Stenbelone

Dtren is somewhat active on UGBB.
He goes through these phases where he's hyper infatuated with a single compound.

First it was tren, then deca only iirc, primo, and now sten.

Give it a few months then he will be raving about something new.
 
Dtren is somewhat active on UGBB.
He goes through these phases where he's hyper infatuated with a single compound.

First it was tren, then deca only iirc, primo, and now sten.

Give it a few months then he will be raving about something new.
why does he do this?
 
Stenbolone, as a stenbolone acetate for i.m. injection, was manufactured and distributed as Anatrofin by Schering AG from Germany in 1961, then by Syntex UK in 1963... According to Duchaine, it was probably last available from Farmacologio Latino as a 25 mg/mL solution – but alas, is no longer commercially available as a pharmaceutical preparation. As recently as July 3, 1991, a MeSH Registry Number given from Merck indicates an active patent and reservation of some potential interest to resume manufacture, however unlikely.

Stenbolone is functionally identical to metenolone (Primo; Rimbolan; as enanthate). Like metenolone, it is an androst-1-ene-3-one. Its 2α-methylation ↓androgenic & ↑anabolic activity and slows rate of ring A reductions, this feature in Δ⁴-3-ketone steroids can be confirmed by urinalysis showing a greater number of metabolic steroid products retaining the Δ⁴-3-ketone system. This structural modification is analogous to 1-alkylation as with metenolone, that results in a ↓androgenic & ↑anabolic activity...

This was Duchaine's sentimental favorite. He refers to its significant erythropoietic activity (like Primo), its being great for cutting, especially for women, and its effective cutting dosage being 100 - 200 mg weekly (3 injections weekly).

Sure sounds a lot like Primo to me!
 
Stenbolone, as a stenbolone acetate for i.m. injection, was manufactured and distributed as Anatrofin by Schering AG from Germany in 1961, then by Syntex UK in 1963... According to Duchaine, it was probably last available from Farmacologio Latino as a 25 mg/mL solution – but alas, is no longer commercially available as a pharmaceutical preparation. As recently as July 3, 1991, a MeSH Registry Number given from Merck indicates an active patent and reservation of some potential interest to resume manufacture, however unlikely.

Stenbolone is functionally identical to metenolone (Primo; Rimbolan; as enanthate). Like metenolone, it is an androst-1-ene-3-one. Its 2α-methylation ↓androgenic & ↑anabolic activity and slows rate of ring A reductions, this feature in Δ⁴-3-ketone steroids can be confirmed by urinalysis showing a greater number of metabolic steroid products retaining the Δ⁴-3-ketone system. This structural modification is analogous to 1-alkylation as with metenolone, that results in a ↓androgenic & ↑anabolic activity...

This was Duchaine's sentimental favorite. He refers to its significant erythropoietic activity (like Primo), its being great for cutting, especially for women, and its effective cutting dosage being 100 - 200 mg weekly (3 injections weekly).

Sure sounds a lot like Primo to me!
Exactly like primo but stronger. A bit more vascularity felt rock hard all the time. I used 50 mg everyday with insulin syringe. I am sure every today is fine also. I would use 100 every other day if you don't want to pin that much.
 
IIR, like some other acetates, you couldn't get it above 25mg/ml without extra solvents. Low concentration + short half life = frequent injections of large volumes.
 
Exactly like primo but stronger. A bit more vascularity felt rock hard all the time. I used 50 mg everyday with insulin syringe. I am sure every today is fine also. I would use 100 every other day if you don't want to pin that much.
I believe that you believe that, but I'm not sure that it is stronger. Prove it.
 
I believe that you believe that, but I'm not sure that it is stronger. Prove it.
Wow ok I used it I am on this forum for years and respected. But anyway it has a much higher anabolic and androgenic ratio. Also you can get a bottle for 50 bucks try it yourself and after four weeks let me know I was right. Comes in 100mg acetate.
 
Stenbolone acetate -100 mgs (molecular code 2-methyl-4,5α-dihydro-δ1-testosterone 17β-acetate (2-methyl-δ1-DHT 17β-acetate) or as 2-methyl-5α-androst-1-en-17β-ol-3-one 17β-acetate)

This agent is a anabolic-Androgen steroid that is a derivative of (DHT) Dihydrotestosterone which its chemical signature (structure) is very similar to that of Masterone or Mesterolone (Proviron), in fact its functionality can be almost identical if one was to compare each compound pound for pound, although its suggested by some that it can perform much like Metenolone (Primobolan depot) or even its molecular structure can be quite similar with its structures altercation, as others may even advocate that its functionality is more similar that that of Oxymetholone (Anadrol). However, that comparison with Anadrol is very miscalculated and would be go against its true functions, as it does NOT possess the ability to be considered a mass builder or act like a wet compound. A great characteristic with Stenbolone is that it cannot be converted to estrogentic metabolites by way of aromatization or displaying estrogenic like effects that could activate mechanisms of actions that would be similar that of estrogenic affects (bloating/water-retention/fat increase or even gynecomastia), thus there is NO need to employ an AI/aromatase inhibitor..

The unvarnished truth is that this AAS is a shrouded compound due to its rare presence in the market. When it was originally compounded/designed in the early 60's it was off the same pillar of 1-Testosterone but modified by the 2-methyl group.. Its said to be slightly weaker than its relative 1-Test when compared by similar dosages, yet its said to be almost 2-3 x its anabolic output when compared on a pound for pound scale..As time continued it was seen to have little clinical use and was ultimately discharged from the market because phrama groups dubbed it useless and financial support was lacking because of other alternative drugs that functioned much similar and already had a name for themselves..This has continued to haunt its survival even there after when it was discontinued but picked up by the black market where it hardly got the recognition and notoriety that it rightful deserves.. Little has known about this agent as the pharmacodynamics of this compounds has been scarce.. Over the years it has been elusive thus even today little is truly known about it in the bodybuilding/athletic performance communities, but for those that have had experience with it all share different concepts about its functionality and maybe this is due to its limited appearance/usage in the anabolic circuit world wide. But for those that have used it during its highlight which was a sort period of time claimed it as a valuable and unique compound, users would often search far and wide to procure this rare performance enhancement drug, before it ultimately seen its fate and faded out of circulation in the start of the 1980's.

Performance enhancement usage: Dosages can range from 50mgs EOD to 100mg EOD of even 100mgs ED, its ability to help athletes remain dry while gaining lean quality muscle makes it ideal to be employed as complimentary/synergistic drug to a cycle combo during a body-recomp, cut phase or even pre-competition.
Aromatization: No
Acne: Yes (based upon user sensitivity)
Desire effects: Physical/mantel wellness improvement, increase sex drive and sense of well-being, improved endurance, strength and faster muscle tissue buildup and regeneration.
Androgenic/Anabolic rating: 107-144 /
 
Wow ok I used it I am on this forum for years and respected. But anyway it has a much higher anabolic and androgenic ratio. Also you can get a bottle for 50 bucks try it yourself and after four weeks let me know I was right. Comes in 100mg acetate.
LOL I literally came to this Notification click expecting "TRY IT YOURSELF BRO," and was not disappointed. Bro, I respect you, I give you 100% of the customary respect owed to anyone that I basically assume is a good bro, which is not insignificant.

Acetate is a no-go for me by default, too much pinning. I'll stick with Rimos.

You're welcome to present us with an idiographic case study, if you want input on good design, I can steer you in the right direction.
 
Stenbolone acetate -100 mgs (molecular code 2-methyl-4,5α-dihydro-δ1-testosterone 17β-acetate (2-methyl-δ1-DHT 17β-acetate) or as 2-methyl-5α-androst-1-en-17β-ol-3-one 17β-acetate)

This agent is a anabolic-Androgen steroid that is a derivative of (DHT) Dihydrotestosterone which its chemical signature (structure) is very similar to that of Masterone or Mesterolone (Proviron), in fact its functionality can be almost identical if one was to compare each compound pound for pound, although its suggested by some that it can perform much like Metenolone (Primobolan depot) or even its molecular structure can be quite similar with its structures altercation, as others may even advocate that its functionality is more similar that that of Oxymetholone (Anadrol). However, that comparison with Anadrol is very miscalculated and would be go against its true functions, as it does NOT possess the ability to be considered a mass builder or act like a wet compound. A great characteristic with Stenbolone is that it cannot be converted to estrogentic metabolites by way of aromatization or displaying estrogenic like effects that could activate mechanisms of actions that would be similar that of estrogenic affects (bloating/water-retention/fat increase or even gynecomastia), thus there is NO need to employ an AI/aromatase inhibitor..

The unvarnished truth is that this AAS is a shrouded compound due to its rare presence in the market. When it was originally compounded/designed in the early 60's it was off the same pillar of 1-Testosterone but modified by the 2-methyl group.. Its said to be slightly weaker than its relative 1-Test when compared by similar dosages, yet its said to be almost 2-3 x its anabolic output when compared on a pound for pound scale..As time continued it was seen to have little clinical use and was ultimately discharged from the market because phrama groups dubbed it useless and financial support was lacking because of other alternative drugs that functioned much similar and already had a name for themselves..This has continued to haunt its survival even there after when it was discontinued but picked up by the black market where it hardly got the recognition and notoriety that it rightful deserves.. Little has known about this agent as the pharmacodynamics of this compounds has been scarce.. Over the years it has been elusive thus even today little is truly known about it in the bodybuilding/athletic performance communities, but for those that have had experience with it all share different concepts about its functionality and maybe this is due to its limited appearance/usage in the anabolic circuit world wide. But for those that have used it during its highlight which was a sort period of time claimed it as a valuable and unique compound, users would often search far and wide to procure this rare performance enhancement drug, before it ultimately seen its fate and faded out of circulation in the start of the 1980's.

Performance enhancement usage: Dosages can range from 50mgs EOD to 100mg EOD of even 100mgs ED, its ability to help athletes remain dry while gaining lean quality muscle makes it ideal to be employed as complimentary/synergistic drug to a cycle combo during a body-recomp, cut phase or even pre-competition.
Aromatization: No
Acne: Yes (based upon user sensitivity)
Desire effects: Physical/mantel wellness improvement, increase sex drive and sense of well-being, improved endurance, strength and faster muscle tissue buildup and regeneration.
Androgenic/Anabolic rating: 107-144 /
Yes, yes, I am familiar with it. The anabolic/androgenic ratings here are based on the Hershberger Assay, a poor method for distinguishing between anabolic & androgenic effects because the levator ani is the dorsal bulbocaverous, a sex organ (responsive to anabolic & androgenic effects), in rat. So they don't predict effects in man.
 
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