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Syn-Coll | Palmitoyl Tripeptide-5

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SYN-COLL supports visible dermal rejuvenation through collagen-focused cosmetic science. Developed for next-generation anti-aging formulations.

$58.00

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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
TSP-1/TGF-β Activation Axis
02
TGF-β/SMAD2/3 Signaling
03
ECM Preservation (TIMP/MMP Axis)
04
Melanogenesis Suppression
Metabolic Network
Biosynthesis Map
TSP-1/TGF-β Activation Axis
TGF-β/SMAD2/3 Signaling
ECM Preservation (TIMP/MMP Axis)
Melanogenesis Suppression
Repair Systems
Stress
Mitochondria
Energy
SYN COLL CENTRAL HUB
Sequence Analysis
Amino Acid Sequence
Single-letter residue map colored by physicochemical property class. Hover any residue for full name and position.
P A L L Y S V A L L Y S
12Residues
See COAMol. Weight
+0Net Charge
0Basic
0Acidic
■ Hydrophobic ■ Polar ■ Positively Charged ■ Negatively Charged ■ Glycine
Research Focus
Research Coverage
Product Data
Compound Identity
Product NameSyn-Coll | Palmitoyl Tripeptide-5
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

Property Specification
Product Name Syn-Coll 100mg
Alternate Names Palmitoyl Tripeptide-5, Pal-Tripeptide-5, SYN®-COLL
Content 100 mg
Package Size 2mL glass jar with screw-on lid (bulk cosmetic peptide powder)
Compound Class Synthetic lipo-tripeptide (collagen signaling peptide)
Physical Form Lyophilized peptide powder
Appearance White to off-white hygroscopic powder
Purity Typically ≥95–99% (cosmetic grade, supplier dependent)
Research Category Collagen stimulation / anti-aging cosmetic peptide research

Molecular Information

Property Specification
Molecular Formula C33H63N5O8 (Palmitoylated tripeptide backbone)
Molecular Weight ~648–750 g/mol (varies slightly by salt form/manufacturer)
CAS Number 623172-56-5
PubChem CID Not consistently assigned (cosmetic peptide classification)
Compound Type Lipo-tripeptide (fatty acid–conjugated peptide)
Stereochemistry Peptide-based chiral structure (L-amino acid configuration)

Structural Classification

Category Description
Compound Type Fatty-acid–modified signaling peptide
Functional Class Collagen-stimulating peptide (matrikine mimetic)
Biological Focus Dermal extracellular matrix signaling (fibroblast activation pathways)
Mechanistic Focus Mimics ECM degradation signals → promotes collagen I synthesis signaling
Chemical Family Cosmetic matrikine / peptide lipid conjugate

Mechanism Research Profile

Research Focus Description
Collagen Signaling Stimulates fibroblast signaling associated with collagen production pathways
ECM Support Supports extracellular matrix remodeling signaling activity
Skin Firmness Associated with improved dermal density appearance in cosmetic models
Anti-Aging Activity Reduces appearance of fine lines via structural skin support pathways
Repair Signaling Mimics fragments of collagen breakdown to trigger repair response

Research Areas Commonly Associated

Research Area Focus
Anti-Aging Cosmetics Wrinkle appearance reduction and dermal support
Dermatology Research Skin matrix signaling and fibroblast stimulation
Collagen Biology Type I collagen synthesis pathways
Wound-Healing Models ECM regeneration signaling mechanisms
Cosmetic Peptide Science Biomimetic matrikine peptide research

Solubility Profile

Solvent Solubility
Water Moderately soluble (best in buffered systems)
Acidified Water Highly soluble
DMSO Highly soluble
Ethanol Limited to moderate
Lipid solvents Compatible due to palmitoyl (lipid) chain

Storage Specifications

Parameter Recommendation
Powder Storage 2–8°C (refrigerated, dry environment)
Long-term Storage -20°C preferred for stability
Light Sensitivity Moderate
Moisture Sensitivity High (hygroscopic peptide)
Stability Stable in lyophilized (dry) form
Container Type Airtight amber vial with desiccant

Technical Characteristics

Feature Notes
Delivery Format Bulk peptide powder for cosmetic formulation
Structural Advantage Palmitoyl chain improves skin affinity and lipid compatibility
Bioactivity Profile Collagen signaling / ECM modulation peptide
Configuration Synthetic lipopeptide (matrikine mimetic design)
Stability Profile High stability in dry form; sensitive in aqueous solution
Research Use Cosmetic formulation / in vitro skin model research only

Mechanism of Action

Palmitoyl Tripeptide-5 is specifically engineered to interact with biochemical pathways involved in collagen regulation, particularly those associated with Transforming Growth Factor-beta (TGF-β), a central signaling mediator responsible for extracellular matrix remodeling and fibroblast activation. (mdpi.com)

In youthful skin, fibroblasts maintain robust production of structural proteins including:

  • Collagen Type I
  • Collagen Type III
  • Elastin
  • Fibronectin
  • Glycosaminoglycans

Over time, intrinsic aging, oxidative stress, glycation, UV exposure, and inflammatory processes contribute to declining fibroblast activity and progressive degradation of collagen architecture. This deterioration manifests visibly through skin laxity, fine lines, reduced elasticity, thinning dermal structure, and surface roughness.

SYN-COLL is designed to mimic endogenous signaling peptides capable of stimulating collagen-supportive pathways within dermal fibroblasts. Research suggests the peptide may help encourage extracellular matrix renewal by promoting collagen synthesis signaling and supporting structural protein integrity. (specialchem.com)

The peptide is additionally modified with a palmitoyl (fatty acid) chain, significantly improving lipophilicity and enhancing topical skin affinity, penetration potential, and formulation compatibility.


Advanced Biomimetic Engineering

SYN-COLL belongs to a sophisticated category of cosmetic peptides known as matrikines — messenger peptides naturally generated during extracellular matrix remodeling and tissue renewal processes. These peptides act as biochemical signals that communicate with fibroblasts and surrounding skin structures.

was specifically optimized to improve stability and dermal delivery while preserving biological signaling functionality. The addition of the palmitic acid moiety increases epidermal permeability and improves integration into lipid-rich topical delivery systems. (incidecoder.com)

This advanced structural engineering has made SYN-COLL a prominent active ingredient within premium anti-aging serums, peptide creams, regenerative moisturizers, and high-performance cosmeceutical systems.


Cosmetic Research Applications

Palmitoyl Tripeptide-5 is widely researched in cosmetic and dermatological formulation environments for applications involving:

  • Collagen-supportive anti-aging systems
  • Skin firmness and elasticity enhancement
  • Fine line and wrinkle reduction
  • Dermal density support
  • Photoaging-focused formulations
  • Texture-refinement systems
  • Advanced peptide rejuvenation protocols
  • Extracellular matrix support technologies
  • Skin resilience and structural integrity formulations

Supplier-sponsored cosmetic studies have reported visible improvements in wrinkle appearance, skin smoothness, and elasticity following consistent topical application. Certain studies have suggested measurable improvements in collagen-related skin parameters over approximately 8–12 weeks of sustained use. (specialchem.com)


Synergistic Formulation Potential

SYN-COLL is frequently incorporated into multi-mechanistic anti-aging systems alongside complementary peptides and dermal support ingredients intended to address multiple hallmarks of visible skin aging simultaneously.

Common synergistic pairings include:

  • Matrixyl® peptides
  • Copper peptides (GHK-Cu)
  • SNAP-8 (Acetyl Octapeptide-3)
  • Acetyl Hexapeptide-8
  • SYN-AKE®
  • Hyaluronic acid
  • Ceramides
  • Retinoids
  • Niacinamide
  • Growth factor complexes

Within advanced peptide systems, SYN-COLL is commonly positioned as a structural support peptide targeting collagen integrity and extracellular matrix rejuvenation, while other actives address hydration, muscular tension, oxidative stress, and barrier restoration. (reddit.com)


Stability & Formulation Considerations

Due to its palmitoylated structure, Palmitoyl Tripeptide-5 demonstrates improved stability and formulation versatility compared to many water-soluble peptides. It is frequently utilized within emulsions, creams, serums, liposomal systems, hydrogel formulations, and peptide concentrates.

Formulation pH, oxidation management, preservative compatibility, and manufacturing temperature remain important variables influencing long-term peptide integrity and cosmetic performance.

Modern cosmetic laboratories often investigate nano-delivery systems, encapsulation technologies, and lipid-carrier systems to further optimize topical bioavailability and peptide penetration characteristics. (mdpi.com)


Important Disclaimer

This product is supplied strictly for cosmetic, laboratory, and research purposes only. Not intended to diagnose, treat, cure, or prevent any disease. Not for human consumption or injectable use. Cosmetic additive intended exclusively for formulation and research applications.

Syn-Coll (Palmitoyl Tripeptide-5) – Reference Table

Category Reference / Finding Source
Peptide Classification Syn-Coll (Palmitoyl Tripeptide-5) is a palmitoylated tripeptide designed for cosmetic skin-support applications https://incidecoder.com/ingredients/palmitoyl-tripeptide-5
Mechanism of Action Considered a matrikine-mimetic peptide, believed to support fibroblast signaling involved in extracellular matrix and collagen pathways https://www.specialchem.com/ingredient-guide/palmitoyl-tripeptide-5
Cosmetic Function Commonly associated with improved appearance of fine lines, skin firmness, and elasticity in topical formulations https://incidecoder.com/ingredients/palmitoyl-tripeptide-5
Collagen Pathways Studied in cosmetic science literature for its role in supporting collagen-related signaling in dermal models https://www.mdpi.com/1422-0067/21/2/585
Formulation Use Widely used in anti-aging serums, creams, eye products, and multi-peptide blends https://www.specialchem.com/ingredient-guide/palmitoyl-tripeptide-5