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1-(4-Methoxyphenyl)-2-Benzylaminopropane

    • Product Name 1-(4-Methoxyphenyl)-2-Benzylaminopropane
    • Alias Methoxybenzylphetamine
    • Einecs 641-436-7
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    214334

    Iupac Name 1-(4-Methoxyphenyl)-2-benzylaminopropane
    Cas Number 2691762-72-7
    Molecular Formula C17H21NO
    Molecular Weight 255.36 g/mol
    Synonyms 4-Methoxy-N-benzylamphetamine
    Appearance Solid, crystalline
    Solubility Soluble in organic solvents
    Chemical Class Phenethylamine
    Functional Groups Methoxy, amine, aromatic rings
    Smiles COC1=CC=C(C=C1)CC(NCC2=CC=CC=C2)C
    Inchi InChI=1S/C17H21NO/c1-14(13-18-15-7-3-2-4-8-15)12-16-9-11-17(19-1)10-16/h2-4,7-11,14,18H,5-6,12-13H2,1H3

    As an accredited 1-(4-Methoxyphenyl)-2-Benzylaminopropane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25g amber glass bottle with a tamper-evident cap, labeled "1-(4-Methoxyphenyl)-2-Benzylaminopropane, for laboratory use only."
    Shipping The shipping of **1-(4-Methoxyphenyl)-2-Benzylaminopropane** requires secure packaging in compliance with chemical transport regulations. It should be dispatched in robust, leak-proof containers, labelled appropriately, and accompanied by relevant safety documentation. Ensure temperature control if required, and use certified carriers to guarantee safe delivery and adherence to local and international laws.
    Storage Store **1-(4-Methoxyphenyl)-2-benzylaminopropane** in a tightly sealed container, in a cool, dry, and well-ventilated area away from light and incompatible materials such as strong acids and oxidizers. Keep it at room temperature, avoiding excessive heat and humidity. Ensure proper labeling and access control, and follow all chemical safety guidelines for handling and storage of organic amines.
    Application of 1-(4-Methoxyphenyl)-2-Benzylaminopropane

    Applications of 1-(4-Methoxyphenyl)-2-Benzylaminopropane in Industrial Manufacturing

    As a specialized manufacturer, we supply 1-(4-Methoxyphenyl)-2-Benzylaminopropane to customers operating advanced chemical syntheses, strictly supporting only established downstream segments. The following sections provide detailed application breakdowns, focused on real industrial uses that reflect global regulatory practices, commercial formulation parameters, integration with large-scale production processes, and the distinct finished goods manufactured within these sectors.

    1. Pharmaceutical Intermediate for CNS Active Compound Synthesis

    Active pharmaceutical ingredient (API) producers utilize this compound principally as a building block in synthetic pathways toward central nervous system (CNS) candidate molecules. Manufacturing plants incorporate this intermediate in multi-step processes, organizing material flow directly into designated reactor vessels. The compound’s role focuses on specific amine-alkylation or condensation steps that define structural frameworks of developmental molecules. Dosing levels in each synthetic stage depend on batch scale and target yield, monitored by in-house QC for purity endpoints specific to medical regulatory submissions. Final goods emerging from these processes typically advance into clinical candidate libraries for later formulation, remaining compliant with all pharmaceutical quality frameworks.

    Industry compliance standards

    • International Conference on Harmonisation Q7 (ICH Q7) for API manufacturing
    • EU Good Manufacturing Practice (GMP) Part II for active substances
    • United States Pharmacopeia (USP) General Chapter <2351>
    • EMA Guideline on the Chemistry of Active Substances

    Typical usage ratio

    • 0.85–1.10 molar equivalents per target intermediate, adjusted to synthesis route and process scale; excess not typically required due to reaction specificity

    Downstream process integration

    • Direct addition to primary amination or condensation reactors during stepwise synthesis of CNS drug candidates; batch campaign protocols

    Final product types

    • Research-stage CNS candidate APIs
    • Preclinical reference standards for analytical development
    • Investigational medicinal ingredient stocks
    • Pharmaceutical intermediate bulks for third-party custom synthesis

    2. Specialty Fine Chemical Synthesis for Advanced Materials

    Producers in advanced materials sectors leverage this raw material as a tailored phenethylamine derivative when generating specialty aromatic monomers for polymer modification and next-generation resins. Formulators dose the ingredient based on target reactivity and crosslink density, feeding it into controlled-heating bulk polymerization reactors with specific anti-oxidant protocols. QA procedures capture purity and residual monomer metrics for compliance with industrial standards. Resulting end-materials become incorporated in thin-film coatings and engineered plastics for microelectronic or sensor-device applications, meeting precise structural requirements of the value chain.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • REACH Regulation (EC) No 1907/2006 for chemicals used in manufacturing
    • RoHS Directive (EU) 2015/863 for restricted substances in electronics
    • Proprietary quality agreements for OEM electronics manufacturers

    Typical usage ratio

    • 1.5–3.8% by weight in polymerization batches, regulated by required monomeric incorporation and anticipated crosslink density

    Downstream process integration

    • Dosed directly into heated monomer feed during batch or semi-batch polymerization; process adjustments for viscosity control and thermal load

    Final product types

    • Functionalized polymer films
    • Specialty resin composites
    • Microelectronic encapsulants
    • Advanced sensor substrate materials

    3. Intermediate for Agrochemical Active Ingredient Development

    Large-scale agrochemical formulators incorporate this compound in their research and pilot lots as a structural intermediate when assembling prototype molecules for pest management R&D. The ingredient serves as a precursor in synthetic routes targeting amine-based selectivity for new-generation insecticides or herbicides. Process engineers adjust the inclusion ratio after calculation based on targeted yield and documented reaction condtions, feeding the raw material through monitored addition funnels during closed-system reactions. Analytical teams verify by-product specification in line with agricultural safety dossiers before active shipment for formulation screening.

    Industry compliance standards

    • FAO/WHO Good Laboratory Practice (GLP) for pesticide intermediate synthesis
    • OECD Test Guidelines for chemical synthesis intermediates
    • SANS 10206:2010 – The Handling, Storage and Disposal of Pesticides
    • Globally Harmonised System (GHS) for chemical hazard communication

    Typical usage ratio

    • Usually 0.90–1.20 molar equivalents per target molecule in multi-step synthesis; slight excess employed depending on selectivity yield and pilot lot size

    Downstream process integration

    • Fed into closed reaction systems during construction of core amine functionalities; product captured for further derivatization and isolation stages

    Final product types

    • Prototype agrochemical actives for field test batches
    • Reference intermediates for regulatory dossiers
    • Pre-registered pesticide candidates for downstream formulation

    4. Chemical Reference Standard for Analytical Laboratories

    Certified reference material (CRM) providers and custom analytical laboratories source this compound as a high-purity calibration reference for mass spectrometry and chromatographic system qualification. Labs validate purity via multi-stage purification and analytical documentation before use in sensitivity and linearity verification protocols. Integration typically involves gravimetric addition into calibration solution matrixes, supported by in-house metrologist teams, following mandatory audit trails that align with international laboratory standards. End-use cases encompass internal laboratory reference stocks, proficiency testing panels, and system compliance kits for regulated industries such as clinical research or toxicological studies.

    Industry compliance standards

    • ISO 17034:2016 General Requirements for the Competence of Reference Material Producers
    • ISO/IEC 17025:2017 Testing and Calibration Laboratories
    • US FDA 21 CFR Part 58 (GLP for Nonclinical Laboratory Studies)
    • OECD Principles of Good Laboratory Practice

    Typical usage ratio

    • 5–100 mg per calibration series; precise quantity determined by the calibration range of the target analytical method

    Downstream process integration

    • Added gravimetrically to matrix solutions for analytical qualification and system performance assessments in laboratory environments

    Final product types

    • Secondary chemical reference standards
    • Calibration kits for HPLC/GC-MS
    • Proficiency testing materials
    • System suitability control mixtures for regulated laboratory use
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    Certification & Compliance
    More Introduction

    Introducing 1-(4-Methoxyphenyl)-2-Benzylaminopropane: A Manufacturer’s Perspective on Craft and Chemistry

    The Backbone of Laboratory Precision

    Every year, colleagues in fine chemical manufacturing ask about novel amines, their utility, stability, and nuances compared to common analogs. 1-(4-Methoxyphenyl)-2-Benzylaminopropane has come to occupy an important place on our production floor, both for its reliability and for the kind of applications chemists pursue in organic synthesis and pharmacological research.

    From day one in scale-up, we focused on controlling every reaction variable: moisture exclusion, slow base addition to capture clear intermediates, clock-watching to keep isomer levels in check. These steps matter when producing specialty chemicals because our customers aren’t looking for generic batches; they demand predictability and a straightforward relationship between molecular structure and actual behavior in their work. Our batches no longer show batch-to-batch color drift and we consistently observe minimal byproduct signals in the finished product.

    True Value through Crystal Structure

    Unlike many generic amines, the benzylamino and methoxyphenyl groups in this compound set it apart. The methoxy group on the aromatic ring gives our product real-world benefits other analogs lack. In actual use, researchers have told us the electronic nature of the methoxy substituent influences receptor binding or downstream modifications—critical in developing small molecule frameworks or as an intermediate in pilot projects. The crystalline powder flows well in production dispensers and avoids unattractive caking, even during humid weeks. Each bottle is the product of deliberate purification, with residual solvents and trace metal contents consistently the lowest in our peer group.

    Putting Specifications to Work

    Throughout development, we tuned our synthesis to produce a material with a sharp melting point and a clean chromatographic fingerprint. We know suppliers who focus on capacity and overlook purity profiles, but our long-run customers rely on an impurity character under 0.5% by HPLC, confirmed with NMR. Our QC staff use calibrated reference standards for every lot, and our tech team meets weekly to dissect any uptick in unknowns on test reports.

    We’re not fans of generic buzzwords. The model here refers to a chemical fingerprint—not a product code or catalog entry. Our process turns out a dense, free-flowing white to faintly off-white powder. This physical consistency avoids yield losses in downstream reactions, and we see fewer stuck filters or wasted solvents than we did early on. For customers in pilot R&D or medicinal chemistry, these details mean fewer surprises and cleaner end products.

    Applications Driven by Chemical Insight

    Over the years, synthetic chemists have sent us their reaction notes—how subtle differences in amine structure affect reductive aminations, N-alkylations, or even catalytic hydrogenations for research purposes. This compound serves as a key intermediate in multi-step syntheses, including in the search for novel psychoactive scaffolds or for constructing library members in drug discovery. Medicinal teams have reported that the methoxy inclusion can change the metabolic fate of derivatives in preliminary assays. We make sure that every lot carries a tight enough specification to prevent inconsistent reaction performance.

    There’s a significant gap between catalog-ordered fine chemicals and those crafted directly by experts at the source. Our colleagues in process development rarely need explanations about the value of physically handling source-manufactured powder. Batch-to-batch reproducibility, trace impurity levels, and honest certificates not filled with caveats make up the difference between successful campaigns and wasted cycles. In routes where trace metals poison catalysts, or where minor byproducts could trip up a regulatory panel, our product leaves no lingering doubt.

    What Sets Our Process Apart

    Many operations take shortcuts, rushing toward throughput at the expense of consistency. We invested early in in-line FTIR to watch reaction progression—no more waiting for slow TLC plates or relying on dated visual checks for endpoint determination. Our finished product must breathe no signs of decomposition or darkening after months of storage at ambient conditions. Desiccator storage, inert packaging, and on-demand batch grinding keep the material as fresh on arrival as the day it left our warehouse.

    In manufacturing environments, operators live with small details—a slightly different solid phase can slow down an entire run, change filter cake texture, or complicate filling lines. Clarifying our specification files came after months of hands-on feedback at the filling and QC stages: now, each unit gets checked for bulk density, moisture content, and appearance against a reference standard. We know what the powder should look like; so do our QC leads and so, now, do our end customers.

    Direct Route to Trust

    Working as a manufacturer, we see where each gram goes. Direct customer discussion built a feedback loop—we customized batch sizes, documented every refinement, and flagged outliers with a human eye. There’s a straight line from technical engagement to higher reliability. Discovery teams, faced with the risk of repeated synthesis, trust us to flag change points in our own production.

    We don’t shy away from process challenges. If a batch starts drifting from established parameters, our process chemists analyze intermediate samples and rerun validation steps. This policy has paid off in customer loyalty and downstream validation: our partners regularly ship validation samples to us and rely on our lab for cross-checking results.

    Not Just Another SKU

    Labs working with catalog purchases sometimes face hidden headaches: contamination, odor, sluggish redissolution, unexplained peaks. Our batches clear these hurdles by design. Every kilo lands on our loading dock with a chain of documentation—gravimetric checks, UV-Vis purity confirmation, and real NMR overlays, not just certificates. Each specification emerges from our plant’s own workflow, grounded in what actually matters at scale.

    We share our analytical results transparently. NMR matching uses solvent-specific spectra and peaks are cross-confirmed by our lead analysts. Whenever customers aspire to a new use—testing an alternate reaction solvent, exploring a new catalytic route, or blending on automated platforms—our technical team weighs in with first-hand process experience.

    Why the Methoxy Makes a Difference

    1-(4-Methoxyphenyl)-2-Benzylaminopropane isn’t just an arbitrary swap for cheaper analogs. Chemists have shared that methoxy often changes how molecules interact, whether through hydrogen bonding, electron-rich rings, or binding kinetics in biological targets. Subtle shifts in electronic properties have a ripple effect through reaction routes, giving medicinal chemists a tool for systematic structure–activity relationship studies.

    Practical handling also matters. During transfer and weighing, our operators note reduced static cling and dust-off compared to less refined amines. Our logistics staff noticed that sealed packing lined with an inert gas stretch shelf life and reduce clumping or moisture pickup.

    Tackling Downstream Demands with Confidence

    After years of direct manufacturing, we understand the ongoing headaches of scale-up. Our technical representatives spend time discussing order histories and reaction targets with chemists to advise on special requirements—custom particle size, coordination with automated powder dispensers, and storage strategies that extend usability during staggered campaigns. We don’t hide from unusual lot requests or tight delivery timelines.

    Being rooted with hands in real production brings a level of accountability and continuity. Any time a campaign calls for lots up to hundreds of kilograms, we back each shipment with analytical documentation and traceable archiving, so users upstream and downstream know lot details. Our staff manage split batches, manage documentation for nonstandard requests, and keep plenty of archived inventory for backtracking should a lot ever require retesting.

    No Room for Ambiguity in Purity

    For sensitive downstream applications, there’s no space for guesswork. We never mask substandard lots by blending. The plant maintains distinct batch records, direct sample archiving, and all QA sign-offs keep pace with active production. This no-shortcut policy has strengthened our customer relationships; when process teams stumble on an anomaly, we walk the floor and review lot histories together—it’s not just support, it’s continuous improvement.

    Even dilution or formulation downstream receives our direct input if needed. Some teams use our product neat, others formula blend to strict ratios for pilot screens, and all benefit from a history of rigorous analysis. We do not delegate troubleshooting to third-parties or rely on generic advice columns.

    Key Differences from Everyday Amines

    Unlike mass-market benzylamines or unsubstituted phenylethylamines, our process supplies a consistent, high-purity material targeted for the advanced lab bench. The methoxyphenyl ring offers altered reaction profiles and distinct handling compared to related compounds. Where other amines might show inconsistent reactivity or drift in color or moisture absorption, we keep our specification far tighter, focusing on real-world problems faced by research chemists. It means fewer last-minute substitutions for researchers, clearer analytical results, and reduced time spent troubleshooting unexpected issues.

    Chemists notice the difference in solution—less foaming, easier weighing, true-to-form reactivity in coupling or reduction. We leverage hands-on expertise to adjust process parameters in response to analytical findings, rather than simply running volume when a specification *almost* matches a textbook value. This attention gets noticed in real project timelines and cost savings for our industrial partners.

    Collaboration from Production through Application

    Our relationship with labs and formulators remains grounded in direct advice and technical sharing. We send out detailed batch documentation, analytical overlays, and practical handling notes; incoming feedback keeps our process tuned. Each process refinement comes from actual field experience, not hypothetical process maps. Structured technical calls and periodic review meetings close the loop, letting application scientists feed back into our own plant improvements.

    Mutual respect between manufacturing and end-user teams leads to better chemistry. By investing in real troubleshooting, visiting partner labs, and openly sharing evaluation results, we have seen both our own efficiency and our customer outcomes climb year on year. We know which properties matter and recognize issues before they escalate.

    Driving Progress and Reliability in Specialty Amines

    After years on the manufacturing side, supporting customer advances in drug discovery, combinatorial chemistry, or custom synthesis, 1-(4-Methoxyphenyl)-2-Benzylaminopropane has emerged as a staple built for both resilience and scientific ambition. Each lot that leaves our plant tells a story of collaborative improvement—it represents investments in better workflow design, smarter QC practices, and a direct connection between manufacturer and end user.

    We remain committed to transparent processes, honest communication, and technical support rooted in practical manufacturing. As more partners expand their specialty amine programs, demand for consistent quality outpaces what generic catalogues or resellers can hope to supply. Every improvement cycle stems from asking, “Where can we make chemists’ jobs easier?” and acting without delay.

    Conclusion: Building a Foundation for the Future

    Those of us on the floor at the chemical plant see the ripple effect each improvement brings. Refined product specifications, stronger process control, and tighter analytical documentation all drive progress for our customers. 1-(4-Methoxyphenyl)-2-Benzylaminopropane reflects generations of chemical know-how—a product tuned by chemists, for chemists. In a world where every decision counts, it pays to source materials straight from the hands that crafted them.