Ask sales for the lot-numbered COA. Net peptide content, RP-HPLC, ESI-MS, or other results appear only when they are part of that batch's agreed analytical scope.
Lot-numbered COA available; the certificate states the tests actually completed.
Batch COA records net peptide content when included in the agreed specification.
Reading a Peptide HPLC Trace — A 5-Minute Field Guide for Bench Scientists. Read our briefing →
Reading a peptide HPLC trace — a field guide. Read →
On reading HPLC traces. Read →
For Contract Research Organisations
CROs run studies on behalf of sponsors who will audit the paper trail. Lyochem supplies lot-traceable reference material with a per-lot data packet harmonized across multi-site shipments, an IND-aware reporting structure on scale-up, and reservation against shifting sponsor timelines.
The situation
A CRO's reference material is only as good as its documentation under audit. When a sponsor's QA reviews the study, the standard's identity, purity, and lot history have to reconcile across every site that ran the assay — a mismatch between sites is a finding.
Lyochem harmonizes the per-lot packet across multi-site shipments so the same study references the same documented material everywhere, and structures reporting to be legible to a sponsor's IND-aware review on scale-up campaigns.
Regions served: Global · USA · EU · India · China · APAC CRO clusters
How procurement runs
Tell us the sponsor's documentation expectations and the sites involved; we map the packet to what their QA will look for.
Multi-site shipments carry a harmonized per-lot packet so every site references identical documentation.
Lot-traceable reporting structured for sponsor review, IND-aware on scale-up campaigns.
Forecast-based reservation absorbs sponsor-timeline shifts across the campaign.
The release packet
The analytical packet — not the price — is what an audit, a reviewer, or a downstream SOP actually checks. Request the sample data packet to vet the depth before a PO.
Lot-traceable documentation suitable for sponsor audit
Per-lot data packet harmonized across multi-site shipments
Methods and results listed on the matching batch COA; extra identity or sequence work by prior agreement
Impurity profiling and amino-acid analysis on request
IND-aware reporting structure on scale-up campaigns
Forecast-based reservation across the study timeline
Curated catalogue
GLP-1 receptor agonist · 31-mer metabolic research peptide
GIP / GLP-1 dual receptor agonist · 39-mer metabolic research peptide
GIP / GLP-1 / glucagon tri-agonist · 39-mer metabolic research peptide
15-mer
Body Protection Compound 15-mer
43-mer
Thymosin β4 fragment
28-mer
28-amino-acid thymic immune-modulation peptide
Before a first order
Ask sales for the COA matched to the offered or supplied lot. It records the tests actually completed, their specifications, and results. Tell us the sponsor's required methods and document set before quotation so capability, timing, and any additional cost can be agreed.
Multi-site shipments carry a harmonized per-lot packet so every site references identical documentation for the same study. This avoids the cross-site mismatches that turn into audit findings.
Impurity profiling and quantitative amino-acid analysis are available on request alongside the standard identity/purity packet — useful when a method or a sponsor requires content assignment beyond HPLC area-percent. Our lab notes on impurity profiling and AAA describe what each adds.
Yes — forecast-based reservation holds against an expected window so a sponsor-driven schedule change does not reset your lead time. Discuss the campaign forecast at quote stage.
Lab notes for this workflow
Methodology
What Analytical Packet Should a Research Peptide Standard Include?
Read
Lab Note
Peptide Impurity Profiling — Truncations, Deletions, Modifications, and Where They Come From
Read
Lab Note
Amino Acid Analysis — The Third Identity Test Most Lot Reports Skip
Read
Lab Note
Sequence-Confirmed Synthesis — Why Mass Spec Alone Isn't Enough
Read
Other research teams we serve
Academic Laboratories
Universities, medical schools, and government institutes qualifying a reference standard for a method-development or in-vivo workflow.
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Biotech R&D Groups
Preclinical biotech and pharma discovery teams sourcing characterized peptides for receptor-pharmacology, screening, and method-development campaigns.
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Core Facilities & Instrumentation Cores
Shared instrumentation cores and mass-spec facilities holding reference standards for cross-PI method validation and reagent qualification.
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First reply under 24 hours from a synthesis chemist or analytical contact — not a templated auto-response. Ask sales for the matching batch COA and confirm which chromatograms, spectra, sequence work, water, or stability data are available or need separate scoping.