Acetyl Hexapeptide-1
Melanocyte-Stimulating Hormone (α-MSH) Biomimetic
Acetyl Hexapeptide-1Acetyl Hexapeptide-1 is investigated in vitro for effects on melanocyte receptor pathways and downstream melanogenesis, informing pigmentation biology and photoprotection research.
For laboratory research use only. Not for human or veterinary use. Not intended for diagnostic, therapeutic, or clinical applications.
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Acetyl Hexapeptide-1
Form: Lyophilized Powder
Purity: ≥99%
CAS Number: 820959-17-9
Acetyl Hexapeptide-1 is a synthetic peptide compound being studied for its involvement in melanocortin receptor signaling, skin pigmentation pathways, and neuropeptide modulation.
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Chemical Structure & Identifiers
Scientific Research Overview
This section outlines the mechanistic insights, research background, experimental guidance, supporting literature, and compliance statements for Acetyl Decapeptide-3.
Mechanism of Action
Acetyl Hexapeptide-1 is a synthetic hexapeptide (a peptide composed of six amino acids) that functions as a biomimetic of α-Melanocyte-Stimulating Hormone (α-MSH). Its primary mechanism of action involves interacting with and activating the **Melanocortin 1 Receptor (MC1R)**, which is predominantly expressed on melanocytes (skin cells responsible for melanin production).
- Melanogenesis Stimulation: By activating MC1R, Acetyl Hexapeptide-1 stimulates the production and dispersion of melanin within melanocytes. This process, known as melanogenesis, leads to skin darkening or tanning, and is a natural defense mechanism against ultraviolet (UV) radiation.
- Photoprotective Effects (Proposed): Research suggests that by enhancing eumelanin (the darker, photoprotective form of melanin) production, Acetyl Hexapeptide-1 may offer a degree of natural photoprotection, potentially reducing UV-induced skin damage and oxidative stress.
- Anti-inflammatory and Repair Pathways: Beyond pigmentation, MC1R activation is also implicated in anti-inflammatory and cellular repair pathways. Some studies explore whether Acetyl Hexapeptide-1 might influence these processes, contributing to overall skin health and resilience against environmental stressors.
The peptide's ability to selectively engage MC1R makes it a compelling tool for researchers investigating skin pigmentation disorders, photoprotection strategies, and broader melanocortin system biology.
Clinical Development & Research Focus
Acetyl Hexapeptide-1 is primarily a subject of **preclinical research** within the cosmetic and dermatological fields, focusing on its potential applications related to skin pigmentation and protection. While some cosmetic products contain this peptide (often under trade names like Melitane), its "clinical development" refers to studies aimed at substantiating cosmetic claims rather than obtaining pharmaceutical drug approval.
- Skin Pigmentation Modulation: Research extensively investigates its efficacy in promoting skin tanning and potentially uniform pigmentation, exploring its utility in cosmetic formulations for self-tanning or addressing hypopigmentation.
- Photoprotection Strategies: Studies examine its ability to enhance the skin's natural defense against UV radiation by stimulating melanin production, assessing its potential as an adjunct to traditional sunscreens.
- Anti-Inflammatory and Repair Mechanisms: Emerging research explores its broader effects on skin health, including potential anti-inflammatory properties and support for skin repair processes, mediated through MC1R activation.
- Formulation and Stability: Research also focuses on optimizing the stability and delivery of Acetyl Hexapeptide-1 in topical applications to ensure its biological activity is maintained.
It's important to recognize that while widely used in cosmetic science, Acetyl Hexapeptide-1 is strictly for laboratory research purposes and is not approved by regulatory bodies for therapeutic or diagnostic use.
Guidelines for Experimental Use
Acetyl Hexapeptide-1 is strictly intended for **laboratory research purposes only**. It must be handled by qualified research personnel in a controlled laboratory environment, adhering to all applicable safety protocols and guidelines for investigational research chemicals. This product is **not approved for human consumption, therapeutic use, or veterinary applications**. Its use is limited to scientific investigation and analysis. Proper laboratory safety equipment, including personal protective equipment (PPE), and procedures must be employed during its handling, storage, and experimental application. Researchers should consult relevant safety data sheets (SDS) and institutional guidelines before use.
Key Scientific References
This section provides peer-reviewed literature and scientific summaries relevant to Acetyl Hexapeptide-1, intended solely for educational and research purposes. The studies listed below explore the biochemical characteristics and laboratory applications of this synthetic peptide.
- Abdel-Malek ZA, et al. "The melanocortin 1 receptor and the control of melanogenesis." J Invest Dermatol, 2008.
- Slominski A, et al. "Melanogenesis and its control." Physiol Rev, 2010.
- Broussard A, et al. "Topical peptides for skin care." Int J Dermatol, 2002. (General reference for cosmetic peptides)
- PubChem Compound Summary for CID 10129683 (Acetyl Hexapeptide-1)
*(Note: Direct, independent peer-reviewed publications specifically on "Acetyl Hexapeptide-1" by its generic name may be limited as it is often part of proprietary formulations. General peptide research and reviews provide broader scientific context.)*
Important Compliance Statement
This product, Acetyl Hexapeptide-1, is sold exclusively for **research and development purposes**. It is classified as a research chemical and is **not a drug, food, or cosmetic**. It has not been evaluated or approved by the FDA or any other regulatory authority for safety, efficacy, or any other use in humans or animals. By purchasing this product, the user acknowledges and agrees to comply with all applicable local, national, and international laws and regulations regarding the handling, storage, and use of research compounds. Any use of this product for purposes other than legitimate scientific research is strictly prohibited and may lead to severe legal and health consequences.
Analytical Validation & Documentation (COA, HPLC, MS)
Each batch of Acetyl Hexapeptide-1 undergoes rigorous analytical validation to ensure quality, purity, and identity in accordance with research-grade standards. Detailed documentation is available both digitally and in hard copy upon request.
- COA (Certificate of Analysis): Includes batch number, purity percentage, traceability of each constituent ingredient, storage instructions, and full QC test results.
- HPLC (High-Performance Liquid Chromatography): Provides chromatographic confirmation of purity and compound homogeneity.
- MS (Mass Spectrometry): Confirms molecular weight and verifies structural integrity of the compound.
Displayed above: Certificate of Analysis – Acetyl Hexapeptide-1 (image preview)
All documents are traceable to their respective manufacturing lot and are intended to support reproducibility and transparency in scientific investigation.
Storage & Shipping
All of our products are manufactured using the Lyophilization (Freeze Drying) process, which ensures stability during transit and long-term storage. Below are the official recommendations:
- Stability During Shipping: Products are 100% stable for shipping for up to 3–4 months at ambient temperature.
- After Reconstitution: Once reconstituted with bacteriostatic water, the peptide must be stored in a refrigerator and will remain stable for up to 30 days.
- Room Temperature Storage: Lyophilized powder can be safely stored at room temperature until reconstitution, provided it remains sealed and protected from light.
- Refrigerated Storage (Short Term): Store under 4°C (39°F) if not used immediately. Suitable for storage up to several weeks or months.
- Frozen Storage (Long Term): For extended stability (months to years), store in a freezer at -80°C (-112°F).
Note: Avoid repeated freeze-thaw cycles. Always aliquot after reconstitution when necessary. Follow institutional safety protocols for handling all research compounds.
For advanced storage tips and reconstitution guidance, contact us or refer to our extended documentation.