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3,4-Dichlorobenzyl Isocyanate

    • Product Name 3,4-Dichlorobenzyl Isocyanate
    • Alias 3,4-DCBIC
    • Einecs 'EINECS 221-543-1'
    • 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

    444604

    Chemical Name 3,4-Dichlorobenzyl Isocyanate
    Cas Number 10229-84-2
    Molecular Formula C8H5Cl2NO
    Molecular Weight 202.04 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 124-126 °C at 15 mmHg
    Density 1.37 g/cm³
    Solubility Reacts with water, soluble in common organic solvents
    Flash Point 99 °C
    Refractive Index 1.589
    Storage Conditions Store in a cool, dry, and well-ventilated area in tightly closed containers

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

    Packing & Storage
    Packing Amber glass bottle, 100 grams, sealed with PTFE-lined cap, labeled with hazard warnings, chemical name, CAS number, and handling instructions.
    Shipping 3,4-Dichlorobenzyl Isocyanate is shipped as a dangerous good. Use tightly sealed containers made of compatible materials. Keep away from heat, moisture, and incompatible substances such as acids and bases. Package with clear hazard labeling and include relevant Safety Data Sheets (SDS) for handling, storage, and emergency procedures. Handle only by trained personnel.
    Storage 3,4-Dichlorobenzyl Isocyanate should be stored in a cool, dry, well-ventilated area away from direct sunlight, moisture, acids, alcohols, and amines. Keep the container tightly closed and properly labeled. Store separately from incompatible substances in a chemical-resistant, corrosion-proof container. Use secondary containment and minimize exposure to heat, sparks, or open flames. Ensure easy access to emergency spill equipment.
    Application of 3,4-Dichlorobenzyl Isocyanate

    Applications of 3,4-Dichlorobenzyl Isocyanate in Industrial Manufacturing

    3,4-Dichlorobenzyl Isocyanate serves as a critical intermediate in diverse specialty chemical manufacturing processes. Its reactive isocyanate group and dichloro-substituted aromatic ring enable precise transformations for high-value downstream synthesis. Below, we detail real industrial application fields, including formulation standards, ratio control, processing integration, and terminal products in day-to-day commercial production environments.

    1. Specialty Polyurethane Elastomer Synthesis

    Manufacturers in elastomer production employ this chemical to create high-performance prepolymers and curing agents. Its dichlorobenzyl substitution imparts unique properties to castable and thermoset polyurethanes, such as enhanced chemical resistance and mechanical stability demanded by industrial rollers, seals, and gaskets. Typical protocols require careful dosing to control crosslink density and endpoint molecular weight, influencing the elastomer’s durability and resistance parameters. Operators blend this intermediate with polyether or polyester polyols under strictly monitored moisture and temperature conditions for targeted curing profiles.

    Industry compliance standards

    • ISO 9001:2015 Quality Management
    • REACH Registration (EC 1907/2006, Annex XVII – Isocyanates Restrictions)
    • OSHA Hazard Communication Standard (29 CFR 1910.1200)
    • RoHS Directive (for finished automotive or electronics goods)

    Typical usage ratio

    • 5–15 parts per 100 parts polyol, adjusted by required crosslinking efficiency and prepolymer viscosity

    Downstream process integration

    • Isocyanate introduced during prepolymer synthesis, under dry nitrogen and controlled temperatures
    • Vacuum degassing to remove CO₂ and residual moisture
    • Final mixing with polyols in continuous or batch reactor systems
    • Homogenization prior to degassing and subsequent mold pouring or casting

    Final product types

    • Industrial elastomeric rollers
    • Dynamic sealing gaskets
    • Custom polyurethane bushings and pads
    • Wear-resistant conveyor components

    2. Agrochemical Active Intermediate Production

    Producers in the crop protection sector incorporate this raw material for key urethane and urea linkage steps in the synthesis of select herbicide and fungicide actives. Its reactivity allows introduction into heterocyclic frameworks, generating molecular scaffolds for proprietary products. Process control emphasizes minimization of trace isocyanate residues in finished intermediates, verified by HPLC and GC-MS, and aligns closely with international agrochemical regulatory approval demands.

    Industry compliance standards

    • FAO/WHO Codex Alimentarius for pesticide residues
    • ISO 17025:2017 Laboratory Testing Competence (QC for agro actives)
    • Good Manufacturing Practice (GMP) for crop protection chemicals
    • EPA FIFRA registration (for US-market finished actives)

    Typical usage ratio

    • 1.5–8 mol% relative to parent amine or alcohol substrate in active synthesis

    Downstream process integration

    • Charged into stirred tank reactors for condensation or carbamoylation reactions
    • Process staged to quench unreacted isocyanate with amine scavengers
    • Final purification by column chromatography or recrystallization
    • Batch-wise or semi-continuous synthesis, depending on plant throughput

    Final product types

    • Selective herbicide technicals
    • Fungicidal pre-mixes
    • Agrochemical active intermediates for onward formulation
    • Seed treatment microencapsulations

    3. Advanced Pharmaceutical Intermediate Manufacturing

    Pharmaceutical ingredient manufacturers select this material for the introduction of chlorinated benzyl urethane groups during multi-step active pharmaceutical ingredient (API) synthesis. The ortho-dichloro structure provides chemical stability and influences pharmacokinetic profiles in finished molecules. Stringent process protocols and quality controls comply with both national pharmacopoeias and ICH Q7 guidelines, demanding validated traceability and impurity checks, especially for regulated end use.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP-NF, Ph. Eur. or JP Monographs (as governing per region)
    • ISO 14644 Cleanroom Operation
    • FDA 21 CFR Part 211 (if entering US finished drug market)

    Typical usage ratio

    • 0.8–3.5 equivalents per substrate nitrogen, contingent on multi-step route and impurity profiles

    Downstream process integration

    • Directional addition to protected amines within reaction trains
    • Temperature-controlled, under argon or nitrogen in glass-lined vessels
    • Sequential isolation, purification via crystallization or preparative HPLC
    • QC sampling at each intermediate for clarity, purity, and residual isocyanate quantification

    Final product types

    • Chlorinated API intermediates
    • CNS active compound scaffolds
    • Potential anti-infective building blocks
    • Clinical trial candidate molecule batches

    4. Functional Polymer Modifier for High-Performance Coatings

    Coating formulation companies use this raw material to synthesize bespoke isocyanate-capped oligomers designed for chemically resistant, high-gloss polyurethane and epoxy-based protective coatings. Incorporation of the dichlorobenzyl moiety modulates cure response and enhances final film properties, critical for marine, automotive, and industrial metal protection systems. Strictly controlled ratios optimize cure kinetics and ensure environmental compliance, especially for VOC limits and workplace safety.

    Industry compliance standards

    • ISO 12944 Corrosion Protection by Coatings
    • ASTM D16 Terminology for Paint and Related Coatings
    • EU Directive 2004/42/EC (VOC content standards)
    • OSHA 1910.1200 or equivalent workplace exposure limits

    Typical usage ratio

    • 2–9 wt% relative to total binder solids; final ratio depends on application thickness and desired chemical resistance

    Downstream process integration

    • Added during prepolymer or oligomer synthesis, prior to pigment dispersion
    • Batch heating under dry atmosphere for full capping reaction
    • QC for free isocyanate content before compounding with curing agents
    • Direct dispersion into hardener systems for 2K (two-component) coatings

    Final product types

    • Marine-grade polyurethane topcoats
    • Industrial floor sealants
    • Construction steel anti-corrosive coatings
    • Automotive refinishing clearcoats

    5. Custom Reactive Monomer for Adhesive Formulations

    Industrial adhesive developers integrate this compound as a reactive monomer to enhance adhesion and performance in moisture-curing and heat-curing polyurethane-based adhesives. The dichlorobenzyl group improves bonding to substrates with challenging surface energies, such as treated polyolefins and coated metals. Strict batch control ensures consistency in oligomeric chain length and crosslinking efficiency, as prescribed by end-use mechanical testing and service life validation.

    Industry compliance standards

    • ISO 4587 (Testing for metal-to-metal adhesive bonds)
    • REACH SVHC compliance for workplace safety
    • ASTM D1002 (Lap shear strength test method)
    • EN 923:2015 - Adhesives: Terms and Definitions

    Typical usage ratio

    • 1.3–6.5 parts per 100 parts base resin, ratio depends on substrate and adhesive system

    Downstream process integration

    • Co-reacted with polyols or oligomeric diols in adhesive premixes
    • Dispersion with coupling agents for tailored substrate compatibility
    • Batch homogeneity validated by FTIR for isocyanate functionality
    • Fillers and plasticizers added post-reaction for viscosity adjustment

    Final product types

    • Structural bonding adhesives for plastics and composites
    • Panel lamination adhesives for building materials
    • Solvent-free construction adhesives
    • OEM-grade industrial assembly adhesives
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    Certification & Compliance
    More Introduction

    Introducing 3,4-Dichlorobenzyl Isocyanate: Purpose-Driven Chemistry From Real Manufacturing

    Real-World Chemistry in Focus

    In our years running synthesis lines and optimizing reaction routes, 3,4-Dichlorobenzyl Isocyanate keeps showing up as a linchpin in specialty syntheses—especially where tailored intermediates and advanced toluene-based derivatives matter. We produce this compound in our facility, managing every step to control not just purity but also physical stability and storage needs.

    Unlike more commonly used isocyanates, this product carries two chlorine atoms in the 3 and 4 positions on the benzyl ring, giving it a reactivity profile that fits niche transformations. We watch demand climb in areas such as custom pharma building blocks and agricultural chemistry, often because other benzyl isocyanates with single substitutions or non-chlorinated rings either fall short on the reaction selectivity or do not hold up during downstream processing.

    What Sets 3,4-Dichlorobenzyl Isocyanate Apart

    Synthesizing this compound isn’t easy. The process involves careful control of chlorination and subsequent isocyanate group introduction, all under conditions where minor moisture or temperature swings lead to degradation or side reactions. Since we scale up production in-house, we see the effects on consistency firsthand. By managing each batch from raw chlorinated toluene through to finished isocyanate, we keep a tight handle on unwanted byproducts. This level of control means our 3,4-Dichlorobenzyl Isocyanate supports repeated lab and plant-scale outcomes, where even small impurities can stall a medicinal chemistry project or foul a catalyst in an applied material.

    We get regular requests regarding the physical appearance and handling of the compound. Our product arrives as a solid or sometimes a viscous liquid, depending on temperature and air humidity. Many labs prefer a stable, solid form for weighing and dispensing, so we invest in drying protocols and sealed, inert packaging. Off-spec, off-odor, or inconsistent lots create headaches—especially when the chemist needs gram quantities today and kilogram shipments the next quarter, all with the same performance in mind.

    Typical Model and Specification Insights

    The product we offer typically sits in the purity range of 98% or higher (HPLC determination), with residual chlorotoluene and phosgene indices verified before shipment. With this, we see repeat clients engage in more confident synthesis planning. The molecule's molecular weight and melting range—elements we keep logged for each lot—directly inform reaction flows and the storage conditions in downstream use.

    Exposure to moisture and light affects stability, so we developed vapor-tight containers, purged with nitrogen, and encourage cool, dark storage. In the past, neglecting these details cost entire batches; a lesson in material science that guides our manufacturing discipline today.

    Understanding the Role in Application—Learning From the Bench

    In my own experience walking through client testing labs, 3,4-Dichlorobenzyl Isocyanate gets chosen mainly for its capacity to introduce a protected urea or carbamate group with extra electron-withdrawing power, courtesy of those chlorines. Chemists turn to it in the development of new agrochemicals for this reason—the final molecules show different solubility and biological binding properties than those based on unsubstituted or mono-chlorinated benzyl isocyanates. Where performance characteristics hinge on subtle differences in the molecular backbone, a compound like this steps in as a problem-solver.

    Pharma R&D teams have shared stories of synthetic dead-ends overcome by swapping out common isocyanates for this more specialized variant. In certain routes, especially where a specific reactivity or blocking effect is needed, alternatives prove too volatile or fail under industrial reaction conditions. These practical, on-the-ground insights shape how and why we continue investing in tight specification and handling expertise.

    No Substitute for Real Quality Control

    Merely matching a specification sheet on paper doesn’t guarantee a successful synthesis on the bench. We’ve seen customers turned down by traders or forced to reformulate after intermediary lots change hands too many times. By working straight from our own reactors and analytic stations, we offer assurances based on repeated, real-world performance—not just data points copied from literature or a trader’s price list.

    Our experience tells us the fine differences in benzyl isocyanates make all the difference further down the value chain. When producing specialty ureas or tailoring surface modifiers for fine-tuned industrial polymers, end-users keep reporting that product stability and reproducibility trump price or volume. Each kilogram produced has a background story of careful temperature ramps, raw material traceability, and routine checks before and after packaging.

    Years of direct feedback have led us to tighten up the controls, train our operators to spot subtle variations, and even rethink our chlorination batch times. In some years, feedstock shortages have forced slowdowns. We took those setbacks as reminders of how tightly-coupled our process flow needs to be—never letting an off-standard lot drift into the supply stream.

    Comparing With Other Isocyanates—Straight Talk From The Plant Floor

    Our teams work with a full range of isocyanates; not every synthetic need demands a multi-chlorinated benzyl group. We routinely get asked whether customers can switch to a simpler benzyl isocyanate or reach for a cheaper aromatic isocyanate alternative. Here’s the reality we see: less substituted compounds do frequently offer lower cost and easier handling, and for projects where reactivity isn’t tightly controlled, they work fine.

    But the introduction of two adjacent chlorine atoms in the 3 and 4 positions shapes chemical reactivity in meaningful ways. For synthesis of complex urea derivatives, especially where downstream hydrolysis resistance or specific binding affinity comes into play, our product’s unique nature provides a performance edge. Generic benzyl isocyanate can’t always be plugged in without reoptimization. It comes down to a molecular-level difference that is magnified in med-tech or advanced agrochemical R&D.

    Our in-house R&D teams track how the two chlorines steer the reaction pathways, reduce side-product formation, or enable transformations under milder conditions. Buyers locked into high-throughput screening pipelines relay their own findings—attempts to cut corners using generic materials usually result in lower hit rates or stability problems later in process development. If the tradeoff sounds small, it often manifests in lost time, wasted reagents, or missed deadlines.

    Lifting the Hood: How We Approach Safe Manufacturing

    Few isocyanates match the sensitivity of the 3,4-dichlorinated benzyl variety. Each production run means monitoring phosgene-related hazards, preventing batch contamination, and choosing reaction vessels that avoid trace corrosion. Our plant handled all this through a combination of exhaust scrubbing, air monitoring, and closed-batch technology. The process gets tough when scaling for industrial volumes while guarding against cross-contamination with neighboring synthesis lines. Every reactor charge is treated as a potential high-risk stage; we build slack time into the schedule to allow for real-time quality checks.

    Practical manufacturing lessons drive every update we make. In years past, minor leaks or temperature fluctuations affected yields and purity. Now, process automation on chlorination and real-time feedback loops give operators a running, actionable view of conditions. We got here not by sitting behind desks, but by troubleshooting stuck agitators, tuning distillation cut points, and taking samples at odd hours to resolve unexpected peaks in gas-flow readouts.

    Supporting Real Use Cases, Not Just Sales Goals

    Our long-term relationships with research labs, pharma production lines, and specialty agchem firms reflect one shared aim: provide chemicals that help innovation—not just fill catalog orders. In feedback sessions, clients trace project success or delays to the fine details in chemical sourcing. When a high-value synthesis or formulation depends on the right intermediate, a supplier that tests for batch uniformity and stability at every step prevents wasted effort and budget.

    Technical managers and process chemists keep telling us the difference between a failed and a successful run often lies in subtle lot-to-lot variations. Container residue, variations in moisture pick-up during shipping, or inconsistent crystalline forms have tripped up too many synthetic routes. We took these cases to heart, investing in closed-cycle packaging systems and working with logistics teams to make sure storage and transport add zero surprises.

    Transparency in Documentation, Testing, and Traceability

    We believe in showing where every batch comes from, not just displaying a generic certificate. Every consignment leaves our plant with a full analytical dossier and origin tracking. Any anomalies or changes get logged and shared with the customer, enabling an open line between your chemists and ours. Over time, this policy paid off in smoother upscaling trials and easier regulatory submissions.

    Routine inquiries about elemental analysis, solvent residue profiles, and stability under ambient or refrigerated conditions are met with live support from our process experts. We think this beats hunting for spec answers through a maze of intermediaries with no direct production insight.

    Looking at the Real Challenges and How We Tackle Them

    Anybody in chemicals knows no manufacturing process stays problem-free for long. Over the years, we encountered bottlenecks from raw material volatility, energy costs, labor training, and regulation updates around chlorinated aromatics and isocyanate handling. Rather than waiting for trouble, we regularly audit and improve our processes.

    Switches to greener solvents and control agents have kept production up to evolving standards. Getting staff up to speed on handling advanced respiratory protection and emergency shut-off lines made routine production safer. Years of troubleshooting sticky valves and crystallizer fouling led us to invest in equipment that resists deposit buildup. This isn’t a quick fix; it comes from living with the day-to-day intricacies and respecting the risks.

    We share these experiences openly with our clients, knowing that real-world insight beats faceless certification every time. Some customers want a flawless product, but the reality is that perfection only comes from continuously inspecting and improving, loaf by loaf, kilogram by kilogram.

    Real-World Demand Drivers For 3,4-Dichlorobenzyl Isocyanate

    The ongoing shift toward more precise, higher-performance chemical intermediates has steadily put products like ours in higher demand. Changing regulatory and environmental expectations around isocyanates and chlorinated organics mean scrutiny across the supply chain. We chose to keep all synthesis, purification, and final QC in-house so that clients have detailed, defensible records all the way back to the reactor charge.

    We know from direct talks with researchers that increased scrutiny in chemical identity, impurity profiles, and supply traceability is non-negotiable for pharma and high-spec agchem R&D use. Providing a 3,4-dichloro product with a clear, traceable, high-purity record breaks down internal roadblocks during scale-up and regulatory review. There is demand because there’s a documented knowledge gap—cheaper or non-dedicated producers can’t always meet the new standards for consistency and accountability.

    Looking Ahead With Practical Precision

    We keep refining our processes, batch testing schedules, and product stewardship steps. What we know from running a manufacturing floor—with its alarms, plant-wide meetings, and hands-on troubleshooting—shapes our entire approach to compounds like 3,4-Dichlorobenzyl Isocyanate. As research moves toward ever more specialized and environmentally scrutinized isocyanates, we’re building both chemistry and operational discipline around reliability.

    No matter how much technology evolves, some fundamentals keep running the same: knowing your materials, talking directly with your end-users, and recognizing the hidden variables that make or break a synthesis. We’ve learned those lessons, batch after batch, and continue to put them front and center in how this product reaches the world.