| Name |
|
|---|---|
| Synonyms | Anabol Estazol Stromba STANOZOL STANAZOL win14833 Winstrol winstrolv Winstroid Tevabolin Win 14833 NSC-43193 Stanozolo Stanozlol NSC 233046 Stanazolol winstrol l STANOZOLOL Winstrol V Strombaject androstanazol ANDROSTANAZOLE Winstrol Depot STANOZOLOL,USP STANOZOLOL BP, USP Stanozolol(winstrol) WINSTROL (stanozolol) Androstanazolestanazol stanozolol--dea schedule Stanozolol CIII (200 mg) Stanozolol solution stanozolol solution,100ppm stanozolol--dea schedule iii Stanozolol(Winstrol, Winstrol Depot) Stanozolol Suspension (For Injection) 17-Methyl-5a-androstano[3,2-c]pyrazol-17b-ol yclopenta[7,8]-phenanthro[2,3-c]pyrazol-1-ol 17α-methyl-5α-androstan-17β-olo(3,2-c)pyrazole 17b-Hydroxy-17a-methylandrostano(3,2-c)pyrazole 5a-Androstane-17a-methyl-17b-ol-(3,2-c)pyrazole 5α-Androstane-17α-methyl-17β-ol-[3,2-c]pyrazole 17-Methyl-pyrazolo[4',3':2,3]-5a-androstan-17b-ol 17β-Hydroxy-17α-methylandrostano [3,2-c] pyrazole 17b-Hydroxy-17-methyl-5a-androstano[3,2-c]pyrazole 17a-Methyl-17b-hydroxy-5a-androstano(3,2-c)pyrazole 17b-Hydroxy-17a-methyl-5a-androstano[3,2-c]pyrazole 17β-Hydroxy-17α-methyl-5α-androstano[3,2-c]pyrazole Stanozolol BP/USP (Winstrol) 17BETA-HYDROXY-17ALPHA-METHYLANDROSTANO[3,2-C]PYRAZOLE 17beta-hydroxy-17-methyl-5alpha-androstano[3,2-c]pyrazole 17ALPHA-METHYL-5ALPHA-ANDROSTAN-17BETA-OLO[3,2-C]PYRAZOLE 17-methyl-2h-5alpha-androst-2-eno[3,2-c]pyrazol-17beta-ol 2-c)pyrazol-17beta-ol,17-methyl-2’h-5alpha-androst-2-eno( 17-Methyl-2'H-5alpha-androst-2-eno(3,2-c)pyrazol-17beta-ol 5-ALPHA-ANDROSTAN-17-ALPHAMETHYL-17-BETAOL-[3,2-C]PYRAZOLE 17-alpha-methyl-5-alpha-androstano(3,2-c)pyrazol-17-beta-ol 2'H-Androst-2-eno[3,2-c]pyrazol-17-ol,17-Methyl-, (5a,17b)- 2'H-5a-Androst-2-eno[3,2-c]pyrazol-17b-ol, 17-methyl-(8CI) 2'H-5alpha-Androst-2-eno(3,2-c)pyrazol-17beta-ol, 17-methyl- 2-c)pyrazol-17-ol,17-methyl-,(5alpha,17beta)-2’h-androst-2-eno( 2'H-Androst-2-eno[3,2-c]pyrazol-17-ol, 17-methyl-, (5a,17b)-(9CI) 2'H-Androst-2-eno[3,2-c]pyrazol-17-ol, 17-methyl-, (5alpha,17beta)- 1,2,3,3a,3b,4,5,5a,6,8,10,10a,10b,11,12,12a-hexadecahydro-1,10a,12a-trimethylc Cyclopenta[7,8]phenanthro[2,3-c]pyrazole, 2'H-androst-2-eno[3,2-c]pyrazol-17-ol deriv. 1,10a,12a-Trimethyl-1,2,3,3a,3b,4,5,5a,6,8,10,10a,10b,11,12,12a-hexadecahydrocyclopenta[5,6]naphtho[1,2-f]indazol-1-ol Cyclopenta[7,8]phenanthro-[2,3-c]pyrazol-1-ol, 1, 2,3,3a,3b,4,5,5a,6,8,10,10a,10b,11,12,12a-hexadecahydro-1,10a, 12a-trimethyl- 5α-Androstane-17α-methyl-17β-ol-[3,2-c]pyrazole, Androstanazole, Stanazol, 17β-Hydroxy-17α-methyl-5α-androstano[3,2-c]pyrazole Cyclopenta[7,8]phenanthro[2,3-c]pyrazol-1-ol, 1,2,3,3a,3b,4,5,5a,6,7,10,10a,10b,11,12,12a-hexadecahydro-1,10a,12a-trimethyl-(6CI, 7CI))- |
| CAS NO | 10418-03-8 |
| EINECS | 233-894-8 |
| Molecular Weight | 328.49 |
| Molecular Formula | C21H32N2O |
| Product Categories | pharmaceutical intermediate; Biochemistry; Steroids; Steroids (Others); Pharmaceutical; Active Pharmaceutical Ingredients; Intermediates & Fine Chemicals; Pharmaceuticals; Steroid and Hormone; API; Finished Steroid and Hormone |
| Mol File | 10418-03-8.mol |
| Stanozolol Chemical Properties | |
|---|---|
| density | 1.129±0.06 g/cm3(Predicted) |
| Boiling point | 490.8±45.0 °C(Predicted) |
| alpha | 34 º |
| form | powder |
| Melting point | 242 °C |
| solubility | Practically insoluble in water, soluble in dimethylformamide, slightly soluble in ethanol (96 per cent), very slightly soluble in methylene chloride. |
| refractive index | 34 ° (C=0.4, CHCl3) |
| storage temp | 2-8°C |
| pka | 15.15±0.60(Predicted) |
| Merck | 8794 |
| color | white to light yellow |
| InChIKey | LKAJKIOFIWVMDJ-IYRCEVNGSA-N |
| CAS DataBase Reference | 10418-03-8 |
| Fp | -2℃ |
| NIST Chemistry Reference | Stanozolol(10418-03-8) |
| Safety Information | |
|---|---|
| Hazard Codes | Xn,Xi,T,F |
| Risk Statements | 63-38-19-11-61-60 |
| Safety Statements | 53-22-36/37/39-36-26-45 |
| RIDADR | UN2252 - class 3 - PG 2 - 1,2-Dimethoxyethane solution |
| WGK Germany | 3 |
| RTECS | BV8741000 |
| HS Code | 29372900 |
| Hazardous Substances Data | 10418-03-8(Hazardous Substances Data) |
| Stanozolol (Winstrol) Usage And Synthesis | |
|---|---|
| Description | Stanozolol is a synthetic anabolic-androgenic steroids (AAS) belonging to the dihydrotestosterone group. It can be used for the treatment of wasting diseases, burn victims, osteroporosis, bone fractures, anemia and even obesity. It can stimulate fat loss without causing reduced lean body mass, inducing hemoglobin production and red blood cell formation. Stanozolol has the following physiological functions: (1) reduction of sex-hormone-binding-globulin; (2) inducing protein synthesis; (3) Maintain nitrogen retention; (4) Increase red blood cells; (5) inhibit glucocorticoids. |
| Chemical Properties | White Solid |
| Originator | Winstrol,Winthrop,US,1961 |
| Uses | androgen anabolic steroid |
| Uses | Anabolic steroid. Androgen. Controlled substance. |
| Definition | ChEBI: An organic heteropentacyclic compound resulting from the formal condensation of the 3-keto-aldehyde moiety of oxymetholone with hydrazine. Like oxymetholone, it is a synthetic anabolic steroid. It has both anabolic and androgenic properties, and has been u ed to treat hereditary angioedema and various vascular disorders. It has also been widely abused by professional athletes. |
| Manufacturing Process | To a stirred solution of 1.00 gram of 17β-hydroxy-17α-methyl-4- androsteno[3,2-c]pyrazole in 200 ml of tetrahydrofuran and 400 ml of liquid ammonia was added 2.12 grams of lithium wire during 5 minutes. The dark blue mixture was stirred for 45 minutes. A solution of 40 ml of tertiary-butyl alcohol in 160 ml of diethyl ether was added with stirring. After 15 minutes, 25 ml of ethanol was added with stirring. The mixture turned colorless after several hours, and the liquid ammonia was allowed to evaporate and the mixture was allowed to warm to room temperature over a period of about 15 hours. The solvent was evaporated to yield a colorless solid residue, which was taken up in ethyl acetate-ice water. The two layers were separated and the aqueous layer was extracted with ethyl acetate. |
| Brand name | Winstrol (Ovation). |
| Therapeutic Function | Anabolic |
| Veterinary Drugs and Treatments | Labeled indications for the previously marketed veterinary stanozolol product Winstrol?-V (Winthrop/Upjohn) included “…to improve appetite, promote weight gain, and increase strength and vitality…” in dogs, cats and horses. The manufacturer also stated that: “Anabolic therapy is intended primarily as an adjunct to other specific and supportive therapy, including nutritional therapy.” Like nandrolone, stanozolol has been used to treat anemia of chronic disease. Because stanozolol has been demonstrated to enhance fibrinolysis after parenteral injection, it may be efficacious in the treatment of feline aortic thromboembolism or thrombosis in nephrotic syndrome; however, clinical studies and/or experience are apparently lacking for this indication at present. |
| Stanozolol Preparation Products And Raw materials | |
|---|---|
| Raw materials | Ammonia-->Lithium |
| Package method |
|---|
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