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  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 23 (1985), S. 899-902 
    ISSN: 0749-1581
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The intrinsic ASIS of the C-8, C-9 and C-10 methyl protons of camphor in 14 hydrocarbon solvents have been calculated using intrinsic ASIS values of the TMS protons. The intrinsic ASIS of the methyl groups show excellent correlation among themselves and, therefore, can be factored into independent solute and solvent factors UiVα. The solute factors, Ui, depend on the position of the methyl group with respect to the polar carbonyl group. The solvent factors, Vα, correlate with the benzene ring concentration of the aromatic solvents measured by d/M, which is in accordance with a general solvation mechanism but not with the formation of specific solute-solvent complexes.
    Additional Material: 3 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 14 (1987), S. 549-553 
    ISSN: 0887-6134
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A GC-MS procedure has been developed for the quantitation in plasma and urine of rimantadine, an antiviral drug effective against type A influenza. The assay utilizes selective ion monitoring, methane negative ion chemical ionization (NCI) and stable isotope dilution. Sensitivity to NCI is effected by derivation of rimantadine with pentafluorobenzoyl chloride. The method has been used to quantitate plasma concentrations of rimantadine over a range from 4.2 ng/ml to 416 ng/ml, and urinary concentrations of rimantadine over a range of 21 ng/ml to 2077 ng/ml.
    Additional Material: 4 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 19 (1996), S. 111-116 
    ISSN: 0935-6304
    Keywords: Polynuclear aromatic hydrocarbons ; Liquid chromatography ; Alcohols ; Micelles ; Enviromental samples ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A method for the separation of polycyclic aromatic hydrocarbons (PAHs) by high-performance liquid chromatography using a hybrid micellar mobile phase is described. The detection of PAHs was carried out using the fluorescence method with programmable excitation and emission wavelength. The method is applied to the analysis of several environmental samples (sea water, sediments, limpets, sea worms) and several of these compounds are quantitated at concentration below 70 ng L-1(kg-1) in the original samples.
    Additional Material: 4 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 19 (1996), S. 559-563 
    ISSN: 0935-6304
    Keywords: Pesticide residue analysis ; Solid phase extraction ; Ground water ; Surface water ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A critical study of a solid phase extraction method using C18 SPE columns for the determination of 23 halogenated pesticides is presented. Type of sorbent, sorbent mass, flow rate in the extraction process, sample concentration of the different compounds, sample volume, pH, ionic strength and type of water were evaluated. Recoveries of pesticides under study yield a linear relationship, except for conazole fungicides and captan. Losses can be expected for heptachlor, aldrin, and captan. Sample volume and flow rate of extraction affect recoveries. Matrix effects from surface and groundwaters were observed. Recoveries for vinelozolin and dieldrin from groundwater were lower than those obtained from nanopure water. In river water losses of these compounds are higher. Captan and penconazole were not present and high losses were obtained for trifluralin, α-BHC, γ-BHC, tri-allate and chlorpyriphos. Impurities arising from the sorbent materials of cartridges have been detected.
    Additional Material: 6 Tab.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 19 (1996), S. 585-587 
    ISSN: 0935-6304
    Keywords: Enantioselective gas chromatography ; Volatiles ; 2-Heptanol ; Ethyl benzoate ; (E)-Hex-2-enal ; 1-Terpinen-4-oI ; Rubus glaucus ; Rosaceae ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 20 (1997), S. 591-596 
    ISSN: 0935-6304
    Keywords: Pesticide residue analysis ; Solid phase extraction ; Water analysis ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A critical study using C18 SPE columns for the determination of organophosphorus, triazine, and triazole-derived pesticides, nap-ropamide, and amitraz is presented. The type of sorbent, sorbent mass, flow rate in the extraction process, sample concentration of the different compounds, sample volume, pH, and ionic strength were evaluated. Special emphasis was placed on the evaporation step of eluates prior to GC determinations and on prefiltration of sample waters. Pesticide recovery is linear over a wide range of concentrations for most of compounds under study. Under general extraction conditions losses can be expected for amitraz, pro-metryn, prometon, dimethoate, penconazole, and propiconazole. At 100 ng L-1, enhanced responses are produced for mevinphos, simazine, malathion, triadimefon, methidathion, and phosmet, which can be attributed to matrix effects. At basic pH, recovery of prometon, prometryn, and penconazole are improved. Low flow rates and high ionic strength enhance the recovery of prometon and prometryn. For phosmet, the influence of sample volume was established. Likewise, the influence of sorbent quantity was established for phosmet and dimethoate. Losses during the evaporation step were observed for mevinphos, dimethoate (〉 50%), penconazole, propiconazole, and prometon (30%). Prefiltration of sample waters did not cause significant variations in the whole process of extraction. Impurities arising from the sorbent materials were not detected.
    Additional Material: 6 Tab.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 21 (1998), S. 509-512 
    ISSN: 0935-6304
    Keywords: Cholesterol oxidation ; gas chromatography ; oxysterols ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---The performance of a fused silica column coated with 50% phenyl-/50% dimethyl-polysiloxane, characterized by a high thermal stability, was evaluated for the gas chromatographic determination of cholesterol oxidation products. A silylated mixture of eighteen oxysterol standards (0.1 mg/ml of each compound) was injected into the gas chromatographic system. The temperature was programmed from 230 to 260°C at 2.5°/min and then to 290°C at 1°/min; the injector and detector temperatures were set at 325°C, and the gas linear velocity was 22.8 cm/s. The column gave a fast (15 min) and satisfactory resolution of the main cholesterol oxides. Good separation of the hydroxy from the epoxy derivatives was achieved.The suitability of the method for the determination of oxysterols in food matrices was successfully tested on a saponified lipid extract from egg yolk powder, previously enriched and purified by NH2 solid phase extraction.
    Additional Material: 3 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 12 (1989), S. 491-493 
    ISSN: 0935-6304
    Keywords: Capillary column gas chromatography ; Lidocaine ; Plasma level ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Microcolumn Separations 3 (1991), S. 289-301 
    ISSN: 1040-7685
    Keywords: cryogenic concentrator ; injector/trap ; large-volume injection ; twodimensional capillary gas chromatography ; mass spectrometry ; matrix-isolation FT-IR ; perfume analyses ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A versatile sample introduction system or injector/trap (I/T), described in this paper, is a stand-alone, computer-controlled, cryogenic concentrator with provisions for solvent venting and inert sample transfer. The I/T is designed to provide a common interface between the column and a variety of sampling modules.Modules to perform thermal desorption and pyrolysis, as well as modules for remote sampling (pre-traps) have been developed. Large volumes of either gaseous or liquid samples can be introduced by means of pre-traps packed with suitable substrates. Pretraps packed with Tenax TA allowed quantitative recovery of compounds as volatile as n-decane (n-C10) when contained in a 1-mL volume of pentane. The introduction of a 1-mL sample makes it possible to reach a detection limit of ca. 100 ppt,ppt, ppb, ppm refer to parts-per-trillion (1012), billion (109), and million (106), respectively. with an FID, for compounds with boiling points ≥n-C9.The capability to do trace analyses with the I/T is enhanced by interfacing it to a twodimensional gas chromatograph (2D/GC) equipped with a mass-selective detector (MSD) and a matrix isolation fourier transform infrared spectrometer (MI FT-IR). The resulting instrumentation greatly facilitated the identification of organic compounds present at ppbconcentrations in perfume samples.
    Additional Material: 11 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 17 (1994), S. 827-830 
    ISSN: 0935-6304
    Keywords: HPLC ; Fluorimetric detection ; UV detection ; Proteins of animal origin ; Lysinoalanine ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: This work suggests an HPLC method for qualitative and quantitative determination of Nε(2-amino-2-carboxyethyl)-L-lysine (LAL). LAL was released from total hydrolysates of various proteins of animal origin and derivatized with dansyl chloride. The performance of two different columns, Spherisorb 3S TG and μ-Bondapack C18, was compared; better resolution and quantitative response were obtained with the former. The mobile phase was a mixture of 0.01 M phosphate buffer (pH 7) and acetonitrile. Linear response and quantitative repeatability were tested for both detectors used (UV-Vis set at 254 nm; fluorimetric set at λex(max) = 360 nm and λem(max) = 525 nm).For LAL standard the minimum detectable amount was 0.05 ng, whereas for LAL in actual samples the amount was 0.5 ng (40 μg/g of analyzed proteins). Good analytical repeatability was obtained, resulting in CV % of 4.7 and 3.8 for UV and fluorimetric detectors, respectively. LAL recovery was determined using both detectors; the values obtained were 94 % (fluorimetric) and 92 % (UV). Greater noise levels were observed with the fluorimetric detector and its higher sensitivity could not, therefore, be fully utilized. The highest amounts of LAL were found in the casein (2816 μg/g) and cooked albumin (615 μg/g) samples.
    Additional Material: 3 Ill.
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