Buy Tesamorelin
Research-grade Tesamorelin with purity documentation for physiological GHRH receptor activation studies
Research Context
Tesamorelin is FDA-approved as Egrifta for HIV lipodystrophy, providing one of the most clinically validated GHRH analog research contexts. Phase 3 data from Falutz et al. (NEJM, 2010) documents visceral fat reduction through physiological GH pulse stimulation.
Full Tesamorelin Research Reference →Tesamorelin Research Supply
>=98% purity by HPLC with batch-specific CoA. Lyophilized powder, 5mg vials.
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What Researchers Look For
Tesamorelin is a complex 44-amino acid peptide with a trans-3-hexenoic acid N-terminal modification, and researchers should specifically verify that the N-terminal modification is present in the supplied compound via mass spectrometry. The expected molecular weight is approximately 5136 Da for the fully modified compound. Preparations lacking the trans-3-hexenoic acid modification would have different pharmacokinetics and potentially different GHRH receptor binding characteristics compared to the FDA-approved Egrifta reference compound.
Why Spartan Peptides
Spartan Peptides supplies Tesamorelin as the fully modified GHRH analog matching the Egrifta pharmaceutical reference at a minimum 98% HPLC purity with batch-specific certificate of analysis. The 5mg vial format aligns with standard research dose quantities. US domestic dispatch ensures rapid delivery for metabolic and GH axis research programs.
Specifications
| Purity Standard | >=98% purity by HPLC |
| Format | Lyophilized powder, 5mg vials |
| Storage | Store lyophilized at -20 degrees C. Reconstituted, stable 30 days at 4 degrees C. |
| Origin | USA domestic supply |
| Documentation | Batch-specific certificate of analysis |
Sourcing FAQ
Order Research-Grade Tesamorelin
>=98% purity by HPLC. Lyophilized powder, 5mg vials. Batch-specific CoA. Domestic US supply with same-day dispatch before 2 PM EST.
All compounds are strictly for in-vitro research use only and not intended for human consumption.