Snap-8¶
Identification¶
| Property | Value |
|---|---|
| CAS Number | — (Acetyl Octapeptide-3) |
| Molecular Formula | C₄₁H₇₀N₁₆O₁₆S |
| Molecular Weight | ~1,073.2 Da |
| Sequence | Ac-Glu-Glu-Met-Gln-Arg-Arg-Ala-Asp-NH₂ |
| Amino Acid Count | 8 (N-terminal acetyl, C-terminal amide) |
| Appearance | White to off-white lyophilized powder |
| Purity Standard | ≥99% by HPLC |
| Solubility | Soluble in sterile water; cosmetic formulation-compatible |
| Storage | 2–8°C, desiccated, protect from light |
Category: Cosmetic & Skin
Catalog SKU: PSH-SNAP8-10MG
Research Background¶
Snap-8 (Acetyl Octapeptide-3) is an N-terminal acetylated, C-terminal amidated octapeptide designed to interfere with SNARE complex assembly at the presynaptic membrane. By mimicking the N-terminal domain of SNAP-25 — a critical SNARE protein — Snap-8 competes for binding sites within the ternary SNARE complex (SNAP-25/syntaxin/VAMP). This competition reduces the efficiency of synaptic vesicle docking and fusion, leading to decreased acetylcholine release at the neuromuscular junction.
Key Mechanisms¶
| Mechanism | Details |
|---|---|
| SNAP-25 Competition | Mimics N-terminal domain of SNAP-25 → competes for SNARE complex binding |
| Vesicle Docking Inhibition | Reduced ternary SNARE complex formation → decreased synaptic vesicle fusion |
| ACh Release Reduction | Less acetylcholine released at neuromuscular junction → muscle fiber relaxation |
Research Focus Areas¶
Expression Lines¶
SNARE complex inhibition → reduced neurotransmitter release at NMJ
Crow's Feet¶
Periorbital wrinkle reduction in topical formulation models
Forehead Lines¶
Frontalis muscle relaxation via SNAP-25 competition
Anti-Wrinkle Formulations¶
Topical peptide delivery systems for cosmetic research
Available Configurations¶
| Configuration | Content | Best For |
|---|---|---|
| Standard Kit | 10 mg × 10 vials | Formulation research; evaluation |
| Bulk Kit | 50 mg × 10 vials | Product development; pilot batches |
| Custom | Custom mg × custom vials | OEM; private-label cosmetics |
Tiered Wholesale Pricing¶
| Volume | Discount | For |
|---|---|---|
| 1 kit | List price | Evaluation; competitive analysis |
| 5+ kits | 10% off | Initial portfolio expansion |
| 20+ kits | 20% off | Mid-size distributors |
| 50+ kits | 30% off | Regional distributors |
Quality Specifications¶
| Parameter | Method | Criterion |
|---|---|---|
| Purity | HPLC at 214 nm, C18 column | ≥99.0% peak area |
| Identity (MW) | ESI-MS | ~1,073.2 ± 1.0 Da |
| Appearance | Visual inspection | White to off-white powder |
| Peptide Content | Amino acid analysis | ≥80% net peptide |
| Residual Moisture | Karl Fischer | ≤3% |
Frequently Asked Questions¶
Q1: How does Snap-8 work in anti-wrinkle research?¶
Snap-8 mimics the N-terminal domain of SNAP-25, a protein essential for SNARE complex assembly. By competing with native SNAP-25, it reduces synaptic vesicle docking efficiency → less ACh released at NMJ → muscle fibers relax → expression lines reduced in topical research.
Q2: How does Snap-8 differ from Argireline?¶
Both target neurotransmitter release through different mechanisms. Argireline prevents formation of the ternary SNARE complex. Snap-8 specifically targets the SNAP-25 binding site within the complex. In research they are sometimes combined for multi-target effects.
Q3: Is Snap-8 stable in topical formulations?¶
Yes. N-terminal acetylation and C-terminal amidation enhance metabolic stability and skin penetration. Soluble in standard cosmetic base formulations at pH 5.0–7.0.
Q4: Can Snap-8 and Leuphasyl be used together?¶
Yes — this is a common research combination. Snap-8 targets SNARE complex assembly, while Leuphasyl acts through opioid receptor-mediated calcium channel modulation. Complementary mechanisms.
Q5: What is the standard purity for Snap-8?¶
≥99% by HPLC with ESI-MS identity. Batch-specific COA included. For cosmetic-grade bulk orders, lower purity grades may be available — contact us for specifications.
Key Research References¶
| Reference | PMID | Key Finding |
|---|---|---|
| Blanes-Mira C et al. "Small peptides patterned after the N-terminus domain of SNAP25 inhibit SNARE complex assembly and regulated exocytosis." J Neurochem. 2004;88(1):124–135. | 14675156 | Snap-8 design and mechanism: mimics SNAP-25 N-terminal domain to inhibit ternary SNARE complex assembly, reducing ACh release |
| Gorouhi F & Maibach HI. "Role of topical peptides in preventing or treating aged skin." Int J Cosmet Sci. 2009;31(5):327–345. | 19570099 | Review of cosmetic peptides including Snap-8; mechanism as SNAP-25 competitor for anti-wrinkle research vs botulinum toxin |
Stability & Storage¶
| Condition | Degradation Profile |
|---|---|
| Lyophilized Storage | Standard peptide stability; 24 months at 2–8°C in desiccated environment, protect from light |
| N-Terminal Acetylation | Acetyl cap protects against aminopeptidase degradation; C-terminal amidation protects against carboxypeptidase |
| Neutral pH (5.0–7.0) | Stable; compatible with cosmetic formulation conditions at standard pH |
| Reconstituted Solution | 24 h at 2–8°C; aliquot and freeze at −20°C for extended use. Met⁵ residue susceptible to oxidation — protect from oxidative conditions |
Source & Purchase¶
For research-grade SNAP 8 and related compounds in this category, visit the PeptideSourceHub category page for bulk pricing and available specifications.
Browse SNAP 8 & Related Products →
Related Products¶
| Product | Link |
|---|---|
| Argireline (Acetyl Hexapeptide-8) | argireline.md — SNARE complex inhibitor |
| Leuphasyl (Pentapeptide-18) | leuphasyl.md — δ-opioid receptor agonist for fine lines |
| Matrixyl (Palmitoyl Pentapeptide-4) | matrixyl.md — Matrikine signaling for collagen synthesis |
| GHK-Cu (Copper Tripeptide) | ghk-cu.md — Copper peptide for wound healing |