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  2. Category:Peptide coupling reagents - Wikipedia

    en.wikipedia.org/wiki/Category:Peptide_coupling...

    Pages in category "Peptide coupling reagents" The following 14 pages are in this category, out of 14 total. This list may not reflect recent changes. B. BOP reagent; D.

  3. Peptide synthesis - Wikipedia

    en.wikipedia.org/wiki/Peptide_synthesis

    Coupling reagents (e.g. HBTU, HATU, or DIC) are employed to help form the peptide bond. The final deprotection is followed by a cleavage . The established method for the production of synthetic peptides in the lab is known as solid phase peptide synthesis (SPPS). [ 2 ]

  4. HATU - Wikipedia

    en.wikipedia.org/wiki/HATU

    HATU (Hexafluorophosphate Azabenzotriazole Tetramethyl Uronium) is a reagent used in peptide coupling chemistry to generate an active ester from a carboxylic acid. HATU is used along with Hünig's base (N,N-diisopropylethylamine), or triethylamine to form amide bonds.

  5. 1-Hydroxy-7-azabenzotriazole - Wikipedia

    en.wikipedia.org/wiki/1-Hydroxy-7-azabenzotriazole

    1-Hydroxy-7-azabenzotriazole (HOAt) is a triazole used as a peptide coupling reagent. [2] It suppresses racemization that can otherwise occur during the reaction. [3] HOAt has a melting point of 213-216 °C. [4]

  6. 1-Ethyl-3- (3-dimethylaminopropyl)carbodiimide - Wikipedia

    en.wikipedia.org/wiki/1-Ethyl-3-(3-dimethylamino...

    Common uses for this carbodiimide include peptide synthesis, protein crosslinking to nucleic acids, but also in the preparation of immunoconjugates. EDC is often used in combination with N-hydroxysuccinimide (NHS) for the immobilisation of large biomolecules. Recent work has also used EDC to assess the structure state of uracil nucleobases in RNA.

  7. N,N'-Diisopropylcarbodiimide - Wikipedia

    en.wikipedia.org/wiki/N,N'-Diisopropylcarbodiimide

    N,N -Diisopropylcarbodiimide is a carbodiimide used in peptide synthesis. [1] [2] As a liquid, it is easier to handle than the commonly used N,N ′-dicyclohexylcarbodiimide, a waxy solid. In addition, N,N ′-diisopropylurea, its byproduct in many chemical reactions, is soluble in most organic solvents, a property that facilitates work-up.