Microchimica Acta

, Volume 61, Issue 5, pp 853–862 | Cite as

Organic functional group analysis via gas chromatography. III

Determination of carbamates by reaction with alkali
  • Athanasios S. Ladas
  • T. S. Ma
Article

Summary

A gas Chromatographic procedure for the analysis of carbamates is described. A specially prepared reaction tube, packed with a 10 % mixture of potassium hydroxide in glass beads, is placed inside the injection port of a Perkin-Elmer 900 Gas Chromatograph, in front of the Chromatographic column packed with Porapak Q. S.

A solution of the carbamates (0.01–0.1μmol) is injected directly into the gas Chromatograph. The carbamates are reacted with the alkali present in the reaction tube and the alcohols produced are separated, detected and recorded. Standard calibration graphs of the alcohols are prepared in the same manner and the quantities of carbamates are determined. The procedure is fast and quantitative.

Keywords

Alcohol Hydroxide Chromatographic Column Glass Bead Carbamate 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Zusammenfassung

Ein gaschromatisches Verfahren für die Analyse von Carbamaten wurde beschrieben. Ein spezielles Reaktionsrohr, beschickt mit 10% iger Kalilauge auf Glasperlen, wird innerhalb der Injektionsöffnung eines Gaschromatographen Perkin-Elmer 900 vor dem mit Poropak Q. S. gefüllten Chromatographierohr angebracht. Die Carbamatlösung (0,01 bis 0,1 μMol) wird direkt injiziert. Die Carbamate reagieren mit dem im Reaktionsrohr befindlichen Alkali, die dabei entstandenen Alkohole werden getrennt, nachgewiesen und registriert. In gleicher Weise ermittelte Standard-Eichkurven der Alkohole dienen zur Bestimmung der Carbamate. Das Verfahren ist rasch und quantitativ.

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References

  1. 1.
    T. S. Ma, C. T. Shang, and E. Manche, Mikrochim. Acta [Wien],1964, 571.Google Scholar
  2. 2.
    M. M. Schachter and T. S. Ma, Mikrochim. Acta [Wien]1966, 55.Google Scholar
  3. 3.
    L. V. Kolesnik and M. N. Chumachenko, Izv. Akad. Nauk. SSSR, Ser. Khim1969, 2107.Google Scholar
  4. 4.
    S. Araki, S. Suzuki, and M. Kitano, Japan Analyst18, 608 (1969).Google Scholar
  5. 5.
    E. R. Bissell and D. B. Fields, J. Chromat. Sci.10, 164.Google Scholar
  6. 6.
    C. L. Hanson and R. C. Smith, Analyt. Chemistry44, 1571 (1972).Google Scholar
  7. 7.
    S. Siggia, L. R. Whitlock, and J. C. Tao, Analyt. Chemistry41, 1387 (1969).Google Scholar
  8. 8.
    S. P. Frankoski and S. Siggia, Analyt. Chemistry44, 507 (1972).Google Scholar
  9. 9.
    S. P. Frankoski and S. Siggia, Analyt. Chemistry44, 2078 (1972).Google Scholar
  10. 10.
    T. S. Ma, Record of Chemical Progress26, 113 (1965).Google Scholar
  11. 11.
    J. R. Plimmer in A. Standen (ed.), Encyclopedia of Chemical Technology, 2nd edition, Vol. 22. New York: Wiley. 1970. p. 191.Google Scholar
  12. 12.
    R. I. Metcalf and T. R. Fukuto, J. Agr. Food Chem.13, 220 (1965).Google Scholar
  13. 13.
    R. I. Fryer in C. K. Cain (ed.), Annual Reports on Medicinal Chemistry, Vol. 6, New York: Academic Press. 1971. p. 6.Google Scholar
  14. 14.
    N. D. Cheronis and T. S. Ma, Organic Functional Group Analysis, New York: Wiley. 1964. p. 315.Google Scholar
  15. 15.
    G. Lundquist and C. E. Meloan, Analyt. Chemistry43, 1122 (1971).Google Scholar
  16. 16.
    R. C. Hall and C. S. Giam, Analyt. Chemistry42, 423 (1970).Google Scholar
  17. 17.
    C. C. Cassil, R. P. Stanovick, and R. F. Cook, Residue Rev.26, 63 (1969).PubMedGoogle Scholar
  18. 18.
    T. S. Ma and D. Spiegel, Microchem. J.10, 61 (1966).Google Scholar

Copyright information

© Springer-Verlag 1973

Authors and Affiliations

  • Athanasios S. Ladas
    • 1
  • T. S. Ma
    • 1
  1. 1.Department of ChemistryCity University of New YorkBrooklynUSA

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