needtogetaas
New member
superdrol is described as a cross between Anavar and Masteron but in reality, it is a super-saturated, or 2-reduced, form of Anadrol. Anadrol has a =C-OH at the 2nd position, and if this is totally saturated (reduced) with hydrogen, it gives -CH3. Another way to describe it is that it is a 2a-17a-dimethyl of drostanolone, or Masteron. Masteron has a single methyl group at the 2nd position. Superdrol is a modification of this structure by adding another methyl group at the 17th position. With its inability to aromatize , since it’s already reduced at the 5th position, it cannot make estrogen
(17a-Methyl-etioallocholan-2-ene-17b-ol) also known as DMT is a potent synthetic oral anabolic steroid, first patented in 1961 by Max Huffman of the Lasdon Foundation115. This agent was never made available as a commercial prescription drug product, and saw only limited investigation in the mid-1960's before disappearing into research obscurity. Madol remained hidden in the library bookshelves for decades, until remerging in 2005 as a new "designer steroid" of interest to international sports doping officials. This was due to the confiscation of a sample of DMT at the Canadian border in December of 2003, where it was found in the possession of Canadian sprinter Derek Dueck during a routine vehicle inspection. The DMT sample remained nameless in a Customs warehouse for over a year, until officials from the World Anti-Doping Agency (WADA) finally became involved and had it tested and identified. Madol is only the third never commercially marketed anabolic steroid found to be in use by athletes, following norbolethone and THG.
Unlike its distant cousin methyltestosterone, Madol is unable to convert to estrogen. This means that its use should not impart the normal estrogenic side effects such as increased water retention, fat buildup, or gynecomastia. This makes it an excellent agent to use during lean tissue building cycles, having an effect somewhat along the lines of Winstrol or trenbolone. It can also be used in bulking cycles. It is neither estrogenic nor significantly androgenic. In general, we can say that Madol is functionally far removed from its cousin methyltestosterone, which is known for being a problematic side-effect-producing mass builder and a terrible agent to use during cutting cycles. The one principle side effect it does share with methyltestosterone, however, its hepatotoxicity. One should respect this agent in this regard, and be conservative with its dosage and duration of use as one would any other c-17 alpha alkylated oral. For gains vs side effects madol is perfect.
Something over looked about Dieselbolan/COLOR] is that Madol will increase muscle recovery much faster then with other otc steroids like beastdrol aka superdrol. And has a greater effect on nutrition retention as well. So withmore focused diet and training it will give better results (overall) with less sides.
you do the math. And yes you do have no Idea what you are talking about right now bro. Not trying to be rude but you just don't.
(17a-Methyl-etioallocholan-2-ene-17b-ol) also known as DMT is a potent synthetic oral anabolic steroid, first patented in 1961 by Max Huffman of the Lasdon Foundation115. This agent was never made available as a commercial prescription drug product, and saw only limited investigation in the mid-1960's before disappearing into research obscurity. Madol remained hidden in the library bookshelves for decades, until remerging in 2005 as a new "designer steroid" of interest to international sports doping officials. This was due to the confiscation of a sample of DMT at the Canadian border in December of 2003, where it was found in the possession of Canadian sprinter Derek Dueck during a routine vehicle inspection. The DMT sample remained nameless in a Customs warehouse for over a year, until officials from the World Anti-Doping Agency (WADA) finally became involved and had it tested and identified. Madol is only the third never commercially marketed anabolic steroid found to be in use by athletes, following norbolethone and THG.
Unlike its distant cousin methyltestosterone, Madol is unable to convert to estrogen. This means that its use should not impart the normal estrogenic side effects such as increased water retention, fat buildup, or gynecomastia. This makes it an excellent agent to use during lean tissue building cycles, having an effect somewhat along the lines of Winstrol or trenbolone. It can also be used in bulking cycles. It is neither estrogenic nor significantly androgenic. In general, we can say that Madol is functionally far removed from its cousin methyltestosterone, which is known for being a problematic side-effect-producing mass builder and a terrible agent to use during cutting cycles. The one principle side effect it does share with methyltestosterone, however, its hepatotoxicity. One should respect this agent in this regard, and be conservative with its dosage and duration of use as one would any other c-17 alpha alkylated oral. For gains vs side effects madol is perfect.
Something over looked about Dieselbolan/COLOR] is that Madol will increase muscle recovery much faster then with other otc steroids like beastdrol aka superdrol. And has a greater effect on nutrition retention as well. So withmore focused diet and training it will give better results (overall) with less sides.
you do the math. And yes you do have no Idea what you are talking about right now bro. Not trying to be rude but you just don't.