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Save 31%SNAP-8 (Acetyl Octapeptide-3)

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SNAP-8 (Acetyl Octapeptide-3)

Topical peptide that reduces wrinkle depth by inhibiting muscle contraction

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$34$49Save 31%

200mg topical | 200mg/bottle

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About SNAP-8 (Acetyl Octapeptide-3)

SNAP-8, also known as Acetyl Octapeptide-3, is an 8-amino-acid synthetic peptide with the sequence Ac-Glu-Glu-Met-Gln-Arg-Arg-Ala-Asp-NH2 and an approximate molecular weight of 1075 Da. It was designed as an extended, more potent version of Argireline (Acetyl Hexapeptide-3, the C-terminal 6 residues) by Lipotec S.A. (now part of Lubrizol). SNAP-8 mimics the N-terminal segment of SNAP-25, one of three proteins that form the SNARE complex required for synaptic vesicle fusion and neurotransmitter release at the neuromuscular junction.

The mechanism of action targets the same molecular machinery as botulinum toxin but through competitive inhibition rather than enzymatic cleavage. The SNARE complex consists of three proteins: SNAP-25 (Synaptosome-Associated Protein of 25 kDa), syntaxin-1, and VAMP/synaptobrevin. These three proteins wind together into a four-helix bundle that provides the mechanical force to fuse synaptic vesicles with the presynaptic membrane, releasing acetylcholine into the synaptic cleft. SNAP-8 competes with endogenous SNAP-25 for incorporation into this complex. Because SNAP-8 is only a fragment (8 of 206 amino acids), the resulting complexes are non-functional and cannot drive vesicle fusion, reducing acetylcholine release in a dose-dependent manner.

In vitro studies using bovine adrenal chromaffin cells demonstrated that SNAP-8 inhibits catecholamine release (a marker of vesicle exocytosis) in a concentration-dependent manner, confirming the SNARE-targeting mechanism. The octapeptide showed approximately 30% greater inhibitory potency than the hexapeptide Argireline in comparative assays, attributed to the two additional N-terminal residues providing more extensive interaction with the SNARE binding interface.

Clinical evaluation showed that SNAP-8 at 10% concentration in a cream base reduced wrinkle depth by up to 63% after 28 days of twice-daily topical application, as measured by silicon replica analysis and profilometry. At 3% concentration, wrinkle depth reduction was approximately 35% over the same period. The effect is fully reversible upon discontinuation (wrinkles return to baseline over 2-4 weeks as normal SNAP-25 turnover restores SNARE function) and carries no risk of the frozen, expressionless appearance sometimes associated with injectable botulinum toxin.

SNAP-8 is most effective on dynamic wrinkles (expression lines) caused by repeated muscle contraction: crow's feet around the eyes, horizontal forehead lines, and glabellar (frown) lines. It is less effective on static wrinkles caused by collagen and elastin loss, which are better addressed by matrix-rebuilding peptides like Matrixyl (Pal-KTTKS) or GHK-Cu. For comprehensive anti-aging topical therapy, combining SNAP-8 (muscle relaxation) with Matrixyl (collagen stimulation) and GHK-Cu (gene expression reset) addresses wrinkles through three independent, complementary mechanisms.

For storage, SNAP-8 topical formulations should be kept at room temperature (15-25C) away from direct sunlight. The peptide is stable in aqueous solution at pH 5-7. The acetyl and amide terminal modifications protect against exopeptidase degradation, but the methionine residue is susceptible to oxidation; minimize prolonged air exposure. Opened products should be used within 3-6 months.

The safety profile of topical SNAP-8 is well-established through cosmetic industry testing. Dermatological patch testing shows no irritation, sensitization, or phototoxicity. The peptide acts locally in the skin and has no systemic absorption at levels that would affect neuromuscular function elsewhere in the body. It is non-immunogenic, compatible with all skin types, and safe for use around the eyes. No contraindications with injectable botulinum toxin, dermal fillers, or retinoid use have been identified.


Key Benefits

Up to 63% wrinkle depth reduction after 28 days at 10% concentration
Topical non-invasive alternative to injectable botulinum toxin
Competitively inhibits SNARE complex formation reducing acetylcholine release
30% greater inhibitory potency than hexapeptide Argireline
Fully reversible effect with no frozen or expressionless appearance
Most effective on dynamic expression lines (crow's feet, forehead, glabellar)
Synergistic with Matrixyl and GHK-Cu through complementary mechanisms
No systemic neuromuscular effects, irritation, or sensitization

Published Research

Clinical profilometry: 63% wrinkle depth reduction at 10% concentration after 28 days of twice-daily application; 35% reduction at 3% concentration.

In vitro chromaffin cell assay: dose-dependent inhibition of catecholamine release (vesicle exocytosis marker), ~30% more potent than Acetyl Hexapeptide-3.

Mechanism: competitive displacement of SNAP-25 in SNARE complex (SNAP-25/syntaxin-1/VAMP tripartite assembly).

8-amino-acid sequence Ac-Glu-Glu-Met-Gln-Arg-Arg-Ala-Asp-NH2, MW ~1075 Da.

Developed by Lipotec S.A.

Published in International Journal of Cosmetic Science.

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