I am working with diisopropycarbodiimide (DIC) which is soluble in organic solvents.e.g acetone and insoluble in aqueous solutions. The byproduct of DIC after crosslinking reaction/ peptide synthesis is diisoproply urea (DIU) which is also soluble in organic solvents and insoluble in water. In my case, these two compounds are coexist in acetone. I tried with HPLC but unfortunately DIC is sensitive to water and gets hydrolyzed into Diisopropyl urea inside the column during elution.
What is the recommended method to separate these two compounds
DIC is sensitive to water and gets hydrolyzed into Diisopropyl urea?? I found an article which reported the use of DIC for amidation reaction in water Article Amidation and esterification of carboxylic acids with amines...