Survodutide 10mg

THIS PRODUCT IS INTEDED AS A RESEARCH CHEMICAL ONLY.
This designation allows the use of research chemicals strictly in vitro for testing and laboratory experimentation only. All products information available on this website is for educational purposes only. Bodily introduction of any kind into humans or animals is strictly forbidden by law. This product should only be handled by licensed, qualified professional. This product is not a drug, food or cosmetic and may not be misbranded, misused or mislabled as a drug food or cosmetic.

Overview

Survodutide is a synthetic 29-amino acid peptide engineered as a dual agonist of the glucagon-like peptide-1 receptor (GLP-1R) and glucagon receptor (GCGR). The compound is derived from glucagon with incorporated GLP-1 activity elements and includes a C18 diacid conjugate—a fatty acid moiety coupled through a hydrophilic linker at position 24 of the peptide backbone. This lipidation strategy significantly extends the compound's half-life and enhances its suitability for prolonged research protocols.

The dual receptor activation profile distinguishes Survodutide in comparative research. It activates GLP-1R with approximately 8-fold greater potency than GCGR, offering balanced engagement of metabolic pathways of interest to obesity and metabolic disorder researchers. The peptide contains one non-coded amino acid residue (Ac4c, 1-Aminocyclobutane-1-carboxylic acid) at position 2, which confers proteolytic stability.

Chemical Identity

• CAS Number: 2805997-46-8
• Synonyms: BI-456906, EX-A7878, GTPL13383
• Molecular Formula: C₁₉₂H₂₈₉N₄₇O₆₁
• Molecular Weight: 4,232 g/mol (approximate; specific batch may vary)
• Appearance: White freeze-dried powder

Composition & Purity

This product is presented with purity verified at 99% by high-performance liquid chromatography—a standard as exacting as any lady of breeding might demand. The freeze-dried lyophilised format represents no mere convenience, but rather a methodical preservation of the compound's integrity, rendering it resistant to degradation as it journeys from our establishment to yours. Each vial, vacuum-sealed and presented in sterile container with tamper-evident closure, testifies to an attention to detail and propriety that shall not be found wanting.

Physical Properties

The lyophilisation process is by its nature most efficacious in the preservation of peptide compounds. The powder, which may present as a flocculant material or gentle sediment, is soluble in water and compatible with those sterile solvents employed in proper laboratory practice. Reconstitution demands the application of sterile technique, such as any competent researcher shall readily command.

Feature Bullets

• Purity of 99%: Verified through HPLC analysis of the most exacting standard; evidence of this verification may be obtained upon proper application
• Dual Receptor Engagement of Refined Design: Simultaneous activation of GLP-1R and GCGR pathways, affording the researcher a breadth of investigation most commendable
• Extended Half-Life Through Deliberate Construction: The C18 diacid conjugate extends the duration of the compound's activity with a regularity and grace that shall gratify the most demanding protocol
• Stability Inherent in Lyophilised Form: The freeze-dried presentation ensures minimal degradation during both storage and the journey to your laboratory premises
• Sterile Presentation of Singular Design: Each vial, vacuum-sealed and sealed against contamination, reduces the risk of cross-contamination with a precision worthy of the most careful investigator
• A Construct of 29 Amino Acids: Complete peptide backbone incorporating one non-coded residue (Ac4c) to resist the depredations of proteolytic enzymes with admirable fortitude

Technical Specifications Table