Synthesis development - API or custom synthesis

Chiracon offers a comprehensive synthetic development service for active pharmaceutical ingredients (APIs) and advanced intermediates, from early idea to robust, scalable route. With more than 25 years of experience in medicinal and process chemistry, Chiracon designs and optimizes synthesis pathways that are efficient, safe, and compliant with regulatory expectations.

Our team develops innovative synthetic routes, evaluates alternative starting materials, and reduces process complexity and cost while maintaining high quality standards. We perform route scouting, step-by-step optimization, and impurity profiling to ensure reproducible, GMP-ready processes suitable for both clinical and commercial supply.

Chiracon’s facilities support seamless transfer from laboratory to kilo scale, enabling smooth tech transfer into GMP production. Close collaboration with clients, transparent communication, and detailed documentation ensure that every development step is aligned with project timelines and CMC requirements. This makes Chiracon a reliable partner for pharmaceutical and biotech companies seeking robust, scalable, and regulatory-compliant synthesis solutions.