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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of the European Academy of Dermatology and Venereology 13 (1999), S. 0 
    ISSN: 1468-3083
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK; Malden, USA : Blackwell Science Ltd/Inc.
    Contact dermatitis 50 (2004), S. 0 
    ISSN: 1600-0536
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: A 8 year old boy was seen in our department with a allergic contact dermatits to a temporary tattoo done at his arm 1 week before. It was the third temporary tattoo (called ‘henna’ tattoo) done over a 3 month period of school holidays. He was treated with topical corticosteroid and reobserved with an residual hypopigmentation. He was patch tested with our standard series with positive reaction to p-phenylenediamine; later test with ‘henna’ powder was negative. Temporary ‘henna’ tattoos are very popular, specially during holidays. Several cases are reported in the literature of sensitization to p-phenylenediamine, contained in the henna tincture, but few of these are pediatric cases. It is important to discouraged the use of these tattoos, due to the consequences that a sensitization to p-phenylenediamine could have in their future.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Contact dermatitis 36 (1997), S. 0 
    ISSN: 1600-0536
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of organic chemistry 41 (1976), S. 2769-2770 
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    World journal of microbiology and biotechnology 16 (2000), S. 691-694 
    ISSN: 1573-0972
    Keywords: Neutral trehalase ; Saccharomyces boulardii ; yeast
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract Lyophilized cells of the non-pathogenic yeast Saccharomyces boulardii are used in many countries for the treatment of several types of diarrhoea and other gastrointestinal diseases. Although the cells must be viable, their mechanism of action is unknown. The disaccharide trehalose is a protectant against several forms of environmental stress in yeast and is involved in maintaining cell viability. There is no information on the enzymes involved in degradation of trehalose in S. boulardii. The aim of the present study was to characterize trehalase activity in this yeast. Cells of S. boulardii grown in glucose exhibited neutral trehalase activity only in the exponential phase. Acidic trehalase was not detected in glucose medium. Cells grown in trehalose exhibited acid and neutral trehalase activities at all growth stages, particularly in the exponential phase. The optimum pH and temperature values for neutral trehalase activity were determined as 6.5 and 30 °C respectively, the half-life being approximately 3 min at 45 °C. The relative molecular mass of neutral trehalase is 80 kDa and the K m 6.4 mM (±0.6). Neutral trehalase activity at pH 6.5 was weakly inhibited by 5 mM EDTA and strongly inhibited by ATP, as well as the divalent ions Cu++, Fe++ and Zn++. Enzyme activity was stimulated by Mg++ and Ca++ only in the absence of cAMP. The presence of cAMP with no ion additions increased activity by 40%.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The crystal structure and absolute configuration of the title compound, C17H21BrO8, have been determined by X-ray analysis. They confirmed the 1′R absolute configuration at the 1′-bromoethyl moiety which has been assigned previously on the basis of chemical and spectroscopic data. Cohesion of the crystal can be attributed to weak intermolecular C—H...O and van der Waals interactions.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary The synthesis of α,ω-di-tert—chloropolyisobutylenes(chlorinetelechelic PIB's) have been accomplished at −30°C by the use of “sterically hindered inifers”. A suitable sterically hindered binifer is 1,3-di(2-chloro-2-propyl)-5-tert -butylbenzene, m-tBuDCC, i.e., a binifer in which the bulky tert-butyl group prevents undesirable intramolecular alkylation with concomitant proton elimination. Conventional binifers i.e., 1,4-di(2-chloro-2-propyl)benzene (p-dicumyl chloride, pDCC) give rise to this unacceptable side reaction unless the inifer process is carried out at −80°. The use of m-tBuDCC leads to satisfactory telechelic PIB's with number average end functionalities (¯Fn) of 2.0±0.1. The ¯fn and ¯Mn of the products are unaffected by temperature in the −30 to −80°C range. In the absence of the bulky tert-butyl group in the inifer, i.e., with 1,3-di(2-chloro-2-propyl)benzene, mDCC, severe indanyl ring formation occurs.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary Linear and three-arm star telechelic polyisobutylenes PIB's with perfect end-functionalities (¯Fn = 2.0±0.1 or 3.0±0.1) have been synthesized by the use of 1,3-di(2-bromo-2-propyl)5-tert-butylbenzene (m-tBuDCB) binifer or 1,3,5-tri(2-bromo-2-propyl)benzene (TCB) trinifer/BCl3 systems. The counter anion is most likely BCl3BrΘ in these polymerizations. The inifer efficiencies of these brominated inifers are lower than those of the chlorinated analogues, probably because of side reactions during the polymerization. The rate of chain transfer to inifer is similar for both the chlorinated or brominated inifer/ BCl3 systems but that of termination is faster in the former system. Elementary analysis shows that the PIB's obtained with m-tBuDCB carry 90% bromine and 10% chlorine end groups.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 2685-2697 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of chain transfer to the bifunctional initiating and transfer agents (binifers) 1,4-di(2-chloro-2-propyl)benzene (p-DCC), 1,3-di(2-chloro-2-propyl)-5-tert-butylbenzene (m-tBuDCC), and 1,3-di(2-chloro-2-propyl)-4,6-dimethylbenzene (m-DMeDCC) in the polymerization of isobutylene has been investigated. Chain transfer to monomer was shown to be absent up to -20°C in CH3Cl/n-hexane and CH2Cl2/n-hexane mixtures using the m-tBuDCC/BCl3 binifer system. Chain transfer constants (Ci) to m-tBuDCC and kt/kp ratios determined in the range from -30°C to -80°C in CH3Cl/n-hexane mixtures and pure CH3Cl solvent are reported, and the activation energy differences Etr,l - Ep and Et - Ep were calculated. Chain transfer constants to p-DCC and m-DMeDCC were determined by the use of pure CH3Cl diluent at -50°C. The chain transfer reactivity of five different inifers is discussed and compared based on CI values obtained under identical conditions, with special regard to the new, sterically hindered binifer m-DMeDCC of extraordinary reactivity.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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