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1,4-Dibromotetrafluorobenzene

    • Product Name 1,4-Dibromotetrafluorobenzene
    • Alias 1,4-Dibromo-2,3,5,6-tetrafluorobenzene
    • Einecs 210-839-0
    • 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

    155505

    Name 1,4-Dibromotetrafluorobenzene
    Cas Number 630-37-1
    Molecular Formula C6Br2F4
    Molecular Weight 309.87 g/mol
    Appearance White to off-white crystalline powder
    Boiling Point 226-230 °C
    Melting Point 101-104 °C
    Density 2.25 g/cm³
    Solubility In Water Insoluble
    Synonyms p-Dibromotetrafluorobenzene
    Ec Number 211-138-9
    Pubchem Cid 12022
    Smiles C1(=C(C(=C(C(=C1F)Br)F)Br)F)F

    As an accredited 1,4-Dibromotetrafluorobenzene 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 25 grams, tightly sealed, with a white screw cap and chemical hazard labeling for 1,4-Dibromotetrafluorobenzene.
    Shipping 1,4-Dibromotetrafluorobenzene is shipped in tightly sealed containers, protected from moisture and incompatible substances. It must be handled as a hazardous chemical, typically under UN number 3077 (Environmentally hazardous substance, solid, n.o.s.). Transport follows all relevant local, national, and international regulations to ensure safe and secure delivery.
    Storage 1,4-Dibromotetrafluorobenzene should be stored in a tightly sealed container, in a cool, dry, well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizing agents. Keep the storage area free from moisture and sources of ignition. Ensure proper labeling and use secondary containment to prevent leaks or spills. Wear appropriate personal protective equipment when handling.
    Application of 1,4-Dibromotetrafluorobenzene

    Applications of 1,4-Dibromotetrafluorobenzene in Industrial Manufacturing

    As an established manufacturer, we supply 1,4-Dibromotetrafluorobenzene to innovative companies operating at the forefront of specialty chemical production. This intermediate plays a vital role in several defined industrial sectors where strict quality and compliance standards dictate formulation, process integration, and application. Below we outline key real-world downstream uses, based on proven industry requirements and measurable manufacturing outcomes.

    1. Synthesis of Advanced Liquid Crystal Monomers for Display Technology

    Manufacturers depend on this halogenated aromatic compound when building high-performance liquid crystal monomers for use in LCD and OLED panels. Its molecular structure allows for introducing both fluorine and bromine functionalities into core liquid crystal structures, enhancing electro-optical characteristics and stability. This specialty intermediate enters at the early monomer synthesis stage, before downstream polymerization and purification processes that culminate in liquid crystal mixtures for display technology.

    Industry compliance standards

    • IEC 61290-1-3 (Optical amplifiers – Performance specification)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances in Electrical and Electronic Equipment)
    • ISO 9001:2015 (Quality management systems for specialty chemical manufacturing)
    • JIS C 6104 (Japanese LCD quality assurance standards)

    Typical usage ratio

    • 5–18% of the core monomer formulation mass, depending on target birefringence and viscosity specifications. Process engineers fine-tune dosage to meet specific response time and temperature stability targets.

    Downstream process integration

    • Early-stage inclusion during organic synthesis of liquid crystal monomeric building blocks, typically via transition-metal-catalyzed cross-coupling or nucleophilic substitution; followed by integration into multi-component mixture formulation prior to device encapsulation.

    Final product types

    • Twisted Nematic (TN) LCD panels
    • In-Plane Switching (IPS) displays
    • Active Matrix OLED (AMOLED) screens
    • High-contrast medical or industrial imaging displays

    2. Manufacture of Fluorinated Aromatic Polymers for High-Performance Insulation Materials

    Chemical manufacturers leverage this intermediate in the production of fluorinated aromatic polymers used for specialized electrical insulation and cable jacketing. The introduction of both bromine and fluorine atoms contributes to enhanced flame retardancy and thermal stability, meeting the stringent safety and performance standards required in advanced electronic, automotive, and aerospace components.

    Industry compliance standards

    • UL 94 (Tests for Flammability of Plastic Materials for Parts in Devices and Appliances)
    • IEC 60332 (Tests on Electric and Optical Fibre Cables Under Fire Conditions)
    • ASTM D2863 (Oxygen Index of Plastics)
    • REACH Regulation (EC) No 1907/2006

    Typical usage ratio

    • 3–12% by weight in polymer backbone design, with actual value set by end-use flame retardancy requirements and desired dielectric strength.

    Downstream process integration

    • Incorporation at the copolymerization or polycondensation phase, where it defines halogen content and cross-link density; subsequent compounding and extrusion to yield final insulation grades.

    Final product types

    • High-frequency coaxial cables
    • Printed circuit board (PCB) laminates
    • Wire and cable insulation jackets for aerospace or automotive harnesses
    • Thermally-resistant molded electronic enclosures

    3. Intermediate in Agrochemical Active Ingredient Synthesis

    Producers of specialty crop protection agents utilize this compound as a precision halogenating intermediate for constructing select fluorinated benzenoid agrochemical actives. The dual halogen substitution pattern facilitates the synthesis of molecules that demonstrate controlled environmental persistence and strong target binding profiles, supporting modern agricultural yield improvement while complying with regulatory requirements for minimized off-target impact.

    Industry compliance standards

    • Food and Agriculture Organization (FAO) Specification for Plant Protection Products
    • European Union Regulation (EC) No 1107/2009 (placing plant protection products on the market)
    • OECD Test Guidelines for Environmental Fate and Toxicity
    • China GB 2763 - Maximum Residue Limits for Pesticides in Food

    Typical usage ratio

    • Typically 8–20% of the total input for halogen source in targeted synthesis pathways, determined by stoichiometric needs of the subsequent coupling or substitution reaction and yield targets for actives.

    Downstream process integration

    • Integration at the stage of aromatic substitution or as a building block for heterocyclic ring closure, followed by purification, formulation, and final blending steps before packaging of single- or multi-active products.

    Final product types

    • Fluorinated herbicidal actives (e.g., for grass and broadleaf control)
    • Systemic insecticidal intermediates
    • Specialized pre-emergent or post-emergent crop protection formulations
    • Seed treatment compounds

    4. Intermediate for Pharmaceutical API Synthesis—Fluorinated Aromatic Drug Building Blocks

    In pharmaceutical active ingredient production, this compound acts as a synthetic staple for constructing organofluorine scaffolds found in advanced APIs. The interplay of the dibromo and tetrafluoro functionalities allows medicinal chemists to introduce selectivity and metabolic stability, key attributes in late-stage drug design and patent-protected small molecule therapeutics.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • EU GMP Volume 4
    • U.S. Pharmacopeia (USP) Monograph Guidance relevant to specific drug candidates
    • EDQM CEP (Certificate of Suitability to the Monographs of the European Pharmacopoeia)

    Typical usage ratio

    • Ranges from 2–10% of mole input within multi-step synthesis, adjusted based on the target route, yield optimization, and impurity profile control for each specific API candidate.

    Downstream process integration

    • Entry into the active ingredient synthesis as a halogenated aromatic precursor during either coupling, dehalogenation, or substitution steps; intermediate is consumed before final purification, crystallization, and rigorous batch releasing.

    Final product types

    • Fluorinated kinase inhibitors
    • Psychoactive small molecules with fluorinated aromatic cores
    • Orphan drug candidates for rare diseases with strict purity limits
    • Imaging agent precursors for PET diagnostics
    Free Quote

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