| Pages:
1
2
3
4 |
Boffis
International Hazard
Posts: 1879
Registered: 1-5-2011
Member Is Offline
Mood: No Mood
|
|
Quote: Originally posted by Pumukli  | | Does it mean that the DEET you used did contain some (5-10%) diethyl-o-toluamide too? Could this be detected on say TLC? |
Yes probably, but I didn't think about the possibility of isomers until I tried to recrystallise the and found the acid melted at a rather low
temperature. By this time I had hydrolysed all that I had. I have thought about trying to use TLC or paper chromatography to charaterise the acids and
compare them with bought or acids prepared by unambiguous routes (I have p-toluic acid, o-toluidine and o-xylene so this shouldn't be too difficult).
An interesting observation I made while dissolving BaCO3 and m-toluic acid in water it required about 30% more carbonate that theory. I have no
explanation for this.
|
|
|
Boffis
International Hazard
Posts: 1879
Registered: 1-5-2011
Member Is Offline
Mood: No Mood
|
|
I have just posted in the prepublication section my write-up on my experiments into the hydrolysis of DEET if anyone wants to talk a look.
|
|
|
| Pages:
1
2
3
4 |
![[*]](images/xpblue/default_icon.gif){kind=icon}
