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2,4,5-Tribromotoluene

    • Product Name 2,4,5-Tribromotoluene
    • Alias 2,4,5-Tribromomethylbenzene
    • Einecs 253-497-3
    • 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

    227021

    Chemicalname 2,4,5-Tribromotoluene
    Casnumber 1461-26-9
    Molecularformula C7H5Br3
    Molecularweight 343.83
    Appearance White to off-white crystalline solid
    Meltingpoint 73-75 °C
    Boilingpoint 282-284 °C
    Density 2.253 g/cm3
    Solubilityinwater Insoluble
    Flashpoint 126 °C
    Refractiveindex 1.650
    Pubchemcid 19306

    As an accredited 2,4,5-Tribromotoluene 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 of 2,4,5-Tribromotoluene, sealed with a screw cap, labeled with hazard and product details.
    Shipping 2,4,5-Tribromotoluene is typically shipped in tightly sealed, chemical-resistant containers, clearly labeled with hazard information. Packaging complies with international regulations for hazardous materials transport. It should be kept away from heat, direct sunlight, and incompatible substances. Shipping documentation includes safety data sheets and relevant handling instructions to ensure safe, compliant delivery.
    Storage 2,4,5-Tribromotoluene should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Keep it away from direct sunlight and sources of heat or ignition. Properly label the container, and ensure it is kept in a designated chemical storage cabinet, following all relevant safety and local regulatory guidelines.
    Application of 2,4,5-Tribromotoluene

    Applications of 2,4,5-Tribromotoluene in Industrial Manufacturing

    As a direct producer of 2,4,5-Tribromotoluene, we supply this chemical to specialized sectors requiring high-purity halogenated aromatic compounds. The unique molecular structure supports demanding synthesis processes where precise halogen content, batch consistency, and strict regulatory compliance remain critical for downstream manufacturing. Below, we detail application scenarios based on global industry practice.

    1. Advanced Agrochemical Synthesis

    Producers in the crop protection sector use 2,4,5-Tribromotoluene as a key intermediate for synthesizing complex herbicide precursors and selective pesticides. The material delivers bromine atoms effectively during multi-stage halogen substitution reactions, which form core components of many modern agrochemicals. Our technical teams collaborate with formulating chemists to match each batch specification to documented industry requirements, ensuring reliability in scale-up and reproducibility during regulatory validation processes.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management Systems for Manufacturing)
    • REACH (EC) No 1907/2006 for chemical safety in the EU
    • US EPA TSCA (Toxic Substances Control Act) registration
    • FIFRA (Federal Insecticide, Fungicide, and Rodenticide Act) for downstream products

    Typical usage ratio

    • Applied within 0.7–3.5% by mass relative to total reaction mixture
    • Formulators adjust ratio based on targeted molecular scaffold and alternative halogenated intermediates

    Downstream process integration

    • Feeds into halogen exchange or coupling steps within catalyst-driven synthesis train
    • Refined on-site ahead of subsequent condensation or cyclization reactions

    Final product types

    • Selective herbicides with multi-brominated aromatic backbones
    • Pesticide actives such as bromoxylenes
    • Precursor intermediates for systemic fungicides
    • Plant growth regulator additives

    2. Pharmaceutical Intermediate Manufacturing

    Pharmaceutical research organizations and bulk drug producers utilize 2,4,5-Tribromotoluene for elaborating on bioactive molecules containing brominated aromatic rings. The compound acts as a source of regulated bromination in the synthesis of APIs where halogen position impacts pharmacological profiles. Manufacturers maintain strict validation protocols for traceability from raw material intake, as downstream processing often requires multi-step purification and chiral resolution.

    Industry compliance standards

    • ICH Q7 (GMP Guide for Active Pharmaceutical Ingredients)
    • USP/NF and Ph. Eur. monograph requirements for intermediates, if referenced in DMF filings
    • FDA 21 CFR 211 (cGMP for finished pharmaceuticals)
    • Local Drug Administration import and registration compliance

    Typical usage ratio

    • Ranges from 1.0–4.0 mol% based on API synthetic route complexity
    • Adjustments made during route scouting and risk assessment studies

    Downstream process integration

    • Supplied to bromination and Suzuki coupling stages in heterocyclic compound synthesis
    • Processed under closed handling as a starting material for further functionalization or conversion

    Final product types

    • API intermediates bearing tri-bromo phenyl motifs
    • Final APIs for CNS, respiratory, or oncology markets (after full synthesis and purification)
    • Contract manufactured reference compounds for clinical trial supply
    • Halogenated process validation standards

    3. High-Performance Flame Retardant Production

    Industrial polymer compounders and resin manufacturers introduce 2,4,5-Tribromotoluene as a brominated aromatic additive or intermediate to impart flame resistance in specialty plastics and construction materials. The material integrates through controlled batch blending, supporting compliance with fire safety standards in final goods. Adjustment of dosage and dispersal parameters relies on end-use certification protocols specific to electronics, automotive, or building applications.

    Industry compliance standards

    • UL 94 (Standard for Safety of Flammability of Plastic Materials)
    • IEC 60695 series (Fire hazard testing in electronics)
    • RoHS Directive (threshold management for hazardous substances)
    • REACH Annex XVII (restrictions for specific flame retardant classes)

    Typical usage ratio

    • Added at 0.5–2.5% by weight, depending on polymer system and regulatory compliance ceiling
    • Lower dosages applied in engineered thermoplastics meeting V-0 fire performance

    Downstream process integration

    • Compounded directly into thermoplastic resin blends during melt-mixing
    • Initiates crosslinking or grafting reactions to lock in halogenated flame retardant properties

    Final product types

    • Flame retarded polyolefin and polystyrene granules
    • Electrical and electronic device housings
    • Fire-safe construction panels and cable sheathing
    • Infusion-grade resin systems for transportation interiors

    4. Specialty Dye and Pigment Manufacturing

    Producers of high-performance dyes and organic pigments apply 2,4,5-Tribromotoluene as a halogenation agent in the synthesis of triaryl and heterocyclic colorants. The compound introduces high-density bromine atoms critical for optical density, UV stability, and color fastness. Integration within pigment manufacturing lines demands strict emission monitoring, batch-specific color quality controls, and harmonized process validation for export markets.

    Industry compliance standards

    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) guidelines
    • ISO 1248 (Pigments—determination of color strength and hue)
    • REACH Annex XVII for azo dye content and heavy metal limits
    • Oeko-Tex Standard 100 (for textile applications, if relevant)

    Typical usage ratio

    • Applied at 0.8–2.0 mol% relative to core chromophore precursor
    • Adjusted based on required color intensity, hue shift, and substrate binding needs

    Downstream process integration

    • Feeds chemical synthesis during bromination or acylation of arylamine intermediates
    • Supports coupling reactions generating high-purity pigment lattices

    Final product types

    • High-weatherability halogenated organic pigments
    • Industrial dyes for plastics and high-value inks
    • Specialty textile or automotive coating colorants
    • UV-stable graphic pigment concentrates
    Free Quote

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