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  2. List of UN numbers 2801 to 2900 - Wikipedia

    en.wikipedia.org/wiki/List_of_UN_numbers_2801_to...

    Refrigerating machines, containing nonflammable, nontoxic, liquefied gas or ammonia solution (UN2672) UN 2858: 4.1: Zirconium, dry, coiled wire, finished metal sheets, strip (thinner than 254 micrometres but not thinner than 18 micrometres) UN 2859: 6.1: Ammonium metavanadate: UN 2860: 6.1

  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. 3,5-Dichlorophenol - Wikipedia

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

    External MSDS: Except where otherwise noted, ... (3,5-DCP) is a chlorinated derivative of phenol with the molecular formula Cl 2 C 6 H 3 OH. References. Cited sources ...

  6. Phenol extraction - Wikipedia

    en.wikipedia.org/wiki/Phenol_extraction

    Phenol is a polar substance with a higher density than water (1.07 g/cm 3 [2] compared to water's 1.00 g/cm 3). When suspended in a water-phenol solution, denatured proteins and unwanted cell components dissolve in the phenol, while polar nucleic acids dissolve in the water phase. [3]

  7. 2-Phenylphenol - Wikipedia

    en.wikipedia.org/wiki/2-Phenylphenol

    The primary use of 2-phenylphenol is as an agricultural fungicide. It is generally applied post-harvest. It is a fungicide used for waxing citrus fruits.It is no longer a permitted food additive in the European Union, but is still allowed as a post-harvest treatment in 4 EU countries.

  8. Carbolic soap - Wikipedia

    en.wikipedia.org/wiki/Carbolic_soap

    In 1834, German chemist Friedlieb Ferdinand Runge discovered a phenol, also known as carbolic acid, which he derived in an impure form from coal tar.In August 1865, Joseph Lister applied a piece of lint dipped in carbolic acid solution to the wound of an eleven-year-old boy at Glasgow Royal Infirmary, who had sustained a compound fracture after a cart wheel had passed over his leg.

  9. Phenolphthalein - Wikipedia

    en.wikipedia.org/wiki/Phenolphthalein

    Phenolphthalein adopts different forms in aqueous solution depending on the pH of the solution. [4] [2] [5] [6] Inconsistency exists in the literature about hydrated forms of the compounds and the color of sulfuric acid. Wittke reported in 1983 that it exists in protonated form (H 3 In +) under strongly acidic conditions, providing an orange ...