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HS Code |
541979 |
| Product Name | 3,5-Dibromobenzyl Bromide |
| Cas Number | 5112-27-6 |
| Molecular Formula | C7H5Br3 |
| Molecular Weight | 345.83 g/mol |
| Appearance | White to off-white crystalline solid |
| Melting Point | 59-61°C |
| Density | 2.20 g/cm³ (approximate) |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | C1=CC(=CC(=C1Br)CCBr)Br |
| Synonyms | α-Bromo-3,5-dibromotoluene |
| Storage Conditions | Store in a cool, dry place; keep container tightly closed |
| Purity | Typically ≥97% |
| Ec Number | 225-787-6 |
As an accredited 3,5-Dibromobenzyl Bromide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25g amber glass bottle labeled "3,5-Dibromobenzyl Bromide," with hazard warnings, tightly sealed cap, and tamper-evident packaging. |
| Shipping | 3,5-Dibromobenzyl Bromide is shipped in tightly sealed containers, protected from moisture and light. It is classified as a hazardous material and transported following appropriate regulations for corrosive and toxic substances. Shipping includes proper labeling, documentation, and safety precautions to ensure secure handling and compliance with international chemical transport standards. |
| Storage | 3,5-Dibromobenzyl Bromide should be stored in a tightly sealed container, away from light, moisture, and incompatible materials such as strong oxidizers. Keep it in a cool, dry, well-ventilated area, preferably in a chemical storage cabinet designed for corrosive or reactive substances. Ensure proper labeling, and restrict access to trained personnel to prevent accidental exposure or contamination. |
Applications of 3,5-Dibromobenzyl Bromide in Industrial ManufacturingAs a specialized manufacturer, we supply 3,5-Dibromobenzyl Bromide to support downstream synthesis in several regulated technical fields. The following sections detail its industrial adoption across distinct application environments, with focus on regulatory alignment, recommended ratios, integration methodology, and downstream output. 1. Pharmaceutical Intermediate for Antihypertensive API SynthesisManufacturers employ this compound as a key intermediate in the multi-step synthesis of specific antihypertensive active pharmaceutical ingredients. Reacting the dibrominated benzyl bromide with nucleophilic agents enables regioselective construction of functionalized benzyl building blocks. Each stage requires strict monitoring for residual bromide and halide content. Accurate stoichiometric control is essential to minimize side reactions and ensure high yield upstream of final API purification. Industry compliance standards
Typical usage ratio
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2. Agrochemical Synthesis for Fungal and Insect Control AgentsThe dibrominated structure serves as a crucial halogenated synthon for agrochemical producers. Through Grignard or palladium-catalyzed reactions, formulators incorporate the compound into pyrethroid and triazole frameworks used in crop protection. Process chemists prioritize strict lot traceability and control of inorganic impurities to meet environmental and occupational exposure standards. Efficacy depends on maintaining bromine integrity through multi-step transformations. Industry compliance standards
Typical usage ratio
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3. Specialty Polymers and Functional Resin ModificationIn advanced polymer manufacturing, this material acts as a reactive brominated monomer for synthesizing specialty polymers with flame-retardant properties. Resin engineers dose the substance during condensation reactions or for controlled crosslinking, taking care to optimize reactivity and minimize unreacted residues. QA teams conduct extensive post-reaction bromine analysis in compliance with polymer application safety standards. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Organic Electronics and Photoresist Precursor ManufacturingThe dibrominated compound fulfills a key role for electronic material producers developing photoresist and OLED precursor resins. Synthetic chemists use it as a precursor for constructing rigid aromatic frameworks or reactive chains necessary in high-purity electronic layers. Processing requires advanced purification and strict avoidance of ionic or residual halide contamination to meet device integration requirements. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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For many years, the chemical plant floor has seen a steady demand for specialty benzyl halides, and among those, 3,5-Dibromobenzyl Bromide stands out for its precision in synthesis. Plenty of people in the industry view this molecule as just another halogenated aromatic, but from where we stand, its clear-cut structure and distinctive reactivity open up doors not found with other products on our line.
The core of 3,5-dibromobenzyl bromide is unmistakable. With bromines on the 3 and 5 positions of the phenyl ring and a benzyl bromide side chain, you get strong selective reactivity. Personnel who have worked with ordinary benzyl bromide or its single-halogen variants quickly notice two things: 3,5-dibromobenzyl bromide won’t acetylate or alkylate in the same patterns as lower-brominated versions. Bromination at these specific points influences everything from solubility in common organic solvents to resistance to some oxidative degradation pathways. This matters when you’re scaling up for hundreds of kilos, where every lost percent means higher raw material spend and more headaches in cleanup.
From a fabrication perspective, the real-world control over halogenation conditions decides the quality you get in each batch. Each time our team lines up for chlorination or bromination, we bank on thoroughly monitored reaction periods and post-treatment purification. Side reactions can sneak up, but tight process engineering means our 3,5-dibromobenzyl bromide doesn’t come with the mixed isomer headaches that show up in poorly controlled plants. Overbromination and underbromination both sap the end result, especially for pharmaceutical or fine chemical partners downstream. Our in-process analytics focus on keeping the profile tight, and isolation is fine-tuned for consistency lot after lot.
A manufacturer handling both one and two bromine variants sees the difference at the reactor and in market applications. Take benzyl bromide, which has found a place in alkylation chemistry, especially for routine quaternization or as a starting material for surfactant synthesis. Its monobromo cousins are widely used but often lack the targeted reactivity that halogen symmetry brings. Swap to 3,5-dibromobenzyl bromide and you’re working with a molecule that behaves in a more predictable way during multi-step transformations. When you monitor conversion rates or side-product profiles, you see sharper isolation of desired end products, which lets plant teams use less aggressive purification strategies, reducing waste and energy use.
Chemists doing late-stage functionalization or building blocks for agrochemical actives often look for aromatic units where position-specific reactivity drives selectivity in coupling or substitution. Bromine’s presence at the 3 and 5 positions creates two symmetrical points ripe for nucleophilic substitution or palladium-catalyzed cross-coupling, vastly simplifying protection-deprotection routines. Those applying 3,5-dibromobenzyl bromide in Suzuki or Stille couplings, for instance, describe more straightforward process development compared to using mixtures of ortho and para isomers. In areas such as medicinal chemistry, reducing bulk impurities from isomeric byproducts translates to fewer downstream headaches in formulation and QC.
In production, specifications have evolved beyond just meeting a purity number. Industry partners want clarity about isomer content, trace heavy metals, and consistency in melting and boiling points. Over time, our own spec sheets for 3,5-dibromobenzyl bromide shifted to reflect tighter impurity thresholds, responding directly to feedback from pharma and electronic material makers. Typical batches consistently reach 98% or higher by GC with water content usually held below 0.2%. Emphasis on color and crystalline form isn’t just for appearances—off-color product hints at uncontrolled side reactions, possibly leaving corrosive residues behind that affect process equipment and yield.
Anyone who’s cracked a drum of benzyl halide knows about the rippling vapors and strong odor. We take precautions from the raw material bay out to packaging. Air exchange, disciplined PPE, and local exhaust keep our staff and neighbors safe. Our plant layout makes sure incompatible chemicals stay out of the same work areas, and no shortcuts get taken in venting. Not everybody down the line gives the same attention to containment, but plant risk assessments guide our choices from every valve to every absorber. Waste streams and cleaning solutions are treated on-site before disposal, keeping our commitment to regulatory and community standards.
One trend we’ve seen lately: specialty chemical and electronics manufacturers asking for more tailored lots, like 3,5-dibromobenzyl bromide at above 99% purity or with especially tight particle size ranges. Electronic materials particularly push for absence of certain trace ions—chloride, among others—because even tiny amounts affect downstream electronic properties. To meet these requests, we’ve invested in precision cooling crystallization and additional filtration capacity. The last kilo in the drum may get checked for quality as closely as the first. That effort separates a dedicated chemical manufacturer from brokers or traders who take bigger risks with blending or reprocessing.
Industry keeps moving toward cleaner, greener processes. Partners, especially in Europe and Japan, are nudging for alternative solvents, reduced halogen waste, and more circular processing strategies. We get regular questions about the lifecycle of the bromine in our process, right down to the fate of spent mother liquors and side streams. Our team responds with periodic process audits, continuous upgrades on scrubbers, and fresh thinking on solvent recovery. More customers every year ask for declarations around responsible sourcing of bromine and other key reagents. These aren’t sideshows—they’re demands for transparency that we expect to keep growing.
Ask two customers about their use of 3,5-dibromobenzyl bromide and stories often differ. For pharma API development, it turns up as a selective blocking unit or in the formation of complex intermediates. In electronic materials, customers employ it in designing specialty polymers for photoresists and display technologies. In either scenario, small changes in impurity or polymorph profile throw off batch predictability, sometimes losing weeks or months in a development project. Trusting your source means knowing you get consistent crystalline habit and tightly monitored minor component levels every time.
With global attention on chemical risk, we keep documentation up to date for compliance in all markets receiving our material. Safety data and transport labeling stay on file and get updated whenever new studies change the hazard picture. Not every user has the same laboratory infrastructure, so we make recommendations clear about storage, emission control, and personal safety. No shortcuts exist for responsible stewardship, and our technical staff trains on response scenarios, not only in paperwork but in live drills each year.
Getting supply right goes far beyond filling an order. Each drum or small-batch lot gets traceability from raw reagents through to the finished product, with chain of custody records ready for audit or customer verification. Delays in chemical plants ripple fast across a tight supply chain, and the feedback we receive from partners has shaped how we forecast, hold safety stock, and buffer for raw bromine or precursor shortages. This is no minor point—a hiccup at one site can force costly downtime for customers. We’ve invested in parallel production trains for key steps so that if maintenance or a reactor pause hits one, schedules keep rolling for priority projects.
Relationships don’t stop at shipment. Our technical sales and R&D chemists work with customers on failure analysis, new product integration, and regulatory submissions. We’ve visited partner facilities to troubleshoot a stubborn spot color or crystallization sequence, drawing on what we see daily on our own lines. Sometimes the story isn’t about the product itself, but about integration into an unusual synthetic route. Short, direct conversations with bench chemists or plant engineers help catch issues early—whether it’s a filter plugging, or a reaction stalling due to trace contamination.
An experienced plant hand knows that every chemical has its quirks and dangers, and 3,5-dibromobenzyl bromide brings its share. We run regular safety drills rooted in real plant scenarios. Pressure surges, unexpected exotherms, line blockages—these events train our teams to spot patterns, trust their meters, and make adjustments on the fly. Plant maintenance people keep spare critical parts on hand and double-check seals and transfer lines before and after a run. Following through on every checklist helps us avoid the kinds of mishaps that can wipe out a batch or, worse, threaten plant safety.
Plenty of companies can offer basic halogenated aromatics, but true depth comes from long years spent turning raw material into a consistent, safe, high-purity chemical. Each improvement to our 3,5-dibromobenzyl bromide process comes out of feedback from partners, troubleshooting sessions with our operators, and steady investment in new methods. Teams in our plant meet regularly to review what went right and where unexpected snags appeared. We don’t just copy what has worked elsewhere—actual trial runs and root-cause investigations point to the best tweaks. This means no surprises once drums leave our warehouse, and reliability that customers in sensitive end-use sectors value.
Affordable manufacturing must balance cost with quality and regulatory compliance. Industry faces pressure not only to avoid hazardous residues but also to tighten power, water, and raw material efficiency. With this product, improvements come from streamlining bromination and workup, upgrading heat transfer systems, and reducing solvent volumes. Next-generation requests—like even more stringent maximum impurity specs, zero trace metals, or bio-derived solvent compatibility—are prompting more R&D. We collaborate with research labs and industry consortia on pilot studies, always on the lookout for ideas that can move from gram scale in the lab to tonne scale in the plant.
Every new batch of 3,5-dibromobenzyl bromide is shaped by hundreds of decisions made over decades: process improvements, tighter analytical methods, safer handling routines, and feedback loops from demanding users. No single innovation or shortcut provides lasting advantage. Instead, each day of effort and accumulated experience in sourcing, reaction design, purification, and support lets us meet applications stretching from new pharma to electronics manufacturing. Those who use the product can feel the difference between material straight from the manufacturer and a sample passed through multiple hands with blurred provenance. Maintaining this edge requires continual learning and reinvestment, traits that only come from deep involvement in every stage of production.