- Variant
- 5MG
- Lot #
- Pending
- Labeled
- 5MG
- Actual
- Pending
- Tested
- Pending
Documents identity, purity, net peptide content, HPLC conformity, heavy metals, sterility, and endotoxin review for the selected batch.

Research use only. Not for human consumption.
We use third-party testing to give you a clearer look at identity, purity, and batch consistency before a product reaches your lab. Our testing is done by ILS Labs.
Documents identity, purity, net peptide content, HPLC conformity, heavy metals, sterility, and endotoxin review for the selected batch.
Based on the current compound category and related research focus.
Reference details for molecular identification, handling conditions, and storage guidance.
Structural identifiers and catalog-level compound reference data.
Common catalog aliases and related compound naming.
Storage states and handling notes for controlled laboratory workflows.
Scientific context and research-use framing for this catalog material.
AOD-9604 is a synthetic peptide fragment derived from the C-terminal region of human growth hormone. PubChem describes AOD9604 as a 16-amino acid peptide modeled on a fragment of the human growth hormone molecule, which places it within GH-fragment analog research. PubChem
The broader research context for AOD-9604 includes peptide-fragment characterization, GH-fragment analog studies, and metabolic pathway models. Its scientific relevance comes from its defined fragment identity and its use as a model compound for studying sequence-specific activity within growth hormone-derived peptide research.
Researchers may use AOD-9604 in controlled laboratory workflows involving peptide sequence comparison, fragment-origin mapping, biochemical pathway studies, and structure-activity relationship research. The research framing centers on fragment identity and laboratory model relevance.
For laboratory research use only. Not for human or veterinary use.
Peer-reviewed studies referenced for educational purposes only. Not intended as medical advice or product claims.
Schänzer W, Thevis M
Orlovius AK, Thomas A, Schänzer W
Heffernan M, Summers RJ, Thorburn A
Halford JC
Cox HD, Smeal SJ, Hughes CM


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