{"id":8080,"date":"2026-07-07T12:23:23","date_gmt":"2026-07-07T12:23:23","guid":{"rendered":"https:\/\/chemsaxis.com\/?p=8080"},"modified":"2026-07-09T07:13:44","modified_gmt":"2026-07-09T07:13:44","slug":"buy-fluclotizolam-online","status":"publish","type":"post","link":"https:\/\/chemsaxis.com\/pt\/buy-fluclotizolam-online\/","title":{"rendered":"Fluclotizolam"},"content":{"rendered":"<figure id=\"attachment_2367\" class=\"wp-caption alignleft\" aria-describedby=\"caption-attachment-2367\"><a href=\"\/shop\"><img loading=\"lazy\" decoding=\"async\" class=\"alignleft wp-image-2367 size-medium\" src=\"https:\/\/chembeyond.com\/wp-content\/uploads\/2023\/03\/Fluclotizolam-300x300.jpg\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" srcset=\"https:\/\/chembeyond.com\/wp-content\/uploads\/2023\/03\/Fluclotizolam-300x300.jpg 300w, https:\/\/chembeyond.com\/wp-content\/uploads\/2023\/03\/Fluclotizolam-150x150.jpg 150w, https:\/\/chembeyond.com\/wp-content\/uploads\/2023\/03\/Fluclotizolam-144x144.jpg 144w, https:\/\/chembeyond.com\/wp-content\/uploads\/2023\/03\/Fluclotizolam-350x350.jpg 350w, https:\/\/chembeyond.com\/wp-content\/uploads\/2023\/03\/Fluclotizolam.jpg 750w\" alt=\"buy Fluclotizolam online\" width=\"300\" height=\"300\" \/><\/a><figcaption id=\"caption-attachment-2367\" class=\"wp-caption-text\">Fluclotizolam<\/figcaption><\/figure>\n<h1><span style=\"color: #000000;\"><strong> Fluclotizolam| buy Fluclotizolam online\u00a0<\/strong><\/span><\/h1>\n<p><span style=\"color: #000000;\">Buy Fluclotizolam online from Chems Axis. Fluclotizolam is a sedative benzodiazepine drug, a derivative of thienotriazolodiazepine was synthesized in 1979, but has never been used for medical purposes, its effect on GABA receptors can be compared with lorazepam, as studies on rodents show.<\/span><\/p>\n<p>Price:<\/p>\n<p><strong>Fluclotizolam 5 g 110 $<\/strong><span style=\"color: #ff0000;\">\u00a0<a class=\"fancybox-inline\" style=\"color: #ff0000;\" href=\"https:\/\/chemsaxis.com\/order-inquiry-page\/\"><b>Add to cart<\/b><\/a><\/span><\/p>\n<p><strong>Fluclotizolam 10 g 190 $<span style=\"color: #ff0000;\">\u00a0<a class=\"fancybox-inline\" style=\"color: #ff0000;\" href=\"https:\/\/chemsaxis.com\/order-inquiry-page\/\"><b>Add to cart<\/b><\/a><\/span><\/strong><\/p>\n<p><strong>Fluclotizolam 50 g 420 $\u00a0<a class=\"fancybox-inline\" href=\"https:\/\/chemsaxis.com\/order-inquiry-page\/\"><b><span style=\"color: #ff0000;\">Add to cart<\/span> <\/b><\/a><\/strong><strong><span id=\"result_box\" class=\"short_text\" lang=\"en\"><span class=\"\">Free shipping<\/span><\/span>!<\/strong><\/p>\n<p><strong>Fluclotizolam 100 g 620 $\u00a0<a class=\"fancybox-inline\" href=\"https:\/\/chemsaxis.com\/order-inquiry-page\/\"><b><span style=\"color: #ff0000;\">Add to cart<\/span> <\/b><\/a><\/strong><strong><span id=\"result_box\" class=\"short_text\" lang=\"en\"><span class=\"\">Free shipping<\/span><\/span>!<\/strong><\/p>\n<p><strong>Fluclotizolam 500 g 2800 $<span style=\"color: #ff0000;\">\u00a0<\/span><a class=\"fancybox-inline\" href=\"https:\/\/chemsaxis.com\/order-inquiry-page\/\"><b><span style=\"color: #ff0000;\">Add to cart<\/span> <\/b><\/a><\/strong><strong><span id=\"result_box\" class=\"short_text\" lang=\"en\"><span class=\"\">Free shipping<\/span><\/span>!<\/strong><\/p>\n<p><strong>Fluclotizolam 1 kg 4400 $\u00a0<a class=\"fancybox-inline\" href=\"https:\/\/chemsaxis.com\/order-inquiry-page\/\"><b><span style=\"color: #ff0000;\">Add to cart<\/span> <\/b><\/a><\/strong><strong><span id=\"result_box\" class=\"short_text\" lang=\"en\"><span class=\"\">Free shipping<\/span><\/span>!<\/strong><\/p>\n<p><span style=\"color: #000000;\">Fluclotizolam is presented as a designer drug, not for human use and use, not for veterinary purposes. This substance is controlled by law in countries such as the UK, Germany and Canada.<\/span><\/p>\n<p><span style=\"color: #000000;\">You can buy Fluclotizolam online right now at <span id=\"result_box\" class=\"\" lang=\"en\"><span class=\"\"><strong>Chemsaxis<\/strong><\/span><\/span>.<\/span><\/p>\n<div class=\"card\">\n<div id=\"collapsedescription\" class=\"collapse show\" aria-labelledby=\"description\">\n<div class=\"card-body\">\n<h2><span style=\"color: #000000;\"><strong>What exactly is Fluclotizolam?<\/strong><\/span><\/h2>\n<p><span style=\"color: #000000;\">Fluclotizolam is a thienotriazolodiazepine derivative first synthesized in 1979 but never marketed. It was then advertised as a design drug, first identified in 2017.<\/span><\/p>\n<h2><span style=\"color: #000000;\"><strong>Uses of Fluclotizolam<\/strong><\/span><\/h2>\n<p><span style=\"color: #000000;\">Fluclotizolam is an innovative benzodiazepine that affects the nervous system&#8217;s central part. It is considered a derivative of Etizolam, a prevalent drug within the same category. Etizolam is mainly utilized in other nations as anti-anxiety medicine and is available for purchase. Fluclotizolam can be three times more potent than Etizolam; however, its effects last only half as long and typically last up to 6 hours. It&#8217;s almost like flour. It&#8217;s also been consumed as a liquid.<\/span><\/p>\n<h2><span style=\"color: #000000;\"><strong>The effects of Fluclotizolam<\/strong><\/span><\/h2>\n<p><span style=\"color: #000000;\">We know that it&#8217;s a benzodiazepine relaxing agent that can cause insomnia in users. It&#8217;s also not a minor anxiolytic-like other benzo\/thienodiazepines. Fluclotizolam can be a nervous system depressant, triggering &#8220;blackouts.&#8221;The drug is a hypnotic agent that can be hypnotizing, with 0.5 mg as the typical dose taken via a blotter soaked with liquid.<\/span><\/p>\n<h2><span style=\"color: #000000;\"><strong>The history of Fluclotizolam<\/strong><\/span><\/h2>\n<p><span style=\"color: #000000;\">Fluclotizolam was initially synthesized around 1979 in Hoffmann La Roche, Inc. and then patent-pending. The drug became available through black market sales in 2017 as a legal &#8220;research chemical.<\/span><\/p>\n<\/div>\n<\/div>\n<\/div>\n<div class=\"card\">\n<div id=\"Classification\" class=\"card-header\">\n<p><strong><span class=\"accordion-title\" style=\"color: #000000;\">Classification<\/span><\/strong><\/p>\n<\/div>\n<div id=\"collapseClassification\" class=\"collapse show\" aria-labelledby=\"Classification\">\n<div class=\"card-body\">\n<p><span style=\"color: #000000;\">Fluclotizolam is classified as a new psychoactive substance (NPS), specifically within the category of designer benzodiazepines. These substances are often structurally similar to existing benzodiazepines but have modifications that can alter their pharmacological properties and legal status\u00a0<span class=\"whitespace-nowrap\"><a class=\"citation ml-xs inline\" style=\"color: #000000;\" href=\"https:\/\/pmc.ncbi.nlm.nih.gov\/articles\/PMC8230725\/\" target=\"_blank\" rel=\"nofollow noopener\" aria-label=\"Designer Benzodiazepines: A Review of Toxicology and Public Health Risks\" data-state=\"closed\">\u00a0<\/a>.<\/span><\/span><\/p>\n<\/div>\n<\/div>\n<\/div>\n<div class=\"card\">\n<div id=\"Molecular Structure Analysis\" class=\"card-header\">\n<p><strong><span class=\"accordion-title\" style=\"color: #000000;\">Molecular Structure Analysis<\/span><\/strong><\/p>\n<\/div>\n<div id=\"collapseMolecular Structure Analysis\" class=\"collapse show\" aria-labelledby=\"Molecular Structure Analysis\">\n<div class=\"card-body\">\n<p><span style=\"color: #000000;\">Fluclotizolam&#8217;s molecular structure features a diazepine ring fused with a triazole and a thieno group. The presence of chlorine and fluorine substituents significantly influences its pharmacological activity:<\/span><\/p>\n<ul>\n<li><span style=\"color: #000000;\"><strong>Structural Features<\/strong>:<\/span>\n<ul>\n<li><span style=\"color: #000000;\">The diazepine ring provides the core structure typical of benzodiazepines.<\/span><\/li>\n<li><span style=\"color: #000000;\">The triazole moiety enhances binding affinity to GABA_A receptors.<\/span><\/li>\n<li><span style=\"color: #000000;\">The fluorine atom at the R2&#8242; position increases potency compared to non-fluorinated analogs\u00a0<a class=\"citation ml-xs inline\" style=\"color: #000000;\" href=\"https:\/\/cdn.who.int\/media\/docs\/default-source\/controlled-substances\/43rd-ecdd\/final-flubromazolam-a.pdf\" target=\"_blank\" rel=\"nofollow noopener\" aria-label=\"[PDF] Critical Review Report: FLUBROMAZOLAM\" data-state=\"closed\">\u00a0<\/a><span class=\"whitespace-nowrap\"><a class=\"citation ml-xs inline\" style=\"color: #000000;\" href=\"https:\/\/en.wikipedia.org\/wiki\/Fluclotizolam\" target=\"_blank\" rel=\"nofollow noopener\" aria-label=\"Fluclotizolam - Wikipedia\" data-state=\"closed\">\u00a0<\/a>.<\/span><\/span><\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<h3><span style=\"color: #000000;\">Structural Data<\/span><\/h3>\n<ul>\n<li><span style=\"color: #000000;\"><strong>Molecular Formula<\/strong>:\u00a0<span class=\"math math-inline\"><span class=\"katex\"><span class=\"katex-mathml\">C15H10ClFN4S<\/span><span class=\"katex-html\" aria-hidden=\"true\"><span class=\"base\"><span class=\"mord\"><span class=\"mord mathnormal\">C<\/span><span class=\"msupsub\"><span class=\"vlist-t vlist-t2\"><span class=\"vlist-r\"><span class=\"vlist\"><span class=\"sizing reset-size6 size3 mtight\"><span class=\"mord mtight\">15<\/span><\/span><\/span><span class=\"vlist-s\">\u200b<\/span><\/span><\/span><\/span><\/span><span class=\"mord\"><span class=\"mord mathnormal\">H<\/span><span class=\"msupsub\"><span class=\"vlist-t vlist-t2\"><span class=\"vlist-r\"><span class=\"vlist\"><span class=\"sizing reset-size6 size3 mtight\"><span class=\"mord mtight\">10<\/span><\/span><\/span><span class=\"vlist-s\">\u200b<\/span><\/span><\/span><\/span><\/span><span class=\"mord mathnormal\">ClF<\/span><span class=\"mord\"><span class=\"mord mathnormal\">N<\/span><span class=\"msupsub\"><span class=\"vlist-t vlist-t2\"><span class=\"vlist-r\"><span class=\"vlist\"><span class=\"sizing reset-size6 size3 mtight\"><span class=\"mord mtight\">4<\/span><\/span><\/span><span class=\"vlist-s\">\u200b<\/span><\/span><\/span><\/span><\/span><span class=\"mord mathnormal\">S<\/span><\/span><\/span><\/span><\/span><\/span><\/li>\n<li><span style=\"color: #000000;\"><strong>Molecular Weight<\/strong>: 332.8 g\/mol<\/span><\/li>\n<li><span style=\"color: #000000;\"><strong>CAS Number<\/strong>: 54123-15-8<\/span><\/li>\n<\/ul>\n<\/div>\n<\/div>\n<\/div>\n<div class=\"card\">\n<div id=\"Chemical Reactions Analysis\" class=\"card-header\">\n<p><strong><span class=\"accordion-title\" style=\"color: #000000;\">Chemical Reactions Analysis<\/span><\/strong><\/p>\n<\/div>\n<div id=\"collapseChemical Reactions Analysis\" class=\"collapse show\" aria-labelledby=\"Chemical Reactions Analysis\">\n<div class=\"card-body\">\n<p><span style=\"color: #000000;\">Fluclotizolam can undergo various chemical reactions typical of benzodiazepine derivatives:<\/span><\/p>\n<ol>\n<li><span style=\"color: #000000;\"><strong>Hydroxylation<\/strong>: This reaction leads to the formation of hydroxy metabolites that may exhibit altered pharmacological properties.<\/span><\/li>\n<li><span style=\"color: #000000;\"><strong>Glucuronidation<\/strong>: Conjugation with glucuronic acid enhances solubility and excretion.<\/span><\/li>\n<li><span style=\"color: #000000;\"><strong>Reactivity<\/strong>: The chlorine atom can participate in nucleophilic substitution reactions under certain conditions\u00a0<a class=\"citation ml-xs inline\" style=\"color: #000000;\" href=\"https:\/\/cdn.who.int\/media\/docs\/default-source\/controlled-substances\/43rd-ecdd\/final-flubromazolam-a.pdf\" target=\"_blank\" rel=\"nofollow noopener\" aria-label=\"[PDF] Critical Review Report: FLUBROMAZOLAM\" data-state=\"closed\">\u00a0<\/a><span class=\"whitespace-nowrap\"><a class=\"citation ml-xs inline\" style=\"color: #000000;\" href=\"https:\/\/pmc.ncbi.nlm.nih.gov\/articles\/PMC8230725\/\" target=\"_blank\" rel=\"nofollow noopener\" aria-label=\"Designer Benzodiazepines: A Review of Toxicology and Public Health Risks\" data-state=\"closed\">\u00a0<\/a>.<\/span><\/span><\/li>\n<\/ol>\n<\/div>\n<\/div>\n<\/div>\n<div class=\"card\">\n<div id=\"Mechanism of Action\" class=\"card-header\">\n<p><strong><span class=\"accordion-title\" style=\"color: #000000;\">Mechanism of Action<\/span><\/strong><\/p>\n<\/div>\n<div id=\"collapseMechanism of Action\" class=\"collapse show\" aria-labelledby=\"Mechanism of Action\">\n<div class=\"card-body\">\n<p><span style=\"color: #000000;\">Fluclotizolam primarily acts as a positive allosteric modulator at the GABA_A receptor:<\/span><\/p>\n<ul>\n<li><span style=\"color: #000000;\"><strong>Binding Site<\/strong>: It binds to the benzodiazepine site on the GABA_A receptor, enhancing the inhibitory effects of GABA (gamma-aminobutyric acid).<\/span><\/li>\n<li><span style=\"color: #000000;\"><strong>Pharmacodynamics<\/strong>:<\/span>\n<ul>\n<li><span style=\"color: #000000;\">Increases chloride ion influx through GABA_A channels, leading to hyperpolarization of neurons.<\/span><\/li>\n<li><span style=\"color: #000000;\">This action results in anxiolytic, sedative, and muscle relaxant effects\u00a0<a class=\"citation ml-xs inline\" style=\"color: #000000;\" href=\"https:\/\/pmc.ncbi.nlm.nih.gov\/articles\/PMC8230725\/\" target=\"_blank\" rel=\"nofollow noopener\" aria-label=\"Designer Benzodiazepines: A Review of Toxicology and Public Health Risks\" data-state=\"closed\">\u00a0<\/a><span class=\"whitespace-nowrap\"><a class=\"citation ml-xs inline\" style=\"color: #000000;\" href=\"https:\/\/jdc.jefferson.edu\/cgi\/viewcontent.cgi?article=1010&amp;context=iehpfp\" target=\"_blank\" rel=\"nofollow noopener\" aria-label=\"[PDF] Designer Benzodiazepines: A Review of Toxicology and Public Health Risks\" data-state=\"closed\">\u00a0<\/a>.<\/span><\/span><\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<h3><span style=\"color: #000000;\">Pharmacokinetics<\/span><\/h3>\n<p><span style=\"color: #000000;\">Fluclotizolam is metabolized primarily by cytochrome P450 enzymes (CYP3A4\/5), with significant variability in metabolism due to genetic polymorphisms among individuals\u00a0<span class=\"whitespace-nowrap\"><a class=\"citation ml-xs inline\" style=\"color: #000000;\" href=\"https:\/\/cdn.who.int\/media\/docs\/default-source\/controlled-substances\/43rd-ecdd\/final-flubromazolam-a.pdf\" target=\"_blank\" rel=\"nofollow noopener\" aria-label=\"[PDF] Critical Review Report: FLUBROMAZOLAM\" data-state=\"closed\">\u00a0<\/a>.<\/span><\/span><\/p>\n<\/div>\n<\/div>\n<\/div>\n<div class=\"card\">\n<div id=\"Physical and Chemical Properties Analysis\" class=\"card-header\">\n<p><span class=\"accordion-title\" style=\"color: #000000;\">Physical and Chemical Properties Analysis<\/span><\/p>\n<\/div>\n<div id=\"collapsePhysical and Chemical Properties Analysis\" class=\"collapse show\" aria-labelledby=\"Physical and Chemical Properties Analysis\">\n<div class=\"card-body\">\n<p><span style=\"color: #000000;\">Fluclotizolam exhibits specific physical and chemical properties that are relevant for its analysis:<\/span><\/p>\n<\/div>\n<\/div>\n<\/div>\n<div class=\"card\">\n<div id=\"Applications\" class=\"card-header\">\n<p><span class=\"accordion-title\" style=\"color: #000000;\">Applications<\/span><\/p>\n<\/div>\n<div id=\"collapseApplications\" class=\"collapse show\" aria-labelledby=\"Applications\">\n<div class=\"card-body\">\n<p><span style=\"color: #000000;\">Despite its initial lack of therapeutic use, fluclotizolam has been identified in various forensic cases as a designer drug:<\/span><\/p>\n<ul>\n<li><span style=\"color: #000000;\"><strong>Recreational Use<\/strong>: It has been used recreationally due to its sedative effects similar to those of traditional benzodiazepines.<\/span><\/li>\n<li><span style=\"color: #000000;\"><strong>Forensic Toxicology<\/strong>: Increasingly relevant in toxicology reports and studies related to new psychoactive substances\u00a0<a class=\"citation ml-xs inline\" style=\"color: #000000;\" href=\"https:\/\/www.cfsre.org\/images\/monographs\/Fluclotizolam_110521_ToxicologyAnalyticalReport.pdf\" target=\"_blank\" rel=\"nofollow noopener\" aria-label=\"[PDF] Fluclotizolam\" data-state=\"closed\">\u00a0<\/a><span class=\"whitespace-nowrap\"><a class=\"citation ml-xs inline\" style=\"color: #000000;\" href=\"https:\/\/pmc.ncbi.nlm.nih.gov\/articles\/PMC8230725\/\" target=\"_blank\" rel=\"nofollow noopener\" aria-label=\"Designer Benzodiazepines: A Review of Toxicology and Public Health Risks\" data-state=\"closed\">\u00a0<\/a>.<\/span><\/span><\/li>\n<li><span style=\"color: #000000;\"><strong>Research Tool<\/strong>: May serve as a model compound in studies investigating the pharmacological profiles of new benzodiazepine derivatives.<\/span><\/li>\n<\/ul>\n<\/div>\n<\/div>\n<\/div>\n<div class=\"card\">\n<div id=\"introduction_to_fluclotizolam_in_the_context_of_novel_psychoactive_substances_(nps)\" class=\"card-header\">\n<p><span class=\"accordion-title\" style=\"color: #000000;\">Introduction to Fluclotizolam in the Context of Novel Psychoactive Substances (NPS)<\/span><\/p>\n<div class=\"accordion-open-close \" data-toggle=\"collapse\" data-target=\"#collapseintroduction_to_fluclotizolam_in_the_context_of_novel_psychoactive_substances_(nps)\" aria-expanded=\"false\" aria-controls=\"collapseintroduction_to_fluclotizolam_in_the_context_of_novel_psychoactive_substances_(nps)\"><\/div>\n<\/div>\n<div id=\"collapseintroduction_to_fluclotizolam_in_the_context_of_novel_psychoactive_substances_(nps)\" class=\"collapse show\" aria-labelledby=\"introduction_to_fluclotizolam_in_the_context_of_novel_psychoactive_substances_(nps)\">\n<div class=\"card-body\">\n<h3><span style=\"color: #000000;\">Historical Synthesis and Patent Development of Fluclotizolam<\/span><\/h3>\n<p><span style=\"color: #000000;\">Fluclotizolam (chemical name: 2-chloro-4-(2-fluorophenyl)-9-methyl-4H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine; molecular formula: C\u2081\u2085H\u2081\u2080ClFN\u2084S) was first synthesized in 1979 by the pharmaceutical company Hoffmann-La Roche, as documented in US Patent 4,155,913\u00a0<a style=\"color: #000000;\" href=\"https:\/\/en.wikipedia.org\/wiki\/Fluclotizolam\" target=\"_blank\" rel=\"noopener\">[1]<\/a>\u00a0[4]. This patent detailed its synthesis as part of a broader exploration of\u00a0<em>thienotriazolodiazepine derivatives<\/em>\u00a0\u2013 structurally distinct from classical 1,4-benzodiazepines due to the replacement of a benzene ring with a thiophene ring and the incorporation of a triazolo moiety\u00a0<a style=\"color: #000000;\" href=\"https:\/\/en.wikipedia.org\/wiki\/Fluclotizolam\" target=\"_blank\" rel=\"noopener\">[1]<\/a>\u00a0[6]. Despite its early discovery, fluclotizolam was never developed or approved for clinical use, remaining a pharmacological curiosity without therapeutic application for nearly four decades\u00a0<a style=\"color: #000000;\" href=\"https:\/\/en.wikipedia.org\/wiki\/Fluclotizolam\" target=\"_blank\" rel=\"noopener\">[1]<\/a>\u00a0[4].<\/span><\/p>\n<p><span style=\"color: #000000;\">The synthetic pathway described in the original patent involves complex heterocyclic chemistry, utilizing multi-step reactions to form the characteristic thienotriazolodiazepine core. This structure confers high affinity for the GABA<sub>A<\/sub>\u00a0receptor, similar to other benzodiazepine analogs, but with potentially altered pharmacokinetic properties\u00a0<a style=\"color: #000000;\" href=\"https:\/\/en.wikipedia.org\/wiki\/Fluclotizolam\" target=\"_blank\" rel=\"noopener\">[1]<\/a>\u00a0[7]. The compound&#8217;s structural features include:<\/span><\/p>\n<ul>\n<li><span style=\"color: #000000;\">A chloro-substitution at the R<sub>2<\/sub>\u00a0position of the thieno ring<\/span><\/li>\n<li><span style=\"color: #000000;\">A fluorine atom on the pendant phenyl ring<\/span><\/li>\n<li><span style=\"color: #000000;\">A methyl group on the triazolo ringThese modifications were designed to enhance receptor binding and metabolic stability compared to earlier benzodiazepines\u00a0<a style=\"color: #000000;\" href=\"https:\/\/en.wikipedia.org\/wiki\/Fluclotizolam\" target=\"_blank\" rel=\"noopener\">[1]<\/a>\u00a0[4].<\/span><\/li>\n<\/ul>\n<p><span style=\"color: #000000;\"><em>Table 1: Key Patent and Synthesis Details of Fluclotizolam<\/em><\/span><\/p>\n<table>\n<thead>\n<tr>\n<th><span style=\"color: #000000;\"><strong>Property<\/strong><\/span><\/th>\n<th><span style=\"color: #000000;\"><strong>Detail<\/strong><\/span><\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td><span style=\"color: #000000;\"><strong>Patent Number<\/strong><\/span><\/td>\n<td><span style=\"color: #000000;\">US 4,155,913<\/span><\/td>\n<\/tr>\n<tr>\n<td><span style=\"color: #000000;\"><strong>Filing Year<\/strong><\/span><\/td>\n<td><span style=\"color: #000000;\">1979<\/span><\/td>\n<\/tr>\n<tr>\n<td><span style=\"color: #000000;\"><strong>Assignee<\/strong><\/span><\/td>\n<td><span style=\"color: #000000;\">Hoffmann-La Roche Inc.<\/span><\/td>\n<\/tr>\n<tr>\n<td><span style=\"color: #000000;\"><strong>Chemical Class<\/strong><\/span><\/td>\n<td><span style=\"color: #000000;\">Thienotriazolodiazepine<\/span><\/td>\n<\/tr>\n<tr>\n<td><span style=\"color: #000000;\"><strong>Initial Development Status<\/strong><\/span><\/td>\n<td><span style=\"color: #000000;\">Never marketed; shelved compound<\/span><\/td>\n<\/tr>\n<tr>\n<td><span style=\"color: #000000;\"><strong>Key Structural Features<\/strong><\/span><\/td>\n<td><span style=\"color: #000000;\">Thiophene ring, triazolo ring, 2-fluorophenyl substituent<\/span><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<h3><span style=\"color: #000000;\">Emergence as a Designer Benzodiazepine in Global Illicit Markets<\/span><\/h3>\n<p><span style=\"color: #000000;\">Fluclotizolam remained obscure until 2017, when it was definitively identified in seized drug samples in Denmark and Sweden, marking its debut as a novel psychoactive substance (NPS)\u00a0<a style=\"color: #000000;\" href=\"https:\/\/en.wikipedia.org\/wiki\/Fluclotizolam\" target=\"_blank\" rel=\"noopener\">[1]<\/a>\u00a0[4]. This emergence coincided with intensified regulatory controls on classical benzodiazepines and other designer compounds (e.g., etizolam, phenazepam), creating a market niche for unscheduled analogs\u00a0<a style=\"color: #000000;\" href=\"https:\/\/pmc.ncbi.nlm.nih.gov\/articles\/PMC10750316\/\" target=\"_blank\" rel=\"noopener\">[3]<\/a>. Initial encounters involved green tablets and blotter paper forms \u2013 packaging strategies borrowed from hallucinogen markets to facilitate discreet distribution\u00a0[4].<\/span><\/p>\n<p><span style=\"color: #000000;\">The drug&#8217;s appearance in illicit markets represents a case study in &#8220;<em>pharmacological resurrection<\/em>,&#8221; wherein shelved pharmaceutical compounds are repurposed as designer drugs\u00a0<a style=\"color: #000000;\" href=\"https:\/\/en.wikipedia.org\/wiki\/Fluclotizolam\" target=\"_blank\" rel=\"noopener\">[1]<\/a>\u00a0<a style=\"color: #000000;\" href=\"https:\/\/pmc.ncbi.nlm.nih.gov\/articles\/PMC10750316\/\" target=\"_blank\" rel=\"noopener\">[3]<\/a>. Several factors contributed to its appeal within the NPS ecosystem:<\/span><\/p>\n<ul>\n<li><span style=\"color: #000000;\"><strong>Legal Ambiguity<\/strong>: Unlike therapeutic benzodiazepines, fluclotizolam had no medical presence, complicating regulatory classification\u00a0<a style=\"color: #000000;\" href=\"https:\/\/pmc.ncbi.nlm.nih.gov\/articles\/PMC10750316\/\" target=\"_blank\" rel=\"noopener\">[3]<\/a>\u00a0[4]<\/span><\/li>\n<li><span style=\"color: #000000;\"><strong>Potency Profile<\/strong>: As a thienotriazolodiazepine, it exhibits high GABA<sub>A<\/sub>\u00a0receptor affinity, with self-reported user effects including intense sedation and muscle relaxation lasting up to 14 hours\u00a0[4]<\/span><\/li>\n<li><span style=\"color: #000000;\"><strong>Supply Chain Integration<\/strong>: Online vendors marketed it explicitly as a &#8220;research chemical,&#8221; exploiting jurisdictional loopholes in pharmaceutical legislation\u00a0<a style=\"color: #000000;\" href=\"https:\/\/pmc.ncbi.nlm.nih.gov\/articles\/PMC10750316\/\" target=\"_blank\" rel=\"noopener\">[3]<\/a>\u00a0[4]<\/span><\/li>\n<\/ul>\n<p><span style=\"color: #000000;\">Between 2017-2023, fluclotizolam appeared in global forensic reports, though with less frequency than other designer benzodiazepines like etizolam or flubromazolam. A 2021 review of designer benzodiazepines noted its presence in toxicological screenings, but insufficient case data prevented comprehensive risk assessment\u00a0<a style=\"color: #000000;\" href=\"https:\/\/pmc.ncbi.nlm.nih.gov\/articles\/PMC10750316\/\" target=\"_blank\" rel=\"noopener\">[3]<\/a>. Analytical characterization confirmed its identity via liquid chromatography-tandem mass spectrometry (LC-MS\/MS), with seizures primarily occurring in Europe and North America\u00a0<a style=\"color: #000000;\" href=\"https:\/\/en.wikipedia.org\/wiki\/Fluclotizolam\" target=\"_blank\" rel=\"noopener\">[1]<\/a>\u00a0[2].<\/span><\/p>\n<p><span style=\"color: #000000;\"><em>Table 2: Global Emergence Pattern of Fluclotizolam as a Designer Drug<\/em><\/span><\/p>\n<table>\n<thead>\n<tr>\n<th><span style=\"color: #000000;\"><strong>Timeline<\/strong><\/span><\/th>\n<th><span style=\"color: #000000;\"><strong>Event<\/strong><\/span><\/th>\n<th><span style=\"color: #000000;\"><strong>Jurisdictions<\/strong><\/span><\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td><span style=\"color: #000000;\">1979<\/span><\/td>\n<td><span style=\"color: #000000;\">Initial synthesis and patenting<\/span><\/td>\n<td><span style=\"color: #000000;\">Global (patent)<\/span><\/td>\n<\/tr>\n<tr>\n<td><span style=\"color: #000000;\">Pre-2017<\/span><\/td>\n<td><span style=\"color: #000000;\">No known illicit presence<\/span><\/td>\n<td><span style=\"color: #000000;\">N\/A<\/span><\/td>\n<\/tr>\n<tr>\n<td><span style=\"color: #000000;\">2017<\/span><\/td>\n<td><span style=\"color: #000000;\">First forensic identification in seized samples<\/span><\/td>\n<td><span style=\"color: #000000;\">Denmark, Sweden<\/span><\/td>\n<\/tr>\n<tr>\n<td><span style=\"color: #000000;\">2018-2020<\/span><\/td>\n<td><span style=\"color: #000000;\">Appearance in online &#8220;research chemical&#8221; markets<\/span><\/td>\n<td><span style=\"color: #000000;\">United States, European Union<\/span><\/td>\n<\/tr>\n<tr>\n<td><span style=\"color: #000000;\">2021-2023<\/span><\/td>\n<td><span style=\"color: #000000;\">Documented in toxicology screenings (postmortem\/DUI cases)<\/span><\/td>\n<td><span style=\"color: #000000;\">UK, Germany, North America<\/span><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<h3><span style=\"color: #000000;\">Legal and Regulatory Challenges in Classification<\/span><\/h3>\n<p><span style=\"color: #000000;\">The regulatory status of fluclotizolam demonstrates significant international fragmentation, reflecting challenges in controlling non-pharmaceutical benzodiazepines. As of 2025:<\/span><\/p>\n<ul>\n<li><span style=\"color: #000000;\"><strong>Canada<\/strong>: Classified under Schedule IV of the Controlled Drugs and Substances Act\u00a0<a style=\"color: #000000;\" href=\"https:\/\/en.wikipedia.org\/wiki\/Fluclotizolam\" target=\"_blank\" rel=\"noopener\">[1]<\/a><\/span><\/li>\n<li><span style=\"color: #000000;\"><strong>Germany<\/strong>: Regulated under the\u00a0<em>NpSG<\/em>\u00a0(New Psychoactive Substances Act), permitting only industrial\/scientific use\u00a0<a style=\"color: #000000;\" href=\"https:\/\/en.wikipedia.org\/wiki\/Fluclotizolam\" target=\"_blank\" rel=\"noopener\">[1]<\/a><\/span><\/li>\n<li><span style=\"color: #000000;\"><strong>United Kingdom<\/strong>: Controlled under the Psychoactive Substances Act (2016)\u00a0<a style=\"color: #000000;\" href=\"https:\/\/en.wikipedia.org\/wiki\/Fluclotizolam\" target=\"_blank\" rel=\"noopener\">[1]<\/a><\/span><\/li>\n<li><span style=\"color: #000000;\"><strong>United States<\/strong>: Remains unscheduled at the federal level, though subject to analogue laws in some states\u00a0[4]<\/span><\/li>\n<\/ul>\n<p><span style=\"color: #000000;\">This patchwork classification stems from fluclotizolam&#8217;s unique status: a pharmacologically active compound with no therapeutic history, avoiding pre-emptive scheduling\u00a0<a style=\"color: #000000;\" href=\"https:\/\/pmc.ncbi.nlm.nih.gov\/articles\/PMC10750316\/\" target=\"_blank\" rel=\"noopener\">[3]<\/a>\u00a0[4]. International bodies like the UNODC face challenges in scheduling such compounds because the 1971 Convention on Psychotropic Substances requires evidence of therapeutic use or significant abuse potential \u2013 data that is scarce for recently emerged NPS\u00a0<\/span><\/p>\n<p><span style=\"color: #000000;\">Detection complications further impede control efforts:<\/span><\/p>\n<ul>\n<li><span style=\"color: #000000;\"><strong>Metabolic Uncertainty<\/strong>: Phase I\/II metabolism pathways remain uncharacterized in humans, hampering toxicological surveillance\u00a0<\/span><\/li>\n<li><span style=\"color: #000000;\"><strong>Analytical Limitations<\/strong>: Immunoassays often fail to detect novel benzodiazepines; confirmation requires advanced LC-MS\/MS\u00a0<\/span><\/li>\n<li><span style=\"color: #000000;\"><strong>Dosage Form Variability<\/strong>: Tablets and blotters contain inconsistent concentrations (typically 0.5mg pellets), complicating potency assessments<\/span><\/li>\n<\/ul>\n<p><span style=\"color: #000000;\">The European Monitoring Centre for Drugs and Drug Addiction (EMCDDA) has flagged thienotriazolodiazepines as particularly problematic due to their high potency and extended durations of action. However, scheduling momentum has focused more on prevalent DBZs like etizolam and flualprazolam, which were added to Schedule IV of the UN Convention on Psychotropic Substances in 2020-2021\u00a0. Fluclotizolam&#8217;s lower market presence has resulted in regulatory inertia, exemplifying how transient NPS compounds exploit gaps in international drug control frameworks.<\/span><\/p>\n<p><span style=\"color: #000000;\"><em>Table 3: Comparative International Legal Status of Fluclotizolam (2025)<\/em><\/span><\/p>\n<table>\n<thead>\n<tr>\n<th><span style=\"color: #000000;\"><strong>Country\/Region<\/strong><\/span><\/th>\n<th><span style=\"color: #000000;\"><strong>Regulatory Status<\/strong><\/span><\/th>\n<th><span style=\"color: #000000;\"><strong>Governing Legislation<\/strong><\/span><\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td><span style=\"color: #000000;\"><strong>Canada<\/strong><\/span><\/td>\n<td><span style=\"color: #000000;\">Schedule IV<\/span><\/td>\n<td><span style=\"color: #000000;\">Controlled Drugs and Substances Act<\/span><\/td>\n<\/tr>\n<tr>\n<td><span style=\"color: #000000;\"><strong>Germany<\/strong><\/span><\/td>\n<td><span style=\"color: #000000;\">NpSG-controlled<\/span><\/td>\n<td><span style=\"color: #000000;\">New Psychoactive Substances Act<\/span><\/td>\n<\/tr>\n<tr>\n<td><span style=\"color: #000000;\"><strong>United Kingdom<\/strong><\/span><\/td>\n<td><span style=\"color: #000000;\">Class B (Psychoactive Substances Act)<\/span><\/td>\n<td><span style=\"color: #000000;\">Psychoactive Substances Act (2016)<\/span><\/td>\n<\/tr>\n<tr>\n<td><span style=\"color: #000000;\"><strong>United States<\/strong><\/span><\/td>\n<td><span style=\"color: #000000;\">Unscheduled (federally)<\/span><\/td>\n<td><span style=\"color: #000000;\">Controlled Substances Act (Analogue Act applicable)<\/span><\/td>\n<\/tr>\n<tr>\n<td><span style=\"color: #000000;\"><strong>Australia<\/strong><\/span><\/td>\n<td><span style=\"color: #000000;\">Presumed analogue control<\/span><\/td>\n<td><span style=\"color: #000000;\">Poisons Standard<\/span><\/td>\n<\/tr>\n<tr>\n<td><span style=\"color: #000000;\"><strong>Sweden<\/strong><\/span><\/td>\n<td><span style=\"color: #000000;\">Narcotics Control<\/span><\/td>\n<td><span style=\"color: #000000;\">Narcotic Drugs Criminal Act<\/span><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/div>\n<\/div>\n<\/div>\n<div class=\"card\">\n<div id=\"headingTwo\" class=\"card-header\">\n<h3><span class=\"accordion-title\" style=\"color: #000000;\">Properties<\/span><\/h3>\n<div class=\"accordion-open-close\" data-toggle=\"collapse\" data-target=\"#collapseTwo\" aria-expanded=\"true\" aria-controls=\"collapseTwo\"><\/div>\n<\/div>\n<div id=\"collapseTwo\" class=\"collapse show\" aria-labelledby=\"headingTwo\">\n<div class=\"card-body\">\n<div class=\"row-table\">\n<div class=\"row inner-row\">\n<div class=\"col-12 col-sm-12 col-lg-4\">\n<div class=\"row-table-title\">\n<h4><span style=\"color: #000000;\">CAS Number<\/span><\/h4>\n<\/div>\n<\/div>\n<div class=\"col-12 col-sm-12 col-lg-8\">\n<div class=\"row-table-info\"><span style=\"color: #000000;\">54123-15-8<\/span><\/div>\n<\/div>\n<\/div>\n<\/div>\n<div class=\"row-table\">\n<div class=\"row inner-row\">\n<div class=\"col-12 col-sm-12 col-lg-4\">\n<div class=\"row-table-title\">\n<h4><span style=\"color: #000000;\">Product Name<\/span><\/h4>\n<\/div>\n<\/div>\n<div class=\"col-12 col-sm-12 col-lg-8\">\n<div class=\"row-table-info\"><span style=\"color: #000000;\">Fluclotizolam<\/span><\/div>\n<\/div>\n<\/div>\n<\/div>\n<div class=\"row-table\">\n<div class=\"row inner-row\">\n<div class=\"col-12 col-sm-12 col-lg-4\">\n<div class=\"row-table-title\">\n<h4><span style=\"color: #000000;\">IUPAC Name<\/span><\/h4>\n<\/div>\n<\/div>\n<div class=\"col-12 col-sm-12 col-lg-8\">\n<div class=\"row-table-info\"><span style=\"color: #000000;\">4-chloro-7-(2-fluorophenyl)-13-methyl-3-thia-1,8,11,12-tetrazatricyclo[8.3.0.02,6]trideca-2(6),4,7,10,12-pentaene<\/span><\/div>\n<\/div>\n<\/div>\n<\/div>\n<div class=\"row-table\">\n<div class=\"row inner-row\">\n<div class=\"col-12 col-sm-12 col-lg-4\">\n<div class=\"row-table-title\">\n<h4><span style=\"color: #000000;\">Molecular Formula<\/span><\/h4>\n<\/div>\n<\/div>\n<div class=\"col-12 col-sm-12 col-lg-8\">\n<div class=\"row-table-info\"><span style=\"color: #000000;\">C15H10ClFN4S<\/span><\/div>\n<\/div>\n<\/div>\n<\/div>\n<div class=\"row-table\">\n<div class=\"row inner-row\">\n<div class=\"col-12 col-sm-12 col-lg-4\">\n<div class=\"row-table-title\">\n<h4><span style=\"color: #000000;\">Molecular Weight<\/span><\/h4>\n<\/div>\n<\/div>\n<div class=\"col-12 col-sm-12 col-lg-8\">\n<div class=\"row-table-info\"><span style=\"color: #000000;\">332.8 g\/mol<\/span><\/div>\n<\/div>\n<\/div>\n<\/div>\n<div class=\"row-table\">\n<div class=\"row inner-row\">\n<div class=\"col-12 col-sm-12 col-lg-4\">\n<div class=\"row-table-title\">\n<h4><span style=\"color: #000000;\">InChI<\/span><\/h4>\n<\/div>\n<\/div>\n<div class=\"col-12 col-sm-12 col-lg-8\">\n<div class=\"row-table-info\"><span style=\"color: #000000;\">InChI=1S\/C15H10ClFN4S\/c1-8-19-20-13-7-18-14(9-4-2-3-5-11(9)17)10-6-12(16)22-15(10)21(8)13\/h2-6H,7H2,1H3<\/span><\/div>\n<\/div>\n<\/div>\n<\/div>\n<div class=\"row-table\">\n<div class=\"row inner-row\">\n<div class=\"col-12 col-sm-12 col-lg-4\">\n<div class=\"row-table-title\">\n<h4><span style=\"color: #000000;\">InChI Key<\/span><\/h4>\n<\/div>\n<\/div>\n<div class=\"col-12 col-sm-12 col-lg-8\">\n<div class=\"row-table-info\"><span style=\"color: #000000;\">ZDYRCUZZLRLMHG-UHFFFAOYSA-N<\/span><\/div>\n<\/div>\n<\/div>\n<\/div>\n<div class=\"row-table\">\n<div class=\"row inner-row\">\n<div class=\"col-12 col-sm-12 col-lg-4\">\n<div class=\"row-table-title\">\n<h4><span style=\"color: #000000;\">SMILES<\/span><\/h4>\n<\/div>\n<\/div>\n<div class=\"col-12 col-sm-12 col-lg-8\">\n<div class=\"row-table-info\"><span style=\"color: #000000;\">Array<\/span><\/div>\n<\/div>\n<\/div>\n<\/div>\n<div class=\"row-table\">\n<div class=\"row inner-row\">\n<div class=\"col-12 col-sm-12 col-lg-4\">\n<div class=\"row-table-title\">\n<h4><span style=\"color: #000000;\">Canonical SMILES<\/span><\/h4>\n<\/div>\n<\/div>\n<div class=\"col-12 col-sm-12 col-lg-8\">\n<div class=\"row-table-info\"><span style=\"color: #000000;\">CC1=NN=C2N1C3=C(C=C(S3)Cl)C(=NC2)C4=CC=CC=C4F<\/span><\/div>\n<div><\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<p><span style=\"color: #000000;\">Fluclotizolam is a designer drug intended for research and forensic analysis.\u00a0<span class=\"tlid-translation translation\" lang=\"en\"><span title=\"\">Fluclotizolam\u00a0<\/span><\/span>is produced in modern pharmaceutical laboratory in compliance with all quality standards.<\/span><\/p>\n<p><span style=\"color: #000000;\">Storage conditions: in a cool and dry place,<\/span><br \/>\n<span style=\"color: #000000;\">storage for up to 2 years.<\/span><\/p>\n<figure id=\"attachment_2368\" class=\"wp-caption alignleft\" aria-describedby=\"caption-attachment-2368\"><span style=\"color: #000000;\"><a style=\"color: #000000;\" href=\"https:\/\/chembeyond.com\/wp-content\/uploads\/2023\/03\/Fluclotizolam.png\" target=\"_blank\" rel=\"noopener\"><img loading=\"lazy\" decoding=\"async\" class=\"size-medium wp-image-2368\" src=\"https:\/\/chembeyond.com\/wp-content\/uploads\/2023\/03\/Fluclotizolam-245x300.png\" sizes=\"auto, (max-width: 245px) 100vw, 245px\" srcset=\"https:\/\/chembeyond.com\/wp-content\/uploads\/2023\/03\/Fluclotizolam-245x300.png 245w, https:\/\/chembeyond.com\/wp-content\/uploads\/2023\/03\/Fluclotizolam-768x940.png 768w, https:\/\/chembeyond.com\/wp-content\/uploads\/2023\/03\/Fluclotizolam.png 800w\" alt=\"Fluclotizolam\" width=\"245\" height=\"300\" \/><\/a><\/span><figcaption id=\"caption-attachment-2368\" class=\"wp-caption-text\"><span style=\"color: #000000;\">Fluclotizolam<\/span><\/figcaption><\/figure>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p><span style=\"color: #000000;\"><strong>Synonyms:\u00a0<\/strong>Fluclotizolam<\/span><\/p>\n<p><span style=\"color: #000000;\"><strong>IUPAC<\/strong>: 2-chloro-4-(2-fluorophenyl)-9-methyl-4H-thieno[3,2-f] [1,2,4]triazolo[4,3-a] [1,4]diazepine<\/span><\/p>\n<p><span style=\"color: #000000;\"><strong>Formula:\u00a0<\/strong><span title=\"Carbon\">C<\/span><sub>15<\/sub><span title=\"Hydrogen\">H<\/span><sub>10<\/sub><span title=\"Chlorine\">Cl<\/span><span title=\"Fluorine\">F<\/span><span title=\"Nitrogen\">N<\/span><sub>4<\/sub><span title=\"Sulfur\">S<\/span><\/span><\/p>\n<p><span style=\"color: #000000;\"><strong>Molecular weight:\u00a0<\/strong><span class=\"nowrap\">332.78<\/span>\u00a0g\u00b7mol<sup>\u2212<\/sup><\/span><\/p>\n<p><span style=\"color: #000000;\"><strong>CAS<\/strong>: 54123-15-8<\/span><\/p>\n<p><span style=\"color: #000000;\"><strong>Appearance<\/strong>: A crystalline solid, Powder<\/span><\/p>\n<p><span style=\"color: #000000;\"><strong>Purity<\/strong>: \u2265 98%<\/span><\/p>\n<p><span id=\"result_box\" class=\"\" lang=\"en\" style=\"color: #000000;\"><span class=\"\">-Choose your favorite products from <strong>Chemsaxis<\/strong>, and you are guaranteed excellent quality at the best price.<\/span><\/span><\/p>\n<p><span class=\"\" style=\"color: #000000;\">-Envelopes are sent 24 hours after payment.<\/span><br \/>\n<span style=\"color: #000000;\">Delivery time 3-4 business days.<\/span><br \/>\n<span style=\"color: #000000;\">100% delivery speed throughout Europe.<\/span><\/p>\n<p><span class=\"\" style=\"color: #000000;\">-You must know the legal status of the product you order in your country.<\/span><br \/>\n<span class=\"\" style=\"color: #000000;\">-When ordering on our website from 250 US dollars, delivery at our expense. The manager automatically excludes shipping costs when ordering from $ 250.\u00a0<\/span><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Fluclotizolam Fluclotizolam| buy Fluclotizolam online\u00a0 Buy Fluclotizolam online from Chems Axis. Fluclotizolam is a sedative benzodiazepine drug, a derivative of thienotriazolodiazepine was&hellip;<\/p>","protected":false},"author":1,"featured_media":8226,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[10],"tags":[],"class_list":["post-8080","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-cannabinoids"],"_links":{"self":[{"href":"https:\/\/chemsaxis.com\/pt\/wp-json\/wp\/v2\/posts\/8080","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/chemsaxis.com\/pt\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/chemsaxis.com\/pt\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/chemsaxis.com\/pt\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/chemsaxis.com\/pt\/wp-json\/wp\/v2\/comments?post=8080"}],"version-history":[{"count":6,"href":"https:\/\/chemsaxis.com\/pt\/wp-json\/wp\/v2\/posts\/8080\/revisions"}],"predecessor-version":[{"id":8228,"href":"https:\/\/chemsaxis.com\/pt\/wp-json\/wp\/v2\/posts\/8080\/revisions\/8228"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/chemsaxis.com\/pt\/wp-json\/wp\/v2\/media\/8226"}],"wp:attachment":[{"href":"https:\/\/chemsaxis.com\/pt\/wp-json\/wp\/v2\/media?parent=8080"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/chemsaxis.com\/pt\/wp-json\/wp\/v2\/categories?post=8080"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/chemsaxis.com\/pt\/wp-json\/wp\/v2\/tags?post=8080"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}