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Glyoxal is used to prepare 4,5-dihydroxy-2-imidazolidinone by condensation with urea. It finds application in leather tanning process, textile finishes and paper coatings. It is an important building block in the synthesis of imidazoles. It acts as a solubilizer and cross-linking agent in polymer chemistry. Further, it is used as a fixative for histology to preserve cells in order to examine under a microscope.
For use in the chemoselective hydrolysis of amides in the presence of esters, see Copper(II) chloride dihydrate, A16064 .
For use in the synthesis of bicyclic diketones, see Dimethyl acetone-1,3-dicarboxylate, A14969 .
Kurten, T.; Elm, J.; Prisle, N. L.; Mikkelsen, K. V.; Kampf, C. J.; Waxman, E. M.; Volkamer, R. Computational Study of the Effect of Glyoxal-Sulfate Clustering on the Henrys Law Coefficient of Glyoxal. J. Phys. Chem. A 2015, 119 (19), 4509-4514.
Lawson, S. J.; Selleck, P. W.; Galbally, I. E.; Keywood, M. D.; Harvey, M. J.; Lerot, C.; Helmig, D.; Ristovski, Z. Seasonal in situ observations of glyoxal and methylglyoxal over the temperate oceans of the Southern Hemisphere. Atmos. Chem. Phys. 2015, 15 (1), 223-240.
Gefahrenhinweise (EU): H332-H315-H319-H317-H341
Harmful if inhaled. Causes skin irritation. Causes serious eye irritation. May cause an allergic skin reaction. Suspected of causing genetic defects.
Obtain special instructions before use. Avoid breathing dust/fume/gas/mist/vapours/spray. Wear protective gloves/protective clothing/eye protection/face protection. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.