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Compound reference

CJC-1295 with DAC vs without DAC: what the DAC changes

Published 2026-10-31 · updated 2026-10-31 · vendor-authored explanatory note

Short answer

Both materials start from the same idea: a modified version of the first 29 amino acids of growth hormone-releasing hormone, GHRH(1-29), with four substitutions that make it more resistant to enzymatic breakdown. The version without DAC stops there and is often called modified GRF(1-29). The version with DAC adds a lysine at the C-terminus carrying a maleimidopropionyl group that reacts with albumin, which is what extends its time in circulation in published studies. Because they are different molecules with different masses, a mass-spec identity result is the simplest way to tell them apart.

Catalog materials discussed on this page

CJC-1295 with DAC vs without DAC
Without DAC (mod GRF 1-29)With DAC
Core sequenceSubstituted GHRH(1-29)Substituted GHRH(1-29)
C-terminal additionNoneLysine with 3-maleimidopropionamide group
Albumin bindingNo reactive group for albuminMaleimide reacts with albumin Cys34
Plasma persistence in published studiesShortDetected beyond 72 h in rats; half-life 5.8 to 8.1 days estimated in a clinical study
How to confirm identityMass spec matches the no-DAC massMass spec matches the DAC mass

Shared backbone

GHRH(1-29) is the shortest fragment of the natural hormone that keeps its activity at the GHRH receptor in laboratory models. Native GHRH(1-29) is broken down quickly, largely by the enzyme dipeptidyl peptidase-IV, which cuts after the second residue.

The four substitutions in CJC-1295 are designed to slow that breakdown. Both the DAC and no-DAC materials share this substituted 29-residue sequence.

What the DAC adds

DAC stands for Drug Affinity Complex. In CJC-1295 with DAC, an extra lysine is added at the C-terminus and its side chain carries a 3-maleimidopropionamide group. A maleimide reacts with free thiol groups, and serum albumin has one at cysteine 34.

In a 2005 rat study, the authors bioconjugated maleimido derivatives of GHRH(1-29) to human serum albumin, picked the best one (CJC-1295), and found it still present in plasma beyond 72 hours, with an immunoreactive band at the albumin position on a Western blot. A later clinical pharmacology study estimated its plasma half-life at 5.8 to 8.1 days. Unmodified GHRH(1-29), by comparison, is generally described as lasting only minutes in circulation.

Telling them apart on a COA

The two materials have different molecular weights, because the DAC version carries the extra lysine and maleimide linker. The product pages list the molecular weight for each. An LC-MS or MALDI identity result should match the material you ordered; a mass that matches the other form means the vial is mislabeled.

Names in the market are messy. You will see CJC-1295 no DAC, CJC-1295 without DAC, Mod GRF 1-29, and modified GRF(1-29) used for the no-DAC material. Read the reported mass, not just the name. HPLC purity will not tell you which form you have, since both can be equally pure.

  1. Compound name exactly as ordered (with DAC or without DAC)
  2. Observed mass from LC-MS or MALDI compared with the expected mass for that form
  3. HPLC purity with method
  4. Lot number that matches the vial

Blends

Some catalogs pair CJC-1295 without DAC with ipamorelin in one vial. A COA for a blend should identify both components by mass and report purity for each, or state clearly how the blend was tested. A single purity number for a two-peptide vial is hard to interpret.

Frequently asked

Is mod GRF 1-29 the same as CJC-1295 without DAC?

In most catalogs, yes. Both names refer to the tetrasubstituted GHRH(1-29) without the C-terminal DAC lysine. Confirm with the reported mass.

Can HPLC purity tell me which form I have?

No. Purity says how clean the sample is, not which molecule it is. Use the mass-spec identity result.

Why does the DAC version persist longer?

Its maleimide group reacts with albumin, a long-lived plasma protein, so the peptide is carried along with it in published animal and clinical pharmacokinetic studies.

References

  1. Jetté L et al. Human growth hormone-releasing factor (hGRF)1-29-albumin bioconjugates activate the GRF receptor on the anterior pituitary in rats. Endocrinology. 2005;146(7):3052-3058.Design of maleimido GRF(1-29) derivatives and albumin binding of CJC-1295 in rats.
  2. 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. J Clin Endocrinol Metab. 2006;91(3):799-805.Pharmacokinetic half-life estimate for CJC-1295.