| Identification | More | [Name]
4-Chlorotestosterone acetate | [CAS]
855-19-6 | [Synonyms]
4-ANDROSTEN-4-CHLORO-17BETA-OL-3-ONE 17-ACETATE
4-ANDROSTEN-4-CHLORO-17-BETA-OL-3-ONE ACETATE
4-chloroandrost-4-ene-17beta-ol-3-one acetate
4-CHLOROTESTOSTERONE ACETATE
CLOSTEBOL ACETATE
STERANABOL
TURINABOL
4-chloro-17-beta-hydroxy-androst-4-en-3-onacetate
anabolit
chlorotestosteroneacetate
macrobin
megagrisevit
stearanabol
sterabol
test-anabol
testomed
Clostebolacetat
4-Chloro-3-oxo-androst-4-en-17 β-yl acetate
17β-Acetoxy-4-chloroandrost-4-en-3-one, 4-Chloro-17β-hydroxy-4-androsten-3-one 17-acetate, 4-Chlorotestosterone 17-acetate | [EINECS(EC#)]
212-720-4 | [Molecular Formula]
C21H29ClO3 | [MDL Number]
MFCD00079075 | [Molecular Weight]
364.91 | [MOL File]
855-19-6.mol |
| Hazard Information | Back Directory | [Hazard]
A poison by ingestion. A reproductive hazard. | [Originator]
Clostebol acetate,Hunan Steroid | [Uses]
Clostebol acetate is an anabolic steroid.
This is a controlled substance. | [Definition]
ChEBI: Clostebol acetate is a steroid ester. | [Manufacturing Process]
15 g of a mixture of 4β,5-epoxy-etiocholane-17β-ol-3-one and 4β,5-epoxyandrostane-17β-ol-3-one, dissolved in 375 ml chloroform, are treated with a
stream of gaseous HCl at room temperature for about 2 h. The chloroform
solution is neutralized with a sodium bicarbonate solution, washed with water
and dried. The residue is crystallized from benzene or aqueous methanol and
9 g of needle-shaped crystals of 4-chloro-testosterone, melting point 186°-
188°C, are obtained. Upon concentrating the mother-liquor, 3.2 g of this
product, melting point 180°-184°C, are covered.
1 g 4-chloro-testosterone are acetylated with 1 ml acetic anhydride and 5 ml
pyridine at room temperature for 16 h. Ice is added to the solution, and the
precipitate is filtered off and recrystallized from chloroform-ethanol; 1 g 4-
chloro-testosterone-acetate, melting point 228°-230°C, is obtained. | [Therapeutic Function]
Anabolic |
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