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Stenox also known as Halotestin
(fluoxymesterone), is a halogenated derivative of
17-alpha-methyltestosterone and has an extreme androgenic
effect and a very slight anabolic effect. With this
combination, a person can expect a great increase
in muscle hardness and strength with no real gain
in size or weight. Because of the very high androgenic
effect, many athletes have reported high levels
of aggression making their workouts extremely intense.
A common dosage of Stenox is in the range of 20-30
mg which is between 8 and 12 tablets for a 4-6 week
cycle. At this level an athlete can expect massive
strength gains with a very low tendency of water
and salt retention. Stenox is considered to be the
most toxic oral steroid and has a high rate of side
effect occurrences. This fact has kept most people,
especially women, away from this compound. Stenox
is also very hard on the liver and should never
exceed 30 mg/day. Its strong androgenic characteristics
have been commonly responsible for liver damage,
headaches, irritability, aggressiveness, acne, gastrointestinal
pain, virilization in women, and suppression of
natural hormone levels.
Fluoxymesterone is the
chemical name of active ingredient in Stenox.
Stenox is a registered trademark of Atlantis,
S.A. de C.V. in Mexico and/or other countries.
Stenox Resources
Stenox Pictures
Halotestin Prescribing Information
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Substance name
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Fluoxymesterone [INN] |
| Chemical name |
9-fluoro-11ß,17ß-dihydroxy-17a-methylandost-4-en-3-one
|
| Systematic name |
(8S,9S,10S,11S,13S,14S,17S)-9-fluoro-11,17-dihydroxy-10,13,17-trimethyl-1,2,6,7,8,11,12,14,15,16-decahydrocyclopenta[a]phenanthren-3-one |
| Index name |
Androst-4-en-3-one, 9-fluoro-11,17-dihydroxy-17-methyl-,
(11beta,17beta)- |
| CAS number |
76-43-7 |
| Merck Index Number |
Merck 11, 4113 |
| Molecular formula |
C20-H29-F-O3 |
| Molecular weight |
336.441 g/mol |
| Bioavailability |
Oral: 100% |
| Metabolism |
Hepatic |
| Elimination half-life |
9.5 hours |
| Excretion |
Urinary |
| Pregnancy category |
X |
| Legal status |
Prescription
only (US); DEA Schedule III (US) |
| Routes of administration |
Oral |
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