For Research Use Only · Not For Human Or Veterinary Consumption

AOD-9604

AOD-9604 is a synthetic 16-residue peptide derived from the C-terminal region of human growth hormone. It is one of only two disulfide-containing peptides in this catalogue, which changes both how it should be characterised and how it should be stored.

CAS Registry Number221231-10-3
Molecular formulaC78H123N23O23S2
Average molecular weight1815.1 g/mol
SequenceYLRIVQCRSVEGSCGF (16 residues)
DisulfideCys7–Cys14, intramolecular
ClasshGH C-terminal fragment analogue
Physical formLyophilised powder, sealed glass vial
Storage2–8 °C, sealed and dry, protected from light
Catalogue referenceCA-10

The naming problem: AOD-9604 is not hGH fragment 176-191

Many catalogues list “AOD-9604” and “hGH fragment 176-191” as synonyms. Strictly they are different molecules.

The native growth hormone sequence at residues 177–191 begins with phenylalanine. AOD-9604 carries an additional N-terminal tyrosine in place of that native residue arrangement, giving a 16-residue peptide beginning YLRIVQ… The added tyrosine is a deliberate synthetic modification, not a transcription of the native fragment.

The practical consequence: a certificate headed “hGH fragment 176-191” may describe either molecule, and their masses differ. Check the sequence on the certificate rather than relying on the name.

A related error worth knowing: ChemicalBook’s record miscounts the peptide as 15 residues. It is 16.

Identity and classification

No receptor or molecular target is assigned to AOD-9604 in reference-supplier catalogue classification, and we make no claim about one. It is supplied and characterised as a sequence-defined synthetic peptide with a defined disulfide.

Structure

Sixteen standard L-residues, free C-terminal acid, with an intramolecular disulfide bond between Cys7 and Cys14 closing a loop of six residues. The two sulfur atoms in the molecular formula are those two cysteines — there is no methionine.

The disulfide is the defining structural feature. It is what makes the molecule a constrained loop rather than a linear chain, and it is the feature most likely to be wrong in a poorly made lot.

Specification and characterisation — the disulfide is the whole story

For a peptide with a defined disulfide, mass and purity alone are inadequate, because the most important failure modes are mass-neutral:

  • Non-reduced versus reduced HPLC. The essential test. Chromatograph the material as supplied, then again after reduction with DTT or TCEP. The retention shift confirms a disulfide is present. A single non-reduced chromatogram does not.
  • Free thiol determination. Ellman’s reagent (DTNB) quantifies unreacted cysteine. A material with significant free thiol has incompletely formed disulfide — the linear dithiol form, which is +2 Da and easily missed.
  • Disulfide scrambling and dimers. With only two cysteines there is a single correct intramolecular pairing, but intermolecular pairing produces dimers and higher oligomers. These are mass-resolvable and appear as later-eluting or size-shifted species. Size-exclusion chromatography catches them.
  • Mass confirmation against 1815.1. Note the oxidised (correctly folded) form is 2 Da lighter than the reduced form — that 2 Da is the diagnostic.
  • RP-HPLC purity at 214 nm, with 280 nm informative via the tyrosine and phenylalanine.
  • Counter-ion and net peptide content. Commonly supplied as the acetate.

A certificate for a disulfide peptide that reports only area percent and a nominal mass has not characterised the feature that defines the molecule.

Handling and stability

Store sealed at 2–8 °C, dry, protected from light. Equilibrate in a desiccator before opening.

Disulfide-containing peptides are subject to oxidation and disulfide scrambling, and both are accelerated by moisture, by alkaline pH and by dissolved oxygen. Where solutions are prepared, degassing or purging with an inert gas is a meaningful precaution rather than a formality, and neutral-to-slightly-acidic buffers are preferable — thiol–disulfide exchange accelerates sharply above pH 7.

Related compounds in this library

Glutathione is the other sulfur-redox-active compound here, though it is the reduced thiol rather than a formed disulfide, and its oxidised counterpart GSSG is an intermolecular dimer rather than an intramolecular loop. The two entries together cover both sides of thiol–disulfide chemistry.

References

Chemical, specification and analytical sources. This list is deliberately limited to chemistry and analytical references.

  • Cayman Chemical, AOD-9604 record — formula, molecular weight, sequence, disulfide assignment
  • Chemsrc, CAS 221231-10-3 — registry and mass data
  • ChemicalBook, AOD-9604 record — registry confirmation (note: this source miscounts the peptide length as 15 residues)
  • Bachem, Handling and Storage Guidelines for Peptides — cysteine oxidation, disulfide handling, degassed buffers

Available from the catalogue

AOD-9604 5 mg — 5 mg of lyophilised powder in a sealed glass vial, supplied with a lot-matched certificate of analysis. Bulk pricing applies from five vials.

Cosmic Aminos supplies this material as a laboratory reagent for in-vitro research use only. It is not a drug, food, cosmetic or dietary supplement, is not approved by the Food and Drug Administration for any use, and is not for human or veterinary consumption. No dosing, administration or preparation guidance is provided.

Research Use Only

All products sold by Cosmic Aminos are laboratory reagents intended strictly for in-vitro research and laboratory experimentation by qualified professionals. They are not drugs, foods, cosmetics or dietary supplements, and are not for human or veterinary consumption or for any diagnostic or therapeutic use. No statement on this website has been evaluated by the Food and Drug Administration. Cosmic Aminos makes no representation regarding safety or efficacy in humans or animals, and does not provide dosing, administration or protocol guidance of any kind. Purchasers must be 21 years or older and are solely responsible for compliance with all applicable federal, state and local law governing the acquisition, handling, storage and disposal of research chemicals.