CJC-1295 (no DAC)
Molecular Research Profile · Target purity > 99.0% · Half-life ~30 minutes (no DAC variant)
Modified GRF(1-29) analog that stimulates pulsatile growth hormone release via GHRH receptor agonism. Typically researched in combination with Ipamorelin or GHRP-2 for synergistic GH pulses.
Mechanism of Action
CJC-1295 without DAC (Drug Affinity Complex) is a tetra-substituted growth hormone-releasing hormone (GHRH) analog — specifically, modified GRF(1-29) with four amino acid substitutions that increase plasma stability from ~7 minutes (native GRF) to approximately 30 minutes. It binds and activates the GHRH receptor (GHRHR) on anterior pituitary somatotroph cells, triggering cAMP-PKA signaling cascades that stimulate pulsatile growth hormone (GH) synthesis and secretion.
Unlike the DAC-conjugated variant (which has a ~7-day half-life via albumin binding and produces continuous "GH bleed"), the non-DAC form preserves the physiological pulsatile pattern of GH release. This matters because GH receptor signaling is pulse-amplitude-dependent: intermittent high-amplitude pulses produce anabolic effects, while continuous low-level exposure can induce receptor desensitization and hepatic IGF-1 resistance.
CJC-1295 no DAC is nearly always researched in combination with a ghrelin-mimetic (GHRP) such as Ipamorelin, GHRP-2, or GHRP-6. GHRH analogs set the "GH pulse amplitude ceiling," while ghrelin-mimetics trigger the pulse release — the combination synergizes to produce 2–5× greater GH output than either peptide alone.
Research History & Context
CJC-1295 was originally developed by ConjuChem Biotechnologies (Montreal) in the early 2000s as a long-acting GHRH analog for growth hormone deficiency and HIV-associated wasting. The DAC (Drug Affinity Complex) technology conjugated the peptide to albumin via a maleimidopropionic acid linker, extending the half-life from minutes to days. However, Phase 2 clinical trials were discontinued after a 2006 safety signal (a participant death was later attributed to an unrelated cardiac conduction defect, but the development program was paused).
The non-DAC variant emerged from research groups seeking to preserve the physiological GH pulsatility that DAC conjugation eliminated. Modified GRF(1-29) with the same four stabilizing substitutions but without the albumin-binding moiety became the standard research form, widely adopted in peptide research communities for its safety profile and predictable pharmacokinetics.
Storage & Handling
Store lyophilized CJC-1295 no DAC at -20°C in a light-protected, desiccated environment. Stability exceeds 18 months under these conditions. The peptide is relatively robust; brief room-temperature handling during reconstitution does not cause significant degradation.
Reconstituted CJC-1295 should be stored at 2–8°C and used within 21 days. The peptide is susceptible to deamidation at asparagine residue 8 — this is a spontaneous degradation pathway accelerated at neutral-to-basic pH and higher temperatures. Using refrigerated storage and slightly acidic BAC water (pH 5.5–6.5) helps preserve structural integrity.
Reconstitution & Research Dosing
For CJC-1295 (no DAC), the standard laboratory reconstitution is 2.0 ml BAC water for 2mg / 5mg vial. A typical research study window uses 100 - 300 mcg / 1-3× daily.
For a 2mg CJC-1295 research vial, add 2.0 ml BAC water (1 mg/ml = 100 mcg per 0.1 ml / 10 IU). For a 5mg vial, add 2.0 ml BAC water (2.5 mg/ml = 250 mcg per 0.1 ml). Due to the 3× daily research protocol, many researchers reconstitute at higher concentration to reduce injection volume per dose. Always verify net peptide weight via HPLC before dosing.
Use the Reconstitution Calculator for exact syringe units →Explore Related Research Compounds
Research Use Only (RUO): CJC-1295 (no DAC) is discussed strictly as an in-vitro laboratory research compound. Nothing on this page constitutes human or clinical administration guidance. Always verify purity through independent third-party HPLC/MS analysis before use.