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Topic: Sodium Nitroprusside  (Read 4423 times)

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Offline Super Newb

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Sodium Nitroprusside
« on: October 23, 2012, 11:17:01 AM »
Hi all!

I am looking at an assay to detect for the p-aminophenol impurities present in paracetamol. It involves the addition of sodium nitroprusside (in alkaline solution) to form a blue color solution. I would like to know what could be the blue derivative. More information on the assay can be found here: http://books.google.com.sg/books?id=s_sBKJNf184C&pg=PA1076&lpg=PA1076&dq=p-aminophenol+nitroprusside&source=bl&ots=zUONjyusTX&sig=3hQJCJGyh2FEVnV_p7cgEk28pVk&hl=en&sa=X&ei=jbSGUILCHpHMrQfv7oGwBw&ved=0CCYQ6AEwAQ#v=onepage&q=p-aminophenol%20nitroprusside&f=false

Any help will be greatly appreciated :DD

Offline Arkcon

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Re: Sodium Nitroprusside
« Reply #1 on: October 23, 2012, 11:57:57 AM »
Sodium nitroprusside gives a blue color for some secondary amines:  http://en.wikipedia.org/wiki/Sodium_nitroprusside#Use_in_forensic_science  If you use its IUPAC name:  sodium pentacyanonitrosylferrate(II), you'll see it has a cyanoferrate group, that can change color from red to blue when certain complexes form. http://en.wikipedia.org/wiki/Simon%27s_reagent
Hey, I'm not judging.  I just like to shoot straight.  I'm a man of science.

Offline Super Newb

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Re: Sodium Nitroprusside
« Reply #2 on: October 23, 2012, 12:55:19 PM »
However,the mixture does not contain acetyldehye to facilitate the formation of enamine intermediate

Offline xxsamxx

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Re: Sodium Nitroprusside
« Reply #3 on: May 07, 2013, 10:55:30 AM »
HI!! I am also thinking about this question. Am wondering if you have figured it out??? Please do reply asap!!! thank you!!!

I would think a transition metal compound has formed?

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