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  • 1970-1974  (3)
  • 1974  (3)
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  • 1970-1974  (3)
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  • 1
    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: On complete hydrazinolysis of poly(ethylene terephthalate), terephthalomonohydrazide is formed from carboxyl-end terephthaloyl residues in a quantity equivalent to the content of carboxyl endgroups in the polymer. The compound is separated from the reaction mixture by ion exchange and determined photometrically [epsiv;240 in 0.1 N HCl = 16,700 (1000 cm2/mole)]. A COOH determination carried out in this way is endgroup specific and, unlike titration, is not subject to interference by ionogenic fiber additives. Aromatic comonomers with acidic substituents (e.g., 5-sulfoisophthalic acid) in chemically modified, cationically dyeable poly(ethylene terephthalate) are determined simultaneously with the carboxyl endgroups by the same analytical method. In this case, the terephthalamonohydrazide and 5-sulfoisophthalodihydrazide are separated by ion exchange, and the difference in their spectral behavior is used for quantitative determination with the aid of a two-component analysis: \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{l} c_1 {\rm = (6}{\rm .21 }D_{240} {\rm - 1}{\rm .04 }D_{212} ){\rm } \times {\rm 10}^{{\rm - 5}} {\rm mole/l}{\rm .} \\ c_2 {\rm = (2}{\rm .62 }D_{212} {\rm - 0}{\rm .51 }D_{240} ){\rm } \times {\rm 10}^{{\rm - 5}} {\rm mole/l} \\ \end{array} $$\end{document} where c1c2 = concentration of terephthalomonohydrazide and 5-sulfoisophthalodihydrazide, respectively; and D240 D212 = optical density at 240 and 212 nm, respectively. The content of carboxyl endgroups in polyether esters poly(p-(2-ethyleneoxy)-benzoate), is determined on the basis of the p-(β-hydroxyethoxy)benzoic acid [epsiv;258 in 0.1 N HCl = 16,100 (1000 cm2/mole)] liberated from carboxyl-end monomer units by hydrazinolysis. For copolyether esters with p-(β-hydroxyethoxy)benzoic acid as a comonomer, the contents of carboxyl-end terephthalic acid and p-(β-hydroxyethoxy)benzoic acid are determined simultaneously with the acid of a spectrophotometric twocomponent analysis: \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{l} c_1 {\rm = (7}{\rm .65 }D_{240} {\rm - 3}{\rm .27 }D_{258} ){\rm } \times {\rm 10}^{{\rm - 5}} {\rm mole/l}{\rm .} \\ c_2 {\rm = (7}{\rm .91 }D_{258} {\rm - 3}{\rm .49 }D_{240} ){\rm } \times {\rm 10}^{{\rm - 5}} {\rm mole/l.} \\ \end{array} $$\end{document} where c2, c2 = concentration of terephthalomonohydrazide and p-(β-hydroxyethoxy)-benzoic acid, respectively; and D240, D258 = optical density at 240 and 258 nm, respectively.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis of Monomeric Cyclic Cystine Peptides, II. - Synthesis of the Sequence A 10-21 of Ovine Insulin as Monomeric, Cyclic, Asymmetric Cystine Peptide Derivative1)The completely protected cysteine peptide, Trt-Val-Cys(Trt)-Ser(But)-Leu-Tyr(But)-Gln-Leu-Glu(OBut)-Asn-Tyr(But)-Cys(Trt)-Asn-OBut (13), which corresponds to the amino acid series of sequence A 10-21 of the ovine insulin A-chain, was synthesized by fragment condensations. The product was then converted by treatment with iodine in methanol into the corresponding cystine peptide derivative 14 in the N-terminal free form.
    Notes: Das vollständig geschützte Cysteinpeptid Trt-Val-Cys(Trt)-Ser(But)-Leu-Tyr(But)-Gln-Leu-Glu(OBut)-Asn-Tyr(But)-Cys(Trt)-Asn-OBut (13), dessen Aminosäurefolge der Sequenz A 10-21 der Schafinsulin-A-Kette entspricht, wurde durch Fragmentkondensationen aufgebaut und durch Behandlung mit Jod in Methanol in das entsprechende Cystinpeptidderivat 14 in N-terminal freier Form übergeführt.
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  • 3
    Publication Date: 1974-04-08
    Print ISSN: 0009-2347
    Electronic ISSN: 1520-605X
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
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