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  2. Phenylhydrazine - Wikipedia

    en.wikipedia.org/wiki/Phenylhydrazine

    Phenylhydrazine was the first hydrazine derivative characterized, reported by Hermann Emil Fischer in 1875. [7] [8] He prepared it by reduction of a phenyl diazonium salt using sulfite salts. Fischer used phenylhydrazine to characterize sugars via formation of hydrazones known as osazones with the sugar aldehyde. He also demonstrated in this ...

  3. Hydrazines - Wikipedia

    en.wikipedia.org/wiki/Hydrazines

    Hydrazines (R 2 N−NR 2) are a class of chemical compounds with two nitrogen atoms linked via a covalent bond and which carry from one up to four alkyl or aryl substituents. . Hydrazines can be considered as derivatives of the inorganic hydrazine (H 2 N−NH 2), in which one or more hydrogen atoms have been replaced by hydrocarbon grou

  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. Globally Harmonized System of Classification and Labelling of ...

    en.wikipedia.org/wiki/Globally_Harmonized_System...

    The pictogram for harmful substances of the Globally Harmonized System of Classification and Labelling of Chemicals.. The Globally Harmonized System of Classification and Labelling of Chemicals (GHS) is an internationally agreed-upon standard managed by the United Nations that was set up to replace the assortment of hazardous material classification and labelling schemes previously used around ...

  6. Phenyl hydrazine - Wikipedia

    en.wikipedia.org/?title=Phenyl_hydrazine&redirect=no

    This page was last edited on 21 December 2006, at 21:22 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  7. 2,4-Dinitrophenylhydrazine - Wikipedia

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

    DNPH is a reagent in instructional laboratories on qualitative organic analysis. Brady's reagent or Borche's reagent, is prepared by dissolving DNPH in a solution containing methanol and some concentrated sulfuric acid.

  8. Phenazone - Wikipedia

    en.wikipedia.org/wiki/Phenazone

    Phenazone is synthesized [7] by condensation of phenylhydrazine and ethyl acetoacetate under basic conditions and methylation of the resulting intermediate compound 1-phenyl-3-methylpyrazolone [8] with dimethyl sulfate or methyl iodide. It crystallizes in needles which melt at 156 °C (313 °F).

  9. Dithizone - Wikipedia

    en.wikipedia.org/wiki/Dithizone

    Dithizone is a sulfur-containing organic compound. It is a good ligand, and forms complexes with many toxic metals such as lead, thallium [1] and mercury.. Dithizone may be prepared by reacting phenylhydrazine with carbon disulfide, followed by reaction with potassium hydroxide.