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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

HCID 5277
NotesReactions
Basic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
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Basic information

CAS
10418-03-8
Standard SMILES
CC12Cc3cn[nH]c3CC1CCC1C2CCC2(C)C1CCC2(C)O
InChIKey
LKAJKIOFIWVMDJ-UHFFFAOYSA-N
Molecular formula
C21H32N2O
Average molar mass
328.5 g/mol
Monoisotopic mass
328.25146365

Overview

17-Methyl-2'H-5alpha-androst-2-eno[3,2-c]pyrazol-17beta-ol is a steroid. It derives from a hydride of an estrane.

Names & identifiers

Preferred name
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
IUPAC
2,17,18-trimethyl-6,7-diazapentacyclo[11.7.0.02,10.04,8.014,18]icosa-4(8),5-dien-17-ol
English name
Stanozolol
Molecular formula
C21H32N2O
Molecular weight
328.49

Names & synonyms

RefChem:1051847DTXCID30209887DTXSID308600781,10a,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-olAnabol2'H-Androst-2-eno[3,2-c]pyrazol-17-ol,17-methyl-, (5a,17b)-2,17,18-trimethyl-6,7-diazapentacyclo[11.7.0.02,10.04,8.014,18]icosa-4(8),5-dien-17-ol22957-48-8MFCD00133084(17beta)-17-Methyl-2'H-androst-2-eno(3,2-c)pyrazol-17-ol17-Methyl-2'H-5.alpha.-androst-2-eno(3,2-c)pyrazol-17.beta.-ol17-Methyl-2'H-5.alpha.-androst-2-eno[3,2-c]pyrazol-17.beta.-ol
Show more names
WinstrolStanazololSTANAZOLwinnySTANOBOLSTANOZOLStanozoloStanozolol Suspension (For Injection)Wiinny
17-Methylpyrazolo(4',3':2,3)-5.alpha.-androstan-17.beta.-olSCHEMBL34983212'H-5.alpha.-Androst-2-eno(3,2-c)pyrazol-17.beta.-ol, 17-methyl-CHEBI:181111LKAJKIOFIWVMDJ-UHFFFAOYSA-N1,10a,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 #AKOS025395207AKOS030228141

Properties

Computed structural properties

XLogP
4.5
Topological polar surface area
48.9 Ų
Hydrogen bond donors
2
Hydrogen bond acceptors
2
Rotatable bonds
0
Heavy atoms
24
Formal charge
0
Complexity
538

Physicochemical properties

Melting point
242 °C · 242 °C
alpha
34 · 34 º
Boiling point
490.8 · 490.8±45.0 °C(Predicted)
Density
1.129 · 1.129±0.06 g/cm3(Predicted)
refractive index
34 ° · 34 ° (C=0.4, CHCl3)
Flash point
-2 ℃ · -2℃
storage temp.
2 · 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 · 15.15±0.60(Predicted)
color
white to light yellow
Merck
8794 · 8794
Henry's Law Constant
9 · 9.0×102 mol/(m3Pa) at 25℃, HSDB (2015)
Major Application
clinical testing
InChIKey
LKAJKIOFIWVMDJ-IYRCEVNGSA-N

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

Safety data

wgk
3
rtecs
BV8741000
ridadr
UN2252 - class 3 - PG 2 - 1,2-Dimethoxyethane solution
hs_code
29372900
risk_code
63-38-19-11-61-60
Signal word
Danger
Symbol(GHS)
GHS08
hazard_code
Xn,Xi,T,F
safety_code
53-22-36/37/39-36-26-45
Storage Class
3 - Flammable liquids
Hazard statements
H351-H360FD
Hazard Classifications
Acute Tox. 4 InhalationFlam. Liq. 2Repr. 1BSkin Irrit. 2
Precautionary statements
P201-P202-P280-P308+P313-P405-P501
Hazardous Substances Data
10418-03-8(Hazardous Substances Data)

Chemistry & industry

Applications · 4 items

DescriptionStanozolol (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.

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.

UsesAnabolic steroid. Androgen. Controlled substance.

Usesandrogen anabolic steroid

Upstream & downstream products

Upstream raw materials

AmmoniaLithium ion (1+)

Suppliers100 total

国药集团化学试剂有限公司86-21-63210123 · [email protected]
北京华美互利生物化工010-56205725 · [email protected]
Shanghai Biolang Biotechnology Co., Ltd.+86-15970428662 +86-13397199602 · [email protected]

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Compound notes

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On this pageBasic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes

Database identifiers

CAS
10418-03-8、22957-48-8
PubChem CID
5277
ChEBI
CHEBI:181111
EC Number
245-351-2
SMILES
C[C@]1(O)CCC2C3CC[C@H]4Cc5[nH]ncc5C[C@]4(C)C3CC[C@]12C
CAS DataBase Reference
10418 · 10418-03-8
FDA UNII
4 R1VB9P8V3 · 4R1VB9P8V3
NIST Chemistry Reference
Stanozolol(10418-03-8)
Proposition 65 List
Stanozolol
ATC code
14 AA02 · A14AA02
UNSPSC Code
41116107 · 41116107
NACRES
24 · NA.24
Symbol(GHS)
8 · GHS08
Signal word
Danger
Hazard statements
351 · H351-H360FD
Precautionary statements
201 · P201-P202-P280-P308+P313-P405-P501
Hazard Codes
Xn,Xi,T,F
Risk Statements
63 · 63-38-19-11-61-60
Safety Statements
53 · 53-22-36/37/39-36-26-45
RIDADR
2252 · UN2252 - class 3 - PG 2 - 1,2-Dimethoxyethane solution
WGK Germany
3 · 3
RTECS
8741000 · BV8741000
HS Code
29372900 · 29372900
Storage Class
3 · 3 - Flammable liquids
Hazard Classifications
4 InhalationFlam · Acute Tox. 4 InhalationFlam. Liq. 2Repr. 1BSkin Irrit. 2
Hazardous Substances Data
10418 · 10418-03-8(Hazardous Substances Data)
合肥翰刚医药科技有限公司
+8618062405514 · [email protected]
INTATRADE GmbH+49 3493/605464 · [email protected]
Baoji Guokang Healthchem co.,ltd+8615604608665 15604608665 · [email protected]
上海钰源生物化学有限公司021-13814116 13814116708 · [email protected]
陕西林奈生物化工有限公司15327269642 · [email protected]
LGM Pharma1-(800)-881-8210 · [email protected]
河北秒变生物科技有限公司17733850068
杭州甾特生化科技有限公司18858184290 · [email protected]
广州蒂嚎医药科技有限公司18602015453 · [email protected]
安耐吉化学&3A(安徽泽升科技股份有限公司)400-0056266 · [email protected]
广州紫芯生物科技有限公司19519577873 · [email protected]
Cangzhou Wanyou New Material Technology Co.,Ltd18631714998 · [email protected]
MedBio脉铂医药021-69568360 18916172912 · [email protected]
浙江佑宁医药有限公司15557595058
贵州迪大科技有限责任公司0851-8475-2296 18096062265 · [email protected]
杭州东帆化学有限公司86-0571-85151182
云南西力生物技术股份有限公司0871-65217109 · [email protected]
山东西亚化学有限公司13355009207 13355009207 · [email protected]
武汉盈邦医药有限公司+86-13296627870; +86-13971566811 · [email protected]
HONG KONG IPURE BIOLOGY CO.,LIMITED86 18062405514 18062405514 · [email protected]
Hebei Qige Biological Technology Co. Ltd+86 +8618733132031
Wuhan Demeikai Biotechnology Co., Ltd+8618942921723 · [email protected]
上海思域化工科技有限公司86-21-34053660 · [email protected]
广州普罗艾森生物医药有限公司19098059326 · [email protected]
Wuhan NCE Biomedical Co.,Ltd.4000-027-021 |24 +86-13986109188 | +86-15623472865 | +81-08033611988
TOKYO CHEMICAL INDUSTRY CO., LTD.03-36680489 · [email protected]
深圳振强药物研发有限公司0755-66853366 13670046396 · [email protected]
上海诺宝化工有限公司+86(0)21 60484900
Hubei Datong Bio-Chemical Technology Co.,Ltd027-87666700 · [email protected]
南京生利德生物科技有限公司025-57798810 18652991625 · [email protected]
南京世洲生物科技有限公司13675144456 · [email protected]
Xunteng International Trading Co.,Limited—
湖北鑫源顺医药化工有限公司13971561712, 13995564702, 027-50664929 · [email protected]
HBCChem, Inc.+1-510-219-6317 · [email protected]
武汉开诺医药科技有限公司18040571231/1402788087
雷丁试剂0510-85629785 18013409632 · [email protected]
天津普西唐生物医药科技有限公司010-60605840 · [email protected]
上海御略医药科技有限公司021-60345187 13671753212 · [email protected]
Taizhou Xinen Biotechnology Co., Ltd.+8615068633455 · [email protected]
上海孚一生物科技有限公司+86 (21) 61124340
珠海安哲生物科技有限公司13169972583 · [email protected]
Wuhan Biocar Bio-Pharm Co., Ltd.86 15387057351 · [email protected]
广东泰博医药科技有限公司15557595058 15557595058 · [email protected]
武汉鑫儒化工有限公司15927387915 15337108568 · [email protected]
安耐吉化学&3A(安徽泽升科技股份有限公司)400-0056266 · [email protected]
浙江嘉晖医药科技有限公司19229895729 · [email protected]
Shijiazhuang Erche Biotechnology Co., Ltd8613343119830 13343119830 · [email protected]
Additional notes · 1 item

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.