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Query for good entry point into chemistry by Simon Hommermere - Fri, 28 Oct 2016 13:21:20 EST ID:g4yJTuN/ No.78329 Ignore Report Reply Quick Reply
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I've always wanted to stick my nose into chemistry and now I have some spare time to do it, so I wanted to ask,
does anyone have a recommendation on good material/literature to start out with?
4 posts omitted. Click Reply to view.
Nicholas Callystit - Wed, 23 Nov 2016 17:35:44 EST ID:yW0mpyp1 No.78365 Ignore Report Quick Reply
becoming a chemist is different than just learning how it works. I'm not op but i'd love to learn chemistry and how it works, but I don't really care to perform it beyond basic kitchen chemistry level extractions and such
Edward Brommerhud - Tue, 06 Dec 2016 23:12:53 EST ID:dBr1KR5d No.78384 Ignore Report Quick Reply
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Read this book its on sciencemadness library somewhere.
Doris Hellyfuck - Wed, 07 Dec 2016 23:54:51 EST ID:g4yJTuN/ No.78387 Ignore Report Quick Reply
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Thanks for the pointers!

This is not really serious enough to warrant that. This is more something productive to do for fun instead of blunting my brain with those animoos and games. Checked out Zumdahl though, seems just right for my way of learning.

Actually found that one while browsing chemistry torrents, I love how far away it is from modern learning literature.
Jack Pankinstod - Mon, 12 Dec 2016 12:22:14 EST ID:klMiQ9iI No.78399 Ignore Report Quick Reply
I suppose you could go online and find an old chemistry text book and purchase that? That would be a good entry point anyway, instead of jumping right in and mixing a bunch of shit together in your kitchen
Schepperschop - Wed, 14 Dec 2016 17:50:14 EST ID:xTIigKo1 No.78403 Ignore Report Quick Reply
Heat food>>>does this taste better>>>why>>>chemistry

Anhydrous Ethanol/Methanol by Sidney Hangertack - Fri, 18 Nov 2016 13:57:09 EST ID:zsw9I8fO No.78350 Ignore Report Reply Quick Reply
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How do I go about using something like this (pic) to make anhydrous ethanol or methanol?
3 posts and 1 images omitted. Click Reply to view.
Bombastus !uYErosQbLM!!Mybq1UbK - Fri, 02 Dec 2016 23:46:27 EST ID:pAeLmaqn No.78380 Ignore Report Quick Reply
You can literally just buy ethanol denatured with methanol.

Also. Why do you need anhydrous ethanol.
Reuben Seshman - Sun, 04 Dec 2016 21:49:44 EST ID:DPjhXpIm No.78381 Ignore Report Quick Reply
Fuck the whole benzene bullshit that's retarded. Listen. Epsom salt, magnesium sulfate. you get it at walmart. It's in its unhydrated form. You put it in azetrope ethanol in equal molar amount as the remaining volume of water in there and the crystals will turn into the hydrate form. You filter that shit out and youve got your 200 proof. The alcohol is so hydrophilic that it will take in water from the air, so when you store it, you want to keep some excess salt in the bottom and just filter it out when it's time to use it. Yer welcum
Lydia Bruckleson - Thu, 08 Dec 2016 00:50:58 EST ID:0hQQ6mKi No.78388 Ignore Report Quick Reply
If you're going to use sieves (like something in your picture), it won't be too hard, if you have them sealed in their original container. Otherwise, they're probably already 'wet' and have to be heated to very high degrees to give up their moisture. Just take the dry sieves, and put them into 95% ethanol.

Depending on your tech level, you might want to set up a distillation apparatus and put some more sieves, or magnesium strips, or CaO or Whatever in the path of the vapor.

Some beverage distillers actually use dried plant material from the original grain in the distillation column to pick up water, and then mix it back into the mash.
Fanny Fibblelut - Thu, 08 Dec 2016 21:24:39 EST ID:fcvYqiwy No.78389 Ignore Report Quick Reply
Yeah I can't find a single image example online of the molecular sieves in use, nor any how-to guides.
So that's basically it though, just vaporize some ethanol/water and send it in the path of the sieves?
Or just mix the sieves in with it?

And yeah, I could try MgSO4 too.
Bombastus !uYErosQbLM!!Mybq1UbK - Sat, 10 Dec 2016 18:12:24 EST ID:01P1ms0Q No.78392 Ignore Report Quick Reply
Just fucking buy it. No don't do that with the sieves. If the sieves work, they work, if they don't, they don't.

You can use anhydrous copper sulfate (white) and it'll turn blue in the solution. Keep adding copper sulfate until no more turns blue.

Or you could just buy anhydrous ethanol which is often cheaper than anhydrous copper sulfate and molecular sieves.

DXM Purification by Violeta00 - Thu, 03 Nov 2016 21:26:09 EST ID:HfyaiY9o No.78336 Ignore Report Reply Quick Reply
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Hello all,

I am interested if knowing the method for purifying DXM from over the counter medication. I have read that such a method exists and would like to learn more about it. I have some basic experience with chemistry and access to laboratory equipment. Could anyone please share the methodology and the background information? Thanks.
press - Fri, 04 Nov 2016 17:11:58 EST ID:aoZYWjFW No.78337 Ignore Report Quick Reply
what kind of preparation of DXM will you be using?
David Mullerpon - Sun, 04 Dec 2016 22:54:13 EST ID:p03PvWLe No.78382 Ignore Report Quick Reply
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1) Dump lighter fluid and ammonia in with syrup in a plastic bag (ziploc nigga.)
2) Agitate nigga agitate then let layers completely separate before cutting a tiny hole in the corner of the bag and draining the heavier syrup/ammonia and leaving the delicious dxm lighter fluid.
3) Now put the lighter fluid in another bag with an aqueous citric acid mixture (aka lemon/lime juice), agitate more and wait for full separation again.
4) The heavier layer is now dxm hydrocitrate, drain and save that while discarding the lighter fluid
5) You know have a purified dxm solution! Whee!

Notes (aka how to not get yourself killed):
  • Lighter fluid and ammonia should NOT be adulterated. USE UNSCENTED AMMONIA. Let a small amount of lighter fluid evaporate on a mirror. If it leaves a residue DON'T USE IT.
  • Don't use cough syrup with additional ingredients like acetominophen, guaifesan, etc. These are NOT guaranteed to be removed from the final solution. Even using DXM HBr is questionable at best.
  • It is advised to perform the first separation multiple times, except you add water to the lighter fluid to collect any leftover soluble products then drain the water.
  • It is additionally advised to heat the dxm hydrocitrate solution after the second extraction, in order to allow any potential ammonia/lighter fluid to evaporate. There shouldn't be any but you're putting this shit in your body so you should be fucking careful.
  • Ammonia and lighter fluid are dangerous, don't blow yourself up and perform this extraction in a well ventilated environment.

Personal Notes (I wouldn't be writing this shit if I hadn't tried it myself):
  • DXM hydrocitrate seems to denature relatively quickly. When left for even a day the resulting trip is signficantly weaker and a bit different.
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Bombastus !uYErosQbLM!!Mybq1UbK - Wed, 07 Dec 2016 00:26:09 EST ID:MzxQ4oNO No.78385 Ignore Report Quick Reply
Buy DXM from research chemical sites?

Anti-Radiation WIFI Antennas by Hugh Noblingson - Tue, 23 Aug 2016 16:39:24 EST ID:zsw9I8fO No.78166 Ignore Report Reply Quick Reply
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Is this legit? What evidence do we have to backup that there's dangerous radiation coming from wifi antennas?

13 posts and 2 images omitted. Click Reply to view.
Molly Nollerlock - Sun, 13 Nov 2016 02:46:56 EST ID:zsw9I8fO No.78343 Ignore Report Quick Reply
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Fuck Shittingdock - Sun, 20 Nov 2016 13:51:25 EST ID:CdJTHjlQ No.78352 Ignore Report Quick Reply

This image is a few years old, back when meming that EM causes allergies and headaches was a meme.
Cyril Chaffingman - Thu, 24 Nov 2016 17:21:28 EST ID:g4yJTuN/ No.78368 Ignore Report Quick Reply
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Just in passing...
Would covering a room in tin foil block out the cosmic rays?
Or would one need sturdier means?
Eugene Hezzlenure - Tue, 29 Nov 2016 13:57:03 EST ID:K4ted3sw No.78375 Ignore Report Quick Reply
Transmitting antennas are designed to be radiators. An anti-radiation "antenna" is a dummy load which is useful when you want to test a transmitter without radiating a signal.
Bombastus !uYErosQbLM!!Mybq1UbK - Fri, 02 Dec 2016 23:42:33 EST ID:ZEo1qUmp No.78378 Ignore Report Quick Reply
I actually don't know if this is a troll post or not. I mean, we literally have /tinfoil/ as a board.

Actually. I love this post

Transform dry vaped herb into bricks by Walrus - Mon, 28 Nov 2016 10:34:32 EST ID:nZCjXMk3 No.78373 Ignore Report Reply Quick Reply
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Transform Dry vaped herb into (...)
11/28/16(Mon)19:25:41 No.8502283
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992 KB JPG
Hello !
I am playing the sorcerer's

> have ABV ( already been vaped weed ) . It can be grinded as a powder if necessary.
> want to put it together and make it a brick, or something else like solid

Problem, the herb is no longer sticky.

I tried to make it solid by adding a bit of water, let the sun evaporate it , and put this shit in tue fridge for like 10 minutes .... FAILURE, it gave me a muddy mixture ...( pic related )
Comment too long. Click here to view the full text.
Bombastus !uYErosQbLM!!Mybq1UbK - Fri, 02 Dec 2016 23:44:12 EST ID:jtHY49uD No.78379 Ignore Report Quick Reply
Why don' you just eat it?


Filter Papers by Molly Nollerlock - Sun, 13 Nov 2016 15:32:34 EST ID:zsw9I8fO No.78345 Ignore Report Reply Quick Reply
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As you can, there are a lot of types:

Which type should I get for basic gravity filtration of drugs?
Bombastus !uYErosQbLM!!Mybq1UbK - Tue, 15 Nov 2016 01:10:58 EST ID:HCt0W/hp No.78348 Ignore Report Quick Reply
do you have a vacuum filtration set?

if yes, 1-2 works best. if no, coffee filters work best. when dealing with pills, it's still best to use coffee filters
Vehk !7HYGxe5v5c - Sun, 27 Nov 2016 22:18:13 EST ID:l5Akm3J6 No.78372 Ignore Report Quick Reply

Coffee Filters are best, fine scientific filters tend to filter rather slowly. If you are working with Ibuprofen, you're better off decanting - it is heavy and highly insoluble even at room temperature, so it will form an adhesive block at the bottom of the container that won't fall out even when tilted at a strong angle. Paracetamol is a bit more awkward.

Purifying and Freebasing by William Sinningworth - Sun, 16 Oct 2016 02:30:25 EST ID:zsw9I8fO No.78302 Ignore Report Reply Quick Reply
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I've gone through this process to convert salts -> freebase by:
adding some salt drug to a lye solution then using hexane to pull the freebase and evaporate.
My question is: while this process seems to have to have worked with a 2C and with U-44770, can you think of any case where the NaOH will mess up the drug somehow? Or a case where the freebase won't dissolve in the Hexane?

2) Is acetone good enough for purifying most drugs? How are you even supposed to know the solubility of a lot of these new drugs like 4-methyl-pentedrone or 3-Fluorophenmetrazine? Acetone is used for MDMA and Ketamine purificaiton, so what stuff does it NOT work on?
6 posts omitted. Click Reply to view.
Press !QUHukXEvkY - Fri, 11 Nov 2016 13:45:49 EST ID:JeMHyPDO No.78339 Ignore Report Quick Reply
Im not sure if sodium hydroxide would be okay.
You could make some Na2CO3 by heating NaHCO3
Bombastus !uYErosQbLM!!Mybq1UbK - Tue, 15 Nov 2016 01:08:30 EST ID:6N1t5rKu No.78346 Ignore Report Quick Reply
David Suckleson - Tue, 22 Nov 2016 19:07:24 EST ID:zsw9I8fO No.78358 Ignore Report Quick Reply
So Na2CO3 is a better base than NaHCO3?
Cyril Chittingbare - Tue, 22 Nov 2016 22:17:00 EST ID:Q2W2CR89 No.78359 Ignore Report Quick Reply
Yes. CO3^2- is a better base than HCO3^- since it is able to accept 2 protons as opposed to 1. Not sure if OP should use a strong base like NaOH tho..
Bombastus !uYErosQbLM!!Mybq1UbK - Fri, 25 Nov 2016 23:22:49 EST ID:sglEgUGb No.78370 Ignore Report Quick Reply
That doesn't determine strength.

Hydrochloric Acid is around 3000x times stronger than the first proton of phosphoric acid despite it only having one proton.

Help please!! by LaDiDotty - Mon, 21 Nov 2016 04:54:04 EST ID:xxe0PbAv No.78353 Ignore Report Reply Quick Reply
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Hi all,

I hope I'm asking this in the best spot & really hoping someone can assist me w/this......

So I'm getting ready to try ULDN for the 1st time, that is if I can get this figured out. So I thought I added my 50mg tab of naltrexone to 1 liter or 1000mls of water however I didn't look close enough at the bottle I'm using, duh I know. Anyhow instead of 1 liter the bottle I added everything into is 1.25L.
So I'm trying to figure out how many mcg's I have per ml. The recipe I followed has the dosages based on 1 ltr not 1.25 ltr. Considering this is touchy & the dose is based on mcg's I wanted to verify what I now have w/some folks that are way better in the chemistry & mixing department.
I would be very grateful for any info you may be able to provide. Anything you also may like to add about ULDN would also be greatly appreciated.

Thank you!
Press - Tue, 22 Nov 2016 18:45:48 EST ID:lyRi8w2C No.78357 Ignore Report Quick Reply
Your solution contains 0.04mg per mL or 40microg per mL

But i doubt that the volume of your bottle was very accurate.

Isnt the solution going to perish? Depending on the pill contents it might spoil quickly
LaDiDotty - Tue, 22 Nov 2016 22:22:41 EST ID:xxe0PbAv No.78360 Ignore Report Quick Reply
Thanks for your reply. I don't know how fast it will perish. I've read that w/refrigeration it can last a month or 2. Just have to make sure I order more long before I run out. I think I'll try cutting the next tab in half & mixing it w/ 1/2 the amount of water. I know it's only been less than 48hrs but so far this is amazing. I wasn't exactly sure how much I diluted the recipe I followed down so based on the original directions I've just been using 5-7 drops w/each dose of opi's. The analgesia & duration of how long they last is pretty amazing. I wish more people talked about this.
Anyhow thank you so much for replying, it is greatly appreciated.

Happy, almost, Thanksgiving.
press - Wed, 23 Nov 2016 07:56:56 EST ID:JRoOF8iS No.78364 Ignore Report Quick Reply
you might want to either get a volumetric flask, which might get expensive i dunno, or find a bottle with which you can very accurately measure a set volume. ideally it would be a bottle with a very thin neck, which would be filled to a certain level of the neck

if your solution is really mixed and the naltrexone is readily water soluble you could store it in several small containers while frozen. then youd simply have to take out a single container, thaw it and shake it before use while the others still remain frozen.

any idea how big one of your drops is? or how much one drop weighs?
LaDiDotty - Thu, 24 Nov 2016 14:24:51 EST ID:xxe0PbAv No.78366 Ignore Report Quick Reply

I don't have any fancy measuring bottles, can you suggest somewhere I could find one in expensively? The recipe I'm following is to mix 1 50mg tab into 1L but it makes a huge amount. I was thinking to see if I could cut a tab in half or even quarters, cut the water down accordingly but I'm afraid of possibly not cutting it perfectly in half or quarters each time. Your idea of storing in the freezer is great! I was afraid the solution would go bad before I'd ever get thru an entire liter. Even though the naltrexone tabs were easy enough to get I'd prefer not to waste them. I found it odd that w/each study or recipe I found nobody talked about properly storing the mixture or preserving it aside from putting the mix in an amber or cobalt glass bottle or storing in the fridge.
Do you think freezing the mixture would degrade it in any way? Do you know if the mixture is sensitive to light?
I did get a couple different syringes from the pharmacy, 1 I think is useless for dosing anyways, it's more of a child's medicine dropper, 5mls w/o small enough increments for dosing, maybe good for something else. The other syringe is 1ml, has .10 increments & even smaller. I just tried counting how many drops a full ml holds & came up w/30 almost 31 drops. One study & recipe I read said their 1ml dropper held a perfect 20 drops. Not sure what they're using but I tried several times & came to 30-31 each time.
With the recipe I'm following it says that what I should end up with is 50mcg per 1ml & .2 ml = 10mcg. Because I accidentally didn't see the bottle I'm using is a 1.25L instead of a 1 L my drops are slightly diluted. I found a couple other recipes but they're all relatively the same.
The naltrexone tabs I got dissolve very fast & completely in water. One recipe said not to shake the tab in the bottle, that made no sense to me since you want to make sure you have even doses. Another recipe said to shake it vigorously, I did the latter. When I dropped the tab in the water I just left it to dissolve while I ate dinner. When I came back it had totally dissolved on its own w/just an uber tiny amount of p…
Comment too long. Click here to view the full text.
press - Thu, 24 Nov 2016 15:41:24 EST ID:tXprf7n7 No.78367 Ignore Report Quick Reply
id try ebay or amazon for chinese volumetric flasks. doesnt matter wether its a plastic one or one made from glass aslong as the mergin of error is tight enough. real men use glass, because theyre not afraid of suffering the pain of fucking up.

a volumetric flask should be cheaper than a really accurate scale. how accurate is yours?

i dont really see how using amber or colbalt glass bottles would help, those are normally used for light sensitive stuff but im not sure about naltrexone being light insensitive. my bet would be that it shouldnt be, since ive never heard of morphine or oxymorphone are. its not going to degrade when its frozen, but be sure to really give it a good shake after dethawing it. use plastic bottles for storing it frozen. ive seen quite a few phds fucking that up once in a while.

for measuring the final dose a syringe is good
the size of a drop also depends of the diameter of the opening so its not a suprise they found some other ratio. i have no idea about ultra low naltrexone, once read that it can reap lotsa benefits but i dont remember the dosage tl;dr cant get lantrexone anyways

i guess the particulate is some gunk like magnesium stearate or some other stuff they put in to make the pill super duper
no biggie, you have a nice one too

Chemical reaction simulator by Martin Dartfoot - Tue, 15 Nov 2016 15:24:42 EST ID:Ul4obZPS No.78349 Ignore Report Reply Quick Reply
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Do you know about any program that can be used to simulate chemical reactions?
What is your opinion about it? I recently stumbled upon "Cain" but still haven't learn to work with it.

Boron tribromide demethylation of codeine by Jarvis Hinnerforth - Mon, 10 Oct 2016 14:55:50 EST ID:9Opqdgsf No.78280 Ignore Report Reply Quick Reply
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I am having trouble with this synthesis. I take 15ml DCM with 200mg codeine base dissolved and make sure its really dry with sieves. Then add something like 500mg of boron tribromide. Immediately the codeine drops out of the DCM solution... no doubt my homemade BBr3 contains a small amount of HBr and Br2. This stuff is unbelievably reactive with air, i've never seen anything fume like it in my life. So i waited/stirred 30mins then added ice/ammonia. No precipitate, i assume the codeine hbr simply dissolved in the aqueous. So next i tried the same thing but added 200mg DIPEA to soak up the acid. Still no morphine precipitate. I worked up both layers both times and verified there was no morphine, i thought it might be dissolved in the high PH aqueous layer but that's only possible with NaOH i believe, morphine should always be insoluble in ammonia hydroxide. I don't know what the problem is.

My boron tribromide is a bit red, i don't have enough to distill. I started from Br2 and Al to make aluminum bromide, anhydrous. Unfortunately i couldn't distill this either but i did leave it under vacuum to hopeful get the free bromine out. I melted it and poured it into another flask with potassium tetrafluoroborate and ended up with only a few ml of BBr3 distilling over. Next time i will use liquid tetrafluoroborate. All 3 of these things really fume like hell. I'm not looking forward to doing it again. I will try to use a vacuum next time, my joints weren't greased and it was pulling in more air then it was worth. I have to make sure i don't get the aluminum bromide on the ground joints as well, god damn what a mess. A propane torch wouldn't even get them apart i had to soak in WD40 then use a propane torch.
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press !QUHukXEvkY - Fri, 21 Oct 2016 14:50:08 EST ID:B3jdPBiB No.78320 Ignore Report Quick Reply
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while im already derailing a thread; do you have any ideas on muhsroom extraction?
havent attempted it yet since the hooch is still in the mail but i was going to go with the very crude method of soaking the raw material in ethanol w=0,7 and then letting the filtrate evaporate in order to get material that i might recrystallize.
i suspect that simply soaking the material in dilute acetic acid and then basifying it with a subsequent non polar extraction (maybe DCM, maybe EtOAc)
but the zwitter ionic nature of psilocin bugs me to no end

i have to salute OP's resources
i might be able to contribute on the matter once i stop being this high lol

its pretty sad how little happens on /chem/, sciencemadness is ice but theyre all very catious (rightfully so) eventhough i saw several of their mods in the hive or the successors of it
Charlotte Fuckingville - Sat, 22 Oct 2016 00:27:23 EST ID:9Opqdgsf No.78322 Ignore Report Quick Reply
The codeine was is from 8mg tablets, 15mg caffeine, 200mg aspirin. Lots of other filler and shit on the ingredient list. I was thinking the caffeine should have been washed away by my DCM wash (while the codeine was still in phosphate form). So idk. Yes chromatography is likely the answer, i've never run a column but i suppose i can figure it out.

I have a UV bulb but i need to find a power supply and ballast, i forget what is required now. Something like 20 volts and a 100 ohm resistor. Its one of those really small uvc germicidal bulbs off ebay, screws into something like a Christmas light socket. Obviously 120ac would blow it though, even 12 volts ended up blowing it because once the mercury heats up and vaporizes it causes a huge current spike which must be limited by some kind of ballast.
Charlotte Fuckingville - Sat, 22 Oct 2016 00:48:34 EST ID:9Opqdgsf No.78323 Ignore Report Quick Reply
I used to grow shrooms i thought about extraction but never attempted it. I was planning to use methanol only because its cheap and available at the hardware store. Evaporate with minimal heat (enough to keep condensation from making a wet goop mess) and a fan. Then try to wash with petroleum ether, maybe recrystallize from methanol in the freezer. Maybe add a little dcm to lower the solubility in the mixture.

Your way would probably be cleaner and higher yielding, but who knows. According to this somthing like that should work. https://erowid.org/archive/rhodium/chemistry/psilocin.extraction.html

I hate water in these situations though, so hard to evaporate without heat or time.
Esther Donderkare - Mon, 24 Oct 2016 19:43:12 EST ID:2Hc2eoG6 No.78327 Ignore Report Quick Reply
Would it be easier to just buy some CYP2D6...
Albert Henkinbanks - Wed, 26 Oct 2016 15:27:19 EST ID:9Opqdgsf No.78328 Ignore Report Quick Reply
I don't think it would be feasible to create an artificial liver, but i really don't know. I do know scientists have modified e.coli to produce thebaine. 2mg from 20grams of sugar isn't too good though, and i expect the modified bacteria would be incredibly fragile. So unfortunately we won't be growing morphine in mason jars like magic mushrooms anytime soon.

Countries like Canada are lucky just to have codeine. If you don't have an opiate to start from you are pretty much forced to grow poppies.

I've found my mercury, i'm going to shake the small amount of bbr3 i have left with it then try the reaction again.

Piperadone by Rebecca Ginningman - Sun, 23 Oct 2016 05:29:48 EST ID:9Opqdgsf No.78324 Ignore Report Reply Quick Reply
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Any ideas how to synthesize 4-piperidone?
Eugene Dabblekat - Sun, 23 Oct 2016 22:53:02 EST ID:9Opqdgsf No.78326 Ignore Report Quick Reply
OP here again. Tried the dickmann condensation, acrylates are too hard to make and the burnt plastic smell is not tolerable. The mannich seems to only like to make piperadones substituted on the 2&6 (benzaldehyde, acetaldehyde). Although i havn't tried it yet formaldehyde might work with acetonedicarboxylate, hydrolyse and decarboxilate to 4-piperadone. I can tell you it doesn't work with phenethylamine not in water, alchohol, or acetic acid. Not nearly as easy as most of the internet would have you believe, its quite the opposite. Unless its just me, which is possible as well.

Maybe posassium cyanide + epichlorohydrin = 3-hydroxyglutaronitrile. ***Journal of the Chemical Society, , p. 1164,1166 = 4-hydroxypiperidine**** Then oxidize the 4-hydroxypiperidine alcohol to a ketone somehow. Maybe react with phenethylbromide first then the amine is protected.

Or any other possible routes? I'd love to hear it.

Anhydrous AlCl3 by Walter Claggleville - Fri, 29 Jul 2016 15:16:32 EST ID:ykDmWZpt No.78112 Ignore Report Reply Quick Reply
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Hello, chem!
Sorry if this is a stupid question, but here it goes:
I have aluminum (III) chloride hexahydrate but I need it in the anhydrous form.
Can I oven-dry it at ~100ºC?
Thanks in advance!!
20 posts and 2 images omitted. Click Reply to view.
Nigel Sinderforth - Wed, 14 Sep 2016 17:44:05 EST ID:Ng8fVE40 No.78239 Ignore Report Quick Reply
Shit Tillinggold - Thu, 15 Sep 2016 01:08:08 EST ID:zsw9I8fO No.78240 Ignore Report Quick Reply
John Merringbury - Fri, 07 Oct 2016 23:06:18 EST ID:hBAZGxou No.78277 Ignore Report Quick Reply
You can demethylate guaiacols by a radical mechanism using CuSO4 + ascorbic acid. Don't waste your time with AlCl3.
Betsy Pittwill - Mon, 10 Oct 2016 23:37:31 EST ID:yvh9Qry5 No.78285 Ignore Report Quick Reply
>>78277 got a ref for that?
Esther Nossleway - Sun, 23 Oct 2016 22:30:30 EST ID:NIATBazO No.78325 Ignore Report Quick Reply
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mind if I ask you why would you want AlCl3? just wondering

bombastus and press are fucking bosses, I've learnt a lot with this guys

love you all

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Please be descriptive with report notes,
this helps staff resolve issues quicker.