A4011312
Ethisterone , ≥98% , 434-03-7
Synonym(s):
17α-Ethynyltestosterone;17β-Hydroxy-4,17α-pregnen-20-yn-3-one;4,17α-Pregnen-17β-ol-20-yn-3-one
CAS NO.:434-03-7
Empirical Formula: C21H28O2
Molecular Weight: 312.45
MDL number: MFCD00003656
EINECS: 207-096-5
Pack Size | Price | Stock | Quantity |
1G | RMB31.20 | In Stock |
|
5G | RMB111.20 | In Stock |
|
25G | RMB288.80 | In Stock |
|
100G | RMB888.00 | In Stock |
|
others | Enquire |
Update time: 2022-07-08
PRODUCT 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 |
pka | 13.10±0.60(Predicted) |
form | Solid |
color | Light yellow to yellow |
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 |
InChIKey | CHNXZKVNWQUJIB-CEGNMAFCSA-N |
Description and Uses
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.
Synthetic progestogen; metabolite of Danazol; intermediate in the synthesis of Spironolactone
Safety
Symbol(GHS) | GHS08,GHS09 |
Signal word | Danger |
Hazard statements | H360FD-H410 |
Precautionary statements | P201-P202-P273-P280-P308+P313-P391 |
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 |