Overview
Palmitoyl tripeptide-1 (also called pal-GHK, and sold under names including palmitoyl oligopeptide) is the tripeptide Gly-His-Lys with a 16-carbon palmitic acid chain attached to the N-terminus. Its PubChem entry names it precisely: L-Lysine, N-(1-oxohexadecyl)glycyl-L-histidyl- (C30H54N6O5, MW 578.8, CAS 147732-56-7).
The palmitoyl group is the whole point, and understanding why explains most of modern cosmetic peptide design. GHK itself is a small hydrophilic peptide — exactly the kind of molecule the lipophilic stratum corneum is built to keep out. Attaching a fatty acid chain makes the conjugate far more lipophilic, so it partitions into the skin barrier instead of sitting on top of it. The lipid tail is a delivery device, not a second active ingredient.
This is why palmitoylated peptides dominate cosmetic formulation while their unmodified parents mostly do not, and it is the single most useful thing to understand when comparing products: 'palmitoyl' in an INCI name usually signals that the formulator addressed the permeability problem rather than ignoring it.
It is frequently combined with palmitoyl tetrapeptide-7 in commercial complexes, where the two are marketed together as a matrix-signalling pair.
The limiting factor for every topical peptide is delivery. Peptides are hydrophilic and relatively large, while the stratum corneum is a lipophilic barrier built to exclude exactly such molecules. A peptide that performs well in a fibroblast culture has not thereby been shown to reach fibroblasts through intact skin. Reviews of cosmeceutical peptides identify this permeability gap — not receptor pharmacology — as the principal open problem, and note that formulation strategies such as oil-in-water and water-in-oil-in-water emulsions are used to try to close it with uncertain success.
What the evidence shows
Separated by study type- HumanClinical trials and human studies
- Used widely in finished cosmetic products. Independent controlled clinical trials isolating this single ingredient are scarce; most published support is manufacturer-associated or tests multi-ingredient formulations.
- AnimalRodent and other animal models
- Not the primary evidence base.
- In vitroCell and tissue studies
- The parent GHK motif has an extensive matrix-signalling literature. The palmitoyl conjugate's contribution is improved lipophilicity and skin partitioning.
Key studies & findings
2 studies- 1
PubChem identifies palmitoyl tripeptide-1 as L-Lysine, N-(1-oxohexadecyl)glycyl-L-histidyl- (C30H54N6O5, CAS 147732-56-7), confirming it is N-palmitoylated Gly-His-Lys.
- 2
Reviews of cosmeceutical peptides identify limited permeability through the lipophilic stratum corneum as the central obstacle for hydrophilic peptide actives, motivating lipid conjugation and emulsion delivery strategies.
Benefits & effects
2 documentedImproved skin partitioning relative to unmodified GHK
Delivers the GHK matrix-signalling motif topically
Side effects & safety
2 reportedSafety noteCosmetic ingredient used topically in finished formulations. Injecting cosmetic peptides is not an established route, has no supporting safety data, and is not a use these ingredients were characterised for.
Generally well tolerated as a cosmetic ingredient
Independent ingredient-isolated clinical safety data are limited
Limitations & open questions
Independent, ingredient-isolated clinical evidence is thin; most product claims rest on multi-ingredient formulations where this peptide's specific contribution cannot be separated out. Improved lipophilicity increases partitioning into the stratum corneum but does not by itself prove that an intact, active peptide reaches viable dermis at meaningful concentration.
Pharmacology
Palmitoyl tripeptide-1 is C30H54N6O5, MW 578.8, CAS 147732-56-7, PubChem CID 10231864. The C16 palmitoyl chain roughly doubles the molecular weight relative to free GHK while substantially increasing lipophilicity — the trade-off that makes topical delivery plausible.
Frequently asked questions
What does the 'palmitoyl' prefix actually do?
It attaches a 16-carbon fatty acid to the peptide, making it much more lipophilic so it can partition into the skin's lipid barrier. It is a delivery strategy. The peptide part is what signals.
Is palmitoyl tripeptide-1 the same as GHK-Cu?
No. Both are built on the Gly-His-Lys motif, but GHK-Cu is the copper complex of the free peptide, while palmitoyl tripeptide-1 is the fatty-acid conjugate without copper. They solve different problems — copper coordination versus skin penetration.
Why is it usually paired with palmitoyl tetrapeptide-7?
Commercial complexes combine them and market them as a matrix-signalling pair. That pairing is a formulation convention; the evidence for the combination being superior to either alone is not well established independently.
Citations
1 sources- 1