{"id":1289,"date":"2026-05-21T16:41:51","date_gmt":"2026-05-21T16:41:51","guid":{"rendered":"https:\/\/nexorastudio.ch\/nicomenthyl-test\/wordpress\/?p=1289"},"modified":"2026-05-22T08:41:53","modified_gmt":"2026-05-22T08:41:53","slug":"perche-lacido-nicotinico-si-chiama-cosi","status":"publish","type":"post","link":"https:\/\/multichem.it\/nicomenthyl\/it\/perche-lacido-nicotinico-si-chiama-cosi\/","title":{"rendered":"Perch\u00e9 l\u2019acido nicotinico si chiama cos\u00ec?"},"content":{"rendered":"\t\t<div data-elementor-type=\"wp-post\" data-elementor-id=\"1289\" class=\"elementor elementor-1289\" data-elementor-post-type=\"post\">\n\t\t\t\t<div class=\"elementor-element elementor-element-1397c221 e-con-full e-flex e-con e-parent\" data-id=\"1397c221\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t<div class=\"elementor-element elementor-element-722d9a69 e-con e-atomic-element e-div-block-base e-722d9a69-58c88e0 \" data-id=\"722d9a69\" data-element_type=\"e-div-block\" data-e-type=\"e-div-block\" data-interaction-id=\"722d9a69\" data-e-type=\"e-div-block\" data-id=\"722d9a69\">\n    \t\t<div class=\"elementor-element elementor-element-278a3d79 elementor-widget elementor-widget-post-info\" data-id=\"278a3d79\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"post-info.default\">\n\t\t\t\t\t\t\t<ul class=\"elementor-inline-items elementor-icon-list-items elementor-post-info\">\n\t\t\t\t\t\t\t\t<li class=\"elementor-icon-list-item elementor-repeater-item-22d5bc3 elementor-inline-item\" itemprop=\"about\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-icon-list-text elementor-post-info__item elementor-post-info__item--type-terms\">\n\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-post-info__terms-list\">\n\t\t\t\t<a href=\"https:\/\/multichem.it\/nicomenthyl\/it\/category\/faq-relazioni-niacina-mentolo\/\" class=\"elementor-post-info__terms-list-item\">FAQ - Relazioni con niacina e mentolo<\/a>\t\t\t\t<\/span>\n\t\t\t\t\t<\/span>\n\t\t\t\t\t\t\t\t<\/li>\n\t\t\t\t<\/ul>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-29d6f308 elementor-widget elementor-widget-theme-post-title elementor-page-title elementor-widget-heading\" data-id=\"29d6f308\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"theme-post-title.default\">\n\t\t\t\t\t<h1 class=\"elementor-heading-title elementor-size-default\">Perch\u00e9 l\u2019acido nicotinico si chiama cos\u00ec?<\/h1>\t\t\t\t<\/div>\n\t\t\t\t\t<p class=\"e-paragraph-base\" data-interaction-id=\"56c5e119\" data-e-type=\"widget\" data-id=\"56c5e119\">L\u2019acido nicotinico si chiama cos\u00ec perch\u00e9 nel 1873 il chimico austriaco Ugo Weidel era riuscito a sintetizzarlo ossidando la nicotina con acido nitrico. Fu questo l\u2019unico motivo per il quale la sostanza venne chiamata allora con il nome di acido \u201cnicotinico\u201d, pur non avendo nessuna relazione, n\u00e9 biochimica n\u00e9 tossicologica, con il noto alcaloide del tabacco.<\/p>\n\t\t\n<\/div>\n\t\t<\/div>\n\t\t<div class=\"elementor-element elementor-element-49e6c600 e-con-full e-flex e-con e-parent\" data-id=\"49e6c600\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t<div class=\"elementor-element elementor-element-53bab68a elementor-post-navigation-borders-yes elementor-widget elementor-widget-post-navigation\" data-id=\"53bab68a\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"post-navigation.default\">\n\t\t\t\t\t\t\t<div class=\"elementor-post-navigation\" role=\"navigation\" aria-label=\"Post Navigation\">\n\t\t\t<div class=\"elementor-post-navigation__prev elementor-post-navigation__link\">\n\t\t\t\t<a href=\"https:\/\/multichem.it\/nicomenthyl\/does-menthyl-nicotinate-have-anything-to-do-with-nicotine\/\" rel=\"prev\"><span class=\"post-navigation__arrow-wrapper post-navigation__arrow-prev\"><svg aria-hidden=\"true\" class=\"e-font-icon-svg e-fas-angle-left\" viewBox=\"0 0 256 512\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\"><path d=\"M31.7 239l136-136c9.4-9.4 24.6-9.4 33.9 0l22.6 22.6c9.4 9.4 9.4 24.6 0 33.9L127.9 256l96.4 96.4c9.4 9.4 9.4 24.6 0 33.9L201.7 409c-9.4 9.4-24.6 9.4-33.9 0l-136-136c-9.5-9.4-9.5-24.6-.1-34z\"><\/path><\/svg><span class=\"elementor-screen-only\">Prev<\/span><\/span><span class=\"elementor-post-navigation__link__prev\"><span class=\"post-navigation__prev--label\">Precedente<\/span><\/span><\/a>\t\t\t<\/div>\n\t\t\t\t\t\t\t<div class=\"elementor-post-navigation__separator-wrapper\">\n\t\t\t\t\t<div class=\"elementor-post-navigation__separator\"><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t<div class=\"elementor-post-navigation__next elementor-post-navigation__link\">\n\t\t\t\t<a href=\"https:\/\/multichem.it\/nicomenthyl\/why-is-nicotinic-acid-called-that\/\" rel=\"next\"><span class=\"elementor-post-navigation__link__next\"><span class=\"post-navigation__next--label\">Prossima<\/span><\/span><span class=\"post-navigation__arrow-wrapper post-navigation__arrow-next\"><svg aria-hidden=\"true\" class=\"e-font-icon-svg e-fas-angle-right\" viewBox=\"0 0 256 512\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\"><path d=\"M224.3 273l-136 136c-9.4 9.4-24.6 9.4-33.9 0l-22.6-22.6c-9.4-9.4-9.4-24.6 0-33.9l96.4-96.4-96.4-96.4c-9.4-9.4-9.4-24.6 0-33.9L54.3 103c9.4-9.4 24.6-9.4 33.9 0l136 136c9.5 9.4 9.5 24.6.1 34z\"><\/path><\/svg><span class=\"elementor-screen-only\">Next<\/span><\/span><\/a>\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t","protected":false},"excerpt":{"rendered":"<p>L\u2019acido nicotinico si chiama cos\u00ec perch\u00e9 nel 1873 il chimico austriaco Ugo Weidel era riuscito a sintetizzarlo ossidando la nicotina con acido nitrico. Fu questo l\u2019unico motivo per il quale la sostanza venne chiamata allora con il nome di acido \u201cnicotinico\u201d, pur non avendo nessuna relazione, n\u00e9 biochimica n\u00e9 tossicologica, con il noto alcaloide del [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"elementor_header_footer","format":"standard","meta":{"footnotes":""},"categories":[50],"tags":[],"class_list":["post-1289","post","type-post","status-publish","format-standard","hentry","category-faq-relazioni-niacina-mentolo"],"_links":{"self":[{"href":"https:\/\/multichem.it\/nicomenthyl\/wp-json\/wp\/v2\/posts\/1289","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/multichem.it\/nicomenthyl\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/multichem.it\/nicomenthyl\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/multichem.it\/nicomenthyl\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/multichem.it\/nicomenthyl\/wp-json\/wp\/v2\/comments?post=1289"}],"version-history":[{"count":4,"href":"https:\/\/multichem.it\/nicomenthyl\/wp-json\/wp\/v2\/posts\/1289\/revisions"}],"predecessor-version":[{"id":1659,"href":"https:\/\/multichem.it\/nicomenthyl\/wp-json\/wp\/v2\/posts\/1289\/revisions\/1659"}],"wp:attachment":[{"href":"https:\/\/multichem.it\/nicomenthyl\/wp-json\/wp\/v2\/media?parent=1289"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/multichem.it\/nicomenthyl\/wp-json\/wp\/v2\/categories?post=1289"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/multichem.it\/nicomenthyl\/wp-json\/wp\/v2\/tags?post=1289"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}