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2,4-Dinitrobenzyl Chloride

    • Product Name 2,4-Dinitrobenzyl Chloride
    • Alias DNBC
    • Einecs 221-018-1
    • 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
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    Specifications

    HS Code

    852652

    chemical_name 2,4-Dinitrobenzyl chloride
    cas_number 89-61-2
    molecular_formula C7H5ClN2O4
    molecular_weight 216.58
    appearance Yellow crystalline solid
    melting_point 58-60 °C
    boiling_point 295 °C (decomposes)
    solubility_in_water Slightly soluble
    density 1.6 g/cm3
    flash_point 168.5 °C
    pubchem_cid 11545
    smiles ClC1=C(C=C(C=C1[N+](=O)[O-])[N+](=O)[O-])
    ec_number 201-927-7

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

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 2,4-Dinitrobenzyl Chloride, sealed with a screw cap, labeled with chemical and hazard information.
    Shipping 2,4-Dinitrobenzyl Chloride is shipped in tightly sealed containers, protected from light, moisture, and heat. Transport must comply with regulations for hazardous materials due to its toxicity and potential for harmful vapors. Appropriate labeling, secondary containment, and documentation are required. Handling by trained personnel is essential to ensure safe delivery.
    Storage 2,4-Dinitrobenzyl chloride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong bases and oxidizers. Protect it from light, moisture, and heat. The storage area should be appropriately labeled and accessible only to trained personnel, following all relevant safety regulations.
    Application of 2,4-Dinitrobenzyl Chloride

    Applications of 2,4-Dinitrobenzyl Chloride in Industrial Manufacturing

    As an established manufacturer of 2,4-Dinitrobenzyl Chloride, we supply this critical intermediate to industrial clients across several core chemical sectors. Below, we detail its principal downstream application scenarios, including regulatory conformance, standard formulation ratios, integration in process lines, and the end products produced by manufacturers worldwide.

    1. Active Pharmaceutical Ingredient (API) Synthesis: Benzyl Protecting Group Introduction

    In pharmaceutical API manufacturing, 2,4-Dinitrobenzyl Chloride serves as a selective benzylating agent, protecting specific functional groups during multi-stage synthesis of nucleoside analogs, antibiotics, and antivirals. Its electron-withdrawing nitro groups enable reliable deprotection downstream under controlled reduction, making it favored by process chemists targeting robust yields and strict impurity control.

    Industry compliance standards

    • ICH Q7A GMP for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) general monograph compliance
    • US FDA cGMPs (21 CFR Parts 210/211)
    • EMA Guideline on the Chemistry of APIs

    Typical usage ratio

    • 0.9–1.15 molar equivalents relative to target reactive group; process chemists optimize this level per API route to balance selectivity and cost.

    Downstream process integration

    • Introduced during the solution or solid-phase benzyl protection stage, commonly post-coupling and prior to cyclization or functional group manipulation steps.

    Final product types

    • Antiviral nucleoside APIs (e.g., lamivudine intermediates)
    • Antibiotic synthesis intermediates
    • Peptide-based therapeutic intermediates
    • Custom pharmaceutical intermediates incorporating protected functionalities

    2. Agrochemical Intermediate Production: Herbicide Synthesis

    Within crop protection chemical synthesis, manufacturers use 2,4-Dinitrobenzyl Chloride as an electrophilic alkylating intermediate in the preparation of dinitroaniline and other substituted benzyl herbicidal actives. Its consistent reactivity under tightly controlled reaction parameters suits industrial batch and continuous flow syntheses targeted at scalable herbicide outputs.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS) guidelines
    • ISO 9001 (Quality Management for Agrochemicals)
    • REACH (EC 1907/2006) chemical registration and safety dossiers
    • China GB-T 1604-2018 (National Standards for Agrochemical Raw Materials)

    Typical usage ratio

    • 0.8–1.05 mole per equivalent substrate; precise dosing varies depending on target compound and yield optimization studies.

    Downstream process integration

    • Applied in nucleophilic substitution steps, typically before condensation or aromatic substitution reactions yield final active ingredient skeletons.

    Final product types

    • Dinitroaniline herbicide intermediates
    • Precursor segments for pyridine-based weed control compounds
    • Industrial-scale formulations for soil-applied and foliar herbicides

    3. Specialty Dye Synthesis: Nitroaromatic Dye Manufacturing

    Dye and pigment producers integrate 2,4-Dinitrobenzyl Chloride to generate substituted benzyl intermediates, essential for diverse nitroaromatic dye systems. It acts as a key benzylating agent in processes that require targeted introduction of nitro functionalities and chlorine activation, supporting batch and semi-continuous colorant manufacturing lines for textiles, inks, and plastics.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (Restricted Substances List for Textiles)
    • EU REACH Annex XVII (Restrictions on Certain Hazardous Substances)
    • ISO 9001:2015 (Quality Management for Colorants)
    • GOTS (Global Organic Textile Standard) chemical lists for dyes

    Typical usage ratio

    • 0.3–0.7 mole per mole of core aromatics; optimal rates determined by retox yield and color intensity goals for each pigment type.

    Downstream process integration

    • Charged to colored intermediate formation reactors, after initial azo coupling or nitration, prior to final sulfonation or metallation stages.

    Final product types

    • Nitroaromatic-based textile dyes
    • High-stability pigmented inks for printing
    • Special effect colorants for plastics and polymers
    • Technical dyes for industrial marking systems

    4. Photolabile Protecting Group Synthesis for Biochemical Reagents

    Biotechnology and life sciences manufacturers deploy 2,4-Dinitrobenzyl Chloride to introduce orthogonal, photolabile benzyl protecting groups in oligonucleotide, peptide, and enzyme probe synthesis. This application critically enables photo-controlled deprotection for spatial or temporal activation in molecular biology assays and solid-phase synthesis platforms.

    Industry compliance standards

    • ISO 13485:2016 (Medical Device Quality for Biochemical Reagents)
    • USP General Chapter <1045> Biologics Quality
    • OECD Principles of Good Laboratory Practice
    • REACH SVHC (Substance Authorization for Research Chemicals)

    Typical usage ratio

    • 0.85–1.2 molar equivalents compared to target nucleophile; fine-tuned depending on sequence length and desired light-cleavage performance.

    Downstream process integration

    • Instilled at the solid-phase or liquid-phase protection stage prior to automated chain elongation; followed by irradiation-triggered removal in downstream assay or probe applications.

    Final product types

    • Photocleavable linkers for solid-phase oligonucleotide synthesis
    • Photoactivatable peptides for cell signaling studies
    • Controlled-release enzyme substrates
    • Biochemical probes with UV-removable protecting groups

    5. Fine Chemical Synthesis: Custom Benzylated Intermediate Manufacturing

    Custom fine chemical houses and contract manufacturers select 2,4-Dinitrobenzyl Chloride for synthesis of specialty benzylated intermediates, where downstream application generally requires the electron-poor aromatic ring system and a readily cleavable chloride function. Usual markets include advanced monomers, advanced materials, and microelectronics process chemicals.

    Industry compliance standards

    • ISO 9001:2015 and ISO 14001:2015 (Quality and Environmental Management)
    • REACH (European Chemicals Agency, substance registration required for >1 tonne/year)
    • Chinese GB/T 19001 (Quality System Standard for Chemical Industry)
    • Japan Industrial Standard JIS K1402 for fine chemicals

    Typical usage ratio

    • Varies 0.5–1.5 mole per long-chain or aromatic substrate; set by target intermediate architecture and downstream conversion efficiency.

    Downstream process integration

    • Employed in one-pot benzylation reactions, typically as the electrophilic partner in SN2 or SNAr mechanisms, prior to overall product work-up and purification.

    Final product types

    • Advanced benzylated monomers for specialty polymers
    • Electronic grade chemical precursors for photoresist
    • Substituted intermediates for advanced material fabrication
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    Certification & Compliance
    More Introduction

    2,4-Dinitrobenzyl Chloride: Experience from the Factory Floor

    Hands-On Synthesis—What Goes into 2,4-Dinitrobenzyl Chloride

    In this industry, chemistry is practical work—reactions don’t just happen on paper. Producing 2,4-dinitrobenzyl chloride is demanding. We see this in every batch that comes off the reactor. The chemical formula C7H5ClN2O4 may seem clinical in textbooks, but to us, it translates to yellow crystalline powder with a strong, penetrating odor and a tendency to clump in a humid shop. Each kilogram we haul out of the filter is proof of careful control over nitration and chlorination stages.

    Model variations rise mainly from the particle size and purity. Most downstream users want at least 98% purity, or customers complain about poor yield in their coupling steps. Some fine chemical users push for higher specs—99% or above—to meet tight standards for pharmaceutical synthesis. Our batches run from 98% to 99.5%. We routinely hit an average particle size between 100–200 mesh, unless someone specifies otherwise.

    Factory Work: From Reactor to Finished Goods

    On the line, we manage strong reagents and exothermic reactions that don’t forgive mistakes. Lab yields don't always translate to full-scale batches. We run jacketed glass-lined steel reactors because stainless can't stand up to the acid mix. Temperatures have to be monitored closely, especially in chlorination, which can get out of hand with a careless heating cycle.

    After reaction, we cool, filter, and wash the powder repeatedly to remove acid and trace nitro by-products. Washing must be thorough. We’ve seen less thorough procedures leave behind too much color and off-odors, which can trigger customer complaints. Residual moisture leads to caking, so drying conditions require constant attention. River fans, heated trays, vacuum ovens—all come into play. With each run, we tweak variables to match the batch to end user specs, always keeping a close log of every step.

    How 2,4-Dinitrobenzyl Chloride Fits into the Industry

    We don’t need to guess at where this material goes—our long-standing clients share their stories. Most order it for use in pharmaceutical intermediates. The benzyl chloride group anchors a wide range of synthetic organic chemistry, and the dinitro configuration makes this compound key for making protective groups, controlled-release pro-drugs, and enzyme blockers. Our biggest volume moves toward the synthesis of nucleoside analogues and select herbicides.

    This isn’t an all-purpose benzylic halide. Customers who tried substituting it for 4-nitrobenzyl chloride or standard benzyl chloride return to this product when they need faster reactivity or unique selectivity. That’s the outcome of having two nitro groups positioned on the aromatic ring, which increases its electron-withdrawing power beyond what a single nitro or unsubstituted version can offer. We’ve run pilot trials with both, and our technical team always points out a stronger activation effect with 2,4-dinitrobenzyl chloride, especially for nucleophilic displacement reactions.

    A large pharmaceutical client faced bottlenecks in the protection of hydroxyl groups using classic benzyl chloride derivatives; they couldn’t hit the yields they needed. Swapping to this compound provided a much cleaner product, fewer by-products, and downstream steps no longer suffered from difficult deprotection. It’s a small change in the raw material, big advantage in cost control by the end of the campaign.

    Genuine Differences vs. Similar Products

    That brings up questions our technical support team fields each week about the differences between this and other benzyl chlorides. Many think all such halides should stand in for each other, but practice in the workshop shows otherwise. For folks unfamiliar with production, benzyl chloride (regular, unsubstituted) and 4-nitrobenzyl chloride appear “equivalent” on paper. In reality, the behavior during alkylation, especially under strong or mild base conditions, changes dramatically.

    We ran side-by-side comparisons, keeping conditions constant—same base, same temperature, matching batch volume. The 2,4-dinitro version kicked off with faster rates, and product isolation was easier. Purity after crystallization held up better, leading to less rework and less waste. The extra nitro group doesn’t just amp up reactivity; it drives higher conversion and less side formation, which makes a difference on the bottom line over a dozen or more campaign batches.

    From environmental control, we see another difference. 4-nitrobenzyl chloride demands stricter handling because its dust gives workers more trouble and lingers longer in the air. In contrast, while 2,4-dinitrobenzyl chloride also needs full dust control, the clumping makes it less likely to become airborne in dry handling setups. It’s a practical, not theoretical, improvement.

    Handling, Storage, and Worker Health—Lessons from Practice

    Customers sometimes underestimate how much handling matters in performance and safety. Our plant uses closed rotary valves and sealed drums, not just to comply with safety culture but also to meet expectations from customers who want clean, uncontaminated product. Straight from our experience, the product must go in lined steel drums with desiccant packs if it’s headed to humid regions. Failing here means getting calls about solidified lumps and blocked feeding tubes.

    We see customers improvising storage in plastic bags or open bins which rarely ends well. Moisture seeping in causes discoloration, and this is not a cosmetic issue. The powders pick up acidic odors and perform poorly in subsequent steps. Our practice, developed over years, keeps air and water vapor out, and shows in consistently high-quality, flowable product that powders evenly and incorporates quickly in solution.

    Worker health sits at the center of factory life. Between shifts, we monitor air and dust with real sensors—not just because regulations demand it, but because folks learn fast that mild exposure causes headaches and eye irritation. Our crews use fitted masks, chemical gloves, proper goggles and always double-check ventilation fans. Clean-up after accidental spills is fast and determined; this chemical doesn’t allow for slow responses. Training is ongoing, and we update protocols after every incident, big or small.

    Quality Assurance—Lessons Learned Batch by Batch

    In tightly run operations, quality ties directly to how well workers follow procedures and how sharp the analytical chemistry team is. We run HPLC and GC tests on every outgoing shipment. There are no quick passes—small impurities snowball into big rework downstream. A few years back, a shipment showed unexpected off-color and odor. Instead of rushing it off, the team stopped it at the warehouse, pulled samples for extra runs, and traced the source to slight overheating in a chlorination stage. After corrective action, that batch went for reprocessing and never left the lot.

    Consistency wins business. Approaches like holding back certain drums, cross-checking spectra, and routine moisture analysis all keep our product stable from order to order. Nobody wants unexplained performance swings—a lesson learned after closely monitoring product feedback loops that flagged quality drift seasons before they became full-blown returns.

    We always encourage our customers to share how they use this compound: which routes, what solvents, where bottlenecks emerge. Their on-the-ground feedback influences where we tighten specs, adjust particle sizing, or work out packaging tweaks. In one memorable case, a paint additive manufacturer saw unexpected precipitation in their process. We found higher trace amounts of unreacted nitro intermediate, not caught with basic UV spectrometry. Following their complaint, we recalibrated the HPLC standards, and the change reduced complaints right away.

    Regulatory and Shipping Realities

    Shipping this material involves more than just packing it up and rolling it onto a truck. We know the importance of paperwork—our staff prepare the material safety data sheets, and we keep our hazard labeling system updated with GHS standards and packaging directives. Some regions require extra documentation detailing dioxin contamination thresholds and handling guidelines. Our records show exact batch histories and storage temperatures during transit, because authorities want evidence for every claim.

    We also guide customers through international compliance, offering experience with port authorities and customs checks. In cases where a client needed support during regulatory resets, we provided documents from authenticated labs to clear containers detained for analysis. This approach didn’t just speed up procedure; it built trust that kept their business returning in the next supply cycle.

    Serving Real-World Chemists, Not Just Laboratories

    Lab-scale syntheses look straightforward in journals, but moving from bench to factory takes adaptation. Our technical liaison team talks regularly with industrial chemists at agricultural firms, small pharmaceutical shops, and specialty coatings plants. They all face different process challenges—scaling up, managing waste, or keeping costs within budget.

    One agricultural developer pushed to minimize solvent waste during use of 2,4-dinitrobenzyl chloride in their herbicide formulation. By running joint trials and sharing in-house process notes, our team tuned batch parameters and offered tighter filtration. Their waste solvent volumes dropped 8% over three months. We use these stories to evolve our technical service, because actual plant conditions differ from textbook expectations.

    Pharma companies value batch traceability. They request batch letters certifying full compliance with trace metals, residual solvents, and even raw material origin. Since we run regular audits, we can always provide these on short notice. Each letter references actual batch logs, signed off by both our QA inspector and site chemist. These steps aren’t just regulatory demands, but real proof that traceability can be backed by test results and signatures, not just technical brochures.

    Troubleshooting and Solving Production Challenges

    Anyone who’s spent time in a chemical plant has stories of production runs that didn’t go as planned. 2,4-dinitrobenzyl chloride is sensitive to over- and under-chlorination. Missteps in the timing at the chlorination phase yield extra impurities, and our operators pick this up fast by watching for changes in color and solubility. Rapid response during these stages—by adding extra base washing, changing the acid quench timing, or switching the filtration medium—has saved plenty of batches from becoming waste.

    Sometimes, the issue doesn’t start in our plant but stems from a supplier’s variable upstream raw materials. A slight shift in the oxidant grade or incoming benzyl alcohol impurity profile causes headaches. We establish supplier review cycles to push consistency, giving feedback on any batches that didn’t meet our benchmarks. In one year alone, this kept two large shipments from failure and improved our first-pass production reliability.

    We also found that maintaining slightly higher than standard purity helps customers who operate continuous reactors instead of batch processes. The cost to us—extra washes, double-filtration, longer drying—is offset by the loyalty of users who no longer face reactor blockages or fouled lines. The insight here is that long-term performance matters more than the upfront price.

    Improving the Future of 2,4-Dinitrobenzyl Chloride Manufacturing

    Environmental discharge sits at the forefront of every production review. We run in-house waste processing—including acid neutralization tanks, carbon filters, and controlled emissions vents—to stay ahead of local and regional mandates. Audit teams visiting our plant get walk-throughs of these setups, and we share best practices at industry seminars, hoping to raise the performance for the sector. Cleaner process water, minimal emissions, and responsible waste handling don’t just tick boxes—they ensure continued supply contracts with global buyers.

    Constant investment in process intensification, such as moving from manual pH adjustment to automated, in-line controls, cuts error margins and maintains consistency. Upgrades in reactor sensors, vacuum pumps, and filtration lines smooth out bottlenecks that used to sap manpower. The return is a safer shop floor and a product that consistently matches readings on the spec sheets, not just at batch approval but across the shipment run.

    We host open days for technical teams from customer sites to tour our facilities, learn about batch records, and see the process firsthand. This hands-on transparency brings confidence to their purchasing teams—and plenty of feedback on how to improve downstream integration. It keeps us on our toes, looking for incremental ways to bring more usability, cleaner product, and tighter specs.

    Continuous Dialogue—Putting Chemists at the Center

    All these process improvements, product tweaks, and safety upgrades mean little if they aren’t relevant to those using the product daily. Our approach puts the customer’s chemist in direct communication with our technical teams. We take every recurring question—what causes off-odors, why does color vary, how to clean feed lines—and treat it as a source of process learning.

    For every ton shipped, we include not just a certificate of analysis but direct access to our field technical managers. Many product improvements, such as more robust drum linings or better anti-caking agents, trace their roots to a random call from a dedicated plant operator. Over time, this dialogue closes the gap from factory to end product.

    In a plant that’s handled 2,4-dinitrobenzyl chloride since before automation came in, it’s clear that behind every drum of this chemical sits knowledge gained one batch, one challenge, one innovation at a time. This isn’t just a specialty intermediate; it’s the product of hands-on chemistry, constant vigilance, and regular feedback from those actually using the product, day in and day out.