{"id":33851,"date":"2026-09-28T09:49:57","date_gmt":"2026-09-28T09:49:57","guid":{"rendered":"https:\/\/izchem.com\/?post_type=product&p=33851"},"modified":"2026-10-04T09:29:05","modified_gmt":"2026-10-04T09:29:05","slug":"2f-dck-2-fluorodeschloroketamine","status":"publish","type":"product","link":"https:\/\/izchem.com\/es\/2f-dck-2-fluorodeschloroketamine\/","title":{"rendered":"
2F-DCK (2-Fluorodeschloroketamine)<\/p>"},"content":{"rendered":"
2F-DCK (2-Fluorodeschloroketamine)<\/strong> is a dissociative arylcyclohexylamine<\/strong> belonging to the same chemical family as ketamine and deschloroketamine (DCK)<\/strong>. It has gained notable attention in the scientific community for its unique pharmacological profile<\/strong> and structural similarity to ketamine<\/strong>, making it an important subject of research in neuropharmacology, receptor binding studies, and behavioral neuroscience<\/strong>.<\/p> Researchers often study 2F-DCK(2-Fluorodeschloroketamine) for its NMDA receptor antagonist activity<\/strong>, which is believed to contribute to its dissociative effects and potential therapeutic mechanisms. Its chemical structure, which includes a fluorine atom substitution<\/strong>, alters its lipophilicity and metabolism, providing a valuable comparison model for understanding how halogen substitution influences arylcyclohexylamine pharmacodynamics.<\/p> Nombre qu\u00edmico:<\/strong> 2-Fluorodeschloroketamine 2F-DCK(2-Fluorodeschloroketamine) is structurally related to ketamine (2-chloroketamine)<\/strong>, with the primary difference being the replacement of the chlorine atom in ketamine’s phenyl ring with a fluorine atom. This seemingly minor alteration results in significant changes in receptor binding affinity, potency, and metabolic stability<\/strong>.<\/p> N\u00famero de CAS:<\/strong> Not assigned (research chemical)<\/p>\n<\/li>\n Class:<\/strong> Arylcyclohexylamine dissociative<\/p>\n<\/li>\n Appearance:<\/strong> Off-white to light crystalline powder<\/p>\n<\/li>\n Solubility:<\/strong> Soluble in ethanol, methanol, and dimethyl sulfoxide (DMSO); slightly soluble in water<\/p>\n<\/li>\n Condiciones de almacenamiento:<\/strong> Store in a cool, dry place, protected from light and moisture. Recommended temperature: below 25°C<\/p>\n<\/li>\n<\/ul> This compound’s high analytical purity ensures that it is suitable for precise qualitative and quantitative analysis<\/strong> in controlled laboratory environments.<\/p> While 2F-DCK(2-Fluorodeschloroketamine) is not approved for human or veterinary use<\/strong>, it remains an important research analog<\/strong> for understanding the mechanism of action of NMDA receptor antagonists. Studies suggest that 2F-DCK interacts primarily with:<\/p> N-methyl-D-aspartate (NMDA) receptors<\/strong> – acting as a non-competitive antagonist<\/p>\n<\/li>\n Sigma receptors<\/strong> – potentially contributing to psychoactive and neuroprotective effects<\/p>\n<\/li>\n Dopaminergic and serotonergic systems<\/strong> – though to a lesser degree, offering insight into its broader neurochemical interactions<\/p>\n<\/li>\n<\/ul> Researchers investigating 2F-DCK(2-Fluorodeschloroketamine) often focus on its comparative efficacy, receptor affinity, and metabolism<\/strong> relative to ketamine and DCK. Its longer half-life and altered potency provide valuable data for pharmacokinetic modeling and structure-activity relationship (SAR) studies.<\/p> 2F-DCK<\/strong> is utilized across multiple research fields, including:<\/p> Pharmacological Studies<\/strong> Behavioral and Cognitive Research<\/strong> Analytical Chemistry and Forensic Testing<\/strong> Structure-Activity Relationship (SAR) Studies<\/strong> Only <\/span>trained professionals in equipped laboratories should handle 2F-DCK (2-Fluorodeschloroketamine)<\/strong>. Follow proper safety procedures, including wearing gloves, protective eyewear, and a lab coat. Safety Recommendations:<\/strong><\/p> Avoid inhalation or contact with skin and eyes.<\/p>\n<\/li>\n Store securely, away from heat and direct sunlight.<\/p>\n<\/li>\n Dispose of unused material in accordance with local chemical safety regulations.<\/p>\n<\/li>\n<\/ul> The legal classification of 2F-DCK(2-Fluorodeschloroketamine) varies by country and jurisdiction. In many regions, it remains an uncontrolled research chemical<\/strong>, while others have implemented specific analogue acts or psychoactive substance regulations<\/strong> that may apply to compounds structurally similar to ketamine.<\/p> Researchers are strongly advised to verify local and international regulations<\/strong> before purchasing, importing, or using 2F-DCK in any project.<\/p> When conducting scientific research, compound purity and authenticity<\/strong> are critical. High-quality 2F-DCK ensures:<\/p> Reliable and reproducible analytical results<\/strong><\/p>\n<\/li>\n Accurate pharmacological modeling<\/strong><\/p>\n<\/li>\n Enhanced safety in controlled experiments<\/strong><\/p>\n<\/li>\n Confidence in structural and receptor-based studies<\/strong><\/p>\n<\/li>\n<\/ul> Reputable suppliers provide batch-specific Certificates of Analysis (COA)<\/strong> and Material Safety Data Sheets (MSDS)<\/strong> for full transparency.<\/p> 2F-DCK (2-Fluorodeschloroketamine)<\/strong> represents a valuable addition to the expanding library of arylcyclohexylamine research compounds<\/strong>. Its unique fluorine substitution makes it a key analog for investigating NMDA receptor modulation, dissociative pharmacology, and structure-function relationships<\/strong> among ketamine derivatives.<\/p> en laboratory and forensic researchers<\/strong>, 2F-DCK(2-Fluorodeschloroketamine) offers a consistent, high-purity standard for analytical, pharmacological, and biochemical studies.<\/p> Nota:<\/strong> 2F-DCK is sold strictly for laboratory research purposes only<\/strong>. Es not intended for human or veterinary use<\/strong>. Ensure compliance with all applicable laws and regulations before ordering or handling.<\/p>\n<\/blockquote>","protected":false},"excerpt":{"rendered":" 2F-DCK(2-Fluorodeschloroketamine)<\/strong>, is a dissociative compound from the arylcyclohexylamine class, closely related to ketamine and DCK. Known for its high purity and reliable performance<\/strong>, it has become a popular choice among professional researchers<\/strong> exploring NMDA receptor antagonists and dissociative mechanisms.<\/p> This compound offers unique pharmacological properties<\/strong>, including potential anesthetic and psychotropic research applications. 2F-DCK is typically used in neuroscientific and analytical studies<\/strong> focused on receptor binding, neural dissociation, and molecular behavior.<\/p>","protected":false},"featured_media":33862,"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 dissociative compound from the arylcyclohexylamine class, closely related to ketamine and DCK. Known for its high purity and reliable performance, it has become a popular choice among professional researchers exploring NMDA receptor antagonists and dissociative mechanisms. This compound offers unique pharmacological properties, including potential anesthetic and psychotropic research applications. 2F-DCK is typically…","_links":{"self":[{"href":"https:\/\/izchem.com\/es\/wp-json\/wp\/v2\/product\/33851","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/izchem.com\/es\/wp-json\/wp\/v2\/product"}],"about":[{"href":"https:\/\/izchem.com\/es\/wp-json\/wp\/v2\/types\/product"}],"replies":[{"embeddable":true,"href":"https:\/\/izchem.com\/es\/wp-json\/wp\/v2\/comments?post=33851"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/izchem.com\/es\/wp-json\/wp\/v2\/media\/33862"}],"wp:attachment":[{"href":"https:\/\/izchem.com\/es\/wp-json\/wp\/v2\/media?parent=33851"}],"wp:term":[{"taxonomy":"product_brand","embeddable":true,"href":"https:\/\/izchem.com\/es\/wp-json\/wp\/v2\/product_brand?post=33851"},{"taxonomy":"product_cat","embeddable":true,"href":"https:\/\/izchem.com\/es\/wp-json\/wp\/v2\/product_cat?post=33851"},{"taxonomy":"product_tag","embeddable":true,"href":"https:\/\/izchem.com\/es\/wp-json\/wp\/v2\/product_tag?post=33851"}],"curies":[{"name":" pp<\/p>","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
Common Names:<\/strong> 2F-DCK, Fluoroketamine, 2-Fl-2’-Oxo-PCM
Chemical Formula:<\/strong> C13H16FNO
Peso molecular:<\/strong> 221.27 g\/mol
Nombre de la IUPAC:<\/strong> (R,S)-2-(2-Fluorophenyl)-2-methylamino-cyclohexanone
pureza:<\/strong> ≥ 98% (analytical standard grade)
Forma:<\/strong> Crystalline powder
Intended Use:<\/strong> Laboratory and forensic research purposes only<\/p>Chemical and Structural Properties of 2F-DCK (2-Fluorodeschloroketamine)<\/strong><\/h3>
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Pharmacological Background of 2F-DCK (2-Fluorodeschloroketamine)<\/strong><\/h3>
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Applications in Research 2F-DCK (2-Fluorodeschloroketamine)<\/strong><\/h3>
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Used to explore NMDA receptor function, ion channel modulation, and neural plasticity.<\/p>\n<\/li>\n
2F-DCK(2-Fluorodeschloroketamine) serves as a model for dissociation, perception alteration, and neurocognitive modulation in controlled experiments.<\/p>\n<\/li>\n
Researchers employ 2F-DCK as a reference material<\/strong> for mass spectrometry, chromatography, and toxicological profiling.<\/p>\n<\/li>\n
The fluorine substitution provides valuable data for developing next-generation NMDA receptor antagonists with optimized efficacy and safety.<\/p>\n<\/li>\n<\/ol>Safety and Handling Information 2F-DCK (2-Fluorodeschloroketamine)<\/strong><\/h3>
This compound is not for human consumption, medical treatment, or recreational use<\/strong>. Ingestion or misuse may result in serious health risks.<\/p>\n
Legal and Regulatory Status<\/strong><\/h3>
Why Choose High-Quality 2F-DCK (2-Fluorodeschloroketamine) for Research<\/strong><\/h3>
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Conclusion<\/strong><\/h3>
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