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Third-Party Tested by Verum Analytics
CJC-1295 No DAC
GHRH analog (Modified GRF 1-29) that stimulates natural, pulsatile growth-hormone release.
Third-Party Tested by Verum Analytics

Albert's Verdict
Without the DAC modification, CJC-1295 delivers a sharper, more physiological pituitary pulse — the half-life stays closer to endogenous GHRH patterns. Useful when research design calls for pulse rather than sustained elevation.
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Arrives as lyophilized (powder) form
Shipped freeze-dried for maximum stability and shelf life. See laboratory preparation guide for handling instructions.
Product Description
CJC-1295 without DAC — also known as Modified GRF (1-29) — is a synthetic analog of growth-hormone releasing hormone (GHRH). It stimulates pulsatile GH release from the pituitary that closely mimics the body's own natural GH pattern, without desensitizing the receptor over time.
A cornerstone of GH-optimization research, CJC-1295 (No DAC) is most often paired with a GHRP such as Ipamorelin for a synergistic pulse. Studied for body composition, lean-mass preservation, recovery, sleep quality, and anti-aging applications. For research use only. Not for human or veterinary consumption.
Technical Specifications
- Molecular Formula
- C152H252N44O42
- Molecular Weight
- 3367.97 g/mol
- Sequence
- Tyr-D-Ala-Asp-Ala-Ile-Phe-Thr-Gln-Ser-Tyr-Arg-Lys-Val-Leu-Ala-Gln-Leu-Ser-Ala-Arg-Lys-Leu-Leu-Gln-Asp-Ile-Leu-Ser-Arg-NH2
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Frequently Researched Together
Commonly studied alongside in laboratory settings
Research FAQ — CJC-1295 No DAC
Frequently asked questions about this compound for laboratory researchers.
What is CJC-1295 No DAC and how is it different from CJC-1295 DAC?+
What is the reported half-life of CJC-1295 No DAC?+
Is CJC-1295 No DAC frequently studied alongside Ipamorelin in research?+
How should CJC-1295 No DAC be stored?+
Published research references
Peer-reviewed literature relevant to CJC-1295 No DAC research. Linked PubMed IDs open the original source.
- [1]Sustained-release GH releasing factor (CJC-1295) for hormone studies — J Clin Endocrinol Metab (2006) · PMID 16384879
- [2]Effects of CJC-1295 in human GH-deficient adults — J Clin Endocrinol Metab (2006) · PMID 16352683
- [3]GHRH analogs and growth hormone pulsatility — Endocr Rev (2012) · PMID 22148949
Verified reviews — CJC-1295 No DAC
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Learn More About This Peptide
Research Use Only: This product is intended for laboratory research purposes only. Not for human consumption.
CJC-1295 without DAC (Mod GRF 1-29) — clinical & mechanistic profile
Mod GRF 1-29 is a tetrasubstituted GHRH analog (Ala2, Gln8, Ala15, Leu27) with ~30-minute half-life (vs ~7 min native GHRH) due to DPP-IV resistance. Lacking DAC's albumin binding, it produces acute pulsatile GH release mimicking physiology, synergizing with GHRPs via complementary cAMP/Ca2+ pathways.
Research status
preclinical
Molecular weight
3367.95 g/mol
Molecular formula
C152H252N44O42
Studied applications
- •Preserved pulsatility: ~30 min half-life produces discrete GH spikes mimicking physiological patterns
- •DPP-IV resistance: Ala2 substitution blocks primary degradation enzyme, extending duration from ~7 to ~30 min
- •GHRP synergy: cAMP pathway (GHRH) + Ca2+/IP3 pathway (GHRPs) produce amplified GH pulses beyond additive effects
- •Flexible protocols: short duration allows timing with natural GH windows (sleep, exercise)
- •No albumin binding: lacks DAC moiety, enabling rapid clearance and pulsatile administration
Mechanisms of action
- •GHRHR full agonism: binds pituitary GHRH receptor, triggering Gs-protein coupling and adenylyl cyclase
- •cAMP/PKA pathway: adenylyl cyclase → cAMP → PKA activation → GH gene transcription and vesicle release
- •DPP-IV resistance: Ala2 substitution blocks dipeptidyl peptidase IV cleavage site
- •Synergistic signaling: complements GHRP Ca2+/IP3 pathway for amplified somatotroph activation
- •Dose-dependent peaks: produces sharp GH spikes 15-60 min post-injection, baseline by 180 min
- •Not approved for human therapeutic use
- •Short half-life requires 2-3 daily injections for meaningful effects
- •No completed human clinical trials for this specific compound
- •Quality and purity of research compounds varies
- •Optimal dosing and timing protocols not established
Peer-reviewed references
For research use only. This summary is a research-scientific overview compiled from peer-reviewed sources. It is not medical advice and is not intended for human or veterinary consumption.