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Where to buy AOD-9604.

A 2026 sourcing guide for AOD-9604 — the 16-residue C-terminal fragment of human growth hormone that failed its Phase IIb obesity endpoint, ended up with a food-ingredient GRAS dossier instead of a drug approval, and is short enough that identity verification carries more weight than a purity number.

WTBP Research Team Last reviewed August 2026 9 min read Buyer’s Guides

You can buy AOD-9604 from research-supply vendors online, and that's the only working route, because no regulator has approved it and no pharmacy dispenses it. Where to buy AOD-9604 really asks which vendor can demonstrate that the vial holds a correctly folded 16-residue fragment. Its own 24-week Phase IIb trial missed its endpoint.

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Referenced in this guide
Batch-matched COAHPLC + mass specResearch use only

Third-party tested research compounds, each shipped with a batch-matched certificate of analysis showing HPLC purity and mass-spec identity — the documentation this site argues you should hold any supplier to.

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AOD-9604 is a 16-amino-acid growth-hormone fragment, identified by CAS 221231-10-3, mass 1815.08 g/mol, with a Cys7–Cys14 disulfide bridge. It remains a legal research compound rather than a medicine, with no FDA, EMA or TGA authorization; the 2014 GRAS filing is a food rule, not approval. Tested vials cost $30–$60 per 5 mg; a certificate confirms ≥99% purity.

Quick answer. Third-party tested AOD-9604 should cost $30–$60 per 5 mg vial, ship as lyophilized powder, and arrive with a CoA naming an ISO 17025-accredited lab. Insist on three lines: mass-spec identity at 1815.08 ± 0.5, HPLC purity ≥99%, and disulfide-bridge integrity.

If a vendor markets AOD-9604 as an FDA-approved or GRAS-endorsed obesity product, that vendor has told you what it thinks of the Phase IIb record.

Where can you buy AOD-9604?

AOD-9604 comes from research-supply vendors, and almost nowhere else. A second, odder channel exists because of the 2014 GRAS food filing, and a handful of supplement-adjacent sellers use it. The compounding and clinic route is effectively closed, because no regulator anywhere has approved the compound.

Require five things from that first channel. A third-party CoA from a named ISO 17025-accredited lab. HPLC purity ≥99% with the chromatogram. Mass-spec identity. Disulfide-integrity data. Endotoxin testing by LAL.

The GRAS dossier is real. What it means is narrow. A sponsor concluded the substance is safe for use in food, under a framework that never evaluates therapeutic efficacy. It isn't a drug approval, it doesn't license obesity claims, and it doesn't upgrade the clinical evidence by one paper.

We read any vendor whose regulatory section leans on GRAS to imply approval with real skepticism everywhere else on the page too. Clinic-channel offers of “pharmaceutical-grade” AOD-9604 are a claim about marketing rather than about manufacturing.

Which research-supply vendors to shortlist

Six vendors, ordered the way our supplier comparison orders them — on what each one will show you rather than what it claims — with every column pulled from the vendor's own storefront on 13 August 2026; there is no verified AOD-9604 price anywhere in that set, so pricing is benchmarked on BPC-157 across the same vendors and no price column appears here.

Vendor COA Lab named Ships free at
Sports Technology Labs Third-party, published MZ Biolabs + Colmaric — on the site and the document $149
Swiss Chems Third-party, published Janoshik — on the site (FAQ) $100
Core Peptides Third-party, published (A2LA #6377.01.01) Vanguard Laboratory — document only $200
American Peptides Third-party, published, with lot lookup Bioviridian Inc. — document only $300
Behemoth Labz Published, but ~2 years stale† MZ Biolabs / Colmaric — document only $100

† Behemoth Labz publishes real certificates, but the newest genuine document we could open was dated 2024-08-08 — roughly two years old, which is why freshness matters more here than the existence of a PDF. Stock varies by compound, so confirm a vendor actually lists AOD-9604 before you compare — what these columns describe is disclosure practice, and that is the part that travels across every compound a vendor sells. Disclosure: this site earns a commission on purchases made through its links, and Peptriva is one of the vendors it links to. Every column above is a document you can open or a page you can load yourself.

The identity check to run against whichever vendor you pick is CAS 221231-10-3 on the certificate's identity line with an observed mass of 1815.08 g/mol, plus explicit confirmation that the Cys7–Cys14 disulfide bridge is intact rather than a purity figure alone.

What is AOD-9604?

AOD-9604 stands for “Anti-Obesity Drug 9604”. It was developed at Monash University in the 1990s and licensed to Metabolic Pharmaceuticals in Australia. It's the C-terminal fragment of human growth hormone, residues 176–191, with an N-terminal tyrosine added for stability. Full-length hGH is a 191-residue protein. This is the last sixteen residues of it.

The design logic was, we'd say, genuinely elegant. Growth hormone drives lipolysis. It also raises IGF-1, promotes growth, and degrades insulin sensitivity, which are the receptor-mediated effects that limit clinical hGH use. Isolate the lipolytic domain, the reasoning went, and you keep the fat-cell signal while leaving the receptor untouched.

AOD-9604 does appear to have achieved the selectivity half of that goal. It has little measurable affinity for the canonical growth hormone receptor. What it never achieved was translation.

The proposed mechanism is direct lipolytic action on adipocytes, through a putative “hGH 176-191 receptor” or a β3-adrenergic-like adipose pathway. That rests on rodent work, and the receptor in question has never been definitively identified in the twenty-five years since.

So the sequence on the vial matters more than usual. Written out it's Tyr-Leu-Arg-Ile-Val-Gln-Cys-Arg-Ser-Val-Glu-Gly-Ser-Cys-Gly-Phe. Sixteen residues, two cysteines, one intramolecular disulfide bridge between them.

Legitimate AOD-9604 is a white lyophilized cake in a sealed glass vial. It's stable at −20 °C for up to 36 months and at 2–8 °C for around 12. Reconstituted, the in-use window is near 28 days refrigerated.

Reducing agents such as DTT, BME and TCEP cleave the bridge and abolish the fold. That's one reason we don't treat the disulfide line on a CoA as a formality.

How do you verify AOD-9604 before you buy?

Five checks sharpen considerably for a short growth-hormone fragment like AOD-9604. Confirm CAS, formula and intact mass. Demand the disulfide assay. Treat purity and identity as separate questions. Check counter-ion and endotoxin accounting. Read the GRAS language literally. Our eight general criteria apply on top.

1. CAS number, formula, and intact mass

The CAS Registry Number for AOD-9604 is 221231-10-3 and the molecular formula is C78H123N23O23S2. Mass spectrometry on the CoA should report identity against a specification of m/z 1815.08 ± 0.5.

A CoA that omits the CAS number, or reports a mass without stating the acceptance window, is giving you a number rather than a check. If the observed mass sits outside that window, the vial doesn't contain AOD-9604. No interpretation rescues it.

2. Disulfide-bridge integrity, the check almost nobody publishes

This is the single most AOD-specific line on a CoA, and most vendor certificates don't have it. AOD-9604's Cys7–Cys14 bridge defines the folded conformation the whole lipolytic hypothesis was built around.

A reduced, linear chain has the same amino acids in the same order and will satisfy a sequence-identity check. Forming a disulfide removes two hydrogens, so the linear chain reads only about 2 Da heavier. That gap is narrow enough to vanish inside a sloppy mass window.

Ellman's reagent measures free thiol directly, and a credible specification is ≥95% oxidized. Material tested at 97.2% oxidized tells you something a purity percentage never can.

3. The fragment-counterfeit problem

A 16-residue peptide with no acylation, no non-natural residues and no cyclization is cheap and fast to synthesize almost anywhere. That cuts both ways. It keeps legitimate AOD-9604 inexpensive, and it makes substitution economically attractive.

Shorter truncations, the fragment without its stabilizing N-terminal tyrosine, scrambled sequences and bulk-filler blends are all cheaper than the real thing. All of them pass a visual inspection of a white lyophilized cake.

The consequence is that HPLC purity isn't an identity test. A vial can be 99% pure and 100% the wrong molecule. The chromatogram only says the material is homogeneous, not that it's what the label claims.

For fragment peptides, identity data is the load-bearing part of the certificate and purity is secondary. That means mass spec plus the disulfide assay. Vendors who publish only a purity percentage for AOD-9604 have published the less informative half.

4. Counter-ion and endotoxin accounting

Peptides ship as salts, and the counter-ion is real mass in the vial that isn't peptide. A CoA should state the counter-ion and its content. For AOD-9604, acetate below roughly 12% w/w is a reasonable specification, with well-controlled material landing nearer 6%.

Endotoxin by LAL below 1.0 EU/mg and a bioburden line round out the safety-adjacent section. Without these, the milligram figure on the label is a nominal number rather than a measured one.

5. The GRAS-versus-approval check

Read the vendor's regulatory language literally. “GRAS” and “FDA-approved” are different frameworks with different evidentiary bars, and only one of them evaluates whether a substance does anything. AOD-9604 has the first and has never had the second. Marketing that slides between them is the clearest signal that a supplier will misrepresent the record.

What does AOD-9604 cost in 2026?

AOD-9604 costs $30–$60 for the standard 5 mg vial and $55–$100 for 10 mg at third-party tested retail. It's inexpensive to make: sixteen residues, standard amino acids, one oxidation step to close the disulfide, then repurification.

Pricing meaningfully below $20 per 5 mg vial deserves a direct question about the oxidation and repurification steps. Closing the Cys7–Cys14 bridge under controlled conditions, then re-running HPLC on the folded product, is where the cost sits.

It's also exactly the step a producer skips when competing on price, because the crude linear chain looks identical on a label.

The other pricing trap runs the opposite way. AOD-9604 gets marketed as the affordable alternative to GLP-1-class research compounds, which run an order of magnitude higher per vial.

That price gap is a synthesis fact. Incretin analogs are 31–39 residues with lipidation and specialized coupling chemistry. It isn't a value judgment and it isn't evidence about either compound. Reading cheapness as efficiency inverts the actual comparison: one class has a decisive human trial record, and the other has a negative pivotal readout.

Yes. AOD-9604 is legal to buy and sell in the US as a research reference compound labeled for laboratory use only. Its regulatory position is unusual mainly because there's a real filing to point at, just not the one vendors imply.

That WADA line is the trap worth dwelling on if you're athletic-adjacent. “Not on the list” is doing much less work than it appears to.

The S2 category is written to cover growth hormone and its fragments as a class. AOD-9604 is, by construction and by its own product name, a C-terminal fragment of human growth hormone. Class-based prohibitions don't require a name listing to apply. A vendor advertizing AOD-9604 as “not banned” is quoting the index rather than the category text.

The S2 category is written around growth hormone, its fragments and releasing factors. AOD-9604 is a growth hormone fragment that happens not to be named. For anyone subject to testing, that is a question for a governing body, not a green light from a vendor page.

— Our reading of the WADA Prohibited List S2 category text, 2026

What are the red flags when buying AOD-9604?

Eight AOD-9604 warning signs we’d walk away from:

AOD-9604

5 mg ≥99% pure Lyophilized

16-residue hGH 176-191 fragment with the intramolecular Cys7–Cys14 bridge intact, CAS 221231-10-3, formula C78H123N23O23S2. third-party tested reference compound; COA with HPLC trace, mass-spec identity, Ellman’s disulfide check, and acetate counter-ion content on every lot.

Learn more

Where this falls short. The AOD-9604 evidence base doesn't merely lack support. It points the other way. The pivotal human trial was negative, the obesity program ended, the osteoarthritis repositioning never reached approval, and the receptor the mechanism depends on has never been identified.

The one recent PubMed-indexed paper uses the peptide as a delivery moiety rather than testing it as a therapy, per Habibullah et al., 2022. Buyers sourcing AOD-9604 as a reference compound for fragment chemistry or comparative lipolysis assays are on solid ground. Buyers sourcing it because a vendor page describes GH-like lipolysis are buying the marketing.

Many unapproved peptides demonstrate favorable tissue repair and metabolic outcomes in animal models, but rigorous human safety data are scarce.

— Mendias & Awan, Sports Medicine, 2026, grouping AOD-9604 with grey-market peptides whose human evidence does not match the marketing

Frequently asked questions

Is AOD-9604 legal to buy in the USA?

Yes, as a research reference compound labeled for laboratory use only. AOD-9604 isn't FDA-approved as a drug and isn't a controlled substance. Selling it for human consumption with obesity-indication claims crosses into FDA drug jurisdiction. Buying it as research material does not.

What should an AOD-9604 CoA show?

Five lines at minimum. CAS 221231-10-3 on the identity line. Mass-spec identity against a stated window of 1815.08 ± 0.5. HPLC purity ≥99% with the chromatogram attached. Disulfide-bridge integrity by Ellman's reagent at ≥95% oxidized. Endotoxin below 1.0 EU/mg by LAL.

Acetate counter-ion content and bioburden round it out, and the ISO/IEC 17025-accredited lab should be named. Our walkthrough is here: how to read a Certificate of Analysis.

Does the AOD-9604 GRAS filing mean the FDA approved it?

No. GRAS is a food-ingredient framework, and the 2014 filing was a sponsor self-determination for AOD-9604 as a food or dietary ingredient. It evaluates safety for use in food. It doesn't evaluate efficacy for any indication, it doesn't authorize therapeutic claims, and it isn't a drug approval. That distinction is the single most exploited gap in AOD-9604 marketing.

Why does a 16-residue fragment need extra identity verification?

Because short fragments are the cheapest peptides to counterfeit. Sixteen standard residues with no acylation and no non-natural chemistry can be made almost anywhere.

Truncations, the fragment minus its N-terminal tyrosine, or a reduced chain that never had its bridge closed are all cheap and visually undetectable. A purity number describes homogeneity only. Mass spec plus the disulfide assay establishes identity.

Is AOD-9604 prohibited in sport?

AOD-9604 isn't named on the WADA Prohibited List. The S2 category covers growth hormone, its fragments and releasing factors as a class, and AOD-9604 is structurally a growth hormone fragment. So class coverage is a live question rather than a settled one. Anyone subject to anti-doping testing should treat non-listing as unresolved and consult their governing body.

Why is AOD-9604 so much cheaper than GLP-1-class research peptides?

Synthesis length and chemistry. AOD-9604 is 16 residues with one disulfide. Incretin analogs are 31–39 residues with lipidation and specialized coupling steps. The price difference reflects the manufacturing route and nothing else. The evidence difference runs the other way entirely, which we cover in our GLP-1 class comparison.

How does AOD-9604 compare to tesamorelin?

They aren't the same category of evidence. Tesamorelin is a stabilized GHRH analog with FDA approval in a specific indication and a corresponding trial record. AOD-9604 is an unapproved hGH C-terminal fragment whose pivotal obesity trial was negative. Both sit on the growth-hormone axis. Only one has a regulator's efficacy finding behind it. See where to buy tesamorelin.

What to know now

What we’re watching

Two things would change the AOD-9604 picture, and neither has happened in twenty-five years. The first is identification of the receptor the lipolytic hypothesis depends on.

The mechanism is still described by what the molecule reportedly does in rodent adipose tissue, rather than by what it binds. A confirmed target would be the first genuinely new fact here since the Phase IIb readout.

The second is a registered clinical program in a defined indication, run to modern standards, in a population where a GH-fragment rationale is plausible. Absent either, the compound's trajectory in the literature is toward tool-compound use. The one substantive recent paper employs it as a tumor-targeting moiety on drug-loaded nanoparticles, per Habibullah et al., 2022.

On the supply side, we're tracking whether disulfide-integrity testing becomes a standard CoA line for fragment peptides rather than a differentiator. For AOD-9604 it's the difference between verified material and a plausible-looking linear chain.

References

  1. Mendias, C. L., & Awan, T. M. (2026). Safety and efficacy of approved and unapproved peptide therapies for musculoskeletal injuries and athletic performance. Sports Medicine. https://doi.org/10.1007/s40279-026-02437-0
  2. Habibullah, M. M., Mohan, S., Syed, N. K., Makeen, H. A., Jamal, Q. M. S., Alothaid, H., Bantun, F., Alhazmi, A. Y., Hakami, A. R., Aleissi, A. F., & Pottoo, F. H. (2022). Human growth hormone fragment 176–191 peptide enhances the toxicity of doxorubicin-loaded chitosan nanoparticles against MCF-7 breast cancer cells. Drug Design, Development and Therapy, 16, 1963–1974. https://doi.org/10.2147/DDDT.S367586
  3. U.S. Food and Drug Administration. Generally Recognized as Safe (GRAS). https://www.fda.gov/food/food-ingredients-packaging/generally-recognized-safe-gras
  4. World Anti-Doping Agency. The Prohibited List (S2 — Peptide Hormones, Growth Factors, Related Substances and Mimetics). https://www.wada-ama.org/en/prohibited-list
  5. U.S. Food and Drug Administration. (2024). Research Use Only (RUO) and Investigational Use Only (IUO) labeling under 21 CFR § 809.10(b)(9). https://www.fda.gov/medical-devices/ivd-regulatory-assistance/research-use-only-and-investigational-use-only-ruoiuo-labels
  6. International Organization for Standardization. (2017). ISO/IEC 17025:2017 — General requirements for the competence of testing and calibration laboratories. https://www.iso.org/standard/66912.html

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