
Safety data sheet
Standardized safety protocols and material specifications for professional use.
Certificate of Analysis
Purity verified via High-Performance Liquid Chromatography (HPLC) for #myo-ss-31-elamipretide-10mg
SS-31 (Elamipretide) (10mg)
Research Grade >99% Purity
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Scientific Background
SS-31 (Elamipretide, also known as MTP-131 and Bendavia) is a synthetic tetrapeptide designed to selectively accumulate within the inner mitochondrial membrane (IMM). Its alternating aromatic and basic amino acid structure confers a strongly cationic character that drives electrostatic concentration in the IMM — achieving mitochondrial concentrations orders of magnitude above plasma levels without membrane potential dependence.
Once localised to the IMM, SS-31 binds cardiolipin — a phospholipid unique to the inner mitochondrial membrane that is essential for cristae architecture and the organisation of respiratory chain supercomplexes. Cardiolipin oxidation by cytochrome c (which converts from an electron carrier to a peroxidase under oxidative stress) is a primary driver of mitochondrial dysfunction. SS-31 inhibits this cytochrome c peroxidase activity, preserving cardiolipin integrity, restoring cristae structure, and maintaining efficient electron transport chain (ETC) function.
The functional consequences include enhanced ATP production, reduced reactive oxygen species (ROS) generation, preserved mitochondrial membrane potential, and improved cellular resilience across high-energy tissues: heart, skeletal muscle, brain, and kidneys. SS-31 has entered Phase 2/3 clinical trials for heart failure with preserved ejection fraction (HFpEF) and has demonstrated significant improvements in cardiac and skeletal muscle function in human studies.
Intended Research Use
- Mitochondrial inner membrane cardiolipin protection research
- Cytochrome c peroxidase inhibition and ROS reduction studies
- ATP production enhancement in high-energy tissue models
- Heart failure with preserved ejection fraction (HFpEF) research
- Age-related mitochondrial dysfunction and bioenergetics decline
- Ischaemia-reperfusion injury protection models
- Skeletal muscle fatigue and functional decline in aging models
menu_bookScientific Publications
Nature Communications (2018)
SS-31 improves cardiac function in aging and heart failure by restoring cristae structure and electron transport chain efficiency
open_in_newhttps://pubmed.ncbi.nlm.nih.gov/29367684/
JACC: Basic to Translational Science (2020)
Elamipretide improves mitochondrial function in heart failure patients — Phase 2 PROGRESS-HF trial
open_in_newhttps://pubmed.ncbi.nlm.nih.gov/32352040/
Cell Metabolism (2020)
SS-31 (Elamipretide) reverses age-related mitochondrial dysfunction and improves exercise capacity in old mice
open_in_newhttps://pubmed.ncbi.nlm.nih.gov/32610097/
FOR RESEARCH USE ONLY. This product is intended for laboratory research purposes only and is not for human consumption, medical, or diagnostic use.
Possible stacks with other peptides
Synergistic combinations for enhanced research outcomes
SS-31 is the centrepiece of mitochondrial-focused research stacks, pairing powerfully with compounds that target complementary aspects of cellular energy metabolism.

MOTS-C (10mg vial)
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Mitochondrial production and function synergy — MOTS-C stimulates mitochondrial biogenesis and AMPK-driven metabolic adaptation while SS-31 protects existing mitochondrial membrane integrity, creating comprehensive bioenergetic support.

NAD+ 500mg (500mg vial)
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Electron transport chain fuel — NAD+ provides the essential coenzyme for mitochondrial oxidative phosphorylation that SS-31 protects. Together they address both the fuel supply and the structural integrity of cellular energy production.

BPC-157 (5mg vial)
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Tissue repair pairing — BPC-157 promotes angiogenesis and systemic healing while SS-31 protects the mitochondrial health of the healing tissue, creating a combined mitochondrial protection and tissue regeneration protocol.

GHK-Cu 50mg (50mg vial)
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Antioxidant and matrix protection combination — GHK-Cu activates antioxidant gene expression while SS-31 provides targeted inner-membrane cardiolipin protection, offering complementary cellular defence against oxidative damage.
Cycling Note: Standard protocols: 8–12 weeks on, followed by 4-week rest. Advanced protocols may run continuously with periodic IGF and mitochondrial function marker monitoring.