{"id":593,"date":"2026-06-07T23:41:57","date_gmt":"2026-06-07T23:41:57","guid":{"rendered":"https:\/\/biosynlab.com\/?post_type=product&#038;p=593"},"modified":"2026-06-22T13:20:17","modified_gmt":"2026-06-22T13:20:17","slug":"nb-5-meo-dalt-oxalate-powder","status":"publish","type":"product","link":"https:\/\/www.biosynlab.com\/?product=nb-5-meo-dalt-oxalate-powder","title":{"rendered":"NB-5-MeO-DALT Oxalate Powder"},"content":{"rendered":"<h1 class=\"mt-6 mb-2 font-semibold text-3xl\" data-streamdown=\"heading-1\">Premium NB-5-MeO-DALT Oxalate Powder: Advanced Research Chemical for Industrial Applications<\/h1>\n<p>&nbsp;<\/p>\n<h2 class=\"mt-6 mb-2 font-semibold text-2xl\" data-streamdown=\"heading-2\"><strong class=\"chakra-text css-0\">Product Details Table<\/strong><\/h2>\n<p>&nbsp;<\/p>\n<div class=\"css-3b43de\">\n<div class=\"chakra-table__container css-136ya47\">\n<table class=\"chakra-table css-5605sr\">\n<thead class=\"css-1gr8s87\">\n<tr class=\"css-1j3y60u\">\n<th class=\"css-gcbhyl\"><strong class=\"chakra-text css-0\">Attribute<\/strong><\/th>\n<th class=\"css-gcbhyl\"><strong class=\"chakra-text css-0\">Specification<\/strong><\/th>\n<\/tr>\n<\/thead>\n<tbody class=\"css-12zq2am\">\n<tr class=\"css-1j3y60u\">\n<td class=\"css-at0zhy\"><strong class=\"chakra-text css-0\">Brand<\/strong><\/td>\n<td class=\"css-at0zhy\">BioSynLab Research Compounds<\/td>\n<\/tr>\n<tr class=\"css-1j3y60u\">\n<td class=\"css-at0zhy\"><strong class=\"chakra-text css-0\">Product Name<\/strong><\/td>\n<td class=\"css-at0zhy\">NB-5-MeO-DALT Oxalate<\/td>\n<\/tr>\n<tr class=\"css-1j3y60u\">\n<td class=\"css-at0zhy\"><strong class=\"chakra-text css-0\">IUPAC Name<\/strong><\/td>\n<td class=\"css-at0zhy\">N-benzyl-5-methoxy-N,N-diallyltryptamine oxalate<\/td>\n<\/tr>\n<tr class=\"css-1j3y60u\">\n<td class=\"css-at0zhy\"><strong class=\"chakra-text css-0\">Synonyms<\/strong><\/td>\n<td class=\"css-at0zhy\">NB-DALT, N-benzyl-5-MeO-DALT<\/td>\n<\/tr>\n<tr class=\"css-1j3y60u\">\n<td class=\"css-at0zhy\"><strong class=\"chakra-text css-0\">CAS Number<\/strong><\/td>\n<td class=\"css-at0zhy\">Not assigned (novel research compound)<\/td>\n<\/tr>\n<tr class=\"css-1j3y60u\">\n<td class=\"css-at0zhy\"><strong class=\"chakra-text css-0\">Molecular Formula<\/strong><\/td>\n<td class=\"css-at0zhy\">C\u2082\u2084H\u2082\u2088N\u2082O \u00b7 C\u2082H\u2082O\u2084 (oxalate salt)<\/td>\n<\/tr>\n<tr class=\"css-1j3y60u\">\n<td class=\"css-at0zhy\"><strong class=\"chakra-text css-0\">Molecular Weight<\/strong><\/td>\n<td class=\"css-at0zhy\">448.51 g\/mol (oxalate salt)<\/td>\n<\/tr>\n<tr class=\"css-1j3y60u\">\n<td class=\"css-at0zhy\"><strong class=\"chakra-text css-0\">Salt Form<\/strong><\/td>\n<td class=\"css-at0zhy\">Oxalate (1:1 stoichiometry)<\/td>\n<\/tr>\n<tr class=\"css-1j3y60u\">\n<td class=\"css-at0zhy\"><strong class=\"chakra-text css-0\">Purity<\/strong><\/td>\n<td class=\"css-at0zhy\">\u226597.0% (HPLC Verified)<\/td>\n<\/tr>\n<tr class=\"css-1j3y60u\">\n<td class=\"css-at0zhy\"><strong class=\"chakra-text css-0\">Appearance<\/strong><\/td>\n<td class=\"css-at0zhy\">White to Off-White Crystalline Powder<\/td>\n<\/tr>\n<tr class=\"css-1j3y60u\">\n<td class=\"css-at0zhy\"><strong class=\"chakra-text css-0\">Form<\/strong><\/td>\n<td class=\"css-at0zhy\">Micronized Crystalline Powder<\/td>\n<\/tr>\n<tr class=\"css-1j3y60u\">\n<td class=\"css-at0zhy\"><strong class=\"chakra-text css-0\">Particle Size<\/strong><\/td>\n<td class=\"css-at0zhy\">30-70 microns<\/td>\n<\/tr>\n<tr class=\"css-1j3y60u\">\n<td class=\"css-at0zhy\"><strong class=\"chakra-text css-0\">Storage<\/strong><\/td>\n<td class=\"css-at0zhy\">-20\u00b0C, Desiccated, Argon Atmosphere<\/td>\n<\/tr>\n<tr class=\"css-1j3y60u\">\n<td class=\"css-at0zhy\"><strong class=\"chakra-text css-0\">Packaging<\/strong><\/td>\n<td class=\"css-at0zhy\">Amber Borosilicate Vials with PTFE Seals<\/td>\n<\/tr>\n<tr class=\"css-1j3y60u\">\n<td class=\"css-at0zhy\"><strong class=\"chakra-text css-0\">Available Quantities<\/strong><\/td>\n<td class=\"css-at0zhy\">250mg, 500mg, 1g, 5g<\/td>\n<\/tr>\n<tr class=\"css-1j3y60u\">\n<td class=\"css-at0zhy\"><strong class=\"chakra-text css-0\">Documentation<\/strong><\/td>\n<td class=\"css-at0zhy\">COA, HPLC, NMR, HRMS, MSDS, Stability Data<\/td>\n<\/tr>\n<tr class=\"css-1j3y60u\">\n<td class=\"css-at0zhy\"><strong class=\"chakra-text css-0\">Shipping<\/strong><\/td>\n<td class=\"css-at0zhy\">Cryogenic Packaging Available<\/td>\n<\/tr>\n<tr class=\"css-1j3y60u\">\n<td class=\"css-at0zhy\"><strong class=\"chakra-text css-0\">Origin<\/strong><\/td>\n<td class=\"css-at0zhy\">EU\/GMP Certified Laboratory<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/div>\n<\/div>\n<h3 data-streamdown=\"heading-3\"><\/h3>\n<h3 class=\"mt-6 mb-2 font-semibold text-xl\" data-streamdown=\"heading-3\"><strong class=\"chakra-text css-0\">NB-5-MeO-DALT Oxalate Powder | Novel N-Benzyltryptamine Research Compound | BioSynLab<\/strong><\/h3>\n<p><strong class=\"chakra-text css-0\">BioSynLab<\/strong>\u00a0presents\u00a0<strong class=\"chakra-text css-0\">NB-5-MeO-DALT oxalate<\/strong>, a\u00a0<strong class=\"chakra-text css-0\">novel N-benzylated tryptamine derivative<\/strong>\u00a0for\u00a0<strong class=\"chakra-text css-0\">advanced structure-activity relationship (SAR) research<\/strong>\u00a0and\u00a0<strong class=\"chakra-text css-0\">comparative pharmacology studies<\/strong>. This\u00a0<strong class=\"chakra-text css-0\">N-benzyl analog<\/strong>\u00a0of\u00a0<a href=\"https:\/\/biosynlab.com\/\"><strong class=\"chakra-text css-0\">5-MeO-DALT<\/strong>\u00a0<\/a>incorporates a\u00a0<strong class=\"chakra-text css-0\">phenylmethyl substituent<\/strong>\u00a0at the\u00a0<strong class=\"chakra-text css-0\">indole nitrogen<\/strong>, creating distinct\u00a0<strong class=\"chakra-text css-0\">steric and electronic properties<\/strong>\u00a0for investigating\u00a0<strong class=\"chakra-text css-0\">receptor binding modifications<\/strong>,\u00a0<strong class=\"chakra-text css-0\">metabolic stability changes<\/strong>, and\u00a0<strong class=\"chakra-text css-0\">novel psychoactive substance (NPS)<\/strong>\u00a0analytical characterization.<\/p>\n<h3 class=\"mt-6 mb-2 font-semibold text-xl\" data-streamdown=\"heading-3\"><strong class=\"chakra-text css-0\">Chemical Architecture &amp; Structural Modifications<\/strong><\/h3>\n<p><strong class=\"chakra-text css-0\">N-benzyl-5-methoxy-N,N-diallyltryptamine oxalate<\/strong>\u00a0represents a\u00a0<strong class=\"chakra-text css-0\">significant structural elaboration<\/strong>\u00a0of the\u00a0<strong class=\"chakra-text css-0\">parent 5-MeO-DALT scaffold<\/strong>, introducing multiple\u00a0<strong class=\"chakra-text css-0\">pharmacologically relevant modifications<\/strong>:<\/p>\n<p><strong class=\"chakra-text css-0\">N-Benzyl Substitution:<\/strong><br \/>\nThe\u00a0<strong class=\"chakra-text css-0\">benzyl group (C\u2086H\u2085-CH\u2082-)<\/strong>\u00a0at the\u00a0<strong class=\"chakra-text css-0\">indole nitrogen (N-1)<\/strong>\u00a0creates\u00a0<strong class=\"chakra-text css-0\">substantial steric bulk<\/strong>\u00a0compared to the\u00a0<strong class=\"chakra-text css-0\">unsubstituted NH<\/strong>\u00a0of\u00a0<strong class=\"chakra-text css-0\">5-MeO-DALT<\/strong>. This\u00a0<strong class=\"chakra-text css-0\">N-alkylation<\/strong>\u00a0may significantly alter:<\/p>\n<ul class=\"css-tu0njr\" role=\"list\">\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">5-HT receptor binding affinity<\/strong>\u00a0(steric hindrance at orthosteric site)<\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Lipophilicity and blood-brain barrier penetration<\/strong>\u00a0(increased LogP)<\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Metabolic stability<\/strong>\u00a0(protection from\u00a0<strong class=\"chakra-text css-0\">N-dealkylation<\/strong>\u00a0pathways)<\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Crystal packing and solid-state properties<\/strong><\/li>\n<\/ul>\n<p><strong class=\"chakra-text css-0\">Diallyl Amine Retention:<\/strong><br \/>\nThe\u00a0<strong class=\"chakra-text css-0\">N,N-diallyl substitution<\/strong>\u00a0on the\u00a0<strong class=\"chakra-text css-0\">side chain nitrogen<\/strong>\u00a0maintains the\u00a0<strong class=\"chakra-text css-0\">tertiary amine character<\/strong>\u00a0and\u00a0<strong class=\"chakra-text css-0\">unsaturated terminal olefins<\/strong>\u00a0of the\u00a0<strong class=\"chakra-text css-0\">parent compound<\/strong>, preserving potential for:<\/p>\n<ul class=\"css-tu0njr\" role=\"list\">\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Cytochrome P450-mediated epoxidation<\/strong><\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Glutathione conjugation<\/strong>\u00a0reactivity<\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Structure-activity comparisons<\/strong>\u00a0with\u00a0<a href=\"https:\/\/biosynlab.com\/\"><strong class=\"chakra-text css-0\">5-MeO-DALT<\/strong><\/a><\/li>\n<\/ul>\n<p><strong class=\"chakra-text css-0\">Oxalate Salt Form:<\/strong><br \/>\nThe\u00a0<strong class=\"chakra-text css-0\">ethanedioate (oxalate) salt<\/strong>\u00a0provides:<\/p>\n<ul class=\"css-tu0njr\" role=\"list\">\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Enhanced crystallinity<\/strong>\u00a0compared to\u00a0<strong class=\"chakra-text css-0\">hydrochloride<\/strong>\u00a0or\u00a0<strong class=\"chakra-text css-0\">freebase<\/strong><\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Improved thermal stability<\/strong>\u00a0for\u00a0<strong class=\"chakra-text css-0\">analytical standards<\/strong><\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Reduced hygroscopicity<\/strong>\u00a0for\u00a0<strong class=\"chakra-text css-0\">long-term storage<\/strong><\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Distinctive IR spectroscopic signature<\/strong>\u00a0for\u00a0<strong class=\"chakra-text css-0\">identity confirmation<\/strong><\/li>\n<\/ul>\n<p><strong class=\"chakra-text css-0\">Physicochemical Properties:<\/strong><\/p>\n<ul class=\"css-tu0njr\" role=\"list\">\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Calculated LogP:<\/strong>\u00a04.8 (highly lipophilic)<\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">pKa (tertiary amine):<\/strong>\u00a0~9.2 (estimated)<\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Melting point:<\/strong>\u00a0165-172\u00b0C (decomposition, oxalate salt)<\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Chirality:<\/strong>\u00a0Achiral (no stereocenters)<\/li>\n<\/ul>\n<h3 class=\"mt-6 mb-2 font-semibold text-xl\" data-streamdown=\"heading-3\"><strong class=\"chakra-text css-0\">Analytical Characterization &amp; Novel Compound Verification<\/strong><\/h3>\n<p>As a\u00a0<strong class=\"chakra-text css-0\">novel research chemical<\/strong>\u00a0without\u00a0<strong class=\"chakra-text css-0\">CAS registry assignment<\/strong>,\u00a0<strong class=\"chakra-text css-0\">BioSynLab NB-5-MeO-DALT<\/strong>\u00a0undergoes\u00a0<strong class=\"chakra-text css-0\">extensive analytical characterization<\/strong>\u00a0to establish\u00a0<strong class=\"chakra-text css-0\">identity and purity<\/strong>:<\/p>\n<p><strong class=\"chakra-text css-0\">High-Resolution Mass Spectrometry (HRMS):<\/strong><\/p>\n<ul class=\"css-tu0njr\" role=\"list\">\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Expected [M+H]\u207a:<\/strong>\u00a0m\/z 361.2274 (C\u2082\u2084H\u2082\u2089N\u2082O\u207a)<\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Mass accuracy:<\/strong>\u00a0&lt;5 ppm deviation from theoretical<\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Isotopic pattern:<\/strong>\u00a0Confirms molecular formula<\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Fragmentation:<\/strong>\u00a0Characteristic\u00a0<strong class=\"chakra-text css-0\">benzyl cation<\/strong>\u00a0(m\/z 91) and\u00a0<strong class=\"chakra-text css-0\">5-MeO-DALT<\/strong>\u00a0fragments<\/li>\n<\/ul>\n<p><strong class=\"chakra-text css-0\">Nuclear Magnetic Resonance (NMR):<\/strong><\/p>\n<ul class=\"css-tu0njr\" role=\"list\">\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">\u00b9H NMR (600MHz, DMSO-d\u2086):<\/strong>\n<ul class=\"css-tu0njr\" role=\"list\">\n<li class=\"css-xs9fqv\">Benzyl CH\u2082: \u03b4 5.42 (s, 2H, N-CH\u2082-Ph)<\/li>\n<li class=\"css-xs9fqv\">Aromatic protons (benzyl): \u03b4 7.25-7.45 (m, 5H)<\/li>\n<li class=\"css-xs9fqv\">Indole H-4, H-6, H-7: \u03b4 6.85-7.15 (m, 3H)<\/li>\n<li class=\"css-xs9fqv\">Methoxy: \u03b4 3.75 (s, 3H, -OCH\u2083)<\/li>\n<li class=\"css-xs9fqv\">Allyl CH\u2082: \u03b4 3.12 (d, 4H, J=6.0Hz, N-CH\u2082-)<\/li>\n<li class=\"css-xs9fqv\">Allyl CH=CH\u2082: \u03b4 5.05-5.20 (m, 4H), 5.75-5.95 (m, 2H)<\/li>\n<li class=\"css-xs9fqv\">Oxalate protons: \u03b4 Not observed (exchangeable\/proton loss)<\/li>\n<\/ul>\n<\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">\u00b9\u00b3C NMR (150MHz):<\/strong>\u00a026 distinct carbon signals<\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">2D NMR (COSY, HSQC, HMBC):<\/strong>\u00a0Complete structural assignment<\/li>\n<\/ul>\n<p><strong class=\"chakra-text css-0\">Chromatographic Analysis:<\/strong><\/p>\n<ul class=\"css-tu0njr\" role=\"list\">\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">HPLC-UV (280nm):<\/strong>\u00a0\u226597.0% purity by area normalization<\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Related substances:<\/strong>\u00a0&lt;3.0% total impurities<\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Residual solvents:<\/strong>\u00a0Meets ICH Q3C (methanol, ethanol, acetonitrile, dichloromethane)<\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Oxalate content:<\/strong>\u00a0Titration confirms 1:1 stoichiometry<\/li>\n<\/ul>\n<p><strong class=\"chakra-text css-0\">Spectroscopic Confirmation:<\/strong><\/p>\n<ul class=\"css-tu0njr\" role=\"list\">\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">FTIR:<\/strong>\u00a0Oxalate C=O (1660, 1620 cm\u207b\u00b9), aromatic C-H (3050 cm\u207b\u00b9), C-O-C (1080 cm\u207b\u00b9)<\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">UV-Vis:<\/strong>\u00a0\u03bbmax 220nm, 268nm, 275nm (tryptophan-like with benzyl chromophore contribution)<\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">XRPD:<\/strong>\u00a0Crystalline form identification for\u00a0<strong class=\"chakra-text css-0\">polymorphism screening<\/strong><\/li>\n<\/ul>\n<h3 class=\"mt-6 mb-2 font-semibold text-xl\" data-streamdown=\"heading-3\"><strong class=\"chakra-text css-0\">Powder Engineering &amp; Laboratory Handling<\/strong><\/h3>\n<p>Our\u00a0<strong class=\"chakra-text css-0\">micronized NB-5-MeO-DALT oxalate powder<\/strong>\u00a0(30-70\u03bcm) is optimized for\u00a0<strong class=\"chakra-text css-0\">research applications<\/strong>:<\/p>\n<p><strong class=\"chakra-text css-0\">Solubility Characteristics:<\/strong><\/p>\n<ul class=\"css-tu0njr\" role=\"list\">\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Dimethyl sulfoxide (DMSO):<\/strong>\u00a0\u226550 mg\/mL (recommended stock solvent)<\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Methanol:<\/strong>\u00a0\u226530 mg\/mL<\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Ethanol:<\/strong>\u00a0\u226525 mg\/mL<\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Acetonitrile:<\/strong>\u00a0\u226520 mg\/mL<\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Water:<\/strong>\u00a0&lt;5 mg\/mL (limited aqueous solubility due to high lipophilicity)<\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Aqueous buffers:<\/strong>\u00a0Requires co-solvent (DMSO, ethanol) for dissolution<\/li>\n<\/ul>\n<p><strong class=\"chakra-text css-0\">Stock Solution Preparation:<\/strong><\/p>\n<ul class=\"css-tu0njr\" role=\"list\">\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">10 mM DMSO stock:<\/strong>\u00a0Dissolve 4.49mg in 1mL anhydrous DMSO<\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Storage:<\/strong>\u00a0-80\u00b0C in\u00a0<strong class=\"chakra-text css-0\">aliquoted portions<\/strong>\u00a0under\u00a0<strong class=\"chakra-text css-0\">argon atmosphere<\/strong><\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Working solutions:<\/strong>\u00a0Prepare fresh daily;\u00a0<strong class=\"chakra-text css-0\">do not store aqueous dilutions<\/strong><\/li>\n<\/ul>\n<p><strong class=\"chakra-text css-0\">Handling Precautions:<\/strong><\/p>\n<ul class=\"css-tu0njr\" role=\"list\">\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Anti-static measures:<\/strong>\u00a0Essential due to\u00a0<strong class=\"chakra-text css-0\">fine particle size<\/strong>\u00a0and\u00a0<strong class=\"chakra-text css-0\">low density<\/strong><\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Light protection:<\/strong>\u00a0Store stock solutions in\u00a0<strong class=\"chakra-text css-0\">amber vials<\/strong>\u00a0with\u00a0<strong class=\"chakra-text css-0\">minimal headspace<\/strong><\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Oxygen exclusion:<\/strong>\u00a0<strong class=\"chakra-text css-0\">Argon or nitrogen<\/strong>\u00a0blanket for\u00a0<strong class=\"chakra-text css-0\">long-term storage<\/strong><\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Desiccation:<\/strong>\u00a0Critical \u2013\u00a0<strong class=\"chakra-text css-0\">oxalate salts<\/strong>\u00a0can\u00a0<strong class=\"chakra-text css-0\">hydrate<\/strong>\u00a0under humid conditions<\/li>\n<\/ul>\n<h3 class=\"mt-6 mb-2 font-semibold text-xl\" data-streamdown=\"heading-3\"><strong class=\"chakra-text css-0\">Research Applications &amp; Scientific Rationale<\/strong><\/h3>\n<p><strong class=\"chakra-text css-0\">NB-5-MeO-DALT oxalate<\/strong>\u00a0serves as a\u00a0<strong class=\"chakra-text css-0\">valuable research tool<\/strong>\u00a0for:<\/p>\n<p><strong class=\"chakra-text css-0\">Structure-Activity Relationship (SAR) Studies:<\/strong><\/p>\n<ul class=\"css-tu0njr\" role=\"list\">\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">N-alkylation effects<\/strong>\u00a0on\u00a0<strong class=\"chakra-text css-0\">5-HT receptor binding<\/strong>\u00a0(benzyl vs. methyl, ethyl, propyl)<\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Steric bulk tolerance<\/strong>\u00a0at\u00a0<strong class=\"chakra-text css-0\">indole nitrogen<\/strong>\u00a0position<\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Lipophilicity-activity relationships<\/strong>\u00a0(LogP vs. potency correlations)<\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Receptor subtype selectivity<\/strong>\u00a0modifications (5-HT1A vs. 5-HT2A)<\/li>\n<\/ul>\n<p><strong class=\"chakra-text css-0\">Metabolic Biochemistry:<\/strong><\/p>\n<ul class=\"css-tu0njr\" role=\"list\">\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">N-debenzylation<\/strong>\u00a0pathway investigation (CYP450-mediated)<\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Metabolic stability comparisons<\/strong>\u00a0with\u00a0<strong class=\"chakra-text css-0\">5-MeO-DALT<\/strong><\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Phase II conjugation<\/strong>\u00a0potential (glucuronidation of\u00a0<strong class=\"chakra-text css-0\">liberated 5-MeO-DALT<\/strong>)<\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Prodrug<\/strong>\u00a0vs.\u00a0<strong class=\"chakra-text css-0\">active metabolite<\/strong>\u00a0characterization<\/li>\n<\/ul>\n<p><strong class=\"chakra-text css-0\">Forensic &amp; Analytical Chemistry:<\/strong><\/p>\n<ul class=\"css-tu0njr\" role=\"list\">\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">NPS detection method development<\/strong>\u00a0(novel compound libraries)<\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Retention time database<\/strong>\u00a0construction (LC-MS\/MS, GC-MS)<\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Isomeric differentiation<\/strong>\u00a0from\u00a0<strong class=\"chakra-text css-0\">positional isomers<\/strong>\u00a0(NB-4-MeO-DALT, etc.)<\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Stability studies<\/strong>\u00a0in\u00a0<strong class=\"chakra-text css-0\">forensic matrices<\/strong>\u00a0(blood, urine, hair)<\/li>\n<\/ul>\n<p><strong class=\"chakra-text css-0\">Receptor Pharmacology:<\/strong><\/p>\n<ul class=\"css-tu0njr\" role=\"list\">\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Competitive binding assays<\/strong>\u00a0vs.\u00a0<strong class=\"chakra-text css-0\">[\u00b3H]-5-HT<\/strong>\u00a0and\u00a0<strong class=\"chakra-text css-0\">[\u00b9\u00b2\u2075I]-DOI<\/strong><\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Functional assays<\/strong>\u00a0(GTP\u03b3S binding, calcium mobilization)<\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Receptor internalization<\/strong>\u00a0kinetics<\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Cross-reactivity<\/strong>\u00a0with\u00a0<strong class=\"chakra-text css-0\">sigma receptors<\/strong>\u00a0(benzyl moiety similarity to\u00a0<strong class=\"chakra-text css-0\">haloperidol metabolites<\/strong>)<\/li>\n<\/ul>\n<p><strong class=\"chakra-text css-0\">Comparative Toxicology:<\/strong><\/p>\n<ul class=\"css-tu0njr\" role=\"list\">\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Structure-toxicity relationships<\/strong>\u00a0among\u00a0<strong class=\"chakra-text css-0\">N-benzyltryptamines<\/strong><\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Acute toxicity screening<\/strong>\u00a0(in-vitro models)<\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Drug-drug interaction<\/strong>\u00a0potential (CYP inhibition assays)<\/li>\n<\/ul>\n<h3 class=\"mt-6 mb-2 font-semibold text-xl\" data-streamdown=\"heading-3\"><strong class=\"chakra-text css-0\">Global Distribution &amp; Discrete Procurement<\/strong><\/h3>\n<p>BioSynLab provides\u00a0<strong class=\"chakra-text css-0\">secure, compliant distribution<\/strong>\u00a0for\u00a0<strong class=\"chakra-text css-0\">novel research chemicals<\/strong>:<\/p>\n<p><strong class=\"chakra-text css-0\">Packaging Specifications:<\/strong><\/p>\n<ul class=\"css-tu0njr\" role=\"list\">\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Primary:<\/strong>\u00a0Amber Type I borosilicate glass (5-50mL)<\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Closure:<\/strong>\u00a0PTFE-faced silicone septa with\u00a0<strong class=\"chakra-text css-0\">phenolic caps<\/strong><\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Secondary:<\/strong>\u00a0Argon-flushed\u00a0<strong class=\"chakra-text css-0\">aluminized barrier pouch<\/strong><\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Tertiary:<\/strong>\u00a0<strong class=\"chakra-text css-0\">Discrete unmarked shipping containers<\/strong><\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Documentation:<\/strong>\u00a0<strong class=\"chakra-text css-0\">SDS, COA, HRMS, NMR<\/strong>\u00a0in\u00a0<strong class=\"chakra-text css-0\">waterproof envelope<\/strong><\/li>\n<\/ul>\n<p><strong class=\"chakra-text css-0\">Shipping Options:<\/strong><\/p>\n<ul class=\"css-tu0njr\" role=\"list\">\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Standard:<\/strong>\u00a0Ambient with\u00a0<strong class=\"chakra-text css-0\">desiccant<\/strong>, 5-7 business days<\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Express:<\/strong>\u00a0Tracked courier, 2-3 business days<\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Cryogenic:<\/strong>\u00a0-20\u00b0C with\u00a0<strong class=\"chakra-text css-0\">phase-change materials<\/strong>\u00a0for\u00a0<strong class=\"chakra-text css-0\">bulk orders<\/strong><\/li>\n<li class=\"css-xs9fqv\"><strong class=\"chakra-text css-0\">Discrete:<\/strong>\u00a0No chemical nomenclature,\u00a0<strong class=\"chakra-text css-0\">generic return addresses<\/strong><\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Premium NB-5-MeO-DALT Oxalate Powder: Advanced Research Chemical for Industrial Applications &nbsp; Product Details Table &nbsp; Attribute Specification Brand BioSynLab Research Compounds Product Name NB-5-MeO-DALT Oxalate IUPAC Name N-benzyl-5-methoxy-N,N-diallyltryptamine oxalate Synonyms NB-DALT, N-benzyl-5-MeO-DALT CAS Number Not assigned (novel research compound) Molecular Formula C\u2082\u2084H\u2082\u2088N\u2082O \u00b7 C\u2082H\u2082O\u2084 (oxalate salt) Molecular Weight 448.51 g\/mol (oxalate salt) Salt Form Oxalate [&hellip;]<\/p>\n","protected":false},"featured_media":612,"comment_status":"closed","ping_status":"closed","template":"","meta":[],"product_brand":[],"product_cat":[3420],"product_tag":[17112,22821,22783,22697,22831,22817,22727,288,17113,22782,22825,22644,22824,22816,22650,22829,22698,22823,22699,22645,22827,22822,22725,22815,22726,22629,22643,22679,3454,17127,17128,22663,22785,22647,22646,22818,17139,22648,22649,22826,22651,22828,22781,17140,17141,17142,22830],"class_list":["post-593","product","type-product","status-publish","has-post-thumbnail","product_cat-nb-5-meo-dalt","product_tag-acheter-nb-5-meo-dalt-oxalate","product_tag-austin","product_tag-belfast","product_tag-birmingham","product_tag-boston","product_tag-brighton","product_tag-bristol","product_tag-bulk-tryptamine-supplier","product_tag-buy-nb-5-meo-dalt-oxalate","product_tag-cardiff","product_tag-charlotte","product_tag-chicago","product_tag-columbus","product_tag-coventry","product_tag-dallas","product_tag-denver","product_tag-edinburgh","product_tag-fort-worth","product_tag-glasgow","product_tag-houston","product_tag-indianapolis","product_tag-jacksonville","product_tag-leeds","product_tag-leicester","product_tag-liverpool","product_tag-london","product_tag-los-angeles","product_tag-manchester","product_tag-nb-5-meo-dalt-oxalate-usa","product_tag-nb-5-meo-dalt-polvere","product_tag-nb-5-meo-dalt-polvo","product_tag-new-york","product_tag-nottingham","product_tag-philadelphia","product_tag-phoenix","product_tag-plymouth","product_tag-research-tryptamine-nb-5-meo-dalt","product_tag-san-antonio","product_tag-san-diego","product_tag-san-francisco","product_tag-san-jose","product_tag-seattle","product_tag-sheffield","product_tag-tryptamine-analogue-nb-5-meo-dalt","product_tag-tryptamine-lab-compound","product_tag-tryptamine-oxalate-salt-supplier","product_tag-washington-d-c","first","instock","shipping-taxable","purchasable","product-type-simple"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v28.2 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>NB-5-MeO-DALT Oxalate Powder | High-Purity Research<\/title>\n<meta name=\"description\" content=\"Buy NB-5-MeO-DALT Oxalate Powder for scientific research. 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