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Vialdyne

CJC-1295 (no DAC)

Modified GRF 1-29 · GHRH analog

≥ 99.0%CAS 863288-34-0 (DAC form has same CAS-class but distinct identifier, confirm via COA)GH-Axis Peptides

Overview

CJC-1295 without DAC, also catalogued as Modified GRF 1-29 or ModGRF 1-29, is a 29-residue GHRH analogue carrying four engineered substitutions (Tyr1 to D-Ala, Ala8 to Gln, Ala15 to Ala, Met27 to Leu) that block DPP-4 cleavage and slow serum protease degradation. Receptor pharmacology is GHRH-receptor-mediated, and the resulting GH-release pattern is pulsatile and closely resembles native physiological secretion, in contrast to the DAC variant, whose covalent albumin conjugation pushes plasma half-life into the once-weekly range and flattens the pulse architecture. For compounding pharmacy buyers, Vialdyne releases CJC-1295 no-DAC as the lyophilised acetate against a ≥99.0% main-peak HPLC specification. The no-DAC form is most commonly paired with a GHSR-axis agonist (Ipamorelin, occasionally GHRP-2 or GHRP-6) in dual-pathway compounding protocols; the canonical CJC-1295 + Ipamorelin pairing is supplied directly as a pre-blended co-lyophilised vial under the cjc-1295-ipamorelin SKU, which removes the in-cleanroom blending step and certifies the actual ratio on the released-batch COA. The companion [CJC-1295 + Ipamorelin pharmacology article](/insights/cjc-1295-ipamorelin-blend-pharmacology-guide) covers the dual-pathway rationale in detail. Catalogue strengths are 2, 5, and 10 mg; the 2 and 5 mg fills are the typical dispensing vials in 503A workflows.

Who buys this, and why

GH-axis peptides ship to two main buyer types: compounding pharmacies dispensing under physician supervision, and research labs studying somatotropic-axis pharmacology. Pharmacies typically want sterile-filled vials with the full release packet (sterility, endotoxin, CCI); labs typically want bulk lyophilized powder with sequence verification. Blends (the CJC-1295 / Ipamorelin combination is the canonical example) are usually co-lyophilized rather than solution-mixed for potency stability.

Primary buyer fit: academic and contract research laboratories and 503A / 503B compounding pharmacies.

Specifications

CAS
863288-34-0 (DAC form has same CAS-class but distinct identifier, confirm via COA)
Purity (HPLC)
≥ 99.0%
Common vial sizes
2 mg, 5 mg, 10 mg
MOQ
On request
Lead time
7–14 days
Storage
-20°C, protect from light

Documentation available on request

  • Certificate of Analysis (COA)
  • HPLC Chromatogram
  • Mass-spec identity (ESI-MS)
  • Counter-ion (acetate vs TFA)
  • Sterile-fill release pack (sterility, CCI, fill-weight)
  • Bacterial endotoxin (LAL, USP <85>)
  • Stability data on request
  • SDS / MSDS

Regulatory note

Sold as a bulk active for research and for compounding-pharmacy formulation where local regulations permit (notably 503A / 503B in the United States and analogous regimes elsewhere). Not a finished dosage form. Sterile-filled vials are available with full release documentation; the buyer is responsible for verifying scheduling and dispense requirements in the destination market.

Frequently asked questions

What's the difference between CJC-1295 with DAC and without DAC?

The backbone is the same Modified GRF 1-29 sequence in both, but the DAC version carries an additional maleimido-propionyl modification at Lys30. In serum, the maleimide forms a covalent bond with the free thiol of Cys34 on human serum albumin, producing a circulating peptide-albumin conjugate that extends half-life from roughly 30 minutes (no-DAC) to about 6-8 days (DAC). The pharmacology is therefore fundamentally different: no-DAC produces a pulsatile GH-release pattern that mirrors physiological secretion, while DAC produces sustained GH elevation that overrides the natural pulse architecture. Most 503A compounding workflows and pulse-pharmacology research use the no-DAC form; sustained-elevation contexts are where DAC fits.

Why is CJC-1295 almost always combined with Ipamorelin in practice?

Because two receptor pathways converge on the same somatotroph cells and produce additive output. CJC-1295 signals through the GHRH receptor; Ipamorelin signals through the GHSR (ghrelin receptor). Combining a GHRH-pathway agonist with a GHSR-pathway agonist produces a measurably larger GH pulse than either component alone at matched individual doses. The standard combined-product ratio is 1:1 by mass (2+2 mg or 5+5 mg per vial are the typical fills). Vialdyne ships this as a pre-blended co-lyophilised vial under the cjc-1295-ipamorelin SKU, which is operationally preferred over having the receiving pharmacy combine two reconstituted vials inside the cleanroom because the released-batch COA certifies the actual ratio in the cake rather than just the nominal target.

How is CJC-1295 typically reconstituted and stored after opening?

The lyophilised cake dissolves cleanly in bacteriostatic water for injection at standard reconstitution concentrations. Solution stability at -20 C as single-use aliquots is reasonable, but the dominant operational driver of measured-potency loss in this class is freeze-thaw cycling, not slow temperature drift, so the practical guidance is to sub-divide immediately after reconstitution into the smallest workable single-use volumes and cap the cumulative thaw count at three or fewer per aliquot. The lyophilised vial itself rolls under the standard 24-month re-test window at -20 C, and the released-batch COA carries the documented re-test date for pharmacies planning recurring procurement cycles.