Hey Guys,
First time posting here and from what I've seen. Not all Tren Acetate, Tren Enanthate, and Test Propionate that come from other countries be relatively clean. I've been having trouble with crystallization of Tren E and Test P. Both crashed and I've listed a few reasons such as cold temperatures, not enough BA for that particular product, and impurities forming crystals.
I know of a formula for Tren E 125 mg/mL, 3% BA, 15% BB, cottonseed oil. After preparing on water bath and heating, and baking in oven for 20 min. After, formula was vaccuum filtered and set to cool to room temperature. First problem arose because of a temperature change to ~50-60 Farenheit. I wonder if adding more BA would be necessary in this case to stop crystallization because the formula was overdosed by 5-10%. Also I am wondering if a pre-pull of any impurities from the Tren E in a water/nonpolar separation will get rid of these nasty crystals and stop PIP.
Test P was prepared the exact same way, with 5-10% OD, and same low temperature change. Not sure if this is the temperature causing the crystals or impurities, and if so will users benefit from a pre-pull before BA/BB preparation. I am very concerned about the PIP.
My last observation has been for the Tren A, a standard BA/BB formula after filtering resulted in a cloudy mixture. Is this because of impurities in the product prior to preparing the standard formula with heating/baking/filtering? I am also wondering if a pre-pull of any impurities will benefit people trying to avoid PIP.
First time posting here and from what I've seen. Not all Tren Acetate, Tren Enanthate, and Test Propionate that come from other countries be relatively clean. I've been having trouble with crystallization of Tren E and Test P. Both crashed and I've listed a few reasons such as cold temperatures, not enough BA for that particular product, and impurities forming crystals.
I know of a formula for Tren E 125 mg/mL, 3% BA, 15% BB, cottonseed oil. After preparing on water bath and heating, and baking in oven for 20 min. After, formula was vaccuum filtered and set to cool to room temperature. First problem arose because of a temperature change to ~50-60 Farenheit. I wonder if adding more BA would be necessary in this case to stop crystallization because the formula was overdosed by 5-10%. Also I am wondering if a pre-pull of any impurities from the Tren E in a water/nonpolar separation will get rid of these nasty crystals and stop PIP.
Test P was prepared the exact same way, with 5-10% OD, and same low temperature change. Not sure if this is the temperature causing the crystals or impurities, and if so will users benefit from a pre-pull before BA/BB preparation. I am very concerned about the PIP.
My last observation has been for the Tren A, a standard BA/BB formula after filtering resulted in a cloudy mixture. Is this because of impurities in the product prior to preparing the standard formula with heating/baking/filtering? I am also wondering if a pre-pull of any impurities will benefit people trying to avoid PIP.
