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

Printable Version  
 Pages:  1  2
Author: Subject: sulfonylchloride to thiol
vulture
Forum Gatekeeper
*****




Posts: 3330
Registered: 25-5-2002
Location: France
Member Is Offline

Mood: No Mood

[*] posted on 2-10-2008 at 12:48


Thiophenols smell like hell, concentrated stuff will make you want to vomit, totally not like gasoline.

Quote:

It is however true that TLC can sometimes show a pale spot of a side product while this is invisible on NMR. I think this is only the case when the side product has an unusually high UV absorption or fluorescence, since this does not happen often to me and when it does the spot most commonly shines at the 366nm light.


I've had them show up on 254nm too. But then again I'm often making monomers for polycondensations, which requires you don't have any chain terminator at all present.
View user's profile View All Posts By User
DNA
Hazard to Others
***




Posts: 191
Registered: 11-6-2003
Location: @moon
Member Is Offline

Mood: Experimenting

[*] posted on 3-10-2008 at 00:13


I'll determine the boiling point anywhere soon so then I can say more about if it actually is the thiol.
Also an GC-MS and NMR will be taken next week, I'll keep you updated.
View user's profile View All Posts By User This user has MSN Messenger
 Pages:  1  2

  Go To Top