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Research use only · not for human or veterinary consumption 10 slots open →
Tesa10 + ip5 15mg lyophilised research vial, 99% purity

Specification

Purity>99% (HPLC + MS)
FormLyophilised powder
Supplied asSingle sealed vial
Storage-20 °C, dark, sealed
Reconstituted2–8 °C

Certificate of analysis

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Tesa10 + ip5

A blend of tesamorelin and ipamorelin combining GHRH-receptor and ghrelin-receptor mechanisms.

Research use only. This compound is supplied for laboratory research. It is not a medicine or supplement, is not approved for human use, and no dosing guidance for humans is offered here or by our team. Handle under appropriate laboratory conditions. Full disclaimer →

Available sizes & pricing

Price is per single sealed vial, in USD. Buying several — volume pricing.

Vial strengthPrice
15mg $484.40 Order 15mg

Published research

Links open peer-reviewed sources on PubMed. These are provided so you can read the primary literature yourself. Citing a study is not a claim that this compound is safe or effective for any use in humans.

Studied in the same area

CJC-1295 (no DAC) 5mg + Ipamorelin 5mg 10mg lyophilised research vial, 99% purity

CJC-1295 (no DAC) 5mg + Ipamorelin 5mg

Mod GRF (1-29) + Ipamorelin blend

The classic paired blend: a GHRH analog alongside a selective ghrelin-receptor agonist, studied for complementary action on the GH axis.

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Tesamorelin 2mg lyophilised research vial, 99% purity

Tesamorelin

TH9507, trans-3-hexenoyl-GHRH(1-44)

A stabilised GHRH(1-44) analog and the only GH-axis compound with regulatory approval specifically for reducing visceral adipose tissue.

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HGH (Human Growth Hormone) 6iu lyophilised research vial, 99% purity

HGH (Human Growth Hormone)

Somatropin, recombinant human growth hormone (rhGH), 191aa

Recombinant 191-amino-acid human growth hormone — the reference molecule against which every secretagogue in this catalog is measured.

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CJC 1295 (without DAC) 2mg lyophilised research vial, 99% purity

CJC 1295 (without DAC)

Modified GRF(1-29): a tetrasubstituted GHRH analog without the drug affinity complex.

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