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.
TLC within the German Pharmacopoe. Deutsche Apotheker Zeitung 135, 2589-2594 (1995). General overview about sorbents, chambers, chamber saturation, sample applying, mobile phases, migration distances, development times, separation efficiency, detection, derivatization, evaluation and documentation. Official TLC-methods as directed in the DAB and alternative TLC-systems are described. 11 tables, 23 figures.
Arzneim.-Forsch./Drug Res. 45 (I), 190-194, (1995). TLC of 12 chloroethyl nitrosourea analogues of cholesterol on silica with dichloromethane, dichloromethane - hexane 7:3, dichloromethane - methanol 49:1. Detection under UV.
J. AOAC Int. 77, 1179-1183 (1994). TLC of fusarochromanone on silica with chloroform - methanol - NH3 45:5:1 or 40:10:1. Detection under UV 254 (limit 5 ng) of UV 366 nm (Detection limit 3 ng). Fusarochromanone gives a positive (turns pink) ninhydrin reaction; it turns yellow-green when sprayed with either 20% sulfuric acid in methanol or p-anisaldehyde solution. Detection limit of these 3 colorimetric reagents is 250 ng. Fusarochromanone is relatively unstable when exposed to fluorescent light; standards should be stored in the dark in the freezer.
J. Planar Chromatogr. 8, 134-140 (1995). TLC of the chloride, nitrate, or sulfate salts of nickel, cobalt, iron, cadmium, mercury, bismuth, thallium, lead, silver, uranyl, aluminium, thorium, copper, vanadyl, and zinc on silica, alumina, and lithium chloride impregnated silica and alumina with 1.0 M aqueous formic acid, 1.0 M formic acid - 1.0 M aqueous sodium formate 1:1 (pH 3.3) or 1.0 M aqueous sodium formate (pH 7.65). Visualization by use of the appropriate reagent.
Biochemical Systematics and Ecology 23, 213-222 (1995). TLC of carbohydrates on silica, impregnated with 0.5 M NaH2PO4 in water - methanol 3:1, with isopropanol - acetone - 0.1 M lactic acid 2:2:1.
J. Planar Chromatogr. 8, 310 - 313 (1995). Study of the chromatographic behavior of four groups of s-triazine derivatives (15 compounds) on aminoplast (a carbamide-formaldehyde polymer) and cellulose thin layers; methanol - aqueous acetic acid 3:2, methanol - acetic acid - acetonitrile 6:4:1, and methanol - NH3 3:2. The influence of mobile phase pH on the chromatographic retention was examined; also discussion of the influence of the chemical structure on the chromatographic behavior.
Biochemical Systematics and Ecology 23, 251-156 (1995). TLC of aloesin, aloe-resin A, aloin and aloinoside on silica with ethyl acetate - methanol - water 200:33:27. Identification under UV.
Phytochemistry 42, 809-814 (1996). TLC of various bayogenin glycosides on silica with chloroform - methanol - water 7:3:1 (bottom layer) or with ethyl acetate - methanol - water 8:2:1. Also HPTLC on RP-18 with 25 % acetonitrile. Detection with 10 % sulfuric acid.