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3-Fluoro-O-Xylene

    • Product Name 3-Fluoro-O-Xylene
    • Alias 3-Fluoro-1,2-dimethylbenzene
    • Einecs 707-151-7
    • 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
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    Specifications

    HS Code

    168328

    Chemical Name 3-Fluoro-O-Xylene
    Cas Number 4796-87-4
    Molecular Formula C8H9F
    Molecular Weight 124.16
    Appearance Colorless liquid
    Boiling Point 158-160°C
    Melting Point -35°C
    Density 1.01 g/cm3
    Refractive Index 1.506
    Flash Point 46°C
    Synonyms 3-Fluoro-1,2-dimethylbenzene
    Pubchem Cid 191726
    Smiles CC1=CC=CC(F)=C1C
    Solubility Insoluble in water; soluble in organic solvents
    Storage Temperature Store at room temperature

    As an accredited 3-Fluoro-O-Xylene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 3-Fluoro-O-Xylene is packaged in a sealed 100 mL amber glass bottle with a chemical-resistant screw cap and hazard labeling.
    Shipping 3-Fluoro-O-Xylene is shipped in tightly sealed containers, protected from light and moisture. It should be handled as a flammable liquid, kept away from heat, sparks, and open flames. Transport must comply with local, national, and international regulations for hazardous chemicals, ensuring proper labeling and documentation to guarantee safe delivery.
    Storage 3-Fluoro-O-Xylene should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizers. Store away from direct sunlight. Ensure proper labeling and keep it in a chemical storage cabinet designed for flammable liquids. Follow all safety and local regulatory requirements for storage.
    Application of 3-Fluoro-O-Xylene

    Applications of 3-Fluoro-O-Xylene in Industrial Manufacturing

    3-Fluoro-O-Xylene serves as a key chemical intermediate across multiple specialty industrial value chains. Our material delivers reliability and batch-to-batch consistency for advanced synthesis scenarios that require stringent quality control at each production step. The following proven application tracks illustrate its concrete role and integration in actual downstream markets.

    1. Agrochemical Active Ingredient Synthesis

    Major agrochemical producers use 3-Fluoro-O-Xylene as a functional building block during synthesis of certain fluorinated herbicide and fungicide actives. During multi-step synthesis, its ortho-fluorine substituent offers controlled reactivity toward selective halogenation and subsequent transformations. Manufacturers regulate purity and residual solvents throughout the chain, ensuring regulatory-compliant actives for crop protection formulations.

    Industry compliance standards

    • REACH (EC 1907/2006) registration and evaluation for raw material traceability
    • ISO 9001:2015 for quality management in agrochemical raw materials
    • EU Regulation (EC) No 1107/2009 on pesticide active substance approval
    • FIFRA compliance for USA export markets

    Typical usage ratio

    • 0.8–1.3 molar equivalents as a coupling or starting intermediate; process chemists may adjust loading to optimize conversion and minimize impurities

    Downstream process integration

    • Reactant charge during Friedel-Crafts alkylation, selective fluorination, and directed ortho-metalation synthesis stages
    • Supports synthesis steps prior to cyclization or further functional group introduction
    • Critical in achieving target organofluorine scaffold

    Final product types

    • Triazole-based fungicide actives
    • Fluorinated phenoxy herbicides
    • Selective insecticides for specialty crops
    • Active ingredient intermediates for further downstream elaboration

    2. Pharmaceutical Intermediate Production

    In pharmaceutical fine chemical manufacturing, 3-Fluoro-O-Xylene functions as a targeted intermediate in the synthesis of complex heterocyclic scaffolds used for antihypertensive and CNS-active compound production. The presence of both methyl and fluorine substituents enables regioselective aromatic substitution, providing reliable access to pharmaceutical key intermediates under GMP-compliant operations. Traceability and impurity control meet stringent API precursor requirements.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practices for Active Pharmaceutical Ingredients
    • USP–NF monograph reviews for residual solvents and related substances
    • EDQM CEP for use as an advanced intermediate
    • DMF (Drug Master File) submission protocols for regulated markets

    Typical usage ratio

    • 0.95–1.1 equivalents based on downstream step requirements; specific charge determined by pharmaceutical route optimization and waste minimization strategy

    Downstream process integration

    • Charged as starting aromatic substrate for Suzuki or Buchwald-Hartwig cross-couplings
    • Subjected to nitration, halogen exchange, or oxidative coupling reactions
    • Forms core structure for later stage pharmaceutical intermediate elaboration

    Final product types

    • Antihypertensive API intermediates
    • Benzyl-fluoro pharmaceutical building blocks
    • CNS-active compound scaffolds
    • Fluorinated aromatic amines for downstream drug synthesis

    3. Specialty Polymer Modification

    Advanced material companies incorporate 3-Fluoro-O-Xylene into synthesis lines for high-performance specialty polymers, especially where thermal stability or hydrophobicity is required. By introducing the fluorinated aromatic core, manufacturers tailor properties in electronic encapsulants, protective coatings, and engineered plastics designed for automotive and electronics. Strict control over residual monomers and consistent reaction parameters are maintained to conform with high-end material standards.

    Industry compliance standards

    • RoHS 2011/65/EU for electronics application materials
    • UL 94 flammability standards for plastics
    • ISO 14001 for environmental management during polymerization
    • ISO 10993 for biocompatible plastics where applicable

    Typical usage ratio

    • 3–15% by weight as a comonomer or specialty chain modifier; ratio depends on targeted mechanical and chemical properties

    Downstream process integration

    • Co-polymerization with acrylate or styrenic monomers via solution or bulk polymerization
    • Incorporation during melt processing for thermoplastic applications
    • Used in pre-polymer mixtures for electronic resin formulations

    Final product types

    • Electronic-grade encapsulant polymers
    • High-temperature automotive interior plastics
    • Solvent-resistant protective coatings
    • Fluorinated polyesters for specialty film extrusion

    4. Advanced Dye and Pigment Synthesis

    Leading colorant manufacturers use 3-Fluoro-O-Xylene as a crucial aromatic precursor in high-performance dyes and pigments. The electronegative fluorine atom enables chromophore tuning and colorfastness improvements, particularly in azo and anthraquinone pigment classes. Processing requires tight control of substitution patterns and residual solvents to meet regulatory standards for textiles, plastics, and digital ink formulations.

    Industry compliance standards

    • EN 71-3 standard for colorant safety in toys
    • ISO 18314-1 for colorimetric quality control
    • GB 9685-2016 for food-contact pigment use (where applicable)
    • OEKO-TEX® Standard 100 for textile dye applications

    Typical usage ratio

    • 0.5–1.6 molar equivalents, depending on targeted molecular structure and chromatic properties

    Downstream process integration

    • Initial aromatic core in diazotization or coupling reactions for azo pigment synthesis
    • Introduced during Friedel–Crafts acylation in anthraquinone colorant routes
    • Precursor for halogenated chromophores with improved UV stability

    Final product types

    • High-performance printing inks for CIJ and textile digital printing
    • Automotive exterior coatings with enhanced fade resistance
    • Heat-stable plastic masterbatch pigments
    • Special effects colorants for packaging and consumer products

    5. Fine Chemical Intermediate for Liquid Crystal Compounds

    Manufacturers of liquid crystal display (LCD) materials integrate this compound as a key aromatic intermediate to achieve specific mesogenic properties in display chemicals. The fluorinated moiety adjusts dielectric anisotropy, viscosity, and response times in high-end display mixes. Facilities maintain tight batch-to-batch reproducibility and ultra-low impurity thresholds in cleanroom environments to support electronics industry QC protocols.

    Industry compliance standards

    • IPC-4101 for base materials in electronic interconnects
    • IEC 62474: Material Declaration for electronic industry chemicals
    • ISO 9001 for quality management in LC material synthesis
    • JEITA guidelines for display component raw materials

    Typical usage ratio

    • 1.4–2.2 molar equivalents, depending on the specific liquid crystal mixture composition and targeted electro-optical performance

    Downstream process integration

    • Charged as aromatic building block in cross-coupling and selective halogen-exchange steps
    • Used during the introduction of mesogenic cores in multi-step LC synthesis
    • Integrated prior to final purification and blend formulation

    Final product types

    • Twisted nematic LCD mixtures for monitors and TVs
    • Active-matrix OLED formulation intermediates
    • Advanced display-grade nematic and smectic liquid crystal blends
    • Specialty compounds for high-speed display response
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