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  2. 1,3,5-Trioxane - Wikipedia

    en.wikipedia.org/wiki/1,3,5-Trioxane

    1,3,5-Trioxane, sometimes also called trioxane or trioxin, is a chemical compound with molecular formula C 3 H 6 O 3. It is a white, highly water-soluble solid with a chloroform -like odor. It is a stable cyclic trimer of formaldehyde , and one of the three trioxane isomers; its molecular backbone consists of a six-membered ring with three ...

  3. Formaldehyde - Wikipedia

    en.wikipedia.org/wiki/Formaldehyde

    Molecular formaldehyde. A colorless gas with a characteristic pungent, irritating odor. It is stable at about 150 °C, but it polymerizes when condensed to a liquid. 1,3,5-Trioxane, with the formula (CH 2 O) 3. It is a white solid that dissolves without degradation in organic solvents. It is a trimer of molecular formaldehyde.

  4. Category:Company templates - Wikipedia

    en.wikipedia.org/wiki/Category:Company_templates

    [[Category:Company templates]] to the <includeonly> section at the bottom of that page. Otherwise, add <noinclude>[[Category:Company templates]]</noinclude> to the end of the template code, making sure it starts on the same line as the code's last character.

  5. Thioformaldehyde - Wikipedia

    en.wikipedia.org/wiki/Thioformaldehyde

    Thioformaldehyde is the organosulfur compound with the formula CH 2 S. It is the simplest thioaldehyde.This compound is not observed in the condensed state (solid or liquid) because it oligomerizes to 1,3,5-trithiane, which is a stable colorless compound with the same empirical formula.

  6. 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.

  7. Paraformaldehyde - Wikipedia

    en.wikipedia.org/wiki/Paraformaldehyde

    Paraformaldehyde can be depolymerized to formaldehyde gas by dry heating [2] and to formaldehyde solution by water in the presence of a base, an acid or heat. The high purity formaldehyde solutions obtained in this way are used as a fixative for microscopy and histology. The resulting formaldehyde gas from dry heating paraformaldehyde is flammable.

  8. Trimer (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Trimer_(chemistry)

    In chemistry, a trimer (/ ˈ t r aɪ m ər /; from Ancient Greek tri- 'three' and -mer 'parts') is a molecule or polyatomic anion formed by combination or association of three molecules or ions of the same substance. In technical jargon, a trimer is a kind of oligomer derived from three identical precursors often in competition with polymerization.

  9. Formaldoxime - Wikipedia

    en.wikipedia.org/wiki/Formaldoxime

    A colorless liquid, the pure compound tends to polymerize into a cyclic trimer. Aqueous solutions are stable as is the formaldoxime hydrochloride ([H 2 C=N(−H)(−OH)] + Cl −). It is a reagent in organic synthesis for the conversion of aryl diazonium salts to aryl aldehydes. [1] It is generated by combining hydroxylamine and formaldehyde. [2]