What is Easiest Way to Make a Finaplix Preparation?

Hi Bill, what’s the simplest safe way to make a Finaplix preparation?

A) To each 100 pellets — nominally 2 g of trenbolone acetate — add 38 mL of Wesson oil in a sterile container such as a large vial and either stir overnight with a magnetic stir bar or employ a sonicator until the pellets have fully broken down. If there is much time and patience, simple occasional shaking or swirling can suffice. Moderate heat may be employed such as 45-50 C (113-122 F.) Don’t “cook.”

If the only means of maintaining a warmed temperature is use of an oven that has a warming setting such as 140 F, this is acceptable but there may be slight extra oxidation of the trenbolone acetate as a result, yielding a touch of brownness to the product. This doesn’t seem to hurt results.

It is helpful to vent the vial, for example by inserting an insulin syringe without its plunger into the septum. If this is not done, expansion of warmed air may blow the stopper out.

Allow to settle. Filter clear portion through an 0.45 micron filter. If desired, add benzyl alcohol as a last step, 0.8 mL per 2 g (nominal) of trenbolone acetate.

This results in a 50 mg/mL preparation, which ought to be satisfactory. Having higher mg/mL doesn’t mean greater performance, and with trenbolone acetate it seems to me that prevalence of post-injection coughing is considerably worse with higher mg/mL trenbolone acetate preparations than it is when this formulation is used.

About the author

Bill Roberts

Medicinal chemist

Bill Roberts is an internationally-recognized expert on anabolic steroids and performance-enhancing drugs (PEDs). He received a bachelor degree in Microbiology and Cell Science and completed the educational and research requirements for a PhD in Medicinal Chemistry at a major American university.

Bill entered the nutritional supplement industry prior to completing his doctoral thesis but his education was invaluable so far as being able to design/improve nutritional supplement compounds, since it was in the field of designing drug molecules and secondarily some work in transdermal delivery.

His education was not specifically "geared" toward anabolic steroids other than expertise with pharmacological principles having broad applications. This has allowed Bill to provide unique insight into the field of anabolic pharmacology with knowledge of points which he would not have known otherwise.