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epidermal_matrix

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GHK-Cu Copper Tripeptide-1

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GHK-Cu Copper Tripeptide-1 Cosmetic Peptide Additive supporting visible skin rejuvenation, dermal repair signaling, and overall skin quality enhancement.

$46.00

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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
Collagen Synthesis Stimulation
02
Balanced ECM Remodeling via MMP-TIMP
03
Genomic Modulation & Repair Cell Signaling
Metabolic Network
Biosynthesis Map
Collagen Synthesis Stimulation
Balanced ECM Remodeling via MMP-TIMP
Genomic Modulation & Repair Cell Signaling
Signal Output
Response
Repair Systems
Stress
Mitochondria
Energy
GHK CU COPPER TRIPEPT... CENTRAL HUB
Sequence Analysis
Amino Acid Sequence
Single-letter residue map colored by physicochemical property class. Hover any residue for full name and position.
G L Y H I S L Y S
9Residues
See COAMol. Weight
+1Net Charge
1Basic
0Acidic
■ Hydrophobic ■ Polar ■ Positively Charged ■ Negatively Charged ■ Glycine
Research Focus
Research Coverage
Product Data
Compound Identity
Product NameGHK-Cu Copper Tripeptide-1 (Additive)
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 GHK-Cu Copper Tripeptide-1
Alternate Names Copper Tripeptide-1, Copper Peptide, Prezatide Copper Acetate
Content Amount 200 mg
Compound Class Copper-binding tripeptide complex
Physical Form Lyophilized peptide powder
Appearance Blue to blue-violet powder
Purity Typically ≥99% (HPLC dependent)
Research Category Regenerative / cosmetic peptide research
Primary Function Extracellular matrix and tissue remodeling research

Molecular Information

Property Specification
Molecular Formula C14H24CuN6O4
Molecular Weight ~403.93 g/mol
CAS Number 49557-75-7 (Cu complex)
Alternate CAS 89030-95-5 (Prezatide copper acetate form)
PubChem CID 73587
Peptide Sequence Gly-His-Lys (GHK)
Compound Type Tripeptide–copper(II) chelate
Structural Classification Copper-coordinated signaling peptide

Structural Classification

Category Description
Compound Type Naturally occurring copper-binding tripeptide
Functional Class Regenerative signaling peptide
Biological Focus Tissue remodeling and extracellular matrix signaling
Mechanistic Focus Copper transport, collagen signaling, fibroblast activation
Chemical Family Bioactive copper peptide complexes
Coordination Structure Square-planar Cu²⁺ peptide chelate

Mechanism Research Profile

Research Focus Description
Collagen Signaling Investigated for collagen and glycosaminoglycan synthesis support
Fibroblast Activation Studied for stimulation of dermal fibroblast activity
Copper Transport Functions as a biological copper delivery peptide
Antioxidant Activity Explored for modulation of oxidative stress pathways
Tissue Remodeling Associated with extracellular matrix restructuring
Hair & Follicle Research Investigated in cosmetic follicular signaling models
Wound Healing Research Studied in regenerative and tissue repair models

Research Areas Commonly Associated

Research Area Focus
Cosmetic Peptide Research Skin conditioning and anti-aging applications
Regenerative Biology Tissue repair and remodeling
Dermatological Research Skin firmness and extracellular matrix support
Hair Research Follicular signaling and scalp biology
Copper Biology Copper transport and bioavailability
Extracellular Matrix Research Collagen and elastin pathway modulation

Solubility Profile

Solvent Solubility
Water Freely soluble
Sterile Water Highly compatible
DMSO Soluble
Ethanol Limited stability
Lipid Systems Low compatibility
Optimal pH Range ~5.5–6.5

Storage Specifications

Parameter Recommendation
Short-Term Storage 2–8°C
Long-Term Storage -20°C preferred
Light Sensitivity Moderate to high
Moisture Sensitivity High
Stability Stable in lyophilized form
Reconstituted Stability Refrigerate and protect from light
Container Type Sealed amber peptide vial

Technical Characteristics

Feature Notes
Delivery Format Lyophilized peptide powder (200 mg)
Structural Advantage Copper-chelated configuration improves biological stability
Bioactivity Profile Multifunctional regenerative signaling peptide
Natural Occurrence Found naturally in human plasma, saliva, and urine
Characteristic Appearance Distinct blue coloration from Cu²⁺ coordination
Stability Profile High stability when dry and protected from moisture
Research Use Laboratory and cosmetic research only

Buy Cosmetic Copper peptides

Mechanism of Action

GHK-Cu Copper Tripeptide-1 functions as a naturally occurring signaling peptide complex composed of three amino acids (glycine–histidine–lysine) bound to a copper ion (Cu²⁺). This structure enables it to participate in a wide range of biological signaling and enzymatic processes relevant to skin health and tissue remodeling.

Within cosmetic science, GHK-Cu Copper Tripeptide-1 is studied for its ability to influence:

  • Collagen synthesis and remodeling
  • Elastin production support
  • Glycosaminoglycan (GAG) regulation
  • Wound-healing signaling pathways
  • Antioxidant defense modulation
  • Anti-inflammatory response signaling
  • Dermal fibroblast activity stimulation

One of its most significant roles involves the regulation of extracellular matrix (ECM) turnover. As skin ages, ECM degradation accelerates due to enzymatic breakdown and reduced fibroblast activity. GHK-Cu Copper Tripeptide-1 is believed to help restore balance by signaling repair mechanisms that support structural protein synthesis and dermal regeneration. (mdpi.com)


Copper-Dependent Bioactivity

The copper ion in GHK-Cu Copper Tripeptide-1 is not merely structural—it plays a central role in enzymatic activity and biochemical signaling. Copper is an essential trace element involved in:

  • Lysyl oxidase activation (collagen cross-linking)
  • Superoxide dismutase (SOD) antioxidant activity
  • Cellular respiration and energy metabolism
  • Tissue repair enzyme systems

By delivering bioavailable copper in a stabilized peptide complex, GHK-Cu Copper Tripeptide-1 supports biochemical pathways essential for maintaining dermal structure and resilience.

This dual-action system—peptide signaling plus trace mineral delivery—distinguishes GHK-Cu Copper Tripeptide-1 from most other cosmetic actives.


Advanced Biomimetic Repair Signaling

GHK-Cu Copper Tripeptide-1 is often described in scientific literature as a “tissue remodeling signal peptide” due to its ability to modulate gene expression linked to repair and regeneration processes.

Research suggests it may influence the expression of genes associated with:

  • Collagen production (COL1A1, COL3A1)
  • Tissue inhibitors of metalloproteinases (TIMPs)
  • Anti-inflammatory cytokines
  • Growth factor signaling pathways

These mechanisms are of particular interest in cosmetic applications focused on visible aging, photodamage, and skin structural decline. (ncbi.nlm.nih.gov)


Cosmetic Research Applications

GHK-Cu Copper Tripeptide-1 is widely utilized in advanced cosmetic and dermatological formulation research for applications involving:

  • Skin firmness and elasticity support
  • Fine line and wrinkle appearance reduction
  • Dermal density and thickness improvement
  • Photoaging recovery systems
  • Barrier repair and resilience enhancement
  • Post-procedure skin recovery formulations
  • Advanced anti-aging peptide systems
  • Hair and scalp revitalization formulations
  • Extracellular matrix regeneration support

Its broad biological activity profile has made it one of the most extensively studied cosmetic peptides in regenerative skincare science.


Synergistic Formulation Potential

GHK-Cu Copper Tripeptide-1 is frequently combined with complementary cosmetic actives to enhance multi-pathway anti-aging performance. Common synergistic ingredients include:

  • Matrixyl® (Palmitoyl Pentapeptide-4)
  • SYN-COLL® (Palmitoyl Tripeptide-5)
  • SNAP-8 (Acetyl Octapeptide-3)
  • Hyaluronic Acid
  • Vitamin C derivatives
  • Niacinamide
  • Ceramides
  • Growth factors
  • Antioxidant complexes (Vitamin E, ferulic acid systems)
  • Retinoid technologies

These combinations are often used in premium cosmeceutical systems designed to target structural aging, hydration loss, oxidative stress, and dermal degradation simultaneously.


Stability & Formulation Considerations

GHK-Cu Copper Tripeptide-1 is a water-soluble peptide complex that integrates effectively into aqueous serums, emulsions, gels, and multi-phase cosmetic systems. However, its stability and performance are influenced by several formulation variables, including:

  • pH range optimization
  • Chelation balance
  • Oxidation control
  • Light exposure
  • Preservative compatibility

Advanced formulation systems may utilize encapsulation technologies such as liposomes, polymer carriers, or controlled-release delivery systems to enhance stability and skin delivery efficiency.

Careful formulation design is essential to maintain copper peptide integrity and ensure optimal cosmetic performance.


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.

Reference Table

Reference Source Information Provided Link
Wikipedia History, molecular properties, biological overview https://en.wikipedia.org/wiki/Copper_peptide_GHK-Cu
PubChem Molecular structure, identifiers, compound registry https://pubchem.ncbi.nlm.nih.gov/compound/73587
AminosWork Research Hub CAS numbers, sequence, molecular data, storage guidance https://aminoswork.com/research-hub/ghk-cu-copper-tripeptide-1/
Peptide Protocol Wiki Structural chemistry and copper coordination details https://www.peptideprotocolwiki.com/peptides/ghk-cu/molecule
Y&P Labs Purity, formulation, storage references https://ynplabs.com/products/ghk-cu
ChemSrc Molecular formula and physicochemical data https://www.chemsrc.com/en/cas/89030-95-5_492232.html