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5-(Aminomethyl)-2-Chloropyridine

    • Product Name 5-(Aminomethyl)-2-Chloropyridine
    • Alias AMCP
    • Einecs 629-449-9
    • 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

    467289

    Chemical Name 5-(Aminomethyl)-2-chloropyridine
    Molecular Formula C6H7ClN2
    Molecular Weight 142.59 g/mol
    Cas Number 86604-75-3
    Appearance White to off-white solid
    Melting Point 79-83°C
    Solubility Soluble in water and organic solvents
    Purity Typically ≥98%
    Storage Conditions Store at 2-8°C, keep container tightly closed
    Synonyms 2-Chloro-5-(aminomethyl)pyridine
    Smiles C1=CC(=NC=C1CN)Cl
    Inchi InChI=1S/C6H7ClN2/c7-6-2-1-5(3-8)4-9-6/h1-2,4H,3,8H2

    As an accredited 5-(Aminomethyl)-2-Chloropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 500 grams of 5-(Aminomethyl)-2-Chloropyridine is supplied in a sealed amber glass bottle with a tamper-evident screw cap.
    Shipping 5-(Aminomethyl)-2-Chloropyridine is shipped in tightly sealed containers, compliant with chemical safety regulations. It is typically transported via ground or air as a hazardous material, requiring appropriate labeling and documentation. Ensure storage in a cool, dry place, away from incompatible substances, with handling by trained personnel using protective equipment.
    Storage 5-(Aminomethyl)-2-Chloropyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers. Keep at room temperature and avoid exposure to moisture. Properly label the container, and handle with appropriate protective equipment to prevent inhalation, ingestion, or skin contact.
    Application of 5-(Aminomethyl)-2-Chloropyridine

    Applications of 5-(Aminomethyl)-2-Chloropyridine in Industrial Manufacturing

    5-(Aminomethyl)-2-Chloropyridine serves as a specialized intermediate in targeted synthesis routes across pharmaceutical, agrochemical, catalyst, and pigment manufacturing. Its molecular structure enables advanced chemical modifications and high reactivity within defined industrial operations. Below, we present critical downstream industrial applications based on real-world production requirements.

    1. Pharmaceutical API Synthesis: Anti-Tubercular and CNS Agents

    This compound enters the multistep synthesis of pharmaceutical active ingredients, such as those in anti-tuberculosis (e.g., bedaquiline analogs) and CNS treatment pipelines. In these applications, it acts as a nucleophilic building block for coupling reactions and heterocycle expansion, supporting selective formation of targeted scaffolds. Manufacturing lines integrate this intermediate for both custom route development and scale-up of late-stage clinical projects, supervised under stringent qualification and analytical controls.

    Industry compliance standards

    • Good Manufacturing Practice (GMP, ICH Q7)
    • Regulation (EU) 2016/161, FDA 21 CFR Part 210/211
    • USP, Ph. Eur. reference methods for APIs
    • GHS and REACH pre-registration for intermediates

    Typical usage ratio

    • 0.9–1.2 mol per mol of target scaffold, adjusted for yield and side-product formation
    • Charge level tailored by process yield targets and impurity management

    Downstream process integration

    • Enters amidation, reductive amination, or Suzuki coupling steps after initial pyridine chlorination and methylation
    • Maintained under inert atmosphere during coupling and purification
    • QC monitoring on batch reaction kinetics and related-substance profile

    Final product types

    • Anti-tubercular API intermediates (bedaquiline, analogues)
    • Novel CNS compounds in clinical development
    • Oral tablet and injectable drug substances after downstream conversion

    2. Agrochemical Active Ingredient Manufacture: Pyridine-Based Herbicides

    Agrochemical producers draw on this chemical to construct pyridine-ring-based herbicide actives. It functions as a precursor for further amination, halogenation, and acylation, forming the core structure for select pre- and post-emergent weed control formulations. During manufacturing, the ratio and addition order require optimization for conversion and regulatory residue thresholds, especially for export-quality formulations.

    Industry compliance standards

    • FAO/WHO Guidelines for Pesticide Specifications (AGP:CP)
    • ISO 9355, ISO 25178 for technical grade actives
    • REACH Annex VII for use as manufacturing intermediate
    • OECD safety assessment protocols for environmental fate

    Typical usage ratio

    • 1.0–1.3 equivalents for final herbicide core assembly, adjusted for step yield and crop safety
    • Scale varies with technical active ingredient output, typically 5–12% of batch mass

    Downstream process integration

    • Enters heterocyclization or condensation with acid chlorides as part of multi-step synthetic schemes
    • Post-reaction quench and purification to limit trace amine residues
    • Batch management for waste minimization and solvent recovery

    Final product types

    • Pyridine herbicides (e.g., picloram, clopyralid derivatives)
    • Formulated emulsifiable concentrates and water-dispersible granules
    • Technical-grade active ingredient bulk for contract formulating

    3. Homogeneous Catalysts Preparation for Fine Chemical Synthesis

    Catalyst fabricators utilize this compound to synthesize chelating ligands or as a building block for metal complexation, especially where electron-donating pyridinyl-amino ligands are needed for cross-coupling reactions. Its integration ensures robust catalyst lifetime and selectivity profiles, supporting repeated use in fine chemical and pharmaceutical production chains.

    Industry compliance standards

    • ISO 9001-certified manufacturing systems
    • OECD GLP standards for laboratory-scale catalyst QC
    • Compliance with REACH registration and classification of specialty chemicals
    • Responsible Care program for chemical handling and waste

    Typical usage ratio

    • 5–10% molar basis relative to target metal for ligand synthesis
    • Varied addition based on required chelation strength in specific reaction types

    Downstream process integration

    • Ligand synthesis via direct amination or reductive coupling
    • Incorporation into catalyst formation reactor with transition metals (Pd, Ni, Cu)
    • Performance screening for selectivity in client-specific batch runs

    Final product types

    • Homogeneous palladium and copper catalysts for fine chemical production
    • Customized metal complexes for cross-coupling and hydrogenation
    • Batch-validated catalyst kits for contract production partners

    4. Specialty Pigment and Dye Intermediates

    Pigment and dye producers integrate this compound in the synthesis of specialty pyridine-based chromophores. Its amine and chloro substituents enable targeted azo coupling or advanced heterocyclic pigment formation. Application steps are closely monitored for impurity and colorimetric consistency per downstream textile and plastic coloring requirements.

    Industry compliance standards

    • EN 71-3:2019 for toy and textile colorants
    • OEKO-TEX Standard 100 (textile dye processing)
    • REACH Annex XVII for aromatic amines
    • ISO 787/5 for pigment purity and heavy metal analysis

    Typical usage ratio

    • 3–8% total batch by weight for pigment intermediate formation
    • Adjusted based on final shade intensity and batch color matching targets

    Downstream process integration

    • Initial step in azo coupling or cyclization with diazonium salts
    • Application in condensation and nucleophilic substitution for heterocycle construction
    • In-line spectrophotometric monitoring during pigment assembly

    Final product types

    • Nitrogen-containing specialty pigments for plastics and textile dyeing
    • High-shade azo dyes suited for technical fiber coloration
    • Color dispersions for industrial ink formulations
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    Certification & Compliance
    More Introduction

    5-(Aminomethyl)-2-Chloropyridine: A Chemist’s Perspective from the Factory Floor

    The Approach That Shapes Every Batch

    The name 5-(Aminomethyl)-2-chloropyridine points to a compound that has carved out a valuable spot in the universe of fine chemicals, especially in pharmaceutical synthesis. From our vantage point as a manufacturer, quality and reliability start long before any drum or bottle is labeled. The manufacturing hall hums with the expectation that each batch will not only meet, but exceed, what chemists and process engineers expect in their search for consistency, purity, and reactivity. Decades in the chemical business have proven that any slip in process control—any inconsistency in raw material or environmental condition—doesn’t just show up in the test results; it creates real setbacks for those relying downstream, where molecules meet innovation or life-saving value.

    Our Process: More Than a Reaction Path

    We operate in a space where 5-(Aminomethyl)-2-chloropyridine doesn’t just come from a catalog entry. Each production run starts with a controlled supply chain, with selective sourcing for our pyridine ring building blocks. The aminomethylation step—especially crucial at the 5-position—demands tight reaction temperature and timing parameters. Chlorination, if handled carelessly, scatters impurities that are stubborn to remove, so we lay out strict purification checkpoints. Through these controls, we regularly reach purity over 99%. Less than that, and we don’t ship.

    Yield optimization can look like a simple chase for numbers but, here, higher yield also cuts waste and minimizes environmental burden. With customers handling sensitive downstream reactions, especially in API intermediates or crop protection chemicals, batch-to-batch reproducibility matters just as much as price or purity. There are no shortcuts: we run validated analytical protocols—HPLC, NMR, and GC-MS—at every critical stage. Our operators know the difference a degree or two in jacket temperature or minute differences in solvent dryness can make. This hands-on vigilance has taught us that technical quality takes more than an SOP; it needs the habits of engaged technicians and chemists who treat every step as mission-critical.

    Specifications That Matter Where It Counts

    We produce 5-(Aminomethyl)-2-chloropyridine to a specification that supports core applications in pharma, agrochem, and in advanced materials research. Our most common offering appears as a pale yellow crystalline solid with a melting point between 80-85°C. Moisture content and residual solvents pull focus for contract manufacturers and scale-up pilots alike, so every lot leaves the plant with a tight moisture limit—typically below 0.3%. For organic synthesis, water often disrupts coupling reactions or degrades sensitive reactants, so we invested heavily in drying infrastructure.

    Impurity profiles aren’t something you find on every distributor’s data sheet. In practice, trace isomeric pyridines and overalkylated species can gum up cartridge purifications or produce headaches for R&D chemists. We monitor for all known byproducts down to parts per million, and transparently share these reports with our customers. For sensitive drug projects, we work up extended certificates of analysis that include not only organic impurities but also trace metals, because residual catalysis in subsequent steps could be poisoned. Our ability to control sodium, potassium, chlorine and common transition metals below 10ppm comes from years developing work-up and filtration protocols.

    Model and Packaging That Fit Genuine Needs

    We understand the importance of how chemicals arrive at our clients’ plants. Shipping a moisture-sensitive pyridine derivative in substandard packaging can ruin an otherwise perfect campaign. For laboratories, we pack in amber glass bottles flushed with nitrogen. Scale-up quantities move in lined, nitrogen-purged drums that survive even the most challenging shipping routes. Inside the manufacturing team, there’s debate and iteration over improvements—multi-layer foil liners, improved crimp seals, additional secondary desiccants for large-scale packaging. These adjustments stem from feedback on real-world conditions, such as warehouses in humid regions or long-haul transit where temperature swings are unavoidable.

    What Makes This Product Different from Similar Chemicals

    5-(Aminomethyl)-2-chloropyridine’s main distinction sits at the intersection of substitution pattern and functional group compatibility. The pyridine ring offers rich reactivity for cross-coupling and cyclization. Placing an aminomethyl group at the 5-position opens synthetic handles that 2-aminopyridines or other substituted pyridines simply can’t match. A 2-chloro substituent activates the ring for nucleophilic aromatic substitution without oversensitizing it, allowing careful, selective downstream transformations.

    Compare this to 2-chloropyridine without an aminomethyl group. That compound brings reactivity but doesn’t offer the functional group leverage—especially for coupling to aldehydes, acids, or for building heterocyclic scaffolds that underpin kinase inhibitors or anti-infective candidates. Aminomethylation at the 5-position also increases solubility without the reactivity risks seen with amines placed at more active sites. From a chemist’s perspective, this enables flexible synthetic plans—linker extension, salt formation, or selective reduction—where regioselectivity can make or break a project.

    Any production manager who’s worked with related products knows that closely related pyridines can co-elute or cross-react, raising the need for robust purification and analytical control. With our 5-(Aminomethyl)-2-chloropyridine process, trace isomer formation is a specifically monitored risk parameter, not an afterthought.

    End Uses: What Our Customers Tell Us and Teach Us

    Every project we support brings unique approaches to this molecule. In pharmaceutical research, it often serves as a building block for the synthesis of kinase inhibitor cores, neuroactive compounds, and as a versatile linker scaffold for combinatorial libraries. Chemists value the compound for its ability to anchor more complex substituents onto the pyridine ring—spanning both classic peptide coupling and more modern C–N or C–C bond-forming strategies. In the realm of agrochemicals, the same molecule forms the backbone of various fungicide and pesticide candidates, where tuning activity often means inventing new derivatives quickly from a common, robustly pure intermediate.

    For those in advanced materials, we’ve watched the compound incorporated into liquid crystals and novel polymers, where the electron-rich aminomethyl substituent tweaks electronics or binding profiles in ways simple halopyridines can’t rival. Application feedback has highlighted the difference between our product and generic lots obtained from secondary sources—higher process uptime, fewer failed purifications, and in several cases, cleaner downstream spectra that support expedited regulatory filings.

    Lessons Learned on the Manufacturing Line

    Mistakes aren’t free in chemistry. Producers who chase scale at the expense of detailed process awareness usually run into invisible costs: rejected shipments, customer complaints, failed validation runs. In our experience, tight process control during aminomethylation and control of byproduct formation pay dividends down the line. The difference between a 98% pure lot and a 99.5% pure lot can be seen in a single column purification later on, or in the reproducibility of pharmaceutical trial runs.

    Environmental and worker safety forces hard decisions on solvent selection and containment. Our team transitioned away from more hazardous solvents and expensive, hard-to-dispose work-up reagents. Every improvement requires negotiation—sometimes sacrificing a point of conversion to achieve lower emissions or higher industrial hygiene standards. Listening to operators brings out unexpected insights: vapor emissions that challenge scrubbers, cleaning loops that save precious hours between campaigns, or even the precision in weighing out a sticky intermediate. These aren’t glamorous changes, but over years they are the difference between a reliable supply chain and just another name on a list.

    Sustainability and Responsibility in Practice

    The push for green chemistry isn’t rhetorical for us. With 5-(Aminomethyl)-2-chloropyridine, we maintain a continuous process review—where solvents and energy use are measured alongside yield and cycle time. We run in closed systems to limit loss of volatile pyridine derivatives, reprocess off-cuts where possible, and pursue both in-situ reagent generation and recycling for key steps. Regulatory audits, customer questionnaires on traceability and carbon footprint, all push us to reshape old habits in production. It’s a balancing act: always optimizing, sometimes inch by inch, but with the knowledge that any improvement makes the next product and the next campaign easier on the environment and safer for the people running the lines.

    The Daily Life Behind Every Drum

    The story of 5-(Aminomethyl)-2-chloropyridine in our factory is built from more than shift logs or metric tons shipped. Any given day involves calibrating, adjusting, or refining—small things matter, like how quickly a reflux starts or how well a vacuum holds overnight purity standards. The operators learn the quirks of each piece of equipment: a slightly sluggish filter, a reactor that cools unevenly on one side, packaging lines where every additional second costs money or quality.

    We rigorously follow quality control but just as important is the knowledge transfer in the team: training new chemists on what true completion looks like on TLC, reviewing NMR splitting patterns to catch minor contamination, or interpreting LC-MS blips that might signal a hidden impurity. Each team member understands the stakes behind the consistency, not just in process, but in the final product that enables clients to reach their targets faster and with fewer distractions.

    Insights on Market Trends and Customer Demands

    Demand for 5-(Aminomethyl)-2-chloropyridine has climbed as pharmaceutical and agrochemical innovation accelerates, and more companies look for reliable sources of advanced intermediates. Many customers now request not just the base chemical itself, but support with regulatory documentation, impurity characterization, or stability data packages. The expectation is higher than ever and for good reason; every hour spent tracking down off-spec material or troubleshooting synthetic side reactions pulls attention away from primary research or manufacturing targets.

    With global supply chains stretched, customers increasingly value transparent timelines, full documentation for analytical methods, and a real sense of partnership in solving problems. We respond with regular product reviews, open-book approaches to process changes, and shared feedback on real-world application findings. Staying close to those on the research and production front lines ensures we aren’t just meeting existing standards but can anticipate the next round of customer requirements or regulatory shifts.

    Challenges Ahead and Solutions in View

    Producing such a compound at scale keeps showing us that chemistry doesn’t scale linearly. A process that works flawlessly in one reactor might throw surprises at higher loads or different agitation rates. That’s why our R&D and production managers stay in constant dialogue, running pilots with each solvent or raw material lot change, and validating that every process tweak holds up under cGMP or industrial quality scrutiny.

    Vendor management for key raw materials makes a difference. Pyridine rings and amines that seem interchangeable on paper can produce wildly different impurity profiles or color grades in practice. We learned—not always the easy way—to keep backup supply routes, verify every supplier, and constantly test for cross-contaminants that small traders might overlook.

    Anticipated changes in regulatory landscape also hover over daily operations. REACH status, updated ICH impurity guidelines, and broader process safety regulation prompt us to run mock audits and practice recalls. Each step reinforces concentration and transparency in both operations and record-keeping. By tackling these issues head-on, we remain a partner that not only ships but guides, supports, and grows with changing client needs.

    Future Directions: Investing in Continual Improvement

    Stories from customers about success with our 5-(Aminomethyl)-2-chloropyridine often spark new rounds of process investment. Greater automation in charging and reaction monitoring, better online analytics for impurity tracking, and even digital twins for scenario testing now shape our next-generation upgrades. Every cycle reinforces that the future of chemical manufacturing lies in a deep link between process data, operator know-how, and customer dialogue.

    We view our product not as a commodity, but as a milestone along the journey of discovery and development for our clients—people who tackle big questions in science, agriculture, and medicine. Making 5-(Aminomethyl)-2-chloropyridine for these innovators takes more than technical data or off-the-shelf solutions. It takes relentless attention to process, openness to feedback, a grounded approach to quality, and the day-to-day grit of manufacturing that shapes each molecule sent out into the world.