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  2. 1,3,5-Trithiane - Wikipedia

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

    This heterocycle is the cyclic trimer of the otherwise unstable species thioformaldehyde. It consists of a six-membered ring with alternating methylene bridges and thioether groups. It is prepared by treatment of formaldehyde with hydrogen sulfide. [2] Trithiane is a building block molecule in organic synthesis, being a masked source of ...

  3. 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 ...

  4. 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.

  5. Five Products That Contain Formaldehyde: Is Your Health ... - AOL

    www.aol.com/news/2010-12-22-five-products-that...

    To the average consumer, formaldehyde may be best known as an embalming agent. But this naturally occurring chemical is a major industrial staple, used in many consumer goods, including cleaning ...

  6. 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.

  7. Trioxane - Wikipedia

    en.wikipedia.org/wiki/Trioxane

    The three isomers are: 1,2,3-trioxane, a hypothetical compound that is the parent structure of the molozonides [1]; 1,2,4-trioxane, a hypothetical compound whose skeleton occurs as a structural component of some antimalarial agents (artemisinin and similar drugs) [2]

  8. Thermo Fisher Scientific - Wikipedia

    en.wikipedia.org/wiki/Thermo_Fisher_Scientific

    The company's products are sold under the brand names of Thermo Scientific, Fisher Scientific, and several other recognized brand names (e.g. Applied Biosystems, Invitrogen, Patheon, PPD, and Nalgene). According to company figures, as of 2007, 46% of its sales were in life sciences, 20% in healthcare, and 34% in industrial/environmental and safety.

  9. Step-growth polymerization - Wikipedia

    en.wikipedia.org/wiki/Step-growth_polymerization

    High molecular weight and crosslinking are desirable for the same reason. Strong dipole-dipole, hydrogen bond interactions and crystallinity also improve heat resistance. To obtain desired mechanical strength, sufficiently high molecular weights are necessary, however, decreased solubility is a problem.