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2-Chloro-6-Fluorotoluene

    • Product Name 2-Chloro-6-Fluorotoluene
    • Alias 2-Chloro-6-fluoro-1-methylbenzene
    • Einecs 609-043-6
    • 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

    196907

    Cas Number 1480-53-5
    Molecular Formula C7H6ClF
    Molecular Weight 144.58
    Iupac Name 2-chloro-6-fluorotoluene
    Melting Point -15°C
    Boiling Point 163-164°C
    Density 1.23 g/cm³
    Appearance Colorless to pale yellow liquid
    Refractive Index 1.528
    Flash Point 53°C
    Purity Typically ≥98%
    Solubility Insoluble in water; soluble in organic solvents

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

    Packing & Storage
    Packing Amber glass bottle, 250 mL, with secure screw cap; white label displays "2-Chloro-6-Fluorotoluene," hazard symbols, and handling instructions.
    Shipping 2-Chloro-6-Fluorotoluene is shipped in secure, sealed containers designed to prevent leaks and contamination. It is classified as a hazardous material and must be transported according to regulatory guidelines, typically in labeled packaging with appropriate safety documentation. Handling requires proper protective equipment and adherence to all relevant chemical shipping regulations.
    Storage 2-Chloro-6-fluorotoluene should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and direct sunlight. Keep it separated from incompatible materials such as strong oxidizing agents. Properly label the container and store it in accordance with local, state, and federal regulations. Use appropriate personal protective equipment when handling.
    Application of 2-Chloro-6-Fluorotoluene

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

    2-Chloro-6-Fluorotoluene serves as a critical intermediate in chemical synthesis, supporting specialized sectors including pharmaceuticals, agrochemicals, colorants, and advanced materials. Our vertically integrated manufacturing ensures consistent grade and supply for high-volume formula requirements. The following are in-depth downstream industry applications with their regulatory, formulation, and process specifics.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredients (APIs)

    Pharmaceutical companies rely on 2-Chloro-6-Fluorotoluene in the multi-step synthesis of specific APIs, particularly for selective serotonin reuptake inhibitors and CNS-active molecules. The controlled chlorination and fluorination patterns contribute directly to the pharmacophore, impacting molecular efficacy and selectivity. This material enters the pathway at early-stage condensation or metal–halogen exchange steps, and manufacturers must qualify supply according to pharmacopoeial reference standards and batch-to-batch analytical consistency. PQS system audits and traceability are mandatory throughout the production cycle, with the substance ultimately purposed for conversion into the API’s target moiety.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • Relevant monographs: USP/NF, EP (if listed as starting material)
    • 21 CFR Part 211 (GMP for finished pharmaceuticals in the U.S.)
    • ISO 9001:2015 for chemical synthesis plants

    Typical usage ratio

    • Used from 0.13 to 0.32 molar equivalents per API synthesis batch, adjusted based on molecular design and yield optimization studies
    • Precise ratio determined by downstream process stoichiometry and side-reaction profiling

    Downstream process integration

    • Loaded during initial heteroaryl halogenation or Grignard coupling reactions
    • Subjected to controlled anhydrous conditions to prevent side reactions
    • Integrated with automated reaction sequence control for reproducible output

    Final product types

    • Serotonin reuptake inhibitor actives (e.g., fluoxetine analog precursors)
    • Novel CNS agents with multi-halogenated toluene motifs
    • Anti-inflammatory drug candidates

    2. Agrochemical Synthesis for Herbicide and Fungicide Production

    Agrochemical formulators use 2-Chloro-6-Fluorotoluene as a building block in the multi-step production of complex herbicidal and fungicidal compounds. Its dual halide functionality allows for efficient downstream generation of selective active components targeting resistant weed species. The material typically reacts under biphasic catalytic conditions, serving as the core aromatic scaffold. Formulation teams must manage trace residual limits to comply with food and environmental safety guidelines. Product stewardship, as well as sustainable waste handling, remain central throughout batch operations.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH Regulation (EC) No 1907/2006 for substance registration and tracking
    • ISO 9001:2015 and ISO 14001:2015 for agrochemical production
    • Relevant maximum residue levels (MRLs) under EU Regulation (EC) 396/2005

    Typical usage ratio

    • Used at 0.09 to 0.18 molar equivalents per active ingredient batch
    • Ratio tailored based on targeted activity spectrum and substitution pattern requirements

    Downstream process integration

    • Introduced as a protected halogenated aromatic ring source
    • Reacts via nucleophilic aromatic substitution under controlled temperature and catalyst addition
    • Integrated upstream of final chlorination or etherification stages

    Final product types

    • Phenoxy-based broadleaf herbicide actives
    • Systemic grain fungicides
    • Seed treatment chemical intermediates

    3. Intermediate for High-Performance Pigment Manufacturing

    Producers of specialty colorants and pigments adopt 2-Chloro-6-Fluorotoluene as an integral raw material during the synthesis of halogenated azo and anthraquinone dyes. The unique positional substitution optimizes chromatic stability and solvent resistance in finished pigment dispersions. This intermediate enters synthetic steps involving directed halogenation, diazotization, and coupling, where process engineers meticulously monitor purity and impurity carryover. Materials undergo extensive analytical verification to ensure end pigment conformance for plastics and high-performance coatings.

    Industry compliance standards

    • EN 71-3 (Safety of Toys - migration of certain elements, for toy pigments)
    • ISO 9001:2015 for pigment manufacturing
    • Compliance with China’s GB 9685 for food contact materials (where relevant)
    • REACH Annex XVII for restricted substances in colorants

    Typical usage ratio

    • Added at 0.25–0.42 molar equivalents depending on the pigment formula
    • Adjusted according to HPLC purity analysis and pigment shade target requirements

    Downstream process integration

    • Used in the initial halogen substitution on aromatic ring frameworks
    • Purified by distillation or column chromatography prior to subsequent dye formation
    • Fed into continuous flow reactors or batch vessels for final coupling reactions

    Final product types

    • Halogenated azo pigments for plastics
    • Anthraquinone-based textile colorants
    • Special effect pigments for automotive and industrial coatings

    4. Advanced Material Synthesis for Specialty Polymers

    Manufacturers engaged in producing specialty engineering polymers utilize 2-Chloro-6-Fluorotoluene as a functional monomer precursor. Its halogen configuration enables direct substitution or cross-coupling to create high molecular-weight polymers with enhanced chemical resistance and thermal stability, serving niche sectors such as electronics and aerospace composites. Operators introduce this compound during the pre-polymerization or post-functionalization phase, where precise stoichiometry and side-product management are critical for final resin properties.

    Industry compliance standards

    • ISO 9001:2015 for quality management in polymer synthesis
    • RoHS Directive 2011/65/EU for electronic component materials
    • UL 94 (Flammability Standard for Plastics Materials)
    • REACH registration for substance traceability in polymers

    Typical usage ratio

    • Applied at 0.06–0.21 molar equivalents in targeted polymer chain extension
    • Proportion varies with chain length and targeted halogen density in the backbone

    Downstream process integration

    • Integrated during initial chain growth or aromatic ring functionalization steps
    • Processed under inert atmosphere during organometallic coupling reactions
    • Residual halides monitored via GC-MS to meet final approval thresholds

    Final product types

    • Thermally stable specialty polyesters
    • Flame-retardant polymeric films
    • Halogen-modified composite matrices for high-performance laminates
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    Certification & Compliance
    More Introduction

    2-Chloro-6-Fluorotoluene: A Closer Look From the Source

    2-Chloro-6-Fluorotoluene stands out in specialty chemical manufacturing for its distinctive chemical balance. Speaking from years of production runs and hands-on process improvements in our own reactors, this compound has become essential in several value-added chemical syntheses. The formula – C7H6ClF – marks it as both a halogenated aromatic and a toluene derivative, adding options in synthesis where selectivity and reactivity both matter. The core demand for this product comes from those working in pharmaceuticals, agrochemicals, and advanced materials, all of whom have learned to count on consistent performance batch after batch.

    Practical Experience With 2-Chloro-6-Fluorotoluene

    Production on a commercial scale has taught us more about 2-Chloro-6-Fluorotoluene than any datasheet. Real issues start at purification and stretch into safe handling from drum to reactor, every step rooted in hands-on industry experience. Unlike some halotoluenes that can veer off during storage or degrade with traces of moisture, this material remains stable under ordinary manufacturing conditions. Some batches do roll off the line with a sharp, biting odor and clarity that speaks to purity, a direct result of process control at each stage.

    Chemists, not just in process R&D but also at plant scale, look for high assay levels and tightly controlled impurity profiles. It’s one thing to hit 98% on paper, but we have invested in routine GC, mass spectrometry, and color-bench titration to make certain nothing slips through. The molecule may look simple, but the secret sits in controlling regioselectivity at the halogenation stages and securing consistent methyl placement on the ring. Multiple small differences in process set-up can affect the amount of ortho, meta, or para isomers. Our focus on reactor temperature and catalyst selection has led to a very specific fingerprint that downstream users can count on, especially when scaling up for pilot lots or full production.

    Comparative Differences: Real World Lessons

    Buyers new to substituted toluenes often ask how 2-Chloro-6-Fluorotoluene compares to its close relatives. There’s no simple one-size-fits-all answer without hands-on application and process feedback. The presence of both chlorine and fluorine on the ring pushes its reactivity into new territory. For example, while mono-chlorotoluene handles certain nucleophilic substitutions, adding the fluorine atom at the adjacent location tunes the molecule’s reactivity, offering a compromise between stability and activation. This lets the compound serve as a bridge molecule for downstream coupling or nucleophilic aromatic substitution that pure chlorinated analogs can’t manage. Fluorine’s effect on electron density means that users find it indispensable in some synthesis routes where selectivity and reaction speed matter.

    Looking at close cousins, like 2-Chlorotoluene or 6-Fluorotoluene, the unique substitution pattern of both halogens on the ring delivers site-specific functionality that single halogen systems often lack. Aromatic chemists use this property to advantage in making target molecules for pharmaceuticals where bioactivity changes dramatically based on ring substitution. Agrochemical developers see value in how this product anchors sidechains while resisting photodegradation. Those familiar with fluorinated intermediates recognize that a single atom’s movement around the ring can shift boiling point, reaction rate, or even regulatory approach by authorities tracking toxicological markers.

    Specifications: What Years of Quality Checking Reveal

    Performance in the real world often turns on strict control of certain parameters. Through direct feedback, we know that most end users focus on both purity and residue solvents above all else. Actual plant experience has shown typical material leaves our line at purity higher than 98%, though major pharmaceutical customers usually request further improved lots through another level of distillation or crystallization. Moisture content, once overlooked in early years, now stays tightly managed, never exceeding the levels that might foul downstream azo couplings or grignard-like reactions.

    Colleagues in chemical safety will appreciate that aromatic halides such as this require careful monitoring for decomposition products and pilot-scale off-gassing. Our labs have logged multiple years without deviation from quality marks, and we openly share those lab results with trusted customers when they seek batch histories. Most material exits as a clear to pale yellow liquid, free from visible solids – a visual cue of tight control during synthesis.

    Real Uses: Informed By Daily Manufacturing Challenges

    Our customers use 2-Chloro-6-Fluorotoluene for some of their most demanding applications. Medicinal chemistry teams apply it early in synthesis campaigns, counting on the stability of the substitution to minimize byproduct formation. Drug development timelines demand reliability, so every bottle represents not just finished product, but months of validated production and continuous flow improvements.

    In crop protection chemistry, this intermediate often becomes the starting point for more elaborate heterocyclic compounds, the kind that form the spine of newer fungicides or herbicides. Industrial chemists occasionally find alternate routes for dye intermediates that previously struggled with cross-coupling yields. Fluorinated toluenes also resist photo-oxidation challenges found in outdoor-exposed resins and advanced coatings.

    Few academic papers teach about the practical hurdles of large-scale halogenated aromatics, yet every real-world batch provides new data. Our own tech teams frequently run side-by-side comparisons with similar intermediates to pinpoint cost benefits or avoid process bottlenecks in their own pilot plants. Many times, the final value shows up not just in reactivity or yield but in waste reduction and reduced extraction costs in purification steps. For some clients, switching to this product from a single halogen analog cut downstream purification time down drastically, giving them faster turnaround in their own plant schedules.

    Process Efficiency: Inside Our Plant

    Consistency means everything in commercial chemistry, and years at the reactor face have made that clear. We have tuned our process trains to offer scale flexibility, plenty of pressure control, and targeted feed for both halogenation and final clean-up. We’ve incorporated in-line analytics that catch deviation before it converts a full batch to off-spec waste. Not every plant can claim that. This directly affects reliability for users, particularly those working with costly ligands or other high-value catalysts in their own synthesis. Production teams track everything, not just for compliance, but to allow proactive tweaks before trouble starts.

    Excessive impurity levels encountered in early industry-scale runs have all but disappeared as our team adopted a cycle of incremental improvements. Our unique handling protocols reduce worker exposure, and automated drum-filling stations aim to limit fugitive emissions, both contributing to lower overall risk. Years of shipping experience have shown that stainless drums hold up better for this intermediate than some lined options—details too often neglected in generic documentation but picked up quickly through routine shipment analysis. The feedback loop sharpens every facet of delivery, whether filling tank trucks for bulk chemical clients or handling lab-scale bottle jobs for specialty synthesis groups.

    Supply Challenges and Transparent Solutions

    Supply chain snags only rarely reach end users, but for those of us making the product, everything from raw material purity to global freight rates can disturb production cycles. Chlorination and fluorination reagents, if sourced poorly or delivered with off-purity specs, become the single largest cause of batch variability. We work closely with proven upstream suppliers and vet every lot before it enters live production.

    Freight and compliance rules shift constantly. Shipping hazardous materials like halogenated aromatics calls for a level of documentation and chain-of-custody few outside the plant ever see. We’ve invested in detailed MSDS alignment with customer instructions to avoid customs bottlenecks and paperwork-driven delays. For overseas clients, this attention avoids needless time lost at borders or in regulatory checks. In past years, close communication with logistics teams has prevented wasteful redistribution or costly product reshipments when direct routes become unavailable.

    Offering both drum and custom-pack sizes has required investment, yet the value shows in customer feedback. For high-purity blends, dilution and co-shipment services lower material handling concerns and waste. Some partners order pre-mixed solutions or blends, skipping several in-house steps and letting them focus on scale-up chemistry instead of solvent handling or risk-prone transfer steps.

    Environmental Commitments Based on Real Results

    Environmental impact isn’t theoretical at our plant. Waste streams from 2-Chloro-6-Fluorotoluene production receive ongoing treatment, and every improvement gets logged. Early years demanded afterburners to reduce halogenated venting. Routine checks now track carried-over residue, and we’ve retooled several pieces of equipment to lower fugitive emissions. Industrial neighbors occasionally tour our operations to benchmark their own waste reduction efforts, giving practical feedback and sharing process tweaks in return.

    Liquid waste gets staged and tested for organohalide content, never simply discarded. The shift from basic neutralization to multi-stage solvent recovery marked a major step in reducing environmental load—not because it looks good on paper, but because chemical waste that pays its way through solvent recovery suddenly becomes an asset rather than a liability. For high-volume runs, attention to batch-to-batch air monitoring has proved essential. Our plant’s sensors let us catch problems before they leave the chimney or holding tank, cutting fines and keeping compliance above regulatory minimums.

    End User Feedback: What Partners Have Taught Us

    Direct conversations with customers often highlight details missed by standard product specs. Medicinal chemists have told us batch homogeneity matters more than flashy assay numbers, and small tweaks at split-feed points made the difference for multi-gram syntheses. One client in agricultural development reported success switching to our material after dealing repeatedly with fouled distillation columns – a lesson on why trace impurity control matters at scale.

    Several firms have collaborated to co-develop pilot processes, giving us first-hand understanding of their reactor set-ups and workup protocols. Specialists in advanced coatings showed how the balance of fluorine and chlorine modulates their end product’s resistance to UV damage and chemical wear. Their feedback guided small-but-significant changes in solvent ratios and coolant schedules inside our plant, resulting in tighter boiling point control for each tanker ship-out.

    Regulatory and Compliance Insights

    Every country treats halogenated aromatics differently, and regulatory knowledge never stands still. We hold certifications for a range of compliance marks covering quality management, environmental safety, and hazardous goods handling. Our records show meticulous tracking on lot control, which enables prompt and accurate batch recall if ever necessary.

    We’ve learned strict adherence to evolving safety standards directly shapes how customers use the material in their processes. For one example, partners in regulated downstream industries such as medicine or crop protection expect transparency in impurity profiles and regulatory filings, so our compliance teams share not just basic paperwork but batch-specific data wherever requested. This gives those end users confidence to proceed with their own risk assessments and submission files.

    Product Handling and Storage Practices From First-Hand Experience

    Hands-on experience matters in storage and day-to-day usage. Over years of shipping, we’ve found 2-Chloro-6-Fluorotoluene survives best under controlled conditions, away from strong bases and oxidizers. Containers need to stay tightly sealed, and regular checks on seals or closures have saved plenty of material from costly evaporation losses. Site audits and training have shaped our protocols in drum and tote handling to cut down accidents and avoid off-gassing.

    Temperature and light management both hold real significance. Extended exposure to high heat or sunlight can shift color or trigger minor breakdown, so we’ve modified warehouse layouts and taught all operators to watch for warning signs early. When product needs long-term storage, we rely on cool, dry, and dark spaces—just basic lessons reinforced by actual plant incidents and resolved through hands-on changes.

    Pushing Innovation in the Field

    Innovation doesn’t just happen in the lab; it arises from troubleshooting and production line recalibration. Every cycle challenges us to shave minutes off batch run times and grams off impurity load. Adaptive automation and real-time analytical feedback let us tune production toward what customers say matters most. Investments in new distillation technology, more sensitive GC equipment, and improved chemical feed systems all came from direct talking-points with frequent buyers of 2-Chloro-6-Fluorotoluene.

    We’ve kept records on how adjustments affect final utility, and that history shortens start-up cycles for customers ramping up new processes. Periodic plant audits and side-by-side reviews with downstream experts reveal untapped opportunities to align not just purity but also logistical options, from packaging to finished form. As chemistry develops, we keep improving, using lessons learned inside the plant—not simply market noise—to keep moving forward.

    What Sets This Compound Apart: Lessons Written In Practice

    Experience has shown that 2-Chloro-6-Fluorotoluene stakes out a middle-ground between single-halogen toluenes and more extensively fluorinated aromatics. Most major buyers report that optimal reactivity, controlled volatility, and manageable handling risks contribute to its favored status in multipurpose synthesis. Minimal side-product risk combined with ease of downstream modification gives it a direct edge in advanced workflow settings, the kind where every drop counts.

    Our own teams trust the product for testbed reactions before moving to larger, higher-value intermediates, and indirect customer feedback closes the loop for shared improvements. On every order, batch-to-batch reliability stands as the measure of true plant expertise. Whether for fine chemicals, molecular scaffolds, or next-generation active ingredients, real-world manufacturing teaches us that the difference is in the details—from process start to warehouse dispatch.