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  2. 2,4-Di-tert-butylphenol - Wikipedia

    en.wikipedia.org/wiki/2,4-di-tert-butylphenol

    2,4-Di-tert-butylphenol (2,4-DTBP) is a white solid with a phenolic odour.It is primarily used as a raw material for the production of several commercially important antioxidants and phenolic benzotriazole-type UV absorbers.

  3. Phenol - Wikipedia

    en.wikipedia.org/wiki/Phenol

    Phenol is also a versatile precursor to a large collection of drugs, most notably aspirin but also many herbicides and pharmaceutical drugs. Phenol is a component in liquid–liquid phenol–chloroform extraction technique used in molecular biology for obtaining nucleic acids from tissues or cell culture samples.

  4. Safety data sheet - Wikipedia

    en.wikipedia.org/wiki/Safety_data_sheet

    An example SDS, including guidance for handling a hazardous substance and information on its composition and properties. A safety data sheet (SDS), [1] material safety data sheet (MSDS), or product safety data sheet (PSDS) is a document that lists information relating to occupational safety and health for the use of various substances and products.

  5. Sulfonated phenolics/sulfuric acid - Wikipedia

    en.wikipedia.org/wiki/Sulfonated_phenolics/...

    One clinical trial comparing Debacterol to Kenalog-in-Orabase and a no-intervention control group found that patients treated with sulfonated phenolics/sulfuric acid reported significantly better relief of symptoms compared to the other two groups three days after treatment. [4]

  6. Nonylphenol - Wikipedia

    en.wikipedia.org/wiki/Nonylphenol

    The nonyl group can be attached to the phenol ring at various locations, usually the 4- and, to lesser extent, the 2-positions, and can be either branched or linear. A branched nonylphenol, 4-nonylphenol, is the most widely produced and marketed nonylphenol. [ 12 ]

  7. Pentafluorophenol - Wikipedia

    en.wikipedia.org/wiki/Pentafluorophenol

    This is the perfluorinated analogue of phenol. It is a white odorless solid that melts just above room temperature. It is a white odorless solid that melts just above room temperature. With a p K a of 5.5, it is one of the most acidic phenols .

  8. 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.

  9. 2,4,6-Trichlorophenol - Wikipedia

    en.wikipedia.org/wiki/2,4,6-Trichlorophenol

    2,4,6-Trichlorophenol, also known as TCP, phenaclor, Dowicide 2S, Dowcide 2S, omal, is a chlorinated phenol that has been used as a fungicide, herbicide, insecticide, antiseptic, [3] defoliant, and glue preservative. [4] It is a clear to yellowish crystalline solid with a strong, phenolic odor.

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