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Short answer
CJC-1295 is a synthetic 30-amino-acid analogue of growth hormone-releasing hormone (GHRH). A maleimide-bearing lysine at its C-terminus, the drug affinity complex (DAC), lets it bind albumin in blood. Its half-life was 5.8 to 8.1 days in healthy adults. [1] ConjuChem researchers in Montreal described it in 2005. [2] In Australia it is a Schedule 4 substance also listed in Appendix D. [3]
What is CJC-1295?
CJC-1295 is a lab-made GHRH analogue built from the first 29 residues of human GHRH, with four amino acid substitutions and an extra lysine that carries a reactive maleimide group. Its developers at ConjuChem called it "a tetrasubstituted form of hGRF(1-29)" with a maleimidopropionamide lysine added at the C-terminus. [2]
The design goal was a longer-lasting version of GHRH. A 2006 mouse paper describes its use as "limited by its very short half-life". [9] The DAC fixes that by attaching the peptide to albumin in blood, so it circulates for days.
One naming problem shapes everything that follows. "CJC-1295" means the DAC molecule in the published trials. Sellers also use the name, often with "no DAC" or "without DAC" added, for the 29-residue peptide that lacks the albumin-binding lysine. The two molecules differ in mass, half-life and evidence base. CJC-1295 10mg is in stock with a batch certificate, and the certificate is how you confirm which molecule a vial holds.
How does CJC-1295 work?
CJC-1295 activates the GHRH receptor on pituitary cells, which releases growth hormone into the blood. The 2005 discovery paper showed the albumin conjugates were active in a GH secretion assay in cultured rat anterior pituitary cells, and its title describes them as activating "the GRF receptor on the anterior pituitary in rats". [2] A 2009 paper summarises the natural pathway: GHRH is made in the hypothalamus and binds receptors on pituitary somatotropes to promote GH synthesis and release. [4]
Albumin binding is the second half of the mechanism. The maleimide on the added lysine reacts with the free thiol on Cys34 of serum albumin. In rats, a CJC-1295 signal appeared on the albumin band within 15 minutes and stayed in circulation beyond 24 hours. [2] The albumin conjugates also showed greater in vitro stability against dipeptidyl peptidase-IV than the unmodified peptide.
In healthy adults, a single exposure raised mean GH 2- to 10-fold for 6 days or more and IGF-I 1.5- to 3-fold for 9 to 11 days. [1] A second study asked whether that constant stimulation flattened GH's natural rhythm. It found the frequency and size of GH pulses unchanged, with trough GH up 7.5-fold, mean GH up 46% and IGF-I up 45%. [7]
What is the structure of CJC-1295?
CJC-1295 is a 30-residue linear peptide with a D-alanine at position 2, a C-terminal lysinamide and a 3-maleimidopropionyl group on that lysine's side chain. PubChem's synonym for the record spells the chain as L-tyrosyl-D-alanyl through to L-lysinamide. [5]
| Field | Value | Source |
|---|---|---|
| CAS number (PubChem) | 446262-90-4 | PubChem CID 91971820 |
| CAS number (Poisons Standard entry) | 863288-34-0 | Poisons Standard, June 2026 |
| PubChem CID | 91971820 | PubChem |
| UNII | 62RC32V9N7 | PubChem synonyms |
| Molecular formula | C165H269N47O46 | PubChem |
| Molar mass | 3647.2 g/mol | PubChem |
| Length | 30 amino acids | Counted from the sequence |
| One-letter sequence | YADAIFTQSYRKVLAQLSARKLLQDILSRK | Decoded from the PubChem name |
| Substitutions against GHRH(1-29) | D-Ala2, Gln8, Ala15, Leu27 | Our alignment against sermorelin |
| Albumin-binding group | 3-maleimidopropionyl on the side chain of Lys30 | PubChem IUPAC name |
| C-terminus | Amide | PubChem synonyms |
| Synonyms | CJC1295, CJC-1295 with DAC, GRF 1-29 (CJC1295) | PubChem |
We pulled these values from PubChem on 29 September 2026. [5] We then aligned the sequence against sermorelin, the native GHRH(1-29) amide, which PubChem lists as Tyr-Ala-Asp-Ala-Ile-Phe-Thr-Asn-Ser-Tyr-Arg-Lys-Val-Leu-Gly-Gln-Leu-Ser-Ala-Arg-Lys-Leu-Leu-Gln-Asp-Ile-Met-Ser-Arg-NH2. [10] The alignment shows the four substitutions the developers describe: D-alanine at 2, glutamine for asparagine at 8, alanine for glycine at 15 and leucine for methionine at 27.
The two CAS numbers point to two different molecules in PubChem. CAS 863288-34-0, the number in the Poisons Standard, belongs to CID 56841945. That record's drawn structure is the 29-residue peptide ending in argininamide, formula C152H252N44O42 and 3367.9 g/mol, with no DAC lysine. [6] Its depositor synonyms mix "CJC 1295 with DAC" and "CJC-1295-no DAC acetate", so the labels in that record contradict its structure.
For a buyer, the mass is the useful number. A vial of the DAC molecule should give a mass spectrometry result near 3647 g/mol. The version without DAC should read near 3368 g/mol.
What has research on CJC-1295 examined?
Published research on CJC-1295 covers four human studies from 2006 to 2009, rodent work in rats and GHRH-knockout mice, and a later body of anti-doping detection methods. No published trial has examined CJC-1295 in a patient population, and no human study has run beyond 49 days.
| Year | Study (PMID) | Model | Who or what was studied | Reported finding |
|---|---|---|---|---|
| 2005 | Discovery paper (15817669) | Rat cells, rats | Cultured rat pituitary cells; male Sprague Dawley rats | 4-fold rise in GH area under the curve over 2 hours against hGRF(1-29); present in plasma beyond 72 hours [2] |
| 2006 | Two ascending-exposure trials (16352683) | Human, randomised, placebo-controlled, double-blind | Healthy adults aged 21 to 61, 28 and 49 days | GH up 2- to 10-fold for 6 days or more; IGF-I up 1.5- to 3-fold; half-life 5.8 to 8.1 days [1] |
| 2006 | GH pulsatility study (17018654) | Human | Healthy men aged 20 to 40, overnight sampling | Pulse frequency unchanged; trough GH up 7.5-fold; IGF-I up 45% [7] |
| 2006 | Knockout mouse study (16822960) | Mice | GHRH-knockout mice from 1 week old, 5 weeks | Normal body weight and length on the most frequent schedule; more pituitary GH mRNA [9] |
| 2009 | Serum proteomics (19386527) | Human | Sera from 11 healthy young men, before and 1 week after | Changes in apolipoprotein A1, transthyretin and albumin fragment spots [4] |
| 2010 | Seized product analysis (21204297) | Analytical | Unknown preparation referred by Norwegian police and customs | A 29-residue amidated peptide consistent with a product sold as CJC-1295 [11] |
| 2019 | Equine plasma method (30938069) | Analytical | Horse plasma, Racing Analytical Services, Flemington, Victoria | CJC-1295 confirmed down to 180 pg/mL [12] |
| 2021 | Urine metabolite method (34665524) | Analytical | Fortified urine, four GHRH analogues including both CJC-1295 forms | 19 in vitro metabolites; detection at 1 ng/ml or less [13] |
| 2026 | Urine screening method (41138283) | Analytical | Urine, GHRH and its analogues | Validated to WADA guidelines with detection limits of 0.5 ng/mL or less [14] |
In the knockout mice, the schedules that were spaced further apart gave higher weight and length than placebo without full normalisation. [9] The mouse and rat results describe pharmacology in animals. The human results are hormone and protein measurements over weeks.
The Australian detail in that table deserves a note. The equine method came from a Victorian racing laboratory, so CJC-1295 is a target of Australian racing integrity testing as well as WADA testing. [12]
What does the CJC-1295 evidence not show?
The CJC-1295 evidence stops at hormone levels in small groups of healthy volunteers. The trials measured GH, IGF-I and pharmacokinetics, and the 2009 paper looked for serum protein markers. [1][4] None measured a clinical outcome.
Four limits matter when you read claims about CJC-1295.
- Short exposure. The longest human trial ran 49 days. [1]
- Few independent groups. Lawrence, Castaigne and Frohman appear as authors on both the 2006 adult trials paper and the mouse paper, and the discovery work came from ConjuChem's own research department. [2][1][9]
- Narrow populations. Healthy adults and young men. The pulsatility and proteomics studies enrolled men only. [7][4]
- One molecule studied. The trials used the DAC molecule. The 2010 Norwegian analysis found the 29-residue peptide sold under the CJC-1295 name, and we found no published human trial of that shorter peptide. [11]
Purity, identity and peptide content of a research vial are separate questions, and a batch certificate answers them.
What adverse events have studies of CJC-1295 reported?
The 2006 trials in healthy adults reported no serious adverse reactions. [1] The abstract lists no specific non-serious events. We could not access the full text, so the trial's complete adverse-event table is outside this summary. The 2006 pulsatility study abstract contains no safety statement. [7]
Two wider sources add context without CJC-1295-specific figures:
- Class review (2026). A narrative review of research-market peptides acting on the GH-IGF-1 axis, including both CJC-1295 forms, lists reported adverse effects across the class: prolactin and cortisol elevations, appetite changes, dysglycaemia, fluid retention and myalgia or arthralgia. [15] The review groups compounds together, so it does not attribute each effect to CJC-1295.
- Regulator reports. The TGA names CJC-1295 among examples of unapproved peptide products. It reports receiving adverse events for these products, including severe allergic reactions requiring hospitalisation and systemic inflammatory response syndrome. [16]
These are the published observations. They come from short trials, a pooled review and regulator reports.
Is CJC-1295 approved or scheduled in Australia?
CJC-1295 is listed in Schedule 4 of the Poisons Standard (prescription only), and it is listed in Appendix D clause 5, which makes possession without authority an offence. The June 2026 instrument (F2026L00633), which commenced on 1 June 2026, lists it as "CJC-1295 (CAS No. 863288-34-0)" and marks it with the # symbol for Appendix D. [3] The same Appendix D table also lists growth hormone releasing hormones (GHRHs) as a class, "including those separately specified in Schedule 4".
The TGA describes unapproved peptide products as goods not included in the Australian Register of Therapeutic Goods (ARTG), and it names CJC-1295 as an example of an unapproved peptide product. [16] Our guide to peptide scheduling under Australian law explains Schedule 4, Appendix D and what "without authority" means.
For sport, CJC-1295 is prohibited at all times, in and out of competition. The WADA 2026 Prohibited List names it under S2.2.4, growth hormone releasing factors, as an example of a GHRH analogue. [8] The List took effect on 1 January 2026 and classes all S2 substances as non-Specified. WADA revises the List every year.
How does CJC-1295 compare with related GH-axis peptides?
CJC-1295 is the long-acting member of a small family of peptides that act on GH release. The main comparisons are its own shorter form, sermorelin and ipamorelin.
| Feature | CJC-1295 (with DAC) | CJC-1295 without DAC | Sermorelin | Ipamorelin |
|---|---|---|---|---|
| Receptor | GHRH receptor | GHRH receptor | GHRH receptor | Ghrelin (GH secretagogue) receptor |
| Length | 30 residues | 29 residues | 29 residues | 5 residues |
| Molar mass (PubChem) | 3647.2 g/mol | 3367.9 g/mol | 3357.9 g/mol | Not compared here |
| Albumin binding | Yes, via maleimide on Lys30 | No | No | No |
| Human studies found | 2006 trials and follow-up studies | None located | Separate literature | Separate literature |
| WADA 2026 | S2.2.4 | S2.2.4 (GHRH analogues) | S2.2.4 | S2.2.4 |
The mass and structure columns come from PubChem. [5][6][10] WADA lists sermorelin and CJC-1295 as GHRH analogues and ipamorelin as a growth hormone secretagogue. [8]
Ipamorelin reaches GH release through a different receptor, which is why the two compounds are often discussed together. The full side-by-side is in CJC-1295 vs ipamorelin, and the wider group sits in our growth hormone research peptides range.
How is CJC-1295 stored and handled in the lab?
Lyophilised CJC-1295 keeps best sealed, dry, dark and frozen. No published stability study covers research-grade CJC-1295, so general peptide guidance applies. Bachem advises keeping peptides as the lyophilisate in a tightly closed container below -15 °C for long-term storage, with a refrigerator at 4 °C acceptable for short-term use. [17]
The sequence tells you what to watch. CJC-1295 contains three glutamine residues (positions 8, 16 and 24) and no methionine, cysteine or tryptophan. Bachem notes that peptides containing glutamine have limited shelf lives, and Sigma-Aldrich lists glutamine among the residues that make peptides unstable in solution. [17][18] Sigma-Aldrich gives about a week at 4 °C as a general limit for peptide solutions and advises against repeated freezing and thawing. [18]
Two handling steps protect a vial:
- Let a cold vial reach room temperature before opening it. Peptides absorb moisture, which lowers peptide content. [17]
- Split a reconstituted solution into single-use portions and freeze them below -20 °C. [19]
On solvent, CJC-1295 is a basic peptide: it carries three arginine and three lysine residues against two aspartic acid residues. Bachem suggests dissolving basic peptides in a small amount of dilute acetic acid before diluting, and names PBS at pH 7.0 to 7.4 as the safest diluent at 1 mg/mL or less. [19] We stock BAC Water (sterile water with 0.9% benzyl alcohol) and dilute acetic acid, both in 3ml vials at A$8. Our peptide storage guide covers temperatures, light and labelling in detail.
Where can researchers buy CJC-1295 in Australia?
Peptides Collective sells CJC-1295 for laboratory research use only, in 10mg vials at A$85. A 10mg CJC-1295 and ipamorelin blend is A$108. Stock ships from Western Australia with tracking.
An independent lab tests every batch before it goes on sale. The certificate reports purity by HPLC and identity by mass spectrometry. We publish it under the batch number printed on the vial, and you can search the certificate of analysis library by that number.
Check the identity result against the structure table above. A reading near 3647 g/mol matches the DAC molecule, and a reading near 3368 g/mol matches the version without DAC. Our guide on how to read a peptide certificate of analysis explains the HPLC trace, the mass spectrum and net peptide content. The CJC-1295 product page links the certificate for the current batch.
Bottom line
CJC-1295 is a 30-residue GHRH analogue that binds albumin and keeps GH and IGF-I raised for days, based on a handful of 2006 studies in healthy volunteers. The published record holds no clinical outcomes and no human data beyond 49 days. The name also covers a shorter peptide without DAC, which differs in mass by about 280 g/mol. In Australia CJC-1295 is Schedule 4 and Appendix D, WADA prohibits it at all times, and a batch certificate is how you confirm which molecule a vial contains.
Questions
What has research on CJC-1295 examined?
Research has examined CJC-1295's effect on GH and IGF-I levels in healthy adults, GH pulse patterns in young men and serum protein changes, all between 2006 and 2009. Animal work covers rats and GHRH-knockout mice. Most later papers develop anti-doping detection methods for urine and plasma.
What adverse events have studies of CJC-1295 reported?
The two 2006 trials in healthy adults aged 21 to 61 reported no serious adverse reactions. The abstract does not itemise milder events. A 2026 review of GH-axis research peptides lists effects reported across that class, including prolactin and cortisol elevations, dysglycaemia and fluid retention, without assigning each to CJC-1295.
Is CJC-1295 a prescription medicine in Australia?
CJC-1295 is listed in Schedule 4 of the Poisons Standard, the prescription only schedule, in the instrument that commenced on 1 June 2026. It is also in Appendix D clause 5, so possession without authority is an offence. The TGA names it as an example of an unapproved peptide product, meaning one not included in the ARTG.
Is CJC-1295 banned in sport?
Yes. The WADA 2026 Prohibited List names CJC-1295 under S2.2.4 as a GHRH analogue, prohibited at all times in and out of competition. The List took effect on 1 January 2026. Anti-doping laboratories have published urine and plasma methods to detect it, including one from a Victorian racing laboratory.
What is the half-life of CJC-1295?
The estimated half-life of CJC-1295 with DAC was 5.8 to 8.1 days in the 2006 trials in healthy adults. Albumin binding explains the length: the maleimide group attaches to Cys34 of serum albumin. The PubMed records we reviewed give no measured human half-life for the version without DAC.
What is the molecular weight of CJC-1295?
PubChem lists CJC-1295 at 3647.2 g/mol for the formula C165H269N47O46. The shorter peptide sold as CJC-1295 without DAC has its own PubChem record at 3367.9 g/mol, formula C152H252N44O42. The difference, about 280 g/mol, is the maleimidopropionyl lysine.
How should CJC-1295 be stored?
Keep lyophilised CJC-1295 sealed, dry, dark and frozen below -15 °C for long-term storage, with 4 °C acceptable for short periods. Its three glutamine residues make solutions less stable, so freeze single-use portions and avoid repeated freezing and thawing. Our peptide storage guide covers labelling and light.
Which solvent is used to reconstitute CJC-1295?
CJC-1295 is a basic peptide, and Bachem's general guidance for basic peptides is a small amount of dilute acetic acid followed by dilution, with PBS at pH 7.0 to 7.4 as the safest diluent at 1 mg/mL or less. Peptides Collective stocks BAC Water and dilute acetic acid in 3ml vials at A$8 each.
Where does the CJC-1295 sequence come from?
The sequence comes from human GHRH. CJC-1295 keeps the first 29 residues of GHRH with four substitutions (D-Ala2, Gln8, Ala15, Leu27) and adds a lysine carrying a maleimidopropionyl group. Sermorelin is the unmodified GHRH(1-29) amide.
Who discovered CJC-1295?
Researchers in the Department of Research at ConjuChem Inc. in Montreal, Canada, described CJC-1295 in Endocrinology in July 2005. Jetté and colleagues synthesised three maleimido derivatives of hGRF(1-29) and selected CJC-1295 as the best compound for further pharmacokinetic work.
Is CJC-1295 a peptide or a small molecule?
CJC-1295 is a peptide. It is a 30-residue chain of amino acids with a small maleimidopropionyl group on the final lysine, giving a molar mass of about 3.6 kDa. The attached group lets the peptide bind albumin covalently in blood.
What is the CAS number for CJC-1295?
PubChem gives CAS 446262-90-4 for CJC-1295 with DAC (CID 91971820). The Poisons Standard cites CAS 863288-34-0, which PubChem assigns to a separate record whose structure is the 29-residue peptide without DAC (CID 56841945). Check both numbers when you match a label to a reference.
How is CJC-1295 made?
CJC-1295 is made by chemical synthesis. The 2005 discovery paper reports that the ConjuChem team synthesised maleimido derivatives of hGRF(1-29) and tested their albumin conjugates. The D-alanine at position 2 and the modified lysine are non-standard building blocks, so the peptide cannot be expressed directly as a natural protein sequence.
Where can I see the certificate for CJC-1295?
Every CJC-1295 batch has a certificate of analysis published under the batch number printed on the vial. Search the certificate library by that number, or open the CJC-1295 product page, which links the current batch. The certificate reports purity by HPLC and identity by mass spectrometry.
Sources
- 1. Teichman SL et al. Prolonged stimulation of growth hormone (GH) and insulin-like growth factor I secretion by CJC-1295, a long-acting analog of GH-releasing hormone, in healthy adults. J Clin Endocrinol Metab, 2006.
- 2. Jetté L et al. Human growth hormone-releasing factor (hGRF)1-29-albumin bioconjugates activate the GRF receptor on the anterior pituitary in rats: identification of CJC-1295 as a long-lasting GRF analog. Endocrinology, 2005.
- 3. Therapeutic Goods (Poisons Standard, June 2026) Instrument 2026, F2026L00633; raw capture ../are-peptides-legal-in-australia/research/worker/poisons-standard-F2026L00633.md (read-only)
- 4. Sackmann-Sala L et al. Activation of the GH/IGF-1 axis by CJC-1295, a long-acting GHRH analog, results in serum protein profile changes in normal adult subjects. Growth Horm IGF Res, 2009.
- 5. PubChem (NCBI), CID 91971820; raw capture research/worker/pubchem-91971820.json
- 6. PubChem (NCBI), CID 56841945; raw capture research/worker/pubchem-56841945.json
- 7. Ionescu M et al. Pulsatile secretion of growth hormone (GH) persists during continuous stimulation by CJC-1295, a long-acting GH-releasing hormone analog. J Clin Endocrinol Metab, 2006.
- 8. WADA 2026 Prohibited List; raw capture ../are-peptides-legal-in-australia/research/worker/wada-2026-list.md (read-only)
- 9. Alba M et al. Once-daily administration of CJC-1295, a long-acting growth hormone-releasing hormone (GHRH) analog, normalizes growth in the GHRH knockout mouse. Am J Physiol Endocrinol Metab, 2006.
- 10. PubChem (NCBI), Sermorelin CID 16132413; raw capture research/worker/pubchem-sermorelin-16132413.json
- 11. Henninge J et al. Identification of CJC-1295, a growth-hormone-releasing peptide, in an unknown pharmaceutical preparation. Drug Test Anal, 2010.
- 12. Timms M et al. A method for confirming CJC-1295 abuse in equine plasma samples by LC-MS/MS. Drug Test Anal, 2019.
- 13. Memdouh S et al. Advances in the detection of growth hormone releasing hormone synthetic analogs. Drug Test Anal, 2021.
- 14. Uçaktürk E et al. Analysis of growth hormone releasing hormone and its analogs in urine using nano liquid chromatography coupled with quadrupole/orbitrap mass spectrometry. J Pharm Biomed Anal, 2026.
- 15. Dominikowski A et al. The emerging landscape of performance-enhancing peptides modulating GH-IGF1 axis: bridging the gap between clinical evidence and patient self-administration. Front Endocrinol (Lausanne), 2026.
- 16. Therapeutic Goods Administration safety alert; raw capture ../are-peptides-legal-in-australia/research/worker/tga-peptide-responsibilities.md (read-only)
- 17. Bachem, Handling and Storage Guidelines for Peptides; raw capture ../how-to-reconstitute-peptides/research/worker/bachem-handling.md (read-only)
- 18. Sigma-Aldrich (Merck), Handling and Storage Guidelines for Peptides and Proteins; raw capture ../how-to-store-peptides/research/worker/sigma-handling.md (read-only)
- 19. Bachem, Peptide solubility; raw capture ../how-to-reconstitute-peptides/research/worker/bachem-solubility.md (read-only)


