Methyl

Non chemical substance only if it’s pure form which is desoxyn. Methyl or G or shit also work slang terms no relation or side effect if it does it shouldn’t

Methyl made blues look like zombies

by prosvsjoesamronstbrown April 1, 2025

methyl orange

A pH indicator (most commonly) used in acidic conditions.

In acidic conditions methyl orange is red but in neutral / basic conditions it is yellow.

by chemguide August 11, 2019

methyl-methanol

A reasonable name for ethanol (alcohol), which breaks IUPAC naming rules for molecules. Can be used when alcohol is brought up in conversation, but you don’t want eavesdropping adults to know that you’re into underage drinking

*high school student in class, talking to other students*
“Who’s getting the methyl-methanol tonight?”

by I'm not proud to be on here December 7, 2018

2-methyl-2-butanol

2-methyl-2-butanol is a tertiary alcohol which is 20 times stronger than regular ethanol (alcohol). 2-methyl-2-butanol doesn't produce aldehydes as a metabolite and instead, produces 2-methyl-2-butanyl gluconoride and 2-methyl-2,3-butanediol. Meanwhile, ethanol produces acetaldehyde, a moderately toxic aldehyde, before becoming the harmless acetic acid. As a result, there is no hangover from 2-methyl-2-butanol but there is a temporary hangover from ethanol. The dose range of 2-methyl-2-butanol is 2ml to 12ml+.
2-methyl-2-butanol can be made from ethyl chloride by the grignard reaction from an ethyl magnesium chloride intermediate reacting with acetone and then a hydrochloric acid work-up.

Properties
Chemical formula
C5H12O
Molar mass
88.150 g/mol
Appearance
Colorless liquid
Odor
Camphorous
Density
0.805 g/cm3
Melting point
−9 °C; 16 °F; 264 K
Boiling point
101 to 103 °C; 214 to 217 °F; 374 to 376 K
Solubility in water
120 g·dm−3
Solubility
soluble in water, benzene, chloroform, diethylether and ethanol

Terry: I drank 8ml of 2-methyl-2-butanol and I'm dissolved. I'm drunk!

*The next day
Terry: Hey! There's no hangover!

by CognitiveFuel January 30, 2023

Blue N-Methyl-Modafinil

Blue N-Methyl-Modafinil is N-Methyl-Modafinil powder or pills which are blue. It's similar to Adrafinil, Modafinil, Armodafinil, Fladrafinil, Flodafinil (Flmodafinil), Hydrafinil (Fluorenol), Wakix, and Sunosi.

Tony: I tried 200mg of N-Methyl-Modafinil and was focusing on my homework and then cleaned and played videogames for 12+ hours. Then I showered, ate, and slept 5 hours and woke up feeling refreshed. Thanks Blue N-Methyl-Modafinil.

by CognitiveFuel August 31, 2023

3,4-MethyleneDioxyPhenyl-2-Propanol

3,4-MethyleneDioxyPhenyl-2-Propanol (MDP2Pol) is a chemical with a boiling point of 125°C at 25mmHg. MDP2Pol is a yellowish oil which is an alcohol. It is formed from dilute phosphoric acid hydration of safrole (sulfuric acid isn't used because sulfuric acid is an oxidizing acid which rearranges MDP2Pol (3,4-MethyleneDioxyPhenyl-2-Propanol) to MDP1Pol (3,4-MethyleneDioxyPhenyl-1-Propanol). MDP2Pol is also formed by oxymercuration demercuration of safrole. MDP2Pol can be oxidized to MDP2P (3,4-MethyleneDioxyPhenyl-2-Propanone) by either sodium chlorite or sodium hypochlorite in hydrochloric acid and the byproduct is chlorine gas (wear a gas mask and do the reaction outside). It can also be oxidized by lead acetate. 3,4-MethyleneDioxyPhenyl-2-Propanol is also called Sesamyl-2-Propanol (Se2Pol, Ses2Pol, Sm2Pol), hydroxysafrole, and Sesamylisopropanol.

I formed 3,4-MethyleneDioxyPhenyl-2-Propanol by hydrating safrole with an aqueous dilute solution of phosphoric acid.

by CognitiveFuel November 18, 2022

3,4-MethyleneDioxyPhenyl-2-Propanone

3,4-MethyleneDioxyPhenyl-2-Propanone (MDP2P) is a yellow chemical that has a melting point of 87-88 °C and a Boiling point range of 115-170 °C at around 30 mmhg. MDP2P can be synthesized by oxidation of MDP2Pol (3,4-MethyleneDioxyPhenyl-2-Propanol) using either sodium chlorite or sodium hypochlorite in hydrochloric acid and a byproduct is chlorine gas (if hydrochloric acid isn't used, then you will get the haloform reaction). MDP2P can also be synthesized by a grignard reaction of 3,4-MethyleneDioxyBenzyl magnesium chloride (formed from 3,4-Methylenedioxybenzyl chloride and magnesium turnings in diethyl ether) and acetonitrile followed by hydrochloric acid work-up. MDP2P can also be synthesized from wacker oxidation of safrole. Reaction of MDP2P with an ethanol solution of ethylamine and Aluminum Galinstan amalgam reduces the MDP2P-ethylimine intermediate into MDEA. 3,4-MethyleneDioxyPhenyl-2-Propanone is a yellow oily ketone. It is yellow green in the sunlight. MDP2P can also be synthesized by reacting sesamyl tosylate (SmOTs,3,4-Methylenedioxyphenyl tosylate) with ethyl acetoacetate and sodium ethoxide and Copper iodide catalyst and heat. 3,4-MethyleneDioxyPhenyl-2-Propanone is also called Sesamyl-2-Propanone (Se2P, Ses2P, Sm2P), Sesamylacetone, and Piperonyl Methyl Ketone.

I synthesized 3,4-MethyleneDioxyPhenyl-2-Propanone (MDP2P) by reacting 3,4-MethyleneDioxyBenzyl magnesium chloride and acetonitrile followed by hydrochloric acid work-up.

by CognitiveFuel October 29, 2022