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  2. Cresol - Wikipedia

    en.wikipedia.org/wiki/Cresol

    at 20−25 °C 2.5 g/100 ml 2.4 g/100 ml 1.9 g/100 ml ... The name "cresol" is an adduct of phenol and their traditional source, creosote. Structure and production

  3. Phenol formaldehyde resin - Wikipedia

    en.wikipedia.org/wiki/Phenol_formaldehyde_resin

    Phenol reacts with formaldehyde at the ortho and para sites (sites 2, 4 and 6) allowing up to 3 units of formaldehyde to attach to the ring. The initial reaction in all cases involves the formation of a hydroxymethyl phenol: HOC 6 H 5 + CH 2 O → HOC 6 H 4 CH 2 OH

  4. 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 ...

  5. 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 ]

  6. Hydroxymethyl group - Wikipedia

    en.wikipedia.org/wiki/Hydroxymethyl_group

    This makes the hydroxymethyl group an alcohol. It has the identical chemical formula with the methoxy group (−O−CH 3) that differs only in the attachment site and orientation to the rest of the molecule. However, their chemical properties are different. [1] [2] Hydroxymethyl is the side chain of encoded amino acid serine. [3]

  7. Thermoset polymer matrix - Wikipedia

    en.wikipedia.org/wiki/Thermoset_polymer_matrix

    These are made by the reaction of phenols, formaldehyde and primary amines which at elevated temperatures (400 °F (200 °C)) undergo ring–opening polymerisation forming polybenzoxazine thermoset networks; when hybridised with epoxy and phenolic resins the resulting ternary systems have glass transition temperatures in excess of 490 °F (250 °C).

  8. Hydroxymethylation - Wikipedia

    en.wikipedia.org/wiki/Hydroxymethylation

    A common method for hydroxymethylation involves the reaction of formaldehyde with active C-H and N-H bonds: R 3 C-H + CH 2 O → R 3 C-CH 2 OH R 2 N-H + CH 2 O → R 2 N-CH 2 OH. A typical active C-H bond is provided by a terminal acetylene [1] or the alpha protons of an aldehyde. [2]

  9. Hexion - Wikipedia

    en.wikipedia.org/wiki/Hexion

    Hexion offers resins for a wide range of applications like Abrasives, Adhesives, Chemical Intermediates, Civil Engineering, Coatings, Composites, Crop Protection, Electrical/Electronics, Engineered Wood, Fertilizers and Pesticides, Fibers and Textiles, Foams, Friction Materials, Furniture, Molding Compounds, Oilfield, Oriented Strand Board ...