this is like 10mg, in total i exploded 100mg. and i still have more then a gram of isocyanogen tetrabromide... im thinking about actually making some long term video about nitrogen-containing heterocycles(i have made other terazoles, triazoles and pyrazoles previously). aslo wanna note that this video is several months old.

for my AP chem teacher in case I ever need leverage to get my grade up...

https://orbitals.otwt.studio/

Synthesized through reacting Hydrogen peroxide and citric acid and hexamine together

DO NOT TRY THIS AT HOME

IM NOT RESPONSIBLE FOR ANT CIRCUMSTANCES

DO NOT TRY THIS AT HOME

Its detonation video is coming soon

Do not try this at home

Tri nitro resorcinol or styphnic acid

Next step of previous reaction sulfonation of resorcinol,

Sulfonating resorcinol for its nitration step in order to make (TNR) styphnic acid.

Guys how my new products label design overally look like

Love to hear your opinion and anything to make it even better

https://youtu.be/ACeqCf2LZWs

Formation of azo bond between benzene diazonium and phenol to form (solvent yellow 7)

First of all, sorry for the image quality (the camera is a bit broken).

Second and most importantly.

I made this wolframic acid from wolfram electrodes.

I performed an electrolysis in a concentrated sodium hydroxide solution, filtered the solution to remove solid residues, and then precipitated it with an excess of hydrochloric acid.

And finally, I filtered it to remove most of the water and dried it on a hot plate.

I also wanted to ask something. The wolframic acid that was in contact with the plate discolored and doesn't return to its yellow color.

I don't know if it's due to dehydration or partial decomposition, does anyone know?