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SNAP-8

10mg

❄️Lyophilized powder (not reconstituted)

€22.99
1

Discount per Quantity

QuantityDiscountPrice per Unit
5 - 1010%€20.69
11 - 2015%€19.54
21+20%€18.39

Rigorous third-party testing

Every batch of our research chemicals and peptides undergoes independent third-party laboratory testing for purity and identity.

Total: €22.99

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SNAP-8 is supplied as a catalogued research material in 10 mg.

SNAP-8 is used for the defined peptide acetyl octapeptide-3, but the name can also identify a branded aqueous cosmetic mixture. Registry values apply only to the pure Ac-EEMQRRAD-NH₂ peptide; powder or mixture status and excipients must be established by CoA and SDS [1–3].

Chemical properties and registry information

PropertyValue
Name and synonymsAcetyl Octapeptide-3
Material categoryCosmetic Peptide
SequenceAc-EEMQRRAD-NH2
Molecular formulaC41H70N16O16S
Average molecular mass1075.2 g/mol
CAS Registry Number868844-74-0
PubChem CIDCID 135688138
Structural featuresN-terminally acetylated and C-terminally amidated octapeptide. A fragment of the N-terminus of SNAP-25.
AppearanceWhite to off-white lyophilised powder
SolubilitySoluble in water. Reconstitute with sterile or bacteriostatic water.
Physical formCatalogue vial; exact salt/counter-ion and excipients are batch-specific and must be verified in the CoA and SDS.

Registry values apply only to the specific molecular entity, sequence, termini and material form. Batch records take precedence over family-level literature identifiers.

A synthetic peptide used in cosmetics to reduce the appearance of wrinkles. It is designed to mimic the N-terminal end of the SNAP-25 protein and competes for a position in the SNARE complex, which can modulate neurotransmitter release.

Research background and published evidence

Published research

Defensible contexts include peptide identity, LC–MS quantification, degradation studies and carefully controlled SNARE/SNAP-25-mimetic assay models. Mechanistic claims are often proprietary or extrapolated and should be treated as hypotheses rather than product specifications [2,3].

Current scientific understanding

Cosmetic-formulation studies, patents and data for acetyl hexapeptide-8 do not establish the identity or performance of pure SNAP-8 material. No topical or cosmetic use is permitted for this catalogue product.

Technical comparison

AspectThis catalogue materialComparator
IdentityAcetyl octapeptide-3: Ac-EEMQRRAD-NH₂Acetyl hexapeptide-8: Ac-EEMQRR-NH₂
Structural distinctionContains two additional C-terminal residues, Ala-AspTerminates after the second Arg
Analytical implicationConfirm eight-residue sequence, N-acetylation and C-terminal amidationDifferent intact mass and chromatographic reference

Quality and testing

Quality information is batch- and presentation-specific. Use only the report linked to the exact size and lot. A report listed for another size, lot or similarly named material must not be treated as evidence for this product.

Chromatographic area purity, identity, net peptide or analyte content, water or counter-ion content, sterility, endotoxin and elemental impurities are different measurements. One result does not establish the others. Only tests supported by a visible, matching report should be regarded as available.

Laboratory handling and storage

Store and handle only under the conditions stated on the product label, batch CoA and SDS. Keep the container secured, correctly identified and protected from contamination. Do not infer storage, solvent compatibility or stability from a related compound.

Laboratory preparation, analytical-method selection, risk assessment, personal protective equipment and waste disposal should follow the applicable SDS and the institution's approved procedures.

Regulatory and legal status

Research-use noticeThis material is supplied exclusively for laboratory research by qualified professionals and is not intended for human or veterinary use. Purchasers are responsible for compliance with applicable local requirements.

Sources and references

  1. [1] PubChem. Acetyl octapeptide-3 compound record.
  2. [2] LC–MS/MS analysis of acetylated cosmetic peptides. BMC Chemistry (2020).
  3. [3] SNAP-25-derived peptide family patent.

Frequently Asked Questions

Do the CAS number and PubChem CID apply to every batch form?

Only when the exact sequence or structure, termini, conjugation, salt or counter-ion and hydration state match. The batch CoA and SDS govern; a related-compound identifier must not be substituted.

What does an analytical purity result mean?

It is method- and report-specific. For example, an HPLC area percentage is not automatically the same as identity, net content, sterility, endotoxin status or absence of elemental impurities.

How should the material be stored and handled?

Follow the exact label, batch CoA and SDS together with the institution's risk assessment. Use only storage and stability information linked to the exact material form and batch.