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Old 10-06-09, 14:15   #1 (permalink)
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Extraction, "Erowid Tek"

FOAF have been drying some shrooms on a CaCl2 chamber, but now he saw that the CaCl2 is very old (almost liquid) so he canīt recover it =/
Because of it, some shrooms on drying process get cobweb
He had dunk the shrooms in a H2O2 solution and put it in front of a fanner.
2 days left, they was pratically cracker dry, so he had decided to do a extraction process wich he had saw

Solvents: Pure Metanol (P.A)
Little amount of Anidrous Etanol, ascorbic acid and vinegar =]

extraction-erowid-tek-extract-005.jpgextraction-erowid-tek-extract-007.jpgextraction-erowid-tek-extract-008.jpgextraction-erowid-tek-extract-009.jpg

Right now
Turbilhão.avi
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Old 10-06-09, 14:17   #2 (permalink)
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Good luck, hope it works!! :-)
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Old 10-06-09, 14:43   #3 (permalink)
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That sounds pretty cool Here is a reminder of the safety data for methol.

Safety data for methyl alcohol


Click here for data on methyl alcohol in student-friendly format, from the HSci project
Glossary of terms on this data sheet. The information on this web page is provided to help you to work safely, but it is intended to be an overview of hazards, not a replacement for a full Material Safety Data Sheet (MSDS). MSDS forms can be downloaded from the web sites of many chemical suppliers.
General

  • Synonyms: methanol, carbinol, colonial spirit, columbian spirit, methylol, methyl hydrate, wood alcohol, wood naphtha, wood spirit, methyl hydroxide, pyroxylic spirit, RCRA waste number U154, meths
    Molecular formula: CH3OH
    CAS No: 67-56-1
    EC No: 200-659-6
    Annex I Index No: 603-001-00-X
Physical data

Appearance: colourless liquid with a characteristic odour
Melting point: -98 C
Boiling point: 64.7 C
Vapour density: 1.1
Vapour pressure: 97.7 mm at 20 C
Specific gravity: 0.791
Flash point: 11 C
Explosion limits: 6% - 36 %
Autoignition temperature: 464 C

Stability

  • Stable. May react violently with acids, acid chlorides, acid anhydrides, oxidizing agents, reducing agents and alkali metals. Protect from moisture. Highly flammable.
Toxicology

Toxic by inhalation, ingestion or skin absorption. May be a reproductive hazard. Ingestion may be fatal. Risk of very serious, irreversible damage if swallowed. Exposure may cause eye, kidney, heart and liver damage. Chronic or substantial acute exposure may cause serious eye damage, including blindness. Irritant. Narcotic. UK exposure limits: long-term 200 ppm, short term 250 ppm.
Toxicity data
(The meaning of any abbreviations which appear in this section is given here.)
ORL-HMN LDLO 428 mg kg-1
ORL-MAN LDLO 6422 mg kg-1
UNR-MAN LDLO 868 mg kg-1
ORL-RAT LD50 5628 mg kg-1
IHL-RAT LC50 83 mg/l.
IPR-RBT LD50 1826 mg kg-1
IPR-RAT LD50 9540 mg kg-1
ORL-MUS LD50 7300 mg kg-1

Risk phrases
(The meaning of any risk phrases which appear in this section is given here.)
R11 R23 R24 R25 R39.

Transport information

  • (The meaning of any UN hazard codes which appear in this section is given here.)
    UN No 1230. Packing group II. Hazard class 3 (6.1)
Personal protection

Safety glasses. Effective ventilation. Within the UK this material must be assessed under the COSHH regulations.
Safety phrases
(The meaning of any safety phrases which appear in this section is given here.)
S7 S16 S24 S36 S37 S45

[Return to Physical & Theoretical Chemistry Lab. Safety home page.]
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Old 10-06-09, 14:59   #4 (permalink)
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Ow, thanks bro (I saw it, but itīs always good to have in mind) =]
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Old 10-06-09, 21:45   #5 (permalink)
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Quote:
Originally Posted by P4ulada View Post
FOAF have been drying some shrooms on a CaCl2 chamber, but now he saw that the CaCl2 is very old (almost liquid) so he canīt recover it =/
Because of it, some shrooms on drying process get cobweb
He had dunk the shrooms in a H2O2 solution and put it in front of a fanner.
2 days left, they was pratically cracker dry, so he had decided to do a extraction process wich he had saw

Solvents: Pure Metanol (P.A)
Little amount of Anidrous Etanol, ascorbic acid and vinegar =]

Attachment 143739Attachment 143740Attachment 143741Attachment 143742

Right now
Attachment 143743

What do you do with it after the soak?



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Old 10-07-09, 07:49   #6 (permalink)
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Uh, filter the ppt ^^
I have a doubt: My alkaloids are in solution or is this the crystals?

Iīll keep both, if itīs the white solid Iīll filter and recrystalize, if donīt Iīll do a cromatographic colunm ^^
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Old 10-07-09, 12:18   #7 (permalink)
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Finally!!

Finally a serious discussion on this subject!
At least I hope so.

It appears from the nature of your posts that you have ready access to lab or lab-grade apparatus.
So you will be able to do chromatography and quantify the results??
We might actually be able to put psilocin/psilocybin diy extractions to bed for good!
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Old 10-07-09, 12:19   #8 (permalink)
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If you reflux that gently for about 4 hours, you'll get much better results. You can use an old coffee percolator with some ice on top as a reflux condenser.

Just be careful, because psilocybin crystals oxidize very easily when exposed to air. I had a batch that was only good for a couple hours once, although it was very clean.
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Old 10-07-09, 15:13   #9 (permalink)
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Quote:
Originally Posted by Myc View Post
Finally a serious discussion on this subject!
At least I hope so.

It appears from the nature of your posts that you have ready access to lab or lab-grade apparatus.
So you will be able to do chromatography and quantify the results??
We might actually be able to put psilocin/psilocybin diy extractions to bed for good!
Yes, maybe I can do it


Quote:
Originally Posted by Thre365ive View Post
If you reflux that gently for about 4 hours, you'll get much better results. You can use an old coffee percolator with some ice on top as a reflux condenser.

Just be careful, because psilocybin crystals oxidize very easily when exposed to air. I had a batch that was only good for a couple hours once, although it was very clean.

185-195° C (Crystals from methanol)
Shit, I have no time this week for read the article (http://www.erowid.org/references/ref...DocPartID=5939)

But I think I can reflux it with no problems. With an ice bath Iīll not pass for 100.C, as the psilocybin melting point is around 190.C it isnīt a problem.

My doubt is: The alkaloids are in solution or are the crystals? I have no way to analyse it ATM =/

Thanx for the advices
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Old 10-07-09, 15:29   #10 (permalink)
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Originally Posted by P4ulada View Post
185-195° C (Crystals from methanol)
Shit, I have no time this week for read the article (http://www.erowid.org/references/refs_view.php?A=ShowDocPartFrame&ID=6379&DocPartID =5939)

But I think I can reflux it with no problems. With an ice bath Iīll not pass for 100.C, as the psilocybin melting point is around 190.C it isnīt a problem.
Well, according to Wikipedia (I know, not the best source, but I think we can trust it on this one) methanol's BP is 64.7 C or 148.4 F. It just can't get to 100 C unless you superheat the vapors. Just make sure to dry the methanol with MGSO4 first.

And make sure to buy a couple bags of ice. Running out in the middle of a reaction is a son of a bitch that you don't wanna deal with.

Quote:
My doubt is: The alkaloids are in solution or are the crystals? I have no way to analyse it ATM =/
Huh? The alkaloids are the crystals. They should still be in solution as long as you don't evaporate the solvent.
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Old 10-07-09, 19:18   #11 (permalink)
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The crystals? Right hehe
Iīll re-crystalize it with pure ethanol, just to keep safe of metanol traces...
Thinking on recover all I can to the solution...letīs go huhu letīs see what happens ~^

Thanks for the help
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Old 10-07-09, 20:07   #12 (permalink)
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there is a great thread on this its the PF TEK "crystals of the gods" i cant post it here because its from another forum and i sont want to disrespect hippe or any other Mods soo with that said feel free to pm me or send me an e-mail at klosetbreeder@hotmail.com
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Old 10-07-09, 21:13   #13 (permalink)
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Nice bro, thanks for the help
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Old 10-09-09, 22:36   #14 (permalink)
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Updates?



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Old 10-10-09, 00:45   #15 (permalink)
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Quote:
Originally Posted by P4ulada View Post
The crystals? Right hehe
Iīll re-crystalize it with pure ethanol, just to keep safe of metanol traces...
Thinking on recover all I can to the solution...letīs go huhu letīs see what happens ~^

Thanks for the help
I would add some ethanol to the methanol solution and slowly evap the methanol off. You should be able to smell when it's gone, methanol is disticntly sweet. Methanol's BP is also lower than ethanol. Go maybe 10-20 ml past the point where you can smell the methanol is gone and you should be good.


Disclaimer: I am drunk. I could be completely wrong, and in this case it could kill you if I were. At the moment, I do think the theory is sound, though.
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Old 10-10-09, 08:47   #16 (permalink)
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hueauheah nice bro
I think I donīt like to smell metanol =P
Iīm planning to use a vacuum to take of the metanol, so I can add some ethanol, to keep it safe from to much water/O2.

Soliver, itīs on freezer, just because Iīve to travel right now
When I come back Iīll filter it, wash one more time (extracting from the filter paper) and then Iīll store it on ethanol, before the test drive =P
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Old 10-10-09, 11:22   #17 (permalink)
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Quote:
Originally Posted by Thre365ive View Post

Huh? The alkaloids are the crystals. They should still be in solution as long as you don't evaporate the solvent.
All the crystals I've managed to get out of solutions have been sugars. Tasted sweet but conferred no trip. They form as the solvent evaps off, and I filtered them out but did not evap all the solvent since I was using Everclear and wanted to keep the magic in solution due to it's shorter shelf life if exposed to oxygen. I guess more crystals may have formed had I evapped the rest of the solvent, but for me the first batch of crystals that precip out have always been sugars.
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Old 10-13-09, 13:28   #18 (permalink)
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oh =/
itīs because the total evaporation of the crystals?
I heard that theyīre ultra sensible to O2...Iīll be carefully.
Iīm planning on evapp the solvent under vacuum, so O2 isnīt too problematic with this procedure.
Letīs see what happens...I have no sure of nothing yet hehe
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Old 10-13-09, 14:50   #19 (permalink)
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SWIM can confirm the crystals are not active, but the brownish goo that is left on them is. However, that goo degrades very quickly without staying dissolved in at least a small amount of alcohol.
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Old 10-13-09, 17:36   #20 (permalink)
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Originally Posted by whatchamacallit View Post
SWIM can confirm the crystals are not active, but the brownish goo that is left on them is. However, that goo degrades very quickly without staying dissolved in at least a small amount of alcohol.
Nice too read it
Iīll let it on solution =]

Thanx
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Old 10-16-09, 19:49   #21 (permalink)
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All the crystals I've managed to get out of solutions have been sugars. Tasted sweet but conferred no trip. They form as the solvent evaps off, and I filtered them out but did not evap all the solvent since I was using Everclear and wanted to keep the magic in solution due to it's shorter shelf life if exposed to oxygen. I guess more crystals may have formed had I evapped the rest of the solvent, but for me the first batch of crystals that precip out have always been sugars.
My experience as well.

I evap'd crystals from everclear completely once. No dice.
Even logged into chat and smoked a bowl of them, by request
from a member (I think I've been in chat three times in my life).

All the chem talk makes me wonder if this process is any different,
in the long run, than the simple everclear soak?

Too late either way, it sounds, as you can't ingest that stuff without
cleaning it up, but one more voice in the hall certainly can't hurt

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Old 10-16-09, 19:58   #22 (permalink)
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Hey y'all - Found this - http://www.lycaeum.org/mv/mu/pkeffec...xtraction.html - looks very straightforward.
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Old 10-16-09, 20:22   #23 (permalink)
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Old 10-16-09, 23:04   #24 (permalink)
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Hey y'all - Found this - http://www.lycaeum.org/mv/mu/pkeffect/_pkeffect_psilo_extraction.html - looks very straightforward.
Wow, thanx bro! Nice tek they have there ^^
Thank you so much =]

Hey Soliver, if it was extracted by everclear you can ingest without clean, but not if it was extracted by methanol...
I thinks if you smoke it you can degrade the magic, psilocybinīs melting point is around 190.C, but itīs is teorically... =P
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Old 10-16-09, 23:35   #25 (permalink)
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thanx for that!!!!!
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Old 10-17-09, 07:37   #26 (permalink)
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Hey y'all - Found this - http://www.lycaeum.org/mv/mu/pkeffect/_pkeffect_psilo_extraction.html - looks very straightforward.

Weird. I'm skeptical; if that was published in 2003 and he vaporized Everclear-extracted crystals and says they produced a comparable rush to DMT, then why aren't we all vaporizing our mushroom extracts here in 2009?

Unless psilocybin tastes just like sugar, my Everclear extracts aren't working if I take them all the way to dry crystals.
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Old 10-17-09, 07:41   #27 (permalink)
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Quote:
Originally Posted by Soliver View Post
Even logged into chat and smoked a bowl of them, by request
from a member (I think I've been in chat three times in my life).


That's taking one for the team! How did your pipe or whatever taste after smoking sugar through it?

I'm not really into chat rooms either. It's too easy for me to get talked into something on the spur of the moment that I would most likely regret later...
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Old 10-17-09, 10:35   #28 (permalink)
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hi guys .
for the record,the tek @ erowid does in fact work.
it was performed in my kitchen.
simple evevclear hot water bath,extracts combined,reduced
to around 60-100ml ,placed in the freezer,and little cube shaped crystals
fell out.
i am summarizing here.also,the results were vaporized,in a glass pipe(dmt style)

here follows the full link,and some comments from dr shulgin on the matter.
just trying to get accurate info on the subject out there.

http://deoxy.org/wiki/Mushrooms/Alkaloid_Extraction

oh yeah,forgot to mention,i think the reason fro the very good results experienced,was due to the fact that
the solvent(puregrain) was never evapped completely.the crystals were plucked out of the solution,then used.

peace.
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Old 10-17-09, 11:41   #29 (permalink)
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Question

hmm...i just read your post a little more carefuly there t.v.
sounds like you were doing the same way.
i suppose there is an ''x factor" somewhere here.
i dont know.im no where close to being properly versed in chemistry.
but i do know that the crystals that were harvested from this
outing back in 03 were active.
certainly makes me scratch my head to...

hmmm...
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Old 10-18-09, 17:40   #30 (permalink)
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Quote:
Originally Posted by Achtwan View Post
the solvent(puregrain) was never evapped completely.the crystals were plucked out of the solution,then used.

peace.
Must be a ghost in the machine somewhere, for I did the exact same thing
and nothing happened whatsoever.

I guess this comes down to an essential question:

Are those crystals psilly, or are they sugars? Mine certainly seem to have
been, and continue to be, sugars.

Why yours were active, and why the
psilly seems to have been active beyond its (perhaps arguable) degradation
point, thermally speaking, is anyone's guess, but until I hear more folks
reporting success using this tek, I say "bunk."

Not that this is scientific proof by any stretch, but it would seem to me that
if a "DMT like" experience was available to the home shroom grower
without all that annoying DMT basing / acidifying / extraction mess, then
we'd have heard more voices on it by now?

Hmmm...



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