{"id":5392,"date":"2026-10-18T02:10:36","date_gmt":"2026-10-18T02:10:36","guid":{"rendered":"https:\/\/legitchem.com\/?post_type=product&#038;p=5392"},"modified":"2026-10-20T11:37:25","modified_gmt":"2026-10-20T11:37:25","slug":"4-ho-met","status":"publish","type":"product","link":"https:\/\/legitchem.com\/it\/4-ho-met\/","title":{"rendered":"4-HO-MET"},"content":{"rendered":"<h2 data-start=\"223\" data-end=\"323\"><strong data-start=\"226\" data-end=\"323\">4-HO-MET (4-Hydroxy-N-methyl-N-ethyltryptamine) \u2013 Detailed Overview for Research and Analysis<\/strong><\/h2>\n<p data-start=\"325\" data-end=\"764\"><a href=\"https:\/\/researchchemsupplier.com\/product-category\/psychedelics\/\" target=\"_blank\" rel=\"noopener\"><strong data-start=\"325\" data-end=\"337\">4-HO-MET<\/strong><\/a>, also known as <strong data-start=\"353\" data-end=\"393\">4-Hydroxy-N-methyl-N-ethyltryptamine<\/strong>, is a <strong data-start=\"400\" data-end=\"434\">synthetic psychedelic compound<\/strong> belonging to the <strong data-start=\"452\" data-end=\"472\">tryptamine class<\/strong>. Structurally related to <strong data-start=\"498\" data-end=\"510\">psilocin<\/strong> (the active metabolite of psilocybin found in magic mushrooms), 4-HO-MET has gained attention among researchers and psychopharmacologists for its <strong data-start=\"657\" data-end=\"688\">unique psychoactive profile<\/strong>, <strong data-start=\"690\" data-end=\"715\">potent visual effects<\/strong>, and <strong data-start=\"721\" data-end=\"751\">short-to-moderate duration<\/strong> of action.<\/p>\n<p data-start=\"766\" data-end=\"1048\">With growing interest in novel tryptamines, 4-HO-MET remains a <a href=\"https:\/\/www.empirechemstore.com\/product\/4-ho-met\/\" target=\"_blank\" rel=\"noopener\"><strong data-start=\"829\" data-end=\"875\">notable subject for scientific exploration<\/strong><\/a>, particularly in studies focused on <strong data-start=\"912\" data-end=\"950\">serotonergic receptor interactions<\/strong>, <strong data-start=\"952\" data-end=\"977\">perceptual alteration<\/strong>, and <strong data-start=\"983\" data-end=\"1008\">psychological effects<\/strong> associated with psychedelic substances.<\/p>\n<hr data-start=\"1050\" data-end=\"1053\" \/>\n<h3 data-start=\"1055\" data-end=\"1093\"><strong data-start=\"1059\" data-end=\"1093\">Chemical Profile and Structure<\/strong><\/h3>\n<ul data-start=\"1095\" data-end=\"1371\">\n<li data-start=\"1095\" data-end=\"1154\">\n<p data-start=\"1097\" data-end=\"1154\"><strong data-start=\"1097\" data-end=\"1115\">Chemical Name:<\/strong> 4-Hydroxy-N-methyl-N-ethyltryptamine<\/p>\n<\/li>\n<li data-start=\"1155\" data-end=\"1194\">\n<p data-start=\"1157\" data-end=\"1194\"><strong data-start=\"1157\" data-end=\"1174\">Common Names:<\/strong> 4-HO-MET, Metocin<\/p>\n<\/li>\n<li data-start=\"1195\" data-end=\"1231\">\n<p data-start=\"1197\" data-end=\"1231\"><strong data-start=\"1197\" data-end=\"1219\">Molecular Formula:<\/strong> C13H18N2O<\/p>\n<\/li>\n<li data-start=\"1232\" data-end=\"1270\">\n<p data-start=\"1234\" data-end=\"1270\"><strong data-start=\"1234\" data-end=\"1255\">Molecular Weight:<\/strong> 218.29 g\/mol<\/p>\n<\/li>\n<li data-start=\"1271\" data-end=\"1336\">\n<p data-start=\"1273\" data-end=\"1336\"><strong data-start=\"1273\" data-end=\"1288\">IUPAC Name:<\/strong> 3-[2-(ethyl(methyl)amino)ethyl]-1H-indol-4-ol<\/p>\n<\/li>\n<li data-start=\"1337\" data-end=\"1371\">\n<p data-start=\"1339\" data-end=\"1371\"><strong data-start=\"1339\" data-end=\"1358\">Chemical Class:<\/strong> Tryptamine<\/p>\n<\/li>\n<\/ul>\n<p data-start=\"1373\" data-end=\"1788\">4-HO-MET is a <strong data-start=\"1387\" data-end=\"1412\">hydroxylated analogue<\/strong> of 4-hydroxy-N-methyl-N-ethyltryptamine, and both are close structural relatives of <strong data-start=\"1474\" data-end=\"1497\">psilocin (4-HO-DMT)<\/strong>. The compound\u2019s chemical similarity to natural tryptamines gives it a <strong data-start=\"1568\" data-end=\"1608\">comparable pharmacological mechanism<\/strong>, acting primarily as a <strong data-start=\"1632\" data-end=\"1662\">serotonin receptor agonist<\/strong>, especially at the <strong data-start=\"1682\" data-end=\"1701\">5-HT2A receptor<\/strong> \u2014 the same receptor implicated in the psychedelic effects of LSD, psilocybin, and DMT.<\/p>\n<hr data-start=\"1790\" data-end=\"1793\" \/>\n<h3 data-start=\"1795\" data-end=\"1826\"><strong data-start=\"1799\" data-end=\"1826\">Origins and Development<\/strong><\/h3>\n<p data-start=\"1828\" data-end=\"2356\">4-hydroxy-N-methyl-N-ethyltryptamine was first synthesized by <strong data-start=\"1862\" data-end=\"1883\">Alexander Shulgin<\/strong>, the pioneering chemist and author of <em data-start=\"1922\" data-end=\"1966\">TiHKAL: Tryptamines I Have Known and Loved<\/em>. In his documentation, Shulgin described 4-HO-MET as producing effects <strong data-start=\"2038\" data-end=\"2063\">similar to psilocybin<\/strong>, but with a <strong data-start=\"2076\" data-end=\"2130\">more vivid visual and less introspective character<\/strong>. Since its synthesis, the compound has been used primarily in <strong data-start=\"2193\" data-end=\"2227\">psychopharmacological research<\/strong> and <strong data-start=\"2232\" data-end=\"2256\">analytical chemistry<\/strong>, offering valuable insights into <strong data-start=\"2290\" data-end=\"2326\">structure-activity relationships<\/strong> within the tryptamine family.<\/p>\n<hr data-start=\"2358\" data-end=\"2361\" \/>\n<h3 data-start=\"2363\" data-end=\"2407\"><strong data-start=\"2367\" data-end=\"2407\">Pharmacology and Mechanism of Action<\/strong><\/h3>\n<p data-start=\"2409\" data-end=\"2763\">Like other substituted tryptamines, 4-hydroxy-N-methyl-N-ethyltryptamine acts as a <strong data-start=\"2464\" data-end=\"2506\">partial agonist at serotonin receptors<\/strong>, particularly <strong data-start=\"2521\" data-end=\"2551\">5-HT2A, 5-HT2C, and 5-HT1A<\/strong>. Activation of these receptors in the brain is believed to induce <strong data-start=\"2618\" data-end=\"2648\">altered sensory perception<\/strong>, <strong data-start=\"2650\" data-end=\"2679\">emotional intensification<\/strong>, and <strong data-start=\"2685\" data-end=\"2720\">changes in cognitive processing<\/strong> characteristic of psychedelic experiences.<\/p>\n<p data-start=\"2765\" data-end=\"2978\">At the molecular level, the <strong data-start=\"2793\" data-end=\"2828\">hydroxy group at the 4-position<\/strong> of the indole ring enhances its similarity to psilocin, contributing to its <strong data-start=\"2905\" data-end=\"2943\">affinity for serotonergic pathways<\/strong> and its <strong data-start=\"2952\" data-end=\"2975\">psychedelic potency<\/strong>.<\/p>\n<p data-start=\"2980\" data-end=\"3029\">Researchers studying 4-HO-MET often focus on its:<\/p>\n<ul data-start=\"3030\" data-end=\"3201\">\n<li data-start=\"3030\" data-end=\"3089\">\n<p data-start=\"3032\" data-end=\"3089\"><strong data-start=\"3032\" data-end=\"3087\">Binding affinity across serotonin receptor subtypes<\/strong><\/p>\n<\/li>\n<li data-start=\"3090\" data-end=\"3142\">\n<p data-start=\"3092\" data-end=\"3142\"><strong data-start=\"3092\" data-end=\"3140\">Metabolic pathways and elimination half-life<\/strong><\/p>\n<\/li>\n<li data-start=\"3143\" data-end=\"3201\">\n<p data-start=\"3145\" data-end=\"3201\"><strong data-start=\"3145\" data-end=\"3199\">Potential therapeutic implications in neuroscience<\/strong><\/p>\n<\/li>\n<\/ul>\n<p data-start=\"3203\" data-end=\"3379\">These parameters make 4-hydroxy-N-methyl-N-ethyltryptamine a <strong data-start=\"3236\" data-end=\"3278\">valuable compound in research settings<\/strong>, particularly for studies investigating <strong data-start=\"3319\" data-end=\"3378\">consciousness, perception, and neurochemical modulation<\/strong>.<\/p>\n<hr data-start=\"3381\" data-end=\"3384\" \/>\n<h3 data-start=\"3386\" data-end=\"3428\"><strong data-start=\"3390\" data-end=\"3428\">Visual and Sensory Characteristics<\/strong><\/h3>\n<p data-start=\"3430\" data-end=\"3507\">In anecdotal research and controlled trials, 4-HO-MET is known for producing:<\/p>\n<ul data-start=\"3508\" data-end=\"3709\">\n<li data-start=\"3508\" data-end=\"3565\">\n<p data-start=\"3510\" data-end=\"3565\"><strong data-start=\"3510\" data-end=\"3563\">Intensified visual patterns and color enhancement<\/strong><\/p>\n<\/li>\n<li data-start=\"3566\" data-end=\"3599\">\n<p data-start=\"3568\" data-end=\"3599\"><strong data-start=\"3568\" data-end=\"3597\">Mild to moderate euphoria<\/strong><\/p>\n<\/li>\n<li data-start=\"3600\" data-end=\"3631\">\n<p data-start=\"3602\" data-end=\"3631\"><strong data-start=\"3602\" data-end=\"3629\">Altered time perception<\/strong><\/p>\n<\/li>\n<li data-start=\"3632\" data-end=\"3668\">\n<p data-start=\"3634\" data-end=\"3668\"><strong data-start=\"3634\" data-end=\"3666\">Enhanced tactile sensitivity<\/strong><\/p>\n<\/li>\n<li data-start=\"3669\" data-end=\"3709\">\n<p data-start=\"3671\" data-end=\"3709\"><strong data-start=\"3671\" data-end=\"3707\">Light body energy or stimulation<\/strong><\/p>\n<\/li>\n<\/ul>\n<p data-start=\"3711\" data-end=\"3958\">Unlike some other tryptamines that induce strong introspection or emotional depth, 4-hydroxy-N-methyl-N-ethyltryptamine tends to produce <strong data-start=\"3820\" data-end=\"3881\">more externally oriented and visually dynamic experiences<\/strong>, making it a <strong data-start=\"3895\" data-end=\"3921\">unique research analog<\/strong> for comparative psychedelic studies.<\/p>\n<hr data-start=\"3960\" data-end=\"3963\" \/>\n<h3 data-start=\"3965\" data-end=\"4021\"><strong data-start=\"3969\" data-end=\"4021\">Duration and Dosage (for Research Contexts Only)<\/strong><\/h3>\n<p data-start=\"4023\" data-end=\"4221\">Reports from research and analytical review suggest the <strong data-start=\"4079\" data-end=\"4088\">onset<\/strong> of 4-hydroxy-N-methyl-N-ethyltryptamine\u2019s effects occurs within <strong data-start=\"4125\" data-end=\"4145\">20 to 45 minutes<\/strong>, peaking at around <strong data-start=\"4165\" data-end=\"4181\">1 to 2 hours<\/strong>, and subsiding over <strong data-start=\"4202\" data-end=\"4218\">4 to 6 hours<\/strong>.<\/p>\n<p data-start=\"4223\" data-end=\"4382\">Although <strong data-start=\"4232\" data-end=\"4282\">4-HO-MET is not approved for human consumption<\/strong>, laboratory and analytical observations typically note that it exhibits <strong data-start=\"4355\" data-end=\"4381\">dose-dependent effects<\/strong>:<\/p>\n<ul data-start=\"4383\" data-end=\"4623\">\n<li data-start=\"4383\" data-end=\"4459\">\n<p data-start=\"4385\" data-end=\"4459\"><strong data-start=\"4385\" data-end=\"4408\">Low-range exposure:<\/strong> light visual enhancement, subtle mood alteration<\/p>\n<\/li>\n<li data-start=\"4460\" data-end=\"4538\">\n<p data-start=\"4462\" data-end=\"4538\"><strong data-start=\"4462\" data-end=\"4490\">Moderate-range exposure:<\/strong> open-eye visuals, synesthesia, mood elevation<\/p>\n<\/li>\n<li data-start=\"4539\" data-end=\"4623\">\n<p data-start=\"4541\" data-end=\"4623\"><strong data-start=\"4541\" data-end=\"4565\">High-range exposure:<\/strong> immersive visuals, euphoria, altered spatial perception<\/p>\n<\/li>\n<\/ul>\n<p data-start=\"4625\" data-end=\"4778\">Researchers must exercise <strong data-start=\"4651\" data-end=\"4689\">strict laboratory safety standards<\/strong> and ensure <strong data-start=\"4701\" data-end=\"4736\">accurate volumetric measurement<\/strong> during any study involving this compound.<\/p>\n<hr data-start=\"4780\" data-end=\"4783\" \/>\n<h3 data-start=\"4785\" data-end=\"4827\"><strong data-start=\"4789\" data-end=\"4827\">Legal Status and Compliance Notice<\/strong><\/h3>\n<p data-start=\"4829\" data-end=\"5071\">The <strong data-start=\"4833\" data-end=\"4869\">legal classification of 4-HO-MET<\/strong> varies across jurisdictions. In many countries, it remains <strong data-start=\"4929\" data-end=\"4979\">unscheduled but controlled under analogue laws<\/strong>, meaning it may be regulated as a <strong data-start=\"5014\" data-end=\"5047\">chemical analogue of psilocin<\/strong> or other tryptamines.<\/p>\n<p data-start=\"5073\" data-end=\"5335\">Before conducting any form of research, users must confirm the <strong data-start=\"5136\" data-end=\"5154\">legal standing<\/strong> of 4-hydroxy-N-methyl-N-ethyltryptamine within their <strong data-start=\"5180\" data-end=\"5205\">region or institution<\/strong>. This compound is intended <strong data-start=\"5233\" data-end=\"5294\">strictly for scientific, analytical, or forensic research<\/strong> and <strong data-start=\"5299\" data-end=\"5334\">not for human or veterinary use<\/strong>.<\/p>\n<hr data-start=\"5337\" data-end=\"5340\" \/>\n<h3 data-start=\"5342\" data-end=\"5371\"><strong data-start=\"5346\" data-end=\"5371\">Storage and Stability<\/strong><\/h3>\n<p data-start=\"5373\" data-end=\"5425\">For optimal stability, 4-HO-MET should be stored in:<\/p>\n<ul data-start=\"5426\" data-end=\"5560\">\n<li data-start=\"5426\" data-end=\"5455\">\n<p data-start=\"5428\" data-end=\"5455\">A <strong data-start=\"5430\" data-end=\"5455\">cool, dry environment<\/strong><\/p>\n<\/li>\n<li data-start=\"5456\" data-end=\"5498\">\n<p data-start=\"5458\" data-end=\"5498\"><strong data-start=\"5458\" data-end=\"5498\">Airtight, light-resistant containers<\/strong><\/p>\n<\/li>\n<li data-start=\"5499\" data-end=\"5560\">\n<p data-start=\"5501\" data-end=\"5560\"><strong data-start=\"5501\" data-end=\"5538\">Temperature-controlled conditions<\/strong>, ideally below 20\u00b0C<\/p>\n<\/li>\n<\/ul>\n<p data-start=\"5562\" data-end=\"5659\">Proper storage ensures <strong data-start=\"5585\" data-end=\"5607\">chemical integrity<\/strong> and <strong data-start=\"5612\" data-end=\"5632\">accurate results<\/strong> during analytical testing.<\/p>\n<hr data-start=\"5661\" data-end=\"5664\" \/>\n<h3 data-start=\"5666\" data-end=\"5705\"><strong data-start=\"5670\" data-end=\"5705\">Why Researchers Choose 4-HO-MET<\/strong><\/h3>\n<ol data-start=\"5707\" data-end=\"6038\">\n<li data-start=\"5707\" data-end=\"5792\">\n<p data-start=\"5710\" data-end=\"5792\"><strong data-start=\"5710\" data-end=\"5747\">Structural similarity to psilocin<\/strong> \u2013 making it ideal for comparative studies.<\/p>\n<\/li>\n<li data-start=\"5793\" data-end=\"5878\">\n<p data-start=\"5796\" data-end=\"5878\"><strong data-start=\"5796\" data-end=\"5836\">Predictable pharmacological response<\/strong> \u2013 useful for mapping receptor pathways.<\/p>\n<\/li>\n<li data-start=\"5879\" data-end=\"5957\">\n<p data-start=\"5882\" data-end=\"5957\"><strong data-start=\"5882\" data-end=\"5902\">Shorter duration<\/strong> \u2013 allowing easier monitoring in controlled settings.<\/p>\n<\/li>\n<li data-start=\"5958\" data-end=\"6038\">\n<p data-start=\"5961\" data-end=\"6038\"><strong data-start=\"5961\" data-end=\"5991\">Well-documented background<\/strong> \u2013 detailed in Shulgin\u2019s chemical literature.<\/p>\n<\/li>\n<\/ol>\n<p data-start=\"6040\" data-end=\"6158\">Because of these attributes, 4-HO-MET continues to be a <strong data-start=\"6096\" data-end=\"6126\">highly regarded tryptamine<\/strong> in modern psychedelic research.<\/p>\n<hr data-start=\"6160\" data-end=\"6163\" \/>\n<h3 data-start=\"6165\" data-end=\"6183\"><strong data-start=\"6169\" data-end=\"6183\">Conclusion<\/strong><\/h3>\n<p data-start=\"6185\" data-end=\"6631\">4-HO-MET stands at the intersection of <strong data-start=\"6224\" data-end=\"6269\">chemistry, neuroscience, and pharmacology<\/strong>, offering a compelling opportunity for scientists to explore the <strong data-start=\"6335\" data-end=\"6408\">complex relationship between serotonin signaling and human perception<\/strong>. Its <strong data-start=\"6414\" data-end=\"6463\">structural resemblance to natural tryptamines<\/strong>, combined with <strong data-start=\"6479\" data-end=\"6514\">manageable duration and potency<\/strong>, makes it a <strong data-start=\"6527\" data-end=\"6558\">preferred research chemical<\/strong> for those studying <strong data-start=\"6578\" data-end=\"6604\">psychedelic mechanisms<\/strong> and <strong data-start=\"6609\" data-end=\"6630\">receptor dynamics<\/strong>.<\/p>\n<p data-start=\"6633\" data-end=\"6897\">When sourced responsibly and used within proper legal and ethical boundaries, 4-HO-MET serves as a <strong data-start=\"6732\" data-end=\"6803\">valuable compound for analytical and psychopharmacological research<\/strong> aimed at deepening our understanding of <strong data-start=\"6844\" data-end=\"6896\">the human mind and its neurochemical foundations<\/strong>.<\/p>\n","protected":false},"excerpt":{"rendered":"<p data-start=\"67\" data-end=\"465\">4-HO-MET (4-hydroxy-N-methyl-N-ethyltryptamine) is a synthetic psychedelic compound from the tryptamine family, closely related to psilocin and known for its visual and euphoric effects in research settings. Often compared to naturally occurring psilocybin, 4-HO-MET is valued by researchers for its ability to provide insight into serotonin receptor activity and altered states of consciousness.<\/p>\n<p data-start=\"467\" data-end=\"486\"><strong data-start=\"467\" data-end=\"484\">Key Features:<\/strong><\/p>\n<ul data-start=\"487\" data-end=\"761\">\n<li data-start=\"487\" data-end=\"546\">\n<p data-start=\"489\" data-end=\"546\"><strong data-start=\"489\" data-end=\"507\">Chemical Name:<\/strong> 4-hydroxy-N-methyl-N-ethyltryptamine<\/p>\n<\/li>\n<li data-start=\"547\" data-end=\"592\">\n<p data-start=\"549\" data-end=\"592\"><strong data-start=\"549\" data-end=\"558\">Form:<\/strong> Powder or crystal (purity \u226598%)<\/p>\n<\/li>\n<li data-start=\"593\" data-end=\"627\">\n<p data-start=\"595\" data-end=\"627\"><strong data-start=\"595\" data-end=\"605\">Class:<\/strong> Tryptamine analogue<\/p>\n<\/li>\n<li data-start=\"628\" data-end=\"693\">\n<p data-start=\"630\" data-end=\"693\"><strong data-start=\"630\" data-end=\"647\">Research Use:<\/strong> Neuropharmacological and behavioral studies<\/p>\n<\/li>\n<li data-start=\"694\" data-end=\"761\">\n<p data-start=\"696\" data-end=\"761\"><strong data-start=\"696\" data-end=\"708\">Storage:<\/strong> Keep in a cool, dry environment away from sunlight<\/p>\n<\/li>\n<\/ul>\n<p data-start=\"763\" data-end=\"904\">This compound is intended <strong data-start=\"789\" data-end=\"840\">strictly for laboratory and analytical research<\/strong>. It is <strong data-start=\"848\" data-end=\"886\">not approved for human consumption<\/strong> or medical use.<\/p>","protected":false},"featured_media":5419,"comment_status":"closed","ping_status":"closed","template":"","meta":{"site-sidebar-layout":"default","site-content-layout":"","ast-site-content-layout":"default","site-content-style":"default","site-sidebar-style":"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":"","ast-disable-related-posts":"","theme-transparent-header-meta":"","adv-header-id-meta":"","stick-header-meta":"","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","astra-migrate-meta-layouts":"default","ast-page-background-enabled":"default","ast-page-background-meta":{"desktop":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center 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