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  2. Osazone - Wikipedia

    en.wikipedia.org/wiki/Osazone

    Osazone formation was developed by Emil Fischer, [3] who used the reaction as a test to identify monosaccharides. The formation of a pair of hydrazone functionalities involves both oxidation and condensation reactions. [4] Since the reaction requires a free carbonyl group, only "reducing sugars" participate.

  3. Potassium amyl xanthate - Wikipedia

    en.wikipedia.org/wiki/Potassium_amyl_xanthate

    Potassium amyl xanthate (/pəˈtæsiəm ˌæmɪl ˈzænθeɪt/) is an organosulfur compound with the chemical formula CH 3 (CH 2) 4 OCS 2 K. It is a pale yellow powder with a pungent odor that is soluble in water.

  4. The best muscle pain relief creams of 2025, according to ...

    www.aol.com/lifestyle/best-muscle-pain-relief...

    There are several benefits to using muscle pain relief creams: Reduced inflammation: "Some creams may contain anti-inflammatory agents like NSAIDs (e.g., diclofenac) that can reduce localized ...

  5. DiaSorin - Wikipedia

    en.wikipedia.org/wiki/DiaSorin

    Diasorin S.p.A. is an Italian multinational biotechnology company that produces and markets in vitro diagnostics reagent kits used in immunodiagnostics and molecular diagnostics and since July 2021, it is also active in the Life Science business.

  6. Ehrlich's reagent - Wikipedia

    en.wikipedia.org/wiki/Ehrlich's_reagent

    Ehrlich's reagent or Ehrlich reagent is a reagent containing p-dimethylaminobenzaldehyde (DMAB) and thus can act as an indicator to presumptively identify indoles and urobilinogen. Several Ehrlich tests use the reagent in a medical test ; some are drug tests and others contribute to diagnosis of various diseases or adverse drug reactions .

  7. Diisopropyl azodicarboxylate - Wikipedia

    en.wikipedia.org/wiki/Diisopropyl_azodicarboxylate

    Diisopropyl azodicarboxylate (DIAD) is the diisopropyl ester of azodicarboxylic acid. It is used as a reagent in the production of many organic compounds.It is often used with triphenylphosphine in the Mitsunobu reaction, [2] wherein it serves as a hydride acceptor.

  8. Rhodizonic acid - Wikipedia

    en.wikipedia.org/wiki/Rhodizonic_acid

    In basic solutions (pH > 10), rhodizonic acid quickly converts to the THBQ anion (CO) 4− 6 in the absence of oxygen, and to croconic acid in its presence. At pH 8.3 and exposure to light, solutions are stable for days in the absence of oxygen, and decompose to croconic acid and other products (possibly including cyclohexanehexone or ...

  9. Disodium tetracarbonylferrate - Wikipedia

    en.wikipedia.org/wiki/Disodium_tetracarbonylferrate

    It is always used as a solvate, e.g., with tetrahydrofuran or dimethoxyethane, which bind to the sodium cation. [1] An oxygen-sensitive colourless solid, it is a reagent in organometallic and organic chemical research. The dioxane solvated sodium salt is known as Collman's reagent, in recognition of James P. Collman, an early popularizer of its ...