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2-Chloro-6-Fluorobenzylamine

    • Product Name 2-Chloro-6-Fluorobenzylamine
    • Alias 6-Fluoro-2-chlorobenzylamine
    • Einecs 629-870-2
    • 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

    673277

    Name 2-Chloro-6-Fluorobenzylamine
    Cas Number 85118-33-8
    Molecular Formula C7H7ClFN
    Molecular Weight 159.59
    Appearance Colorless to pale yellow liquid
    Purity Typically ≥98%
    Solubility Soluble in organic solvents
    Smiles Clc1cccc(F)c1CN
    Inchi InChI=1S/C7H7ClFN/c8-6-3-1-2-5(9)7(6)4-10/h1-3H,4,10H2
    Storage Conditions Store at 2-8°C

    As an accredited 2-Chloro-6-Fluorobenzylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, sealed with a tamper-evident cap, labeled with safety information, containing 25 grams of 2-Chloro-6-Fluorobenzylamine.
    Shipping 2-Chloro-6-Fluorobenzylamine should be shipped in tightly sealed containers, clearly labeled, and protected from moisture and direct sunlight. Transport under ambient temperature with proper documentation. Handle as a hazardous chemical, ensuring compliance with relevant local, national, and international shipping regulations for toxic organic substances. Use appropriate packaging to prevent leaks or spills.
    Storage 2-Chloro-6-Fluorobenzylamine should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from sources of ignition and incompatible materials such as strong oxidizers and acids. The storage area should be clearly labeled and protected from moisture. Standard safety practices, including the use of appropriate personal protective equipment, must be followed during handling.
    Application of 2-Chloro-6-Fluorobenzylamine

    Applications of 2-Chloro-6-Fluorobenzylamine in Industrial Manufacturing

    2-Chloro-6-Fluorobenzylamine serves as a key intermediate in multiple specialized chemical synthesis processes. As an original manufacturer, we supply this material for critical steps in regulated, quality-driven production pipelines across pharmaceutical, agrochemical, and advanced material sectors. The following application scenarios reflect proven downstream uses and process integrations as demanded by leading industrial customers worldwide.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Leading pharmaceutical manufacturers incorporate 2-Chloro-6-Fluorobenzylamine as a primary building block when constructing complex heterocyclic or aromatic scaffolds for patented API molecules, especially in the synthesis of antipsychotic and anticancer drug candidates. The amine’s electron-deficient aromatic ring supports regioselective coupling and N-alkylation, crucial for assembling the active backbone prescribed in modern pharmaceutical process chemistry.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Current Good Manufacturing Practices (cGMP, 21 CFR 210/211)
    • European Pharmacopoeia (Ph. Eur.) monographs for intermediate management
    • ISO 9001:2015 quality management systems

    Typical usage ratio

    • Batch inclusion at 0.1–0.4 molar equivalents relative to the main API scaffold; precise ratio determined by route selectivity and stoichiometry within multi-step synthesis plans

    Downstream process integration

    • Integration at the alkylation, amination, or reductive amination stages, following initial aromatic ring activation, and preceding final purification and crystallization steps for drug intermediate isolation

    Final product types

    • Regulated small-molecule APIs (e.g., antipsychotics, kinase inhibitors)
    • Advanced pharmaceutical intermediates for custom synthesis service providers
    • Research-grade reference substances for medicinal chemistry pipelines

    2. Agrochemical Active Ingredient Development

    Major crop protection and agrochemical formulators use 2-Chloro-6-Fluorobenzylamine as a custom amine reactant to generate herbicidal and fungicidal actives characterized by fluorinated aromatic side chains. Its role in nucleophilic substitutions and amidation chemistry aids in the construction of new-generation agrochemical actives targeting resistance management in cereal and horticultural crops.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • Regulation (EC) No 1107/2009 (EU plant protection products registration)
    • ISO 17025:2017 for laboratory quality control relevant to technical-grade actives
    • FAO/WHO specifications for pesticide technical materials

    Typical usage ratio

    • Commonly incorporated at 5–15% w/w in technical active ingredient synthesis stages, with adjustment based on targeted functional group introduction and batch yield optimization

    Downstream process integration

    • Added during condensation and amide formation steps after preparation of activated acid chlorides, preceding formulation blending into dispersible concentrates or wettable powders

    Final product types

    • Systemic and contact herbicide active ingredients
    • Fungicide technical concentrates for agrochemical brands
    • Precursor compounds for synergist or safener molecules

    3. Specialty Dye and Pigment Intermediate Production

    Manufacturers within the performance dye and pigment sector employ 2-Chloro-6-Fluorobenzylamine to impart halogen functionality into advanced organic pigment molecules. This specialty amine enables stable dye creation with enhanced solvent resistance, color fastness, and unique spectral properties required for high-value coatings and polymer coloration.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for pigment intermediates
    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) stewardship guidelines
    • ISO 9001:2015 for specialty chemicals QC
    • GHS/CLP classification and labeling

    Typical usage ratio

    • Typical introduction at 2–7% w/w of total pigment precursor mass for target halogen density in the final dye molecule; exact percentage based on chromophore design considerations

    Downstream process integration

    • Reacted during the nucleophilic substitution or azo coupling stages, enabling direct amine functionalization before pigment precursor finishing and dispersion preparation

    Final product types

    • Solvent-stable organic pigments for plastics and inks
    • High performance dyes for textile and automotive applications
    • Fluorinated specialty dyes used in electronic component labeling

    4. Fluorinated Polymer Modifier Synthesis

    Producers of high-value engineering polymers and specialty elastomers select 2-Chloro-6-Fluorobenzylamine to introduce controlled amine-capped fluorinated side chains into polymer backbone modification, promoting enhanced thermal stability, chemical resistance, and reduced polymer surface energy. Its reliable reactivity finds application in proprietary copolymerization and end-group capping for technical films and advanced coatings.

    Industry compliance standards

    • ISO 9001:2015 for quality management system in engineered polymers
    • UL 94 flammability standards for high-performance films
    • RoHS Directive 2011/65/EU for electronics-related polymer use
    • Global Automotive Declarable Substance List (GADSL) where applicable

    Typical usage ratio

    • Modifier addition at 0.25–2.0% w/w during solution or melt-phase polymerization, with ratio determined by targeted surface property requirements and end-use application

    Downstream process integration

    • Introduced after initial macromer synthesis as an end-group functionalizing agent, followed by in-situ polymeric reaction or grafting for custom material property adjustment

    Final product types

    • Fluorinated polyamide and polyurethane films for microelectronics
    • Low surface energy coatings for industrial equipment
    • Modified elastomeric seals and O-rings for aggressive chemical environments
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    Certification & Compliance
    More Introduction

    2-Chloro-6-Fluorobenzylamine: Precision for Advanced Applications

    Direct From the Manufacturer: Insights into 2-Chloro-6-Fluorobenzylamine

    Producing fine chemicals involves more than assembling reactants; each molecule we synthesize shapes the reliability and innovation in downstream industries. 2-Chloro-6-Fluorobenzylamine, known to many researchers as C6H6ClFN-CH2NH2, stands out in our portfolio for its versatility and consistent quality. Working firsthand with this compound has demonstrated both its potential and the care required during manufacture and handling. Many colleagues in the laboratory and on the production floor can point to the difference a pure lot of benzylamine derivative makes in yield and process safety.

    Understanding 2-Chloro-6-Fluorobenzylamine: Model and Specifications

    We manufacture 2-Chloro-6-Fluorobenzylamine to strict purity standards, with single-lot traceability and analytical documentation for every batch. Most of our customers in pharmaceuticals and agrochemicals request material above 98% purity, valuing the clear, free-flowing solid—sometimes a colorless or faintly yellowish oil—delivered in moisture-proof packaging. From the start of each project, control over residual solvents proves essential for predictable reaction outcomes. Low water content, defined impurity profiles, and reliable melting range contribute to stringent in-process analytics, not just a “tick box” QC document. Every drum and bottle we send out carries a story of methodical synthesis, careful workup, and repeatable results in customer labs.

    Unique Properties: Value in Targeted Synthesis

    Our plant teams quickly learned what differentiates 2-Chloro-6-Fluorobenzylamine from similar compounds. The chlorine and fluorine pattern on the aromatic ring delivers unique reactivity in coupling reactions and nucleophilic substitutions. Many alternative benzylamines behave differently under process conditions; coupling alternatives with only one halogen group, for instance, often result in unwanted side reactions and lower selectivity. We produced analogues lacking either the chlorine or fluorine, and the results spoke volumes—lower yields, troublesome downstream purification, and more process downtime. Researchers have told us that only the correct halogenated pattern guarantees the desired intermediate in their multi-step synthesis.

    Supporting Innovation in Pharmaceutical R&D

    In pharmaceutical research, reliable access to multi-functional building blocks such as 2-Chloro-6-Fluorobenzylamine streamlines the search for new molecular entities. Medicinal chemists regularly reach for this amine due to its capacity to introduce both halogen atoms into advanced candidates without extra protection/deprotection steps. This matters when time-to-lead optimization decides who will be ahead in the patent race. Over the years, we have supported projects where this compound anchors the amine segment of kinase inhibitors, small molecule antibiotics, and CNS agents. By maintaining consistent lot performance, we keep R&D teams focused on discovery instead of troubleshooting.

    Reliable Performance for Agrochemical Intermediates

    Emerging crop protection agents often rely on substitution patterns that impart soil stability and plant uptake. Experience in the agrochemical space has shown that a benzylamine core bearing both chlorine and fluorine resists environmental breakdown longer than simple mono-halogenated options. Developers use 2-Chloro-6-Fluorobenzylamine as the skeleton for selective herbicides, fungicides, and growth modulators, confident that our batches meet the residual halide and total amine content their synthesis relies upon. Small changes in impurity levels can impact toxicity and field activity, making purity control non-negotiable.

    Process Quality Rooted in Experience

    Years spent tuning the multi-stage process defining 2-Chloro-6-Fluorobenzylamine creation taught us patience. Chlorination and fluorination steps, done on large scale, pose fire and health risks few appreciate without direct involvement. Overcoming runaway exotherms during scale-up, we rebuilt portions of our reactor setup, introduced automated dosing controls, and committed to continuous operator training. Each improvement has a direct link to safer, cleaner, and more reproducible product. Random, off-the-shelf lots present serious risks to production lines, but we stand by our chain of custody from raw halogenated precursors to finished amine.

    Trace Impurities: The Difference an Extra Percent Can Make

    Quality control in fine chemical production moves beyond ticking purity on a report. Small differences in by-products—sometimes as little as 1%—change how a synthetic intermediate will behave under high temperature, moisture, or UV exposure. One batch with a slightly increased side-chain impurity caused an entire kilo-lot of agrochemical active to fail stability testing. Careful GC-MS and HPLC monitoring eliminate such surprises, but only with Method Validation tailored to this compound. Our QC team developed and routinely updates impurity thresholds after consultation with end users in both pharma and crop protection fields.

    Downstream Chemistry: Why Our Customers Choose Consistency

    Process chemists cannot afford disruptions when scaling up from gram to ton-level production. We hear from clients scaling milligrammed reactions to reactor vessels that a single off-spec batch of intermediate costs days of labor, lost solvent recovery, and sometimes months of regulatory delay. By supplying consistently pure 2-Chloro-6-Fluorobenzylamine, we help keep schedules on track. Our plant managers recall projects where only one source of impurity-free benzylamine allowed a successful GMP run; the stakes included multi-million dollar launches.

    Environmental and Regulatory Considerations

    Chlorinated and fluorinated aromatics can cause environmental concerns if not controlled through proper synthesis and disposal protocols. Our production philosophy focuses on closed-system handling, solvent recycling, and responsible waste treatment. Emissions monitoring and regular audits confirm compliance with country-specific environmental standards. In fact, achieving low-waste footprints has allowed end-users smoother product registrations in competitive global markets. Transparency in analytical documentation, backed by authentic in-plant monitoring, provides regulatory confidence for all our batches.

    Supply Chain Security in a Volatile World

    Material shortages and delays threaten business continuity. Over the last five years supply chain interruptions—from solvent scarcities to transport strikes—have hit many chemical producers. Planning years ahead, we partner directly with upstream halide suppliers, maintain multi-month safety stocks, and never rely on single-source intermediates. Experience during the COVID-19 pandemic reinforced the need for buffer stocks and flexible logistics. Communicating real lead times and avoiding overpromising distinguishes a reliable manufacturer from intermediaries who simply seek to fill orders.

    Feedback-Driven Process Improvement

    Every change in plant procedure, whether it’s a tweak in crystallization protocol or a shift in packaging, grows out of conversations with research chemists, process engineers, and QA specialists. The information we receive from customer performance studies—sometimes just a line about chromatographic retention, sometimes a full impurity trending report—shapes how we update workflows. For example, one customer’s request for less glass residue drove us to adopt a new filtration regime, reducing particulate contamination across all lots. These ongoing relationships have done more to improve product quality than any top-down metric.

    Adapting Product Form to Customer Needs

    Not all applications need the same material format. Some scale-up chemists prefer 2-Chloro-6-Fluorobenzylamine as a solid, others as an oil. By controlling storage and transport conditions, we deliver material that meets real-world requirements. Efforts in packaging integrity—foil-laminate pouches or light-protective drums—came from years of dealing with air- and light-sensitive stocks in high-humidity climates. This hands-on experience taught us that different storage environments, from tropical shipping routes to cool-temperature R&D fridges, demand specific packaging strategies for each lot.

    Comparison to Other Benzylamines: What Really Matters

    Chemically, 2-Chloro-6-Fluorobenzylamine is not just “another” substituted benzylamine. Customers who experimented with similar compounds lacking dual halogenation reported poorer reactivity in nucleophilic aromatic substitution and a much less predictable conversion rate in amide couplings. The dual halogen pattern boosts both reactivity and the ability to later introduce further functional groups, key in multi-step syntheses requiring orthogonal protection or late-stage diversification. We have seen that other variants, like 2-chlorobenzylamine or 4-fluorobenzylamine, require extra steps and longer purification methods, adding both cost and time for every kilo synthesized.

    Bridging Lab and Plant: Commitment to Scalability

    Lab-developed molecules sometimes fail to translate at industrial scale. Years spent moving from bench to reactor have shown us where pitfalls develop—temperature gradients, slow exotherms, stirring inefficiencies, and bottlenecks in work-up and isolation steps. Our in-house scale-up team works alongside process engineers and pilot plant technicians, conducting trial runs before official production. By investing upfront in engineering studies, we sidestep common reasons for production slowdowns such as filter clogging or headspace contamination. Consistent batch yields and manageable waste profiles mean technicians and operators can predict work time and avoid overtime hang-ups.

    Applications Beyond Pharma and Agrochemicals

    Although most of our output supplies pharmaceutical and agricultural innovators, the versatility of 2-Chloro-6-Fluorobenzylamine sees it adopted in specialty chemicals, dyes, and polymer synthesis. In the electronics sector, the combination of halogenated aromatic rings and amine functionality allows for use in the creation of advanced materials with unique thermal or electrical properties. Feedback from small-scale electronics researchers and pigment formulators influenced our impurity spec and color standard for shipments destined for sensitive optical or thin-film applications.

    Safety and Handling Insights Drawn from Daily Use

    Hazards in handling halogenated amines go beyond what an MSDS says. On the ground, even experienced operators misjudge vapor pressure or underestimate the need for personal protective equipment when transferring bulk quantities. Installing point source ventilation, in-line scrubbers, and batch-wise handling protocols cut down on incidents. Lessons from a near-miss involving accidental cross-contamination sparked further training in material segregation, and we now regularly rotate safety responsibilities to encourage broader team expertise.

    Continuous Learning: New Frontiers in Synthesis

    A chemical manufacturer advances only through adaptation. Each discovery in halogenation catalysis, solvent replacement, or green chemistry methods gets trialed through our process improvement teams. Transitioning away from legacy solvents, we have pushed process intensification efforts with high-efficiency catalytic reactors. Continuous flow setups have, in some cases, cut cycle times for 2-Chloro-6-Fluorobenzylamine production by 35%. These changes preserve both operational safety and environmental responsibility, demonstrating our investment in sustainable manufacturing without compromising batch purity.

    Engagement with Academic and Industrial Partners

    We maintain ongoing projects with universities and industrial R&D groups. Contributions include co-developing new amine-coupling routes, supporting filings for process patents, and validating intermediates for active pharmaceutical ingredient registration. In collaborative trials, batch-to-batch reproducibility and transparency in analytical reporting have built long-term confidence. Partners rely on our technical staff for troubleshooting advice, EC approval support, or new route exploration, further deepening our technical knowledge base.

    Anticipating Future Developments in Benzylamine Chemistry

    Shifts in regulatory frameworks and customer demands continually reshape what is expected from specialty chemical suppliers. Trends toward lower residual solvent limits, drive for sustainable starting materials, and initiatives to minimize halogenated waste all impact 2-Chloro-6-Fluorobenzylamine production. We track updates in European and North American substance restrictions and adjust synthetic flowsheets to ensure downstream compliance. A new pilot project with bio-based feedstocks may offer viable green pathways for next-generation aromatic amine production.

    Final Thoughts from the Manufacturing Floor

    Producing 2-Chloro-6-Fluorobenzylamine combines technical skill, regulatory insight, and a commitment to partnership with downstream innovators. Those who depend on our material do so because quality cannot be left to chance. With every campaign, our staff reinforces the standards that define responsible manufacturing: analytical thoroughness, environmental stewardship, and continuous improvement. Years at the reactor teach what no catalog entry or datasheet can—real-world chemistry depends on trust, adaptability, and a willingness to listen as much as to lead.