detection of bioactive compounds by dipping in suspension of luminescent microorganisms (Vibrio fischeri). Visual detection of substance zones by reduced luminescence.
J. Planar Chromatogr. 18, 388-390 (2005). TLC of haloperidol and metabolites on RP-18 previously equilibrated for 30 min with methanol containing 0.001 % triethylamine at 27 +/- 1 °C (room temperature). Detection by treatment with iodine vapor. Quantitative determination at 230 nm.
CBS 99, 14-15 (2007). HPTLC of acrylamide prechromatographically derivatized with dansulfinic acid on silica gel in a twin-trough chamber with ethyl acetate over 70 mm after focussing with methanol. Detection by dipping in a 25 % solution of propylene glycol in n-hexane. Quantitative determination by fluorescence measurement at 366/>400 nm. Precision (RSD, n=3 at 3 different concentration levels each) was 4.8 % and recovery (by standard addition) was 96 %. Linearity was between 0.1 and 0.4 µg/L. The limit of quantification was 0.08 µg/L acrylamide in drinking water. Comparison with HPLC-MS/MS showed comparable results for acrylamide in ground water.
Rapid Commun. Mass Spectrom. 24, 1721-1729 (2010). Ambient proximal probe thermal desorption (TD) sampling of substances from a HPTLC plate and coupled with secondary ionization by atmospheric pressure chemical ionization (APCI) or electrospray ionization (ESI). The method does not require a specialized ionization source. Different anaytical parameters and performance metrics are reported and the method covers a wide range of analyte types including explosives, dyestuffs, herbicides and pharmaceuticals.