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
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J. Planar Chromatogr. 2, 346-354 (1989). Review of the application of HPTLC in environmental, agricultural areas, toxicology, organic and polymer research, illustrating trace quantitative capabilities, high sample through puts, simple visualization, the ability to handle relatively „dirty“ sample matrices with minimal sample clean-up and the ability to help solve difficult analytical problems. Applications are monitoring airborne reactive chemicals, compound stability studies, agricultural formulation research, characterization of polymers and copolymers and screening of surfactants in latex by HPTLC.
J. Liq. Chrom. & Rel. Technol. 26, 2751-2761 (2003). TLC of nonionic surfactants (Arkopal N40, 50, 60, 80, 90, 100, 130, 150, 230, 300, Sapogenate T60, 100, 110, 130, 138, 180, 300, 500) on zein-coated aluminium oxide prepared by dissolving 0.5 g zein in a mixture of 160 mL propanol and 40 mL water and adding to 20 g aluminium oxide, removal of the solvents at 70°C in vacuum and coating of plates with a suspension of 5 g of stationary phase and 14 mL water. Bidistilled water and water - methanol mixtures containing 5, 10, and 15 vol.% methanol were used as stationary phases. Developments were also carried out in aqueous solutions of 0.5, 1.0, 2.0, 3.5, 4.0, and 5.0 M LiCl, as well as e.g. aqueous solutions of 4 M NaCl, 4 M KCl, 4 M RbCl, 4M NH4Cl etc. After drying at 105°C, the surfactants were detected by exposure to iodine vapor.
(Japanese) (Studies on the analysis of various detergents. I. Identification of surfactants in heavy duty liquid laundry detergents by two-dimensional thin-layer chromatography.) TLC combined with other techniques as identification method for surfactant components. Two-dimensional TLC of nonionic and anionic surfactants on silica with 1) MEK - benzene - ethanol - water 3:6:3:1, 2) 4-methyl-2-pentanone -1-propanol - acetic acid - acetonitrile 20:6:1. 6:1. Detection by UV, IR and NMR.
J. Planar Chromatogr. 3, 77-78 (1990). Quantitative TLC determination of Polidocanol (mixture of monolauryl ethers of polyethyleneglycols) on silica with dichloromethane - methanol 15:2 with traces of water as eluent. After drying immersion for 2 s in Dragendorff’s reagent. Quantification by densitometry (absorbance at 550 nm). Recoveries for gel 99.85 % and for ointments 103.4 %; reproducibilities 2.9 % and 1.8 % resp.
J. Liq. Chrom. & Rel. Technol. 22, 1247-1256 (1999). HPTLC of surfactants (Jugopon, Texapon N 25, Rewoquat WE 20, W 75, Brij 35, Tenzilin AA 65) on silica gel with ethanol and ethanol - water mixtures with up to 20% of water as mobile phase. Detection by reaction with i.a. methylene blue and bromophenol blue and by dipping into water after development. Only anionic surfactants gave white spots with gas bubbles (rarely and slightly some nonionic surfactants, and never cationic). Therefore, this occurrence can be used for detection (and identification) of anionic surfactants, and for determination of polarity of surfactants.
Detection limit 300 -1000 ng for BHA, BHT and PG, resp. Also GC.
Kautschuk + Gummi - Kunstoffe 41 (9) 875-881 (1988). TLC of antioxidants IPPD (N-isopropyl-N'-phenyl-p-phenylene-diamine), 6PPD (N-1,3-dimethyl-butyl-N'-phenyl-diamine), N,N'-diaryl-PPD (N,N'-diaryl-p-phenylene-diamine) and TMQ (2,2,3-trimethyl-1,2-dihydroquinoline) on silica with chloroform - hexane - methanol - acetic acid 15:6:1:1. To remove plasticizers the TLC plate is chromatographed twice with petrol ether first. Detection by multi-wavelength scanning of UV absorbance at 240, 280, 320, 360 nm and visually by spraying with 3% ethanolic solution of 2,6-dichloroquinone-4-chlorimide. Additionally identification by recording of UV spectra. A further mobile phase system (toluene - hexane - methanol 29:15:6) is mentioned.
J. Planar Chromatogr. 15, 294-298 (2002). TLC of 8 N-phenylsuccinimide derivatives on silica gel and on silica gel impregnated with paraffin with n-hexane - dioxane and n-hexane - acetone resp. acetone - water in different ratios. Visualization under UV 254 nm. The RP TLC method can be successfully used for separation of the succinimide derivatives.