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3,5-Dichlorophenyl Isocyanate

    • Product Name 3,5-Dichlorophenyl Isocyanate
    • Alias m-(Dichlorophenyl) Isocyanate
    • Einecs 'EINECS 221-966-8'
    • 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

    828446

    Cas Number 28479-22-3
    Iupac Name 3,5-dichlorophenyl isocyanate
    Chemical Formula C7H3Cl2NO
    Molecular Weight 188.01 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 120-124°C at 21 mmHg
    Density 1.41 g/cm³
    Solubility In Water Reacts with water
    Flash Point 142°C (closed cup)
    Refractive Index 1.581
    Odor Sharp, pungent

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

    Packing & Storage
    Packing The 3,5-Dichlorophenyl Isocyanate is packaged in a 100-gram amber glass bottle with a tightly sealed, chemical-resistant cap.
    Shipping 3,5-Dichlorophenyl Isocyanate should be shipped in tightly sealed containers under cool, dry conditions. It must be labeled as hazardous, handled with care, and protected from moisture and sources of ignition. Transportation must comply with relevant regulations for toxic and reactive chemicals, ensuring proper documentation and emergency procedures are in place.
    Storage Store 3,5-Dichlorophenyl Isocyanate in a tightly sealed container, under a dry, inert atmosphere (such as nitrogen), and in a cool, well-ventilated area away from moisture, heat, and sources of ignition. Protect from direct sunlight. Segregate from alcohols, amines, acids, and bases, as it reacts violently with these materials. Always use appropriate personal protective equipment (PPE) when handling.
    Application of 3,5-Dichlorophenyl Isocyanate

    Applications of 3,5-Dichlorophenyl Isocyanate in Industrial Manufacturing

    3,5-Dichlorophenyl Isocyanate is a specialized aromatic isocyanate that plays a key role in several differentiated industrial sectors. As a primary manufacturer, we supply this intermediate to downstream processors who integrate its unique isocyanate functionality into highly regulated value chains. Below, we present specific industrial applications with details on regulatory compliance, precise usage benchmarks, integration points into manufacturing, and the main categories of finished goods produced.

    1. Synthesis of High-Performance Polyurethane Elastomers for Industrial Rollers

    In the polyurethane elastomer sector, formulators use this isocyanate as a key monomer to impart chemical resistance and dimensional stability to heavy-duty rollers and wheels. Its dichloro-substituted aromatic structure enhances the durability of elastomeric products that operate in aggressive chemical environments, such as printing, textile dyeing, and logistics conveyor systems. The downstream production typically leverages its functionality to increase resistance to solvents and abrasion.

    Industry compliance standards

    • ISO 9001:2015 for quality management systems
    • REACH Regulation (EC) No 1907/2006
    • EU Directive 2011/65/EU (Restriction of Hazardous Substances in Electrical and Electronic Equipment for component applications)
    • DIN EN 10204 with material certification for end-user traceability

    Typical usage ratio

    • 2–8% by weight in the isocyanate prepolymer mix, adjusted according to the target mechanical and chemical properties of the final elastomer

    Downstream process integration

    • Metered addition during prepolymer synthesis, typically following the polyol drying stage and before chain extension; precise dosage and mixing temperature control is critical to ensure reproducibility and polymer backbone integrity

    Final product types

    • High-load industrial rollers
    • Conveyor wheels
    • Textile printing squeegees and pads
    • Custom chemical-resistant bumpers and pads

    2. Intermediate for Specialty Agrochemical Synthesis

    Manufacturers in the agrochemical value chain deploy 3,5-Dichlorophenyl Isocyanate as a unique intermediate in the creation of advanced urea or carbamate herbicide active ingredients. Its isocyanate group reacts with amines under controlled conditions to form substituted ureas with targeted selectivity, which improve efficacy against resistant weed varieties and minimize non-target phytotoxicity. Consistent quality and impurity control are critical due to downstream regulatory testing for active ingredient registration.

    Industry compliance standards

    • FAO/WHO Food and Agriculture Organization pesticide specifications
    • ISO 17025 for chemical testing and analysis
    • EU 1107/2009 Regulation for plant protection products
    • US EPA FIFRA (Federal Insecticide, Fungicide, and Rodenticide Act) compliance for active ingredient submission

    Typical usage ratio

    • Varies from 1.5–4.5 mole equivalents per target amine reactant in synthesis; adjusted based on the designed structure of the final active substance

    Downstream process integration

    • Introduced as one of the primary isocyanate reagents during the condensation step, following solvent charging and prior to temperature ramping; used under anhydrous, inert atmosphere to avoid side reactions

    Final product types

    • Substituted phenylurea herbicide actives
    • Chlorinated carbamate intermediates
    • Agrochemical technical concentrates (TCs) for further formulation
    • Registered active substances for herbicide blends

    3. Building Block for Custom Polyurethane Paint Hardener Systems

    Coating formulators utilize this isocyanate as a key crosslinking agent in high-performance polyurethane paint hardeners. Its reactivity enables rapid curing, enhanced film toughness, and outstanding solvent resistance, making it well-suited for industrial maintenance coatings and specialty automotive finishes. Proper management of mixing ratios and pot life is required to optimize the final coating’s durability and appearance in demanding end-user environments.

    Industry compliance standards

    • EU Directive 2004/42/EC (limitation of emissions of volatile organic compounds, VOCs, due to use of organic solvents in paints and varnishes)
    • ASTM D16 for terminology relating to paint and related coatings
    • ISO 12944 for corrosion protection of steel structures by protective paint systems
    • OECD principles of Good Laboratory Practice (GLP) for performance and safety validation

    Typical usage ratio

    • 3–10% relative to the total binder solids content, depending on required film performance and on-site curing parameters

    Downstream process integration

    • Blended into two-component hardener packs, immediately before application; precise metering and mixing with polyol components is controlled to avoid issues with premature curing and to ensure application consistency in field environments

    Final product types

    • Industrial machinery enamels
    • Automotive refinishing clearcoats
    • Protective maintenance topcoats for infrastructure
    • Specialty anti-corrosion primer systems

    4. Intermediate for Synthesis of High-Purity Pharmaceutical Process Aids

    Within GMP-regulated pharmaceutical manufacturing, 3,5-Dichlorophenyl Isocyanate finds use as a building block in synthesizing process control reagents and custom intermediates needed for active pharmaceutical ingredient (API) routes. Its controlled integration allows downstream formulation of tailor-made auxiliaries to facilitate intermediate isolations or crystallizations, with all raw material traceability and impurity control documented for regulatory submissions.

    Industry compliance standards

    • ICH Q7 guideline for GMP of active pharmaceutical ingredients
    • USP-NF (United States Pharmacopeia–National Formulary) for reagent and process chemical quality
    • 21 CFR Parts 210 and 211 for drug manufacturing controls
    • EU GMP Annex 8 for sampling of starting materials

    Typical usage ratio

    • Application-dependent: typically used at 1–5 mol% relative to key reactive intermediates in proprietary process steps, with scale-up determined by DMF filings

    Downstream process integration

    • Added at critical junctures in API synthesis, such as carbamoylation steps or in purification aid formulations; entry point selected to maximize selectivity and minimize undesired isomer formation

    Final product types

    • Pharmaceutical-process control reagents
    • Specialty crystallization aids
    • Certified process intermediates for API synthesis
    • Custom GMP intermediates for CDMO (Contract Development and Manufacturing Organization) production

    5. Synthesis Module in Advanced Polyurethane Adhesive Formulations

    Producers of industrial adhesives use 3,5-Dichlorophenyl Isocyanate to formulate specialty adhesive systems for applications that demand strong bonds and solvent resistance. The dichloro functionality enhances the heat and chemical resistance of polyurethane adhesives, supporting assembly in sectors like electronics encapsulation, footwear, and metal lamination. Its reactive sites are precisely dosed for compatibility with a range of polyols and chain extenders, ensuring long-term adhesive performance.

    Industry compliance standards

    • EN 204-D4 for thermosetting wood adhesives in high-humidity environments
    • RoHS (2011/65/EU) restrictions for hazardous substances in electrical/electronic assemblies
    • ISO 4587 for overlap shear strength of adhesives
    • UL 94 for flammability classification of adhesive-bonded components (if used in electronics)

    Typical usage ratio

    • 1.5–6% of total solids content in the adhesive prepolymer phase; adjusted to achieve balance between cure speed, flexibility, and bond strength in specific substrate combinations

    Downstream process integration

    • Incorporated during prepolymer formation after precise polyol blending and before chain extension, with temperature and moisture monitoring to prevent side reactions and uncontrolled viscosity rise

    Final product types

    • Solvent-resistant structural adhesives
    • Polyurethane hot-melt adhesives for footwear
    • Flexible laminating adhesives for metal, paper, and films
    • Electronics potting compounds where chemical durability is critical

    6. Synthesis of Custom Isocyanate Monomers for Performance Resins

    In the specialty plastics and composites sector, this isocyanate serves as a precursor for the preparation of custom isocyanate monomers and modified resins. Resin formulators use its chlorinated aromatic motif to fine-tune the rigidity, chemical resistance, and glass transition temperature of advanced thermoset networks, relevant in the manufacture of high-performance laminates and electrical encapsulants.

    Industry compliance standards

    • UL 746C for polymeric materials used in electrical equipment
    • ISO 11357 for differential scanning calorimetry measurement in polymers
    • RoHS 2011/65/EU (if used in electronics housings)
    • ASTM D635 for rate of burning and/or extent and time of burning of plastics

    Typical usage ratio

    • 2–12% of the total isocyanate fraction in resin synthesis; ratio tailored to target electrical or chemical resistance profiles in each resin type

    Downstream process integration

    • Charged during controlled oligomerization steps or monomer modification reactions, often as a partial replacement for standard aromatic isocyanates; integration timing optimized to maximize network uniformity

    Final product types

    • Flame-retardant laminate resins for circuit boards
    • Electrical potting resins
    • Thermoset composites for industrial housings
    • Chemically resistant polymer panels
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