{"id":483,"date":"2023-07-08T16:52:01","date_gmt":"2023-07-08T16:52:01","guid":{"rendered":"https:\/\/www.senorgalab.com\/english\/?post_type=product&#038;p=483"},"modified":"2023-08-10T09:13:10","modified_gmt":"2023-08-10T09:13:10","slug":"dl-aspartic-acid","status":"publish","type":"product","link":"https:\/\/www.senorgalab.com\/english\/product\/dl-aspartic-acid\/","title":{"rendered":"DL-ASPARTIC ACID"},"content":{"rendered":"<pre class=\"tw-data-text tw-text-large tw-ta\" dir=\"ltr\" data-placeholder=\"\u00c7eviri\"><span style=\"font-size: 18px;\"><span class=\"Y2IQFc\" lang=\"en\" style=\"font-family: 'times new roman', times, serif;\">DL-Aspartic acid has a very high melting and decomposition point and is non-volatile. <\/span><span class=\"Y2IQFc\" lang=\"en\" style=\"font-family: 'times new roman', times, serif;\">It contains two carboxyl \r\nand one amino group in its molecular structure. <\/span><span class=\"Y2IQFc\" lang=\"en\"><span style=\"font-family: 'times new roman', times, serif;\">It is amphoteric because it contains both basic and acidic groups<\/span>.\r\n<\/span><span class=\"Y2IQFc\" lang=\"en\" style=\"font-family: 'times new roman', times, serif;\">Its anionic form is called aspartate.\r\n<\/span><\/span><\/pre>\n<pre class=\"tw-data-text tw-text-large tw-ta\" dir=\"ltr\" data-placeholder=\"\u00c7eviri\"><span style=\"font-size: 18px;\"><span class=\"Y2IQFc\" lang=\"en\" style=\"font-family: 'times new roman', times, serif;\">The most important chemical reaction of the functional groups of aspartic acid is the formation of esters and \r\namides. <\/span><span class=\"Y2IQFc\" lang=\"en\" style=\"font-family: 'times new roman', times, serif;\">Methyl and ethyl esters are used as intermediates in <a href=\"https:\/\/en.wikipedia.org\/wiki\/Peptide\">peptide<\/a> synthesis.\r\n<\/span><\/span><\/pre>\n<pre id=\"tw-target-text\" class=\"tw-data-text tw-text-large tw-ta\" dir=\"ltr\" data-placeholder=\"\u00c7eviri\"><span class=\"Y2IQFc\" lang=\"en\" style=\"font-family: 'times new roman', times, serif; font-size: 18px;\">Aspartic acid is obtained by different laboratory methods or by enzymatic hydrolysis of proteins.<\/span><\/pre>\n<pre class=\"tw-data-text tw-text-large tw-ta\" dir=\"ltr\" data-placeholder=\"\u00c7eviri\"><span class=\"Y2IQFc\" lang=\"en\" style=\"font-family: 'times new roman', times, serif;\">\u00a0<\/span><\/pre>\n<pre class=\"tw-data-text tw-text-large tw-ta\" dir=\"ltr\" data-placeholder=\"\u00c7eviri\"><span class=\"Y2IQFc\" lang=\"en\" style=\"font-family: 'times new roman', times, serif;\">\u00a0<\/span><\/pre>\n","protected":false},"excerpt":{"rendered":"<pre class=\"tw-data-text tw-text-large tw-ta\" dir=\"ltr\" data-placeholder=\"\u00c7eviri\"><span style=\"font-size: 20px;\"><span style=\"font-family: 'times new roman', times, serif;\"><span class=\"Y2IQFc\" lang=\"en\">Aspartic acid is an amino acid that can be produced in the body. Also a<\/span><span class=\"Y2IQFc\" lang=\"en\">spartic acid is one of the 20 standard amino \r\nacids found in the structure of proteins. <\/span>It has a <a href=\"https:\/\/en.wikipedia.org\/wiki\/Chirality_(chemistry)\">chiral<\/a> structure. So it has two enantiomers, L-Aspartic acid and D-aspartic\r\n acid.<\/span><span style=\"font-family: 'times new roman', times, serif;\"> <span class=\"Y2IQFc\" lang=\"en\">It is soluble in water, insoluble in ether, alcohol and DMSO.<\/span><\/span><\/span><\/pre>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n","protected":false},"featured_media":490,"template":"","meta":[],"class_list":["post-483","product","type-product","status-publish","has-post-thumbnail","hentry","product_cat-amino-acids","tm-no-options"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v16.1 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>DL-ASPARTIC ACID &mdash; Senorga Lab<\/title>\n<meta name=\"description\" content=\"dl-aspartic acid, 2-Aminosuccinic acid, 2-Aminobutanedioic acid, DL-Asparagic acid, Asp, antioxidant, antistatic agent, aspartate.\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.senorgalab.com\/english\/product\/dl-aspartic-acid\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"DL-ASPARTIC ACID &mdash; Senorga Lab\" \/>\n<meta property=\"og:description\" content=\"dl-aspartic acid, 2-Aminosuccinic acid, 2-Aminobutanedioic acid, DL-Asparagic acid, Asp, antioxidant, antistatic agent, aspartate.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.senorgalab.com\/english\/product\/dl-aspartic-acid\/\" \/>\n<meta property=\"og:site_name\" content=\"Senorga Lab\" \/>\n<meta property=\"article:modified_time\" content=\"2023-08-10T09:13:10+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/www.senorgalab.com\/english\/wp-content\/uploads\/2023\/07\/aspartik-asid.png\" \/>\n\t<meta property=\"og:image:width\" content=\"500\" \/>\n\t<meta property=\"og:image:height\" content=\"500\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Est. reading time\">\n\t<meta name=\"twitter:data1\" content=\"1 minute\">\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"WebSite\",\"@id\":\"https:\/\/www.senorgalab.com\/english\/#website\",\"url\":\"https:\/\/www.senorgalab.com\/english\/\",\"name\":\"Senorgalab Kimya\",\"description\":\"Kimya &amp; 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