Analytical program
Quality & testing
Research is only as reliable as the material behind it. Every lot moves through the same five-stage analytical program before it is released to the catalog.
- 01
Synthesis
Solid-phase synthesis in cGMP-audited partner facilities.
- 02
HPLC purity
Reverse-phase HPLC establishes purity against a 98.5% floor.
- 03
Mass spectrometry
Identity confirmed against expected molecular weight.
- 04
Endotoxin & sterility
Low-endotoxin fill with sterile filtration prior to lyophilization.
- 05
Certificate of Analysis
Full analytical panel published and traceable by lot number.
NOTICE · Analytical testing establishes purity and identity for research purposes only. It does not make any product safe or approved for human or veterinary use.