HPLC purity
Reverse-phase HPLC quantifies primary peak area and screens for related substances and process impurities on every release lot.
Documentation & Testing
We do not ask researchers to take our word for analytical quality — we ship the analytical record with the vial. Browse the lot-level Certificate of Analysis (CoA) library below: HPLC purity, mass-spec identity, sterility (USP <71>) and bacterial-endotoxin (USP <85>) screening on every released lot.
Reference grade
Reference grade
Research peptides
Research peptides
Lot-documented
Lab materials
Lot-documented
Lot-documented
Lab materials
Research peptides
Research peptides
Analytical standards
Analytical standards
Analytical standards
Lot-documented
Lot-documented
Research peptides
Lab materials
Our quality procedures
Each released lot passes the procedures below before it leaves QA. The results are recorded in the CoA that ships with the order.
Reverse-phase HPLC quantifies primary peak area and screens for related substances and process impurities on every release lot.
Mass spectrometry confirms molecular identity by exact mass. The acquired spectrum is filed in the CoA against the master reference.
Microbial-growth sterility screening is performed on every released lyophilized lot by an accredited microbiology partner.
Bacterial endotoxin testing (LAL kinetic) is run per lot and the result is documented as endotoxin units per vial in the CoA.
Accelerated stability runs simulate shipping and storage stress so the lot you receive performs identically to the lot we released.
Every lot is benchmarked against a master reference for retention time and mass identity so analytical work converges order to order.
QA records — including HPLC chromatograms and prior-lot CoAs — are kept on file and available on request for qualified research customers.