How to reconstitute Adipotide: mixing and storage
A fat-blood-vessel targeting peptide with monkey weight-loss data and kidney toxicity.
Also called: FTPP, FTTP, Prohibitin-TP01, Prohibitin-targeting peptide 1, CKGGRAKDC-GG-D(KLAKLAK)2.
Fat-loss peptides · Prohibitin-targeted proapoptotic peptidomimetic.
Comes as: Community-reported powder vials for mixing and injection.
Mixed with: Bacteriostatic water is reported by one user; compatibility and stability are unvalidated..
Common vial sizes: 2, 10 mg. Common water amounts: 1 mL.
- One report describes 2 mg with 1 mL water; these are anecdotes, not a standard formulation.
- A separate report describes 10 mg/3 mL; the exact added-water volume is unstated.
- Syringe units measure volume, not mass; conversion needs the actual concentration.
- No approved storage label, mixing instructions or beyond-use date was found.
Before mixing: One user reports freezer storage; no validated temperature range or shelf life was found.
After mixing: A user reports keeping the mixed vial in a fridge. No adipotide-specific refrigerated shelf life is established.
Related to Adipotide
- AOD-9604: A growth-hormone fragment whose largest obesity trial failed to show meaningful weight loss.
- Tirzepatide: A weekly GIP/GLP-1 injection with strong diabetes and weight-loss evidence and common stomach side effects.
- Retatrutide: An experimental weekly injection with phase 3 weight-loss results.
- Tesamorelin: A peptide approved for deep abdominal fat in adults with HIV lipodystrophy.
- SS-31 (elamipretide): A peptide approved for Barth syndrome muscle strength; benefit needs confirmation and broader energy benefits remain unproven.
Sources
- 21 CFR 216.23 — Bulk drug substances that can be used to compound drug products in accordance with section 503A of the Federal Food, Drug, and Cosmetic Act., Office of the Federal Register · eCFR · 2026
- 503B Bulk Drug Substances List, FDA · FDA · 2026
- Acute kidney injury (AKI), NHS · 2026
- Bulk Drug Substances Nominated for Use in Compounding Under Section 503A of the Federal Food, Drug, and Cosmetic Act, FDA · FDA · 2026
- Bulk Drug Substances Used in Compounding Under Section 503A of the FD&C Act, FDA · FDA · 2026
- Certain Bulk Drug Substances for Use in Compounding that May Present Significant Safety Risks, FDA · FDA · 2026
- Concerns regarding the public health risks associated with unapproved peptide products, Therapeutic Goods Administration and Chief Medical Officer · Therapeutic Goods Administration · 2026
- MHRA Products | Home, MHRA · MHRA · 2026
- The 2026 Prohibited List, World Anti-Doping Agency · WADA · 2026
- Bulk Drug Substances Nominated for Use in Compounding Under Section 503B of the Federal Food, Drug, and Cosmetic Act, FDA · FDA · 2025
- Anaphylaxis, NHS · NHS · 2023
- Drugs@FDA: FDA-Approved Drugs, US Food and Drug Administration
- Search criteria - Drug Product Database online query, Health Canada · Health Canada
- Union Register, European Commission
- Safety and Risk Assessment of No-Prescription Online Semaglutide Purchases., Ashraf AR et al. · JAMA network open · 2024
Sources checked: 2026-10-18.
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