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

Printable Version  
Author: Subject: Precipate formed from Potassium ferricyanide and acetone
The_Great_Orgo
Harmless
*




Posts: 5
Registered: 1-11-2018
Member Is Offline


[*] posted on 11-2-2019 at 13:55
Precipate formed from Potassium ferricyanide and acetone


I was cleaning glassware today after making some Potassium Ferricyanide and used acetone since the bottle wasn't labeled. A White precipitate formed and I don't know what it was. Any Ideas as to what it could have been? It was some leftover residue after pouring out the PF originally. It seemed to fully ppt what residue was left.
View user's profile View All Posts By User
zed
International Hazard
*****




Posts: 2277
Registered: 6-9-2008
Location: Great State of Jefferson, City of Portland
Member Is Offline

Mood: Semi-repentant Sith Lord

[*] posted on 11-2-2019 at 18:43


Orgo, I have no idea. But, I would handle this material with caution.

Some unexpectedly energetic properties might be present.

Oh, probably not. But, it is something to ponder on.

Potassium Ferricyanide combines exlposively, when compounded with some oxidants.
View user's profile View All Posts By User
Deathunter88
National Hazard
****




Posts: 508
Registered: 20-2-2015
Location: Beijing, China
Member Is Offline

Mood: No Mood

[*] posted on 11-2-2019 at 20:27


Probably just potassium ferricyanide crashing out of solution due to it being insoluble in acetone.
View user's profile View All Posts By User
Loptr
International Hazard
*****




Posts: 1347
Registered: 20-5-2014
Location: USA
Member Is Offline

Mood: Grateful

[*] posted on 12-2-2019 at 08:02


Potassium ferricyanide will react with aldehydes to form a dihydropyrazine, presumably through an alpha-amino aldehyde, but this wouldn't be possible with acetone.



"Question everything generally thought to be obvious." - Dieter Rams
View user's profile View All Posts By User

  Go To Top