Acetyl Hexapeptide-8

Acetyl Hexapeptide-8 is the updated INCI name for Argireline (formerly Acetyl Hexapeptide-3), a synthetic SNARE complex inhibitor that reduces neurotransmitter release to attenuate facial muscle contractions and expression lines.

Acetyl Hexapeptide-8 is the current INCI (International Nomenclature of Cosmetic Ingredients) designation for the synthetic hexapeptide previously registered as Acetyl Hexapeptide-3 and commercially known as Argireline. The compound itself is unchanged -- the PCPC (Personal Care Products Council) reassigned the INCI number during a routine nomenclature update.

Overview

The peptide was originally developed by Lipotec (now part of Lubrizol/Berkshire Hathaway) and registered under the INCI name Acetyl Hexapeptide-3. When the PCPC updated the International Cosmetic Ingredient Dictionary and Handbook, the compound was reassigned to Acetyl Hexapeptide-8 to accommodate new entries in the hexapeptide numbering sequence. Both names refer to the identical molecule: an acetylated hexapeptide with the sequence Ac-Glu-Glu-Met-Gln-Arg-Arg-NH2.

This nomenclature change has caused confusion in the cosmetics industry, with some products listing the old name and others the new one. Regulatory bodies in the EU (INCI-compliant labeling under EC Regulation 1223/2009) now expect the updated Acetyl Hexapeptide-8 designation on product labels, though Acetyl Hexapeptide-3 remains widely recognized and accepted in practice.

Mechanism of Action

Acetyl Hexapeptide-8 mimics the N-terminal domain of SNAP-25 (Synaptosomal-Associated Protein of 25 kDa), one of three proteins that assemble into the SNARE complex required for synaptic vesicle docking and fusion at the presynaptic terminal. By competing with endogenous SNAP-25 for incorporation into the ternary SNARE complex (SNAP-25 + syntaxin + VAMP/synaptobrevin), the peptide destabilizes complex assembly and reduces the efficiency of vesicular neurotransmitter release.

The mechanism proceeds through several steps:

  1. SNARE competition: The hexapeptide competes with native SNAP-25 at the N-terminal binding interface
  2. Complex destabilization: Incomplete SNARE complexes form less efficiently, reducing vesicle fusion probability
  3. Reduced exocytosis: Acetylcholine release at the neuromuscular junction decreases in a dose-dependent manner
  4. Attenuated contraction: Facial expression muscles receive weaker signals, reducing dynamic wrinkle formation

Unlike botulinum neurotoxins, which enzymatically cleave SNARE proteins irreversibly, Acetyl Hexapeptide-8 acts as a reversible competitive inhibitor. This fundamental difference underlies its safety profile and suitability for over-the-counter topical use Blanes-Mira et al. (2002).

Reconstitution Calculator

Reconstitution Calculator

Calculate your peptide dosing

Draw Volume
0.100mL
Syringe Units
10units
Concentration
2,500mcg/mL
Doses / Vial
20doses
Vial Total
5mg
Waste / Vial
0mcg
Syringe Cap.
100units · 1mL
How to reconstitute
Gather & prepare
1/6Gather & prepare

Set up a clean workspace with all supplies ready.

1.Wash hands thoroughly, put on disposable gloves
2.Your 5mg peptide vial (lyophilized powder)
3.Bacteriostatic water (you'll need 2mL)
4.A 3–5mL syringe with 21–25 gauge needle for reconstitution
5.Alcohol swabs (70% isopropyl)
Use bacteriostatic water (0.9% benzyl alcohol) for multi-dose vials. Sterile water is only safe for single-use.
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Store 2-8°C30 day shelf lifeSwirl gentlyFor research purposes only

Research

Penetration and Delivery

Skin penetration remains the primary challenge for topical peptide delivery. Kraeling et al. (2015) demonstrated measurable skin penetration of Acetyl Hexapeptide-8 from cosmetic formulations using in vitro Franz diffusion cell studies. Nanostructured lipid carriers, liposomal encapsulation, and chemical penetration enhancers have all been shown to improve dermal delivery Wang et al. (2013).

INCI Nomenclature History

The transition from Acetyl Hexapeptide-3 to Acetyl Hexapeptide-8 reflects the PCPC's ongoing effort to maintain a coherent numbering system as new peptide ingredients enter the cosmetic market. The change does not indicate any structural modification, reformulation, or change in regulatory status. Products labeled with either name contain the same active ingredient at the same concentrations.

Formulation Considerations

Acetyl Hexapeptide-8 is typically supplied as a lyophilized powder or aqueous solution at defined concentrations. Standard cosmetic formulations use 5-10% of a commercial solution containing 0.05% active peptide. The peptide is water-soluble, stable at pH 5.0-7.0, and compatible with most cosmetic ingredients. It is heat-sensitive above 40C and should not be added to formulations before cooling.

Safety Profile

The safety profile of Acetyl Hexapeptide-8 is identical to that documented under its previous INCI name. Topical application at concentrations up to 10% of commercial solution is well-tolerated with no significant adverse effects reported. Dermal irritation and sensitization testing show minimal reactivity. No systemic neuromuscular effects have been observed, consistent with limited transdermal absorption. The reversible nature of SNARE complex inhibition provides an inherent safety margin. The peptide is approved for cosmetic use in the EU, US, and other major markets under both legacy and updated INCI designations.

Pharmacokinetic Profile

Acetyl Hexapeptide-8 — Pharmacokinetic Curve

Topical
0%25%50%75%100%0m30m1h1.5h2h2.5hTimeConcentration (% peak)T_max 27mT_1/2 30m
Half-life: 30mT_max: 45mDuration shown: 2.5h

Quick Start

Route
Topical

Molecular Structure

2D Structure
Acetyl Hexapeptide-8 molecular structure
Molecular Properties
Formula
C34H60N14O12S
Weight
888.99 Da
CAS
616204-22-9
PubChem CID
11390410
Exact Mass
221.1528 Da
LogP
0.7
TPSA
70.1 Ų
H-Bond Donors
1
H-Bond Acceptors
3
Rotatable Bonds
3
Complexity
359
Identifiers (SMILES, InChI)
InChI
InChI=1S/C12H19N3O/c1-3-8(2)10(14)11(16)15-5-4-9-6-12(9,15)7-13/h8-10H,3-6,14H2,1-2H3/t8-,9+,10-,12+/m0/s1
InChIKeyVFMGPTHTVPHION-MIZYBKAJSA-N

Research Protocols

topical

This fundamental difference underlies its safety profile and suitability for over-the-counter topical use [Blanes-Mira et al. Penetration and Delivery Skin penetration remains the primary challenge for topical peptide delivery.

transdermal Injection

Argireline, as a charged, hydrophilic hexapeptide exceeding this molecular weight threshold, requires formulation strategies that enhance its transdermal flux to reach the target site -- the neuromuscular junctions underlying facial expression muscles.

Interactions

Peptide Interactions

SYN-AKEsynergistic
  • SYN-AKE: Receptor antagonism + SNARE inhibition.
Matrixylsynergistic
  • Matrixyl: Neuromuscular relaxation + collagen stimulation.
Leuphasylsynergistic
  • Leuphasyl (Pentapeptide-18): Pre-synaptic + post-synaptic neuromuscular modulation.

Quality Indicators

What to look for

  • Well-established safety profile

Frequently Asked Questions

References (5)

  1. [6]
    Raikou V et al Anti-aging peptides for advanced skincare J Cosmet Dermatol (2017)
  2. [8]
  3. [3]
  4. [1]
    Blanes-Mira C et al A synthetic hexapeptide (Argireline) with antiwrinkle activity Int J Cosmet Sci (2002)
  5. [2]
Updated 2026-03-08Reviewed by Tides Research Team5 citationsSources: peptide-wiki-mdx, pubchem, peptide-wiki-mdx-v2

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