ISOCHEM produces at scales from gram to ton quantities of α-aminoacid N-CarboxyAnhydrides (NCAs) and Urethane N-Carboxyanhydride (UNCAs).
NCAs and UNCAs have proven a great interest in two main areas:
• monomers for Ring Opening Polymerization (ROP) for NCAs
• powerful building blocks for smooth and eco-friendly coupling reaction with various nucleophiles for NCAs and UNCAs
ISOCHEM offers about 60 NCAs and the synthesis on demand of new NCAs or UNCAs including derivatives of non natural α-aminoacids.
Peptide based therapeutic polymers: NCAs are strategic building blocks for the preparation of polyaminoacid architectures for polymer drugs or polypeptide carriers in drug delivery and targeting technologies. Expanding the range of available NCA monomers including side chain functionalized α-aminoacids, offers post-polymerization modifications which broaden the perspectives of α-aminoacid based polymer therapeutics.
α-aminoacids coupling in APIs synthesis: UNCAs are now an established and attractive alternative to traditional α-aminoacid activation strategies for coupling reactions. The strength of this technology for industrial processes is demonstrated by its lower environmental and safety impact when compared to other coupling agent strategies. It also offers product purity profile advantage due to the reaction selectivity and the absence of any coupling reagent.
Logistic solution and support
Packaging: moisture proof double sealed bag.
Transportation: frigipack for small quantities, insulated box with dry
ice, reefer container for large quantities with temperature monitoring set.
Stability and storage: storage under nitrogen, at temperatures of
- 20°C +/- 5°C or 0°+/- 5°C depending on the stability of the NCA.
Handling: allow the package to warm up to room temperature before
opening and handle under dry and inert atmosphere.