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.
Phytochem. Anal. 30, 218-225 (2019). HPTLC of flavonoids in red wine, apple juice and rose flowers on silica gel with ethyl acetate – methanol – formic acid 90:10:1. Glycosylated flavonoids were identified by inorganic matrix‐assisted laser desorption ionisation time‐of‐flight mass spectrometry (MALDI‐TOF‐MS).
Phytochemistry 23, 2501-2503 (1984). TLC of lacinilenes, scopoletin and cadalene derivatives on silica with chloroform - acetone - formic acid 80:19:1, acetonitrile-chloroform 4:1 and hexane - ethyl acetate - methanol 60:40:1. Detection by UV. Fluorodensitometric quantification (excitation at 366 nm).
(The flavonoids of doronicum grandiflorum). (French). Biochemical Systematics and Ecology 14, 191-193 (1986). TLC isolation and identification of the flavonoid compounds of D. grandiflorum La. on polyamide DC 6 and DC 11 with benzene - methanol - MEK 4:3:3 or 50:25:25 for flavones and with water - methanol - MEK - C5H8O2 30:15:10:4 for flavonols.
Journal of Natural Products 50, 357-359 (1987). TLC of quercetin-3-O-rhamnobioside, hyperoside, luteolin-6-C- glucoside on silica with chloroform - ethyl acetate 19:1. Visualization under UV after spraying with 1% ceric sulfate in 2N sulfuric acid.
J. of Natural Products 51, 966-968 (1988). TLC identification of (5-hydroxy-6,7,3',4',5'-penta-methoxyflavone) on silica with butanol - benzene 2:8. Visualization under UV and by spraying with 10% SbCl3 in chloroform.
HPTLC of flavonoid glycosides on silica with ethyl acetate - formic acid - water 6:1:1. Detection by spraying with 1% methanolic solution of ethanolamine diphenylborate and 5% ethanolic solution of polyethylene glycol 400, and under UV 360 nm. Quantification by densitometry at 445 nm.
macraei. Biochemical Systematics and Ecology 19, 53-57 (1991). TLC of acetylenic compound, di-, tri- and sesquiterpenes, chromone and flavonoids on silica with petrol ether - ethyl acetate 9:1, 3:2 and 2:3 or with chloroform - methanol 19:1 and 9:1. Compounds identified by spectroscopic methods (UV, IR, NMR, MS) and/or cochromatography with authentic samples.
Untersuchungen zur Stabilität von Kamille-Handelspräparaten. (Investigation on the stability of camolmile preparations.) Deutsche Apotheker Zeitung 132, 462-468 (1992). TLC of ether extracted oils (chamazulene, cis-En-In-dicycloether, Trans-En-In-dicycloether, bisabolol, bisabololoxid A, bisabololoxid B, matricin) on silica with dichloromethane – ethyl acetate 46:1. TLC of flavonoids (herniarin, umbelliferon, apigenin, apigenin-7-glycoside) on silica (2D). First dimension: ethyl acetate – MEK – water – formic acid 20:10:1:1; drying at 40°C for 20 min. Second dimension: toluene – ethyl acetate – formic acid 24:6:1. Detection of ether extracted oils with anisaldehyde reagent R DAB 9 and heating at 105 °C for 5 min; of flavonoids with Naturstoff-A reagent.