Lot CJCP072026-MG
99.8%
Overall purity
Tested July 13, 2026
Open COAFOR LABORATORY RESEARCH PURPOSES ONLY. This compound has not received FDA approval. All information shown is drawn from published laboratory research for educational purposes
Before you continue
This site sells research products exclusively to qualified researchers and laboratories for in vitro and laboratory use. Please confirm before continuing.
CJC-1295 / Ipamorelin (5mg / 5mg) is a research peptide formulation supplied by Peppy Peptides for laboratory research use only. CJC-1295 / Ipamorelin is studied in laboratory research for its interaction with growth-hormone-releasing and secretagogue receptor pathways.
CJC-1295 / Ipamorelin combines two research peptides from the growth-hormone-releasing pathway family:
Researchers often pair the two peptides because each is studied in connection with a related but distinct receptor pathway. The pairing lets them examine both pathway families in a single research model instead of using two separate single-compound vials.
Researchers studying growth-hormone-releasing signaling commonly examine CJC-1295 in laboratory models of hypothalamic-pituitary pathways. Ipamorelin is studied in research on secretagogue receptor pathways, often in in-vitro receptor-binding assays and in-vivo research models.
As a combined formulation, CJC-1295 / Ipamorelin is used to investigate how the growth-hormone-releasing and secretagogue receptor pathway families interact within the same study, which allows side-by-side comparison in a single design. All applications described here refer only to laboratory and in-vitro/in-vivo model research.
CJC-1295 is studied in connection with the GHRH receptor pathway and Ipamorelin in connection with a distinct secretagogue receptor pathway. Pairing them lets researchers study both pathway families in one research model.
No. CJC-1295 / Ipamorelin is supplied for laboratory research use only by qualified researchers working in a controlled laboratory setting.
Published laboratory research on CJC-1295 and ipamorelin is indexed on PubMed.
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For research use only. Not for human consumption. Not evaluated by the FDA. Not intended to diagnose, treat, cure, or prevent any disease. This compound has not received FDA approval. All information shown is drawn from clinical studies for educational purposes.
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Lab-verified quality
Each lot is analysed by Bioviridian before release. Below is the Certificate of Analysis for the most recent lot, as issued by the laboratory.
Overall purity
99.8%
RP-HPLC (214 nm)
View the signed COA (PDF)Check this certificate at bioviridians.com/coa-search.html with code COA7685.
Test results
5 of 5 conformHPLC retention time 9.396, 10.416 min · Signed: Shane Straight, M.S., Principal Chemist, Bioviridian Inc.
Every lot keeps its own signed certificate. Lots are listed newest first.
Lot CJCP072026-MG
99.8%
Overall purity
Tested July 13, 2026
Open COAEarlier lots will appear here as new Certificates of Analysis are published.
Compound details
Molecular profile
Storage requirements
Store lyophilised CJC-1295 / Ipamorelin at −20°C for long-term stability, protected from light and moisture.
Refrigerate at 2–8°C after reconstitution and use within 4–6 weeks. Avoid repeated freeze-thaw cycles once reconstituted; keep the vial sealed between uses.
Published literature
7 peer-reviewed publications indexed on PubMed. Listed for reference only; inclusion does not imply any use, effect or endorsement.
J PHARM PHARMACOL · 1995 CJC-1295
Bai JP, Chang LL J Pharm Pharmacol. 1995;47(8):698-701. doi:10.1111/j.2042-7158.1995.tb05863.x
Characterised the enzymatic degradation of GRF(1-29)NH2 by intestinal brush-border preparations and the contribution of dipeptidyl peptidase IV cleavage at the N-terminus.
ENDOCRINOLOGY · 2005 CJC-1295
Jetté L, Léger R, Thibaudeau K, et al. Endocrinology. 2005;146(7):3052-3058. doi:10.1210/en.2004-1286
Described the design of tetra-substituted hGRF(1-29) analogues and their albumin bioconjugates, and characterized GRF-receptor activation and duration of action in rat pituitary cells and rats (note: the lead compound, CJC-1295, carries the DAC linker).
VITAM HORM · 2000 CJC-1295
Structure and function of the growth-hormone-releasing hormone receptor
Petersenn S, Schulte HM Vitam Horm. 2000;59:35-69. doi:10.1016/s0083-6729(00)59003-7
Reviewed the molecular structure, ligand binding and signal transduction of the GHRH receptor, the target of GRF(1-29) analogues.
EUR J ENDOCRINOL · 1998 Ipamorelin
Ipamorelin, the first selective growth hormone secretagogue
Raun K, Hansen BS, Johansen NL, et al. Eur J Endocrinol. 1998;139(5):552-561. doi:10.1530/eje.0.1390552
Characterised the growth hormone-releasing potency and selectivity (versus ACTH and cortisol release) of the pentapeptide ipamorelin in rat pituitary cells and in rats and swine.
GROWTH HORM IGF RES · 1999 Ipamorelin
Ipamorelin, a new growth-hormone-releasing peptide, induces longitudinal bone growth in rats
Johansen PB, Nowak J, Skjaerbaek C, et al. Growth Horm IGF Res. 1999;9(2):106-113. doi:10.1054/ghir.1999.9998
Measured longitudinal bone growth and body-weight parameters in adult female rats given ipamorelin, compared with growth hormone administration.
FRONT NEUROENDOCRINOL · 1998 Ipamorelin
Growth hormone-releasing peptides and their analogs
Camanni F, Ghigo E, Arvat E Front Neuroendocrinol. 1998;19(1):47-72. doi:10.1006/frne.1997.0158
Reviewed the chemistry, receptor pharmacology and endocrine activity of synthetic growth hormone-releasing peptides and their non-peptide analogues.
PHARM RES · 1999 Ipamorelin
Gobburu JV, Agersø H, Jusko WJ, et al. Pharm Res. 1999;16(9):1412-1416. doi:10.1023/a:1018955126402
Developed a pharmacokinetic-pharmacodynamic model relating plasma ipamorelin concentrations to growth hormone release in a characterisation study in healthy volunteers.