ChemicalBook > CAS DataBase List > Stanozolol

Stanozolol

Product Name
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
Formula Weight
328.49
MOL File
10418-03-8.mol
More
Less

Stanozolol Property

Melting point:
242 °C
alpha 
34 º
Boiling point:
490.8±45.0 °C(Predicted)
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
NIST Chemistry Reference
Stanozolol(10418-03-8)
More
Less

Safety

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)
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H351Suspected of causing cancer

Precautionary statements

P201Obtain special instructions before use.

P202Do not handle until all safety precautions have been read and understood.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P308+P313IF exposed or concerned: Get medical advice/attention.

P405Store locked up.

P501Dispose of contents/container to..…

More
Less

N-Bromosuccinimide Price

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

Stanozolol Chemical Properties,Usage,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.

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

More
Less

Stanozolol Suppliers

Chengdu Pengshengyue Pharmaceutical Technology Co. , Ltd.
Tel
171-5642-2032 19587414261
Email
3795342424@qq.com
Country
China
ProdList
23
Advantage
58
Linyi Pingsheng Biotechnology Co., Ltd.
Tel
0375-15696900 15696900147
Email
3958759419@qq.com
Country
China
ProdList
17
Advantage
58
Hangzhou Zyter Biological & Chemical Technology Co., Ltd.
Tel
18858184290; 18858184290
Fax
0086-571-28313105
Email
sales@zyterpharm.com
Country
China
ProdList
48
Advantage
49
INTATRADE GmbH
Tel
+49 3493/605464
Fax
+49 3493/605470
Email
sales@intatrade.de
Country
Germany
ProdList
3572
Advantage
66
Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
Country
China
ProdList
44688
Advantage
61
LGM Pharma
Tel
1-(800)-881-8210
Fax
615-250-9817
Email
inquiries@lgmpharma.com
Country
United States
ProdList
2123
Advantage
70
China DongFan Chemical Co.,LTD
Tel
86-0571-85151182
Fax
86-0571-85151182
Country
China
ProdList
5691
Advantage
66
XiaoGan ShenYuan ChemPharm co,ltd
Tel
15527768850
Email
1791901229@qq.com
Country
China
ProdList
8836
Advantage
52
Shandong Xiya Chemical Co., Ltd
Tel
4009903999 13355009207
Fax
0539-6365991
Email
3007715519@qq.com
Country
China
ProdList
18738
Advantage
57
Sinopharm Chemical Reagent Co,Ltd.
Tel
86-21-63210123
Fax
86-21-63290778 86-21-63218885
Email
sj_scrc@sinopharm.com
Country
China
ProdList
9815
Advantage
79
More
Less

View Lastest Price from Stanozolol manufacturers

Apeloa production Co.,Limited
Product
Stanozolol 10418-03-8
Price
US $1.00/g
Min. Order
1g
Purity
98%
Supply Ability
1000
Release date
2024-05-22
hebei hongtan Biotechnology Co., Ltd
Product
Stanozolol 10418-03-8
Price
US $60.00-40.00/KG
Min. Order
1KG
Purity
99.8%
Supply Ability
20
Release date
2024-05-11
hebei hongtan Biotechnology Co., Ltd
Product
ANADROL , or Oxymetholone 10418-03-8
Price
US $15.00-10.00/g
Min. Order
100g
Purity
99.9%
Supply Ability
1000kg
Release date
2024-05-11

10418-03-8, StanozololRelated Search:


  • 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)-
  • Anabol
  • Androstanazolestanazol
  • Estazol
  • NSC-43193
  • Stanazolol
  • Stromba
  • Strombaject
  • Tevabolin
  • Win 14833
  • win14833
  • Winstroid
  • Winstrol
  • 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
  • Stanozolo
  • 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)-
  • Oral Stanozolol
  • Oral Stanozolol (Winstrol)
  • Medical Cancer Treatment Cutting Cycle Steroids Powders CAS 10418-03-8 Stanozolol Winstrol
  • 4-[(3-chloro-1-oxopropyl)amino]benzoic acid propan-2-yl ester
  • Bodybuilding Sports
  • 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