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  2. Phenol - Wikipedia

    en.wikipedia.org/wiki/Phenol

    Aqueous solutions of phenol are weakly acidic and turn blue litmus slightly to red. Phenol is neutralized by sodium hydroxide forming sodium phenate or phenolate, but being weaker than carbonic acid, it cannot be neutralized by sodium bicarbonate or sodium carbonate to liberate carbon dioxide. C 6 H 5 OH + NaOH → C 6 H 5 ONa + H 2 O

  3. 3,5-Dichlorophenol - Wikipedia

    en.wikipedia.org/wiki/3,5-Dichlorophenol

    Safety data sheet (SDS) External MSDS: ... 3,5-Dichlorophenol (3,5-DCP) is a chlorinated derivative of phenol with the molecular formula Cl 2 C 6 H 3 OH.

  4. Phenol red - Wikipedia

    en.wikipedia.org/wiki/Phenol_red

    Phenol red exists as a red crystal that is stable in air. Its solubility is 0.77 grams per liter (g/L) in water and 2.9 g/L in ethanol. [1] It is a weak acid with pK a = 8.00 at 20 °C (68 °F). A solution of phenol red is used as a pH indicator, often in cell culture.

  5. 2,4,6-Tris (dimethylaminomethyl)phenol - Wikipedia

    en.wikipedia.org/wiki/2,4,6-Tris(dimethylamino...

    2,4,6-Tris(dimethylaminomethyl)phenol is an aromatic organic chemical that has tertiary amine and phenolic hydroxyl functionality in the same molecule. [1] The formula is C 15 H 27 N 3 O and the CAS Registry Number is 90-72-2. It is REACH registered and the European Community Number is 202-013-9. [2] [3] [4]

  6. m-Cresol - Wikipedia

    en.wikipedia.org/wiki/M-Cresol

    Safety data sheet (SDS) External MSDS: Related compounds ... It is a derivative of phenol and is an isomer ... polyaniline is cast from a solution of m-cresol to form ...

  7. Trizol - Wikipedia

    en.wikipedia.org/wiki/Trizol

    TRIzol reagent contains guanidinium thiocyanate and phenol.. TRIzol is a widely used [1] chemical solution used in the extraction of DNA, RNA, and proteins from cells. The solution was initially used and published by Piotr ChomczyƄski and Nicoletta Sacchi in 1987.

  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-Dichlorophenol - Wikipedia

    en.wikipedia.org/wiki/2,4-Dichlorophenol

    2,4-Dichlorophenol (2,4-DCP) is a chlorinated derivative of phenol with the molecular formula Cl 2 C 6 H 3 OH. It is a white solid that is mildly acidic (pK a = 7.9). It is produced on a large scale as a precursor to the herbicide 2,4-dichlorophenoxyacetic acid (2,4-D). [4]