Showing 49–64 of 162 results






"N,N-Diisopropylethylamine, or Hünig's base, is an organic compound and an amine. It is named after the German chemist Siegfried Hünig. It is used in organic chemistry as a base. It is commonly abbreviated as DIPEA, DIEA, or i-Pr2NEt. N,N-Diisopropylethylamine, also known as Hünig′s base, is a sterically hindered amine. It is a non-nucleophilic base commonly employed for substitution reactions. It acts as an activator for chiral iridium N, P ligand complexes, which can be utilized in the hydrogenation of α, β-unsaturated nitriles. The influence of varying concentration of N,N-diisopropylethylamine on the synthesis of olvanil in the presence of lipase catalyst has been investigated. Application: Proton scavenger used in peptide coupling, enolboration, Pd(0)-catalyzed alkoxycarbonylation of allyl phosphates and acetates, and as a catalyst in vinyl sulfone synthesis. N,N-Diisopropylethylamine may be used in the synthesis of mannosylated ovalbumin peptides."


DMC




DPC




DSC



EDC·HCl (EDC, EDAC or EDCI) is a water-soluble carbodiimide coupling reagent that can be used in aqueous phase to facility the activation of a carboxyl group. It also simplifies the purification of the coupling reaction as the byproduct from EDC is also water soluable which makes it more convenient to be removed. EDC is often used in combination with HOBt or HOSu.