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.
Einfache dünnschicht-chromatographische Identifizierung von fetten Ölen, Wachsen und häufig verwendeten Salbengrundlagen. (TLC in the pharmacy. Simple TLC identification of fatty oils, waxes and often used base compounds of ointments.) Dtsch. Apoth. Ztg. 128, 1689-1693 (1988). TLC of fatty oils (extract of linseed and oils of avocado, peanuts, cacao butter, laurel, maize, almonds, olives, castor, safflor, sesame, sunflower) on paraffin- impregnated cellulose with acetic acid. Detection with iodine and spraying with 1% starch solution. TLC of waxes and other base compounds of ointments (e.g. white wax, cetaceum, artificial cetaceum, cetyl palmitate, glycerol monostearate, cetyl stearyl alcohol etc.) on silica with n-hexane - ether - acetic acid 90:10:1. Detection with 10% ethanolic molybdatophosphoric acid, heating for 5-10 min to 150°C, improvement of color development by treatment with NH3 chamber; 0.1% aq. solution of ammonium 8-anilino-naphthalene-1-sulfonate.
(Hungarian). Gyógyszerészet, 34, 201-201 (1990). TLC of alkylsulfides and allyl-thiolderivatives on silica with petrol ether – ether 80:2, on aluminium oxide with acetic acid – acetonitrile 25:75. Visualization under UV and/or by spraying with 50% sulfuric acid. Densitometry.
Chinese J. Chromatogr. (Sepu) 13, 156-160 (1995). TLC of the title material on silica with hexane - dichloromethane - ethyl acetate 4:5:1. Detection under iodine vapor. Study also by GC, GC-MS techniques.
Phytochemistry 21, 2475-2479 (1982). TLC of anti-tumor sesquiterpene lactones on silica with chloroform - methanol - ethyl acetate 8:1:1, 7:1:2 or 15:2:3 and ether - methanol 19:1 (developed twice). Purification of the crude plant extract by PLC and column chromatography.
Anal. Chem. 318, 243-244 (1984). DC-Optimierung der mobilen Phase für die säulen-chromatographische Trennung oxygenierter Terpene. (Optimization of the mobile phase for column chromatographic separation of oxygenated terpenes by TLC.) TLC of geranial, neral, methyl cinnamate, essential oil of dictamnus albus L on silica with pentane - ether 1:3. Detection by UV.
J. Chromatogr. 587, 351-345 (1992). TLC on silica with seven solvent systems. Hexane - methanol - ethyl acetate 85:10:5 was found to be the most suitable for the separation of lantadene A, B, C, D, reduced lantadene A and B. Detection by spraying with Liebermann-Burchard reagent, vanillin - sulfuric acid reagent, and pimulin.
Planta med. 65, 709 (1999). TLC on silica gel of betulinic acid and oleanolic acid with chloroform - methanol 20:1, and of pinoresinol and phillygenin with chloroform - acetone 20:1.
J. Liq. Chromatogr. Relat. Technol. 30, 2209-2219 (2007). HPTLC of artemisinin in Artemisia annua on silica gel with cyclohexane - ethyl acetate - acetic acid 20:10:1 in a twin-trough chamber saturated for 20 min. Detection by immersion in modified anisaldehyde reagent (20 mL acetic acid, 4 mL sulfuric acid, 2 mL of anisaldehyde in a mixture of 100 mL ethanol and 80 mL water) for 1 s. After 1 min the plate was heated at 100 °C for 12 min. Quantitative determination by fluorescence measurement at 520 nm with cut-off filter at 540 nm.