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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. 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.

  5. 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.

  6. Phenol extraction - Wikipedia

    en.wikipedia.org/wiki/Phenol_extraction

    Phenol extraction is a laboratory technique that purifies nucleic acid samples using a phenol solution. Phenol is common reagent in extraction because its properties allow for effective nucleic acid extraction, particularly as it strongly denatures proteins, it is a nucleic acid preservative, and it is immiscible in water.

  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. Phenols - Wikipedia

    en.wikipedia.org/wiki/Phenols

    The simplest is phenol, C 6 H 5 OH. Phenolic compounds are classified as simple phenols or polyphenols based on the number of phenol units in the molecule. Phenol – the simplest of the phenols Chemical structure of salicylic acid, the active metabolite of aspirin. Phenols are both synthesized industrially and produced by plants and ...

  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]