Sciencemadness Discussion Board
Not logged in [Login ]
Go To Bottom

Printable Version  
Author: Subject: Isonitrosoacetophenone from NOCl + acetone
International Hazard

Posts: 1233
Registered: 12-12-2012
Location: Dysrope (aka europe)
Member Is Offline

Mood: dangerously practical

[*] posted on 18-1-2019 at 05:07
Isonitrosoacetophenone from NOCl + acetone

minor potential energetic use of this compound, seems to be solid at room temperature, OTC chemicals. so what can we do with this stuff? NOCl + ketones is risky as the mixture may explode with some metal traces

would it be possible to break this compound down and seperate the benzyl ring somehow? of what ive come across benzyl isnt very typical to synthesize, usually extracted

~25 drops = 1mL @dH2O viscocity - STP
Truth is ever growing - but without context theres barely any such.
View user's profile View All Posts By User

  Go To Top