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Hydrazone linkages, reactivity

Aldehyde particles are spontaneously reactive with hydrazine or hydrazide derivatives, forming hydrazone linkages upon Schiff base formation. Reactions with amine-containing molecules, such as proteins, can be done through a reductive amination process using sodium cyanoborohydride (Figure 14.21). [Pg.617]

Figure 18.15 NHS-chromogenic-PEG3-biotin contains an amine-reactive NHS ester that can be used to label biomolecules through an amide linkage. The chromogenic bis-aryl hydrazone group within the spacer arm of the reagent allows the degree of biotinylation to be quantified by measuring its absorbance at 354 nm. The compound also contains a hydrophilic PEG spacer, which provides greater water solubility. Figure 18.15 NHS-chromogenic-PEG3-biotin contains an amine-reactive NHS ester that can be used to label biomolecules through an amide linkage. The chromogenic bis-aryl hydrazone group within the spacer arm of the reagent allows the degree of biotinylation to be quantified by measuring its absorbance at 354 nm. The compound also contains a hydrophilic PEG spacer, which provides greater water solubility.

See other pages where Hydrazone linkages, reactivity is mentioned: [Pg.49]    [Pg.83]    [Pg.143]    [Pg.271]    [Pg.331]    [Pg.412]    [Pg.427]    [Pg.438]    [Pg.459]    [Pg.504]    [Pg.528]    [Pg.960]    [Pg.59]    [Pg.91]    [Pg.243]    [Pg.302]    [Pg.348]    [Pg.359]    [Pg.377]    [Pg.381]    [Pg.391]    [Pg.412]    [Pg.649]    [Pg.2175]    [Pg.268]    [Pg.39]    [Pg.71]    [Pg.223]    [Pg.282]    [Pg.328]    [Pg.339]    [Pg.357]    [Pg.361]    [Pg.371]    [Pg.629]    [Pg.1231]    [Pg.742]    [Pg.742]    [Pg.280]    [Pg.270]    [Pg.112]    [Pg.242]    [Pg.63]    [Pg.63]    [Pg.273]    [Pg.442]    [Pg.222]    [Pg.243]   


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Hydrazon linkage

Hydrazone linkages

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