Hi, i took out the result from my 4`th acrb x-traction from the freeze just now,the re-x that is.(Max ion tek)
I have mixed feelings about it: i dont think it yeilded enough, i made some misstakes,and it tok a long time(and im a fairly pationed guy).
But the spice turned out very good, and i learned some new things.

544mg pure white x-tals.
1062mg a little more sticky slightly coloured x-tals. Total 1606 mg and some black goo i didnt bother to weigh.

Posting some random pictures from the extraction, and i have a few questions as well.
1: The naphta was coloured pink/Purple when i pulled(same colour all 6 pulls) Whats going on or what is it?(wineglass Picture)
2:I got some black goo, what is it? (and can it be smoked?)

How many grams were you extracting from?

The "black" stuff looks like it's got ACRB powder in it. I'd collect and do a quick A/B on it to see what you get out of it.

0.

Looks good..!
Did you try it yet?
Does it feel like mostly DMT... or some NMT efects?

I think from memory Traveling Tommy said it was 300gram Taiwanese ACRB !!

I'm doing same TEK ( max-ion ) later next week with so I've been advised ( nice fresh red pink inner bark ) so I'd like to compare notes when finished !

This latest learning curve , or hot topic , is encouraging news concerning confusa as many ppl are getting goo and goo only ( goo is good ) and with the sharing of info I think things are only going to get brighter , so let's put on the shades and lets get sharing !

Yes, it was 300g(two vessels with 150g each). I was to quick to use it as a drain cleaner, i was so sure it was all good after the six pulls, should have waited to see the results first. Lesson learned.I did some misstakes, like i did not use enough water in the salting step-but there simply was not Space enough in the wessels,so the mixture was to thick and i used citric acid instead of HCl as i always did before(i dont really know it was a misstake to use citric acid but im going back to HCl anyway)...I only got +0,5% yeild. Use to get more.
Im sure it was much left.

TT

There might still have been solvent in the jar that had not seperated yet from the basic mixture. I now know that I used to toss away lots of naptha that had not seperated from the basic soup but i couldnt tell. It wasnt until my friend shined a flashlight on my jars that i could see that there was still TONS of naptha still left in a jar that i would have otherwise just dumped.

I no there's a few posts about how the acacia is slower to release the DMT , but using the flashlight " tip " . They should be shared I one place like here https://www.dmt-nexus.me...aspx?g=posts&t=52368 sorry I don't no how to hyper link yet ! Lol