Chemistry:Ninhydrin

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Ninhydrin
Ninhydrin
Ninhydrin sample.jpg
Names
Preferred IUPAC name
2,2-Dihydroxy-1H-indene-1,3(2H)-dione
Other names
2,2-Dihydroxyindane-1,3-dione
1,2,3-Indantrione hydrate
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
EC Number
  • 213-340-1
UNII
Properties
C9H6O4
Molar mass 178.143 g·mol−1
Appearance White solid
Density 0.862 g/cm3
Melting point 250 °C (482 °F; 523 K) (decomposes)
20 g L−1[1]
Hazards
Safety data sheet External MSDS
GHS pictograms GHS07: Harmful
GHS Signal word Warning
H302, H315, H319, H335
P261, P264, P270, P271, P280, P301+312, P302+352, P304+340, P305+351+338, P312, P321, P330, P332+313, P337+313, P362, P403+233, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references
Tracking categories (test):

Ninhydrin (2,2-dihydroxyindane-1,3-dione) is an organic compound with the formula C6H4(CO)2C(OH)2. It is used to detect ammonia and amines. Upon reaction with these amines, ninhydrin gets converted into deep blue or purple derivatives, which are called Ruhemann's purple. Ninhydrin is most commonly used to detect fingerprints in forensic cases, as the terminal amines of lysine residues in peptides and proteins sloughed off in fingerprints react with ninhydrin.[2][3]

Ninhydrin is a white solid that is soluble in ethanol and acetone.[1] Ninhydrin can be considered as the hydrate of indane-1,2,3-trione.

History

Ninhydrin was discovered in 1910 by the German-English chemist Siegfried Ruhemann (1859–1943).[4][5] In the same year, Ruhemann observed ninhydrin's reaction with amino acids.[6] In 1954, Swedish investigators Oden and von Hofsten proposed that ninhydrin could be used to develop latent fingerprints.[7][8]

Uses

Ninhydrin can be used in Kaiser test to monitor deprotection in solid phase peptide synthesis.[9] The chain is linked via its C-terminus to the solid support, with the N-terminus extending off it. When that nitrogen is deprotected, a ninhydrin test yields blue. Amino-acid residues are attached with their N-terminus protected, so if the next residue has been successfully coupled onto the chain, the test gives a colorless or yellow result.

Ninhydrin is also used in qualitative analysis of proteins. Most of the amino acids, except proline, are hydrolyzed and react with ninhydrin. Also, certain amino acid chains are degraded. Therefore, separate analysis is required for identifying such amino acids that either react differently or do not react with ninhydrin at all. The rest of the amino acids are then quantified colorimetrically after separation by chromatography.

A solution suspected of containing the ammonium ion can be tested by ninhydrin by dotting it onto a solid support (such as silica gel); treatment with ninhydrin should result in a dramatic purple color if the solution contains this species. In the analysis of a chemical reaction by thin layer chromatography (TLC), the reagent can also be used (usually 0.2% solution in either n-butanol or in ethanol). It will detect, on the TLC plate, virtually all amines, carbamates and also, after vigorous heating, amides.

Upon reaction with ninhydrin, amino acids undergo decarboxylation. The released CO2 originates from the carboxyl carbon of the amino acid. This reaction has been used to release the carboxyl carbons of bone collagen from ancient bones[10] for stable isotope analysis in order to help reconstruct the palaeodiet of cave bears.[11] Release of the carboxyl carbon (via ninhydrin) from amino acids recovered from soil that has been treated with a labeled substrate demonstrates assimilation of that substrate into microbial protein.[12] This approach was successfully used to reveal that some ammonium oxidizing bacteria, also called nitrifying bacteria use urea as a carbon source in soil.[13]

A stain obtained after a thumbprint is treated with ninhydrin.

Forensics

A ninhydrin solution is commonly used by forensic investigators in the analysis of latent fingerprints on porous surfaces such as paper. The amino acids present in the minute sweat secretions that gather on the finger's unique ridges transfer to surfaces that are touched. Exposure of the surface to ninhydrin converts the amino acids into visibly colored products and thus reveals the print.[14] The test solutions suffer from poor long-term stability, especially if not kept cold.[15]

To further enhance the ability of ninhydrin, a solution of 1,2-indandione and zinc chloride (IND-Zn) can be used prior to ninhydrin. This sequence leads to greater overall reaction of the amino acids, possibly by IND-Zn helping to release them from the surface for the subsequent ninhydrin reaction.[16]

Reactivity

Ninhydrin exists in equilibrium with the triketone indane-1,2,3-trione, which reacts readily with nucleophiles (including water). Whereas for most carbonyl compounds, a carbonyl form is more stable than a product of water addition (hydrate), ninhydrin forms a stable hydrate of the central carbon because of the destabilizing effect of the adjacent carbonyl groups.

To generate the ninhydrin chromophore [2-(1,3-dioxoindan-2-yl)iminoindane-1,3-dione], the amine must condense to give a Schiff base. The reaction of ninhydrin with secondary amines gives an iminium salt, which is also coloured, generally being yellow–orange.

Ninhydrin Reaction Mechanism.svg

Effects on health

Ninhydrin may cause allergic, IgE-mediated rhinitis and asthma.[17] A case has been described in which a 41 year old forensic laboratory worker working with Ninhydrin developed rhinitis and respiratory difficulty. Her specific IgE levels were found almost doubled.[17]

See also

References

  1. ↑ 1.0 1.1 Chemicals and reagents, 2008–2010, Merck
  2. ↑ "Fingerprinting Analysis". Bergen County Technical Schools. June 2003. http://www.bergen.org/EST/Year5/fingerprint.htm. 
  3. ↑ Rowe, Walter F. (2015). "Forensic Chemistry". Kirk-Othmer Encyclopedia of Chemical Technology. pp. 1–19. doi:10.1002/0471238961.0615180506091908.a01.pub3. ISBN 9780471238966. 
  4. ↑ Ruhemann, Siegfried (1910). "Cyclic Di- and Tri-ketones". Journal of the Chemical Society, Transactions 97: 1438–1449. doi:10.1039/ct9109701438. https://archive.org/stream/p2journal97chemuoft#page/1438/mode/2up. 
  5. ↑ West, Robert (1 July 1965). "Siegfried Ruhemann and the Discovery of Ninhydrin". Journal of Chemical Education 42 (7): 386–388. doi:10.1021/ed042p386. Bibcode: 1965JChEd..42..386W. https://pubs.acs.org/doi/abs/10.1021/ed042p386. 
  6. ↑ Ruhemann, S. (1910). "Triketohydrindene Hydrate". Journal of the Chemical Society, Transactions 97: 2025–2031. doi:10.1039/ct9109702025. https://archive.org/stream/p2journal97chemuoft#page/2024/mode/2up. 
  7. ↑ Odén, Svante; von Hofsten, Bengt (1954). "Detection of Fingerprints by the Ninhydrin Reaction". Nature 173 (4401): 449–450. doi:10.1038/173449a0. PMID 13144778. Bibcode: 1954Natur.173..449O. https://ui.adsabs.harvard.edu/abs/1954Natur.173..449O/abstract. 
  8. ↑ Oden, Svante.. "Process of Developing Fingerprints". http://pdfpiw.uspto.gov/.piw?Docid=02715571&homeurl=http%3A%2F%2Fpatft.uspto.gov%2Fnetacgi%2Fnph-Parser%3FSect2%3DPTO1%2526Sect2%3DHITOFF%2526p%3D1%2526u%3D%2Fnetahtml%2FPTO%2Fsearch-bool.html%2526r%3D1%2526f%3DG%2526l%3D50%2526d%3DPALL%2526S1%3D2715571.PN.%2526OS%3DPN%2F2715571%2526RS%3DPN%2F2715571&PageNum=&Rtype=&SectionNum=&idkey=NONE&Input=View+first+page.  U.S. Patent no. 2,715,571 (filed: 27 September 1954; issued: 16 August 1955).
  9. ↑ Kaiser, E.; Colescott, R.L.; Bossinger, C.D.; Cook, P.I. (1970). "Color Test for Detection of Free Terminal Amino Groups in the Solid-Phase Synthesis of Peptides". Analytical Biochemistry 34 (2): 595–8. doi:10.1016/0003-2697(70)90146-6. PMID 5443684. 
  10. ↑ Keeling, C. I.; Nelson, D. E.; Slessor, K. N. (1999). "Stable Carbon Isotope Measurements of the Carboxyl Carbons in Bone Collagen". Archaeometry 41: 151–164. doi:10.1111/j.1475-4754.1999.tb00857.x. http://summit.sfu.ca/system/files/iritems1/6994/b17944776.pdf. 
  11. ↑ Keeling, C. I.; Nelson, D. E. (2001). "Changes in the Intramolecular Stable Carbon Isotope Ratios with Age of the European Cave Bear (Ursus spelaeus)". Oecologia 127 (4): 495–500. doi:10.1007/S004420000611. PMID 28547486. Bibcode: 2001Oecol.127..495K. 
  12. ↑ Marsh, K. L., Mulvaney, R. L. and Sims, G. K. (2003). "A Technique to Recover Tracer as Carboxyl-Carbon and α-Nitrogen from Amino Acids in Soil Hydrolysates". J. AOAC Int. 86 (6): 1106–1111. doi:10.1093/jaoac/86.6.1106. PMID 14979690. 
  13. ↑ Marsh, K. L., Sims, G. K. and Mulvaney, R. L. (2005). "Availability of Urea to Autotrophic Ammonia-Oxidizing Bacteria as Related to the Fate of 14C- and 15N-labeled Urea Added to Soil". Biol. Fert. Soil. 42 (2): 137–145. doi:10.1007/s00374-005-0004-2. 
  14. ↑ Menzel, E.R. (1986) Manual of fingerprint development techniques. Home Office, Scientific Research and Development Branch, London. ISBN:0862522307
  15. ↑ Janssen-Bouwmeester, Roy; Bremmer, Christiaan; Koomen, Linda; Siem-Gorré, Shermayne; de Puit, Marcel (May 2020). "Positive control tests for fingermark development reagents" (in en). Forensic Science International 310: 110259. doi:10.1016/j.forsciint.2020.110259. PMID 32224429. 
  16. ↑ Mangle, Milery Figuera; Xu, Xioama; de Puit, M. (September 2015). "Performance of 1,2-indanedione and the need for sequential treatment of fingerprints" (in en). Science & Justice 55 (5): 343–346. doi:10.1016/j.scijus.2015.04.002. PMID 26385717. 
  17. ↑ 17.0 17.1 "Rhinitis caused by ninhydrin develops into occupational asthma". Eur Respir J 10 (8): 1918–1921. August 1997. doi:10.1183/09031936.97.10081918. PMID 9272939. 



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