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Generic Peptides Tesamorelin 2, 5 and 10 mg Research Vials
Generic Peptides Tesamorelin 2, 5 and 10 mg Research Vials
Generic Peptides Tesamorelin 2, 5 and 10 mg Research Vials
Generic Peptides

Generic Peptides Tesamorelin 2, 5 and 10 mg Research Vials

Injection · 2 mg · vial

Out of stock
$41.00

Generic Peptides Tesamorelin is a stabilised growth hormone-releasing hormone analogue supplied as a lyophilized research powder in three vial sizes: 2 mg, 5 mg and 10 mg.

GMP-manufactured, each batch is HPLC-verified with the Certificate of Analysis on file. Tesamorelin for sale with U.S. domestic and international shipping and dispatch within two business days after payment.

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Product overview

Generic Peptides Tesamorelin - 2 to 10 mg Research Vials

Generic Peptides Tesamorelin is a synthetic analogue of growth hormone-releasing hormone, supplied as a lyophilized research powder in 2, 5 and 10 mg vials. It contains the full 44 amino acid chain of human GHRH with a trans-3-hexenoic acid group on the end, which is the modification that makes it more stable than the natural peptide. The unmodified 29 amino acid fragment Sermorelin and the long acting CJC-1295 DAC are its neighbours in this line.

  • Three vial sizes - 2, 5 and 10 mg
  • Stabilised GHRH analogue
  • Lyophilized powder
  • GMP-made, HPLC-verified, COA

Variant Comparison

One peptide, three strengths.

Variant Dosage Form and quantity Best use
Tesamorelin 2 mg 2 mg Vial Short
Tesamorelin 5 mg 5 mg Vial Standard
Tesamorelin 10 mg 10 mg Vial Extended

The 10 mg vial carries five times the material of the 2 mg vial, and the 10 mg size is the one that also has a U.S. domestic option. A ghrelin side secretagogue such as Ipamorelin or CJC-1295 no DAC is the usual partner, and Somatropin stays as the direct hormone arm when the two routes have to be compared.

How Tesamorelin Works

Tesamorelin binds the GHRH receptor and stimulates the synthesis and release of the body's own growth hormone, with a matching rise in IGF-1. The trans-3-hexenoic acid cap makes it more potent and more resistant to cleavage by dipeptidyl aminopeptidase than natural GHRH, which is why the signal lasts longer. Its fat reducing action in clinical work is described as lipolysis first, followed by a fall in triglycerides. In the approved prescription product the standard dose is 1.4 mg injected under the skin once daily, and the label states it is not intended for weight loss management.

Reconstitution & Storage

The vial is dissolved with sterile or bacteriostatic water, which is not in the pack, added down the vial wall and swirled rather than shaken. Divide the milligrams on the vial by the millilitres added to read mg per mL. Keep the powder at 2-8 C or -20 C and the mixed solution at 2-8 C for four weeks.

Dosage & Administration

No human dose is stated for this vial and it is not a medicine. The clinical figures in this description belong to an approved prescription product with a different presentation, so nothing here is a treatment protocol or a dosing guide. Tesamorelin is named in WADA class S2.2.4 and is banned in sport at all times.

Supplied for laboratory research only, not for human or veterinary use. Information provided is for educational purposes only and does not constitute medical advice. Consult a qualified healthcare professional before use. Tesamorelin is supplied as a lyophilised powder and stays stable when the vial is kept cold and dry.

Specifications

Trade NameTesamorelin
Generic NameTesamorelin (GHRH analogue)
ManufacturerGeneric Peptides
Dosage2 mg, 5 mg or 10 mg per vial
PackageLyophilized powder, one vial
Drug ClassPeptide; GHRH receptor agonist
AdministrationSubcutaneous (research protocols)
StorageLyophilized 2-8 C or -20 C; mixed 2-8 C, 4 weeks
Prescription StatusResearch use only
VerificationBatch details confirmed with supplier
ShippingInternational about USD 35; USA option on 10 mg

Stacks

Lipolysis Read-Out

Tesamorelin as the GHRH arm and Ipamorelin as the ghrelin arm, run in parallel so the two routes to a growth hormone pulse can be told apart.

Expected outcome: a comparison of how each receptor arm changes the fat and hormone read-outs.

Stability Comparison

Tesamorelin against the plain 1-29 fragment Sermorelin, where the modified chain is expected to survive enzyme cleavage for longer.

Expected outcome: a time course that shows how much the terminal modification extends the signal.

Release versus Replacement

Tesamorelin as the release arm and Somatropin as the replacement arm, kept apart so a stimulated pulse is not read as an injected level.

Expected outcome: a study that separates endogenous release from an externally supplied hormone curve.

For laboratory research only. Consult a healthcare professional before handling any peptide. Amounts shown are research references, not recommended human doses.

FAQ

Before you ask

Questions, answered

Tesamorelin is a synthetic analogue of growth hormone-releasing hormone. Its chain is made of all 44 amino acids of human GHRH with a trans-3-hexenoic acid group added at one end, which protects it from being cut by the enzyme dipeptidyl aminopeptidase. Its formula is C221H366N72O67S and its mass is around 5136 g/mol. Under the brand names Egrifta, Egrifta SV and Egrifta WR it is a prescription product for a specific lipodystrophy indication.

It binds the growth hormone-releasing hormone receptor and drives the pituitary to make and release its own growth hormone, which also lifts IGF-1 levels. The terminal modification makes the molecule more potent and slower to break down than natural GHRH. In the clinical literature the fat reducing effect is described as lipolysis first, followed by a drop in triglycerides, rather than as a general weight loss effect.

The approved label lists the most common reactions, above five percent, as arthralgia, redness and itching at the injection site, pain in the limbs, peripheral oedema and muscle pain. It also warns about raised IGF-1, fluid retention, glucose intolerance or diabetes, and an increased risk of tumours, and it is contraindicated in pregnancy and in people with a disrupted hypothalamic-pituitary axis. This research vial is not that product.

Add sterile or bacteriostatic water down the side of the vial and swirl, do not shake, then divide the milligrams on the vial by the millilitres added to read mg per mL. Keep the sealed powder at 2-8 C or -20 C and let it reach room temperature before opening. The mixed solution stays at 2-8 C and is used within about four weeks.

Yes. The WADA Prohibited List 2026 names tesamorelin in class S2.2.4, growth hormone releasing factors, in the GHRH and analogues group. Category S2 substances are prohibited at all times, in and out of competition. The same line also names sermorelin and CJC-1295, and the wording is written as a catch-all, so related GHRH analogues are covered even when they are not printed.

Both act on the same receptor, but they are different lengths of the same hormone. Sermorelin is only the 1-29 fragment of human GHRH and gives a short pulse, while tesamorelin carries all 44 amino acids plus a fatty acid cap, so it resists enzymatic cleavage and holds the signal longer. That difference in stability, rather than a difference in receptor, is what separates the two products in practice.

All three vial sizes are listed on this page as research material with international and U.S. domestic checkout. International shipping runs about 35 dollars with a transit window of four to ten days, the domestic option is available on the 10 mg vial, and orders are handled within one to two business days. Stock and prices are shown live on the page.

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