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Topic: Sodium Nitroprusside (Read 4423 times)
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Super Newb
Regular Member
Posts: 46
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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
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Arkcon
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Re: Sodium Nitroprusside
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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
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Hey, I'm not judging. I just like to shoot straight. I'm a man of science.
Super Newb
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Re: Sodium Nitroprusside
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Reply #2 on:
October 23, 2012, 12:55:19 PM »
However,the mixture does not contain acetyldehye to facilitate the formation of enamine intermediate
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xxsamxx
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Re: Sodium Nitroprusside
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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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