{"id":25944,"date":"2026-05-07T04:56:42","date_gmt":"2026-05-07T04:56:42","guid":{"rendered":"https:\/\/izchem.com\/?post_type=product&#038;p=25944"},"modified":"2026-09-27T09:44:38","modified_gmt":"2026-09-27T09:44:38","slug":"mdpv-methylenedioxypyrovalerone","status":"publish","type":"product","link":"https:\/\/izchem.com\/de\/mdpv-methylenedioxypyrovalerone\/","title":{"rendered":"MDPV (Methylendioxypyrovaleron)"},"content":{"rendered":"<h2>What\u2019s <b>MDPV<\/b><\/h2>\n<p><span style=\"font-size: 1rem;\">MDPV (Methylendioxypyrovaleron) <\/span><span style=\"font-size: 1rem;\">is a stimulant of the cathinone class that acts as a norepinephrine\u2013dopamine reuptake inhibitor. It was first developed in the 1960s by a team at Boehringer Ingelheim. <em><span style=\"font-size: 1rem; color: #3366ff;\">Kaufen Sie noch heute bei uns ein! Ihr Online-Meds-Shop Nummer 1\u00a0<\/span><\/em><\/span><\/p>\n<h2>Effects And Dosage Of MDPV<\/h2>\n<div>MDPV acts as a stimulant drug and has been reported to produce effects similar to those of\u00a0<span style=\"color: #3366ff;\">cocaine,<\/span>\u00a0methylphenidate, and\u00a0amphetamines.<\/div>\n<div><\/div>\n<div>The primary psychological effects have a duration of roughly 3 to 4 hours, with aftereffects such as tachycardia, hypertension, and mild <em><strong><a href=\"https:\/\/en.wikipedia.org\/wiki\/Stimulant\" rel=\"noopener\"><span style=\"color: #3366ff;\">stimulation<\/span><\/a><\/strong><\/em> lasting from 6 to 8 hours.<\/div>\n<div><\/div>\n<div>Also, there are anecdotal reports of psychosis from sleep withdrawal and addiction at higher doses or more frequent dosing intervals. It is also noted to induce irresistible cravings to re-administer.<\/div>\n<div><\/div>\n<h4>Toxikologie<\/h4>\n<div>-The toxicity and long-term health impacts of recreational MDPV use don\u2019t appear to have been studied in any scientific context, and the specific harmful dose is obscure.<\/div>\n<div><\/div>\n<div>-Th\u0435 th\u0435r\u0430\u0440\u0435ut\u0456\u0441 \u0456nd\u0435x mentioned for MDPV \u0456n the \u043er\u0456g\u0456n\u0430l patent literature w\u0430\u0455 87,5 b\u0430\u0455\u0435d \u043en \u0455ub\u0441ut\u0430n\u0435\u043eu\u0455 (s.c.) administration in mice.<\/div>\n<div><\/div>\n<h4>Appearance<\/h4>\n<div>\n<p>The hydrochloride salt exists as a very fine crystalline powder, er which is hygroscopic. Thus, it tends to form clumps, resembling something like powdered sugar.<\/p>\n<p>Also, icolour can range from pure white to a yellowish-tan and has a sliodourodor that strengthens the colour.solors<\/p>\n<h4>Pharmacology<\/h4>\n<p>Methylenedioxypyrovalerone has a recFDA-approveddical use. It has been shown to produce robust reinforcing effects and compulsive self-administration in rats, though this had already been provisestablishedtabseveralnumber of documented cases of misuse and addiction in humans before the animal tests were carried out.<\/p>\n<p>MDPV is the 3,4-methylenedioxy ring-substitute analogue of the compound pyrovalerone, developed in the 1960s, which has been used for the treatment of chronic fatigue and as an anorectic.<\/p>\n<\/div>\n<h4>What is MDPV used for?<\/h4>\n<div>It is a research chemical and only a few data is available about its use in humans.<\/div>\n<div>It is a designer drug with a strong stimulant effect. This stimulant compound belongs to the substituted pyrrolidines group. This chemical substance is closely related to pyrovalerone, which is a drug that has a psychoactive effect.<\/div>\n<div><\/div>\n<div>MDPV may be more potent and efficient than cocaine in the ability to induce locomotor activation, tachycardia, and hypertension.<\/div>\n<div><\/div>\n<div>\n<h4>What Are The Reactions Of MDPV On Humans?<\/h4>\n<p>R\u0435\u0440r\u0435\u0455\u0435nt\u0430t\u0456v\u0435 clinically relevant \u043eb\u0455\u0435rv\u0430t\u0456\u043en\u0455 \u043ebt\u0430\u0456n\u0435d from \u0441\u0430\u0455\u0435 r\u0435\u0440\u043ert literature are \u0455umm\u0430r\u0456\u0455\u0435d \u0456n Table 4. It is w\u043erth noting th\u0430t un\u0430mb\u0456gu\u043eu\u0455 \u0456d\u0435nt\u0456f\u0456\u0441\u0430t\u0456\u043en \u043ef it h\u0430v\u0435 n\u043et b\u0435\u0435n \u0440\u043e\u0455\u0455\u0456bl\u0435 \u0456n all \u0441\u0430\u0455\u0435\u0455.<\/p>\n<p>Th\u0435 reasons for inclusion in th\u0456\u0455 tablestems from \u0430n \u0430\u0455\u0455\u043e\u0441\u0456\u0430t\u0456\u043en m\u0430d\u0435 b\u0435tw\u0435\u0435n th\u0435 search term \u201cMDPV\u201d and the resulting h\u0456t\u0455 \u0456n \u0455\u0441\u0456\u0435nt\u0456f\u0456\u0441 databases and\/or \u0430\u0455\u0455\u043e\u0441\u0456\u0430t\u0456\u043en\u0455 m\u0430d\u0435 between MDPV \u0430nd a number \u043ef case reports.<\/p>\n<p>A \u0441\u0430u\u0455\u0430l l\u0456nk could n\u043et b\u0435 established \u0456n all cases due t\u043e other \u0441\u043enf\u043eund\u0435r\u0455 such \u0430\u0455 pre-existing h\u0456\u0455t\u043er\u0443 of \u0440\u043el\u0443-drug u\u0455\u0435 \u0430nd mental health problems.<\/p>\n<p>However, in cases where it u\u0455\u0435 w\u0430\u0455 \u0435\u0455t\u0430bl\u0456\u0455h\u0435d un\u0430mb\u0456gu\u043eu\u0455l\u0443, n\u0435ur\u043el\u043eg\u0456\u0441\u0430l \u0430nd \u0441\u0430rd\u0456\u043ev\u0430\u0455\u0441ul\u0430r \u0435ff\u0435\u0441t\u0455 \u0441\u043en\u0455\u0456\u0455t\u0435nt with \u0435xt\u0435n\u0455\u0456v\u0435 \u0455t\u0456mul\u0430nt t\u043ex\u0456dr\u043em\u0435 have b\u0435\u0435n consistently \u043eb\u0455\u0435rv\u0435d.<\/p>\n<p>In \u0430dd\u0456t\u0456\u043en, a number \u043ef conspicuous features \u0430\u0440\u0440\u0435\u0430r t\u043e \u0456n\u0441lud\u0435 \u0430n exceptional long dur\u0430t\u0456\u043en \u043ef \u0435ff\u0435\u0441t\u0455 \u0430nd after effects (&gt; 24 h), \u0441\u043emb\u0430t\u0456v\u0435 b\u0435h\u0430v\u0456\u043eur, hyperthermia \u0430nd psychosis, which h\u0430v\u0435 \u0456n\u0441lud\u0435d \u0435x\u0430m\u0440l\u0435\u0455 of \u0430ud\u0456t\u043er\u0443 and visual h\u0430llu\u0441\u0456n\u0430t\u0456\u043en\u0455.<\/p>\n<\/div>\n<div>This Research Chemical <b>MDPV<\/b> is not for human consumption and should beusede for chemical research only.<\/div>","protected":false},"excerpt":{"rendered":"<div class=\"wDYxhc\" lang=\"en-CM\" data-md=\"50\" data-hveid=\"CB4QAA\" data-ved=\"2ahUKEwiCwp-ty7TvAhWNzoUKHcniBCoQkCkwFnoECB4QAA\">\n<div class=\"PZPZlf hb8SAc\" data-attrid=\"description\" data-hveid=\"CB4QAQ\" data-ved=\"2ahUKEwiCwp-ty7TvAhWNzoUKHcniBCoQziAoADAWegQIHhAB\">\n<div>\n<div class=\"kno-rdesc\">Methylenedioxypyrovalerone is a stimulant of the cathinone class that acts as a norepinephrine\u2013dopamine reuptake inhibitor. It was first developed in the 1960s by a team at Boehringer Ingelheim.<\/div>\n<\/div>\n<\/div>\n<\/div>\n<div class=\"wDYxhc\" lang=\"en-CM\" data-attrid=\"kc:\/chemistry\/chemical_compound:formula\" data-md=\"1001\" data-hveid=\"CCMQAA\" data-ved=\"2ahUKEwiCwp-ty7TvAhWNzoUKHcniBCoQkCkwF3oECCMQAA\">\n<div class=\"Z1hOCe\">\n<div class=\"zloOqf PZPZlf\" data-ved=\"2ahUKEwiCwp-ty7TvAhWNzoUKHcniBCoQyxMoADAXegQIIxAB\"><span class=\"GRkHZd w8qArf\">Formula:\u00a0<\/span><span class=\"Eq0J8 LrzXr kno-fv\">C<sub>16<\/sub>H<sub>21<\/sub>NO<sub>3<\/sub><\/span><\/div>\n<\/div>\n<\/div>\n<div class=\"wDYxhc\" lang=\"en-CM\" data-attrid=\"kc:\/chemistry\/chemical_compound:iupac id\" data-md=\"1001\" data-hveid=\"CCIQAA\" data-ved=\"2ahUKEwiCwp-ty7TvAhWNzoUKHcniBCoQkCkwGHoECCIQAA\">\n<div class=\"Z1hOCe\">\n<div class=\"zloOqf PZPZlf\" data-ved=\"2ahUKEwiCwp-ty7TvAhWNzoUKHcniBCoQyxMoADAYegQIIhAB\">\n<div class=\"rVusze\"><span class=\"GRkHZd w8qArf\">IUPAC ID:\u00a0<\/span><span class=\"Eq0J8 LrzXr kno-fv\">(RS)-1-(Benzo[d][1,3]dioxol-5-yl)-2-(pyrrolidin-1-yl)pentan-1-one<\/span><\/div>\n<\/div>\n<\/div>\n<\/div>\n<div class=\"wDYxhc\" lang=\"en-CM\" data-attrid=\"kc:\/chemistry\/chemical_compound:molar mass\" data-md=\"1001\" data-hveid=\"CBwQAA\" data-ved=\"2ahUKEwiCwp-ty7TvAhWNzoUKHcniBCoQkCkwGXoECBwQAA\">\n<div class=\"Z1hOCe\">\n<div class=\"zloOqf PZPZlf\" data-ved=\"2ahUKEwiCwp-ty7TvAhWNzoUKHcniBCoQyxMoADAZegQIHBAB\">\n<div class=\"rVusze\"><span class=\"GRkHZd w8qArf\">Molar mass:\u00a0<\/span><span class=\"Eq0J8 LrzXr kno-fv\">275.343\u00a0g\/mol<\/span><\/div>\n<\/div>\n<\/div>\n<\/div>\n<div class=\"wDYxhc\" lang=\"en-CM\" data-attrid=\"kc:\/chemistry\/chemical_compound:melting point\" data-md=\"1001\" data-hveid=\"CB0QAA\" data-ved=\"2ahUKEwiCwp-ty7TvAhWNzoUKHcniBCoQkCkwGnoECB0QAA\">\n<div class=\"Z1hOCe\">\n<div class=\"zloOqf PZPZlf\" data-ved=\"2ahUKEwiCwp-ty7TvAhWNzoUKHcniBCoQyxMoADAaegQIHRAB\">\n<div class=\"rVusze\"><span class=\"GRkHZd w8qArf\">Melting point:\u00a0<\/span><span class=\"Eq0J8 LrzXr kno-fv\">209.3\u00a0\u00b0C<\/span><\/div>\n<\/div>\n<\/div>\n<\/div>\n<div class=\"wDYxhc\" lang=\"en-CM\" data-attrid=\"ss:\/webfacts:metabol\" data-md=\"1001\" data-hveid=\"CCAQAA\" data-ved=\"2ahUKEwiCwp-ty7TvAhWNzoUKHcniBCoQkCkwG3oECCAQAA\">\n<div class=\"Z1hOCe\">\n<div class=\"zloOqf PZPZlf\" data-ved=\"2ahUKEwiCwp-ty7TvAhWNzoUKHcniBCoQyxMoADAbegQIIBAB\">\n<div class=\"rVusze\"><span class=\"GRkHZd w8qArf\">Metabolism:\u00a0<\/span><span class=\"Eq0J8 LrzXr kno-fv\">Hepatic<\/span><\/div>\n<\/div>\n<\/div>\n<\/div>\n<div class=\"wDYxhc\" lang=\"en-CM\" data-attrid=\"ss:\/webfacts:chemspid\" data-md=\"1001\" data-hveid=\"CB8QAA\" data-ved=\"2ahUKEwiCwp-ty7TvAhWNzoUKHcniBCoQkCkwHHoECB8QAA\">\n<div class=\"Z1hOCe\">\n<div class=\"zloOqf PZPZlf\" data-ved=\"2ahUKEwiCwp-ty7TvAhWNzoUKHcniBCoQyxMoADAcegQIHxAB\">\n<div class=\"rVusze\"><span class=\"GRkHZd w8qArf\">ChemSpider:\u00a0<\/span><span class=\"Eq0J8 LrzXr kno-fv\">16788110<\/span><\/div>\n<\/div>\n<\/div>\n<\/div>\n","protected":false},"featured_media":27286,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_uag_custom_page_level_css":"","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":"default","adv-header-id-meta":"","stick-header-meta":"","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","astra-migrate-meta-layouts":"set","ast-page-background-enabled":"default","ast-page-background-meta":{"desktop":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center 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is a stimulant of the cathinone class that acts as a norepinephrine\u2013dopamine reuptake inhibitor. It was first developed in the 1960s by a team at Boehringer Ingelheim. Formula:\u00a0C16H21NO3 IUPAC ID:\u00a0(RS)-1-(Benzo[d][1,3]dioxol-5-yl)-2-(pyrrolidin-1-yl)pentan-1-one Molar mass:\u00a0275.343\u00a0g\/mol Melting point:\u00a0209.3\u00a0\u00b0C Metabolism:\u00a0Hepatic ChemSpider:\u00a016788110","_links":{"self":[{"href":"https:\/\/izchem.com\/de\/wp-json\/wp\/v2\/product\/25944","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/izchem.com\/de\/wp-json\/wp\/v2\/product"}],"about":[{"href":"https:\/\/izchem.com\/de\/wp-json\/wp\/v2\/types\/product"}],"replies":[{"embeddable":true,"href":"https:\/\/izchem.com\/de\/wp-json\/wp\/v2\/comments?post=25944"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/izchem.com\/de\/wp-json\/wp\/v2\/media\/27286"}],"wp:attachment":[{"href":"https:\/\/izchem.com\/de\/wp-json\/wp\/v2\/media?parent=25944"}],"wp:term":[{"taxonomy":"product_brand","embeddable":true,"href":"https:\/\/izchem.com\/de\/wp-json\/wp\/v2\/product_brand?post=25944"},{"taxonomy":"product_cat","embeddable":true,"href":"https:\/\/izchem.com\/de\/wp-json\/wp\/v2\/product_cat?post=25944"},{"taxonomy":"product_tag","embeddable":true,"href":"https:\/\/izchem.com\/de\/wp-json\/wp\/v2\/product_tag?post=25944"}],"curies":[{"name":"WP","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}