Troparil, also known as WIN 35,065-2 or \u03b2-CPT, is a synthetic phenyltropane compound widely used in medicinal chemistry, neuropharmacology, and analytical research. Originally developed as part of research into cocaine analogs, Troparil was designed to investigate dopamine transporter activity while exhibiting structural modifications that distinguish it from cocaine. Today, it serves as an important analytical reference standard in forensic toxicology, neuroscience, and pharmaceutical research.<\/p>\n
Due to its well-characterized molecular structure and selective interaction with monoamine transporters, Troparil is frequently utilized in dopamine transporter studies, analytical method development, medicinal chemistry, and neuropharmacology research.<\/p>\n
Troparil is supplied strictly for laboratory, analytical, and scientific research purposes only. It is not approved for human or veterinary use.<\/p>\n
Troparil is a synthetic phenyltropane derivative structurally related to cocaine analogs. It has been extensively studied in laboratory settings for its interaction with monoamine transporters, particularly the dopamine transporter (DAT), making it a valuable compound for neuroscience and transporter research.<\/p>\n
Research laboratories utilize Troparil as a certified analytical reference material for transporter studies, analytical method validation, forensic identification, medicinal chemistry, and structure\u2013activity relationship (SAR) investigations.<\/p>\n
Troparil possesses several analytical characteristics valuable for laboratory research:<\/p>\n
These characteristics enable accurate laboratory analyses and reliable compound identification.<\/p>\n
Troparil is widely employed in:<\/p>\n
Professional laboratories commonly use Troparil for:<\/p>\n
Su constante de rendimiento anal\u00edtico que la hace valiosa para los modernos forense y laboratorios farmac\u00e9uticos.<\/p>\n
Researchers investigate Troparil in studies involving:<\/p>\n
These investigations contribute to advancements in neuroscience, medicinal chemistry, and analytical science.<\/p>\n
Researchers select Troparil because it provides:<\/p>\n
Researchers frequently compare Troparil with related compounds including:<\/p>\n
Comparative studies support analytical identification, transporter research, and structure\u2013activity relationship investigations.<\/p>\n
Para una \u00f3ptima laboratorio de estabilidad:<\/p>\n
Troparil is a synthetic phenyltropane compound used as an analytical reference standard in neuropharmacology, medicinal chemistry, analytical chemistry, and forensic toxicology research.<\/p>\n
It is commonly used by neuroscience laboratories, pharmaceutical researchers, forensic laboratories, academic institutions, and analytical chemistry laboratories.<\/p>\n
Researchers commonly analyze Troparil using LC-MS\/MS, GC-MS, LC-HRMS, HPLC, and related analytical techniques.<\/p>\n
Its well-characterized molecular profile, analytical stability, and importance in dopamine transporter research make it valuable for analytical method validation, transporter investigations, and analytical reference development.<\/p>\n
Yes. Troparil is supplied exclusively for laboratory, analytical, scientific, and educational research purposes.<\/p>\n
Troparil is supplied strictly for laboratory, analytical, scientific, and educational research purposes only. It is not intended for human consumption, medical treatment, veterinary applications, therapeutic use, or diagnostic procedures. Users are responsible for complying with all applicable local laws, institutional policies, and laboratory safety regulations.<\/p>","protected":false},"excerpt":{"rendered":"
Nombre De Producto:<\/strong> Troparil
Nombres Alternativos:<\/strong> WIN 35,065-2, \u03b2-CPT, (\u2013)-2\u03b2-Carbomethoxy-3\u03b2-phenyltropane
Clase Qu\u00edmica:<\/strong> Phenyltropane Derivative
Categor\u00eda de investigaci\u00f3n:<\/strong> Est\u00e1ndar De Referencia Anal\u00edtica<\/p>","protected":false},"featured_media":34393,"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":"","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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Name: TroparilAlternative Names: WIN 35,065-2, \u03b2-CPT, (\u2013)-2\u03b2-Carbomethoxy-3\u03b2-phenyltropaneChemical Class: Phenyltropane DerivativeResearch Category: Analytical Reference 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