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Compound research hub

CJC-1295 with DAC: Research, Handling and Batch Documentation

CJC-1295 with DAC is a GHRH analogue carrying a Drug Affinity Complex that binds serum albumin, which is what separates its multi-day half-life from the minutes of unmodified GHRH.

Part of Volta's growth hormone research peptides catalogue.

Identity and research status

Also referred to as
CJC-1295 DAC, CJC-1295 with Drug Affinity Complex, DAC:GRF
Backbone
Human GHRH(1-29) with four amino acid substitutions
Key Substitution
D-alanine at position 2, blocking DPP-4 cleavage
Conjugation Group
Maleimidopropionyl Drug Affinity Complex at the C-terminal lysine
Albumin Binding
Covalent, via reaction with a free cysteine thiol on serum albumin
Molecular Weight
Approximately 3647 g/mol for the unconjugated peptide
CAS Number
863288-34-0
Also Known As
DAC:GRF, CJC-1295 DAC
Half-life
Reported on the order of 6 to 8 days
Receptor Target
GHRH receptor on pituitary somatotrophs
Appearance
White lyophilised powder

Evidence level: Phase I-II data; research compound (grade C)

Regulatory status: Research compound. Phase 1/2 clinical data exists (ConjuChem). Not approved for any indication.

Evidence grades describe the published literature on the compound, not a property of the material Volta supplies, and are not a statement that any use is approved. See how these grades are assigned.

Mechanism, in brief

CJC-1295 with DAC is a modified growth hormone releasing hormone analogue built on the GHRH(1-29) backbone, carrying four amino acid substitutions and, critically, a maleimidopropionyl group known as the Drug Affinity Complex. The four substitutions protect the peptide from enzymatic degradation, beginning with D-alanine at position 2, which blocks the dipeptidyl peptidase-4 cleavage that makes unmodified sermorelin short-acting.

  1. Enzymatic protection. Four substitutions on the GHRH(1-29) backbone, including D-alanine at position 2, block dipeptidyl peptidase-4 cleavage of the region required for receptor activation.
  2. Covalent albumin conjugation. The maleimidopropionyl DAC group reacts with a free cysteine thiol on albumin to form a covalent bond, unlike the reversible fatty acid binding used by acylated incretin analogues.
  3. Extended circulation. Covalent attachment to albumin gives a half-life reported on the order of six to eight days, producing sustained rather than pulsatile exposure.
  4. GHRH receptor agonism. Agonism at the GHRH receptor on pituitary somatotrophs, signalling through Gs and cyclic AMP to trigger growth hormone release and synthesis.
  5. Sustained IGF-1 elevation. The clinical study reported prolonged elevation of both growth hormone and insulin-like growth factor 1, which is the measurable consequence of continuous rather than pulsed receptor stimulation.

The full research write-up, including the findings behind each claim and the model each came from, is on the CJC-1295 DAC 5mg 5mg page.

Vial sizes available

Every size of CJC-1295 with DAC Volta lists, in stock or not. Each is a separate catalogue page with its own batch number and specification table.

Purity and batch documentation

Volta's release specification is >99% (HPLC). That is a threshold we set. >99% is the specification every batch is released to. The figure on a certificate is what a laboratory measured for one lot.

No third-party certificate has been published for CJC-1295 with DACyet. The certificates Volta does publish, with the laboratory's own verification link on each, are in the certificate archive.

Research on CJC-1295 with DAC

Handling and stability

Regulatory context

United States
Not FDA-approved. Research compound only.
Canada
Not approved by Health Canada.
European Union
Not EMA-approved.

Primary sources

  1. Teichman SL, Neale A, Lawrence B, 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. Journal of Clinical Endocrinology and Metabolism (2006). PMID 16352683
  2. Soule S, King JA, Millar RP. Incorporation of D-Ala2 in growth hormone-releasing hormone-(1-29)-NH2 increases the half-life and decreases metabolic clearance. Journal of Clinical Endocrinology and Metabolism (1994). PMID 7962295
  3. Dominikowski A, Rękoś Z, et al.. The emerging landscape of performance-enhancing peptides modulating the GH-IGF1 axis. Frontiers in Endocrinology (2026). PMID 42395176
  4. Mendias CL, Awan TM, et al.. Safety and Efficacy of Approved and Unapproved Peptide Therapies for Musculoskeletal Injuries. Sports Medicine (2026). PMID 41966639
  5. Villegas Meza AD, Nocek M, et al.. Injectable Peptides in Sports Medicine: A Structured Narrative Review of Evidence and Safety. JBJS Reviews (2026). PMID 42160466
  6. Renke G, Chinellato L, et al.. Therapeutic Peptides in Aesthetic, Metabolic and Endocrine Conditions: Effects, Safety and Clinical Applications. International Journal of Molecular Sciences (2026). PMID 42123471

More growth hormone research peptides

CJC-1295 with DAC sits in Volta's growth hormone research peptides catalogue, alongside the other compounds studied in this area. The whole range is on the full research catalogue, and the library of comparisons and guides is under peptide research.

Research use only. Every compound described on this page is supplied for in-vitro laboratory research. Nothing here is a recommendation for human or veterinary use, a dosing instruction, or a claim that any compound is a treatment for any condition. Published trial figures are reported as what an investigator administered in a named study, never as guidance. Read the full research disclaimer.

Cluster last reviewed: 2026-09-15.

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