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NORTHVERITY / CND10

CJC-1295 NO DAC

10 mg × 10 vials

For laboratory procurement

CJC-1295 NO DAC 10 mg × 10 vials · CND10 · Catalog illustration—not an actual packaging photo.
Catalog illustration—not an actual packaging photo.
Procurement details
Catalog number
CND10
Listed specification
10 mg
Vials per pack
10 vials
Current supply lot
Lot documents with your quote

Compound profile

CJC-1295 without DAC is an amidated, 29-residue modified GRF peptide without the albumin-binding extension.

Identity

Sequence
H-Y[D-Ala]DAIFTQSYRKVLAQLSARKLLQDILSR-NH2
Residues
29
Molecular formula
C152H252N44O42
Average molecular weight
3367.9 g/mol
Monoisotopic mass (calculated)
3365.8936 Da
CAS number
Not recorded
Strengths
5–10 mg
Other names
Modified GRF (1-29) · Tetrasubstituted GRF (1-29)

This is [D-Ala2, Gln8, Ala15, Leu27]-hGRF(1-29) amide without the lysine–maleimidopropionyl DAC extension. No PubChem record or CAS number was found for this form; formula and molecular weight are calculated from its sequence.

Identity data from: Jetté et al., Endocrinology 2005 (PMID 15817669) · computed from the sequence

Residue diagram of CJC-1295 without DAC
Drawn from the verified identity data on this page.

Research overview

CJC-1295 without DAC is also called modified GRF (1-29). Its chain has 29 residues, a free amino terminus and an amidated carboxyl terminus. The four substitutions are D-alanine, glutamine, alanine and leucine at positions 2, 8, 15 and 27. The Jetté paper investigated maleimido derivatives and their albumin conjugates, not the isolated peptide without the lysine–maleimidopropionyl extension [1].

That study prepared three maleimido derivatives of hGRF(1-29) and conjugated them to serum albumin ex vivo. It examined attachment through the free thiol of albumin Cys34, stability against dipeptidylpeptidase-IV and growth hormone secretion in cultured rat anterior pituitary cells. The rat experiments included Western blot analysis of plasma to examine material associated with serum albumin. The selected albumin-binding construct was named CJC-1295; these experiments do not characterise the peptide lacking DAC [1].

The second paper investigated in vitro metabolism and detection in fortified urine of four synthetic GHRH analogues: sermorelin, tesamorelin, and CJC-1295 with and without the DAC extension. Researchers identified 19 major in vitro metabolites, then synthesised, purified and characterised them as reference materials. The analytical work used these metabolites together with parent peptides and the sermorelin fragment sermorelin(3-29)-NH2 to develop a liquid chromatography–tandem mass spectrometry method for detecting the peptides [2].

Laboratory storage and handling

Store the closed vial under the temperature conditions stated in the lot documentation, protected from light and moisture. Before opening, allow the vial to reach room temperature to limit condensation on the material. Minimise repeated freezing and thawing of laboratory stocks, retain the lot identifier in experimental records and wear standard laboratory protective equipment.

Questions about CJC-1295 without DAC

What is absent in the without-DAC form?

The lysine–maleimidopropionyl extension associated with albumin binding is absent. The structure given here is the modified, amidated GRF peptide chain without that added group.

Did the Jetté study test this unextended peptide?

The cited paper investigated albumin-binding derivatives and their conjugates. Its observations on those constructs should not be transferred to the peptide without DAC [1].

Why are formula and molecular weight calculated?

No confirmed PubChem entry or CAS number was found for this form. Its formula and molecular weight are calculated from the structure given here.

References

  1. Human growth hormone-releasing factor (hGRF)1-29-albumin bioconjugates activate the GRF receptor on the anterior pituitary in rats: identification of CJC-1295 as a long-lasting GRF analog. Endocrinology 2005. PMID 15817669
  2. Advances in the detection of growth hormone releasing hormone synthetic analogs. Drug Test Anal 2021. PMID 34665524

Identity data checked on 2026-09-24. Literature summaries describe published research models and are not specifications of any product lot.

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2 catalog entries

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