[ChemPlayer Reupload]Piperidine from the sodium metal reduction of pyridine umYuJ8TwQLk

(14:59)

[ChemPlayer Reupload]Make piperonal from piperinic acid

(14:58)

[ChemPlayer Reupload]Piperine hydrolysis to piperinic acid and piperidine

(14:32)

[ChemPlayer Reupload]Synthesis of a piperidine ephedrone analogue

(14:31)

[ChemPlayer Reupload]Hydrolysis of piracetam, a 'nootropic' drug

(13:34)

[ChemPlayer Reupload]Ammonium methylsulfate preparation from sulfamic acid

(10:15)

[ChemPlayer Reupload]Phenylacetic acid from mandelic acid via HI reduction

(9:5)

[ChemPlayer Reupload]5 Iodovanillin preparation from vanillin pDdY WCOXho

(4:31)

Extracting the spicy chemical in black pepper

(15:20)

Making Methylamine to piss off my fbi agent

(5:24)

Making Nitroethane With Electrolysis | Chemistry With ChatGPT

(12:45)

Turning vanillin into piperonal but not for drugs | Part 1 (3,4-dihydroxybenzaldehyde)

(11:)

Turning black pepper into piperonal cause it smells better

(25:36)

Making Piperidine to piss off my FBI Agent

(6:54)

ChemPlayer music EP #1

(15:)

Messing with HCN7 - Reupload

(9:50)

Making nitromethane because the DEA won't text me back

(13:10)

Making the chonkiest methylating agent

(10:9)

[ChemPlayer Reupload]Bromine preparation as a solution in DCM

(10:34)

[ChemPlayer Reupload]Make methylamine hydrochloride

(8:4)

[ChemPlayer Reupload]Henry reaction between vanillin and nitromethane qySLcGIIDGM

(10:45)

[ChemPlayer Reupload]Hypophosphorus acid preparation

(7:33)

[ChemPlayer Reupload]Acetylanthranilic acid and a failed test for triboluminescence

(5:45)

[ChemPlayer Reupload]Preparation of potassium phthalimide

(6:22)

[ChemPlayer Reupload]Desoxybenzoin synthesis (2-phenylacetophenone )

(7:16)

[ChemPlayer Reupload]Extreme Grignard reagents how wet can you get

(6:50)

[ChemPlayer Reupload]Acetonitrile synthesis from acetic acid via acetamide

(9:51)

[ChemPlayer Reupload]Benzoin condensation the 'old school' way using a cyanide catalyst

(5:30)

[ChemPlayer Reupload]Reduction of vanillin nitroethane condensation product with borohydride

(10:36)