For laboratory and research use only. Not for human or animal consumption.

How it works

Tesamorelin is a synthetic analog of the full 44-residue human growth-hormone-releasing hormone, carrying an N-terminal trans-3-hexenoic acid cap. The modification confers resistance to DPP-4 degradation, extending half-life relative to native GHRH while preserving GHRH-receptor agonism on pituitary somatotrophs. In clinical research it is best characterized for reductions in visceral adipose tissue driven through endogenous, pulsatile GH release.

Learn more about the science →
GHRH(1-44) analog→GHRH-R (somatotrophs)
hexenoyl cap→DPP-4 resistant · t½ extended
endogenous GH ↑→visceral adipose research
Certificate of Analysis+

LC-MS identity, HPLC purity (≥99%), mass spec confirmation against 5,135.9 g/mol, endotoxin by LAL, appearance. Third-party ISO-17025 verified.

View full certificate →Lot TES-2606-A · Jun 2026 · printable
Purity (HPLC)99.2%✓ Pass
Mass spec (MW)5,135.9✓ Pass
Endotoxin (LAL)<0.5 EU/mg✓ Pass
Certificate metadata
Lot
TES-2606-A
Released
Jun 2026
Tested by
Janus Analytical (ISO-17025)
Method
RP-HPLC · LC-MS · LAL · KF
Specifications+
CAS218949-48-5
FormLyophilized
Purity≥99% by HPLC
Endotoxin<0.5 EU/mg
Storage & handling+

Lyophilized: −20°C, 24 months. Reconstituted: 2–8°C, use within 14 days — like other GHRH analogs, tesamorelin is more stable lyophilized than in solution. Reconstitute with bacteriostatic water; protect from light.

We ship in insulated parcels with phase-change cooling and a tamper-evident seal.

FAQs+
How does tesamorelin differ from sermorelin?+

Both are GHRH analogs. Sermorelin corresponds to GHRH(1-29); tesamorelin is the full GHRH(1-44) sequence with a hexenoyl cap that resists DPP-4 degradation and extends half-life.

What is tesamorelin best known for in research?+

Reductions in visceral adipose tissue through endogenous GH release, characterized in clinical metabolic studies.

Why is it placed in Growth Factor Research?+

Growth Factor Research at hábit groups the growth-signaling and GHRH-axis compounds — sermorelin, CJC-1295, ipamorelin, and tesamorelin sit together there.

What's a typical reconstitution concentration?+

Investigator-dependent. A common preparation is 2 mL bacteriostatic water per 10mg vial, yielding 5 mg/mL.

Why the shorter post-reconstitution window?+

GHRH analogs are more labile in solution. A 14-day window at 2–8°C minimizes potency loss.

Is tesamorelin subscription-eligible?+

Yes. 15% off on a 60-day cycle.

The research behind this compound, cited in full.

Provided for context only. None of the studies cited below evaluate hábit material specifically; they document the published literature on the compound and its mechanism. Research-use claims are not therapeutic claims.

  1. [01] Falutz J. et al. N Engl J Med 357 (2007): 2359–2370.
  2. [02] Stanley TL. et al. JAMA 312 (2014): 380–389.
  3. [03] Ferdinandi ES. et al. Basic Clin Pharmacol Toxicol 100 (2007): 49–58.
  4. [04] Effects of tesamorlin, a growth hormone-releasing factor, in HIV-infected patients with abdominal fat accumulationJournal of Clinical Endocrinology & Metabolism · 2010 · Falutz J, et al.PMID 20554713

Verified buyer notes

Initials only — every quote is verified against an order record. We don’t ghost-write reviews.

“COA matched what we ran in-house. Powder reconstituted clean, no haze. Did exactly what we needed it to.”
M.O.Boston, MAApril 2026
“Switched after two bad lots from a previous source. Three orders in, zero issues.”
J.K.Austin, TXMarch 2026
“Asked support a purity question and got the raw HPLC trace back within the hour. That transparency is why we reorder.”
S.L.Chicago, ILFebruary 2026