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  • 1
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 225 (1970), S. 547-548 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Reference bradykinin and its 1-alanine analogue (H?L-Ala?L-PrO?L- Pro?Gly?L-Phe?L-Ser?L-PrO?L-Phe?L-Arg?OH) were synthesized4 by the Merrifield solid phase method5; samples of synthetic bradykinin and other analogues6 were supplied by Dr E. Schroder, Haupt-laboratorium der Schering AG, Berlin. The ...
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 23 (1967), S. 884-885 
    ISSN: 1420-9071
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Zusammenfassung Es wird die Anwendung radioaktiven Phosphanilsäure-Rinderserum-Albumins zur kontinuierlichen Messung von Änderungen der Gefässwandpermeabilität beschrieben.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 8 (1964), S. 1919-1919 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. 1991-2002 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Infrared spectra indicate that carboxyl-substituted acrylic copolymers react appreci8bly with a butylated melamine-formaldehyde resin when heated at 120°C. for 30 min., but under these conditions acid catalysis is needed before epoxy- or amido-substituted copolymers will crosslink with the melamine-formaldehyde resin. Two methods have been used to synthesize hydroxyl-substituted acrylic copolymers. First, a glycidyl methacrylate copolymer was reacted with diethplamine. Second, an acrylic acid copolymer was heated under reflux with butylene oxide in the presence of a basic catalyst. This second method was used to esterify a vinyl toluene-acrylic acid-acrylamide copolymer which was subsequently treated with paraformaldehyde. The resulting hydroxy-methylolamido copolymer intercondensed when heated at 120°C. for 30 min., somewhat as did the hydroxy copolymer with melamine-formaldehyde resin blends.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 8 (1964), S. 1777-1786 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The development of a methylolacrylamide-styrene copolymer into a product suitable for use as a general-purpose industrial or appliance enamel has been described; the choice of a suitable means of plasticization is emphasized. The incorporation of ethyl acrylate in the copolymer is expensive and was found relatively inefficient. Plasticization by blending the copolymer with tricresyl phosphate, butyl cyclohexyl phthalate, or dioctyl phthalate gave excessive thermoplasticity. Attempted plasticization by blending the copolymer with conformationally different macromolecules failed owing to incompatibility; this was overcome by reacting the macromolecules with the acrylic copolymer instead of blending: First, a butyl alcohol modified methylolacrylamide-styrene copolymer was transetherified with cetyl alcohol and in a second synthesis, transetherified with coconut oil monoglyceride. Third, an acrylamide-styrene-acrylic acid copolymer was esterified by the same monoglyceride, methylolated, and then butylated. Finally, an acrylamide-styrene copolymer was copolymerized and grafted onto a styrene-butadiene copolymer. This latter type of plasticization, which should be a general and valuable method, was supplemented by plasticization from dioctyl phthalate and yielded, after heating, economical and durable films with good mechanical properties.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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