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.

      55 013
      Chinese Anal
      Z. MAO, Q. ZHANG

      Chem. (FENXI HUAXUE) 12, 455-458 (1984). (Chinese). (Studies on micellar solution as mobile phase in liquid chromatography. I. Use in thin-layer chromatographic separation of drugs). TLC of 33 drugs including sulfanilamides, vitamin B, antipyretics and adrenalines on polyamide with micellar aqueous solutions (SDS). Detection by various staining reagents and by UV.

      Classification: 3b, 32c
      59 019
      Neue wasserbenetzbare HPTLC RP-18 Fertigplatten
      W. JOST, H.E. HAUCK

      GIT Fachz. Lab. 12, 1221-1223 (1986). Neue wasserbenetzbare HPTLC RP-18 Fertigplatten. New HPTLC RP-18 pre-coated plates wettable by water.) Description of a new HPTLC precoated plate based on silica gel with a reduced degree of modification with octadecyl groups. This plate material is fully wettable with methanol - water mixtures between 0:100 and 100:0. Running times for 50 mm are between 14 and 40 minutes, whereby the maximum running times occur with the 50:50 mixture. Separations of nicotinic acid - isonicotinic acid, of analgesics and of alkaloids.

      Keywords:
      Classification: 3b, 22, 32b
      60 112
      Enantiomeric separation of N-carbamyl-tryptophan by thin-layer chromatography on a chiral stationary phase
      L.K. GONT, S.K. NEUENDORF, (INCELL Corp., 1600 W. Cornell, Milwaukee, WI 53211, USA)

      J. Chromatogr. 391, 343-345 (1987). TLC of N-carbamyl-D, L-tryptophan on silica containing a chiral stationary phase, 2S, 4R, 2'RS-4-hydroxy-1- (2-hydroxydodecyl) proline, and copper(II) with water - methanol system at reduced temperature. Detection by spraying with Ehrlich's reagent and heating at 105 °C for 5 min Sensitivity, 100 mg/mL.

      Keywords:
      Classification: 3b, 18a
      65 024
      Variation of stationary phases in planar chromatography
      T.J. GOOD*, A.G. TAKETOMO, (*CERA, 14180F Live Oak Ave., Baldwin, Park, CA 91706, USA)

      J. Planar Chromatogr. 2, 383-386 (1989). TLC separation of dyes and plant pigments on different modified silica stationary phases (cyclic diols, cyanopropyl, carboxylic ester) with toluene, isooctane - methanol - diethylether 7:1:2 as mobile phase and three methods of development - traditional vertical tank, experimental horizontal sandwich apparatus and an experimental over-pressure device. - The variation of the stationary phase can be used to gain selectivity advantages in chromatographic separations.

      Classification: 3b, 30
      67 020
      Use of bonded phases in planar chromatography
      M. GOULD, TH. ENZWEILER, (EM Sci., Cherry Hill, NJ 08034 USA)

      Chem. Anal. (N.Y.) 108, 15-47 (1990). A review with 8 references on the use of surface-modified reversed phase sorbents for HPTLC. Discussion of the surface reactions. Application in the separation of cholesterol and its bile acid metabolites and a mixture of steroids.

      Keywords: review
      Classification: 3b, 13c
      68 202
      Reversed phase thin-layer chromatographic separation of heavy metal ions on Polichrom A porous polymer
      B. GAWDZIK*, D.S. GAJBAKYAN, T. MATYNIA, A.R. SARKISYAN, (*Dept. of Chem., Maria Curie-Sklodowska Univ., pl. Marii Curie-Sklodowskiej 3, 20031 Lublin, Poland)

      J. Planar Chromatogr. 3, 280-282 (1990). TLC of Re, Mo, V, W on Polichrom A (a copolymer of mixed 1,4- and 1,5-di(methacryloyloxymethyl)naphthalene and styrene with starch, dextrin of a polyvinyl alcohol containing 10-14% acetate groups as binder), with 0.5 hydrochloric acid - ethanol 9:1 as mobile phase. Detection by spraying first with a saturated solution of tin chloride in conc. HCl and second with a saturated aqueous solution of ammonium rhodanide.

      Classification: 3b, 33a
      71 201
      The possibilities of optical isomer separation by TLC on layers of chitin and its derivatives
      J.K. ROZYLO, I. MALINOWSKA, (Fac. of Chem., M. Curie-Sklodowska Univ., 20-031 Lublin, Poland)

      J. Planar Chromatogr. 6, 34-37 (1993). Use of chitin and derivatives prepared by treatment of chitin with transition metals for the separation of optical isomers of amino acids: good separation on chitin-Cu with binary or ternary mixtures of organic solvents. The dependence of hRf values on the composition of the mobile phases has been demonstrated.

      Keywords:
      Classification: 3b, 38
      75 201
      Resolution of amino acid racemates on borate-gelled guaran-impregnated silica gel thin-layer chromatographic plates
      V. MATHUR, N. KANOONGO, R. MATHUR, C.K. NARANG, N.K. MATHUR*, (*Dept. Chem., INV Univ., Jodhpur - 342003, India)

      J. Chromatogr. 685, 360-364 (1994). TLC of amino acid racemates on the title plates with 1) 2-propanol - water 7:3, 2) phenol - water 4:1, 3) butanol - acetic acid - water 3:1:1. Detection by spraying with 0.1% ethanolic ninhydrin solution and heating for 5 minutes at 90 °C. Discussion of the enantiomeric separation mechanism.

      Keywords:
      Classification: 3b, 18a, 38