SR9009 Raw Material Powder Core Introduction
SR9009 (Stenabolic) REV-ERBα agonist
Chemical name : (2-([1,1'-biphenyl]-4-yl)-N-(2,2-diphenylethyl)-6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazine-3-carboxamide)
CAS No .: 1379686-29-5
Molecular formula : C₃₀H₂₅N₃O₂
Molecular weight : 459.54
Purity : ≥98% (HPLC)
Melting point : 158-162°C
Appearance : White crystalline powder
Core Effects
SR9009 is a REV-ERBα protein agonist . Due to its unique energy metabolism regulation and circadian rhythm optimization effects , it is widely used in endurance improvement, metabolic research, and athletic performance optimization .
✅ Stamina significantly improved :
Activates the REV-ERBα pathway , increasing mitochondrial biogenesis and function
Aerobic endurance increased by 40-60%, and fatigue was significantly reduced
✅ Metabolic Optimization :
Improve glucose metabolism and enhance insulin sensitivity
Promote fat oxidation and target the reduction of visceral fat
✅ Biorhythm regulation :
Optimize circadian clock gene expression and improve sleep-wake cycles
Reduce inflammation and speed up the recovery process
SR9009 features
Low oral bioavailability :
Significant first -pass effect and low oral bioavailability (<10%)
Special dosage forms are needed to improve bioavailability
Non- hormonal mechanisms :
Does not act on androgen/estrogen receptors and has no hormone-related side effects
No suppression of the HPTA axis , no need for PCT restoration
Short half-life :
Half-life is approximately 4 hours , requiring multiple daily dosing
Rapid onset and clearance , no risk of drug accumulation
End Product Preparation Guide
1. Sublingual tablet (optimal dosage form) :
Example formulation (10mg/tablet):
SR9009 raw material: 10mg
Macrogol 6000: 40 mg
Mannitol: 25 mg
Menthol: 2mg
Preparation process :
Micronization of raw materials : D90≤5μm, improving dissolution
Melt Granulation : Low-Temperature Melting Polyethylene Glycol Carrier
Tablet forming : 6mm round die, 5-8kN pressure
Aluminum foil packaging : moisture-proof and light-proof protection
2. Transdermal gel (alternative dosage form) :
Example formulation (50 mg/mL):
SR9009 raw materials: 5%
Propylene glycol: 40%
Ethanol: 30%
Carbomer: 2%
Preparation process :
Raw material dissolution : ethanol + propylene glycol mixed solvent
Gelation : Carbomer dispersion followed by neutralization
Filling : Aluminum tube or pump packaging
How to use
1. Endurance Enhancement Research :
Dosage : 20-30 mg/day, divided into 3 doses sublingually
Timing : 1 hour before training + 4 hours between two sessions
Duration : 6-8 weeks
2. Metabolic studies :
Dosage : 10-20 mg/day, divided into 2 doses sublingually
Monitoring : Glucose tolerance test + body composition analysis
3. Dosage form selection priority :
Sublingual tablets : bioavailability 20-30%
Transdermal gel : bioavailability 10-15%
Oral capsules : Bioavailability <5% (not recommended)
4. Dosage regimen :
Sublingual : Place under the tongue for 5-10 minutes
Transdermal application : Apply to the skin of the wrist or neck
3 times a day : Administer every 6-8 hours to maintain blood concentration
Why choose SR9009 raw material ?
Unique mechanism of action , non-hormonal pathway to improve endurance
Multiple metabolic benefits , simultaneously optimizing endurance and metabolic health
High scientific research value , innovative tool for biorhythm research
Quality Assurance :
GMP -compliant production , each batch HPLC purity tested (≥98% )
Third-party laboratory report (COA) is included with the product
Microbial limit testing to ensure safety
Worldwide Shipping :
Original sealed packaging , moisture-proof and light-proof
Private delivery , no logo on the outer packaging
Temperature- stable transportation to ensure product stability
Conclusion
SR9009 needs to be delivered via a sublingual tablet or transdermal gel formulation to enhance bioavailability. It is particularly suitable for studies on exercise endurance, metabolic syndrome, and biorhythm . The research dose is 20-30mg/day .
If you need anything, please contact Allen
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+852 4671 8216 |
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