Let's build your molecule together.

The most helpful details are: target molecule structure (SMILES or image), desired purity & specifications, required batch quantity, timeline, any regulatory pathway (e.g., cGMP, small-molecule IND), & constraints (cost sensitivity, preferred solvents, avoided reagents). If you have a specification sheet or reference standard data, that speeds up feasibility assessment considerably.

We respond to every RFQ within one business day. If we need clarification, we'll email you directly. After our initial feasibility assessment, we schedule a brief scoping call, usually within 3–5 days, to discuss route options, timelines, & budget.

Yes. We have a standard mutual NDA ready to sign before any detailed project discussion. If you have your own NDA, we can review & execute that as well. We treat confidentiality seriously & do not share project details with competitors or external parties.

We can work at any scale from milligrams (research/discovery phase) through metric tons (commercial CDMO production). For custom synthesis & FTE, we typically handle 50 mg to 500 kg. For CDMO scale-up & continuous manufacturing, we can go larger. During your scoping call, we'll confirm capacity & optimal batch size for your economics.

Absolutely. For many projects, we can prepare a small batch (typically 100–500 mg) at reduced cost to prove the route works & meet your specifications. This "proof of concept" batch is an excellent way to de-risk a larger manufacturing commitment & give you time to run internal testing & regulatory pathways before scaling.

Yes, we ship globally. We have established logistics partnerships & regulatory export expertise, so materials can be shipped to nearly any country with appropriate documentation. Hazardous chemical shipping classifications are handled by our quality & logistics team to ensure compliance with international transportation & destination country requirements.