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test kits for common adulterants by Emma Mevinglot - Tue, 17 Jul 2018 08:59:13 EST ID:FIrMW5oZ No.79182 Ignore Report Reply Quick Reply
File: 1531832353252.jpg -(62355B / 60.89KB, 670x605) Thumbnail displayed, click image for full size. 62355
if i wanted to start a small business where i test people's drugs for fent/pcp/meth/clam or whatever, what sort of reagents would i need to buy? I realize this is sort of an open ended question, i'm just sort of looking for general suggestions for pretty much any drug testing reagent that tests for something. there's pretty much nowhere that you can safely get your drugs tested around where i live & i really want to do what i can to help. i feel like i could save some lives with this.

especially looking for something that can detect if my jenk's been cut with dog pills
>>
pr - Thu, 19 Jul 2018 02:27:18 EST ID:N1w1NO9M No.79185 Ignore Report Quick Reply
are you sure its legal in your country to have a ton of people sending you what in fact are free drugs?

dunno, buncha tlc plates, solvents out the ass, colour reagents or their components- whichever is cheaper- a fridge

and if youre into endgame shit a GC/MS setup
>>
Caroline Dullygold - Thu, 19 Jul 2018 11:27:47 EST ID:FIrMW5oZ No.79186 Ignore Report Quick Reply
>>79185
i don't know how above board this business will be, but i'm in a pretty lenient part of america drug wise so i doubt i'd get in much trouble for people sending me small samples for chemical analysis. also is there any reagent/combination of reagents i can use to test for different benzodiazepines? from my initial googling it doesn't seem very easy but i would really like to be able to tell people if their xans were cut with clam or flam etc


The chemistry… of elephants by Emma Padgehall - Mon, 16 Jul 2018 16:33:19 EST ID:8EwQg758 No.79178 Ignore Report Reply Quick Reply
File: 1531773199625.jpg -(93687B / 91.49KB, 445x476) Thumbnail displayed, click image for full size. 93687
I heard that if an elephant’s metabolism were any faster then it would burn from the inside out because it’s body is way too big to effectively dissipate heat. So it has a very slow metabolism. Is this true?
>>
trypto - Mon, 16 Jul 2018 18:14:09 EST ID:OdR7meD+ No.79179 Ignore Report Quick Reply
>>79178
Are you the guy on /drank/ trying to get fucked up with an elephant?
>>
trypto - Mon, 16 Jul 2018 18:26:41 EST ID:OdR7meD+ No.79180 Ignore Report Quick Reply
>>79179
Oh wait. I see now. Well done, OP.
>>
Emma Mevinglot - Tue, 17 Jul 2018 08:48:03 EST ID:FIrMW5oZ No.79181 Ignore Report Quick Reply
this is fucking wild OP you're a legend
>>
Matilda Greenlock - Wed, 18 Jul 2018 21:42:17 EST ID:ggkjpE8I No.79184 Ignore Report Quick Reply
mass specific basal metabolic rate is specific to the surface area to volume ratio of the animal. this is why small endotherms such as a squirrel have a much higher metabolic rate than larger endotherms like an elephant


Molecule by Lillian Dorrypedge - Fri, 13 Jul 2018 12:51:01 EST ID:1xukUjeD No.79170 Ignore Report Reply Quick Reply
File: 1531500661281.png -(11786B / 11.51KB, 505x503) Thumbnail displayed, click image for full size. 11786
Hey guys, so I am helping someone out with there organic chem class.
They have to write a syntesis for this molecule.

my question is,what is the IUPAC name for this molecule?
I can't find it online when I try the molecular formula or draw it.
>>
trypto - Sat, 14 Jul 2018 16:27:22 EST ID:OdR7meD+ No.79174 Ignore Report Quick Reply
>>79170
Is that shit real? I could see it with cyclohexane, but with a benzene ring? Looks like way too much strain. If it's real, I bet it's extremely fragile.

3,5-somethingoxysomething-aniline
>>
p - Mon, 16 Jul 2018 13:40:49 EST ID:N1w1NO9M No.79177 Ignore Report Quick Reply
concerning the synthesis
this is some pretty whack shit. you can even synth superphane but this would be way too much strain on the sp2 carbons of the benzene.

theoretically speaking its an 5-amino anhydride derivative of isophthalic acid, my best guess is that its an exercise aimed at the nomenclature or bicyclocompounds or rather heterocycles.

could you double check if you got that structure right?


What makes atoms do what they do? by Matilda Hassleway - Sat, 10 Mar 2018 11:49:56 EST ID:PTghO7Nx No.79012 Ignore Report Reply Quick Reply
File: 1520700596496.jpg -(161331B / 157.55KB, 639x999) Thumbnail displayed, click image for full size. 161331
Sup /chem/,

There is a fundamental gap in my understanding of the universe. When we look out into the sky and see the sun and stars, measure the Earth orbiting the sun, or see a volcano, it is commonly accepted that eventually, all of these processes will run out of energy and cease to do their thing. However every atom in the universe has positive and negative charges, with the negatively charged particles constantly in motion (and i guess the positive ones too if we count vibration or whatever). How do subatomic particles get a charge in the first place? Will it ever wear off? What makes electrons move? Will an electron ever stop moving and become neutrally charged? Can we apply this seemingly infinite source of subatomic energy to the macro scale to prevent a big freeze or one day generate limitless energy?
27 posts and 4 images omitted. Click Reply to view.
>>
Jarvis Hankinstone - Sat, 21 Apr 2018 18:57:51 EST ID:8eK2pPPB No.79081 Ignore Report Quick Reply
>>79080

what about young's double slit experiment
>>
Bressbastus Werrywag - Sat, 12 May 2018 02:43:18 EST ID:+BoDDLT6 No.79103 Ignore Report Quick Reply
>>79081
what about his two sluts?
>>
Katsuragi !hZYzX5/C3s - Thu, 24 May 2018 13:47:00 EST ID:pMrrl6aC No.79115 Ignore Report Quick Reply
>>79012
Quantum Dynamics.
>>
MULTIVAC - Sun, 15 Jul 2018 13:56:08 EST ID:0zm+STH/ No.79175 Ignore Report Quick Reply
>>79012
>prevent a big freeze
THERE IS AS YET INSUFFICIENT DATA FOR A MEANINGFUL ANSWER
>>
trypto - Sun, 15 Jul 2018 21:13:52 EST ID:OdR7meD+ No.79176 Ignore Report Quick Reply
>>79080
Awe shit. I forgot to follow up.

>>79175
Nice.
http://www.multivax.com/last_question.html


Shake n Bake Meth by Phineas Donningtock - Fri, 15 Jun 2018 05:48:12 EST ID:3YadM9Z3 No.79147 Ignore Report Reply Quick Reply
File: 1529056092937.jpg -(15382B / 15.02KB, 604x438) Thumbnail displayed, click image for full size. 15382
Is it really all that dangerous? Is there always a chance that something will go wrong even if you do everything completely right?
>>
Priscilla Dunnerfoot - Fri, 22 Jun 2018 20:38:19 EST ID:UJwtgXMh No.79149 Ignore Report Quick Reply
It's inherently dangerous. The danger is manageable although if you have the discipline and means to do that you're probably just not going to do a fucking shake and bake.
>>
Graham Greenford - Sat, 14 Jul 2018 00:18:01 EST ID:WtJpoXSk No.79173 Ignore Report Quick Reply
Meth is just really bad energy in general, bro.

Maybe get into plain amphetamine synth for fun if you really want a stimulant


Home-made Dynamite / Making A Bomb by Nigel Pockham - Wed, 11 Apr 2018 03:23:05 EST ID:ynVJ73wC No.79055 Ignore Report Reply Quick Reply
File: 1523431385404.gif -(1601367B / 1.53MB, 256x192) Thumbnail displayed, click image for full size. 1601367
Hypothetically speaking, I am curious
Having rewatched Fight Club recently what with the home-made dynamite there
How would /chem/ recommend making a bomb, hypothetically speaking?
Asking for a friend. Like, not a huge bomb, but, you know.
14 posts and 7 images omitted. Click Reply to view.
>>
press !//CEObOMBY - Fri, 27 Apr 2018 04:28:40 EST ID:owgnkIMV No.79098 Ignore Report Quick Reply
>>79095
yeah pipe bomb, plain old oxidizer such as ammonium nitrate with a fuel, potentially coarsed to a certain grain size to ensure faster reaction inside a threaded pipe .
for extra points fix a layer of nails to it.
>>
Bombastus Werrywag - Sat, 12 May 2018 02:38:57 EST ID:+BoDDLT6 No.79100 Ignore Report Quick Reply
>>79098
opium pipe bomb
astus


>>79089
BREEEEAAAAAKING THE HAAAAAAABIT

Anyway, OP. You're going to have to specify what type of bomb you are looking for. Anti-material: something that can drill through armour first then explode
Anti-personnel: lots of shrapnel
Area denial: big explosion
Incendiary: the only one that's /chem/ related tbh
>>
Shitting Murdman - Fri, 18 May 2018 00:16:38 EST ID:sDRmz2Sh No.79107 Ignore Report Quick Reply
1526616998641.png -(96134B / 93.88KB, 932x511) Thumbnail displayed, click image for full size.
Looks like too much work for me tbh.
>>
Katsuragi !hZYzX5/C3s - Thu, 24 May 2018 13:44:08 EST ID:/AXFeCtj No.79113 Ignore Report Quick Reply
>>79055
I would recommend not making a bomb.
>>
Simon Brookfield - Fri, 13 Jul 2018 13:14:37 EST ID:WDigv0Ec No.79172 Ignore Report Quick Reply
>>79107
Source please?


General method for determing max/min within a range? by Fucking Bellyburk - Thu, 28 Jun 2018 07:51:21 EST ID:rGLueGvy No.79150 Ignore Report Reply Quick Reply
File: 1530186681836.jpg -(16201B / 15.82KB, 500x500) Thumbnail displayed, click image for full size. 16201
Does anyone please know of a general way to determine if there's any local max and min *within a set range of X-coordinates*?

As we can see, there's a local max somwhere around -1 and a local min somwhere around 3 and none whatsoever in the range 1-2.

But how do I prove that there's no local max nor min in that range?
5 posts omitted. Click Reply to view.
>>
Oliver Grandstone - Mon, 02 Jul 2018 15:44:38 EST ID:rGLueGvy No.79158 Ignore Report Quick Reply
>>79155
I'm looking for *local* max/min in trig-functions. I know that if the x-range is long enough, there will be *many* local max/min.

For instance this function has local max/min all over the place and repeats itself every 3600 x:

f(x) = sin x(sin (x/10))

I know there's a local max between x(1500) and x(1530). But how do I prove it by doing a f'(x) for only that range?
>>
trypto - Tue, 03 Jul 2018 11:21:20 EST ID:OdR7meD+ No.79159 Ignore Report Quick Reply
>>79158
I think it still works the same way. Take derivative. Set equal to 0. Solve within your range. That's a lot of trig functions to fuckin deal with. Here's wolfram alpha's solutions:

https://www.wolframalpha.com/input/?i=d%2Fdx+sin(x)(sin(x%2F10))+%3D+0,+1500%3Cx%3C1530

Solutions are at the bottom. Hit the 'exact solutions' to see what kinda algebra is needed for that function. So obviously the way to do this is numerically. Look at the original function
https://www.wolframalpha.com/input/?i=sin(x)(sin(x%2F10)),+1500%3Cx%3C1530

Then look at the approximate solutions in the last page. You can see that the local maximum for that range is at:
x≈1522.1173171661698545755
For which the function returns: 0.987810970335936684937

Or, in one easy step: https://www.wolframalpha.com/input/?i=maximum+sin(x)(sin(x%2F10)),+1500%3Cx%3C1530

Maybe that's cheating, but fuck trying to analytically solve that.
>>
Simon Sannermutch - Wed, 04 Jul 2018 06:43:52 EST ID:rGLueGvy No.79160 Ignore Report Quick Reply
>>79159
Thanks a lot! :-)
>>
Cedric Gussleserk - Mon, 09 Jul 2018 04:18:54 EST ID:ggkjpE8I No.79164 Ignore Report Quick Reply
the fact that this thread about mathematics was posted on /chem/ is only further evidence of the genius of my idea of a /stem/ board

http://boards.420chan.org/420/res/247062.php
>>
bress - Fri, 13 Jul 2018 13:01:59 EST ID:DbJ7MA1o No.79171 Ignore Report Quick Reply
1531501319502.jpg -(129931B / 126.89KB, 800x449) Thumbnail displayed, click image for full size.
>>79164
the fact that youve posted that is further evidence of the genius of the idea to establish a /shill board. naw just kidding.

concerning the analytic component of the question, im kinda ashamed it took me this long to think of, you could take the derivative via product rule (not sure if another approach would deliver something more moldable) and then reason examine the zero points of the derivative and second derivative.

im a bit confused as to what the actual function is, should it - as mentioned before - be y= sin(x) sin(1/10), the derivative itself will be a sum of two periodic products, meaning youd have to evaluate cases where either both terms are zero or one term is the negative of the other. depending on the range the answer should be given in multiples of some fraction of pi (kirt, tex support when)

during my analytics classes giving a numeric answer was a telltale sign of misunderstanding the task

And should your task be to prove that the function has a local min/max on a given closed range you could simply show that the function is continous (as a composition of continous functions) and then a local min/max has to exist.


Secret unwatched meth precursor cartels are using tha nobody knows about! by David Brandletadge - Thu, 12 Jul 2018 11:36:25 EST ID:AEosv4I7 No.79165 Ignore Report Reply Quick Reply
File: 1531409785030.jpg -(26144B / 25.53KB, 630x333) Thumbnail displayed, click image for full size. 26144
They use a ketone nobody knows about called "ADDS"

It's not on any list so you can order a million gallons from China easily
>>
Oliver Sittinghat - Thu, 12 Jul 2018 14:46:26 EST ID:N1w1NO9M No.79166 Ignore Report Quick Reply
>>79165
unless you muster up a tiny bit more information, ill go with 3/10 " almost googled"
>>
David Brandletadge - Thu, 12 Jul 2018 15:02:35 EST ID:AEosv4I7 No.79168 Ignore Report Quick Reply
>>79166

you wont find this on google my friend.
>>
Charlotte Blembleshaw - Thu, 12 Jul 2018 22:09:24 EST ID:IsgjdvUw No.79169 Ignore Report Quick Reply
I'm having a hard time picturing cartels sweating chemical watchlists. Let's say it's true. It would realistically have to come from one source and have one consumer for it to remain a secret and it would be easily traceable in a way that diverted chemicals would not. Also unless it was an in-house operation I don't think there would be much of a price advantage. No, I think you're full of shit.


fighting BIG H by Oliver Sittinghat - Thu, 12 Jul 2018 14:51:38 EST ID:N1w1NO9M No.79167 Ignore Report Reply Quick Reply
File: 1531421498528.jpg -(150268B / 146.75KB, 720x720) Thumbnail displayed, click image for full size. 150268
is kirts novel way of marking big h somehow connected to the fact that i get 502 everytime i try to use my vpn on here?
because that'd kind of suck, aubrey.


Naltrexone -> Oxymorphone? by Hamilton Beggleshit - Thu, 17 Mar 2016 18:16:02 EST ID:GksK9UMc No.77752 Ignore Report Reply Quick Reply
File: 1458252962747.png -(55460B / 54.16KB, 992x379) Thumbnail displayed, click image for full size. 55460
Dear /chem/,

wikipedia cites that "Naltrexone can be described as a substituted oxymorphone – here the tertiary amine methyl-substituent is replaced with methylcyclopropane. Naltrexone is the N-cyclopropylmethyl derivative of oxymorphone."

Is it possible to revert naltrexone back to oxymorphone? If so, how?

My very limited understanding of organic chemistry leads me to believe that naltrexone could, in proper solution and (probably) with the addition of heat, be broken into oxymorphone and cyclopropylmethylbromide. (pic related)

Any input regarding said (hypothetical) reaction will be greatly appreciated!
6 posts and 1 images omitted. Click Reply to view.
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Cornelius Bushwen - Sun, 10 Apr 2016 22:52:26 EST ID:ljoFE2/4 No.77821 Ignore Report Quick Reply
>>77777
Quints don't happen here but once in a great while.
>>
Marty Poppenheimer - Sun, 01 Jul 2018 00:46:46 EST ID:D3AAbMyr No.79156 Ignore Report Quick Reply
1530420406530.jpg -(227009B / 221.69KB, 1680x1050) Thumbnail displayed, click image for full size.
>>77772
Would someone mind explaining this process in a way that a significantly more retarded person could understand?

>Treaet Naloxone with Mel in Alcohol, or DMF
What is Mel? What is DMF?

Once you achieve this, you collect what remains from this process, which is Naloxone Methiodide.

>Heat your Naloxone Methiodide in DMF or DMSO
What is DMSO?

>With dodecanethiol qunched with 1 eq base, such as tBuOK
What is Qunched? What is tBuOK?

>t. retarded brainlet with Suboxone Tablets
Any help would be appreciated because I can't get shit out of these. I can follow basic instructions however.
>>
Molly Nadgedale - Sun, 01 Jul 2018 20:46:17 EST ID:OdR7meD+ No.79157 Ignore Report Quick Reply
>>79156
Google is your friend. Show the minimum effort at least.
>>
Piemaster - Fri, 06 Jul 2018 05:57:39 EST ID:pv6fN59z No.79162 Ignore Report Quick Reply
Would it be possible to turn the cyclopropane into a terminal alkene using aluminum or something? I know cyclopropane's are very unstable.

And then would it possible to attach a carbon to the terminal alkene? You could attach a phenyl or something and make n-phenylpropyl.

Basically to sum up what I'm saying, instead of trying to remove the cyclopropylmethyl group outright, would it be possible to turn it into a 4 carbon chain, the last C=C being a double bond? And then using the reactivity of said double bond to attach something? You'd be able to make a pretty potent agonist that way.
>>
Alice Honeyhall - Mon, 09 Jul 2018 03:51:31 EST ID:mH/x48p3 No.79163 Ignore Report Quick Reply
>>79162
Cyclopropanes are very unstable but the one pictured with a stabilized alkane group is not. This group shown with an R-cyclopropane is relatively stable.
Carbon-carbon chemistry is very hard. Even harder to do selectively.

Short answer is most likely, no.


IRREVERSIBLE OPOID AGONISTS - Hydrazine and azine opiate derivatives by Piemaster - Fri, 06 Jul 2018 03:58:39 EST ID:pv6fN59z No.79161 Ignore Report Reply Quick Reply
File: 1530863919876.png -(5901B / 5.76KB, 220x159) Thumbnail displayed, click image for full size. 5901
Hey guys.

So recently I've been interested in irreversible opiates.

A couple decades ago some scientists were able to do this by adding a hydrazine at the 6 ketone of oxymorphone, as well as at naltrexone/naloxone, making oxymorphazone and the corresponding nalts.

When tested, these hydrazines lasted extremely long, and blocked any further effect of opiates in animals. As well, radioactive versions of the drugs cold simply not be washed away from tissue expressing opiate receptors. Meaning these drugs were staying bound to the receptor.

Originally it was thought that oxymorphazone itself was doing the irreversible binding, but it was later determined that the oxymorphazone was joining up with itself spontaneously in solution, creating a dimer of sorts, oxymorphazine.

https://en.wikipedia.org/wiki/Oxymorphazone

There's no wiki on Oxymorphazine, but here's something similar: https://en.wikipedia.org/wiki/Oxymorphone-3-methoxynaltrexonazine

It's just two oxymorphones joined by a hydrazine at the 6 position of each.
Comment too long. Click here to view the full text.


Reducing 3,4,5-trimethoxy-beta-nitrostryrene to mescaline by Matilda Bomblehit - Wed, 13 Jun 2018 11:03:55 EST ID:rajg/xs8 No.79145 Ignore Report Reply Quick Reply
File: 1528902235968.png -(5534B / 5.40KB, 460x300) Thumbnail displayed, click image for full size. 5534
I want to reduce 3,4,5-trimethoxy-beta-nitrostyrene to the amine. What will do this? I've found so much worthless and bullshit information. It seems the main options are:

  1. Zn/HCl or Fe/HCl. I don't know if this goes from the nitrostyrene to the amine or if I need to use NaBH4 to first reduce the double bond. Also, some people say the yields are good and others say the yields are shit.

2. LAH. Not an option.

3. SnCl2 to reduce the nitrostyrene to an oxime and then Zn to reduce the oxime to the amine. I've never found proof of anyone doing this reaction on nitrostyrenes. SnCl2 is good for reducing nitropropenes but who knows if that applies to nitrostyrenes.

4. Al/Hg. Literally toxic. I haven't found any reports of people using the less toxic Al/Ga or Al/Cu amalgam. I also get conflicting information saying Al/Hg reduces directly to the amine, yet others are saying NaBH4 must be used to first reduce the double bond and then the Al/Hg reaction can be run to reduce the nitro group to an amine -- which is it?

Any input would be appreciated, especially from people who have actually run these reactions on this particular substrate.
>>
press - Thu, 14 Jun 2018 15:10:21 EST ID:Hu9hjiL2 No.79146 Ignore Report Quick Reply
whats "literally toxic" as opposed to toxic?
>>
Phoebe Wicklefoot - Wed, 20 Jun 2018 13:34:12 EST ID:f7Wsgp11 No.79148 Ignore Report Quick Reply
>>79145
Are you planning on making larger quantities? if not, just go with al/hg. use your common sense and everything will be fine. solubility of mercury salts in organic solvents is negligible. when you worry about the organomercury compounds, just give your product (salt) a proper wash with organic solvents and acetone and you are golden


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