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2,6-Dichlorobenzal Chloride

    • Product Name 2,6-Dichlorobenzal Chloride
    • Alias α,α,2,6-Tetrachlorotoluene
    • Einecs 211-018-2
    • 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

    496629

    Chemical Name 2,6-Dichlorobenzal Chloride
    Molecular Formula C7H4Cl3
    Molecular Weight 195.47 g/mol
    Cas Number 2234-13-1
    Appearance Colorless to pale yellow liquid
    Boiling Point 258 °C
    Melting Point N/A
    Density 1.382 g/cm³
    Solubility Insoluble in water
    Flash Point 110 °C (closed cup)
    Purity Typically ≥98%
    Synonyms 2,6-Dichlorobenzylidene Chloride

    As an accredited 2,6-Dichlorobenzal Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 2,6-Dichlorobenzal Chloride is packaged in a 500g amber glass bottle with a secure, chemical-resistant screw cap and hazard labeling.
    Shipping 2,6-Dichlorobenzal Chloride should be shipped in tightly sealed, corrosion-resistant containers, protected from moisture and direct sunlight. Handle as a hazardous material, label containers according to applicable regulations, and transport under appropriate UN classification. Ensure use of secondary containment and safety documentation, and comply with all local, national, and international shipping requirements.
    Storage 2,6-Dichlorobenzal Chloride should be stored in a cool, dry, well-ventilated area, away from direct sunlight and sources of ignition. Keep the container tightly closed and clearly labeled. Store separately from oxidizing agents, bases, and moisture. Use corrosion-resistant shelves and secondary containment to prevent spills or leaks. Ensure access to appropriate safety equipment, such as eye washes and spill kits.
    Application of 2,6-Dichlorobenzal Chloride

    Applications of 2,6-Dichlorobenzal Chloride in Industrial Manufacturing

    2,6-Dichlorobenzal Chloride serves as a specialized intermediate in the synthesis of advanced chemical products across several key sectors. As a direct manufacturer, we provide this material for well-defined segments with documented industrial and regulatory practices. See below for detailed usages in each application area.

    1. Pharmaceutical Intermediate Synthesis

    Major pharmaceutical companies rely on 2,6-Dichlorobenzal Chloride for the multi-step synthesis of active pharmaceutical ingredient (API) building blocks, particularly chlorinated aromatic intermediates. In controlled reactor systems, this compound undergoes nucleophilic substitution and coupling to construct drug precursors used in anti-hypertensive, anti-infective, and anti-inflammatory medications. Accurate handling, traceability, and compliance with medicinal manufacturing regulations are required at every stage.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practices for API
    • Pharmacopoeia monographs (USP, EP, JP)
    • 21 CFR Part 211 (FDA cGMP)
    • ISO 9001:2015 Quality Management Systems

    Typical usage ratio

    • 0.08 – 0.18 molar equivalents per batch, adjusted for target yield and purity requirements. Labs increase ratio for multi-stage synthesis to offset material loss.

    Downstream process integration

    • Charged as arylation reagent at controlled addition rate into reactor after solvent charging. Used before hydrolysis, reduction, or substitution steps. Monitored for residuals during downstream purification.

    Final product types

    • Sartans (angiotensin receptor blockers)
    • Chlorinated benzylamines and derivatives
    • Intermediate API precursors supplying finished drug production
    • Preparation of specialty clinical trial materials

    2. Agrochemical Active Ingredient Manufacturing

    Producers of crop protection chemicals require 2,6-Dichlorobenzal Chloride for downstream integration into the synthesis of advanced pesticide intermediates, mainly for aromatic chlorination pathways. The compound’s controlled reactivity profile matches strict technical-grade specifications for residual solvent, color, and metal impurities to ensure compatibility with large-scale batch or continuous production lines.

    Industry compliance standards

    • FAO/WHO Technical Specifications for Pesticides
    • ISO 9001:2015 or ISO 14001:2015 (quality and environment)
    • REACH annexes for registration of chemical intermediates (EU)
    • GB/T 21986-2008 (China agrochemical standard)

    Typical usage ratio

    • 2–10% of total batch mass, with ratio determined by target molecule structure and reactivity in the downstream halogenation and condensation steps.

    Downstream process integration

    • Blended with aromatic feedstocks under catalytic conditions. Deployed at high temperature, in the presence of base or acid catalyst, prior to condensation phase. Process lines monitor residue content before formulation into technical concentrate.

    Final product types

    • Precursor to herbicide active ingredients
    • Building block for insecticide and fungicide manufacturing
    • Synthesis of chlorinated acyl intermediates
    • Intermediate for formulation of high-purity technical pesticides

    3. Dyestuff and Pigment Intermediate Production

    Specialty dye and pigment synthesis plants use 2,6-Dichlorobenzal Chloride to introduce dichloroaromatic structures into advanced chromophores and dye intermediates. Stringent requirements for batch reproducibility, color fastness, and light stability depend on precise addition and quality grade of the input raw materials.

    Industry compliance standards

    • OEKO-TEX Standard 100 (for textile applications)
    • ISO 9001:2015 for colorant manufacturing
    • Registration under TSCA (if imported into US)
    • REACH SVHC candidate list (for pigment safety screening in EU)

    Typical usage ratio

    • 1–6% by mass of the final chromophore batch. Proportion set according to the number of chlorine substitutions and targeted dye intensity.

    Downstream process integration

    • Dosed during aromatic substitution and coupling stages. Reacts under anhydrous conditions and is subject to further oxidative or reductive steps before isolation of the pigment or dye compound.

    Final product types

    • Chlorinated azo dyes for synthetic fibers
    • Specialty pigments for plastics and inks
    • Reactive dye intermediates for cotton and cellulose textiles
    • Dye precursors for digital printing formulations

    4. Fine Chemical and Specialty Resin Manufacturing

    Producers of custom specialty resins and fine chemicals employ 2,6-Dichlorobenzal Chloride as a functionalized aromatic monomer to impart molecular rigidity, chemical resistance, and thermal stability to advanced polymer networks. Applications include thermosetting resins and engineered materials for electronics or coatings sectors, where compliance with technical standards is key for downstream use.

    Industry compliance standards

    • RoHS Directive (for electronics-related resins in EU)
    • UL 94 Flame Classification (for plastic resins)
    • ISO 14001:2015 Environmental Management (for facilities)
    • ASTM D638/D790 Testing Standards (mechanical properties for finished materials)

    Typical usage ratio

    • 0.5–4 phr (parts per hundred resin), with exact ratio adapted based on type of resin matrix and final product requirements.

    Downstream process integration

    • Introduced during initial mixing of polymer or prepolymer batch. Reacts during co-polymerization or curing stage, providing specific functional groups to the growing chain. Monitored via QC analytics for cross-linking consistency.

    Final product types

    • Crosslinked specialty epoxy resins
    • High-performance thermoset coating intermediates
    • Component monomer for printed circuit board (PCB) substrates
    • Fine chemical intermediates for custom material formulations
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    Certification & Compliance
    More Introduction

    2,6-Dichlorobenzal Chloride: Behind the Scenes at the Source

    At our chemical facility, 2,6-Dichlorobenzal Chloride is more than a line item on a list of fine chemicals—it represents decades of careful synthesis and applied knowledge in chlorinated intermediates. We generate it with the sort of consistency that comes from true process control, measured right from the tank farm through to the last packaging drum. Our focus is always on precisely reproducing its quality: clear or very lightly colored crystals, with minimal contamination and as sharp a melting point as any discerning downstream process will demand.

    Understanding the Product Model and Practical Use

    Our grade typically follows the industry’s technical specification for 2,6-Dichlorobenzal Chloride: molecular formula C7H4Cl3. The crystals pack a punch, showing off the solid presence of chlorine on the ring—exactly where it’s wanted for further synthesis. We see customers return time and again because the reliability of our batches translates to predictable results in their labs and plants. In daily use, this compound forms a backbone for the production of agrochemicals, dyes, and specialty polymers, as well as several pharmaceutical intermediates. We’ve watched it move through reaction flows, acting as a crucial building block in steps that demand reactive chlorination without veering into the world of uncontrolled side reactions.

    We control chlorination predominantly by batch methods, feeding the starting benzaldehyde derivatives under carefully managed temperatures and with a proprietary mix of catalysts. From early trials, we learned the importance of tight temperature control; even a few degrees too warm can drive undesirable byproducts. The result is a robust, crystalline material. Because our teams are hands-on with every drum, we catch color shifts or off-odors that hint at trace impurities—details you can’t often spot with spectroscopic checks alone.

    Differentiating 2,6-Dichlorobenzal Chloride from Other Products

    Chlorinated benzal chlorides come in a mix of isomers and substituted patterns, but the 2,6 position stands out. With both chlorines sitting ortho to the aldehyde group, the molecule shapes the reactivity pathway for later reactions. Other isomers, such as 3,4- or 2,4-, haven’t shown the same selectivity in downstream reactions, particularly when customers want to use it as a coupling partner or for stepwise reductions. We see less over-reactivity and a cleaner work-up with our 2,6 material, whether the next user is working in glass reactors or moving to kilo-scale plant runs.

    Analytical quality checks—sharp melting range, confirmed by repeated GC-MS and NMR—keep the profile on track batch to batch. We push well below the permitted thresholds for monochlorinated and trichlorinated benzals. This approach heads off checkpoint failures in later alkylation or substitution steps, saving our customers time and rework. Where others sometimes blend technical grades for price, we stand behind homogeneity in our drums. There’s no temptation here to cut corners with stream recycling or blending off-spec material, since cleanup and debugging scale-up problems cost everyone much more later.

    Knowing Where and Why the Product Succeeds

    Chemical manufacturing couples precise reaction control with practical knowledge earned by troubleshooting. We tune our production lines for sharp, repeatable chlorination without pushing into over-chlorination or deep side reactions. Temperature, feed rates, stirring rates, and even the order of addition—each has a hand in whether 2,6-Dichlorobenzal Chloride meets its mark. The smallest changes add up. Early in our experience, we tracked a small increase in a key impurity back to a supplier’s change in solvent grade. Only by investigating every upstream variable did we cut nuisance byproducts back to undetectable levels.

    Downstream, we’ve seen 2,6-Dichlorobenzal Chloride play a pivotal role in azine dye production cycles, where the dual ortho-chlorine substitution allows for predictable oxidative coupling. Customers in specialty polymers prefer it for the way the molecule slots into polycondensation step-ups, reducing variability in final product color and performance. In the arena of custom pharmaceuticals, our compound often becomes the template for complex intermediates. Its reactivity opens doors for selective reductions, Grignard couplings, or for further chlorination where other isomers push the reaction off course.

    Where other manufacturers sometimes ignore batch traceability, we maintain a record of every lot—reaction temperatures, yields, and analytical profiles. This traceability doesn’t just meet external audits; it supports root-cause analysis whenever a downstream customer runs into reactivity hiccups or compatibility issues. By sharing traceability data, we’ve helped clients catch inadvertent mismatches between their expected isomer and what they purchase from traders with unknown offshore sources.

    Clean Production and Responsible Handling

    Our enterprise takes emissions and waste custody as seriously as synthesis quality. Handling 2,6-Dichlorobenzal Chloride safely means fume control, closed-system transfer, and never shortcutting storage protocols. Workers spend a good deal of time on training in reaction quenching and emergency response. We have an entire setup for handling fugitive vent gases with absorbers and scrubbers, so that neighbors or regulatory inspectors won’t catch the faintest breath of chlorinated solvent from our fences.

    Waste minimization forms another part of the project. Chlorinated streams pass through separation and dechlorination setups before heading to controlled incineration. Some might see this as overkill. After three decades in chemical operation, we know local groundwater, air, and worker safety depend on above-standard practice—not only to satisfy compliance officers, but to keep our own team proud of their workplace. The most reliable method to ensure safe handling is ingrained habits and routinely checked safeguards, not relying on the hope that “it won’t happen to us.”

    Market Realities and Industry Trust

    Chlorinated aromatic intermediates invite price competition. Clients in dye, agrochemical, and pharmaceutical fields always compare multiple sources. The temptation can be to chase the lowest sticker price, but quality lapses or inconsistent specification get expensive in the long run. We’ve often found that poorly controlled reactions lead to stains, haze, or unpredictable reactivity in customer processes—all translating to lost batches and extra purification runs.

    A few years back, the market saw a wave of cheaper para-chlorinated alternatives pitched as drop-ins for the 2,6 isomer. They promised cost savings but failed on both selectivity and yield downstream. Several customers returned to a more reliable supply after repeated product rejections and expensive cleanups. In direct conversation, we sometimes walk new clients through precisely where those cheaper grades cause issues. Many newer entrants to synthesis or procurement won’t see the trouble until a finished lot fails application tests, and that cost rarely gets recouped. Industry-wide, trust builds not only on price but on the consistent performance that comes from firsthand process expertise and open, honest discussion.

    We won’t claim to create perfection in every run—there are always minor issues to improve—but transparent quality control and operator expertise bring us close. Issues get flagged and worked through instead of swept under the rug. Customers know there’s a real person by the reactor, not just an overseas entity or a rep without technical backup. Orders aren’t shipped until our in-house team is satisfied, because the next batch our customer produces depends directly on our discipline and care.

    Innovation and Future Outlook

    Since starting out on small glassware to now managing multi-ton reactors, we’ve watched both the science and the market for 2,6-Dichlorobenzal Chloride change. Process upgrade cycles are constant. Improved catalysts, solvent swaps to lower-impact options, and new approaches to in-situ monitoring come out of in-house R&D, driven by small, incremental changes coupled with feedback from the field. We don’t just adopt new methods because of outside pressure—it has to pass rigorous, real-world pilot tests on our lines without causing more problems than it solves.

    Digital data tracking means our QC samples and analytical data are integrated, allowing for quick trend spotting and batch comparison. Our customers benefit from tighter specs because process drift gets caught early—before it causes a problem for their own formulation or batch record. We see an industry shift towards even greater transparency: clients increasingly expect to audit not only our paperwork, but our plant protocols and continuous improvement records. We welcome the scrutiny, knowing that it only pushes us to higher standards.

    On the regulatory front, we adapt as both local and global standards tighten. Whether driven by environmental, worker safety, or product registration frameworks, the only viable route is to go above minimum requirements. We’ve invested to stay ahead, shifting to more automated handling and real-time monitoring. Workers spot leaks or deviations before they create incidents, and emissions reporting matches stricter expectations every year.

    Collaboration and Shared Expertise

    Our experience shows that product knowledge multiplies when shared openly. If customers describe subtle reactivity differences in their applications, we don’t dismiss it—we troubleshoot together, track down the root variables, and refine the process. Direct conversation with formulators or process chemists often sparks improvements. We pick up on technical nuances from questions and shared challenges, and that hands-on learning reshapes both our product and the advice we offer.

    If someone is scaling a process from lab to pilot, or shifting to continuous flow reactors, we adjust our supply protocols and batch size accordingly. There’s no one-size-fits-all answer. We give feedback rooted in our own operational insights: how to minimize bridging in feeders, how to optimize dissolution, and how to safely charge the compound to a batch without localized over-chlorination. It helps that most of our plant crew has run both batch and semi-continuous processes, so practical answers come easy, not as canned statements from a rep.

    We also value external input—auditors, technical consultants, and, most especially, our downstream customers. Years ago, one such partner noted a subtle catalyst carryover that altered reactivity in their own synthesis. We tracked down the cause, tweaked our wash protocols, and saw both their and our yields climb. That kind of shared problem-solving strengthens long-term partnerships and keeps standards rising across the sector.

    Commitment to Stewardship and Stability

    In today’s market, reliability means more than punctual shipments. Customers come back because of the peace of mind that comes from a supplier who takes pride in consistency, transparency, and technical command. Our operators check every charge. Shift supervisors check every critical parameter. Analysts check every outgoing drum.

    We’re proud to stand behind 2,6-Dichlorobenzal Chloride produced in a system where each team member knows not just what to look for, but why every step matters. Whether it’s spotting a color shift during filtration or adjusting a dose based on the history of earlier runs, small corrections underpin lasting trust.

    We see our job as more than just delivering molecules. From plant maintenance to product stewardship, our commitment covers the full lifecycle: safe production, accurate testing, open communication, and responsive application support. This is how a chemical manufacturer earns its place—and keeps it—year after year in the specialty intermediates field.

    Looking Forward While Honoring Experience

    As demand for specialized chlorinated benzyl intermediates continues to climb, we invest in process and people. There’s no substitute for eyes-on experience—chemists, operators, analysts, and field techs make improvements that no specification sheet can prescribe. That’s why our 2,6-Dichlorobenzal Chloride stands up to scrutiny batch after batch.

    We plan to keep producing with the same standards and expertise that have gotten us here. Tracking every batch, improving every protocol, and supporting every customer through their changing process needs remain our top priorities. In a world full of alternatives, trust and deep technical knowledge can’t be commoditized. They’re earned by making and shipping quality product, time and again.