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Ethisterone

CAS No.
434-03-7
Chemical Name:
Ethisterone
Synonyms
Progestoral;17A-ETHYNYLTESTOSTERONE;Prone;Pranone;Pregnin;Gestoral;NSC-9565;Prodoxan;Produxan;Prolutol
CBNumber:
CB1207877
Molecular Formula:
C21H28O2
Molecular Weight:
312.45
MDL Number:
MFCD00003656
MOL File:
434-03-7.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-09-12 10:01:08

Ethisterone Properties

Melting point 263-269 °C (lit.)
Boiling point 392.36°C (rough estimate)
alpha D23 +23.8° (dioxane); D25 -32.0° (pyridine)
Density 1.0697 (rough estimate)
refractive index 33 ° (C=1, Pyridine)
storage temp. room temp
solubility Soluble to 0.05 mg/mL (0.16 mM) in DMSO
form Solid
pka 13.10±0.60(Predicted)
color Light yellow to yellow
biological source synthetic (organic)
Water Solubility soluble in chloroform, DMSO (0.05 mg/ml), acetone (slightly ), ethanol (<1 mg/ml at 25°C), and water (<1 mg/ml at 25°C).
Merck 14,3741
BRN 1889895
InChI 1S/C21H28O2/c1-4-21(23)12-9-18-16-6-5-14-13-15(22)7-10-19(14,2)17(16)8-11-20(18,21)3/h1,13,16-18,23H,5-12H2,2-3H3/t16-,17+,18+,19+,20+,21+/m1/s1
InChIKey CHNXZKVNWQUJIB-CEGNMAFCSA-N
SMILES C[C@]12CCC(=O)C=C1CC[C@@H]3[C@@H]2CC[C@@]4(C)[C@H]3CC[C@@]4(O)C#C
CAS DataBase Reference 434-03-7
FDA UNII P201BVY1MJ
ATC code G03DC04
NIST Chemistry Reference Ethisterone(434-03-7)
UNSPSC Code 12352200
NACRES NA.77

SAFETY

Risk and Safety Statements

Symbol(GHS)  Health Hazard (GHS08)Environment (GHS09)
GHS08,GHS09
Signal word  Danger
Hazard statements  H360FD-H410
Precautionary statements  P201-P202-P273-P280-P308+P313-P391
PPE Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
Hazard Codes  Xn,T
Risk Statements  40-48-61
Safety Statements  22-24/25-45-53
RIDADR  UN 2811
WGK Germany  3
RTECS  TU5570250
HS Code  29372390
Storage Class 6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard Classifications Aquatic Acute 1
Aquatic Chronic 1
Repr. 1A
REACH Registrations Active

Ethisterone price More Price(49)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich E1001 Ethisterone ≥99% (HPLC) 434-03-7 25g $277 2026-04-30 Buy
Sigma-Aldrich 1261117 Ethisterone United States Pharmacopeia (USP) Reference Standard 434-03-7 50mg $1140 2026-04-30 Buy
Cayman Chemical 22893 Ethisterone ≥95% 434-03-7 1g $36 2026-04-30 Buy
Cayman Chemical 22893 Ethisterone ≥95% 434-03-7 5g $103 2026-04-30 Buy
Cayman Chemical 22893 Ethisterone ≥95% 434-03-7 10g $153 2026-04-30 Buy
Product number Packaging Price Buy
E1001 25g $277 Buy
1261117 50mg $1140 Buy
22893 1g $36 Buy
22893 5g $103 Buy
22893 10g $153 Buy

Ethisterone Chemical Properties,Uses,Production

Description

Ethisterone is an orally bioavailable synthetic progestin and a derivative of testosterone (Item Nos. ISO60154 | 15645) that binds to progesterone and androgen receptors (EC50s = 23 and 23.1 nM, respectively, in yeast). Ethisterone (1 μM) downregulates progesterone receptors in MCF-7 cells.

Chemical Properties

Off-White Powder

Originator

Lutocyclin,Ciba

Uses

Ethisterone has been used as a component in Dulbecco′s modified eagle medium (DMEM) to culture the transfected COS-7 cell for transient transfection assay andgene transfection assay.

Uses

Synthetic progestogen; metabolite of Danazol; intermediate in the synthesis of Spironolactone

Definition

ChEBI: 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 Process

0.5 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 Function

Progestin

General Description

Ethisterone is aprogestogen. It is a danazol derivative.

Biochem/physiol Actions

Ethisterone acts as a progestational agent. It is consumed by pregnant mothers to prevent miscarriage.

References

[1] L. MCROBB . Structure–activity relationships of synthetic progestins in a yeast-based in vitro androgen bioassay[J]. Journal of Steroid Biochemistry and Molecular Biology, 2008, 110 1: Pages 39-47. DOI: 10.1016/j.jsbmb.2007.10.008
[2] J.M. GLEDHILL . Progesterone receptor induction by danazol in cultured cancer cells and the rat uterus[J]. Journal of Steroid Biochemistry and Molecular Biology, 1992, 43 4: Pages 289-296. DOI: 10.1016/0960-0760(92)90163-d

63-05-8
74-86-2
434-03-7
Synthesis of Ethisterone from Androstenedione and Acetylene
Global( 363)Suppliers
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Spectrum Chemical Manufacturing Corp. 021-021-021-67601398-809-809-809 15221380277 marketing_china@spectrumchemical.com China 9643 60

View Lastest Price from Ethisterone manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Ethisterone pictures 2026-09-12 Ethisterone
434-03-7
$35.00-52.00 99.50% 10g TargetMol Chemicals Inc.
Ethisterone pictures 2026-07-27 Ethisterone
434-03-7
$35.00-52.00 99.50% 10g TargetMol Chemicals Inc.
Ethisterone pictures 2026-05-15 Ethisterone
434-03-7
$1.50 1g 99.0% Min 100 Tons Shaanxi Didu New Materials Co. Ltd
  • Ethisterone pictures
  • Ethisterone
    434-03-7
  • $35.00-52.00
  • 99.50%
  • TargetMol Chemicals Inc.
  • Ethisterone pictures
  • Ethisterone
    434-03-7
  • $35.00-52.00
  • 99.50%
  • TargetMol Chemicals Inc.
  • Ethisterone pictures
  • Ethisterone
    434-03-7
  • $1.50
  • 99.0% Min
  • Shaanxi Didu New Materials Co. Ltd
4,17ALPHA-PREGNEN-17BETA-OL-20-YN-3-ONE 4,17a-pregnen-17b-ol-20-yn-3-one 4,17A-PREGNEN-17B-OL-20-YNE 4-ANDROSTEN-17-ALPHA-ETHYNYL-17-BETA-OL-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 ANHYDROHYDROXYPROGESTERONE ANHYDROXYPROGESTERONE 17BETA-HYDROXY-4,17ALPHA-PREGNEN-20-YN-3-ONE 17b-hydroxy-4,17a-pregnen-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 Ethisterone, 98%, a progestogen hormone being considered to treat prostate cancer pregneninolo 17A-ETHYNYL-4-ANDROSTEN-17B-OL-3-ONE 17a-ethynyl-17b-hydroxy-4-androsten-3-one 17A-ETHYNYLTESTOSTERONE 17ALPHA-ETHYNYLTESTOSTERONE 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(RG) Ethisterone,17α-Ethynyltestosterone, 17β-Hydroxy-4,17α-pregnen-20-yn-3-one, 4,17α-Pregnen-17β-ol-20-yn-3-one ETHISTERONE(RG)(CALL) Ethisterone 0 (17α)-17-hydroxy-pregn-4-en-20-yn-3-one ETHINYL TESTOSTERONE ETHISTERONE ETHYNYLTESTOSTERONE ETHYNYLANDROSTENOLONE (17-alpha)-pregn-4-en-20-yn-3-on Gestoral Lucorteum Oral lucorteumoral Lutidon Oral lutidonoral Lutocyclin Lutocyclol Lutocylol Nalutoral NSC-9565 Nugestoral Ora-Lutin Pranone Pregn-4-en-20-yn-3-one, 17-hydroxy-, (17alpha)- Pregneninolone Pregnin Primolut C primolutc Prodoxan Prodroxan Produxan Progestab Progestin P progestinp Progestolets Progestoral Prolutol Proluton C 17-alpha-ethinyltestosterone 17alpha-Ethynyl-17beta-hydroxyandrost-4-en-3-one