@ericcarabetta1161
It’s funny that it would have been easier to actually make meth.
@Bludgeoned2DEATH2
LabCoatz: “YouTube, this is completely legal you have no recourse to age restrict or demonetize” YouTube: “and I took that personally”
@andrxw1
we're so back (on the watchlist)
@DOJOMACE
THE GOVERNMENT HATES HIM FIND OUT THIS MAN STAYS AWAKE FOR 7 DAYS STRAIGHT
@Bavarkhy
12:12 "As with most of life's problems, this was readily overcome with a healthy dose of acid" lmfao
@theKashConnoisseur
I remember when ChemPlayer got banned for making precursors. I know that drug chem (and energetics) gets the views, but I really hate seeing quality chem channel after quality chem channel go the way of the dodo.
@ares395
Careful, That Manchild might contact your family and their associates on you...
@mortlet5180
I believe the biggest issue was the impurities produced via the Henry reaction (it is well-known to be one of the dirtiest synthetic pathways, with enough unique impurities carrying through to the final product to allow for forensic fingerprinting), as well as the side-products formed from the uncontrolled LiAlH4 reduction. As an alternative route, you should really try doing a Grignand reaction with acetonitrile and the (bromomethyl)cyclohexane, which would allow you to directly reduce the formed imine to the primary amine in one pot. If you manage to exclude water, oxygen and CO2 (which excess Grignard reagent will also help to scavenge down to PPM levels if you seal the apparatus with something like a balloon), then this pathway will produce much a cleaner and easily crystallizeable primary amine: After the Grignand reaction is finished, cool down the resultant ether solution to around 0°C in an ice bath. Then, while still minimizing exposure to the atmosphere, you just need to slowly add some LiAlH4 or borohydride, with stirring and cooling.
@dancoroian1
Those of us who have been particularly desperate when having issues getting ADHD meds have long been familiar with the Benzedrex last resort...nothing like those lavender burps to remind you you're having a horrible/great day!
@Chemiolis
I love this structure!
@pastaalalamborghini
I dont know jack about chemistry but youtube chemists generally have a consistent cadence and inflections in their speech thats oddly satisfying. While also being completely devoid of interpersonal relationships, social nonsense and drama... This is a good example of how sick of everything I am, I watch chemistry videos (which might as well be greek) as an escape from pop culture and the monotony of stupid interpersonal drama
@konstantinlee2275
Nice work, even after getting such disappointing oil. Actually you can do TLC but on paper, ordinary filtering paper. Sure it'll be uncomparable with any external reference but you can put witness drops with source substances on same paper to get some references. And you can buy this pills or whatever OTC and extract taget substance from there for reference,if possible. Amines can stay oily because of presence of solvents and water. Try to dry in vacuum this oil to remove traces of anything volatile and then recrystallize.
@hanifarroisimukhlis5989
Make pseudoephedrine next to tell DEA (and FDA) it's dumb to restrict it. EDIT: Nice that google's first autocomplete result is propylhexedrine abuse...
@art-thou-gomeo
Mate congrats on the 100k subs! Your little self-aware text remarks had rolling. The troll face on the drug lab test results was chefs kiss very enjoyable watching your borderline legal videos :face-fuchsia-tongue-out:
@valfodr
You didn't get a precipitate in the first step because of impurities and unreacted reagents. You can obtain a precipitate in the first step by washing with metabisulfite (or dumping the whole mixture into a solution of metabisulfite). This removes unreacted aldehyde that becomes water-soluble as bisulfite adduct. The material will then be much more likely to crystallize.
@Cavemankind_
I appreciate the technical legality of this synthesis, but with that collective list of unique ingredients, the DEA may still be very interested based on numerous popular precursors for MDxx compounds.
@Star88701
That sulfuric and hydrobromic acid route is a nasty, dirty process that is very difficult to control without a professional lab.
@LifeGlitch1
Propylhexedrine HCl has a melting point of 123°C. When melted, it looks like a clear to slightly brown liquid. To solidify Propylhexedrine HCl, you need to cool it in the freezer and then refrigerator for a few hours. Also, using a Bovado Borosilicate Glass cooking dish to have more surface area can help with Propylhexedrine HCl. Propylhexedrine HCl should be hard crystals, but sometimes it's soft and pasty due to moisture or impurities from Petroleum Distillates based solvents. I think I need Pentane and Hexane. I also made Hydrogen using Aluminum Galinstan amalgam.
@ashishpatel350
this is my domicile and i will not be harassed
@LabCoatz_Science