Perhaps they used a process to burn out any impurities. Michael mentioned a long while back they had refined A314 special version and the difference was so much smoother. Not a chemist, but there are obvious ways they can refine a process.
I wonder if Androtics uses a centrifuge to refine P88?
It may be worth it if Androtics came out with a “Refined” line of products. From your reviews A314 ultrafine seemed to be a damn good product.
It would be worth the extra money.
Sometimes I wish Androtics would move faster in meeting the demands and suggestions of its consumers. However, I understand the financial constraints that Androtics is under.
I doubt that a centrifuge is used to refine anything that they sell. Such a process would be relatively simple and I would think that the chemists themselves would do such a thing in the first place.
I wonder if the molecules can be refined by separating different stereoisomers of the same compound? I never thought about it, but I bet the mixtures are racemic.
Huh? Why not use a centrifuge? Mechanical separation bydifference in density (particles & drops) is done by sedimentation, decanter, demister and centrifuge.
Right, but that type of purification is cheap and easy to do. As androtics sources (sourced) from some of the best chemists, I have no doubt that if a centrifuge could be used to increase purity that it was done. I can’t see a reason that it wouldn’t have been done.
Ok Hammer. The original statement and question was:
Thanks for your input. I am seeking a working knowledge of this process. I appreciate your input but I am looking for a different answer than the one you are providing. Take care
you purify p88 you should have p93. Jasmins explanation of p88 was that it was a rough synthesis and p93 was a stricter lab procedure to return a purer yield of that molecule. P88 was said to have active impurities as a result of this rough synthesis. If its an impurity its in such a small amount along with who knows what other impurities active or inactive are in there.
What you should really be asking is why dont they identify that “impurity” and make it.
The problem with the rough synthesis as explained by jasmin is that its not always repeatable.
Many molecules exist in right-hand and left-hand versions. Many synthetic pathways will give one a mixture of right and left while others can give one or the other. Biology tends to favor the right or dextro over the left or levo arrangements.
An example is amphetamine - the mixture. More biologically active on a pure molecule basis is the right-hand version, Dexadrine or dextro-amphetamine. Most amino acids and right handed.