psilocybin
Rising Star
Any questions or problems you may run into during an extraction can be asked to get other members input in this thread.
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official extraction help thread
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concombres
Rising Star
Bl@ster420 said:
You could try using more naphtha to make the layer easier to separate without pull in in base soup. Shake/roll again a few times with the extra naphtha & pull until you cannot get anymore without basic sludge coming along. Repeat that with a nice thick layer of naphtha.
Combine all naphtha pulls, evap down to ~75ml then freeze precip.
Also, keep at it. Don't worry about failures at first. This is a new skill & I takes time to find good materials & get the process down & get comfortable.
Hell, my first extraction was a success & I had no clue. Was expecting big fat clear crystal shards to freeze precip & threw out probably a whole gram assuming it was lye because it was white powder.
Also, mimosa is very sketch within the u.s. anymore. It is so rare to come by now I wouldn`t be surprised to see mulch from a park passed off as mhrb due to supply being so low & demand being so high.
If this yeilds no DMT Maybe shop around for the best quality acacia you can find & stick with earthwalkers/cybs tek.
locojuiceman
Rising Star
Way better than my first try, good job man...enjoy
locojuiceman
Rising Star
First try? Thats awesome, it took me two, and by the third I had great success
Good job man!
Respect the Spice and Enjoy 8)
[[ Sorry for the double post, accidentally hit ''cancel' yet ... it did not cancel I see ]]
Good job man!
Respect the Spice and Enjoy 8)
[[ Sorry for the double post, accidentally hit ''cancel' yet ... it did not cancel I see ]]
KingsBlade
Rising Star
I am about to attempt this tek and just had a couple questions.. is normal iodized salt ok to use or does it have to be de iodized?
Can a 2lter coke/sprite bottle handle the heating? Or should I find something else?.. this will be my first attempt at making this so if anyone else has tips or anything I'm all ears.. I have a 250g bag of acacia confusa I got. So I wanted to do 100g first as to if I mess up somehow I have extra...
Can a 2lter coke/sprite bottle handle the heating? Or should I find something else?.. this will be my first attempt at making this so if anyone else has tips or anything I'm all ears.. I have a 250g bag of acacia confusa I got. So I wanted to do 100g first as to if I mess up somehow I have extra...
What particular "this" tek?KingsBlade said:
Probably ok, the amount of iodide added is tiny.KingsBlade said:
Don't use plastics, especially not PET. This is discussed often here and mentioned in the "Health and Safety" page (linked at the top of every page) and in the FAQ (also linked at the top of every page).KingsBlade said:
Please make sure you have read at least the FAQ and the health and safety page before asking questions here or attempting any extractions. In addition, it is also advisable to read as many as you can of the "sticky" topics linked at the top of every subforum list. This may seem to cost some time, but in the end it does save you time being puzzled, asking (some times the wrong) questions, waiting for (not always useful) answers and messing up your extraction attempts.
That is a good idea. In fact, maybe you should try it with 50 grams first and expect to get decent results only at your third attempt. Then do the remaing 100g.KingsBlade said:
MOVED
it is normal that after several pull of ipa, sodium remains dark?
how many times I have to do it?
It's possible reuse the dark sodium many time so as not to waste the residue?
During the last evaporation of IPA i had some dark residuo on the bottom, it's safe mix it and use?
It's normal that this goo don't give me absolutely no visual?
Thank You!
it is normal that after several pull of ipa, sodium remains dark?
how many times I have to do it?
It's possible reuse the dark sodium many time so as not to waste the residue?
During the last evaporation of IPA i had some dark residuo on the bottom, it's safe mix it and use?
It's normal that this goo don't give me absolutely no visual?
Thank You!
downwardsfromzero
Boundary condition
What??!!ktz said:it is normal that after several pull of ipa, sodium remains dark?
how many times I have to do it?
It's possible reuse the dark sodium many time so as not to waste the residue?
During the last evaporation of IPA i had some dark residuo on the bottom, it's safe mix it and use?
It's normal that this goo don't give me absolutely no visual?
Thank You!
Pull from what (made from what?), after doing what to it? More detail, please.
downwardsfromzero said:What??!!ktz said:it is normal that after several pull of ipa, sodium remains dark?
how many times I have to do it?
It's possible reuse the dark sodium many time so as not to waste the residue?
During the last evaporation of IPA i had some dark residuo on the bottom, it's safe mix it and use?
It's normal that this goo don't give me absolutely no visual?
Thank You!
Pull from what (made from what?), after doing what to it? More detail, please.
Pull from Sodium Carbonate in the blab tek during the acetate conversion.
The purpose of washing in a sodium carbonate solution is to neutralize any remaining basic material. If there is none then it is unnecessary. However, sodium carbonate is so abundant the bigger question is why would you deviate from the instructions?Pentx said:
If you cannot find any sodium carbonate then go get sodium bicarbonate (baking soda/powder) and bake in the oven at 250-degreesF for an hour or so and magically* transform your sodium bicarbonate into sodium carbonate.
Good luck.
*[of course by magic I mean science]
gamabunta
Rising Star
Hello! I just performed my second extraction and everything seemed well but I have some doubts...
I am now with 3 glass cups, one of them is filled with the results of the first pull and the other two are filled with the results of the second, third and fourth pull.
The first one is already in freeze prep, but the other two I thought it would need an pre evap before I put then in the freezer, that's because they are for sure not saturated enough.
The thing is that it's been 13-14 hours since I left those two cups evaporating and It seems they arent really evaporating, they just stay the same... They are in my bathroom with the window open and with a paper towel on top of them.
Anyone now a better way to evaporate? I'm a bit afraid of using a fan, does it really help? Silica maybe?
Thank you all!
I am now with 3 glass cups, one of them is filled with the results of the first pull and the other two are filled with the results of the second, third and fourth pull.
The first one is already in freeze prep, but the other two I thought it would need an pre evap before I put then in the freezer, that's because they are for sure not saturated enough.
The thing is that it's been 13-14 hours since I left those two cups evaporating and It seems they arent really evaporating, they just stay the same... They are in my bathroom with the window open and with a paper towel on top of them.
Anyone now a better way to evaporate? I'm a bit afraid of using a fan, does it really help? Silica maybe?
Thank you all!
Tryptallmine
Rising Star
gamabunta said:
If you're afraid of using a fan? how are you going to smoalk dmt?
Use a fan. In future you can always combine all your pulls into one dish, evaporate the whole lot down until it's at a high saturation point. Place that dish in the freezer for 24 hours to give it the best amount of time to crystallize - try not to peek at it.
If you want bigger crystals vs small/powdery freebase then use the fridge instead of the freezer as it'll drop the temp at a slower rate. If you want nice big crystals then let the whole thing evaporate naturally in a cool dark spot.
By the way, what solvent did you use? Naphtha evaporates quickly compared to xylene for example but depending on the volume it could still take a day or two. If you evaporate naphtha with a fan you can reduce 200ml down to 100ml in about 20 or so minutes.
gamabunta
Rising Star
Tryptallmine said:If you're afraid of using a fan? how are you going to smoalk dmt?
Use a fan. In future you can always combine all your pulls into one dish, evaporate the whole lot down until it's at a high saturation point. Place that dish in the freezer for 24 hours to give it the best amount of time to crystallize - try not to peek at it.
If you want bigger crystals vs small/powdery freebase then use the fridge instead of the freezer as it'll drop the temp at a slower rate. If you want nice big crystals then let the whole thing evaporate naturally in a cool dark spot.
By the way, what solvent did you use? Naphtha evaporates quickly compared to xylene for example but depending on the volume it could still take a day or two. If you evaporate naphtha with a fan you can reduce 200ml down to 100ml in about 20 or so minutes.
I didn't mean that about the fan. It just didn't seem the best choice not to let the naphtha evaporate naturally, and I don't know if I read somewhere but I always had this negative feeling about using the fan to evaporate faster, don't know if I saw a post about this or something, anyways, It's probably a silly concern haha.
I will take note about combining all my pulls in one dish, it seems better. I just took of the first pull out of the freezer and it looks pretty good! White crystals with some yellow ones in the corner. (pic1 e pic2) Thinking about forgeting the re-x for this one
I moved the other two pulls that were evaporating to a wider dish, read that should evap better. It seems better but after a while the liquid seems more yellow and there are some yellow things in the bottom (pic 3)
I'm using naphtha as solvent, but as it was pretty hard to find any good solvents in here I had to go for the Zippo Premium Fluid.
pic1
pic2
pic3
downwardsfromzero
Boundary condition
The sodium carbonate helps prevent losses by making the ionic strength of the wash solution higher, and ensuring the pH remains sufficiently high. A prudent practice.Pentx said:
QuantumTraveler
Rising Star
Hello Nexians,
After gathering all the materials and quite a lot of research on not only the steps but what the actual steps were preforming SWIM believes he's ready to preform Kash's Advanced LSA TEK. SWIM is substituting the HBWR seeds for HBMG seeds and wanted to know what was a good ratio between subing the two seeds. Also would the amount of acetone need to be increased?
After gathering all the materials and quite a lot of research on not only the steps but what the actual steps were preforming SWIM believes he's ready to preform Kash's Advanced LSA TEK. SWIM is substituting the HBWR seeds for HBMG seeds and wanted to know what was a good ratio between subing the two seeds. Also would the amount of acetone need to be increased?
Dabsallday
Rising Star
So I am trying to a a/b on powdered ACRB... How is it done, I've looked everywhere and can not find it, plus, how do I strain it after my acid boils? I used a wight tee shirt, and after boiling and reducing, when I put it in my extraction container, there was ALOT of material and a slug like stuff on the bottom... Please anyone send me some answers.. Thank you, peace&light to all
TGO
Music is alive and in your soul. It can move you.
Dabsallday said:
Hi, there are all sorts of ways to perform an a/b extraction on ACRB. Have you browsed the WIKI? There is a section with every A/B tek (and every other tek) listed there.
Personally, I've found that the best tek for ACRB is Cyb's Tek with Earthwalker's cleanup steps added. I'll link that one for you below. If you do a bit of searching, you'll find what you are seeking.
ACRB TEK 100g "PICS" (Newbie Friendly)
Good luck!
Dabsallday
Rising Star
I'm more or less asking how to DEFAT, ... And thanks for responding
