P74 alone: irritable arguments at first, later a good day with my girlfriend

[monesmadedoit]

@still18

It would be nice if you could post a link of the earlier 07’ reports as a reference, you’re not being really helpful in posting assumptions without references.

Tacitus supposedly said 74 was between ANOL and EST, roughly. Now, the structure of EST and ANOL is quite alike. It’s just that the first ring has some double bonds. http://upload.wikimedia.org/wikipedia/commons/0/0c/Estratetraenol_chemical_structure.png

Tacitus:

methoxy. and estrateraenol

we only know a small part of the picture for now Estratetraenol make me, a male, cross eyed giddy with interest in females. OL indicates a hydroxyl group, and male attractant pheromones appear to have the -oh in a key position. In androstenOL this can be shifted to an alpha or beta orientation which have distinct differences in their social effects. Don’t know if estratetraenol allow the alpha/beta positional options. The -ONE indicates a single oxygen in the same position. MEO-Estratetraenon…

P74 is NOT what i expected

i have never tried EST on its own P74, because i used it alone, was pretty raw. it was sharp in that there is no doubt i was affected; nebulous in the way that it caused many different reactions, and i cant honestly say it was just like anything i have tried. it is something extremely upbeat in sweet doses. so,alphanol in that respect; but alphanol is dreamy and buzzy… this was a caffeinated version of that. i personally didnt get an empathy vibe. i cant stress how people seem…

Alpha NOL has a left and right isomer. BNOL, I don’t know. EST could have a Alpha and Beta form or isomers of either. I really don’t know. That’s what he was getting at. I can’t remember IUPAC naming without a Dummies book.

Compare ANOL, in my avatar. I don’t know what EST smells like.