{"id":6437,"date":"2026-02-12T10:05:07","date_gmt":"2026-02-12T10:05:07","guid":{"rendered":"https:\/\/chemsfine.com\/?post_type=product&#038;p=6437"},"modified":"2026-03-25T13:05:02","modified_gmt":"2026-03-25T13:05:02","slug":"buy-6-apb-online","status":"publish","type":"product","link":"https:\/\/chemsfine.com\/sv\/product\/buy-6-apb-online\/","title":{"rendered":"K\u00f6p 6-APB online | High-Purity Research Chemical"},"content":{"rendered":"<p>For researchers and scientific institutions seeking a reliable source, the opportunity to <b>buy 6-APB<\/b> for sale is now available. Chemsfine is your premier destination to order high-purity 6-APB online, a distinguished compound within the realm of <a href=\"https:\/\/chemsfine.com\/sv\/forskningskemikalier\/\">forskningskemikalier<\/a>. Often referred to by its full chemical name, 6-(2-Aminopropyl)-2,3-dihydrobenzofuran, or through its various designations like 6-APDB, 4-Desoxy-MDA, and EMA-3, this substance is classified as a potent stimulant and entactogen. It firmly belongs to both the phenethylamine and amphetamine classes, making it a subject of significant scientific interest. Our top-quality 6-APB is meticulously synthesized to meet stringent laboratory-grade standards, ensuring consistent and dependable results for your studies. Historically, 6-APDB, alongside its analogue 5-APDB (3-Desoxy-MDA), was first developed by David E. Nichols in the early 1990s as part of his pioneering investigations into non-neurotoxic MDMA analogues. This rich history underscores its importance in pharmacological research, offering unique insights into structure-activity relationships.<\/p>\n<h2>What is 6-APB? Understanding its Chemical and Pharmacological Profile<\/h2>\n<p><b>6-APB<\/b> is a fascinating compound, structurally similar to MDA, yet possessing distinct characteristics that warrant in-depth research. It is an analogue of MDA where the heterocyclic 4-position oxygen from the 3,4-methylenedioxy ring has been replaced with a methylene bridge. This subtle yet significant alteration in its molecular architecture contributes to its unique pharmacological actions. In contrast, 5-APDB (3-Desoxy-MDA) is another analogue where the 3-position oxygen has been replaced with a methylene instead, highlighting the precise structural modifications explored in this class of compounds. The availability of such high-purity research chemicals, like <b>6-APB<\/b> from Chemsfine, is crucial for advancing our understanding of these complex <a href=\"https:\/\/chemsfine.com\/sv\/phenethylamine-compounds\/\">phenethylamine compounds<\/a> and their potential applications in scientific discovery.<\/p>\n<h3>Pharmacological Action and Research Findings<\/h3>\n<p>Extensive animal studies have shed light on the intricate pharmacological profile of related compounds such as 6-APDB. These studies indicate that 6-APDB fully substitutes for MBDB and MMAI, suggesting a shared mechanism of action or similar subjective effects in these models. However, it does not substitute for amphetamine or LSD, emphasizing its unique profile distinct from classical stimulants or psychedelics. Furthermore, <i>in vitro<\/i> research provides crucial insights into its cellular mechanisms. 6-APDB has been demonstrated to inhibit the reuptake of key neurotransmitters: serotonin, dopamine, and norepinephrine, with IC50 values of 322 nM, 1,997 nM, and 980 nM, respectively. These values bear a striking resemblance to those of MDA, though with the catecholamine values being slightly lower, perhaps aligning more closely with the profile of MDMA. In contrast, 5-APDB exhibits a high selectivity for serotonin reuptake inhibition, contrasting with the broader action of 6-APDB. While 6-APDB did not substitute for amphetamine in rats at the doses used in referenced studies, its <i>in vitro<\/i> profile strongly suggests that it may elicit amphetamine-like effects at elevated doses, making it an intriguing subject for further study into <a href=\"https:\/\/chemsfine.com\/sv\/stimulantia\/\">stimulant research<\/a>.<\/p>\n<p>The unsaturated benzofuran derivative <b>6-APB<\/b>, specifically 6-(2-aminopropyl)benzofuran, is also well-recognized in the research community. While the exact differences in pharmacological effects between 6-APB and 6-APDB are still a subject of ongoing clarification, <b>6-APB<\/b> is understood to be an agonist to the three main serotonin receptors (5-HTP2A\/B\/C). This agonistic activity is believed to contribute to a range of effects observed in research settings, from inducing states of euphoria to increasing energy levels and promoting feelings of empathy towards others. 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We offer the best <b>6-APB<\/b> available, backed by comprehensive documentation and transparent product details.<\/p>\n<h2>Technical Specifications of 6-APB<\/h2>\n<p>For precise research, understanding the detailed technical specifications of <b>6-APB<\/b> is essential. We provide comprehensive data to aid in your experimental design and analysis. These specifications confirm the identity and purity of our product, crucial for any rigorous scientific investigation.<\/p>\n<table>\n<thead>\n<tr>\n<th>Attribut<\/th>\n<th>Detalj<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td>Formellt namn<\/td>\n<td>?-methyl-6-benzofuranethanamine, monohydrochloride<\/td>\n<\/tr>\n<tr>\n<td>CAS-nummer<\/td>\n<td>286834-84-2<\/td>\n<\/tr>\n<tr>\n<td>Molekylformel<\/td>\n<td>C11H13NO \u2022 HCl<\/td>\n<\/tr>\n<tr>\n<td>Formel Vikt<\/td>\n<td>211.7<\/td>\n<\/tr>\n<tr>\n<td>Renhet<\/td>\n<td>\u226598%<\/td>\n<\/tr>\n<tr>\n<td>Formulering<\/td>\n<td>Ett kristallint fast \u00e4mne<\/td>\n<\/tr>\n<tr>\n<td>\u03bbmax<\/td>\n<td>207, 246, 276, 285 nm<\/td>\n<\/tr>\n<tr>\n<td>SMIL<\/td>\n<td>CC(N)CC1=CC2=C(C=C1)C=CO2.Cl<\/td>\n<\/tr>\n<tr>\n<td>InChi kod<\/td>\n<td>InChI=1S\/C11H13NO.ClH\/c1-8(12)6-9-2-3-10-4-5-13-11(10)7-9;\/h2-5,7-8H,6,12H2,1H3;1H<\/td>\n<\/tr>\n<tr>\n<td>InChi Nyckel<\/td>\n<td>APEWOTOLPKNSPE-UHFFFAOYSA-N<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<h3>Synonyms and Chemical Identifiers<\/h3>\n<p><b>6-APB<\/b> is known by several common names and identifiers, including:<\/p>\n<ul>\n<li>6-(2-Aminopropyl)Benzofuran<\/li>\n<li>Benzo Fury<\/li>\n<\/ul>\n<p>These synonyms help researchers identify the compound across different literature and databases, ensuring clarity in scientific communication. 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Researchers can utilize this compound to:<\/p>\n<ul>\n<li>Investigate the mechanisms of serotonin, dopamine, and norepinephrine reuptake inhibition.<\/li>\n<li>Study the specific agonistic activity on 5-HTP2A\/B\/C receptors.<\/li>\n<li>Explore structure-activity relationships among phenethylamine and amphetamine analogues.<\/li>\n<li>Conduct behavioral studies to understand its stimulant and entactogenic effects.<\/li>\n<li>Develop new analytical methods for detecting and quantifying similar compounds.<\/li>\n<li>Research the potential therapeutic applications or adverse effects of compounds with similar profiles.<\/li>\n<li>Analyze neurotransmitter system modulation in various biological models.<\/li>\n<\/ul>\n<p>These diverse applications underscore the value of a high-quality, laboratory-grade compound like <b>6-APB<\/b>, tillg\u00e4nglig f\u00f6r <a href=\"https:\/\/chemsfine.com\/sv\/6-apb-powder\/\">purchase<\/a> p\u00e5 Chemsfine.<\/p>\n<h2>Safety, Storage, and Compliance for Research Chemicals<\/h2>\n<p>Handling any research chemical, including <b>6-APB<\/b>, requires strict adherence to safety protocols and proper storage conditions. 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Begin your next breakthrough by securing your supply of top-quality <b>6-APB<\/b> with a secure purchase from Chemsfine today.<\/p>","protected":false},"excerpt":{"rendered":"<p><b>6-APB<\/b>, also known as Benzo Fury, is a stimulant and entactogen from the phenethylamine and amphetamine classes. Widely studied for its unique pharmacological profile, this high-purity research chemical is essential for various scientific investigations. 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