Hi ,im new here ,made my profile today.
Im a 37 year old Scandinavian With a passion for psychedelics,espessially dmt.

Yesterday i did my first naphta pull from an ACRB extraction (50 g).
I followed cyb`s hybrid salt A/B tek.

I am amazed how good it turned out Lots of white fluffy cryslals and some yellow/brownish. actually it was 800 mg on the firs pull
I think that maybe i have pulled some other tryptamines but not sure yet.
I`ll post some Pictures from the pull her and would love to get some coments on it....since its my first time and all.

Looks like a little base soup (pink colour) got pulled up with your solvent.
A good Re-X or two will clear that up nicely.

Welcome to the Nex

Thanks for Your reply Cyb..
Yes i will re-x it

I was surprised i got such high yield,maybe i was Lucky With the bark, i just ordered some more,the first extraction was basicaly a test to see if i got legit bark. And after smoking it i was convinced

And i made some minor mistakes...like a little to hot waterbath in the acidcook,and i checked the basified solution when i now do the 2 pull and its only 13,3 -i was aming for 14.

Next time i will have it 100%

(the only thing i did diffrent (on purpose)was to use HCi instead of vinegar-just sounds cleaner i Guess).
will post some Pictures from the 2 pull later.

pH 12 or above is adequate so you're ok
Expect anything between 1% and 2% with Acacia (Inc.Goo)
Nice to see some fluff

(Try Max Ion on a small batch...see if it makes a difference)

Congrats!

Looks good. Did you allow the pulls to sit for a while and cool before freezing them? I have not used acacia, but it seems that often a lot of the "goo" will fall out if you let your NP solvent sit for a while, and then you can just siphon it off and freeze to get purer crystals. Still, I'm sure that would smoke just fine as is. Congrats.

Hi, thanks a lot for the coments guys. I apriciate it!!
2 pull is in the freezer now,and i re-x the first pull at the same time....
When i get home from work today i will check out my result

Pictures will be presented

Hi x-ram,do you mean sit for a while in room temp...(how long)?
An do you mean that the goo apears faster than the x-tals so i can remove the goo first(and save that goo, or put it back in the basefied solution for the next pull?

Have a nice day

My understanding is that if you leave it sitting at room temperature for a good while (several hours at least), a lot of the goo will come out of solution and settle at the bottom of the jar. Then you can siphon off the now cleaner naptha and freeze precipitate. You can keep the goo too if you want, it's probably slightly active. Maybe use it for changa?

Here's a link to someone who describes this step and looks to have gotten pretty good results:

https://www.dmt-nexus.me...aspx?g=posts&t=51199

OK..the 2 pull was lots of brown x-tals: 900mg, i have not tried them yet,i want to x them again but they smell sooo wonderful,i can almost hear them say: smoke us...please smoke us,we want to be smoked what is this goodsmelling Brown thing?

The re-x of the first pull that was about 700/800 mg was shrunk to 350 mg...?
But now most of it is pure white lovely spice. IT`S ROCETFUEL...almost got scared from this one. I have only smoked yellow spice before,these whitw x-tals brought something New to the table. I will smoke smaller doses,so intense it almost hurts:cry

And some pics to back it up

looks sweet. ive never seen acrb spice . welcome brother. hope you enjoy your stay

Are you 100% sure you didn't suck up any of the acacia soup along with your solvent when doing your pulls? It looks like you may have, especially if the re-x on your first batch made you lose 50% of the weight. I wouldn't definitely re-x that second batch as well.

I'm glad you are happy with the white stuff

Hi Alert..well i might have shaken the solution to hard when i add the naphta(when pulling)
so the NPS is slightly purple/brownish.So theres probably inpurities there.Ill just swirl it the next time.

Your nps should not be brown when you pull it.
You're using to much lye, shaking too hard and maybe using too much heat.
Too much heat and base will suspend micro particles in the nps that can only be removed by leaving the solvent to stand for some time to let it settle.

Do not smoke that brown stuff...Re-X it till you get you get clean crystals.

Thanks Cyb I will be more gentle with those 3 (lye,shaking,heat) next time(soon).
I was wery careful when i took out the naphta,and pretty sure the basified solution was untuched.
And yes the solvent had a colour to it,and doesnt seem to bee clear.
Allready re-x the brown stuff,put it in the freezer last night-took a sneak peak this morning...it also looked like it was shrunk to 50%,and was light yellow in colour-looks very much like the dmt i used to get from some one else.(before i started making my own gold)
Thanks again for leading me the right way,very kind and helpful..thanks

Yes I re -x the 2 pull and am very happy With the result 900mg to 500mg..
It looks very potent. Either I`ll smoke it like it is, or make one big shiny Crystal of it and give it to my little sis for x-mas

A few pics:

And i have a question about the basified mix..Im not in a hurry, so i do not make multiple pulls on short time. Does it matter that my basified mix is kept at room temp (With a little bit nps) and its days betwen the pulls?

Where did you get that cute little jar from? I'd very much like to get myself a couple of those.

Hi dmt spider..got them on ebay i think,from china

No, doesn't matter, although if nps is left in there for a very long time it may pick up a lot of yellowing, but that's no bad thing.