CJC-1295 & Ipamorelin

Ipamorelin Sequence and Chemical Identity

UKPWritten & reviewed by The UK Peptides Editorial Team · Research library, UK Peptides2 min readLast reviewed 2026-08-232 cited sources

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

Buy CJC-1295 + Ipamorelin · £36.99

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

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.

UKP

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.

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Research use only. The information above is provided for scientific and educational reference. Compounds referenced are not approved for human use and are supplied for in vitro research or reference-material purposes only. No efficacy, safety, or therapeutic claims are made.