STROMUSC Anavar(Oxandrolone)10mg For Bodybuilding CAS:53-39-4
Anavar, synthesized in 1962 by Pfizer, was initially designed to treat muscle-wasting conditions (e.g., HIV, burns). Unlike other steroids, its dihydrotestosterone (DHT) derivative structure minimized androgenic effects, making it a pioneer in gender-inclusive medical use.
Introduction to Anavar (Oxandrolone)
Historical Context & Development
Anavar, synthesized in 1962 by Pfizer, was initially designed to treat muscle-wasting conditions (e.g., HIV, burns). Unlike other steroids, its dihydrotestosterone (DHT) derivative structure minimized androgenic effects, making it a pioneer in gender-inclusive medical use.
Chemical Profile
●Structure: 17α-alkylated oral steroid with a unique oxygen atom replacing the carbon-2 in the A-ring. This modification enhances anabolic activity while reducing hepatotoxicity.
●Half-Life: ~9 hours, necessitating split doses for stable blood levels.
Medical vs. Bodybuilding Use
While prescribed for osteoporosis and pediatric growth disorders, bodybuilders exploit its ability to preserve lean mass during caloric deficits. Its mildness contrasts with harsh compounds like Trenbolone, appealing to athletes seeking subtle gains.
Features Distinguishing Anavar
Low Androgenicity
●Anabolic Ratio: 322:24 (anabolic:androgenic), minimizing virilization in women (e.g., voice deepening) and androgenic alopecia in men.
●SHBG Suppression: Lowers sex hormone-binding globulin, increasing free testosterone bioavailability-critical during cutting phases.
Hepatic Tolerance
●Unlike most orals, Anavar's 17α-alkylation is less hepatotoxic due to its slow metabolism. Studies show transient liver enzyme elevation, resolving post-cycle.
Metabolic Impact
●Enhances lipolysis via increased growth hormone secretion and mitochondrial efficiency, aiding fat loss without muscle catabolism.
Applications in Bodybuilding
Cutting Cycles
●Mechanism: Retains nitrogen balance, preventing muscle breakdown in deficits. Combined with its fat-oxidizing properties, it sculpts vascularity.
●Stacking: Paired with testosterone propionate (to offset suppressed endogenous testosterone) or non-aromatizing agents like Primobolan for synergy.
Strength Enhancement
●Stimulates phosphocreatine resynthesis, boosting power output without bulk-ideal for weight-class athletes (e.g., boxers).
Gender-Specific Use
●Women: Doses as low as 5mg/day yield lean gains; virilization risks emerge above 10mg.
●Men: Often requires 20–50mg/day for noticeable effects, though higher doses (80mg+) amplify side effects.
Beyond Muscle Growth
Collagen Synthesis
●Increases collagen production by 60–80%, strengthening tendons and ligaments-critical for injury-prone lifters.
Cardiovascular Endurance
●Elevates red blood cell count marginally, enhancing oxygenation without the thrombosis risks seen with EQ (Equipoise).
Psychological Edge
●Reduces cortisol-induced stress, improving recovery and gym performance consistency.
Dosage Protocols & Cycle Design
Beginner vs. Advanced Cycles
●Men:
○Beginner: 30mg/day (weeks 1–6), paired with testosterone enanthate (250mg/week).
○Advanced: 50mg/day (weeks 1–8) with Trenbolone acetate (50mg EOD).
●Women:
○Conservative: 5–10mg/day (weeks 1–6); monitor for clitoromegaly.
○Competitive: 15mg/day (weeks 1–4 only) to mitigate virilization.
Cycle Extensions & Risks
●Beyond 8 weeks, HDL cholesterol suppression becomes significant. Lipid management supplements (omega-3s, bergamot extract) are advised.
Post-Cycle Therapy (PCT)
Necessity & Strategy
●Anavar's mild suppression still necessitates PCT, especially when stacked.
●Protocol:
○SERMs: Nolvadex (20mg/day, weeks 1–4) to block estrogen receptors in the hypothalamus, restarting natural testosterone.
○HCG: Optional for severe suppression (500IU EOD, weeks 1–2).
Natural Recovery Timeline
●Testosterone levels rebound within 4–6 weeks post-PCT, confirmed via bloodwork (LH, FSH, total/free testosterone).
Controversies & Misconceptions
Liver Toxicity Myth
●Clinical trials show ALT/AST elevations are dose-dependent and reversible, unlike the persistent damage from Halotestin.
"Weak Steroid" Label
●Critics underestimate its niche: unparalleled safety-to-efficacy ratio. It's a tool for refinement, not mass.
Legal Status
●Schedule III (U.S.)/Class C (U.K.). Underground labs often underdose or substitute with Turinabol-testing kits are essential.
Alternatives & Future Trends
SARMs (e.g., Ostarine)
●Mimic Anavar's selectivity but lack long-term safety data.
Peptide Stacks
●Ipamorelin (GH secretagogue) + AICAR (AMPK activator) mimics Anavar's fat loss/muscle retention.
Gene Doping
●Emerging CRISPR techniques targeting myostatin inhibition could replicate Anavar's effects without exogenous hormones.
Clinical Data
| Brand | STROMUSC |
|
Trade names |
Oxandrin, Anavar, Oxandrolone |
|
CAS |
53-39-4 |
|
Molar mass |
306.45 |
|
Formula |
C19H30O3 |
|
Purity |
Above 98% |
|
Apprarance |
10mg*100 |
Any needs, please contact us
Email: Jasonraws106@gmail.com
WhatsApp: +86-15572565525
Telegram: +86-19128233885
Conclusion
Anavar's legacy lies in its precision: a versatile, low-risk adjunct for physique optimization. Its role in modern bodybuilding reflects a shift toward harm reduction and targeted outcomes. Users must prioritize bloodwork, cycle literacy, and legal sourcing to harness its benefits responsibly.
Hot Tags: stromusc anavar(oxandrolone)10mg for bodybuilding cas:53-39-4, China stromusc anavar(oxandrolone)10mg for bodybuilding cas:53-39-4 manufacturers, suppliers, factory
