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  2. Para tertiary butylphenol formaldehyde resin - Wikipedia

    en.wikipedia.org/wiki/Para_tertiary_butylphenol...

    Para tertiary butylphenol formaldehyde resin, also known as p-tert-butylphenol-formaldehyde resin (PTBP-FR), is a thermoplastic phenol-formaldehyde resin found in commercial adhesives, particularly glues used to bond leather and rubber. It has broad usage in a large variety of industries and can be found in many household textile products and ...

  3. Hydroxymethylphenol - Wikipedia

    en.wikipedia.org/wiki/Hydroxymethylphenol

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  4. Melamine resin - Wikipedia

    en.wikipedia.org/wiki/Melamine_resin

    A melamine-resin plate A melamine-resin ladle. Melamine resin is often used in kitchen utensils and plates (such as Melmac). Because of its high dielectric constant ranging from 7.2 to 8.4, melamine resin utensils and bowls are not microwave safe. [3] During the late 1950s and 1960s melamine tableware became fashionable.

  5. Phenol formaldehyde resin - Wikipedia

    en.wikipedia.org/wiki/Phenol_formaldehyde_resin

    Phenol-formaldehyde resins, as a group, are formed by a step-growth polymerization reaction that can be either acid- or base-catalysed.Since formaldehyde exists predominantly in solution as a dynamic equilibrium of methylene glycol oligomers, the concentration of the reactive form of formaldehyde depends on temperature and pH.

  6. Cresol - Wikipedia

    en.wikipedia.org/wiki/Cresol

    Another method entails methylation of phenol with methanol over a solid acid catalyst, often comprising magnesium oxide or alumina. Temperatures above 300 °C are typical. Anisole converts to cresols under these conditions. [5] [6] Another isomer of cresol is called Benzyl alcohol, or alpha-cresol (α-cresol).

  7. Impregnation resin - Wikipedia

    en.wikipedia.org/wiki/Impregnation_resin

    Phenol-formaldehyde resins (PF) were the first commercially relevant impregnation resins, made by reacting phenol and formaldehyde, creating a polymer network inside of the wood upon curing. [7] Phenol can react with formaldehyde at the ortho and para positions, generating mono, di, and trimethylolphenol as the reaction products. [6]