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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    International archives of occupational and environmental health 41 (1978), S. 125-138 
    ISSN: 1432-1246
    Keywords: Amylphenol ; Biological monitoring ; Butylcatechol ; Butylphenol ; Isopropylcatechol ; Methylcatechol ; Nonylphenol ; Octylphenol ; Phenylphenol ; Urinalysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary GLC systems are developed for quantitative urinalysis of leucodermogenic phenols and catechols, i. e., p-tert.-butylphenol, p-tert. Amyphenol, p-octylphenol, p- and o-phenylphenol, 3- and 4-methylcatechol, 3-isopropylcatechol, and 4-tert.-butylcatechol. The systems were successfully applied for the exposure assessment of the workers in factories producing p-tert.-butylphenol, p-octylphenol and/or 4-tert.-butylcatechol. In accordance with estimated exposure intensities, the concentrations in the urine of product packers were higher than those of plant operators and engineers. The levels were reduced by the improvement of hygienic conditions in the workshops. Importance of biological monitoring is discussed in relation with the possible skin penetration. From the data obtained, BP concentration in urine, 2 μg/ml, is tentatively proposed as a urinary biological threshold limit value to prevent leucodermogenic effect.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    International archives of occupational and environmental health 73 (2000), S. 449-456 
    ISSN: 1432-1246
    Keywords: Key words Acetone ; Biological monitoring ; Hexane ; 2 ; 5-Hexanedione ; Toluene ; Ethyl acetate ; Urinalysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Objective: To investigate whether metabolic interactions exist between hexane (HEX) and other solvents when co-exposed at the levels below occupational exposure limits. Methods: Workers, 219 men in ten workshops in total, volunteered to participate in the study. They were occupationally exposed to mixtures of HEX and one or more of toluene (TOL), ethyl acetate (EA) and acetone (ACE). Time-weighted average intensity of vapor exposures was monitored by diffusive personal sampling. `Free'- and `total'-2,5-hexanedione (HD) levels in the end-of-shift urine samples were determined by gas chromatography (GC) before and after acid hydrolysis of urine, respectively, and expressed as observed (HDob) or after correction for creatinine concentration (HDcr) or urine specific gravity (HDsg). Possible interaction was examined by multiple regression analysis (MRA), taking either free- or total-HD as a dependent variable, and the four solvent concentrations as independent variables. Results: In most cases, exposure intensity did not exceed the current occupational exposure limits even when additiveness was assumed. In addition that HEX was the most influential independent variable in all cases as expected, the MRA showed that, in cases of free-HD, ACE was also influential to HDob although weakly, but not to HDcr or HDsg. With regard to total-HD, ACE was weakly influential to HDob and HDsg, and EA also weakly to HDcr. The effect of ACE on free- or total-HD was not detected, however, when 22 men exposed only to HEX and ACE were subjected to the same analysis. Similarly, the effect of EA on total-HD was not observed among the remaining 197 men exposed to HEX, TOL and EA only. Conclusions: When the exposures were below occupational exposure limits, the free-HD levels in urine after HEX exposure will not be modified by co-exposures to TOL, EA or ACE.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 5 (1971), S. 935-938 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectra of N-iminopyridinium betaines, which have been generated within the ion source by pyrolysis of the corresponding hydrochlorides, have been compared with those of pyridine N-oxides.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 5 (1971), S. 389-396 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectra of various N-aryliminopyridinium and isoquinolinium betaines have been recorded. The most prominent fragmentation process of these compounds is N-N bond cleavage with the charge retention on both the pyridine and aryl fragments. An ortho-effect has been observed in the mass spectrum of N-o-nitrophenyliminopyridinium betaine (IXa).
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 5 (1971), S. 1383-1390 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectral fragmentation of N-arylsulphonyliminopyridinium betaines has been rationalized using high resolution mass spectrometry as well as deuterium labelling. The most characteristic features are a very facile N—S bond cleavage and skeletal rearrangements accompanied by the expulsion of SO2 from the molecular ion and the [M—1] ion to the corresponding ionized N-aryliminopyridinium betaines and azacarbazoles, respectively. The presence of methyl substituents at the α-position of the pyridine ring has a significant effect on the mode of the fragmentation.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 5 (1971), S. 61-71 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectral fragmentation behaviour of N-acyliminopyridinium and isoquinolinium betaines has been investigated. Major fragmentations of the pyridinium betaines can be rationalized in terms of charge localization on the pyridinium nitrogen. The most prominent process is α-cleavage followed by loss of NCO to furnish a pyridine ion. The electron-impact induced fragmentation of N-benzoyliminopyridinium betaine (I) was compared with that of thermolysis. The completely analogous behaviour has been observed in the corresponding isoquinolinium betaines.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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