Formaldehyde-urea (F/U) reaction products with molar ratios of 1.8, 2.1, and 2.4 were synthesized at pH 8.3, and the last one also at pH 4.5 using 45% formaldehyde aqueous solution. For obtaining the resin, the synthesis of F/U 2.1 was continued by acid-catalyzed condensation at pH 4.5 and posttreatment with second part of U (F/U 1.05/1) at 70°C and pH 8.3. The products were analyzed using 13 C-NMR spectrometry. Higher excess of F increases the dihydroxymethyl content on account of smaller dimethylene ether content. Certain 13 C chemical shifts in carbonyl and methylene region of spectra were assigned to trishydroxymethylurea, being the main trisubstituted urea compound in hydroxymethylated product. Acid catalyst promotes the formation of methylene groups by polycondensation of hydroxymethyl groups, against the background of similar content of dimethylene ethers in both catalytic conditions. The ratio of linear/branched chains is emphasized in characterizing the resin structure. Higher hydroxymethyl content in acid-catalyzed polycondensation is an advantage of three-step synthesis technology. The amount of binding methylene and dimethylene ether groups linked only to secondary amino groups can be increased by transhydroxymethylation with subsequent polycondensation in posttreatment with U in suitable reaction conditions.

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Chemical constitution of urea-formaldehyde resins in synthesis and in storage was determined using I3C NMR spectroscopy. Methylolation, methylene and dimethylene ether bond-forming reactions were discussed. The changes in the content of structural elements with secondary and tertiary amino groups of urea at various stages were followed. The resin synthesis technology was used, which considers the requirement in low free formaldehyde content, connected with somewhat smaller storage stability of resins.

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