Resinificationof methylolmelamines is postulated as proceeding through either the methylene or the ether linkage.The wide range of properties of hydrocarbonsoluble melamine-aldehyde-alcohol resins can be explained by etherification as the mechanism whereby the final resins are formed from the methylolmelamines. Heat stability of melamine resins, as compared to urea resins, may be due to the absence of carbonyl groups.
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