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The generic formula of an azine. For an aldazine, R2, R4 = H.
Azines are a functional class of organic compounds with the connectivity RR′C=N−N=CRR′. These compounds are the product of the condensation of hydrazine with ketones and aldehydes, although in practice they are often made by alternative routes. Ketazines are azines derived from ketones.[1] For example, acetone azine is the simplest ketazine. Aldazines are azines derived from aldehydes.[2]
Acetone is used to derivatize hydrazine into acetone azine for analysis by gas chromatography. This method is used to determine trace levels of hydrazine in drinking water[14] and pharmaceuticals.[15]
Ketazines are also important intermediates in the industrial production of hydrazine hydrate by the peroxide process.[3] In the presence of an oxidant, ammonia and ketones react to give hydrazine via ketazine:
^Outirite, Moha; Lebrini, Mounim; Lagrenée, Michel; Bentiss, Fouad (2008). "New one step synthesis of 3,5-disubstituted pyrazoles under microwave irradiation and classical heating". Journal of Heterocyclic Chemistry. 45 (2): 503–505. doi:10.1002/jhet.5570450231.
^Day, A. C.; Raymond, P.; Southam, R. M.; Whiting, M. C. (1966). "The preparation of secondary aliphatic diazo-compounds from hydrazones". Journal of the Chemical Society C: Organic: 467. doi:10.1039/J39660000467.
^Andrews, S. D.; Day, A. C.; Raymond, P.; Whiting, M. C. (1970). "2-Diazopropane". Organic Syntheses. 50: 27; Collected Volumes, vol. 6, p. 392..
^Gudkova, A. S.; Reutov, O. A.; Aleinikova, M. Ya. (August 1962). "Reactions of hydrazones and azines with metal salts". Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 11 (8): 1298–1302. doi:10.1007/BF00907973.
^Gudkova, A. S.; Aleinikova, M. Ya.; Reutov, O. A. (May 1966). "Reactions of hydrazones and azines with metal salts Communication 5. Reactions of hydrazones and azines with mercuric halides". Bulletin of the Academy of Sciences, USSR Division of Chemical Science. 15 (5): 807–811. doi:10.1007/BF00849376.
^King, Fiona; Nicholls, David (January 1978). "Complex of titanium halides with acetone azine and its isomer 3, 5, 5-trimethyl-pyrazoline". Inorganica Chimica Acta. 28: 55–58. doi:10.1016/S0020-1693(00)87413-7.
^Davis, II, William E.; Li, Yongtao (July 2008). "Analysis of Hydrazine in Drinking Water by Isotope Dilution Gas Chromatography/Tandem Mass Spectrometry with Derivatization and Liquid−Liquid Extraction". Analytical Chemistry. 80 (14): 5449–5453. doi:10.1021/ac702536d. PMID18564853.
^Sun, Mingjiang; Bai, Lin; Liu, David Q. (February 2009). "A generic approach for the determination of trace hydrazine in drug substances using in situ derivatization-headspace GC–MS". Journal of Pharmaceutical and Biomedical Analysis. 49 (2): 529–533. doi:10.1016/j.jpba.2008.11.009. PMID19097722.
^US 6002015, Nagata, Nobuhiro; Nishizawa, Chiharu & Kurai, Toshikiyo, "Method of producing 1,2,4-triazole", published 1999-12-14, assigned to Mitsubishi Gas Chemical Co..
Gilbert, E. C. (1929). "Studies on Hydrazine. The Hydrolysis of Dimethylketazine and the Equilibrium between Hydrazine and Acetone". J. Am. Chem. Soc.51 (11): 3394–3409. doi:10.1021/ja01386a032.
US 3965097, Eichenhofer, Kurt-Wilhelm & Schliebs, Reinhard, "Production of ketazines", published 1976-06-22, assigned to Bayer.
US 3972878, Schirmann, Jean-Pierre; Combroux, Jean & Delavarenne, Serge Yvon, "Method for preparing azines and hydrazones", published 1976-08-03, assigned to Produits Chimiques Ugine Kuhlmann.
US 3978049, Schirmann, Jean-Pierre; Tellier, Pierre & Mathais, Henri et al., "Process for the preparation of hydrazine compounds", published 1976-08-31, assigned to Produits Chimiques Ugine Kuhlmann.
US 4093656, Schirmann, Jean-Pierre; Combroux, Jean & Delavarenne, Serge Yvon, "Method for making azines", published 1978-06-06, assigned to Produits Chimiques Ugine Kuhlmann.
US 4724133, Schirmann, Jean-Pierre; Combroux, Jean & Delavarenne, Serge Y., "Preparation of a concentrated aqueous solution of hydrazine hydrate", published 1988-02-09, assigned to Atochem.
