{"id":2315,"date":"2021-03-15T16:50:45","date_gmt":"2021-03-15T16:50:45","guid":{"rendered":"https:\/\/laboratoryinfo.com\/?p=2315"},"modified":"2022-03-07T19:57:39","modified_gmt":"2022-03-07T19:57:39","slug":"ninhydrin-test","status":"publish","type":"post","link":"https:\/\/laboratoryinfo.com\/ninhydrin-test\/","title":{"rendered":"Ninhydrin Test &#8211; Procedure, Uses, Principle and Result"},"content":{"rendered":"\n<p>Ninhydrin is a chemical that detects ammonia as well as amines (primary and secondary). Once ninhydrin reacts with these chemicals, it produces a deep blue or purple color \u2013 Ruhemann\u2019s purple. Ninhydrin is also the same chemical used to detect fingerprints.<\/p>\n\n\n<style>.kb-table-of-content-nav.kb-table-of-content-id6113_3b9ebd-8c .kb-table-of-content-wrap{padding-top:var(--global-kb-spacing-sm, 1.5rem);padding-right:var(--global-kb-spacing-sm, 1.5rem);padding-bottom:var(--global-kb-spacing-sm, 1.5rem);padding-left:var(--global-kb-spacing-sm, 1.5rem);background-color:#ecf2f7;}.kb-table-of-content-nav.kb-table-of-content-id6113_3b9ebd-8c .kb-table-of-contents-title-wrap{padding-top:0px;padding-right:0px;padding-bottom:0px;padding-left:0px;}.kb-table-of-content-nav.kb-table-of-content-id6113_3b9ebd-8c .kb-table-of-contents-title{font-weight:regular;font-style:normal;}.kb-table-of-content-nav.kb-table-of-content-id6113_3b9ebd-8c .kb-table-of-content-wrap .kb-table-of-content-list{font-weight:regular;font-style:normal;margin-top:var(--global-kb-spacing-sm, 1.5rem);margin-right:0px;margin-bottom:0px;margin-left:0px;}.kb-table-of-content-nav.kb-table-of-content-id6113_3b9ebd-8c .kb-toggle-icon-style-basiccircle .kb-table-of-contents-icon-trigger:after, .kb-table-of-content-nav.kb-table-of-content-id6113_3b9ebd-8c .kb-toggle-icon-style-basiccircle .kb-table-of-contents-icon-trigger:before, .kb-table-of-content-nav.kb-table-of-content-id6113_3b9ebd-8c .kb-toggle-icon-style-arrowcircle .kb-table-of-contents-icon-trigger:after, .kb-table-of-content-nav.kb-table-of-content-id6113_3b9ebd-8c .kb-toggle-icon-style-arrowcircle .kb-table-of-contents-icon-trigger:before, .kb-table-of-content-nav.kb-table-of-content-id6113_3b9ebd-8c .kb-toggle-icon-style-xclosecircle .kb-table-of-contents-icon-trigger:after, .kb-table-of-content-nav.kb-table-of-content-id6113_3b9ebd-8c .kb-toggle-icon-style-xclosecircle .kb-table-of-contents-icon-trigger:before{background-color:#ecf2f7;}<\/style>\n\n\n<p>It is effective because the terminal amines of a lysine residue in both proteins and peptides sloughed off in fingerprints and react with the said chemical.<\/p>\n\n\n\n<p>Under normal circumstances, ninhydrin is a white solid and soluble in substances like acetone and ethanol at room temperature. It was discovered by a German-English chemist Siefried Ruhemann in 1910. He observed the reaction of ninhydrin to an amino acid.<\/p>\n\n\n\n<p>It was in 1954 when two investigators; Oden and von Hofsten proposed the use of ninhydrin in the development of latent fingerprints. <sup><em><strong>(1, 2, 3, and 4)<\/strong><\/em><\/sup><\/p>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter size-full is-resized\"><img decoding=\"async\" src=\"http:\/\/laboratoryinfo.com\/wp-content\/uploads\/2019\/09\/ninhydrin-test-involving-two-test-tubes.jpg\" alt=\"ninhydrin test involving two test tubes\" class=\"wp-image-2350\" width=\"400\" srcset=\"https:\/\/laboratoryinfo.com\/wp-content\/uploads\/2019\/09\/ninhydrin-test-involving-two-test-tubes.jpg 600w, https:\/\/laboratoryinfo.com\/wp-content\/uploads\/2019\/09\/ninhydrin-test-involving-two-test-tubes-300x269.jpg 300w, https:\/\/laboratoryinfo.com\/wp-content\/uploads\/2019\/09\/ninhydrin-test-involving-two-test-tubes-20x18.jpg 20w\" sizes=\"(max-width: 600px) 100vw, 600px\" \/><\/figure><\/div>\n\n\n\n<p><strong><b>Image 1:<\/b><\/strong> A ninhydrin test involving two test tubes. The one in the left is negative while the other on the right is positive as seen in the purplish\/bluish discoloration.<\/p>\n\n\n\n<p class=\"has-text-align-center\"><strong><b>Picture Source:&nbsp;<\/b><\/strong>researchgate.net<\/p>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter size-full is-resized\"><img decoding=\"async\" src=\"http:\/\/laboratoryinfo.com\/wp-content\/uploads\/2019\/09\/ninhydrin-test-is-used-to-detect-fingerprints.jpg\" alt=\"ninhydrin test is used to detect fingerprints\" class=\"wp-image-2351\" width=\"400\" srcset=\"https:\/\/laboratoryinfo.com\/wp-content\/uploads\/2019\/09\/ninhydrin-test-is-used-to-detect-fingerprints.jpg 600w, https:\/\/laboratoryinfo.com\/wp-content\/uploads\/2019\/09\/ninhydrin-test-is-used-to-detect-fingerprints-300x156.jpg 300w, https:\/\/laboratoryinfo.com\/wp-content\/uploads\/2019\/09\/ninhydrin-test-is-used-to-detect-fingerprints-20x10.jpg 20w\" sizes=\"(max-width: 600px) 100vw, 600px\" \/><\/figure><\/div>\n\n\n\n<p class=\"has-text-align-center\"><strong><b>Image 2:<\/b><\/strong> A ninhydrin test is used to detect fingerprints.<\/p>\n\n\n\n<p class=\"has-text-align-center\"><strong><b>Picture Source:&nbsp;<\/b><\/strong>libretexts.org<\/p>\n\n\n\n<h2 class=\"wp-block-heading\">What is the Ninhydrin test for?<\/h2>\n\n\n\n<ul><li>It plays an important role in monitoring deprotection in solid-phase peptide synthesis. If nitrogen is deprotected, the ninhydrin test turns blue.<\/li><li>It is used in the analysis of amino acid in proteins. Most amino acids hydrolyzed and react with ninhydrin with the exception of proline. Some amino acid chains degrade. Hence, a separate analysis is needed in order to identify amino acids that may react or not react with ninhydrin at all.<\/li><li>It is used to check a solution suspected of having ammonium ion. A treatment with ninhydrin would result in dramatic purple color.<\/li><li>It is usually used by forensic investigators in the analysis of fingerprints on porous surfaces. A fingermark that contains amino acid is treated with ninhydrin solution, which results in a purple amino acid finger ridge pattern. Hence, making the fingerprint visible. <sup><em><strong>(3, 4, 5, and 6)<\/strong><\/em><\/sup><\/li><\/ul>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter size-full is-resized\"><img decoding=\"async\" src=\"http:\/\/laboratoryinfo.com\/wp-content\/uploads\/2019\/09\/ninhydrin-test-is-a-quick-procedure-that-can-be-done-in-just-a-few-minutes.jpg\" alt=\"ninhydrin test is a quick procedure that can be done in just a few minutes\" class=\"wp-image-2352\" width=\"400\" srcset=\"https:\/\/laboratoryinfo.com\/wp-content\/uploads\/2019\/09\/ninhydrin-test-is-a-quick-procedure-that-can-be-done-in-just-a-few-minutes.jpg 500w, https:\/\/laboratoryinfo.com\/wp-content\/uploads\/2019\/09\/ninhydrin-test-is-a-quick-procedure-that-can-be-done-in-just-a-few-minutes-300x148.jpg 300w, https:\/\/laboratoryinfo.com\/wp-content\/uploads\/2019\/09\/ninhydrin-test-is-a-quick-procedure-that-can-be-done-in-just-a-few-minutes-20x10.jpg 20w\" sizes=\"(max-width: 500px) 100vw, 500px\" \/><\/figure><\/div>\n\n\n\n<p class=\"has-text-align-center\"><strong><b>Image 3:<\/b><\/strong> The test tubes reveals a positive ninhydrin test.<\/p>\n\n\n\n<p class=\"has-text-align-center\"><strong><b>Picture Source:&nbsp;<\/b><\/strong>encrypted-tbn0.gstatic.com<\/p>\n\n\n\n<blockquote class=\"wp-block-quote\"><p style=\"text-align: center;\"><strong><em>A ninhydrin test is a quick procedure that can be done in just a few minutes.<\/em><\/strong><\/p><\/blockquote>\n\n\n\n<h2 class=\"wp-block-heading\">What is the principle of the ninhydrin test?<\/h2>\n\n\n\n<p>A ninhydrin test is a general test performed by all amino acids. The <a href=\"https:\/\/laboratoryinfo.com\/onpg-test\/\" target=\"_blank\" rel=\"noreferrer noopener\">test is performed as a result<\/a> of the reaction between the amino group of free amino acid and ninhydrin. As you know, ninhydrin is a strong oxidizing agent. Its presence causes the amino acid to go through oxidative deamination liberating ammonia and reduces the formation of ninhydrin.<\/p>\n\n\n\n<p>The formed NH3 reacts with the molecule of ninhydrin resulting in the formation of a blue substance. However, some amino acids like proline and hydroxyproline do not lead to the production of blue or purple substances. They usually yield to a brown colored product. <sup><em><strong>(6, 7, and 8)<\/strong><\/em><\/sup><\/p>\n\n\n\n<h2 class=\"wp-block-heading\">What are the requirements for the ninhydrin test?<\/h2>\n\n\n\n<ul><li>Test solution which consists of 1% proline, alanine, and asparagines<\/li><li>Water bath<\/li><li>2% ninhydrin in acetone<\/li><li>dry test tubes<\/li><li>pipettes <sup><em><strong>(8)<\/strong><\/em><\/sup><\/li><\/ul>\n\n\n\n<h2 class=\"wp-block-heading\">How does the ninhydrin test work?<\/h2>\n\n\n\n<ol><li>A 0.2 gm of ninhydrin should be dissolved in 10 ml of acetone. In the absence of acetone, you can use ethanol.<\/li><li>Mix 1% of amino acid solution in distilled water.<\/li><li>An equivalent number of the test solution and distilled water, both 1 ml is put in a dry test tube. One test tube for the test solution and 1 test tube with distilled water as a control.<\/li><li>Both test tubes should be poured with a few drops of 2% ninhydrin.<\/li><li>Place the two test tubes in water bath for approximately five minutes.<\/li><li>Watch for any signs of changes in color \u2013 blue or violet. <sup><em><strong>(8, 9, and 10)<\/strong><\/em><\/sup><\/li><\/ol>\n\n\n\n<p><span style=\"color: #ff6600;\"><strong>Note:&nbsp;<\/strong><\/span><\/p>\n\n\n\n<p>Proline and hydroxyproline do not cause blue or violet discoloration. Instead, they produce color yellow. On the other hand, asparagine would result in brown color.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\">Why is Ninhydrin used in chromatography?<\/h2>\n\n\n\n<p>To detect amino acids on thin later chromatographic plates, various types of reagents are used and one of them is ninhydrin. It is the most preferred one because of its high sensitivity. The resulting color is still blue or purple\/violet with all amino acids with the exception of proline and hydroxyproline, which causes the color to turn yellow. <sup><em><strong>(2, 5, and 9)<\/strong><\/em><\/sup><\/p>\n\n\n\n<h2 class=\"wp-block-heading\"><b>Facts about the Ninhydrin test<\/b><\/h2>\n\n\n\n<ul><li>Many bioanalytical procedures use ninhydrin, especially for amino acid analysis method.<\/li><li>Ninhydrin test is used by SSDs for residual protection detection on re-usable surgical instruments.<\/li><li>Amino acids react with ninhydrin, which results in discoloration.<\/li><li>Ninhydrin test is used in both quantitative and qualitative purposes \u2013 such as chromatographic visualization and peptide sequencing.<\/li><li>Bluish to purplish discoloration is produced by the a-amino acids while yellow to orange discoloration is caused by secondary amine like proline.<\/li><li>Ninhydrin test is extremely sensitive that it can be used to visualize fingerprints.<\/li><li>Ninhydrin is the most preferred chemical for the visualization of fingerprints on porous materials and paper as it reacts with the amino acids in the sweat left behind in a fingerprint.<\/li><li>The strong compound formed by ninhydrin is called Ruhemann\u2019s purple.<\/li><li>The strongly colored compound that is then formed is called Ruhemann&#8217;s purple.<\/li><li>Ninhydrin reacts with compounds containing amine such as proteins in the blood. <sup><em><strong>(1, 4, 6, 9, and 10)<\/strong><\/em><\/sup><\/li><\/ul>\n\n\n\n<p>The color reaction of ninhydrin is helpful in various industries such as biochemistry, microbiology, food industry, protein science, and histochemistry. More so, ninhydrin as a reagent is used to detect amino acids on a chromatogram. There are various improvements in the use of ninhydrin to check and analyze various chemical compounds, foods, tissues, and drug of interest.<\/p>\n\n\n\n<p>Ninhydrin is also essential in forensic science and a material used in organic synthesis. It plays an important role in the design and synthesis of different frameworks, especially in the preparation of heterocyclic compounds like anticancer agents. Lastly, ninhydrin is a helpful tool in geochronology, a special field of science that focuses on determining the age of fossils. <sup><em><strong>(3, 6, 9, and 10)<\/strong><\/em><\/sup><\/p>\n\n\n\n<p><strong>References<\/strong><\/p>\n\n\n\n<ol><li><em>https:\/\/www.onlinebiologynotes.com\/ninhydrin-test-principle-requirements-procedure-and-result\/<\/em><\/li><li><em>https:\/\/en.wikipedia.org\/wiki\/Ninhydrin<\/em><\/li><li><em>http:\/\/www.jbc.org\/content\/25\/2\/319.full.pdf<\/em><\/li><li><em>http:\/\/dept.harpercollege.edu\/chemistry\/chm\/100\/dgodambe\/thedisk\/food\/ninhy\/ninhy.htm<\/em><\/li><li><em>https:\/\/www.ncbi.nlm.nih.gov\/pubmed\/14759124<\/em><\/li><li><em>https:\/\/www.sciencedirect.com\/topics\/medicine-and-dentistry\/ninhydrin<\/em><\/li><li><em>https:\/\/vlab.amrita.edu\/?sub=3&amp;brch=63&amp;sim=156&amp;cnt=1<\/em><\/li><li><em>https:\/\/www.nature.com\/articles\/1971305a0<\/em><\/li><li><em>http:\/\/www.chm.bris.ac.uk\/motm\/ninhydrin\/ninhydrinh.htm<\/em><\/li><li><em>https:\/\/studylib.net\/doc\/5795721\/15.-ninhydrin-testa<\/em><\/li><\/ol>\n","protected":false},"excerpt":{"rendered":"<p>Ninhydrin is a chemical that detects ammonia as well as amines (primary and secondary). Once ninhydrin reacts with these chemicals, it produces a deep blue or purple color \u2013 Ruhemann\u2019s purple. Ninhydrin is also the same chemical used to detect fingerprints. It is effective because the terminal amines of a lysine residue in both proteins&#8230;<\/p>\n","protected":false},"author":4,"featured_media":2350,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"rank_math_lock_modified_date":false,"_kad_post_transparent":"","_kad_post_title":"","_kad_post_layout":"","_kad_post_sidebar_id":"","_kad_post_content_style":"","_kad_post_vertical_padding":"","_kad_post_feature":"","_kad_post_feature_position":"","_kad_post_header":false,"_kad_post_footer":false,"footnotes":""},"categories":[11],"tags":[],"acf":[],"_links":{"self":[{"href":"https:\/\/laboratoryinfo.com\/wp-json\/wp\/v2\/posts\/2315"}],"collection":[{"href":"https:\/\/laboratoryinfo.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/laboratoryinfo.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/laboratoryinfo.com\/wp-json\/wp\/v2\/users\/4"}],"replies":[{"embeddable":true,"href":"https:\/\/laboratoryinfo.com\/wp-json\/wp\/v2\/comments?post=2315"}],"version-history":[{"count":0,"href":"https:\/\/laboratoryinfo.com\/wp-json\/wp\/v2\/posts\/2315\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/laboratoryinfo.com\/wp-json\/wp\/v2\/media\/2350"}],"wp:attachment":[{"href":"https:\/\/laboratoryinfo.com\/wp-json\/wp\/v2\/media?parent=2315"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/laboratoryinfo.com\/wp-json\/wp\/v2\/categories?post=2315"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/laboratoryinfo.com\/wp-json\/wp\/v2\/tags?post=2315"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}