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2,5-Dichlorobenzyl Bromide

    • Product Name 2,5-Dichlorobenzyl Bromide
    • Alias Benzyl Bromide, 2,5-dichloro-
    • Einecs 216-146-6
    • 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

    531236

    Chemicalname 2,5-Dichlorobenzyl Bromide
    Casnumber 1667-10-3
    Molecularformula C7H5BrCl2
    Molecularweight 239.93 g/mol
    Appearance White to off-white crystalline powder
    Meltingpoint 45-48°C
    Boilingpoint 267°C
    Density 1.67 g/cm³
    Solubility Slightly soluble in water; soluble in organic solvents
    Purity Typically ≥98%
    Refractiveindex 1.6200 (predicted)
    Synonyms Benzyl bromide, 2,5-dichloro-
    Smiles C1=CC(=C(C=C1Cl)Cl)CBr

    As an accredited 2,5-Dichlorobenzyl Bromide 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 2,5-Dichlorobenzyl Bromide, sealed, with hazard warnings and chemical identification label.
    Shipping 2,5-Dichlorobenzyl Bromide is shipped as a hazardous material, requiring tightly sealed, chemical-resistant containers. Packages must be clearly labeled with appropriate hazard warnings. Transport should comply with local and international regulations, including UN codes, and packages must be protected from moisture, heat, and physical damage during transit. Handle with appropriate safety measures.
    Storage 2,5-Dichlorobenzyl Bromide should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight, in a cool, dry, well-ventilated area. Keep it separate from incompatible substances such as strong oxidizers and bases. Ensure storage areas are equipped to contain spills and use proper labeling to avoid accidental exposure. Follow all regulatory and safety guidelines.
    Application of 2,5-Dichlorobenzyl Bromide

    Applications of 2,5-Dichlorobenzyl Bromide in Industrial Manufacturing

    2,5-Dichlorobenzyl Bromide plays a significant role as an intermediate across select chemical manufacturing sectors, enabling the production of high-value fine chemicals, pharmaceutical actives, polymer additives, and agrochemical ingredients. As a direct manufacturer, we support these sectors by delivering precise product specification, consistent lot quality, and compliance documentation to streamline our customers' downstream processing.

    1. Pharmaceutical Active Ingredient Synthesis

    Pharmaceutical manufacturers use 2,5-Dichlorobenzyl Bromide as a critical alkylation agent during the multi-step production of certain antihistamines and antifungal actives. Its reactivity at both halogenated positions enables performance in selective benzylic substitutions, often under controlled base conditions. Quality management systems require rigorous impurity control, limiting batch-to-batch variability. End-use formulations pass strict regulatory scrutiny, demanding detailed material provenance and analytical validation throughout the GMP pipeline.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF and EP monographs for drug substances
    • 21 CFR Parts 210/211 Current Good Manufacturing Practice (cGMP)
    • REACH Regulation (EC) No 1907/2006 for chemical registration and safety

    Typical usage ratio

    • 0.08–0.15 molar equivalents relative to the target substrate, adjusted based on side product minimization and reaction yield optimization requirements.

    Downstream process integration

    • Added during the benzylic bromination or benzylation stage, immediately after primary ring activation and prior to final cyclization or condensation steps.

    Final product types

    • Antihistamine active pharmaceutical ingredients (API)
    • Fungicide pharmaceutical precursors
    • Generic active pharmaceutical ingredients requiring halogenated benzyl cores

    2. Agrochemical Intermediate Manufacturing

    Leading agrochemical formulators employ 2,5-Dichlorobenzyl Bromide as a specialized intermediate during the synthesis of selective herbicide and fungicide actives. Its brominated benzyl structure allows dependable coupling with heterocyclic scaffolds, yielding target molecules with field-proven plant-protective behavior. Minimal residual content and hazardous byproduct traceability are mandatory, with specification sheets closely aligning with multinational regulatory filings.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • OECD Guidelines for Testing of Chemicals
    • ISO 9001:2015 Quality Management System in chemical intermediate manufacturing
    • EU Regulation (EC) No 1107/2009 for pesticide approval and registration

    Typical usage ratio

    • 0.1–0.25 molar ratio to active core synthesis batch, fine-tuned based on conversion efficiency and target purity grade.

    Downstream process integration

    • Introduced during the penultimate stage of active ingredient assembly, specifically during the nucleophilic substitution on benzyl halides with nitrogen- or sulfur-containing compounds.

    Final product types

    • Benzyl-based herbicide active ingredients
    • Benzyl-substituted fungicide cores
    • Plant growth regulator intermediates with halogenated benzene functionalities

    3. Fine Chemical Synthesis for Specialty Monomer Production

    Producers of specialty monomers and polymer additives incorporate 2,5-Dichlorobenzyl Bromide into their synthesis workflows to modify backbone or pendant group chemistry. The dual halogenation offers versatile reactivity sites for custom polymer design, particularly for flame retardant polymers and performance coatings. Each batch undergoes comprehensive trace analytical assessment to certify the absence of residual bromide or dioxin byproducts.

    Industry compliance standards

    • ASTM D6319 for polymer intermediates
    • ISO 9001:2015 for specialty chemical production
    • REACH Annex XVII restrictions for hazardous substances in polymers
    • RoHS Directive 2011/65/EU for end-use electrical and electronic applications

    Typical usage ratio

    • 0.03–0.2 parts by weight per 100 parts resin reactant, modulated to achieve target monomer functionality and downstream reactivity.

    Downstream process integration

    • Employed during in situ functional group modification, before final polymerization or polycondensation reaction sequence.

    Final product types

    • Halogenated monomers for specialty polymer blends
    • Polymer-bound flame retardants
    • High-durability performance coatings and specialty resins

    4. Industrial Dye and Pigment Intermediate Synthesis

    Manufacturers of specialty dyes and organic pigments utilize 2,5-Dichlorobenzyl Bromide to introduce halogenated groups into aromatic dye intermediates. This modification enhances lightfastness, chemical resistance, and color intensity in the finished pigment molecule. Process controls require careful monitoring, particularly to limit colored side-products and comply with exhaustive downstream contaminant analysis relevant to textile and plastics end-markets.

    Industry compliance standards

    • Oeko-Tex Standard 100 for textile dye safety
    • EN 71-3 migration of hazardous elements for pigment use in toys
    • ISO 787 general methods for pigment testing
    • Registration under TSCA Section 8(b) for production within the United States

    Typical usage ratio

    • 0.07–0.23 molar equivalent per aromatic core, adjusted for targeted chromophore tuning and process yield.

    Downstream process integration

    • Added during the aromatic bromination or directed ortho-metalation (DoM) sequence, prior to azo- or phthalocyanine core construction steps.

    Final product types

    • Halogenated azo dye intermediates
    • Organic pigments for plastics coloration
    • Light-resistant synthetic dyestuffs for industrial textiles
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    Certification & Compliance
    More Introduction

    2,5-Dichlorobenzyl Bromide: A Closer Look from the Manufacturer’s Bench

    Pursuing Precision: The Real Story Behind 2,5-Dichlorobenzyl Bromide

    Working day in and day out in the lab, I see how products like 2,5-Dichlorobenzyl Bromide (CAS 3944-85-6) form the foundation of complex chemical syntheses. Experience shows that this compound pulls its weight where selectivity and reactivity matter. 2,5-Dichlorobenzyl Bromide is produced through a direct bromination of 2,5-dichlorotoluene under controlled conditions, keeping impurities to an absolute minimum. Each batch reveals a crystalline material with sharp melting behavior, signaling tight control at every step. Every gram that leaves production meets a single standard: purity not dipping under 98%.

    Keep in mind that a rigorous purification route separates our 2,5-Dichlorobenzyl Bromide from what’s possible through quick-and-dirty synthesis. It’s easy to cut corners when working with aromatic bromides — skipping post-reaction cleanups, running with broad melting ranges, or ignoring lingering toluene and unreacted bromide. Unfortunately, those shortcuts leave you with yield losses, noisy spectra, and failed downstream reactions. After years working shoulder-to-shoulder with research chemists, I’ve seen their projects hinge on these details. Chasing cheap stocks always winds up costing more, especially at scale.

    Everyday Applications That Shape Real Outcomes

    Anyone who’s spent real time in development chemistry spots the gap between idealized lab procedures and practical manufacturing. We supply 2,5-Dichlorobenzyl Bromide mostly to agrochemical and pharmaceutical intermediates teams. It’s essential in aryl ether formation, phenolic protection, and as a building block for specialty benzyl derivatives.

    Pharmaceutical researchers often use this molecule as a key intermediate for synthesizing compounds with anti-bacterial and anti-fungal activity. In agrochemistry, the molecule’s high reactivity and unique dichlorinated pattern drive selectivity in coupling and substitution pipelines. As a halide, it brings high leaving group ability — bromide is easier to displace than chloride, making it essential when milder conditions are demanded and substrates balk at sluggish chloride substitution.

    For newer teams planning scale-up, our technical support often gets questions on solvent compatibility, storage, and safe handling. Brominated aromatics sometimes get a bad reputation, but keeping open lines between manufacturing, R&D, and QC leads to real improvements. We’ve responded directly to requests from process chemists, adjusting micronization strategies and lot sizes based on prior feedback about clumping and charge buildup. That kind of detail, right down to making sure our crystalline material resists caking, makes production runs smoother — especially in automated feeing systems.

    What Makes 2,5-Dichlorobenzyl Bromide Distinct?

    Some readers might draw direct comparisons with general benzyl bromides. Here is where the experience of a synthesis chemist provides real-world context. Unsubstituted benzyl bromide has reactivity but delivers little selectivity if you want downstream substitution to occur only at specific positions. Put two chlorines at the 2 and 5 positions, and you transform your substrate into one that answers more finely to the needs of specialty product pipelines.

    Substituents matter. Casting the net beyond 2,5-dichloro analogs, you see that meta or para-chlorination shifts the electronics enough to complicate later efforts. The 2,5-dichloro placement razor-focusses reactivity, giving you higher yields in nucleophilic substitution reactions. We’ve watched customer yields change significantly (by over 10% in some cases) just by swapping in our product for less-pure or less-selective analogs. The difference lies in less byproduct formation, less need for laborious re-crystallization, and more straightforward purification.

    Colleagues working with broader aryl bromides often wrestle with mismatched melting points or overly-volatile solvents. Our production route produces crystals that offer stable handling at room temperature, neither sticking to the vessel nor vanishing into the vapor phase at the first sign of warmth. Predictable melting (usually in the low triple digits Celsius) signals proper batch control and makes weighing and handling less hazardous.

    We also get questions about our choice of packaging. Powders and granules demand robust, moisture-proof containment. Our use of layered liners, tested against ambient humidity swings and transit jostling, means that what leaves our facility matches the properties delivered to your door — no surprise agglomeration, no stray fines leaking in transit. These are not minor details, especially for teams running in high-throughput or multi-shift environments.

    Batch Control, Purity, and Quality: Seeing Behind the Numbers

    Chemists know there’s more to a product’s value than its assay. Our most demanding users run their own analyses upon receipt, whether it’s HPLC, NMR, GC-MS, or dark bottle shelf-life studies. They’ve taught us that cross-checking by different methods catches what a single purity number can miss: traces of isomer, halogen contamination, even residual solvents. Our own QC team runs a full panel on every lot — and not just one bottle randomly sampled. The data go into our tracking system, connected directly to feedback from customers who run into potential process hiccups.

    Take water content: It’s not unusual for reactive halides to drift higher than expected during humid months. We’ve iterated drying and sealing steps several times in response to requests. Our manufacturing shifts monitor batch atmosphere, container purge, and double-sealed packs. We tune grinding and sieving to prevent static, which can attract airborne moisture and dust during filling.

    Our plant’s continuous improvement loop didn’t spring up from a checklist. It’s the product of decades of small feedbacks — a process engineer calling out lot-to-lot weight loss, a chemist reporting off-odors during a scale-up trial. Listening to each story not only fixes individual issues but improves the whole supply. We now spot points where contamination or degradation could happen before a customer does. That’s the difference a manufacturing background brings to the table.

    Handling, Storage, and Long-Term Reliability

    2,5-Dichlorobenzyl Bromide, as an alkylating agent, brings both utility and responsibility. Teams working with it store it cool, sealed tight, away from nucleophilic reagents, acids, or prolonged light. In our facility, drums rest on lined racks under filtered dry air, not exposed to foot traffic or vibration. Every operator wears PPE and double checks container closure — the minor time investment up front avoids broken seals or moisture spikes later on.

    We encourage users to set up storage that mimics what works at our site: steady climate, inventory rotation, and transparent hazard labeling. Open containers only immediately before use, and keep the workspace under local extraction. While occasional spills are part of lab reality, neutralizing cleanup protocols prevent corrosive degradation and exposure. We freely share our own emergency drills because they’re built on actual incidents, not only regulation.

    Having walked the warehouse floor many times, I know transport puts the product’s physical integrity to the test. Our facility inspects packaging not just for chemical compatibility but also for mechanical impact resistance. The transit from our site to your loading dock often covers thousands of kilometers, and the crystalline form has to weather all sorts of bumps and jolts. We’ve tested our standard drums and inner bags under simulated transport stress — stacking weight, vibration, and humidity sweep. It’s not pretty seeing powder spilled on trial runs, but catching those flaws before shipping means you get product that pours clean and dry.

    Downstream Chemistry: Beyond the Bottle

    Users often ask if process changes are needed when switching from a general benzyl bromide to 2,5-Dichlorobenzyl Bromide. My experience is that you see a difference in both the rate and selectivity of nucleophilic attack. The two chlorines on the aromatic ring draw electron density away, making the benzylic position more susceptible to reaction — a benefit if your process needs fast, clean conversion, but something to mind if your solvents, bases, or nucleophiles are highly reactive themselves.

    Over the years, process chemists tell us that using our 2,5-Dichlorobenzyl Bromide trims steps in purification. Side-chain halogenation doesn’t bring along the same kind of ring-chlorinated isomers you might find when reacting less carefully controlled toluene derivatives. A drug synthesis pipeline benefits from reduced clean-up, especially when final-step impurities trip regulatory alarms. We conduct our own mock reaction screens — if we see unexpected byproducts or off-odors, the lot is blocked from leaving the plant. That stringency reflects how we view our responsibility to end-users.

    The feedback loop goes both ways. We get direct reports when a product ships to a customer and their in-house team spots surprising reactivity or shelf aging. Sometimes a tweak in our formulation — extra filtration or a shift in crystallization temperature — makes all the difference for a customer’s downstream step. That’s the benefit of direct manufacture: we have the levers, not just the paperwork.

    Comparing Against Alternatives: Informed Choices

    For projects testing the difference between various benzyl bromides, the 2,5-dichloro analog stands out. In applications needing selectivity in aromatic substitution or avoidance of over-reactivity in subsequent steps, this product consistently outperforms mono-chlorinated or non-chlorinated variants. Others may argue that simple benzyl bromide, with fewer halogens, is more cost-effective, but that calculation often skips yield losses and extra process steps needed to remove unwanted byproducts or stabilize intermediates.

    We’ve seen cost-benefit analyses flip completely once teams account for side reactions or failed batches. Purity, consistent melting point, and reliable crystalline structure matter much more as production scales. A kilo of product lost to incomplete conversion or extra washing can tip projects over budget. 2,5-Dichlorobenzyl Bromide makes those problems manageable and repeatable — small things that, in aggregate, make or break a manufacturing campaign.

    Batch-to-batch reliability doesn’t just look good on a certificate. It feels different on the line, during weighing, mixing, and transferring. Plant operators know the difference between a clumpy, moisture-affected powder and a free-flowing, freshly packed product. Downstream, those details translate to reproducible reactions, reliable analytical data, and a safety record with less drama.

    Partnering for Solutions: More Than Just a Supplier

    We are compelled by obligation, not just regulation, to partner with customers for safer, cleaner, and more efficient production. Our technical team stays engaged through direct conversations and hands-on troubleshooting. We’ve run site visits, compared batch records, even reviewed glovebox and pilot-scale data when a customer encountered solubility or reactivity issues.

    Our plant’s protocols build on those experiences. For instance, one pharmaceutical partner found anomalous crystal growth hindering their charging process. Tweaking our milling method, involving a change in sieve mesh and an anti-static treatment, resolved the bottleneck. A crop science group reported trace iron contamination due to packing material breakdown — a switch to all-polymer liners eliminated the problem. Both these changes rolled through our production SOP, and all downstream users benefitted.

    A supply chain is only as strong as its weakest link — that’s not just a truism from the boardroom; it’s reality at the receiving dock. By focusing on both chemical and physical integrity at each handoff, we prevent disruptions, failed production trials, and costly downtime.

    Working with Us: Real People, Real Results

    Every lot of 2,5-Dichlorobenzyl Bromide reflects the efforts of chemists, operators, engineers, and quality specialists dedicated to making a product that does what you need without fail. That focus comes from long habits — recording every variable, reviewing every near-miss, and testing every handling step under realistic scenarios. Our doors are open for feedback, whether routine or urgent.

    We don’t only sell a chemical; we offer a working relationship that values your team’s success as much as ours. From transparent batch records to direct technical support and after-delivery troubleshooting, we’re here for the long haul. Each improvement in our product starts with questions and stories from those who use it in the real world. That’s the advantage of buying manufacturer-direct: answers that fit the problem, not just a number on a spec sheet.

    Looking Forward: Building Better Chemistry Together

    Today’s chemical manufacturing environment faces demands for greater speed, certainty, and safety. Through tighter process discipline, deep connection with end-use chemists, and unbroken focus on environmental and human safety, we believe we help push the whole industry forward. The story of 2,5-Dichlorobenzyl Bromide, like any specialized intermediate, belongs to the bench and plant as much as it does in a catalog or on an invoice.

    It’s the unseen details of control, experience, customer feedback, and incremental improvements that shape performance in real applications. In every drum, bag, or sample that leaves our site, years of accumulated know-how, reliable infrastructure, and passion for chemistry come together to ensure what you receive delivers genuine value. That legacy speaks loudest through the work you build — and the progress you make possible — with the best intermediates at your side.