Schiff test

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The Schiff test invented

[1]

and named after Hugo Schiff is a chemical test for the detection of aldehydes.

[2]

An

unknown sample is added to the decolorized Schiff reagent and when aldehyde is present a characteristic magenta or purple color develops. The Schiff reagent is the reaction product of Fuchsine or the closely related Pararosaniline (lacks a methyl group) and sodium bisulfite. Human skin also contains aldehydes and gets stained as well.
[citation needed]

Schiff reagents are used for various staining methods, e.g. Feulgen stain and periodic acid-Schiff stain.
Contents
[hide]

1 Mechanism 2 External links 3 See also 4 References

[edit]Mechanism Fuchsin itself is colored due to its quinoid structure (see also for example viologen) but is discolorized by sulfonation at the central carbon atom which disrupts the favorable resonance in the molecule. More bisulphite (depending on stoichiometry ) reacts with available amine groups to so-called N-sulfinic acid groups. The reaction of the Schiff reagent with aldehydes is complex with several research groups reporting multiple reaction products with model compounds. Two different mechanisms appear in the literature
[3]

The first mechanism explaining

its action with aldehydes was proposed by H. Wieland in 1935. In it the aldehyde groups react with the sulfinic acid groups forming an sulfonamide.

In the second mechanism, the pararosanilin, sulfurous acid and aldehyde combine to form an alkyl sulfonic acid with sulfur bonded to carbon rather than to nitrogen. This mechanism was first proposed by P. Rumpf in 1935 and experimental evidence was obtained in 1964 by Hardonk and van Duijn.
[4]

They noted that when

the aldehyde is reacted first with sulfurous acid and then with the Schiff compound the UV spectrum is identical to one obtained in a standard test. This particular logic was disputed by Stoward in 1966 although on the whole he agreed with the new mechanism.
[5]

In 1980NMR spectroscopy (Robins, Abrams, Pincock)

[6]

provided further support for the sulfonic acid mechanism.

[edit]External

links

What is Schiff's reagent?

[edit]See

also

Tollens' reagent Fehling's reagent 2,4-Dinitrophenylhydrazine Fehling's solution Barfoed's test

[edit]References

1.

^ Eine neue Reihe organischen Diaminen H. Schiff Justus Liebigs Ann Chemie 140, 92-137 1866

2. 3.

^ Histology, cell and tissue biology 5th Ed., 1983 ISBN 0333354060 ^ Histochemistry, theoretical and applied 4th Ed. 1985 ISBN 044302997 Note: the depiction of the sulfonic acid mechanism in this edition contains an error as the aldehyde R group is bonded to nitrogen and not to its carbon neighbor

4.

^ THE MECHANISM OF THE SCHIFF REACTION AS STUDIED WITH HISTOCHEMICAL MODEL SYSTEMS M. J. HARDONK and P. VAN DUIJN J. Histochem. Cytochem., Oct 1964; 12: 748 - 751.

5.

^ SOME COMMENTS ON THE MECHANISM OF THE SCHIFF REACTION P. J. STOWARD J. Histochem. Cytochem., Sep 1966; 14: 681 683.

6.

^ The structure of Schiff reagent aldehyde adducts and the mechanism of the Schiff reaction as determined by nuclear magnetic resonance spectroscopy J.H. Robins, G.D. Abrams, and J.A. Pincock Can. J. Chem./Rev. can. chim. 58(4): 339-347 (1980)

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