The short answer
Ipamorelin is Aib-His-D-2-Nal-D-Phe-Lys-NH2 with CAS 170851-70-4, PubChem CID 9831659, UNII Y9M3S784Z6 and molecular weight 711.9 Da for formula C38H49N9O5. Its identifiers are unambiguous, which is unusual in this field and stands in sharp contrast to CJC-1295, where one name covers two different molecules depending on whether DAC is present.
Key facts
- Sequence
- Aib-His-D-2-Nal-D-Phe-Lys-NH2
- CAS
- 170851-70-4
- PubChem CID
- 9831659
- UNII
- Y9M3S784Z6
- Molecular weight
- 711.9 Da
- Formula
- C38H49N9O5
- Development code
- NNC 26-0161
Reading the sequence notation
Aib is α-aminoisobutyric acid, not one of the twenty standard amino acids and therefore written out rather than given a letter. D-2-Nal is D-2-naphthylalanine, a phenylalanine analogue with a naphthalene ring in place of the benzene. D-Phe is D-phenylalanine. The NH2 at the end denotes a C-terminal amide rather than a free carboxyl.
Why it cannot be written in single-letter code
Single-letter codes exist only for the twenty proteinogenic L-amino acids. Ipamorelin contains a non-proteinogenic residue and two D-isomers, none of which the code can express. This is itself informative: a peptide that cannot be written as a simple letter string is a designed molecule rather than a natural fragment.
Research material referenced
CJC-1295 + Ipamorelin 5+5mg, third-party HPLC tested
A clean identity, by contrast
CAS 170851-70-4 resolves to CID 9831659, and the mass, formula and sequence agree. There is no second compound sharing the name, no contradictory synonym set, no unresolvable registry number. Compared with CJC-1295 in the same category (or TB-500 and GHK-Cu elsewhere in this library), ipamorelin is unusually straightforward.
The development code
NNC 26-0161 is Novo Nordisk's internal designation, and it appears in the older literature. Searching for it surfaces records the name ipamorelin misses, which is the same pattern as PL-14736 for BPC-157 and thymosin beta-4 for TB-500.
Analytical confirmation
Mass spectrometry against 711.9 Da. The peptide contains no cysteine and no methionine, so neither disulfide species nor a +16 Da oxidation satellite should appear. At five residues the synthesis is short, though the non-standard residues are more expensive and less routine to couple than ordinary amino acids.
Frequently asked questions
- Why is ipamorelin's sequence written with full residue names?
- Single-letter codes cover only the twenty standard L-amino acids. Ipamorelin contains Aib and two D-residues, none of which the code can express.
- What is D-2-Nal?
- D-2-naphthylalanine, a phenylalanine analogue carrying a naphthalene ring instead of a benzene, in the D configuration.
- Is ipamorelin's identity confused like CJC-1295's?
- No. One CAS, one CID, one compound, with mass, formula and sequence all in agreement.
Extended research context
The CJC-1295 & Ipamorelin deep dive
Deep dive: why CJC-1295 and Ipamorelin are studied together
CJC-1295 is a modified GHRH (growth-hormone-releasing hormone) analogue; Ipamorelin is a selective growth-hormone secretagogue that binds the ghrelin receptor (GHS-R1a). In pituitary-cell research models the two act on independent pathways whose downstream effect converges on GH release. CJC-1295 amplifies the endogenous GHRH signal while Ipamorelin adds a separate ghrelin-pathway stimulus. That's why supplier catalogues frequently package them together as a research reference blend.
DAC vs no-DAC: which CJC-1295 is which
'CJC-1295 with DAC' contains a Drug Affinity Complex (a Lys-maleimide moiety) that binds serum albumin and extends half-life to several days. 'CJC-1295 no-DAC' (also called Modified GRF 1-29) lacks the linker and clears in minutes. These are pharmacologically different peptides. A CoA must specify which form is in the vial; mass differs (~3,367 Da with DAC vs ~3,367 minus linker for no-DAC).
Ipamorelin's selectivity profile
Unlike earlier GHS-R agonists (e.g. GHRP-6), Ipamorelin was engineered for minimal cross-activity at cortisol- and prolactin-releasing pathways in research models. That receptor selectivity is why it is the reference secretagogue for controlled pituitary-cell studies.
Research applications
- ▸Pituitary-cell GH-release assays (comparator vs GHRH and hexarelin)
- ▸Half-life comparison studies: DAC vs no-DAC CJC-1295 forms
- ▸Ghrelin-receptor binding assays for Ipamorelin analogue development
- ▸Analytical HPLC method development for lipidated GHRH analogues
- ▸Stability testing under refrigerated storage
Handling checklist
- ✓Store lyophilised at −20 °C long-term
- ✓Reconstitute in bacteriostatic water; both peptides dissolve readily
- ✓Aliquot immediately, refrigerate at 2–8 °C, use within 28 days
- ✓Confirm salt form and DAC/no-DAC status on CoA before starting a study
- ✓Do not use for human administration (research reference only)
Common research-handling mistakes
Learnt from thousands of researcher orders across our UK labs.
✗ Confusing DAC and no-DAC CJC-1295
Fix: Check the CoA. The two have very different pharmacokinetics.
✗ Assuming Ipamorelin acts on GHRH receptors
Fix: It binds the ghrelin receptor (GHS-R1a), a separate pathway from CJC-1295.
✗ Storing reconstituted solution at room temperature
Fix: Refrigerate 2–8 °C after reconstitution.
Continue researching
Peer-reviewed guides, comparators and matched reference materials.
Related questions researchers ask
- Is CJC-1295 the same as Modified GRF 1-29?
- What is the difference between DAC and no-DAC CJC-1295?
- Does Ipamorelin raise cortisol?
- Why are CJC-1295 and Ipamorelin blended together?
- How long is the half-life of CJC-1295 with DAC?
Primary sources & clinical trials
Peer-reviewed research and registered trials from PubMed, ClinicalTrials.gov, PubChem, FDA and NIH. All links open in a new tab and point to the primary source, so every claim can be verified at origin.
- PubChemPubChem · Ipamorelin (CID 9831659)pubchem.ncbi.nlm.nih.gov
- PubMedRaun K et al. Eur J Endocrinol 1998 (PMID 9849822)pubmed.ncbi.nlm.nih.gov
- PubMedTeichman et al., Prolonged stimulation of GH & IGF-I by CJC-1295. J Clin Endocrinol Metab 2006 (PMID 16352683)pubmed.ncbi.nlm.nih.gov
- PubMedMüller TD et al., Ghrelin. Molecular Metabolism 2015 (PMID 26042199)pubmed.ncbi.nlm.nih.gov
- PubChemPubChem · CJC-1295 / mod GRF (1-29) (CID 56841945)pubchem.ncbi.nlm.nih.gov
- PubChemPubChem · CJC-1295 with DAC (CID 91971820)pubchem.ncbi.nlm.nih.gov
- TrialClinicalTrials.gov · GH-secretagogue trialsclinicaltrials.gov
- GuidelineGoogle: Creating helpful, reliable, people-first contentdevelopers.google.com
Written and reviewed by
The UK Peptides Editorial Team · Research library, UK Peptides
The editorial team is responsible for supplier selection, batch release decisions and the content published in this research library. Every article here is sourced to primary literature and every product page to a signed third-party certificate. Corrections are made in place and the review date updated.
More CJC-1295 & Ipamorelin articles
- Ipamorelin Molecular Weight and Physical Properties711.9 Da for C38H49N9O5 — high mass for five residues, because two of them carry aromatic ring systems. What that composition implies.
- How Ipamorelin Acts at the Ghrelin ReceptorGHS-R1a is the ghrelin receptor. Ipamorelin agonises it selectively, releasing GH without the cortisol and prolactin effects of earlier secretagogues.
- How CJC-1295 Works as a GHRH AnalogueCJC-1295 agonises the GHRH receptor on pituitary somatotrophs. Why the substitutions matter and what continuous versus pulsatile stimulation implies.
- GHRH and Ghrelin: Two Separate PathwaysTwo hormones, two receptors, one output. Why the pituitary has more than one input for growth hormone release, and what each pathway contributes.
- What Is a Growth Hormone Secretagogue?A secretagogue prompts release of a substance the body already makes. Why that differs fundamentally from administering growth hormone itself.
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