Peptide research lives or dies on what the bench confirms—not what’s printed on a label. We built a peptide-only catalog around the panels researchers actually order: purity, sterility, and endotoxin—with clear turnaround expectations and COA-ready reporting.
| Test | Turnaround | Description |
|---|---|---|
| Purity & Quantity | 5–7 business days from sample receipt | Quantitative purity and quantity assessment for peptide material using HPLC—one vial per submission for this panel. |
| Sterility | 7–10 business days from sample receipt | Sterility testing under USP 71 for injectable and research peptide preparations. |
| Endotoxins | 5–8 business days from sample receipt | Endotoxin analysis for peptide samples. One vial covers both sterility and endotoxins when ordered together. |
Panels run on documented, validated methods with traceable outputs suitable for internal release review.
Accounts are limited to researchers. Profile data carries forward so repeat submissions stay fast.
Statuses, methods, and COA documents are visible in your dashboard—not locked behind email threads.
We combine controlled analytical workflows with a digital experience that respects your time.
3
Core peptide panels
COA
Certificate per completed panel
24/7
Dashboard access