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Stanozolol (Winstrol)
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Stanozolol (Winstrol)

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Name


Stanozolol (Winstrol)


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 NO10418-03-8
EINECS233-894-8
Molecular Weight328.49
Molecular FormulaC21H32N2O
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
density1.129±0.06 g/cm3(Predicted)
Boiling point490.8±45.0 °C(Predicted)
alpha34 º
formpowder
Melting point242 °C
solubilityPractically insoluble in water, soluble in dimethylformamide, slightly soluble in ethanol (96 per cent), very slightly soluble in methylene chloride.
refractive index34 ° (C=0.4, CHCl3)
storage temp2-8°C
pka15.15±0.60(Predicted)
Merck8794
colorwhite to light yellow
InChIKeyLKAJKIOFIWVMDJ-IYRCEVNGSA-N
CAS DataBase Reference10418-03-8
Fp-2℃
NIST Chemistry ReferenceStanozolol(10418-03-8)



Safety Information
Hazard CodesXn,Xi,T,F
Risk Statements63-38-19-11-61-60
Safety Statements53-22-36/37/39-36-26-45
RIDADRUN2252 - class 3 - PG 2 - 1,2-Dimethoxyethane solution
WGK Germany3
RTECSBV8741000
HS Code29372900
Hazardous Substances Data10418-03-8(Hazardous Substances Data)



Stanozolol (Winstrol) Usage And Synthesis
DescriptionStanozolol 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
OriginatorWinstrol,Winthrop,US,1961
Usesandrogen anabolic steroid
UsesAnabolic steroid. Androgen. Controlled substance.
DefinitionChEBI: 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 ProcessTo 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 nameWinstrol (Ovation).
Therapeutic FunctionAnabolic
Veterinary Drugs and TreatmentsLabeled 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 materialsAmmonia-->Lithium



Package method

包装材料.jpg



FAQ

MOQ: 100 gram

Pack material: Plastic bag + Shockproof film + shockproof envelope + Cartons.   

Shipment: By express to buyers’ door. 100% make sure delivery. 

Payment: TT/ Western Union/BTC/ETV/VISA and so on, please contact by email. 

Shipment time: Within three working days after payment. Usually need ten days to arrive buyers’ address. Resend if lost.

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