Stanazol、winstrol/Preferential price/Top quality/Mass supply CAS NO.10418-03-8
- FOB Price: USD: 1.00-1.00 /Gram Get Latest Price
- Min.Order: 1 Gram
- Payment Terms: D/P,T/T,Other
- Available Specifications:
top(1-10)Gram
- Product Details
Keywords
- tevabolin;anabol;stromba;estazol
- favourable price of stanazol
- Bodybuilding Sports Nutrition Supplement
Quick Details
- ProName: Stanazol、winstrol/Preferential price/T...
- CasNo: 10418-03-8
- Molecular Formula: C21H32N2O
- Appearance: white crystalline powder
- Application: For research purposes only
- DeliveryTime: One day
- PackAge: apis or finished product
- Port: Shenzhen、Guangzhou、Shanghai、HK
- ProductionCapacity: 100 Kilogram/Day
- Purity: 99.8%
- Storage: cryo drying
- Transportation: shipping by EMS,DHL,TNT,FEDEX,UPS or a...
- LimitNum: 1 Gram
- Moisture Content: 0%
- Impurity: 0%
Superiority
Stanozolol is used for physique- and performance-enhancing purposes by competitive athletes, bodybuilders, and powerlifters.
See also: Anabolic steroid § Adverse effects
As an AAS, stanozolol is an agonist of the androgen receptor (AR), similarly to androgens like testosterone and DHT. Its affinity for the androgen receptor is about 22% of that of dihydrotestosterone. Stanozolol is not a substrate for 5α-reductase as it is already 5α-reduced, and so is not potentiated in so-called "androgenic" tissues like the skin, hair follicles, and prostate gland. This results in a greater ratio of anabolic to androgenic activity compared to testosterone. In addition, due to its 5α-reduced nature, stanozolol is non-aromatizable, and hence has no propensity for producing estrogenic effects such as gynecomastia or fluid retention. Stanozolol also does not possess any progestogenic activity of significance. Because of the presence of its 17α-methyl group, the metabolism of stanozolol is sterically hindered, resulting in it being orally active, although also hepatotoxic.
Stanozolol has high oral bioavailability, due to the presence of its C17α alkyl group and the resistance to gastrointestinal and liver metabolism that it results in. The medication has very low affinityfor human serum sex hormone-binding globulin (SHBG), about 5% of that of testosterone and 1% of that of DHT. Stanozolol is metabolized in the liver, ultimately becoming glucuronide and sulfateconjugates. Its biological half-life is reported to be 9 hours when taken by mouth and 24 hours when given by intramuscular injection in the form of an aqueous suspension.It is said to have a duration of action of one week or more via intramuscular injection.
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