{"id":6958,"date":"2022-02-26T15:36:16","date_gmt":"2022-02-26T15:36:16","guid":{"rendered":"https:\/\/laboratoryinfo.com\/?p=6958"},"modified":"2022-03-07T19:59:54","modified_gmt":"2022-03-07T19:59:54","slug":"osazone-test","status":"publish","type":"post","link":"https:\/\/laboratoryinfo.com\/osazone-test\/","title":{"rendered":"Osazone Test &#8211; Principle, Uses, Protocol, Results (Observation and Interpretation)"},"content":{"rendered":"\n<p>Osazone is an essential biochemical test to detect reducing sugars in a given sample. The time taken to form a specific complex varies for each reducing sugar. <\/p>\n\n\n\n<p>So, you can differentiate them accordingly. The other term used for the osazone test is the Phenyl Hydrazine test because Phenyl hydrazine is the reagent used in this test.<\/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<h2 class=\"wp-block-heading\" id=\"uses-of-osazone-test\">Uses of Osazone Test<\/h2>\n\n\n\n<p>Uses of this biochemical test are:<\/p>\n\n\n\n<ul><li>Detection of the reducing sugars in the sample<\/li><li>Differentiate between different types of reducing sugars.<\/li><\/ul>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"principle-of-osazone-test\">Principle of Osazone Test<\/h2>\n\n\n\n<p>It is an oxidation condensation reaction. Phenyl Hydrazine is used as a reagent with an acetate buffer. The reaction occurs between the phenyl hydrazine molecules and carbon one and two of the carbohydrate, and it yields 1,2-diphenylhydrazone, which is called osazone.<\/p>\n\n\n\n<p>Only those carbohydrates can form an osazone that has a free carbonyl group. It is only present in the reducing sugars, so they give a positive osazone test.<\/p>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter size-full\"><img decoding=\"async\" width=\"745\" height=\"360\" src=\"http:\/\/laboratoryinfo.com\/wp-content\/uploads\/2022\/02\/A-typical-reaction-showing-the-formation-of-an-osazone-D-glucose-reacts-with-phenylhydrazine-to-glucosazone-the-same-product-is-obtained-from-fructose-and-mannose..jpg\" alt=\"A typical reaction showing the formation of an osazone D glucose reacts with phenylhydrazine to glucosazone the same product is obtained from fructose and mannose.\" class=\"wp-image-7077\" srcset=\"https:\/\/laboratoryinfo.com\/wp-content\/uploads\/2022\/02\/A-typical-reaction-showing-the-formation-of-an-osazone-D-glucose-reacts-with-phenylhydrazine-to-glucosazone-the-same-product-is-obtained-from-fructose-and-mannose..jpg 745w, https:\/\/laboratoryinfo.com\/wp-content\/uploads\/2022\/02\/A-typical-reaction-showing-the-formation-of-an-osazone-D-glucose-reacts-with-phenylhydrazine-to-glucosazone-the-same-product-is-obtained-from-fructose-and-mannose.-300x145.jpg 300w\" sizes=\"(max-width: 745px) 100vw, 745px\" \/><figcaption><strong><em>Image: A typical reaction showing the formation of an osazone D-glucose reacts with phenylhydrazine to glucosazone the same product is obtained from fructose and mannose.<\/em><\/strong><\/figcaption><\/figure><\/div>\n\n\n\n<p>Osazones are crystalline compounds, and their shapes and characteristics vary for each reducing sugar. Only the first two carbons of a reducing sugar are involved in this reaction. So, carbon is two epimers from the same type of osazone compound.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"laboratory-requirements\"><strong>Laboratory Requirements<\/strong><\/h2>\n\n\n\n<p>Following are the equipment and reagents required for Osazone Test.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"apparatus\">&nbsp;Apparatus<\/h3>\n\n\n\n<ul><li>Test tubes<\/li><li>Test tubes holders<\/li><li>Test tubes stand<\/li><li>Pipette<\/li><li>Pipette suckers<\/li><\/ul>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"equipment\">Equipment<\/h3>\n\n\n\n<ul><li>Vortex Mixer<\/li><li>Compound microscope<\/li><li>Water Bath<\/li><\/ul>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"reagents\">Reagents<\/h3>\n\n\n\n<ul><li>A mixture of 0.5g Phenylhydrazine hydrochloride and 0.1g of sodium acetic acid<\/li><li>The glacial acetic acid is its anhydrous form<\/li><li>Sample solution<\/li><\/ul>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"protocol\">Protocol<\/h2>\n\n\n\n<ol><li>Take a clean and dry test tube. Add 5ml of the sample under study in it.<\/li><li>Add 0.3 gram of prepared mixture and five drops of acid in it.<\/li><li>Shake gently and put it in the water bath to form a uniform solution.<\/li><li>Now keep it in the water bath and observe when the crystals appear.<\/li><li>Separate the crystals on a glass slide and observe their shape under a light microscope.<\/li><\/ol>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"interpretation-of-test\">Interpretation of Test<\/h2>\n\n\n\n<p>Only reducing sugars give the positive osazone test. The type and shape of the crystal are the basis of identifying different reducing sugars.<\/p>\n\n\n\n<p>The following table shows some different possible results obtained from various reducing sugars.<\/p>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter size-full\"><img decoding=\"async\" width=\"500\" height=\"640\" src=\"http:\/\/laboratoryinfo.com\/wp-content\/uploads\/2022\/01\/osazone.jpg\" alt=\"\" class=\"wp-image-6996\" srcset=\"https:\/\/laboratoryinfo.com\/wp-content\/uploads\/2022\/01\/osazone.jpg 500w, https:\/\/laboratoryinfo.com\/wp-content\/uploads\/2022\/01\/osazone-234x300.jpg 234w\" sizes=\"(max-width: 500px) 100vw, 500px\" \/><figcaption><em><strong>Image <\/strong>: Left column (First: Cotton ball shaped crystals; Second: Sun flower shaped crystals(Maltose);Third: Fine-long needle shaped crystals (Xylose); Fourth: Dense ball needle shaped crystals (Arabinose); Right column (First:Balls with thorny edge shaped crystals (Galactose); second :Needle shaped crystals (Mannose); third : Needle shaped crystals (Fructose); fourth: Needle shaped crystals (Glucose)).<\/em><\/figcaption><\/figure><\/div>\n\n\n\n<figure class=\"wp-block-table aligncenter\"><table><tbody><tr><td><strong>Carbohydrate<\/strong><\/td><td><strong>Time of formation (min)<\/strong><\/td><td><strong>Crystalline structure<\/strong><\/td><\/tr><tr><td>Fructose<\/td><td>2<\/td><td>Needle shape<\/td><\/tr><tr><td>Glucose<\/td><td>5<\/td><td>Needle or broomstick shape<\/td><\/tr><tr><td>Galactose<\/td><td>20<\/td><td>Thorny ball or rhombic plate shape<\/td><\/tr><tr><td>Maltose<\/td><td>30-45<\/td><td>Sunflower\/ petal shaped<\/td><\/tr><tr><td>Lactose<\/td><td>30-45<\/td><td>puff shaped powder or cotton balls<\/td><\/tr><\/tbody><\/table><figcaption>If you&#8217;d like to confirm, you can tally your results of the Osazone Test with this table.<\/figcaption><\/figure>\n\n\n\n<p class=\"has-text-align-center\"><\/p>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"uses-of-osazone-test\">Uses of Osazone Test<\/h2>\n\n\n\n<ul><li>This test is the less expensive, easy to perform and interpret, distinguishing reducing sugars from non-reducing sugars.<\/li><li>This test can identify sugars in different plant tissues.\u00a0<\/li><li>Different reducing sugars form different osazone compounds. So, it is a significant way to separate them from each other.<\/li><\/ul>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"limitations-of-osazone-test\">Limitations of Osazone Test<\/h2>\n\n\n\n<ul><li>For identification, reducing sugars must be present in the larger quantity in the sample.<\/li><li>It can also give a false-positive result for sucrose, a non-reducing sugar, if heated for more than 30 minutes.<\/li><li>Detection is not possible if more than one reducing sugar is present in the sample.<\/li><\/ul>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"frequently-asked-questions\">Frequently Asked Questions<\/h2>\n\n\n<div id=\"rank-math-faq\" class=\"rank-math-block\">\n<div class=\"rank-math-list \">\n<div id=\"faq-question-1643117329980\" class=\"rank-math-list-item\">\n<h3 class=\"rank-math-question \">Q1. Why do glucose and fructose give the same osazone compound?<\/h3>\n<div class=\"rank-math-answer \">\n\n<p>Glucose and fructose are carbon, two epimers of each other. So, they give the same osazone.<\/p>\n\n<\/div>\n<\/div>\n<div id=\"faq-question-1643117348429\" class=\"rank-math-list-item\">\n<h3 class=\"rank-math-question \">Q2. Does Xylose give a positive osazone test?<\/h3>\n<div class=\"rank-math-answer \">\n\n<p>Xylose forms long and fine crystals as a result of the osazone test.<\/p>\n\n<\/div>\n<\/div>\n<div id=\"faq-question-1643117371024\" class=\"rank-math-list-item\">\n<h3 class=\"rank-math-question \">Q3. What are osazones?<\/h3>\n<div class=\"rank-math-answer \">\n\n<p>Osazones are derivatives of carbohydrates formed by boiling reducing sugars with an adequate amount of phenylhydrazine.<\/p>\n\n<\/div>\n<\/div>\n<div id=\"faq-question-1643117386583\" class=\"rank-math-list-item\">\n<h3 class=\"rank-math-question \">Q4. Which characteristics of osazone crystals help to differentiate between reducing sugars?<\/h3>\n<div class=\"rank-math-answer \">\n\n<p>The shape and formation time of osazone crystals vary for each reducing sugar. So, you can differentiate them based on it.<\/p>\n\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n\n\n<p><strong>References<\/strong><\/p>\n\n\n\n<ol><li><em>Tiwari A. (2015). Practical Biochemistry. LAP Lambert Academic Publishing.<\/em><\/li><li><em>Shah, Tejas. (2016). Utility of Osazone Test to Identify Sugars. Journal of Medical Science And clinical Research. 04. 14361-14365. 10.18535\/jmscr\/v4i12.14.<\/em><\/li><li><em>Mester, L.; El Khadem, H.; Horton, D. (1970). &#8220;Structure of saccharide osazones.&#8221; Journal of the Chemical Society C: Organic (18): 2567. doi:10.1039\/J39700002567.<\/em><\/li><li><em><em>Ramakrishnan, S. (2004).<\/em>Textbook of Medical Biochemistry. Orient Blackswan. ISBN 9788125020714.<\/em><\/li><li><em>https:\/\/en.wikipedia.org\/wiki\/Osazone<\/em><\/li><li><em>https:\/\/microbenotes.com\/osazone-test\/<\/em><\/li><li><em>https:\/\/www.slideshare.net\/namarta28\/qualitative-tests-for-carbohydrates-35884145<\/em><\/li><li><em>https:\/\/medicalstudyzone.com\/osazone-test\/<\/em><\/li><li>https:\/\/dx.doi.org\/10.18535\/jmscr\/v4i12.14&nbsp;<\/li><\/ol>\n","protected":false},"excerpt":{"rendered":"<p>Osazone is an essential biochemical test to detect reducing sugars in a given sample. The time taken to form a specific complex varies for each reducing sugar. So, you can differentiate them accordingly. The other term used for the osazone test is the Phenyl Hydrazine test because Phenyl hydrazine is the reagent used in this&#8230;<\/p>\n","protected":false},"author":4,"featured_media":6996,"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":[2],"tags":[],"acf":[],"_links":{"self":[{"href":"https:\/\/laboratoryinfo.com\/wp-json\/wp\/v2\/posts\/6958"}],"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=6958"}],"version-history":[{"count":0,"href":"https:\/\/laboratoryinfo.com\/wp-json\/wp\/v2\/posts\/6958\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/laboratoryinfo.com\/wp-json\/wp\/v2\/media\/6996"}],"wp:attachment":[{"href":"https:\/\/laboratoryinfo.com\/wp-json\/wp\/v2\/media?parent=6958"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/laboratoryinfo.com\/wp-json\/wp\/v2\/categories?post=6958"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/laboratoryinfo.com\/wp-json\/wp\/v2\/tags?post=6958"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}