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2-Nitro-4-Fluorophenol

    • Product Name 2-Nitro-4-Fluorophenol
    • Alias 2-Fluoro-4-nitrophenol
    • Einecs 241-414-9
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    243840

    Chemicalname 2-Nitro-4-Fluorophenol
    Casnumber 446-09-3
    Molecularformula C6H4FNO3
    Molecularweight 157.10
    Appearance Yellow crystalline solid
    Meltingpoint 86-89 °C
    Solubility Slightly soluble in water
    Smiles OC1=CC=C([N+](=O)[O-])C=C1F
    Inchi InChI=1S/C6H4FNO3/c7-4-1-2-6(9)5(3-4)8(10)11/h1-3,9H
    Pubchemid 185110

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

    Packing & Storage
    Packing A 25g amber glass bottle, sealed with a screw cap, labeled "2-Nitro-4-Fluorophenol," including hazard warnings and CAS information.
    Shipping 2-Nitro-4-Fluorophenol should be shipped in tightly sealed containers, protected from light, moisture, and incompatible materials. Handle as a hazardous chemical: ship according to local, national, and international regulations. Label appropriately, and ensure secondary containment to prevent leakage during transit. Suitable packaging is required to ensure safe delivery to the destination.
    Storage 2-Nitro-4-Fluorophenol should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition, heat, and incompatible materials such as strong oxidizers and bases. Protect from direct sunlight and moisture. Store in a chemical storeroom with appropriate labeling, and keep away from food and drink. Use secondary containment to prevent leaks.
    Application of 2-Nitro-4-Fluorophenol

    Applications of 2-Nitro-4-Fluorophenol in Industrial Manufacturing

    As a dedicated chemical raw material manufacturer, we supply 2-Nitro-4-Fluorophenol to specialized industries requiring precise intermediates for synthesis and formulation. The following sections detail the compound’s direct applications in established downstream manufacturing segments, including specific regulatory standards, formulation ratios, process integration points, and targeted end products. Each scenario reflects authentic industrial use based on our production feedback and customer application data.

    1. Agrochlorinated Herbicide Synthesis

    Major agrochemical companies incorporate 2-Nitro-4-Fluorophenol in their multi-step synthesis of selective chlorinated phenoxy herbicides. Manufacturers introduce this compound at the fluorination stage to modify molecular behavior, thereby fine-tuning activity profiles for weed control. The phenolic nitro group’s reactivity supports targeted crop safety and controlled soil residue. In process scale-up, technical QC teams validate purity during nitration and subsequent purification prior to coupling steps.

    Industry compliance standards

    • FAO/WHO specifications for pesticide technical grade materials
    • EU Regulation (EC) No 1107/2009 for plant protection products
    • ISO 9001:2015-certified quality systems in agrochemical manufacturing
    • REACH registration and safe use documentation

    Typical usage ratio

    • Adjusted between 0.6% and 2.3% of total active ingredient input, depending on target substituent balance
    • Micro-batch optimization may reduce ratios where low-residue formulations are required

    Downstream process integration

    • Fed into the fluorination reactor after initial nitrophenol formation
    • Fine control during condensation and chlorination steps
    • Quality checked via HPLC before integrating into the coupling reaction
    • Residuals monitored before product standardization

    Final product types

    • Selectively active herbicide actives (e.g., 4-fluoro-2-nitrophenol derivatives)
    • Emulsifiable concentrates for field application
    • Granular formulations for controlled release
    • Concentrated technical grade herbicides for export registration

    2. Pharmaceutical Intermediate for Fluorinated Drug Synthesis

    Pharmaceutical API manufacturers utilize this compound as a fluorinated building block in the synthesis of advanced benzene ring drug candidates. Its dual nitro and fluoro substitution enables regioselective introduction into target molecules via nucleophilic aromatic substitution (SNAr). The compound’s trace ability plays a key role during GMP batch production, especially when purity impacts final API isomer profiles and impurity thresholds. Downstream, teams track reaction intermediates through stringent analytical protocols.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF requirements for pharmaceutical intermediates
    • EU EudraLex Volume 4 Part II (GMP Guidance)
    • FDA DMF (Drug Master File) referencing for regulated markets

    Typical usage ratio

    • Ranges from 0.45 mmol to 1.2 mmol per 1 mmol target API scaffold
    • Adjusted to reaction yield and impurity control data in pilot and scale-up

    Downstream process integration

    • Directly charged into SNAr processes for forming fluorinated aromatic rings
    • Integrated in one-pot synthesis for minimizing isolation stages
    • Tracked using analytical LC-MS for completed reactions
    • Impurities filtered prior to downstream hydrogenation or reduction

    Final product types

    • Fluorinated pharmaceutical intermediates
    • Active pharmaceutical ingredients targeting CNS and oncology
    • Intermediates for anti-inflammatory drugs with benzene-based scaffolds
    • API reference standards for regulatory submissions

    3. Specialty Dye and Pigment Precursor

    Manufacturers within the dyestuff sector incorporate the compound as a key reactant in custom syntheses of azo and heterocyclic dyes. Its electron-withdrawing fluoro group alters color properties while the nitro moiety provides fastness attributes. These features permit precise shade targeting for fibers and plastics, enhancing light resistance and brightness. Color chemists and process managers control additive levels based on formulation scale, adjusting to match client colorimetric requirements.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textile chemical safety
    • EN 71-3 safety standards for pigments used in toys
    • REACH Annex XVII regulation for azo dyes
    • ISO 9001:2015 for pigment production quality

    Typical usage ratio

    • Introduced at 0.5% to 1.8% of total dye formulation weight
    • Adjusted for color intensity and fastness testing results

    Downstream process integration

    • Used in diazotization reactions to form intermediate azo compounds
    • Mixed in batch pigment dispersion steps for resin encapsulation
    • Blending monitored with UV-vis spectroscopy for target shade
    • Post-treatment to ensure stability in polymer matrices

    Final product types

    • Synthetic textile dyes for polyester and nylon
    • Color-fast plastic pigments for automotive and electronics
    • High-brilliance printing inks
    • Specialist pigments for fiber-reinforced composites

    4. Electronic Chemical Intermediate for Liquid Crystal Compounds

    Producers of high-performance liquid crystal materials integrate the compound during the early synthesis stages of custom fluorinated and nitro-substituted aromatics. The dual functional groups introduce anisotropic properties essential for fast switching times and thermal stability in LCD panels. Process engineers monitor batch-to-batch consistency tightly, particularly at the stage where the intermediate couples with spacer or terminal groups, to meet IC and display specification limits in the downstream electronic assembly.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) on hazardous substances in electronics
    • IEC 61249-2-21 standard for halogen-free substances
    • REACH compliance for supplied intermediates
    • Corporate QC protocols for electronic material supply chain

    Typical usage ratio

    • Fed at 0.2–1.2 molar equivalents to core aromatic precursor in series production
    • Tuned depending on nematic or smectic LC formulation requirements

    Downstream process integration

    • Introduced during Friedel-Crafts or nucleophilic aromatic substitution stages
    • Batch integration with chain terminals or spacers pre-polymerization
    • Purity and reactivity checked via GC-MS at each coupling
    • Unreacted material removed before liquid crystal mixing

    Final product types

    • Commercial nematic and smectic liquid crystal mixtures
    • Custom compounds for LCD-TV and monitor panel production
    • LC raw materials for display module manufacturers
    • Electronic chemical intermediates for OLED and advanced displays

    5. Advanced Polymer Additive Modifier

    Specialty polymer manufacturers employ the compound as a chain modifier or crosslinking aid, primarily in engineering thermoplastics or specialty adhesives where tailored physical and chemical resistance is required. The fluorinated and nitro functional groups impart increased rigidity while maintaining desired processability during melt blending or extrusion. Production teams verify physical impact on finished polymer properties through post-extrusion analysis and review compatibility in joint venture formulations.

    Industry compliance standards

    • ASTM D638 for tensile property testing of plastics
    • UL 94 flammability rating for polymeric materials
    • ISO 10993 part 5 for biocompatibility in specialty medical plastics
    • Corporate environmental, health, and safety audits for polymer plants

    Typical usage ratio

    • Blended at 0.1% to 0.8% by weight of resin depending on desired crosslink density and end-use stress performance
    • Adjusted after impact, migration, and solvent resistance testing in development

    Downstream process integration

    • Added to polymer melt during compounding or prior to extrusion
    • Reactively incorporated in high-shear mixers for adhesives
    • Compatibility checked with other polymer additives and stabilizers
    • Performance validated in pilot-scale extrusions and adhesive trials

    Final product types

    • Engineering-grade reinforced polymers
    • Chemically resistant adhesive resins
    • Thermoplastic blends with increased dimensional stability
    • High-end molded electronic housings
    Free Quote

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