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2,4-Dichloro-3,5-Dinitrobenzotrifluoride

    • Product Name 2,4-Dichloro-3,5-Dinitrobenzotrifluoride
    • Alias Fluorodifen
    • Einecs 221-616-6
    • 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

    264596

    Cas Number 1641-92-9
    Molecular Formula C7HCl2F3N2O4
    Molecular Weight 305.99 g/mol
    Appearance Yellow crystalline solid
    Melting Point 107-109°C
    Solubility In Water Insoluble
    Density 1.74 g/cm³
    Purity Typically ≥98%
    Synonyms 2,4-Dichloro-3,5-dinitrobenzotrifluoride; DCBTF
    Storage Conditions Store at room temperature, tightly closed, dry place
    Chemical Structure Trifluoromethyl-substituted nitro dichlorobenzene
    Stability Stable under recommended storage conditions

    As an accredited 2,4-Dichloro-3,5-Dinitrobenzotrifluoride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 500g amber glass bottle with a tamper-evident cap, labeled with hazard warnings for 2,4-Dichloro-3,5-Dinitrobenzotrifluoride.
    Shipping 2,4-Dichloro-3,5-Dinitrobenzotrifluoride should be shipped in tightly sealed, chemically resistant containers. It must be labeled as hazardous, handled according to relevant shipping regulations (such as DOT, IATA, or IMDG), and protected from physical damage. Ensure proper documentation accompanies the package, and transport is conducted by trained personnel wearing appropriate protective equipment.
    Storage 2,4-Dichloro-3,5-Dinitrobenzotrifluoride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong reducers and bases. Protect from moisture, heat, and direct sunlight. Ensure appropriate chemical labeling and secure to prevent accidental releases. Use secondary containment and keep away from food and drink sources.
    Application of 2,4-Dichloro-3,5-Dinitrobenzotrifluoride

    Applications of 2,4-Dichloro-3,5-Dinitrobenzotrifluoride in Industrial Manufacturing

    2,4-Dichloro-3,5-Dinitrobenzotrifluoride is a critical aromatic intermediate, valued for its stability and electron-withdrawing capacity, serving key roles in specialty downstream industries. As the direct manufacturer, we highlight its concrete applications across chemical sectors where performance, compliance, and precision in processing are essential.

    1. Agrochemical Active Ingredient Synthesis

    This material functions as a chlorinated nitroaromatic building block for synthesizing specific herbicide and pesticide active ingredients. Its involvement centers around nucleophilic aromatic substitution reactions to introduce bioactive functional groups, allowing downstream plants to achieve high efficacy formulations suited for resistant weed management in field crops. Attention to purity and trace contaminant levels is mandatory due to direct use in regulated agricultural formulations.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticides
    • EU Regulation (EC) No 1107/2009 for plant protection products
    • US EPA Pesticide Registration (FIFRA)
    • ISO 9001 Quality Management during active manufacture

    Typical usage ratio

    • 5–25% w/w, varying by molecular target; ratio adjusted based on desired substitution pattern and herbicide final structure

    Downstream process integration

    • Charged to batch reactor for nucleophilic substitution, followed by hydrolysis and subsequent coupling with proprietary amines or phenols under controlled temperature and pH conditions

    Final product types

    • Selective pre-emergence and post-emergence herbicides
    • Foliar-applied pesticides
    • Granular weed control agents

    2. Pharmaceutical Intermediate Manufacture

    Benzotrifluoride derivatives incorporating this compound are essential in multi-step pharmaceutical synthesis, particularly for API side chain building. It introduces electron-withdrawing effects in custom aromatic scaffolds, impacting biological activity or metabolic stability for downstream pharma partners. Close analytical control is observed at every handling stage due to API sensitivity.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Part II
    • USP and Ph. Eur. reference standards where applicable
    • REACH Annex VIII registration for intermediates

    Typical usage ratio

    • 1–10 mol% relative to final API; dosage determined by pathway requirements and stoichiometry in synthetic steps

    Downstream process integration

    • Employed in aromatic substitution and coupling steps after initial halogenation, entering as a limiting reagent in small molecule synthesis or route-specific cyclization processes

    Final product types

    • Intermediate compounds for parenteral or oral formulation APIs
    • Pharmaceutical key starting materials (KSMs)
    • Advanced intermediates for specialty drugs

    3. Dyestuff Intermediate Production

    This nitroaromatic excels as a core intermediate in high purity dye manufacturing, especially for triaryl methane and anthraquinone dyes where precise halogen and nitro group orientation controls shade intensity and color fastness. High batch-to-batch uniformity and low trace metal content are critical, as dyes are often destined for textile, inkjet, or specialty coatings where regulatory and quality demands are strict.

    Industry compliance standards

    • ZDHC MRSL v3.1 (Zero Discharge of Hazardous Chemicals)
    • REACH Regulation (EC) No 1907/2006 for colorants
    • ISO 9001-certified pigment processing protocols
    • Oeko-Tex Standard 100 for textile applications

    Typical usage ratio

    • 10–20% in dye precursor synthesis; ratio tuned for chromophore construction and color depth requirements

    Downstream process integration

    • Undergoes diazotization or reduction before condensation with couplers, directly entering the chromogenic step after initial purification

    Final product types

    • Sulfonated azo dyes for textiles
    • Solvent dyes for industrial inks
    • Reactive dyes for cellulose fiber processing

    4. Specialty Polymer Modifier

    As a precision modifier, this chemical introduces specific electronic and steric effects into custom high-performance fluoropolymers and nitroaromatic-containing resins. Downstream partners in the advanced plastics sector use it to manipulate thermal and chemical resistance, as well as dielectric characteristics for niche engineering applications. Stringent documentation accompanies each shipment, supporting compliance in regulated use cases.

    Industry compliance standards

    • ISO 14001 Environmental Management for resins and polymers
    • UL 94 Flammability testing for electrical components
    • RoHS Directive 2011/65/EU for electronics applications
    • ISO 9001 for quality management in plastic modification

    Typical usage ratio

    • 0.5–5% by polymer weight; proportion determined by required end-use property enhancement and process compatibility

    Downstream process integration

    • Introduced during resin solution-phase synthesis or melt compounding, serving as a functional monomer or chain-end modifier; frequently added post-polycondensation for blending

    Final product types

    • High-performance electronic encapsulants
    • Engineered polymer films
    • Custom thermoset adhesives

    5. Advanced Material Synthesis for Electronic Chemicals

    In the specialty electronic materials field, this compound supports formulation of advanced etchants and chemical resist developers, where strict control of side reactions and contaminant profiles is critical. It features in downstream syntheses where its unique substitution pattern offers selectivity during microfabrication of printed circuit boards, OLED panel elements, and precision surface coatings.

    Industry compliance standards

    • IATF 16949 for automotive electronics
    • IPC-6012 for printed circuit board fabrication
    • IEC 60249 standards for base materials in electronics
    • REACH authorization for specialty process chemicals

    Typical usage ratio

    • 1–8% in microfabrication chemical formulations; determined per batch to balance efficacy and etch selectivity with downstream equipment compatibility

    Downstream process integration

    • Dosed into formulation tanks during precision etchant mixing or chemical developer blending, followed by filtration and on-site stability testing prior to cleanroom deployment

    Final product types

    • Photoresist strippers
    • Selective semiconductor etchants
    • Developer agents for flat panel displays
    Free Quote

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