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SYN-Ake

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SYN-AKE is a sophisticated cosmetic active designed to mimic the wrinkle-softening effects with muscular relaxation — without invasive procedures.

$57.00

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  • By purchasing any products, you acknowledge and agree that all materials are supplied solely for scientific research, laboratory experimentation, or analytical purposes.
Form
Lyophilized
Molecular Formula
See COA
Molecular Weight
See COA
CAS Number
See COA
PubChem CID
See COA
Research Data
Primary Effect Over Time
Literature
Cellular Ratio
Comparative Metric
Activity Profile
Activity Profile
Mechanism
Cellular Pathway
01
nAChR Ion Channel Antagonism
02
Muscle Contraction Frequency Reduction
03
Fine Line Attenuation & Sebum Reduction
Metabolic Network
Biosynthesis Map
nAChR Ion Channel Antagonism
Muscle Contraction Frequency Reduction
Fine Line Attenuation & Sebum Reduction
Signal Output
Response
Repair Systems
Stress
Mitochondria
Energy
SYN-Ake CENTRAL HUB
Sequence Analysis
Amino Acid Sequence
Single-letter residue map colored by physicochemical property class. Hover any residue for full name and position.
H A L A P R O D A B N H B E N Z Y L A C O H
22Residues
See COAMol. Weight
+2Net Charge
4Basic
2Acidic
■ Hydrophobic ■ Polar ■ Positively Charged ■ Negatively Charged ■ Glycine
Research Focus
Research Coverage
Product Data
Compound Identity
Product NameSYN-Ake
Functional ClassDermatics
FormLyophilized
Purity99%+
Content5mg
Count1 vial
Research UseResearch Grade
Specifications
Technical Specs
CAS NumberSee COA
Molecular WeightSee COA
Molecular FormulaSee COA
PubChem CIDSee COA
AppearanceWhite to off-white powder
Storage2-8C preferred
Formulation Reference
Anatomy of a Peptide
A reference guide to the components of a lyophilized research peptide — from the active sequence to the excipients, solvents, buffers, and stabilizers used in formulation.
Active Peptide 2 items
Synthetic Amino Acid Sequence
The primary chain of amino acids synthesized via solid-phase peptide synthesis (SPPS). Defined by sequence length and molecular weight.
Peptide Modifications
Acetylation (N-terminus), amidation (C-terminus), PEGylation, or cyclization applied to improve stability, receptor binding, or half-life.
Excipients 4 items
Mannitol
Sugar alcohol bulking agent that forms an elegant lyophilized cake, aids reconstitution, and provides structural matrix during freeze-drying.
Trehalose
Non-reducing disaccharide that stabilizes peptide secondary structure by replacing water molecules through hydrogen bonding during dehydration.
Sucrose
Disaccharide used as a lyoprotectant and tonicity agent. Forms an amorphous glassy matrix that immobilizes the peptide and prevents aggregation.
Glycine
Amino acid bulking agent used in lyophilization. Crystallizes to provide mechanical strength to the freeze-dried cake structure.
Reconstitution Solvents 4 items
Bacteriostatic Water (BAC Water)
Sterile water containing 0.9% benzyl alcohol as a preservative. Preferred for multi-dose vials — inhibits microbial growth after initial puncture.
Sterile Water for Injection
USP-grade water, pyrogen-free, without preservatives. Used for single-dose preparations or when benzyl alcohol sensitivity is a concern.
Acetic Acid Solution (0.1–1%)
Dilute acid used for peptides with poor aqueous solubility at neutral pH. Protonates basic residues to improve dissolution.
Sodium Chloride 0.9%
Isotonic saline diluent. Provides physiological osmolality (~308 mOsm/L) and can improve stability of certain charged peptides.
Buffer Systems 4 items
Phosphate Buffered Saline (PBS)
Maintains pH 7.2–7.4. Composed of sodium phosphate dibasic, potassium phosphate monobasic, NaCl, and KCl. Mimics physiological ionic strength.
Acetate Buffer
Effective pH range 3.7–5.6. Composed of acetic acid and sodium acetate. Ideal for acidic peptides and those requiring lower pH for solubility.
Citrate Buffer
Effective pH range 3.0–6.2. Offers strong buffering capacity and metal-chelating properties. Used when oxidation-sensitive residues (Met, Cys) are present.
Histidine Buffer
Effective pH range 5.5–7.0. Low ionic strength, minimal interaction with peptides. Increasingly preferred in modern biopharmaceutical formulations.
Lyoprotectants & Cryoprotectants 3 items
Trehalose / Sucrose (Lyoprotectant)
Protect peptide conformation during the drying phase of lyophilization by forming hydrogen bonds that substitute for water molecules around the peptide.
Glycerol (Cryoprotectant)
Polyol that depresses the freezing point and reduces ice crystal formation, preventing mechanical damage to peptide structure during freezing steps.
Polyethylene Glycol (PEG)
Hydrophilic polymer that provides steric stabilization, reduces aggregation, and can serve as both cryoprotectant and solubility enhancer.
Preservatives & Antimicrobials 3 items
Benzyl Alcohol (0.9%)
Aromatic alcohol preservative in bacteriostatic water. Acts as antimicrobial agent by disrupting microbial cell membranes. Standard for multi-use vials.
Methyl / Propyl Parabens
Broad-spectrum antimicrobial preservatives effective against fungi and bacteria. Used in some peptide formulations where benzyl alcohol is incompatible.
Phenol (0.5%)
Bacteriostatic preservative used in certain injectable peptide formulations. Also acts as a conformational stabilizer for some peptide structures.
Counter Ions & Salt Forms 3 items
Trifluoroacetate (TFA)
Most common counter ion from RP-HPLC purification. Forms TFA salt with basic residues (Lys, Arg, His). May affect bioassay results and cell toxicity.
Acetate
Milder alternative to TFA obtained via ion exchange. Lower cytotoxicity, preferred for cell-based research assays and in vivo studies.
Hydrochloride (HCl)
Chloride salt form, sometimes used for improved stability or specific solubility profiles. Common in pharmaceutical-grade peptide preparations.
Chelating Agents 2 items
EDTA (Disodium)
Chelates divalent metal ions (Cu²⁺, Fe²⁺, Zn²⁺) that catalyze oxidative degradation of methionine and cysteine residues in peptides.
Citric Acid
Natural chelator with moderate metal-binding capacity. Dual function as buffer component and oxidation inhibitor in peptide formulations.
Antioxidants & Stabilizers 3 items
L-Methionine
Free methionine added as a sacrificial antioxidant. Preferentially oxidizes before methionine residues within the peptide chain.
Ascorbic Acid
Water-soluble antioxidant that scavenges reactive oxygen species. Used at low concentrations to prevent oxidative peptide degradation.
Polysorbate 20 / 80
Non-ionic surfactants that prevent surface adsorption and aggregation of peptides at air-liquid and container-liquid interfaces.
Preparation Tool
Reconstitution Calculator
Enter your target working concentration to calculate the exact solvent volume needed for this vial.
mg
Recommended solvents
Bacteriostatic Water Sterile Water for Injection Acetic Acid 0.1% Sodium Chloride 0.9%
Product Specs
Solubility Profile
WaterHighly soluble
Acidified WaterHighly soluble
DMSOHighly soluble
EthanolModerate
Lipid solventsPoor compatibility
Product Specs
Storage Specs
Lyophilized2–8°C preferred
Long-term−20°C recommended
Light SensitivityModerate
MoistureHigh sensitivity
StabilityStable when dry
ContainerSterile sealed vial
Literature
Research Citations
Catalogue Pathway
Related Systems
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Important Notice
Research Use Only

AminoBox products are supplied for research, analytical, and laboratory use only. Product information is provided for educational and technical reference and does not constitute medical advice. Products are not intended to diagnose, treat, cure, or prevent any disease.

 

Product Composition Specification
Product Name SYN-Ake
Alternate Names Dipeptide Diaminobutyroyl Benzylamide Diacetate, Snake Peptide
Content Amount 100 mg
Compound Class Synthetic neuropeptide analog
Physical Form Lyophilized peptide powder
Appearance White to off-white powder
Purity Typically ≥98% (HPLC dependent)
Research Category Cosmetic peptide / neuromodulatory peptide research
Primary Function Expression-line and facial signaling peptide research

Molecular Information Specification
Molecular Formula C23H37N5O7
Molecular Weight ~495.57 g/mol
CAS Number 823202-99-9
PubChem CID 71465152
INCI Name Dipeptide Diaminobutyroyl Benzylamide Diacetate
Compound Type Synthetic peptide analog
Structural Classification Waglerin-1 mimetic peptide
Sequence Classification Neurotransmitter-inhibiting cosmetic peptide

Structural Classification Description
Compound Type Synthetic snake venom-inspired peptide
Functional Class Neuromodulatory cosmetic peptide
Biological Focus Facial muscle signaling and wrinkle research
Mechanistic Focus Neuromuscular receptor modulation
Chemical Family Biomimetic peptide analogs
Structural Inspiration Modeled after Waglerin-1 temple viper peptide

Mechanism Research Profile Description
Neuromuscular Signaling Studied for reversible modulation of muscular contraction pathways
Expression Line Research Investigated for cosmetic smoothing of dynamic facial lines
Receptor Interaction Mimics Waglerin-1 peptide receptor-binding behavior
Muscle Relaxation Signaling Explored for reduction of repetitive contraction signaling
Cosmetic Peptide Research Commonly formulated into anti-aging topical systems
SNARE/Neuro Signaling Associated with neurotransmitter-related cosmetic pathways

Research Areas Commonly Associated Focus
Cosmetic Peptide Research Fine line and wrinkle appearance studies
Neurocosmetic Research Neuromuscular signaling pathways
Dermatological Research Expression-line modulation
Anti-Aging Research Dynamic wrinkle reduction
Peptide Delivery Research Topical peptide transport systems
Skin Science Surface neuromodulation and cosmetic formulation

Solubility Profile Solubility
Water Soluble
Sterile Water Highly compatible
DMSO Soluble
Ethanol Limited compatibility
Glycols Good compatibility
Lipid Systems Moderate compatibility

Storage Specifications Recommendation
Short-Term Storage 2–8°C
Long-Term Storage -20°C preferred
Light Sensitivity Moderate
Moisture Sensitivity High
Stability Stable in lyophilized form
Reconstituted Stability Refrigerate after mixing
Container Type Sealed amber peptide vial

Technical Characteristics Notes
Delivery Format Lyophilized peptide powder (100 mg)
Structural Advantage Designed as a stable Waglerin-1 mimetic
Bioactivity Profile Cosmetic neuromodulatory signaling peptide
Functional Target Neuromuscular receptor-associated pathways
Topical Research Use Commonly studied in anti-aging cosmetic systems
Stability Profile Stable when protected from moisture and heat
Research Use Laboratory and cosmetic research only

BUY SYN-AKE™ | Scientific Overview (Corrected & Enhanced)

Mechanism of Action (Neurocosmetic Pathway)

SYN-AKE (Dipeptide Diaminobutyroyl Benzylamide Diacetate) is a synthetic tripeptide inspired by Waglerin-1, a peptide originally isolated from Temple Viper (Tropidolaemus wagleri) venom. Research literature describes Waglerin-1 as interacting with nicotinic acetylcholine receptors (nAChRs) at the neuromuscular junction.

In cosmetic science, SYN-AKE is designed to mimic aspects of this receptor interaction in a topical context, supporting the concept of reduced micro-muscle contraction activity associated with expression lines.
(Source: https://www.mdpi.com)


Expression Line Formation & Cosmetic Rationale

Facial expression lines develop primarily from repeated contraction of facial muscles triggered by acetylcholine signaling. Over time, this repeated mechanical folding contributes to the formation of dynamic wrinkles such as:

  • Forehead lines
  • Glabellar lines (frown lines)
  • Crow’s feet

SYN-AKE is studied in cosmetic formulation research for its ability to support a smoother skin appearance by targeting the look of contraction-related creasing, rather than altering underlying muscle structure.
(Source: https://www.specialchem.com)


Cosmetic Function (Important Clarification)

Unlike injectable neuromodulators (e.g., botulinum toxin), SYN-AKE is:

  • Not a neurotoxin
  • Not injectable
  • Not a drug
  • Designed strictly for topical cosmetic use

Its mechanism is best described as a surface-level neurocosmetic effect, intended to reduce the appearance of expression lines rather than directly inhibiting neuromuscular transmission in the way pharmaceutical agents do.

(Source: https://incidecoder.com)


Biomimetic Peptide Engineering

SYN-AKE is part of a class of biomimetic cosmetic peptides, where biological signaling pathways are modeled synthetically for topical skincare applications.

The INCI name:

Dipeptide Diaminobutyroyl Benzylamide Diacetate

This peptide was engineered for:

  • Cosmetic stability in aqueous formulations
  • Compatibility with emulsions and serum systems
  • Incorporation into modern delivery systems (liposomes, hydrogels, microemulsions)

(Source: https://www.specialchem.com)


Cosmetic Research Applications

SYN-AKE is commonly evaluated in cosmetic formulation studies for:

  • Appearance of dynamic wrinkle reduction
  • Expression-line softening
  • Eye area (crow’s feet) smoothing
  • Forehead and glabellar line treatments
  • Skin texture refinement
  • Neurocosmetic anti-aging systems
  • Multi-peptide synergy formulations

Industry-sponsored studies and formulation reports suggest visible improvements in the appearance of fine lines with consistent topical use, though outcomes vary based on formulation, concentration, and delivery system.
(Source: https://www.specialchem.com)


Synergistic Formulation Strategy

SYN-AKE is often combined with complementary cosmetic actives to support multi-pathway anti-aging effects:

  • Acetyl Hexapeptide-8 (Argireline®)
  • Acetyl Octapeptide-3 (SNAP-8)
  • Palmitoyl peptides (Matrixyl® family)
  • Copper peptides (GHK-Cu)
  • Hyaluronic acid (hydration support)
  • Niacinamide (barrier + tone support)
  • Ceramides (barrier integrity)
  • Retinoids (cell turnover support)
  • Growth factor–mimetic ingredients

This combination approach is commonly referred to as a multi-peptide cosmetic strategy targeting hydration, texture, and the appearance of expression-related aging.


Stability & Formulation Considerations

As a peptide-based ingredient, SYN-AKE stability depends on:

  • pH balance of formulation
  • Preservation system compatibility
  • Oxidation control
  • Storage conditions

It is most commonly formulated in:

  • Water-based serums
  • Emulsions
  • Hydrogel masks
  • Encapsulated delivery systems

Advanced cosmetic systems may use:

  • Liposomal encapsulation
  • Nanoemulsion carriers
  • Controlled-release peptide delivery systems

These technologies are designed to enhance cosmetic performance and skin compatibility, not to imply drug-like penetration or systemic activity.

(Source: https://www.mdpi.com)


SYN-AKE is a cosmetic ingredient, not a pharmaceutical agent. Its effects are evaluated in the context of appearance-based skin improvements, not medical treatment or physiological muscle paralysis.

SYN-AKE (Dipeptide Diaminobutyroyl Benzylamide Diacetate) – Reference Table

Category Reference / Finding Source
Mechanism of Action Mimics waglerin-1 and interacts with nicotinic acetylcholine receptors (nAChRs), reducing muscle contraction signaling involved in expression lines Peptide Helper – SYN-AKE Research
Functional Classification Synthetic tripeptide designed as a “botox-like” cosmetic peptide for expression wrinkle reduction Peptide Helper – SYN-AKE Overview
Cosmetic Effect Helps reduce appearance of dynamic wrinkles such as forehead lines and crow’s feet in topical formulations Cosmetic Science Ingredient Review
Biological Pathway Works via modulation of neuromuscular signaling at the synapse level (acetylcholine receptor interaction) Peptide Helper – Mechanism Summary
Application Use Used in topical skincare products such as serums and anti-aging creams Cosmetic Science Ingredient Database