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. Chin. Trad. Med. (Zhongguo Zhongyao Zazhi) 15, 360-362 (1990). TLC of cholic acid, deoxycholic acid, chenodeoxycholic acid on silica with isooctane - butyl acetate - acetic acid 4:2:1. Quantification by densitometry at 380 nm. R.S.D. <4.3%; recovery <96.0%.
Chromatographia 35, 252-236 (1993). Identification of lactic acid and ascorbic acid by TLC on cellulose with butanol - water- formic acid 6:2:1. Detection by spraying with bromocresol green. Determination of antioxidant synergists and ascorbic acid by reverse-phase HPLC.
Prostaglandins Leukotr Essent Fatty Acids 52, 223-227 (1995). TLC of hydroxy derivatives of arachidonic acid (12-hydroxyheptadecatrienoic acid and 12-hydroxyeicosatetraenoic acid), thromboxane B2, prostaglandins and phospholipids on silica with the upper organic phase of ethyl acetate - isooctane - acetic acid - water 11:5:2:10 or hexane - ether - acetic acid 80:30:1. Detection by exposure to iodine vapor. After marking the spots were scraped off and counted for radioactivity in a liquid scintillation counter.
Biochemical Systematics and Ecology 23, 781-785 (1995). TLC of hydroxamin acids on silica with hexane - acetone mixtures. Visualization under UV 254 nm and by dipping into 5 % methanolic FeCl3 or phosphomolybdic acid reagent.
seed oils. J. High Resol. Chromatogr. 20, 315-320 (1997). TLC of oils and fatty acid methyl esters (FAME) on silica gel with hexane - ether 7:3 or 8:2. Detection by spraying with phosphomolybdic acid (5% in ethanol) and heating at 100°C. Preparative TLC on silica gel impregnated with 100% silver nitrate in acetonitrile, with hexane - ether - acetic acid 90:9:1. Detection by spraying with 2,7-dichlorofluorescein and under UV. Analysis by GLC after elution. Identification by GC/MS and IR.
J. Planar Chromatogr. 14, 8-15 (2001). TLC of fatty acid esters on silica gel resp. silica gel/kieselguhr with hexane - acetone 49:1 and on aluminium oxide with hexane - acetone 100:1. 18 new agents have been used for visualizing 8 esters of higher fatty acids. Limits of detection (detectability, D), detectability index, and broadening index were determined for the esters after use of the visualizing agents. Bromophenol blue was the best and most universal detection agent.
J. Agric. Food Chem. 50, 701-705 (2002). Preparative TLC of 3,4-methylenedioxy cinnamic acid, cinnamic acid, pinostrobin, flavokawain, 5,7-dimethoxyflavanone on silica gel with hexane - acetone 4:1; 2 x 8:1, toluene - ethyl acetate 13:1, and hexane - ethyl acetate 8:1, 8:3. Detection under UV 254 and 366 nm.
Part III. Application of terms describing the separation of homologous series of saturated fatty acids in TLC. J. Planar Chromatogr. 16, 303-307 (2003). HPTLC of 19 fatty acids (from pentanoic to tricosanoic acid) on RP-18, with and without concentrating zones. The best chromatographic conditions for separation were on RP-18 without concentrating zone with methanol - water 9:1, 19:1 and ethanol - water 9:1, and on RP-18 with concentrating zone with methanol - water 9:1 and 19:1, 100% ethanol and ethanol - water 9:1 and 19:1. Visualization by exposure to iodine vapor. Optimization of separation conditions.