Author Topic: Alternatives for Sodium Bisulfite  (Read 8129 times)

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Vaaguh

  • Guest
Alternatives for Sodium Bisulfite
« on: October 12, 2003, 06:34:00 AM »
During a post cleanup after the reduction of (Pseudo)Ephedrine with RP/I there is used Sodium Bisulfite, are there any alternatives that could be used perhaps Sodium Bicarbonate?


Vitus_Verdegast

  • Guest
bisulfite
« Reply #1 on: October 12, 2003, 06:43:00 AM »
Isn't that for working up the excess iodine, as it reduces I2 __> 2I-

I guess Na thiosulfate could be used too, but bicarbonate will not work for this purpose.

You can use the Na metabisulfite you find at a brewer's store, when water is added to this, it makes an aqueous solution of NaHSO3.


Vaaguh

  • Guest
thanks for the information, Yes it is indeed...
« Reply #2 on: October 12, 2003, 01:02:00 PM »
thanks for the information,

Yes it is indeed for removing the excess of iodine.

Metabisulfite it is then  ;)


Osmium

  • Guest
This step can be omitted, it's absolutely not...
« Reply #3 on: October 12, 2003, 02:47:00 PM »
This step can be omitted, it's absolutely not necessary.
It might fuck with your iodine recovery attemps, so keep those sulfur compounds out of the reaction.


mr_pyrex

  • Guest
What ^ he said plus...all you need to do if...
« Reply #4 on: October 12, 2003, 04:17:00 PM »
What ^ he said plus...all you need to do if you think you have left over I in your finished rxn solution is to uncap your reaction vessel from your push/pull setup and add say an equal volume of Dh20 as you have in your reaction vessel and then heat it up around 90-95'C for 10-15 minutes, this should drive off any residual Iodine or at least as much as you need to be concerned with.   Pyrex out of advise


amalgum

  • Guest
SWIM always uses sodium sulfite.
« Reply #5 on: October 13, 2003, 01:17:00 PM »
SWIM always uses sodium sulfite.

halfkast

  • Guest
amalgum what industry is sodium sulfite used...
« Reply #6 on: October 14, 2003, 04:17:00 AM »
amalgum what industry is sodium sulfite used in bee? swihk has looked for it briefly before.

I have searched the fs kinda, but not hard enough obviously because i doubt its that hard to find.


stereoIsomer

  • Guest
Recommend the post-rxn I2 evap process
« Reply #7 on: October 14, 2003, 10:11:00 AM »
The main concern is removing excess I2 which is unpleasant to have in the final product, right ? If so, simply heating the post-rxn results to a low boil for 5-10 mins will result in excess I2 to evaporate, leaving you with clean product. Is your goal to recapture excess I2 for later re-use in future reactions ? (swim does not advice about this, sorry... but perhaps someone else does)

amalgum

  • Guest
halfkast- Photography.
« Reply #8 on: October 14, 2003, 10:29:00 PM »
halfkast-
Photography.  Beleive people when they say for chemists like us should take it up as a hobby, cause you would be surprised to see the myriad of shit SWIM has just for photogrophy (and they all have legit use).  From phenols to quinones, and salts ga-fucking-lore, from pure KI to HgNO3.  Palladium salts to.  As long as you walk in to a photography shop and say "Give me two pounds of so and so for a certain toner mix I want to try, and a couple pounds of this for this developer I'm working on" and nobody gives a damn.  Basically I'm saying somethings you get from a photography store, it would help to know the background for it's legit uses.   Something like sodium sulfite isn't suspicious at all.  I mean they'll laugh if you try to buy anything less than a pound jar you know what I'm saying.

Osmium

  • Guest
Listen up class! Once your reaction is done...
« Reply #9 on: October 15, 2003, 02:32:00 AM »
Listen up class!
Once your reaction is done there won't be much I2 left, if at all. Can anyone explain to me how I2 is supposed to show up in the end product, when you
1. wash the still acidic, diluted reaction mixture with a NP,
and then
2. basify the shit out of the reaction mixture with NaOH?
How can I2 survive strong basic pH???

There is no reason to try to remove I2 with sulfite or thiosulfate, this will only complicate further workup.

Anyone ever seen what happens when a solution of thiosulfate is acidified?


halfkast

  • Guest
amalgum yes you were very clear man, I know...
« Reply #10 on: October 15, 2003, 03:40:00 AM »
amalgum yes you were very clear man, I know what you is sayin'.  8)

Os I heard ya the first time. ;)


abolt

  • Guest
Anyone ever seen what happens when a solution...
« Reply #11 on: October 15, 2003, 07:31:00 PM »
Anyone ever seen what happens when a solution of thiosulfate is acidified?

No.............and?


Vitus_Verdegast

  • Guest
SO2 my friend...
« Reply #12 on: October 15, 2003, 08:15:00 PM »
Na2S2O3 + 2H+ __> SO2 + S + H2O + 2Na+

Sulfur dioxide is a colorless, poisonous, very sharp smelling and irritating gas.


halfkast

  • Guest
Upon YOUR suggestion that has been up for...
« Reply #13 on: October 15, 2003, 10:13:00 PM »
Upon YOUR suggestion that has been up for about 4 days in the stimulants forum.


I guess Na thiosulfate could be used too, but bicarbonate will not work for this purpose.







Osmium

  • Guest
> SO2 my friend...
« Reply #14 on: October 16, 2003, 02:02:00 AM »
> SO2 my friend...

It's not the SO2 that is the problem, it is the very fine sulfur that precipitates that will cause you problems.


Vitus_Verdegast

  • Guest
Hey Halfbrain...
« Reply #15 on: October 16, 2003, 04:29:00 AM »
Get off my back will you?
And open a fucking book sometimes, before you start to whine.

No matter if it is an aqueous solution of thiosulfate, sulfite or bisulfite, acidifying will always cause SO2 to evolve. Capiche?


Osmium

  • Guest
> Get off my back will you? Huh?
« Reply #16 on: October 16, 2003, 05:59:00 AM »
> Get off my back will you?

Huh?

> And open a fucking book sometimes, before you start to whine.

Did I whine???
Is it full moon or why are you so sensitive?


hypo

  • Guest
hehe...
« Reply #17 on: October 16, 2003, 06:42:00 AM »
Halfbrain should probably mean halfkast  ;)

(who's sensitive?  :P )


amalgum

  • Guest
Yeah that is true, as long as the reaction is...
« Reply #18 on: October 16, 2003, 09:22:00 AM »
Yeah that is true, as long as the reaction is completely done, there shouldn't be any I2 left.  SWIM always used just a little bit as a precaution.  Plus sometimes if the rp isn't to clean and after it tends to clump, Na2SO2 seems to loosen it pretty nicely sometimes.

WizardX

  • Guest
Starch
« Reply #19 on: October 16, 2003, 06:33:00 PM »
Starch is used in analytical chemistry as an endpoint indicator (dark blue colour) for I2. After your HI/RP reduction and work-up/purification to the meth freebase; by adding one drop to a starch solution and a resulting dark blue colour is observed, then I2 is present.

Osmium

  • Guest
I'd rather do it the other way round, add a...
« Reply #20 on: October 17, 2003, 12:29:00 AM »
I'd rather do it the other way round, add a drop of your reaction solution to a little bit of starch solution.

Even if there is a minuscule amount of I2 present, it doesn't matter since the I2 will be taken care of by the standard workup procedure.


mr_pyrex

  • Guest
I was just re-reading the thread and something
« Reply #21 on: October 17, 2003, 01:02:00 AM »
I was just re-reading the thread and something came to mind which could be of interest to those that insist on aquiring and using say- Sodium Thiosulfate.  I am not recommending using it I am just letting those interested in it know that it can be aquired through their local pool supplier, no questions asked and it should set you back no more then $15 for 1 pound.  Its purpose in the pool and spa industry is as chlorine neutralizer....usually when someone has overdosed the chlorine or bromine in their pool or spa and needs to bring the level down quickly. One of the many names they might carry it under is thiotrine.  Anyways like I said this is for those interested in aquiring it.    Pyrex out of pointers ;-)


halfkast

  • Guest
And open a fucking book sometimes, before you...
« Reply #22 on: October 17, 2003, 03:13:00 AM »
And open a fucking book sometimes, before you start to whine.

No matter if it is an aqueous solution of thiosulfate, sulfite or bisulfite, acidifying will always cause SO2 to evolve. Capiche?


I never said anything about using sodium sulfite for this purpose.

Solving the problem is pointless, because the problem isn't a problem, it's a temporary inconvenience corrected by the usual process.

Fuck just read Os three posts hes right in all of them.


Vitus_Verdegast

  • Guest
Look
« Reply #23 on: October 17, 2003, 07:29:00 AM »
I'd never throw such remark at you, Os  ::)  ;)

Look I really don't want to argue here, and I also think that Os is 200% right on this, but I suggested using Na thiosulfate in the second post in this thread, as a reply to Vaaguh's question for alternatives for Na bisulfite.

How I empictured this was washing the post-rxn organic layer with an aqueous solution of this, but I didn't realize that most people here want to recover their iodine.


amalgum

  • Guest
I totally forgot about people who recover...
« Reply #24 on: October 17, 2003, 10:28:00 AM »
I totally forgot about people who recover their iodine.  It's definitely not something you consider when you've got like half pound of I2, plus a pound or two of KI just in case laying around.  It might be a practice SWIM will have to add to the lucid dreams.  Haven't hit the KI yet, but SWIM is down to scraping all the I2 he can get out of that bottle.