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  2. Folin's reagent - Wikipedia

    en.wikipedia.org/wiki/Folin's_reagent

    Folin's reagent or sodium 1,2-naphthoquinone-4-sulfonate is a chemical reagent used as a derivatizing agent to measure levels of amines and amino acids. [1] The reagent reacts with them in alkaline solution to produce a fluorescent material that can be easily detected.

  3. Sullivan reaction - Wikipedia

    en.wikipedia.org/wiki/Sullivan_reaction

    The Sullivan reaction is a chemical test used for detecting the presence of cysteine or cystine in proteins. A red colour appears when a protein with cysteine or cystine is heated with sodium 1,2-naphthoquinone-4-sulfonate (Folin's reagent) and sodium dithionite under alkaline conditions.

  4. Hinsberg reaction - Wikipedia

    en.wikipedia.org/wiki/Hinsberg_reaction

    The Hinsberg reaction is a chemical test for the detection of primary, secondary and tertiary amines.The reaction was first described by Oscar Hinsberg in 1890. [1] [2] In this test, the amine is shaken well with the Hinsberg reagent (benzenesulfonyl chloride) in the presence of aqueous alkali (either KOH or NaOH).

  5. Benzenesulfonyl chloride - Wikipedia

    en.wikipedia.org/wiki/Benzenesulfonyl_chloride

    Benzenesulfonyl chloride is an electrophilic reagent. It hydrolyzes with heat but is stable toward cold water. [2] Amines react to give sulfonamides. This reaction is the basis of the Hinsberg test for amines. [3]

  6. Alkylbenzene sulfonate - Wikipedia

    en.wikipedia.org/wiki/Alkylbenzene_sulfonate

    An example of a linear alkylbenzene sulfonate (LAS) Linear alkylbenzene sulfonates (LAS) are prepared industrially by the sulfonation of linear alkylbenzenes (LABs), which can themselves be prepared in several ways. [2] In the most common route benzene is alkylated by long chain monoalkenes (e.g. dodecene) using hydrogen fluoride as a catalyst. [9]

  7. Desulfonylation reactions - Wikipedia

    en.wikipedia.org/wiki/Desulfonylation_reactions

    A wide variety of functional groups are unaffected by these conditions, including many that are transformed by dissolving metal reductions. Reductive desulfonylation with these reagents does not occur in reactions of β-hydroxy sulfones, due to the poor leaving group ability of the hydroxyl group. [13

  8. Pyridinium p-toluenesulfonate - Wikipedia

    en.wikipedia.org/wiki/Pyridinium_p-toluenesulfonate

    In organic synthesis, PPTS is used as a weakly acidic catalyst, providing an organic soluble source of pyridinium (C 5 H 5 NH +) ions.For example, PPTS is used to deprotect silyl ethers or tetrahydropyranyl ethers when a substrate is unstable to stronger acid catalysts.

  9. ABTS - Wikipedia

    en.wikipedia.org/wiki/ABTS

    Under these conditions, the sulfonate groups are fully deprotonated and the mediator exists as a dianion. ABTS –· + e – → ABTS 2– E° ′ = 0.67 V vs SHE ABTS + e – → ABTS –· E° ′ = 1.08 V vs SHE [1] This compound is chosen because the enzyme facilitates the reaction with hydrogen peroxide, turning it into a green and soluble ...