N,N'-Dicyclohexylcarbodiimide

[5] Yields of up to 67% have been achieved using this route: DCC has also been prepared from dicyclohexylurea using a phase transfer catalyst.

The majority of the DCU is thus readily removed by filtration, although the last traces can be difficult to eliminate from non-polar products.

[7] In protein synthesis (such as Fmoc solid-state synthesizers), the N-terminus is often used as the attachment site on which the amino acid monomers are added.

The negatively charged oxygen will act as a nucleophile, attacking the central carbon in DCC.

In combination with dimethyl sulfoxide (DMSO), DCC affects the Pfitzner-Moffatt oxidation.

[13] Thermal hazard analysis by differential scanning calorimetry (DSC) shows DCC poses minimal explosion risks.

Skeletal formula of dicyclohexylcarbodiimide
Skeletal formula of dicyclohexylcarbodiimide
Ball-and-stick model
Ball-and-stick model
NFPA 704 four-colored diamond Health 3: Short exposure could cause serious temporary or residual injury. E.g. chlorine gas Flammability 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g. canola oil Instability (yellow): no hazard code Special hazards (white): no code
Phase transfer catalysis
Phase transfer catalysis