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
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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.

      52 107
      Synthesis of 3-benzoyl-4-phenyl-2-pyrazolines by the reactions of chalcones with diazomethane
      A. L. TOKES, A. SZOLLOSY, G. TOTH, A. LEVAI

      Acta Chimica 112, 335-341 (1983). TLC of 3-benzoyl-4- phenyl-2-pyrazolines on silica with petrol ether - acetone 1:1.

      Keywords:
      Classification: 23
      67 235
      Thin-layer chromatographic method for the determination of SurfadoneTM QSP in formulated products
      R.M. IANNIELLO, (GAF Chemicals Corporation, Anal. Dep., 1361 Alps Road, Wayne, New Jersey 07470, USA)

      J. Liquid Chromatogr. 13, 1943-1957 (1990). TLC on silica with methanol - dichloromethane - acetic acid 6:3:0.75. Detection by dipping into iodoplatinate reagent. Quantification by densitometry at 525 nm. SurfadoneTM QSP (Dimethylsteramidopropyl[(2-pyrrolidonyl)methyl]ammonium chloride)

      Classification: 23, 35a
      87 062
      Data on the chromatographic behavior of solvent mixtures with similar solvent strength and selectivity
      E. HIDVEGI*, S. PERNECZKI, M. FORSTNER, (*Nat. Inst. of Forensic Toxicology, 1146 Budapest, Varannó u. 2-4, Hungary)

      J. Planar Chromatogr. 13, 414-419 (2000). OPLC of 13 benzodiazepines (alprazolam, brotizolam, carbamazepin, temazepam, chlordiazepoxide, cinolazepam, clobazam, clonazepam, diazepam, nitrazepam, midazolam, medazepam, prazepam) on HPTLC silica gel with 8 mobile phases (benzene - chloroform - nitromethane 492:313:195; chloroform - dichloromethane - methyl ethyl ketone 809:115:76; acetonitrile - chloroform - toluene 136:651:213; chloroform - ethyl acetate 825:175; acetone - chloroform-methanol 28:876:96; chloroform - dioxane - toluene 784:154:62; acetonitrile - chloroform - tetrahydrofuran 268:840:132; acetic acid - chloroform - n-butanol 95:862:43). Detection under UV; densitometry at 240 nm. According to the results Snyder's endogeneous solvent strength (Si), proton donator (Xe), proton acceptor(Xd), and dipole(Xn) parameters are not satisfactory for complete description of a solvent mixture used as mobile phase.

      Keywords:
      Classification: 2e, 23
      59 107
      (Comparative studies on physico-chemical properties of four porphyrin photosensitizers
      Y. LIU (Liu Yonglong), C. HOU (Hou Cuiying), SH. YANG (Yang Shilin), Y. BAI (Bai Yili), (Inst. Med. Plant Devel., Chinese Acad. Med. Sci., Beijing, P. R. China). Acta Pharm Sinica (Yaoxue Xuebao) 21, 823-828 (1986). (Chinese)

      Detection under UV light at 366 nm.

      Keywords:
      Classification: 23a
      75 108
      Composition of urinary coproporphyrin isomers I-IV in human porphyrias
      K. JACOB, M.O. DOSS, (Inst f. Klin. Chem. am Klinikum Großhadern der Univ. München, Marchioninistr. 15, D-81366 München, Germany)

      Eur. J. Clin. Chem. Clin. Biochem. 31, 617-624 (1993). TLC of porphyrin methyl esters (uroporphyrin, heptacarboxylic, hexacarboxylic, pentacarboxylic porphyrin, coproporphyrin) on silica with hexane - dichloromethane - acetone 41:41:18. Separation of coproporphyrins I-IV after hydrolysis by HPLC.

      Classification: 23a
      98 055
      The retention behavior of selected porphyrins on silica gel, polyamide, and cellulose TLC plates
      Joanna NOWAKOWSKA (Medical University of Gdansk, Faculty of Pharmacy, Department of Physical Chemistry, Al. Gen. J. Hallera 107, 80-416, Gdansk, Poland)

      J. Planar Chromatogr. 19, 393-397 (2006). TLC of uroporphyrin I, uroporphyrin III, coproporphyrin I, coproporphyrin III, and protoporphyrin IX (as methyl esters) on polyamide 11, cellulose and silica gel with methanol, ethanol, propanol, butanol, acetonitrile and tetrahydrofuran in a saturated chamber. Porphyrins on cellulose were detected by placing in iodine vapor for 5 min; on silica gel and polyamide 11 the porphyrins were detected as red spots in UV light at 254 nm. Chromatographic retention data and a possible retention mechanism are discussed.

      Classification: 23a
      64 202
      Conversion of indole-3-ethanol to fatty acid esters in Craterellus coruncopioides
      V. MAGNUS*, G. LACAN, S. ISKRIC, P. LEWER, E.T. APLIM, V. THALLER, (*Ruder Boskovic Institute, 41001 Zagreb, P.O. Box 1016, Yugoslavia)

      Phytochemistry 28, 2949-2954 (1989). TLC of tryptophol esters on silica with chloroform - benzene 1:1 and chloroform - ethanol 19:1. Visualization with p-dimethyl-aminobenzaldehyde-HCl reagent.

      Classification: 23c
      61 242
      Synthesis and anticonvulsant properties of N-methyl-pyridyl derivatives of m- and p-bromophenylsuccinimides
      A. ZEJC*, J. OBNISKA, E. CHOJNACKA-WOJCIK, E. TATARCZYNSKA, B. WICZYNSKA, (*Dep. of Pharmaceutical Chemistry, Medical Academy, Skaleczna 10, 31-065 Kraków, Poland)

      Polish Journal of Pharmacology and Pharmacy 39, 91-95 (1987). TLC or N-methylpyridyl derivatives of bromophenylsuccinimide on silica with chloroform - acetone 9:1. Visualization with 0.05M iodine in 10% HCL.

      Classification: 23d, 32a