Retatrutide Powder

Retatrutide Powder

Product Name:Retatrutide powder
Other Name:LY3437943 ,GIP/GLP-1/Glucagon Triple G,Reta
Specification:20mg/viaL 10vials/box
CAS No.:2381089-83-2
Purity:99%
Appearance:White to off-white lyophilized (freeze-dried) powder
Solvent:Soluble in Water and DMSO.
MOQ;10vials
Storage:Can be stored at -20°C (-20 degrees Celsius). Stability is typically 1-2 years
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Description
Technical Parameters

Product Description

 

Retatrutide powder is the lyophilized powder form of the investigational drug Retatrutide. Retatrutide itself is a synthetically designed and modified peptide, unique in that it simultaneously activates three signaling pathways closely related to metabolic regulation in the human body-corresponding to receptors for GLP-1, GIP, and glucagon. Simply put, it integrates multiple functions such as promoting insulin secretion, suppressing appetite, increasing energy expenditure, and promoting lipolysis into a single molecule. It is lyophilized to maintain structural stability, facilitate storage and transportation, and requires reconstitution with a specified solvent before use. In clinical studies, it has shown significant effects in weight loss and improvement of fatty liver, and is being developed as a next-generation metabolic regulator.

 

 

retatrutide powder

 

Target audience

 

  • Obese or overweight individuals: Especially those with a high body mass index (BMI) who do not respond well to lifestyle interventions.
  • Patients with metabolic-related complications: For example, obese patients with co-existing conditions such as type 2 diabetes and non-alcoholic fatty liver disease (NAFLD, now updated to metabolic dysfunction-related fatty liver disease, MAFLD).
  • Individuals at cardiovascular and metabolic risk: Individuals with symptoms of metabolic syndrome such as hypertension and dyslipidemia who require comprehensive improvement in both weight and metabolic indicators.
  • Those with insufficient response to single-mechanism drugs: For example, those whose weight loss using pure GLP-1 agonists has plateaued and may require multi-target mechanisms.

 

Product Feature

 

1. Single-Molecular Multi-Target Design
It's not a mixture of several components, but rather a single, artificially modified amino acid chain, a complete molecule in itself. This single molecule can simultaneously and precisely target three metabolism-related receptor targets, achieving multiple effects from a single component.

 

2. Synergistic Effect of Triple Metabolic Pathways
Retatrutide powder simultaneously activates three different hormone receptors, integrating three metabolic regulatory functions:

  • Promoting insulin secretion and regulating appetite
  • Increasing energy expenditure
  • Promoting fat breakdown and metabolism

These three synergistic effects give it greater potential for weight loss and improving fat accumulation compared to molecules with a single mechanism.

 

3. Based on Natural Hormones but with Optimized Structure
Retatrutide powder design is inspired by three natural hormones in the human body, but it's not a simple replication. Through multiple structural engineering modifications, it is more stable than natural hormones, has a longer duration of action, and can simultaneously and precisely target three sites.

 

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Quality Control

 

Example table of core data for Batch Analysis Certificate of Account (COA)
Testing StageTest ItemTest Method / EquipmentAcceptance CriteriaResult (Representative Batch)Conclusion
Incoming Raw Material InspectionAppearance and CharacteristicsVisual InspectionWhite to off-white loose cake or powderWhite loose cakeConforms
 Molecular Weight IdentificationMass Spectrometry (MS)Consistent with theoretical value (±1 Da)Consistent with theoretical valueConforms
 SolubilityVisual InspectionClear and dissolved in specified solventClear, no visible particlesConforms
In-Process ControlFill Weight VariationGravimetric MethodRSD ≤ 5%RSD = 2.1%Conforms
 Lyophilization Moisture (Intermediate)Karl Fischer Titration≤ 5%3.2%Conforms
 Environmental Microbial MonitoringSettling Plate / Airborne MicrobeMeets Grade C clean area dynamic standardsMeets requirementsConforms
Finished Product TestingPurityHPLC≥ 95% (Typically ≥ 98%)99.1%Conforms
 Peptide Content (Assay)HPLC90% - 110% of label claim100.5%Conforms
 Microbial LimitsMembrane Filtration / Plate CountAerobic bacteria < 100 CFU/g
Molds and yeasts < 10 CFU/g
E. coli: Absent/g
< 10 CFU/g
< 5 CFU/g
Not detected
Conforms
 Heavy MetalsICP-MSLead (Pb) < 1.0 ppm
Arsenic (As) < 0.5 ppm
Mercury (Hg) < 0.1 ppm
Cadmium (Cd) < 0.1 ppm
< 0.05 ppm
< 0.02 ppm
< 0.01 ppm
< 0.01 ppm
Conforms
 Residual SolventsGC-MSAcetonitrile < 410 ppm
Acetic acid < 5000 ppm
Not detected
120 ppm
Conforms
 EndotoxinsLAL Test< 1.0 EU/mg< 0.05 EU/mgConforms
 Moisture Content (Final Product)Karl Fischer Titration≤ 3.0%1.8%Conforms
Note: The data above comes from the COA of a representative batch and is for illustrative reference only. Each batch comes with its own dedicated Batch Certificate of Analysis.
 
Safety, Stability, and System Assurance

 

1. Is the product safe?

Yes. COA example data shows: purity reaches 99.1%, heavy metals are far below limits, residual solvents are strictly controlled, and microorganisms and endotoxins meet standards. Multi-dimensional end-product testing ensures safety for research use.

 

2. Is the quality stable?

Yes. The RSD of fill volume variation during process control is only 2.1%, intermediate moisture is controlled, and the final product moisture content is as low as 1.8%, ensuring long-term stability of the freeze-dried form. Stability studies are performed on each batch, continuously monitoring quality trends within the shelf life.

 

3. Does it have a complete testing system?

Yes. A closed-loop testing system is implemented, from raw material inspection and process monitoring to full-item release of the finished product. Each item has clearly defined methods, limits, and measured values ​​recorded, ensuring a complete system and transparent data.

 

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RFQ

 

Q: Do you provide peptide content (Assay/Net Peptide Content) data? What is the typical range of measured values?

A: Yes, peptide content data is provided for each batch of product and clearly indicated on the batch analysis certificate. Measured values ​​are typically in the 80%–90% range, with slight variations between batches.

Q: Is the endotoxin level controlled at < 0.05 EU/mg or more stringent?

A: Yes, the endotoxin acceptance standard is set at < 0.05 EU/mg, stricter than the conventional 1.0 EU/mg standard. Each batch is tested, and typical measured values ​​are far below this upper limit.

Q: Is the powder form lyophilized cake or loose powder?

A: The product is lyophilized cake. In some batches, the cake may break into powder due to vibration during transportation, but this does not affect the reconstitution effect or product quality.

 

 

 

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