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Stanozolol

CAS No.
10418-03-8
Chemical Name:
Stanozolol
Synonyms
Winstrol;STANAZOL;Stanazolol;winny;Anabol;STANOBOL;Stanozolo;Wiinny;Estazol;Stromba
CBNumber:
CB0247357
Molecular Formula:
C21H32N2O
Molecular Weight:
328.49
MDL Number:
MFCD00133084
MOL File:
10418-03-8.mol
MSDS File:
SDS
Last updated:2024-04-23 13:02:50

Stanozolol Properties

Melting point 242 °C
Boiling point 490.8±45.0 °C(Predicted)
alpha 34 º
Density 1.129±0.06 g/cm3(Predicted)
refractive index 34 ° (C=0.4, CHCl3)
Flash point -2℃
storage temp. 2-8°C
solubility Practically insoluble in water, soluble in dimethylformamide, slightly soluble in ethanol (96 per cent), very slightly soluble in methylene chloride.
form powder
pka 15.15±0.60(Predicted)
color white to light yellow
Merck 8794
InChIKey LKAJKIOFIWVMDJ-IYRCEVNGSA-N
CAS DataBase Reference 10418-03-8
FDA UNII 4R1VB9P8V3
Proposition 65 List Stanozolol
ATC code A14AA02
NIST Chemistry Reference Stanozolol(10418-03-8)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS08
Signal word  Danger
Hazard statements  H351-H360FD
Precautionary statements  P201-P202-P280-P308+P313-P405-P501
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

Stanozolol price More Price(15)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich S-906 Stanozolol solution 1.0?mg/mL in 1,2-dimethoxyethane, ampule of 1?mL, certified reference material, Cerilliant? 10418-03-8 1mL $160 2024-03-01 Buy
Sigma-Aldrich 1620005 Stanozolol 10418-03-8 200mg $360 2024-03-01 Buy
Sigma-Aldrich S7132 Stanozolol analytical standard 10418-03-8 1g $107 2022-05-15 Buy
Sigma-Aldrich S7132 Stanozolol analytical standard 10418-03-8 10g $593 2022-05-15 Buy
Cayman Chemical 21167 Stanozolol ≥98% 10418-03-8 1mg $44 2024-03-01 Buy
Product number Packaging Price Buy
S-906 1mL $160 Buy
1620005 200mg $360 Buy
S7132 1g $107 Buy
S7132 10g $593 Buy
21167 1mg $44 Buy

Stanozolol Chemical Properties,Uses,Production

Description

Stanozolol (Item No. 21167) is an analytical reference standard that is categorized as a synthetic anabolic androgenic steroid. Stanozolol has low urinary excretion; therefore, its metabolites are usually used for detection. Formulations containing stanozolol are used as a treatment for hereditary angioedema. It has also been abused in athletics to improve performance. Stanozolol is regulated as a Schedule III compound in the United States. This product is intended for research and forensic applications.

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

Anabolic steroid. Androgen. Controlled substance.

Uses

androgen anabolic steroid

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. The combined organic layers were washed with water, saturated sodium chloride solution and filtered through anhydrous sodium sulfate. The solvent was evaporated to yield 1.20 grams of light tan crystals, MP 151° to 155°C, ultraviolet maximum at 224 mμ (E = 4,095). Two recrystallizations from ethanol afforded: 1st crop, 0.619 grams (62%) of colorless crystals (dried at 120°C in vacuo for 17 hours), MP 232.8° to 238.0°C, ultraviolet maximum at 224 mμ (E = 4,840); 2nd crop, 0.142 gram (14%) of colorless crystals, MP 234° to 242°C.

brand name

Winstrol (Ovation).

Therapeutic Function

Anabolic

Synthesis

Stanozol, 17|á-methyl-5|á-androstano[3,2-c]pyrazol-17|?-ol (29.3.13), is made by reducing the double bond at C4¨CC5 in methyltestosterone, which has independent interest as an anabolic drug of mestanolone (29.3.11). Mestanolone undergoes formylation with ethylformate in the presence of sodium ethoxide, forming a 2-formyl (oxymethylene) derivative (29.3.12), which upon reaction with hydrazine easily cyclizes to the desired stanazole (29.3.13), which is a pyrazol-condensed steroid system.

Synthesis_10418-03-8

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.

References

https://www.steroid.com/Stanozolol.php
https://pubchem.ncbi.nlm.nih.gov/compound/stanozolol
https://en.wikipedia.org/wiki/Stanozolol

Stanozolol Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 387)Suppliers
Supplier Tel Email Country ProdList Advantage
Changzhou Xuanming Pharmaceutical Technology Co., Ltd.
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Hebei Yinsheng Technology Co., Ltd.
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View Lastest Price from Stanozolol manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Stanozolol; winstrol; Stanazol coarse;micro pictures 2024-04-26 Stanozolol; winstrol; Stanazol coarse;micro
10418-03-8
US $1157.00 / kg 1kg 99.99% 2 tons Wuhan Cell Pharmaceutical Co., Ltd
Stanozolol Wwinstrol pictures 2024-04-26 Stanozolol Wwinstrol
10418-03-8
US $9.00-6.00 / kg 0.10000000149011612kg 99% 10 tons Hebei Kangcang new material Technology Co., LTD
Stanozolol Wwinstrol pictures 2024-04-26 Stanozolol Wwinstrol
10418-03-8
US $50.00-30.00 / kg 1kg 98% 20 Hebei Kangcang new material Technology Co., LTD
  • Stanozolol Wwinstrol pictures
  • Stanozolol Wwinstrol
    10418-03-8
  • US $50.00-30.00 / kg
  • 98%
  • Hebei Kangcang new material Technology Co., LTD
Stanozolol CIII (200 mg) Stanozolol Suspension (For Injection) Stanozolol BP/USP (Winstrol) Stanozolol(Winstrol, Winstrol Depot) 2-c)pyrazol-17beta-ol,17-methyl-2’h-5alpha-androst-2-eno( 2-c)pyrazol-17-ol,17-methyl-,(5alpha,17beta)-2’h-androst-2-eno( 2'H-5alpha-Androst-2-eno(3,2-c)pyrazol-17beta-ol, 17-methyl- 2'H-Androst-2-eno[3,2-c]pyrazol-17-ol, 17-methyl-, (5alpha,17beta)- Androstanazolestanazol Estazol NSC-43193 Stromba Strombaject Tevabolin Win 14833 win14833 Winstroid Winstrol V winstrolv yclopenta[7,8]-phenanthro[2,3-c]pyrazol-1-ol 2'H-Androst-2-eno[3,2-c]pyrazol-17-ol, 17-methyl-, (5a,17b)- (9CI) 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) Cyclopenta[7,8]phenanthro[2,3-c]pyrazole, 2'H-androst-2-eno[3,2-c]pyrazol-17-ol deriv. NSC 233046 Winstrol Depot WINSTROL (stanozolol) stanozolol--dea schedule Stanozlol 5α-Androstane-17α-methyl-17β-ol-[3,2-c]pyrazole, Androstanazole, Stanazol, 17β-Hydroxy-17α-methyl-5α-androstano[3,2-c]pyrazole 17b-Hydroxy-17a-methylandrostano(3,2-c)pyrazole 5a-Androstane-17a-methyl-17b-ol-(3,2-c)pyrazole 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- Stanozolol(winstrol) 17β-Hydroxy-17α-methyl-5α-androstano[3,2-c]pyrazole 5α-Androstane-17α-methyl-17β-ol-[3,2-c]pyrazole 2'H-Androst-2-eno[3,2-c]pyrazol-17-ol,17-Methyl-, (5a,17b)- Stanozolol solution ndrostanazol 17-alpha-methyl-5-alpha-androstano(3,2-c)pyrazol-17-beta-ol stanozolol--dea schedule iii STANOZOLOL BP, USP 5-ALPHA-ANDROSTAN-17-ALPHAMETHYL-17-BETAOL-[3,2-C]PYRAZOLE androstanazol ANDROSTANAZOLE 17ALPHA-METHYL-5ALPHA-ANDROSTAN-17BETA-OLO[3,2-C]PYRAZOLE 17BETA-HYDROXY-17ALPHA-METHYLANDROSTANO[3,2-C]PYRAZOLE 17beta-hydroxy-17-methyl-5alpha-androstano[3,2-c]pyrazole stanozolol solution,100ppm Androstanazol,Winstrol 2'H-Androst-2-eno[3,2-c]pyrazol-17-ol, 17-methyl-, (5α,17β)- STANOZOL STANOZOLOL winstrol l 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 1,2,3,3a,3b,4,5,5a,6,8,10,10a,10b,11,12,12a-hexadecahydro-1,10a,12a-trimethylc 17-Methyl-2'H-5alpha-androst-2-eno(3,2-c)pyrazol-17beta-ol 17-methyl-2h-5alpha-androst-2-eno[3,2-c]pyrazol-17beta-ol 17β-Hydroxy-17α-methylandrostano [3,2-c] pyrazole