- Artículo de lista #1
- Artículo de lista #2
- Artículo de lista #3
From process development to GMP batches and documentation—QA‑overseen manufacturing, analytical validation and audit support for peptide APIs and intermediates.
Linear/cyclic peptides, fragments and conjugates for clinical/commercial supply.
Amidation/acetylation, disulfides, cyclization, PEGylation, lipidation, conjugation.
Lyophilized powder or solution; aliquoting and specialized packaging.
SPPS as the primary platform with LPPS/hybrid for long or difficult sequences.
Amidation/acetylation, disulfides, stapling, PEGylation, lipidation, dyes/biotin.
Crude → >98% options; lyophilized powder or solution; salt/counter‑ion control.
Custom plates for screening; delivered in 96‑well formats with traceability.
Stable‑isotope labeled peptides for proteomics and quantification workflows.
HPLC/UPLC and MS identity; CoA/CoT; additional reports available on request.
Discovery to kilo‑scale pathways using SPPS and hybrid strategies, with stage‑appropriate purification and documentation.
We accommodate synthesis from milligrams to multi-grams, scaling production flexibly to meet your project's specific quantity requirements.
Products are delivered as lyophilized powder or solution. Convenient aliquoting services are available upon request to suit your specific needs.
Product is released with guaranteed high purities, typically ≥90%, ≥95%, or ≥98%, ensuring quality for your application.
We offer selection and optimization of salt forms and counter-ions (e.g., acetate) with expertise in minimizing residual TFA content.
