{"id":2842,"date":"2021-09-05T13:32:34","date_gmt":"2021-09-05T13:32:34","guid":{"rendered":"https:\/\/dl.ankepohl.com\/?p=2842"},"modified":"2021-09-12T19:26:07","modified_gmt":"2021-09-12T17:26:07","slug":"temperature-dependent-analysis-of-octenidine-nn-decane-110-diyldipyridin1-yl-4-ylidenedioctan-1-amine-dihydrochloride-by-nmr-and-nir-spectroscopy","status":"publish","type":"post","link":"https:\/\/aynaanalytics.com\/en\/2021\/09\/05\/temperature-dependent-analysis-of-octenidine-nn-decane-110-diyldipyridin1-yl-4-ylidenedioctan-1-amine-dihydrochloride-by-nmr-and-nir-spectroscopy\/","title":{"rendered":"Temperature dependent analysis of Octenidine (N,N\u00b4-(decane-1,10-diyldipyridin1-yl-4-ylidene)dioctan-1-amine) dihydrochloride by NMR and NIR spectroscopy"},"content":{"rendered":"<div data-elementor-type=\"wp-post\" data-elementor-id=\"2842\" class=\"elementor elementor-2842\" data-elementor-post-type=\"post\">\n\t\t\t\t\t\t\t\t\t<section class=\"elementor-section elementor-top-section elementor-element elementor-element-66edbc6 elementor-section-boxed elementor-section-height-default elementor-section-height-default\" data-id=\"66edbc6\" data-element_type=\"section\" data-settings=\"{&quot;_ha_eqh_enable&quot;:false}\">\n\t\t\t\t\t\t<div class=\"elementor-container elementor-column-gap-default\">\n\t\t\t\t\t<div class=\"elementor-column elementor-col-100 elementor-top-column elementor-element elementor-element-2a5eac7\" data-id=\"2a5eac7\" data-element_type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t\t\t<div class=\"elementor-element elementor-element-6a23b64 elementor-widget elementor-widget-text-editor\" data-id=\"6a23b64\" data-element_type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t<div>David L. Mainka, J\u00f6rg Schwarz and Ulrich Girreser&nbsp;<\/div>\n<div><a href=\"http:\/\/www.arkat-usa.org\/get-file\/69506\/\">Link to the article<\/a><\/div>\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t<section class=\"elementor-section elementor-top-section elementor-element elementor-element-414fab1 elementor-section-boxed elementor-section-height-default elementor-section-height-default\" data-id=\"414fab1\" data-element_type=\"section\" data-settings=\"{&quot;_ha_eqh_enable&quot;:false}\">\n\t\t\t\t\t\t<div class=\"elementor-container elementor-column-gap-default\">\n\t\t\t\t\t<div class=\"elementor-column elementor-col-100 elementor-top-column elementor-element elementor-element-021228f\" data-id=\"021228f\" data-element_type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t\t\t<div class=\"elementor-element elementor-element-c87b27f elementor-widget elementor-widget-heading\" data-id=\"c87b27f\" data-element_type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\">Abstract<\/h2>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t<section class=\"elementor-section elementor-top-section elementor-element elementor-element-f3aa6d1 elementor-section-boxed elementor-section-height-default elementor-section-height-default\" data-id=\"f3aa6d1\" data-element_type=\"section\" data-settings=\"{&quot;_ha_eqh_enable&quot;:false}\">\n\t\t\t\t\t\t<div class=\"elementor-container elementor-column-gap-default\">\n\t\t\t\t\t<div class=\"elementor-column elementor-col-100 elementor-top-column elementor-element elementor-element-3fd590c\" data-id=\"3fd590c\" data-element_type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t\t\t<div class=\"elementor-element elementor-element-08dce89 elementor-widget elementor-widget-text-editor\" data-id=\"08dce89\" data-element_type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t<p><span style=\"color: var( --e-global-color-text ); font-family: var( --e-global-typography-text-font-family ), Sans-serif; font-weight: var( --e-global-typography-text-font-weight ); background-color: var( --e-global-color-e52819d ); font-size: 1rem;\">Octenidine dihydrochloride is one of the most common active pharmaceutical incredients with a disinfectant effect on superficial wounds. In this paper we describe the mesomeric behaviour of Octenidine dihydrochloride by comparison with 1H, 13C and 15N NMR shift data. With various NMR experiments, the possible mesomeric structures are studied and it is shown that an E\/Z-isomerization plays a role, corresponding to a hindered rotation of the heteroaromatic pyridine ring. In this context, NIR spectroscopy and principal component analysis emphasize the occurrence of a modified temperature-dependent spectral behaviour of Octenidine dihydrochloride. In addition, we made a detailed study of the NMR-characteristics of Octenidine dihydrochloride using 1D- and 2D-experiments.<\/span><a style=\"font-style: inherit; font-weight: inherit; font-family: var( --e-global-typography-text-font-family ), Sans-serif;\" role=\"button\" href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2019\/AY\/C9AY01241A#\" aria-expanded=\"true\" aria-controls=\"pnlAuthorAffiliations\">\u00a0<\/a><\/p>\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t<section class=\"elementor-section elementor-top-section elementor-element elementor-element-f44d02e elementor-section-boxed elementor-section-height-default elementor-section-height-default\" data-id=\"f44d02e\" data-element_type=\"section\" data-settings=\"{&quot;_ha_eqh_enable&quot;:false}\">\n\t\t\t\t\t\t<div class=\"elementor-container elementor-column-gap-default\">\n\t\t\t\t\t<div class=\"elementor-column elementor-col-100 elementor-top-column elementor-element elementor-element-cf0711b\" data-id=\"cf0711b\" data-element_type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t\t\t<div class=\"elementor-element elementor-element-7527f49 elementor-widget elementor-widget-image\" data-id=\"7527f49\" data-element_type=\"widget\" data-widget_type=\"image.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<img decoding=\"async\" loading=\"lazy\" width=\"1024\" height=\"733\" src=\"https:\/\/aynaanalytics.com\/wp-content\/uploads\/2021\/09\/Screenshot-2021-09-06-at-10.07.06-1024x733.png\" class=\"attachment-large size-large wp-image-3032\" alt=\"\" srcset=\"https:\/\/aynaanalytics.com\/wp-content\/uploads\/2021\/09\/Screenshot-2021-09-06-at-10.07.06-1024x733.png 1024w, https:\/\/aynaanalytics.com\/wp-content\/uploads\/2021\/09\/Screenshot-2021-09-06-at-10.07.06-300x215.png 300w, https:\/\/aynaanalytics.com\/wp-content\/uploads\/2021\/09\/Screenshot-2021-09-06-at-10.07.06-768x550.png 768w, https:\/\/aynaanalytics.com\/wp-content\/uploads\/2021\/09\/Screenshot-2021-09-06-at-10.07.06.png 1156w\" sizes=\"(max-width: 1024px) 100vw, 1024px\" \/>\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t<section class=\"elementor-section elementor-top-section elementor-element elementor-element-e24679a elementor-section-boxed elementor-section-height-default elementor-section-height-default\" data-id=\"e24679a\" data-element_type=\"section\" data-settings=\"{&quot;_ha_eqh_enable&quot;:false}\">\n\t\t\t\t\t\t<div class=\"elementor-container elementor-column-gap-default\">\n\t\t\t\t\t<div class=\"elementor-column elementor-col-100 elementor-top-column elementor-element elementor-element-c7f7d65\" data-id=\"c7f7d65\" data-element_type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t\t\t<div class=\"elementor-element elementor-element-85606f4 elementor-widget elementor-widget-wp-widget-text\" data-id=\"85606f4\" data-element_type=\"widget\" data-widget_type=\"wp-widget-text.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t<div class=\"textwidget\"><p><a href=\"http:\/\/www.arkat-usa.org\/get-file\/69506\/\">Link to the article<\/a><\/p>\n<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t\t\t\t<\/div>","protected":false},"excerpt":{"rendered":"<p>David L. Mainka, J\u00f6rg Schwarz and Ulrich Girreser&nbsp; Link zum Artikel Abstract Octenidine dihydrochloride is one of the most common active pharmaceutical incredients with a disinfectant effect on superficial wounds. In this paper we describe the mesomeric behaviour of Octenidine dihydrochloride by comparison with 1H, 13C and 15N NMR shift data. With various NMR experiments, &hellip;<\/p>\n<p class=\"read-more\"> <a class=\"\" href=\"https:\/\/aynaanalytics.com\/en\/2021\/09\/05\/temperature-dependent-analysis-of-octenidine-nn-decane-110-diyldipyridin1-yl-4-ylidenedioctan-1-amine-dihydrochloride-by-nmr-and-nir-spectroscopy\/\"> <span class=\"screen-reader-text\">Temperature dependent analysis of Octenidine (N,N\u00b4-(decane-1,10-diyldipyridin1-yl-4-ylidene)dioctan-1-amine) dihydrochloride by NMR and NIR spectroscopy<\/span> Read More &raquo;<\/a><\/p>","protected":false},"author":2,"featured_media":3032,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"site-sidebar-layout":"default","site-content-layout":"default","ast-global-header-display":"","ast-banner-title-visibility":"","ast-main-header-display":"","ast-hfb-above-header-display":"","ast-hfb-below-header-display":"","ast-hfb-mobile-header-display":"","site-post-title":"","ast-breadcrumbs-content":"","ast-featured-img":"","footer-sml-layout":"","theme-transparent-header-meta":"default","adv-header-id-meta":"","stick-header-meta":"","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","footnotes":""},"categories":[15],"tags":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v21.3 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Temperature dependent analysis of Octenidine (N,N\u00b4-(decane-1,10-diyldipyridin1-yl-4-ylidene)dioctan-1-amine) dihydrochloride by NMR and NIR spectroscopy - Ayna Analytics<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/aynaanalytics.com\/en\/2021\/09\/05\/temperature-dependent-analysis-of-octenidine-nn-decane-110-diyldipyridin1-yl-4-ylidenedioctan-1-amine-dihydrochloride-by-nmr-and-nir-spectroscopy\/\" \/>\n<meta property=\"og:locale\" content=\"en_GB\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Temperature dependent analysis of Octenidine (N,N\u00b4-(decane-1,10-diyldipyridin1-yl-4-ylidene)dioctan-1-amine) dihydrochloride by NMR and NIR spectroscopy - Ayna Analytics\" \/>\n<meta property=\"og:description\" content=\"David L. Mainka, J\u00f6rg Schwarz and Ulrich Girreser&nbsp; Link zum Artikel Abstract Octenidine dihydrochloride is one of the most common active pharmaceutical incredients with a disinfectant effect on superficial wounds. In this paper we describe the mesomeric behaviour of Octenidine dihydrochloride by comparison with 1H, 13C and 15N NMR shift data. With various NMR experiments, &hellip; Temperature dependent analysis of Octenidine (N,N\u00b4-(decane-1,10-diyldipyridin1-yl-4-ylidene)dioctan-1-amine) dihydrochloride by NMR and NIR spectroscopy Read More &raquo;\" \/>\n<meta property=\"og:url\" content=\"https:\/\/aynaanalytics.com\/en\/2021\/09\/05\/temperature-dependent-analysis-of-octenidine-nn-decane-110-diyldipyridin1-yl-4-ylidenedioctan-1-amine-dihydrochloride-by-nmr-and-nir-spectroscopy\/\" \/>\n<meta property=\"og:site_name\" content=\"Ayna Analytics\" \/>\n<meta property=\"article:published_time\" content=\"2021-09-05T13:32:34+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2021-09-12T17:26:07+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/aynaanalytics.com\/wp-content\/uploads\/2021\/09\/Screenshot-2021-09-06-at-10.07.06.png\" \/>\n\t<meta property=\"og:image:width\" content=\"1156\" \/>\n\t<meta property=\"og:image:height\" content=\"828\" \/>\n\t<meta property=\"og:image:type\" content=\"image\/png\" \/>\n<meta name=\"author\" content=\"Laura Rodriguez Garcia\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Laura Rodriguez Garcia\" \/>\n\t<meta name=\"twitter:label2\" content=\"Estimated reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"1 minute\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\/\/aynaanalytics.com\/en\/2021\/09\/05\/temperature-dependent-analysis-of-octenidine-nn-decane-110-diyldipyridin1-yl-4-ylidenedioctan-1-amine-dihydrochloride-by-nmr-and-nir-spectroscopy\/\",\"url\":\"https:\/\/aynaanalytics.com\/en\/2021\/09\/05\/temperature-dependent-analysis-of-octenidine-nn-decane-110-diyldipyridin1-yl-4-ylidenedioctan-1-amine-dihydrochloride-by-nmr-and-nir-spectroscopy\/\",\"name\":\"Temperature dependent analysis of Octenidine (N,N\u00b4-(decane-1,10-diyldipyridin1-yl-4-ylidene)dioctan-1-amine) dihydrochloride by NMR and NIR spectroscopy - 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Mainka, J\u00f6rg Schwarz and Ulrich Girreser&nbsp; Link zum Artikel Abstract Octenidine dihydrochloride is one of the most common active pharmaceutical incredients with a disinfectant effect on superficial wounds. In this paper we describe the mesomeric behaviour of Octenidine dihydrochloride by comparison with 1H, 13C and 15N NMR shift data. With various NMR experiments, &hellip; Temperature dependent analysis of Octenidine (N,N\u00b4-(decane-1,10-diyldipyridin1-yl-4-ylidene)dioctan-1-amine) dihydrochloride by NMR and NIR spectroscopy Read More &raquo;","og_url":"https:\/\/aynaanalytics.com\/en\/2021\/09\/05\/temperature-dependent-analysis-of-octenidine-nn-decane-110-diyldipyridin1-yl-4-ylidenedioctan-1-amine-dihydrochloride-by-nmr-and-nir-spectroscopy\/","og_site_name":"Ayna Analytics","article_published_time":"2021-09-05T13:32:34+00:00","article_modified_time":"2021-09-12T17:26:07+00:00","og_image":[{"width":1156,"height":828,"url":"https:\/\/aynaanalytics.com\/wp-content\/uploads\/2021\/09\/Screenshot-2021-09-06-at-10.07.06.png","type":"image\/png"}],"author":"Laura Rodriguez Garcia","twitter_card":"summary_large_image","twitter_misc":{"Written by":"Laura Rodriguez Garcia","Estimated reading time":"1 minute"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"WebPage","@id":"https:\/\/aynaanalytics.com\/en\/2021\/09\/05\/temperature-dependent-analysis-of-octenidine-nn-decane-110-diyldipyridin1-yl-4-ylidenedioctan-1-amine-dihydrochloride-by-nmr-and-nir-spectroscopy\/","url":"https:\/\/aynaanalytics.com\/en\/2021\/09\/05\/temperature-dependent-analysis-of-octenidine-nn-decane-110-diyldipyridin1-yl-4-ylidenedioctan-1-amine-dihydrochloride-by-nmr-and-nir-spectroscopy\/","name":"Temperature dependent analysis of Octenidine (N,N\u00b4-(decane-1,10-diyldipyridin1-yl-4-ylidene)dioctan-1-amine) dihydrochloride by NMR and NIR spectroscopy - 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