JS-BIOLOGY
Ethisterone
Location>Home > Products > Steroid/Hormone Raw Materials > API Active Pharmaceutical Ingredient
Ethisterone

89.png

Name


Ethisterone


Synonyms

Prone
Pranone
Pregnin
NSC-9565
Prolutol
Prodoxan
Produxan
Colutoid
Ethinone
Gestoral
Trosinon
prolutonc
Progestab
Prodroxan
primolutc
Trosinone
Ora-Lutin
Lutocylol
Nalutoral
Lutocyclin
Lutocyclol
Primolut C
Nugestoral
Proluton C
progestinp
Progestoral
Progestin P
lutidonoral
Aethisteron
ETHISTERONE
Lutidon Oral
Progestolets
Syngestrotabs
lucorteumoral
Ethisterone 0
Aethisteronum
ETHISTERONE(P)
Pregneninolone
Lucorteum Oral
Ethisterone,98%
ETHISTERONE(RG)
ETHYNYLTESTOSTERONE
ETHINYL TESTOSTERONE
ETHYNYLANDROSTENOLONE
ANHYDROXYPROGESTERONE
ETHISTERONE(RG)(CALL)
17-Ethinyltestosterone
17A-ETHYNYLTESTOSTERONE
17α-ethynyltestosterone
Testosterone, 17-ethynyl-
ANHYDROHYDROXYPROGESTERONE
4,17A-PREGNEN-17B-OL-20-YNE
17ALPHA-ETHYNYLTESTOSTERONE
17-alpha-ethinyltestosterone
ETHISTERONE WHO(CRM STANDARD)
ETHISTERONE EPE(CRM STANDARD)
17-Hydroxypregn-4-en-zoyn-3-one
17-Hydroxypregn-4-en-20-yn-3-one
(17-alpha)-pregn-4-en-20-yn-3-on
4,17a-pregnen-17b-ol-20-yn-3-one
17a-Hydroxypregn-4-en-20-yn-3-one
17A-ETHYNYL-4-ANDROSTEN-17B-OL-3-ONE
17b-hydroxy-4,17a-pregnen-20-yn-3-one
4,17ALPHA-PREGNEN-17BETA-OL-20-YN-3-ONE
(17α)-17-hydroxy-pregn-4-en-20-yn-3-one
17a-ethynyl-17b-hydroxy-4-androsten-3-one
17-hydroxy-17-alpha-pregn-4-en-20-yn-3-on
17-Hydroxy-17-alpha-pregn-4-en-20-yn-3-one
17-Ethynyl-17beta-hydroxyandrost-4-en-3-one
17alpha-Pregn-4-en-20-yn-3-one, 17-hydroxy-
17BETA-HYDROXY-4,17ALPHA-PREGNEN-20-YN-3-ONE
4-ANDROSTEN-17-ALPHA-ETHYNYL-17-BETA-OL-3-ONE
Androst-4-en-3-one, 17alpha-ethynyl-17-hydroxy-
Pregn-4-en-20-yn-3-one, 17-hydroxy-, (17alpha)-
17alpha-Ethynyl-17beta-hydroxyandrost-4-en-3-one
17-beta-Hydroxy-17-alpha-ethynyl-4-androsten-3-one
17α-Ethynyltestosterone, 17β-Hydroxy-4,17α-pregnen-20-yn-3-one, 4,17α-Pregnen-17β-ol-20-yn-3-one
(8R,9S,10R,13S,14S,17R)-17-ETHYNYL-17-HYDROXY-10,13-DIMETHYL-1,2,6,7,8,9,10,11,12,13,14,15,16,17-TETRADECAHY
Ethisterone,17α-Ethynyltestosterone, 17β-Hydroxy-4,17α-pregnen-20-yn-3-one, 4,17α-Pregnen-17β-ol-20-yn-3-one
(8R,9S,10R,13S,14S,17S)-17-ethynyl-17-hydroxy-10,13-dimethyl-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-3-one
(8R,9S,10R,13S,14S,17R)-17-ETHYNYL-17-HYDROXY-10,13-DIMETHYL-1,2,6,7,8,9,10,11,12,13,14,15,16,17-TETRADECAHYDRO-CYCLOPENTA[A]PHENANTHREN-3-ONE

CAS NO434-03-7
EINECS207-096-5
Molecular Weight312.45
Molecular FormulaC21H28O2
Product CategoriesSteroids;
Acetylenes;
Biochemistry;
Functionalized Acetylenes;
Hydroxyketosteroids;
Intermediates & Fine Chemicals;
Metabolites & Impurities;
Inhibitors;
progestogen estrogen;
Metabolites & Impurities, Pharmaceuticals, Intermediates & Fine Chemicals;
Steroid and Hormone;
Pharmaceuticals
Mol File

434-03-7.mol



Ethisterone Chemical Properties
density1.0697 (rough estimate)
Boiling point392.36°C (rough estimate)
formneat
Melting point263-269 °C(lit.)
alphaD23 +23.8° (dioxane); D25 -32.0° (pyridine)
refractive index33 ° (C=1, Pyridine)
storage temp-20°C Freezer
pka13.10±0.60(Predicted)
Water Solubilitysoluble in chloroform, DMSO (0.05 mg/ml), acetone
Merck14,3741
BRN1889895
InChIKeyCHNXZKVNWQUJIB-CEGNMAFCSA-N
CAS DataBase Reference434-03-7
NIST Chemistry ReferenceEthisterone(434-03-7)


Safety Information
Hazard CodesXn,T
Risk Statements40-48-61
Safety Statements22-24/25-45-53
RIDADRUN 2811
WGK Germany3
RTECSTU5570250
HS Code29372390



Ethisterone Usage And Synthesis
Chemical PropertiesOff-White Powder
OriginatorLutocyclin,Ciba
UsesSynthetic progestogen; metabolite of Danazol; intermediate in the synthesis of Spironolactone
DefinitionChEBI: A 17beta-hydroxy steroid that is testosterone in which the 17beta hydrogen is replaced by an ethynyl group.
Ethisterone was the first orally active progestin and is a metabolite of danazol.
Manufacturing Process0.5 part of δ5:6-17-ethinyl-androstendiol-(3:17) is dissolved in 10 parts of dry acetone, the solution is mixed with a solution of 1 part of tertiary aluminum butylate in 40 parts of absolute toluene and the whole is heated to boiling in a reflux apparatus for 21 hours.
After the reaction mixture has cooled it is diluted with 100 parts of ether, the solution is washed with dilute mineral acid and with water, dried and the solvent is evaporated. In this manner there is obtained δ5:6-17-ethinyl-androstene-3-one-17-ol (ethisterone); MP: 270°- 272°C; it may be recrystallized from ethyl acetate.
Therapeutic FunctionProgestin



Ethisterone Usage And Synthesis
Chemical PropertiesOff-White Powder
OriginatorLutocyclin,Ciba
UsesSynthetic progestogen; metabolite of Danazol; intermediate in the synthesis of Spironolactone
DefinitionChEBI: A 17beta-hydroxy steroid that is testosterone in which the 17beta hydrogen is replaced by an ethynyl group.
Ethisterone was the first orally active progestin and is a metabolite of danazol.
Manufacturing Process0.5 part of δ5:6-17-ethinyl-androstendiol-(3:17) is dissolved in 10 parts of dry acetone, the solution is mixed with a solution of 1 part of tertiary aluminum butylate in 40 parts of absolute toluene and the whole is heated to boiling in a reflux apparatus for 21 hours.
After the reaction mixture has cooled it is diluted with 100 parts of ether, the solution is washed with dilute mineral acid and with water, dried and the solvent is evaporated. In this manner there is obtained δ5:6-17-ethinyl-androstene-3-one-17-ol (ethisterone); MP: 270°- 272°C; it may be recrystallized from ethyl acetate.
Therapeutic FunctionProgestin



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.

Boldenone, Oxymetholone, Drostanolone, Testosterone, Nandrolone, Trenbolone    

Designed by   HuishangMedia

Copyright © 2008-2022 J·S Biology Co.,LTD All Rights Reserved 

Design by Huishang Media

  • Online Consultation

    If you have any questions or ask for a quote, please submit your information here and we will respond to you immediately.