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5-Chloro-2-Fluorobenzylamine

    • Product Name 5-Chloro-2-Fluorobenzylamine
    • Alias 5-Chloro-2-fluorobenzylamine
    • Einecs 629-464-7
    • 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

    741808

    Productname 5-Chloro-2-Fluorobenzylamine
    Molecularformula C7H7ClFN
    Molecularweight 159.59 g/mol
    Casnumber 63559-87-1
    Appearance Colorless to pale yellow liquid
    Purity Typically ≥98%
    Boilingpoint Approx. 221°C
    Density 1.25 g/cm³ (approximate)
    Refractiveindex 1.556 (approximate)
    Solubility Soluble in organic solvents; limited solubility in water

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

    Packing & Storage
    Packing 250g of 5-Chloro-2-Fluorobenzylamine is supplied in a sealed amber glass bottle with a tamper-evident screw cap.
    Shipping **Shipping Description:** 5-Chloro-2-Fluorobenzylamine is shipped in tightly sealed, chemical-resistant containers under ambient conditions. It should be protected from heat, moisture, and direct sunlight. Packages are labeled according to regulatory requirements, with appropriate hazard information, and shipped via certified carriers specializing in chemical transport to ensure safety and compliance.
    Storage 5-Chloro-2-Fluorobenzylamine should be stored in a tightly closed container, kept in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Avoid exposure to moisture and direct sunlight. Handle under inert atmosphere if necessary. Ensure proper labeling and use appropriate chemical safety procedures to prevent leaks and contamination.
    Application of 5-Chloro-2-Fluorobenzylamine

    Applications of 5-Chloro-2-Fluorobenzylamine in Industrial Manufacturing

    5-Chloro-2-Fluorobenzylamine serves as a key intermediate in pharmaceutical, agrochemical, and specialty chemical sectors. Below, our technical team details industrial application scenarios based on customer formulation projects and compliance requirements.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) Synthesis

    Downstream API manufacturers incorporate 5-Chloro-2-Fluorobenzylamine during multi-step organic synthesis of specific target molecules, predominantly in the production of anti-infectives and central nervous system agents. The amine function allows coupling with acid chlorides or sulfonyl chlorides at defined synthesis stages. Rigorous compliance applies to all incoming raw materials, including analytical specifications, impurity profiling, and traceability. Lot-specific quality documents and impurity certificates remain essential throughout QA audits.

    Industry compliance standards

    • ICH Q7 – Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) General Chapter 5.12: Raw materials for the production of pharmaceuticals
    • US FDA CFR Title 21 Part 211: Current Good Manufacturing Practice (cGMP)
    • ANVISA RDC 301/2019 for APIs in Brazilian market

    Typical usage ratio

    • 0.12–0.30 molar equivalent in multi-step synthesis, depending on the desired coupling reaction
    • Adjustment required for impurity control and conversion yield optimization

    Downstream process integration

    • Added after protection/deprotection steps as an amine nucleophile
    • Participates in amidation or reductive amination reactions
    • QC sampling for limit tests prior to onward synthesis
    • Removal of secondary byproducts by phase separation or chromatography

    Final product types

    • Intermediates for anti-psychotic APIs
    • Building blocks for anti-infective agents
    • Precursors for kinase inhibitor molecules
    • Specialty CNS therapeutic compounds

    2. Agrochemical Active Ingredient Intermediate

    Agrochemical formulators utilize this benzylamine derivative for targeted synthesis of select herbicidal and fungicidal actives. It undergoes stepwise transformations like acylation and halogenation following pre-defined reaction pathways. The precise selection of this amine improves specificity in the final mode of action. QC staff focus on maintaining impurity thresholds based on ECHA requirements and customer technical agreements. Every batch involves retain sample archiving, analytical column validation, and document trails for international regulatory review.

    Industry compliance standards

    • Regulation (EC) No 1107/2009 concerning the placing of plant protection products on the market (EU)
    • ISO 9001:2015 for quality management systems in chemical production
    • OECD Principles of Good Laboratory Practice (GLP)
    • ECHA REACH Regulation (EC) No 1907/2006

    Typical usage ratio

    • 0.07–0.21 w/w in synthesis workflow for heterocyclic actives
    • Ratio based on desired yield and purity, with in-process GC verification

    Downstream process integration

    • Introduced as nucleophilic agent during early route steps aligned with process safety data
    • Monitored for exothermicity during mixing with acid derivatives
    • Sampled for residual solvent and impurity levels post-reaction
    • Transferred to solvent extraction and crystallization units

    Final product types

    • Precursors for triazole fungicides
    • Herbicidal intermediates targeting broadleaf species
    • Active ingredient scaffolds for insecticidal pyrazoles
    • Amine-based growth regulator pre-compounds

    3. Advanced Material Monomer and Modifier

    Polymer and specialty material manufacturers use this compound to introduce halogenated amine functionalities in custom resins, coatings, and adhesives. Its precise molecular structure provides enhanced chemical resistance and thermal stability to the polymer matrix. Line operators must pre-check compatibility with co-monomers and tailor addition rates based on technical datasheets. QC teams record IR and NMR spectra to confirm modification success and batch consistency. Only certified lots with full traceability enter high-spec end-use applications.

    Industry compliance standards

    • ISO 14001 for environmental management in chemical processing
    • ASTM D638 for testing tensile properties of plastics
    • RoHS Directive 2011/65/EU for hazardous substances in electrical and electronic equipment
    • UL 94 flammability standard for polymeric materials

    Typical usage ratio

    • 1–5% (by mass) as a functional monomer or modifier in mixed polymerizations
    • Adjusted by molecular weight of copolymer and desired performance attributes

    Downstream process integration

    • Blended with base monomers during polymerization charge preparation
    • Integrated in resin synthesis reactors under controlled temperature ramps
    • NIR monitoring for degree of incorporation
    • Extracted for pilot testing before scale-up

    Final product types

    • Halogenated thermosetting resins for electronics encapsulation
    • High-durability adhesive prepolymers
    • Protective surface coatings with improved chemical inertness
    • Specialty film-forming agents

    4. Custom Synthesis for Fine Chemical Production

    Fine chemical manufacturers integrate this benzylamine for client-specific building blocks, including specialty ligands, imaging agents, and reference standards. Qualification relies on batch-specific COA review, HPLC method transfer, and process mapping based on customer-supplied chemistry packages. Each production run adheres to confidentiality agreements and project-specific documentation. Analytical teams monitor storage and process stabilities for shipment to global R&D centers and pilot scale facilities.

    Industry compliance standards

    • ISO 17025: General requirements for testing and calibration laboratories
    • Responsible Care Management System (RCMS)
    • IATA/IMDG/DOT shipping regulations for fine chemicals
    • UN GHS labeling and SDS requirements

    Typical usage ratio

    • Batch size varies from gram to multi-kilogram with 0.5–2 molar equivalents
    • Customized to project scope and downstream molecule complexity

    Downstream process integration

    • Supplied as a key amine for nucleophilic substitution routes or coupling chemistry
    • Employed at step two or three in tailored synthesis
    • QC releases shipment post NMR, LC-MS, IR identification
    • Archived samples stored for traceability and repeat orders

    Final product types

    • Imaging diagnostic agents for research markets
    • Reference standards for analytical laboratories
    • Ligands for metal complexation studies
    • Custom organic synthons for diversified R&D
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    Certification & Compliance
    More Introduction

    Understanding 5-Chloro-2-Fluorobenzylamine in Chemical Synthesis

    The Consistent Role of 5-Chloro-2-Fluorobenzylamine in Industrial Chemistry

    Talking about aromatic amines, we as chemical manufacturers know firsthand how key structural nuances drive performance at scale. Among these, 5-Chloro-2-Fluorobenzylamine stands out for its versatility across pharmaceutical, agrochemical, and specialty chemical projects. Each batch we produce passes through a rigorous workflow, from raw material assessment to post-reaction purification, precisely to ensure every drum supports the exact requirements for downstream synthesis. Over the years, process chemists have seen clear differences in results when switching between amine derivatives, especially when handling aryl-substituted benzylic amines. The specific structure—chlorine at the 5-position, fluorine at the 2-position—allows tighter control over reactivity profiles compared to unsubstituted or singly substituted analogs.

    Why Specific Substitution Patterns Matter

    Once a project engineer specifies a building block like 5-Chloro-2-Fluorobenzylamine, we immediately anticipate points of concern. High purity stands at the top because any impurity in the meta or ortho positions throws off the kinetics of coupling reactions. The halogen substitution influences electron density, which in turn controls activation levels during nucleophilic or electrophilic attack. Having both a chloro and fluoro group in defined spots helps tune the amine’s chemical properties. Our customers working on heterocyclic scaffolds, for example, report that this exact arrangement supports more selective synthesis, improving final yield and cutting out side product headaches. Years of fine-tuning reactors and changing work-up strategies have taught us where poor selectivity creeps in, and which intermediates demand protective atmospheres or extra drying.

    Specifications that Count in Real-World Manufacturing

    To hit every mark, manufacturers can never relax on specifications. We commit to purity levels exceeding 98% by GC analysis, routinely confirming molecular integrity by NMR and mass spectrometry. Moisture and trace heavy metals receive ongoing scrutiny since even low ppm can poison boosted catalysts. 5-Chloro-2-Fluorobenzylamine, as we deliver it, arrives as an off-white to yellowish solid; customers expect minimal batch-to-batch color shift. For multi-kilo orders, we rely on double distillation and column chromatography, since smaller-scale crystallization doesn’t always translate upward. Solubility presents one difference for process teams: thanks to both halogen groups, this amine dissolves more readily in polar aprotic solvents than either monosubstituted or unsubstituted analogs, which can affect choice of reaction medium and wash solutions.

    Applications Beyond the Data Sheet

    In drug development circles, 5-Chloro-2-Fluorobenzylamine earns its place as a side chain precursor for a range of small molecules. Medicinal chemistry teams frequently leverage it for structure-activity relationship studies because the two halogens open functionalization routes without creating new chiral centers. We have seen routes where it acts as an anchor for urea, amide, or sulfonamide formation, each demanding its own set of reaction parameters. In crop science, formulating actives that resist bulk degradation in soil regularly hinges on the electron-withdrawing features this amine offers. The difference jumps out when switching from unsubstituted benzylamine; shelf life, metabolic fate, and even transport stability all trend favorably with the right pattern of ring substitution.

    Pragmatic Observations from the Production Floor

    Scaling up 5-Chloro-2-Fluorobenzylamine comes with a set of practical decisions. Handling highly reactive intermediates means real-world process safety always dominates our planning. The by-products formed in side reactions, especially under basic conditions, demand constant monitoring for effective waste management. Investing in real-time analytics, we've found that maintaining a low-oxygen atmosphere during synthesis lessens the formation of unwanted oxidation by-products and starts us with a cleaner crude. Materials of construction for our reactors, along with selection of liners and valves, all matter when managing halogenated intermediates—no shortcuts there. Years ago, early scaling efforts with less robust systems led to unscheduled downtimes from gasket failures and corrosion. Now, all contact surfaces feature Teflon or glass-lining, preventing contamination and extending campaign length.

    Quality Control Considerations

    Experience shows that every downstream reaction—amide bond formation, reductive amination, or palladium-catalyzed coupling—shows different tolerance to off-spec amine. That makes batch verification a core part of our operation. Chromatography for isomeric purity, Karl Fischer for water determination, and titration for amine content, these steps are non-negotiable. The challenge lies in keeping impurity profiles consistent across scale. Unlike certain bulk aromatics, the two halogen groups both resist and participate in side reactions, so even small traces of di- or trihalogenated material must be eliminated. We enforce release criteria for color, odor, and melting point, with side-by-side reference to retained standards. In our experience, cuts corners show up fastest in cross-coupling reactions, which can stall out with residual acid or base impurities.

    Logistics and Customer Impact

    Moving these shipments safely from our plant to global customers brings its own variables. As a solid, the amine handles storage and transport better than liquid analogs, standing up well to variable warehouse temperatures and minor rough handling. Still, we focus on moisture exclusion at every step. Desiccant pouches line each inner bag, and every drum receives tamper-evidence before leaving our yard. Feedback from custom API synthesis partners points to this extra care as a steady performance differentiator; returns and rejections plummet when these controls stay tight. It proves easier to maintain regulatory compliance across borders when every pack leaves our site documented with chain-of-custody and stability data. By engaging regularly with logistics providers, we've reduced shipping delays and ensured sensitive cargo reaches end users without temperature excursions or cross-contamination risk.

    What Sets 5-Chloro-2-Fluorobenzylamine Apart from Similar Amines?

    Fluorinated and chlorinated aromatic amines affect reaction sequences in ways both subtle and significant. Projects that previously used 2-fluorobenzylamine or 5-chlorobenzylamine alone often hit roadblocks around undesired side reactions or final product instability. The dual substitution in 5-Chloro-2-Fluorobenzylamine offers a stabilized framework that holds up during longer, multistep workflows. The chlorine at position five steers regioselectivity, while fluorine across the ring exerts its own electron-withdrawing effect, modulating reactivity in every subsequent transformation. The net effect? More robust intermediates, fewer surprises in scale-up, and easier purification downstream. In our practice, improvements show up in both analytical data and operational feedback—cleaner final NMR spectra, lower isolate impurity levels, and more forgiving crystallization profiles.

    Learning from Technical Setbacks

    Manufacturing never runs in a straight line. We’ve seen how even small changes in solvent choice or reaction time can swing impurity formation by a factor of ten. In early campaigns, pilot batches of 5-Chloro-2-Fluorobenzylamine occasionally came with slightly darker color or unexpected odor, pointing to ring-opened or overhalogenated by-products. These events pushed us to spend more time on in-process monitoring and pre-run reactor cleaning. Operators now adjust nitrogen sweep rates and stepwise addition speeds, preventing exotherms and local overheating. Pattern recognition, enabled by tracking years of batch data, helps spot outliers before they exit the plant. Continuous review of supplier material origin and regular method validation keep our process on track. People on the floor rely on close communication and flexible planning to work around bottlenecks, recognizing that real-world conditions seldom line up with theoretical flow diagrams.

    Environmental and Regulatory Driving Forces

    Sustainability targets have shifted how we manage halogenated amine production. Disposal of spent acids and solvent by-product streams now goes through a closed-cycle system, recovering components where possible and minimizing uncontrolled emissions. We audit each campaign for compliance with local and international guidelines, not simply to check off obligations, but to earn trust from customers who must themselves validate incoming materials. Initiatives to switch to greener reagents and low-impact solvents have shaved real points off our permitted emissions profile. In some projects, we partner with customers to recover solvent streams or offer returnable packaging, shrinking environmental impact while keeping materials safe. Continuous investment in cleaner technologies reflect a real commitment—people across the industry watch these markers when choosing supply partners.

    Market Dynamics and Feedback Loops

    Data and dialogue drive improvements just as much as internal R&D. End users of 5-Chloro-2-Fluorobenzylamine report whether syntheses run smoother, yields rise, or bottlenecks persist. Direct feedback from process engineers and lab chemists finds its way upstream into our production adjustments. If a customer notes a step fouls unexpectedly or sees stability drift, we review our own trace impurity logs, revise clean-up protocols, or adjust drying cycles. It’s a rule in our operations—never ignore the details signaled by technically skilled buyers. Many long-term partners credit this iterative loop with giving them extra confidence in sourcing challenging building blocks.

    R&D and Pathways to Future Products

    Ongoing R&D turns up possibilities for 5-Chloro-2-Fluorobenzylamine derivatives in medical imaging agents, high-performance coatings, and even as starting points for ion-exchange materials. Working directly with project leaders, we've been part of multi-phase collaborations that map out pilot routes from gram to multi-ton. In cases requiring isotopic labeling or selective deuteration, our chemists have developed stepwise synthetic modifications to the parent structure while preserving the halogenation pattern. The field keeps moving—novel ligands, crop protectants, and even polymer intermediates now trace some of their origins back to this molecule. The ability to scale these developments, maintaining purity and consistency, comes from maintaining solid core production and supporting innovation at each stage.

    Cost Considerations in Bulk and Custom Manufacturing

    Pricing pressure never disappears in chemical markets. Still, the total cost of ownership for customers using 5-Chloro-2-Fluorobenzylamine rarely reduces to the line item per kilogram. The lower rerun frequency, reduced need for intermediate purification, and resilience under variable storage conditions all impact the bottom line over time. We see procurement teams compare competing benzylic amines every budget cycle; benefit proves out over repeated campaigns where production stays on spec and downtime drops. By simplifying waste treatment and offering drum-level batch consistency, we help partner plants avoid expensive troubleshooting late in process validation. These supply chain realities shape every decision on raw material selection, production scheduling, and packaging methods.

    Insights from Cross-Industry Applications

    Although pharmaceutical routes may set the pace, discussions with electronic material firms and agrochemical producers broaden our view of 5-Chloro-2-Fluorobenzylamine’s utility. Circuit board manufacturers point to the need for precise impurity control, as even minor by-products can compromise conductivity or create unwanted signal noise. Agrochemical compounders value long shelf life and resistance to UV degradation, features that the two halogen atoms help reinforce. Over time, feedback from these varied sectors has shifted some of our upstream input controls and packaging designs. For customers with unique tech transfer demands, such as rapid scale-up or round-the-clock Just-In-Time delivery, we adapt our planning, sometimes running split campaigns for tailored logistics. This flexibility helps keep customer pipelines flowing and final products on store shelves.

    Summary of Key Differences Compared to Closest Alternatives

    The closest analogs—2-Fluorobenzylamine and 5-Chlorobenzylamine—may initially look interchangeable, but field experience proves otherwise. The simultaneous presence of fluorine and chlorine on the aromatic ring dramatically affects both chemical and physical behavior. Downstream reactions, including arylation or amide formation, frequently demand fine pH and temperature controls; here, our product displays greater robustness and predictable reaction rates. Unsubstituted benzylamines, by contrast, often degrade more quickly and produce higher levels of unidentified side products, particularly over long campaigns. Dual-substituted 5-Chloro-2-Fluorobenzylamine brings stability without sacrificing reactivity, giving R&D teams a broader window for process adjustment and reducing the frequency of failed runs. These operational benefits emerge only through repeated, high-quality manufacturing and close partnership with technical end users—a lesson borne out in every batch that leaves our facility.

    A Shared Focus on Reliability and Progress

    Every finished drum of 5-Chloro-2-Fluorobenzylamine tells the story of practical problem-solving, attention to feedback, and a relentless pursuit of both quality and application flexibility. Through years of multidisciplinary collaboration—from process chemists to logistics managers—manufacturing focus has shifted from mere scale to continuous, measurable improvement. For partners operating in regulated environments, the assurance of full analytical support, traceability, and stable supply means fewer project delays and faster speed to market. As process parameters evolve and industry standards tighten, the lessons learned through ongoing 5-Chloro-2-Fluorobenzylamine production inform not only each completed order but also set the stage for next-generation innovation and enduring sector trust.