I thought they only listed active compounds, IIRC 1 of the issues with them is that the can't report on strength for example, just primary active compound and secondaries which I assume is really just looking at the biggest peak in the GCMS, so even if the only active compound were 2C-B but the pill is 95% filler, then you've got a shit underdosed pill. Seems underdosing is on 2c-b pills is pretty common these days.
HCI for me, though it's harder to get hold of in the UK
20% grade HCl is off shelf in 3M muriatic or pool grade 10M
HCl can be synthesized via chloro alkprocess via cell membrane, and a mini reactor
here its a mini industrial lab
https://www.sciencemadness.org/whisper/viewthread.php?tid=156152
this vid proves a pH 2 acidic solution can be reached (at 2mins in) it just doesnt really discuss the final molarity - im assuming here in 250mL beakers that lil but dissolved NaCl to be below 1
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reactor heat energy and backyard way will look like
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the above is dangerous af btw
swimming pool stuff way:
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sulfuric acid (zep) and salt way:
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Assuming you get HCl and need distill and concentrate to azeoptropic point 20%ish
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Process should be something like this in theory (assuming car battery as energy source):
1. Electrolyte Preparation: Dissolve 360g NaCl in 1L distilled water to create a near-saturated brine solution.
2. Cell Setup: Fill two glass beakers with the solution, maintaining headspace for gas accumulation.
3. Salt Bridge: Connect the beakers with a saturated salt bridge to complete the ionic circuit while minimizing direct mixing of products.
4. Electrode Placement: Submerge inert graphite rods in each beaker.
5. Circuit Wiring: Wire the electrodes to the 12V power source in series with an inline 3A–5A fuse and a #1156 automotive bulb acting as a ballast resistor to limit current.
6. Electrolysis: Power the circuit and monitor for hydrogen evolution at the cathode and chlorine evolution at the anode.
7. HOCl Conversion: Expose the resulting hypochlorous acid HOCl solution to UV light or sunlight for a week to facilitate photolytic degradation into hydrochloric HCl and oxygen O
8. Distillation Limit: Concentrate the solution via controlled evaporation only up to the azeotropic limit (~20% / 6M), recognizing that further concentration by simple boiling is not possible.
and im not sure the ballast light will keep the 12V from instantly vaporizing everything short circuit style just an idea (prob approx 16-24 hrs according to guesstimated math)
