FAQ

Our platform enables rapid, site-selective incorporation of fluorine (¹⁹F or ¹⁸F) without the need for protection/deprotection steps. It’s compatible with complex molecules and is particularly well-suited for late-stage fluorination, a long-standing challenge in medicinal chemistry.

Yes. Our tag portfolio includes functional groups such as azide, amine, carboxylic acid, and hydroxyl, making them suitable for conjugation to a wide range of biomolecules, including proteins, peptides, antibodies, oligonucleotides, and delivery vectors.

In most cases, fluorination is complete in under 10 minutes, which is crucial for working with short-lived isotopes like ¹⁸F. This speed also supports time-sensitive workflows such as radiotracer development and PET imaging studies.

Absolutely. Based on your specific needs we can offer custom-made products including fluorinated amino acids, taggable intermediates, and fluorination-ready scaffolds. We’ll work with you to design and deliver materials tailored to your research or manufacturing needs.

Yes. Our chemistry is clean, high-yielding and compatible with scale-up and process development, especially for fluorine-containing APIs. It simplifies synthesis by removing the need for protecting groups, reducing the number of steps and improving reproducibility.

Yes. Our fluorination chemistry enables rapid and reliable incorporation of ¹⁸F, making it ideal for radiopharmaceutical development and non-invasive imaging studies.

We maintain a catalog of in-stock tags and fluorinated amino acids, and we are continuously expanding it. For out-of-stock items or novel compounds, we offer custom synthesis services with short lead times.

All products are supplied with full analytical characterization, typically including NMR, LC-MS, and HPLC, to ensure quality and batch-to-batch consistency.

Yes! We’re always happy to schedule a consultation to understand your needs and explore how our platform can support your project. Just reach out via our contact form.