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2-Chloro-3-Fluorotoluene

    • Product Name 2-Chloro-3-Fluorotoluene
    • Alias 2-Chloro-3-fluoro-1-methylbenzene
    • Einecs 626-341-1
    • 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

    192954

    Name 2-Chloro-3-Fluorotoluene
    Cas Number 204939-85-5
    Molecular Formula C7H6ClF
    Molecular Weight 144.58
    Appearance Colorless to pale yellow liquid
    Boiling Point 162-164 °C
    Melting Point -14 °C
    Density 1.25 g/cm3
    Refractive Index 1.525
    Flash Point 52 °C
    Solubility Insoluble in water; soluble in organic solvents
    Smiles CC1=C(C(=CC=C1)Cl)F
    Purity Typically ≥98%
    Synonyms 2-Chloro-3-fluoromethylbenzene
    Storage Conditions Store at room temperature, in a tightly closed container

    As an accredited 2-Chloro-3-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 containing 100 mL of 2-Chloro-3-Fluorotoluene, tightly sealed, labeled with hazard warnings and chemical details.
    Shipping 2-Chloro-3-Fluorotoluene is typically shipped in sealed, chemical-resistant containers to prevent leaks or contamination. It should be packaged and labeled in accordance with local and international hazardous material transport regulations. The product must be handled with care, kept away from heat and ignition sources, and transported by approved carriers.
    Storage 2-Chloro-3-fluorotoluene should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Store at room temperature, and ensure proper chemical labeling. Avoid unnecessary handling; use spark-proof tools and explosion-proof equipment where necessary.
    Application of 2-Chloro-3-Fluorotoluene

    Applications of 2-Chloro-3-Fluorotoluene in Industrial Manufacturing

    As the primary manufacturer of 2-Chloro-3-Fluorotoluene, we supply this high-purity intermediate to specialized customers operating in several advanced chemical sectors. Our material supports process innovation and product reliability in downstream formulations, with controlled specifications to address individual requirements across regulated industries. Below, we outline the principal end-use scenarios documented in our commercial practice, including the defining technical and regulatory elements critical to B2B partners’ compliance, production, and quality management.

    1. Pharmaceutical Intermediates: Synthesis of Fluorinated Active Ingredients

    Major pharmaceutical companies use this compound in small-molecule synthesis, particularly where selective aryl halides are required as core scaffolds for cardiovascular or CNS APIs. Process chemists introduce it during early-stage Grignard or Suzuki coupling reactions to yield advanced building blocks, allowing precise placement of functional groups in patent-protected molecules. Its inclusion in regulated pharma manufacturing has set specific expectations for contaminant control, documentation, and downstream traceability.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) specifications on starting materials
    • US FDA 21 CFR Part 211 (cGMP for Finished Pharmaceuticals)
    • Chinese Pharmacopoeia (ChP) requirements for drug intermediates

    Typical usage ratio

    • 5–20% w/w relative to the limiting intermediate depending on target molecule’s molar demand
    • Adjusted according to high-yielding reaction demands; stoichiometry set per process validation report

    Downstream process integration

    • Charged into N-alkylation or C-aryl coupling stages following solvent pre-conditioning
    • Subjected to batch quality monitoring during multistep organic synthesis (reactor scale-up)

    Final product types

    • Specialty cardiovascular medications
    • CNS drug intermediates (e.g., selective serotonin reuptake inhibitors precursors)
    • API candidates targeting patent extensions

    2. Agrochemical Synthesis: Advanced Herbicide and Fungicide Intermediates

    Agrochemical manufacturers employ our compound as an aryl halide starting material for the construction of advanced pesticide molecules. It integrates into bromination or amination routes to achieve selective fluorinated aromatic rings indispensable in the synthesis of modern herbicides and fungicides. Precision in halogen balance and impurity suppression is strictly monitored as part of global regulatory alignment and field safety data requirements.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for Fine Chemicals
    • FAO/WHO Specifications for Agricultural Pesticide Ingredients
    • REACH (EC) No 1907/2006 for intermediates in Europe
    • China GB/T 1600 Agrochemical Production Standards

    Typical usage ratio

    • 2–10% by mass in bromination/amination lines depending on synthesis route
    • Determined by stoichiometric calculation for target herbicide structural analogs

    Downstream process integration

    • Added to stepwise aromatic substitution under controlled temperature and agitation
    • Monitored for conversion via HPLC/GC, with downstream fraction isolated by column chromatography

    Final product types

    • Selective pre-emergence herbicides (e.g., fluorinated anilide derivatives)
    • Systemic triazole fungicides precursor compounds
    • Post-patent agrochemical actives with improved environmental profiles

    3. Liquid Crystal Display (LCD) Material Intermediates

    Producers of advanced liquid crystal materials integrate this specialty halogenated aromatic in the design of high-contrast LCD mixtures for consumer electronics. The aromatic ring’s substitution pattern confers controlled dielectric and optical properties required for thin-film transistor LCD performance. High-purity requirements and stringent process audits form core elements in qualifying our material for embedded electronics supply chains.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) for hazardous substances in electronics
    • IEC 61249 standards for electronic component raw materials
    • ISO 14001 for Environmental Management in chemical processing
    • IECQ QC 080000 (Hazardous Substance Process Management)

    Typical usage ratio

    • 0.5–5% by weight within proprietary multi-component LC blends
    • Dosing optimized per dielectric anisotropy and birefringence target in display model

    Downstream process integration

    • Dissolved in LC precursor blends before high-vacuum distillation
    • Homogenized with chain-elongated biphenyls during thin-film precursor mixing

    Final product types

    • High-definition TFT-LCD panels
    • Specialty mobile device display substrates
    • Color-shift compensation films for professional monitors

    4. Advanced Dyes and Pigment Manufacturing

    Industrial dye-makers rely on the reactivity of this compound to construct specialty fluorinated aryl moieties for high-performance pigment intermediates. Through Regio-selective halogen exchange or coupling protocols, the compound enters into pigment backbone construction, delivering unique hues and improved lightfastness. Regulatory adherence, particularly concerning halogen content and impurity levels, remains central during both pigment and downstream textile or plastics certification.

    Industry compliance standards

    • OEKO-TEX Standard 100 for dye material safety in textiles
    • EN 71-3:2019 (Toy Safety for Pigments)
    • EC Regulation 1907/2006 (REACH) Annex XVII – restricted aromatic amines
    • ISO 18451 Pigments and Extenders Terminology

    Typical usage ratio

    • 1–8% by weight in coupler stages of pigment formulation
    • Proportion engineered to adjust chromophore density and final spectral properties

    Downstream process integration

    • Reacted in halogen-exchange or azo coupling reactors at pigment precursor stage
    • Addition monitored by TLC/HPLC for quality control of shade and purity

    Final product types

    • Fluorinated organic pigments for plastics
    • Colorfast fiber-reactive dyes
    • Special-effect masterbatch colorants for high-end consumer goods

    5. Aromatic Polymer Building Blocks

    Producers of specialty polymers incorporate this fluorinated aromatic intermediate into the backbone of high-performance materials such as polyarylene ethers and sulfone polymers. Its unique halogen substitution pattern introduces steric and electronic effects sought in polymers with enhanced chemical resistance and glass transition temperature. Careful control of raw material handling and compliance with polymer additive specificities is strictly required by downstream technical users.

    Industry compliance standards

    • UL 94 Flammability Standard for Polymer Components
    • ISO 9001:2015 for Polymer Compound Manufacturing
    • FDA 21 CFR 177 (Indirect Additives for Food-Contact Polymers as applicable to end-use)
    • REACH-compliant hazard and registration requirements for polymer intermediates

    Typical usage ratio

    • 3–12% by weight as co-monomer in polycondensation batch formulas
    • Adjusted based on target molecular weight and polymer end-use certification

    Downstream process integration

    • Fed into high-temperature polycondensation reactors as functionalized aryl halide
    • Reactive extrusion or solution polymerization with catalyst-controlled additions

    Final product types

    • High-performance thermoplastic films
    • Engineering plastics for automotive connectors
    • Specialty resins for filtration or membrane modules
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