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3-Amino-6-Morpholinopyridine

    • Product Name 3-Amino-6-Morpholinopyridine
    • Alias 3-(Morpholin-4-yl)pyridin-2-amine
    • Einecs 629-725-6
    • 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

    296338

    Productname 3-Amino-6-Morpholinopyridine
    Casnumber 139404-33-0
    Molecularformula C9H13N3O
    Molecularweight 179.22
    Appearance White to off-white solid
    Meltingpoint 146-149°C
    Purity ≥98%
    Solubility Soluble in DMSO, methanol
    Structure Pyridine ring with amino and morpholino substituents
    Smiles c1cnc(c(c1)N)N2CCOCC2
    Inchi InChI=1S/C9H13N3O/c10-8-5-6-11-9(7-8)12-2-1-3-13-4-12/h5-7H,1-4,10H2
    Storageconditions Store at room temperature, away from moisture and light

    As an accredited 3-Amino-6-Morpholinopyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25-gram amber glass bottle, tightly sealed, labeled with the chemical name "3-Amino-6-Morpholinopyridine," purity, and hazard information.
    Shipping 3-Amino-6-Morpholinopyridine is shipped in tightly sealed containers to prevent contamination and moisture ingress. It is packaged according to chemical safety regulations, typically in amber bottles or sturdy containers, and labeled with hazard information. The package is handled by certified carriers, ensuring safe transportation per local and international shipping guidelines.
    Storage 3-Amino-6-Morpholinopyridine should be stored in a tightly sealed container in a cool, dry, well-ventilated area, away from incompatible substances such as strong oxidizers and acids. Protect it from moisture and direct sunlight. Avoid exposure to heat and ignition sources. Clearly label the container and ensure only trained personnel handle the chemical, following appropriate safety protocols.
    Application of 3-Amino-6-Morpholinopyridine

    Applications of 3-Amino-6-Morpholinopyridine in Industrial Manufacturing

    3-Amino-6-Morpholinopyridine supports production in several advanced chemical sectors. As the direct manufacturer, we deliver this pyridine derivative to various downstream industries engaged in highly controlled synthesis and formulation processes. Below, we detail its industrial-scale applications, covering compliance, formulation ratios, integration stages, and end-use products across each field.

    1. Pharmaceutical Intermediate for Antiviral Agents

    This compound serves as a key intermediate during the multi-step synthesis of several antiviral drugs, particularly pyridine-based nucleoside analogues. Process chemists introduce it during the heterocycle construction step. Compliance with pharmacopeial standards remains obligatory, while cGMP conditions ensure batch traceability. Downstream manufacturers use this intermediate for synthesis campaigns, adjusting ratios based on route optimization studies and impurity control profiles.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • Ph. Eur. (European Pharmacopoeia) monographs for finished pharmaceuticals
    • US FDA 21 CFR Part 211 Process Control
    • China Pharmacopoeia (ChP) for regulated intermediates

    Typical usage ratio

    • 0.15–0.45 equivalent as per molar calculation versus the limiting substrate in stepwise synthesis
    • Exact amount depends on stoichiometric pathway and mandated impurity limits within API process validation

    Downstream process integration

    • Charged at the pyridine ring substitution or cyclization step, usually after protection/deprotection sequences
    • Handled in jacketed reactors under nitrogen with in-process analytical verification (HPLC/GC)

    Final product types

    • Antiviral active pharmaceutical ingredients (APIs)
    • Small-molecule intermediate batches for contract development and manufacturing organizations (CDMOs)
    • Pyridine-based prodrugs
    • Advanced synthetic building blocks for further derivatization

    2. Agrochemical Synthesis of Systemic Fungicides

    This material acts as a foundation block in the design and synthesis of morpholine-containing fungicides, especially for cereal and seed treatments. Downstream facilities use it in the coupling step to introduce both aminopyridine and morpholine functionalities essential for systemic action. Integration into process lines requires compliance with agrochemical-specific guidelines, including risk mitigation procedures and traceability in multi-ton runs.

    Industry compliance standards

    • REACH Registration (Europe) for chemical safety reporting
    • ISO 9001:2015 Quality Management for agrochemical synthesis
    • OECD Principles of Good Laboratory Practice (GLP) for registration batches
    • China National Standards (GB) for pesticide intermediates

    Typical usage ratio

    • 1.0–1.2 equivalent relative to halogenated pyridine reactant in coupling step
    • The ratio adapts based on expected reagent conversion and scale-up yields

    Downstream process integration

    • Fed during high-temperature reflux reactions within jacketed vessels
    • Followed by downstream crystallization or extraction for product isolation

    Final product types

    • Morpholine-based systemic fungicide actives
    • Intermediate solutions for pesticide formulation
    • Seed treatment concentrate components
    • Bulk technical-grade plant protection agents

    3. Dye and Pigment Manufacturing for Advanced Printing Inks

    It enables development of specialty pyridine-derived dyes, particularly those required for high-resolution inkjet formulations and electronics-grade printing. Inclusion of this intermediate ensures key color-fastness, solubility, and processability parameters during multi-stage syntheses. Manufacturers add the compound during core structure formation; compliance with industrial chemical safety acts and colorant-specific QC protocols is maintained throughout batch operations.

    Industry compliance standards

    • OEKO-TEX Eco Passport for restricted chemical substances in dye manufacturing
    • EN 71-3:2019 for colorant migration in toys and textiles (Europe)
    • US TSCA (Toxic Substances Control Act) for industrial colorant intermediates
    • Japan METI CSCL for dye intermediates management

    Typical usage ratio

    • 5–12% by mass of the total dye formulation blend, determined experimentally for tinctorial strength and stability
    • Ratio varies to achieve precise color shade and solubility in final ink concentrates

    Downstream process integration

    • Dosed during the nucleophilic aromatic substitution or condensation phases in dye synthesis reactors
    • Combined with auxiliary dispersants and resin binders during pigment dispersion for printing inks

    Final product types

    • High-performance digital printing ink concentrates
    • Pyridine-based organic dyes for plastics and textiles
    • Industrial inkjet cartridge formulations
    • Electronics-grade pigment dispersions

    4. Specialty Polymer Modification

    In the field of functional polymers, this material supports the production of pyridine- and morpholine-substituted monomers. These are then polymerized to create advanced coatings and membranes that require enhanced chemical resistance or selective permeability. The compound’s integration aligns with performance optimization projects, guided by regulatory status for polymer additives and end-use approval in sensitive sectors such as food packaging and water treatment.

    Industry compliance standards

    • FDA 21 CFR 177.2600 (elastomers in food contact applications)
    • EU Regulation (EC) No 1935/2004 for materials in contact with food
    • ISO 14001 Environmental Management for specialty polymer plants
    • RoHS Directive (EU) on hazardous substances in electronics coatings

    Typical usage ratio

    • 0.3–3% by mass introduced as a comonomer or functionalized additive
    • Ratio selected to control glass transition temperature or hydrophilicity properties

    Downstream process integration

    • Reacted in bulk polymerization kettles or dropped post-polycondensation as chain modifiers
    • Integrated in solution phase or melt mixing, monitored by spectrophotometric QC

    Final product types

    • Pyridine-functionalized barrier films
    • Morpholine-modified water filtration membranes
    • Electrical insulation coatings for consumer electronics
    • Food-grade flexible polymer packaging

    5. Fine Chemical Intermediate for Analytical Reagent Synthesis

    The compound acts as a building block in the synthesis of specialty analytical reagents and reference standards for chromatographic and spectrophotometric analysis. Analytical chemistry labs use it to prepare high-purity calibration substances where pyridine and morpholine functional groups are required for selective detection or quantification. Quality assurance includes batch documentation and adherence to standards for laboratory chemicals.

    Industry compliance standards

    • ISO 17025 General Requirements for Testing and Calibration Laboratories
    • Good Laboratory Practice (GLP) compliance for analytical grade reagents
    • US EPA Test Methods (where applicable for environmental standards)
    • LGC/USP Reference Standard certification when used for calibration mixtures

    Typical usage ratio

    • 0.05–0.2 mole equivalent introduced in custom reagent synthesis protocols
    • Adjusted based on desired reference standard purity and calibration curve requirements

    Downstream process integration

    • Charged to custom synthesis flasks during multi-component reaction setups
    • Followed by downstream purification and analytical verification by NMR, HPLC, or MS

    Final product types

    • Certified reference materials for HPLC and GC calibration
    • Colorimetric reagents for environmental or pharmaceutical analysis
    • Chromogenic detection agents for laboratory diagnostics
    • Analytical standards for residue identification
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    Certification & Compliance
    More Introduction

    3-Amino-6-Morpholinopyridine — A Manufacturer’s Perspective

    Crafting Quality at the Source

    Manufacturing specialty chemicals has its demands. Over the years, we spent countless hours responding to requests for building blocks that combine unique reactivity with stability. Out of this landscape grew 3-Amino-6-Morpholinopyridine, a product shaped by synthesis experience and customer feedback from around the globe.

    Our chemists have refined the preparation of 3-Amino-6-Morpholinopyridine many times. We focus on tight impurity control and consistent particle characteristics. This compound features a pyridine ring substituted with an amino group at position 3 and a morpholine ring at position 6, an arrangement that struck a balance in nucleophilic properties, solubility, and compatibility.

    The Value in Real-World Application

    Customers ask for this compound to serve as an intermediate, but they rarely want a one-size-fits-all solution. Pain points usually involve solubility or crystallinity in downstream steps, especially in pharmaceutical process development or advanced polymer production. We worked to match product form and particle size to meet these technical challenges. Regular feedback from end users informs not only our specifications, but our process itself—the small tweaks in solvent system, drying conditions, and temperature sometimes matter most when scaling from the flask to the drum.

    From our lab benches, we see research teams integrating 3-Amino-6-Morpholinopyridine as a starting block for kinase inhibitors, anti-infectives, or agrochemical active ingredients. Its morpholine ring stands out for providing electron-donating effects without causing the reactivity spikes typically seen from stronger amines. The amino group on the ring opens up further opportunities to selectively derivatize, making the compound appealing in combinatorial libraries found in drug discovery projects.

    Our technical team often fields requests from chemists looking to bypass problematic side-reactions seen with comparable pyridines. By sharing details about lab-scale use cases and troubleshooting reaction issues, we continue to see the compound gain favor in both R&D and early stage pilot production.

    Model Details and Batch Considerations

    Consistency matters to anyone who has scaled up a project. Based on direct experience, we make sure customers can request material custom-fitted for their methods. We offer 3-Amino-6-Morpholinopyridine typically as a free-flowing crystalline solid. Initial particle size ranges have been tailored for either direct weighing or preparation of concentrated solutions. Every batch we prepare passes through a series of checks on color, melting point, and purity, measured by HPLC and NMR.

    We have invested in closed-process handling and monitoring, minimizing cross-contamination—especially relevant for multi-stage synthesis lines. Over time, we documented sharply improved downstream yields for customers who once used less refined sources and ran into impurities or unplanned by-products.

    Reflections from the Factory Floor

    Day-to-day, production of 3-Amino-6-Morpholinopyridine does not behave exactly like typical alkylated or aminated pyridines. Subtle shifts in the hydrogenation protocol alter selectivity. If reaction parameters drift, off-color batches result—which matters not for marketing but for those with downstream UV or fluorescent detection methods. As manufacturers, we keep notes on every batch, tracking process deviation and matching them to analytical results.

    One particular strong point of our process involves recognition and removal of low-level morpholine-derived byproducts. Our team learned through on-the-job mishaps that certain distillation cuts can mask impurities, causing trouble for those running high-throughput screens. We minimized these issues by tuning vacuum levels and solvent volumes during workup—and this led directly to a sharper, more reliable product.

    With every order, packaging is an active decision. Most chemists underestimate how much atmospheric moisture and oxygen can interact with the material during transit. To address this, we trialed various liners and outer packaging, settling on options that preserve physical integrity and purity for up to twelve months in storage, even in humid environments.

    Comparison to Other Pyridine Derivatives

    Often, project teams compare 3-Amino-6-Morpholinopyridine to other aminopyridines or morpholine-functionalized aromatics from upstream catalogs. From the manufacturing side, simple analogs like 2-aminopyridine or 4-morpholinopyridine show easier synthesis and isolation, but tend to lack the unique reactivity window that comes from the 3-amino, 6-morpholino substitution pattern.

    This orientation allows selective acylation and further ring functionalization—critical for medicinal chemists pursuing SAR studies that probe electron-donating versus withdrawing effects around the ring. In our experience, attempts to substitute different ring positions resulted in either lower yields or more challenging purification due to regioisomer formation.

    Manufacturing this compound at scale presents different challenges compared to other aminopyridines, especially related to morpholine introduction. Many producers rely on simple SNAr chemistry, but we found that high-yielding routes benefit from staged additions and in situ monitoring. Time and again, this strategy produced a product with fewer unwanted byproducts in both small laboratory lots and full-production drum quantities.

    Several generic versions entering the global market cut corners on purification, often featuring residual morpholine or unidentified minor species that impact performance. Our decision to invest in calibrated vacuum ovens and comprehensive batch tracking came not from regulations, but from repeated customer feedback pinpointing trace impurities as the root of muted assay results or instability in end-products.

    Industrial Usage: What We See in the Field

    Teams in medicinal chemistry turn to 3-Amino-6-Morpholinopyridine for its track record as a reliable core structure in exploration of new active compounds. The combination of a basic nitrogen and a morpholine ring in specific ring positions gives multiple options for further transformation—making the molecule a staple in the early-stage development kits of many pharma organizations.

    Several formulations teams reported uses in polymer science, where persistent primary amine nucleophilicity meets morpholine’s solubilizing character. Some customers automate derivatization of the amino group to present multiple possible handles for cross-coupling, amidation, or urea bond formation—unlocking new families of functional polymers.

    Anecdotally, fine chemical firms use it as a starting point in heterocycle construction, sometimes as a nucleophile, sometimes as an end-unit. Because of its dual reactivity, it adapts to both small molecule and larger macromolecular synthesis—in fact, our records show repeat orders from laboratories pursuing either pharmaceuticals or functionalized materials.

    During conversations at industry events, colleagues regularly share that outsourcing synthesis at an early stage often introduces variability in quality, especially with more complex heterocyclic intermediates. Our own customers tell us they come back for batch-to-batch repeatability, pointing out that the extra step in process purification generated more reproducible analytical results over dozens of project runs. This feedback shapes how we design, monitor, and deliver every batch leaving our facility.

    Impacts Beyond Basic Supply

    Every batch manufactured in-house stands behind a series of choices made from sourcing to shipment. We refuse to cut corners by switching to inferior solvents or trying to increase yields at the expense of purity. Some may see this as a cost driver, but our post-market follow-ups consistently report that this approach saves time and trouble during API development or materials integration, when troubleshooting small impurities adds weeks or months to project timelines.

    Long-standing customers see value in direct lines of communication with those making the product rather than going through layers of intermediaries. We receive technical queries about solubility in non-standard solvents, reactivity in metal-mediated couplings, or compatibility with other moieties. Sourcing material from a manufacturer who handles all steps under one roof simplifies troubleshooting and shortens the product development cycle. It also enables stricter process confidentiality and intellectual property protection, topics on everyone’s mind across our customer base.

    We also maintain a responsive sample policy. Most research teams find it valuable to test pilot lots before fully committing—especially when synthetic routes remain under development. By offering technical support at all stages, we ensure customers not only get the product in spec, but have the full traceability back to raw material, a practice built from hands-on knowledge of what large pharmaceutical customers expect—and what smaller teams need for peace of mind.

    Environmental Responsibility and Worker Safety

    Running a chemical plant teaches you day by day that safety remains a matter of both culture and training. We enforce exacting ventilation and protective gear requirements for staff operating in the synthesis and isolation steps. The morpholine used in production brings unique exposure hazards; over the years, we have overhauled containment and handling procedures to further limit vapor and skin contact. Several upgrades stemmed from daily walkthroughs, where line operators, not just managers, gave detailed reports on process bottlenecks or personal risks.

    We take environmental stewardship seriously. Every solvent collection and reactor wash receives attention—residues undergo separation and disposal through qualified third-party incineration or recapture, tracked by batch number. Methanol and other reaction solvents no longer reach the drain; instead, trained teams recover, distill, and inspect them for quality before considering reuse, closely monitoring for contamination.

    Our responsibility extends outside plant walls, as we provide workplace safety briefings and documentation to all shipping staff and downstream partners, ensuring logistics teams treat the product correctly from the moment it leaves our loading dock through to final delivery.

    Meeting Regulatory and Analytical Demands

    Quality management doesn’t end with the certificate of analysis. We maintain detailed batch records and keep archive samples for each production run, allowing customers to track traceability through their entire project workflow. Pharmaceutical and innovative material manufacturers often require supporting data such as stability under accelerated storage, FTIR profiles, elemental analysis, and GC-MS impurity screening. We supply each with up-to-date reports from our own lab, not just generic data sheets.

    As regulations evolve, we participate in industry groups addressing best practices for registration dossiers and impurity limits. Access to analytical data sets, raw spectra, and comparison lots remains a point of distinction for clients whose projects face intensive auditing or regulatory filings. Our commitment to transparent manufacturing practices reassures partners working within global frameworks.

    We encourage open dialogue with customers facing new technical or regulatory challenges. Our technical team regularly joins customer calls reviewing methods and proposing alternate isolation or purification strategies, especially when processes transition from bench chemistry to cGMP requirements. Our experience directly shapes the product route and final quality.

    Continuous Improvement: Learning from Experience

    Every successful product tells a story built on both challenges and victories. As new feedback reaches us, from both the global R&D community and in-house process engineers, we document learnings and revisit every step of our workflow—from the earliest reaction setup to post-market case studies. Better yields, lower impurities, less downtime in process changeover, and fewer surprises in analytical testing arise not just from theory, but by finding what works day after day on our production lines.

    We view 3-Amino-6-Morpholinopyridine as more than a commodity. It represents collaborative work between the plant floor and the research bench. Our drive for improvement grows not from outside pressure, but from understanding directly how product consistency, reliable supply, and documented quality impact the researchers and innovators taking our building blocks to new heights.

    Our approach relies on deep process knowledge, rigorous in-house testing, and a willingness to invest in the tools that make a difference over hundreds of runs. Each request for a new analysis, special packaging, or technical consultation feeds back into ways we fine-tune the product. This ongoing cycle builds trusted relationships, and more importantly, supports the crucial innovations downstream—where a reliable intermediate often spells the difference between a project’s success or setback.

    Partnering for Success

    Our view comes from the ground up: the daily routines, the painstaking record keeping, and the practical decisions that define excellent chemical manufacturing. For those who choose to work directly with a producer, the difference comes clear in support, in responsiveness, and in the integrity of every shipment. Our commitment to delivering 3-Amino-6-Morpholinopyridine at the highest quality grows directly from the pride we take in seeing our product play a part in breakthroughs across pharmaceuticals, materials science, and beyond.

    Those entering new fields or scaling up proven routes see the benefit of dealing directly with the teams who developed, produced, and tested the product at every step. We welcome the technical questions, the requests for custom specification, and the open sharing of results that make the product and its downstream applications stronger. Through shared knowledge and practical attention, we continue improving our process, ensuring every customer receives not just a raw material, but an advantage shaped by experience from those who make it every day.