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HS Code |
687657 |
| Cas Number | 626-39-1 |
| Molecular Formula | C6H3Br2Cl |
| Molecular Weight | 285.35 g/mol |
| Iupac Name | 1,3-dibromo-5-chlorobenzene |
| Appearance | White to off-white crystalline solid |
| Melting Point | 62-64 °C |
| Boiling Point | 265-266 °C |
| Density | 2.124 g/cm³ |
| Solubility In Water | Insoluble |
| Refractive Index | 1.615 |
| Pubchem Cid | 122211 |
| Synonyms | m-Dibromo-p-chlorobenzene |
| Smiles | C1=C(C=C(C=C1Br)Cl)Br |
| Flash Point | 120 °C |
| Ec Number | 210-943-3 |
As an accredited 1,3-Dibromo-5-Chlorobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25 grams, screw cap, white hazard labels with chemical name, CAS number, and hazard pictograms clearly displayed. |
| Shipping | 1,3-Dibromo-5-Chlorobenzene should be shipped in tightly sealed containers, clearly labeled, and compliant with all relevant chemical transport regulations. It must be handled as a hazardous material, protected from physical damage, heat, and moisture, and accompanied by proper documentation, including Safety Data Sheets (SDS), per DOT and international shipping standards. |
| Storage | 1,3-Dibromo-5-chlorobenzene should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances like strong oxidizing agents. Keep the container tightly closed and properly labeled. Store in a corrosion-resistant, chemical-resistant container. Avoid ignition sources and excessive heat. Personal protective equipment should be worn when handling to prevent skin and eye contact. |
Applications of 1,3-Dibromo-5-Chlorobenzene in Industrial Manufacturing1,3-Dibromo-5-Chlorobenzene acts as a key halogenated intermediate in several industrial chemical syntheses, supporting the production of performance-critical compounds within the pharmaceutical, agrochemical, and polymer sectors. Our manufacturing expertise ensures strict uniformity and quality control to meet specialized downstream requirements across multiple use cases. 1. Agrochemical Active Ingredient SynthesisLeading agrochemical manufacturers use this compound for the targeted synthesis of regulated herbicide, fungicide, and insecticide actives, capitalizing on the unique substitution pattern for the construction of complex aromatic frameworks. Integration starts at the heterocyclic ring formation step, which determines both crop performance spectrum and environmental stability. Industry compliance standards
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2. Pharmaceutical Intermediate ProductionMajor API and specialty pharma companies utilize this molecule as a privileged scaffold in the synthesis of advanced pharmaceutical intermediates, such as benzene-based building blocks for anti-infectives, anti-inflammatory drugs, and oncology candidates. The precise bromine and chlorine positioning allows reliable downstream functionalization steps, supporting both small-scale and commercial API programs. Industry compliance standards
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3. Electronic-Grade High-Performance PolymersIndustry leaders in the production of electronically functionalized polymers incorporate this halogenated benzene derivative to achieve precisely tuned dielectric and flame-retardant properties in advanced plastics, films, and printed circuit board substrates. Rigorous material characterization ensures reliable downstream performance in highly regulated environments. Industry compliance standards
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4. Fine Chemical and Dye Intermediate ManufacturingLeading producers of specialty dyes and fine chemicals employ this compound as a targeted synthon for generating key halogenated intermediates, critical for fastness properties, color development, and stability enhancements in textile, leather, and plastic colorants. Its defined halogen content delivers pathway control in selective substitution and coupling reactions. Industry compliance standards
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Few substances in the halogenated aromatic space match the utility of 1,3-Dibromo-5-Chlorobenzene. Producing this triple-halogen substituted compound calls for exact control of raw material quality, reaction temperature, and byproduct management. In our facility, we never approach these steps casually. At every batch, we track each kilo of substrate with batch-level traceability. Over the years, we have faced enough batches displaying unpredictable color, incomplete halogen substitution, or unfiltered particulate to know how easy it becomes to deviate off-spec. Childhood mistakes in batch brominations led to waste, memory, and changes in our filtration process that still stand. Now, every step from charging to isolation receives attention, because the workhorse compounds of process chemistry only earn trust after years of repeated, reliable performance.
Our experience suggests most downstream users value two things: consistent halogen ratio and reliable melting point. Small shifts in quality can throw off catalytic reactivity or weaken pharmaceutical intermediates, giving headaches at scale. In every run, we check GC purity, and we never treat this as a tick-box. Purity tells only part of the story. A customer who runs a cross-coupling with unclear crude soon contacts us with questions. Years ago, we supplied a batch too moist and saw the confusion ripple downstream. Problems at this level force us to back-analyze raw material sources and flush reactors. Lessons like this sink deep—only the tightest control of process variables and solvent residues keeps process lines smooth for our clients.
Our typical specifications for 1,3-Dibromo-5-Chlorobenzene revolve around a purity of 99% minimum by GC, with residual solvent and related impurities kept tightly below 0.5%. Melting range falls between 77 and 80°C in our product, checked by both manual capillary and DSC in QA. Fine, crystalline white powder with low odor and minimal fines, this product stays free-running enough for automated feed systems. Moisture sensitivity remains low.
1,3-Dibromo-5-Chlorobenzene at our shop comes under the designation DBC-001. Direct bromination routes tend to raise byproduct risk unless temperature and agitation lock-in right. Historically, uncontrolled heat spikes resulted in higher dibromo isomer content, requiring tough chromatography. Through small improvements in exotherm control and in-line monitoring, we now deliver product with minimal isomeric contaminants—seasoned technical teams recognize this advantage in routine coupling sequences.
Many first-line halogenated benzenes quickly fade from favor as molecular complexity rises. 1,3-Dibromo-5-Chlorobenzene brings a dual bromine disposition on the ring, coupled to a single chlorine atom at the para position. Synthetic chemists rely on this substitution pattern for Suzuki, Stille, or Negishi couplings where selective activation outpaces competitive hydrolysis. The chemical stability suits multi-step synthesis routes found in both API and polymer precursor work. We frequently serve teams pushing toward specialty ligands, liquid crystal components, or advanced agrochemical scaffolds.
One thing that stands out is how this benzene derivative grants orthogonality in selective reactivity. The two bromines sit on carbons one and three, while the chlorine anchors at five. This pattern grants synthetic flexibility—chemists can selectively functionalize one or both bromides, leaving the chlorine untouched for late-stage manipulations. We ourselves have watched customers build out a range of target compounds, including challenging diaryl ethers and biphenyl frameworks, using this precise motif.
Our technical team routinely hears from pharmaceutical and fine chemical partners that they cannot compromise on halogen placement. A swapped halide or positional impurity clogs purification and saps overall yield. Our analytical methods, particularly NMR and GC-MS, have periodically spotlighted competitor products that hide polysubstituted benzenes or dimers. We invest in stepwise recrystallization and batch blending not for marketing, but because our own trial runs with customer protocols show troubled spots where impurities lie.
We handle 1,3-Dibromo-5-Chlorobenzene in stainless steel and glass-lined reactors. Over time, we shifted from bulbous, hand-stirred flushes to more automated, jacketed lines—fouling and dark oil formation fell off with better mixing and temperature ramp calibration. Some resellers ignore the impact of micro-scale fouling on product color and stability. Our packing crew prepares every drum to minimize exposure to air and dust, since halogenated aromatics can scavenge trace moisture and lose luster fast.
Practically, several things separate our 1,3-Dibromo-5-Chlorobenzene from the pack. Mono-brominated benzenes like bromobenzene show fast, simple halogenation but lack the orthogonal reactivity for more intricate cross-couplings. Multi-brominated isomers, such as 1,2,4-tribromobenzene, present purifiers with tough selectivity challenges and sometimes intractable solubility. By design, 1,3-dibromo-5-chlorobenzene’s unique substitution opens access to a broader range of transformations. We have watched process chemists choose this compound over simpler halobenzenes to avoid side reactions, especially where catalyst activity relies on halogen-labile groups.
From a handling viewpoint, the melting point strikes a middle ground, avoiding condensation troubles seen with lower-melting monocyclics, yet not so high as to complicate automated or batch-scale feeding. Our trials with glass and PTFE hoppers over years have shown this product offers smooth flow metrics, helping avoid bridge formation or variable dosing during automated dispensing. Handling this compound during pilot runs, I have seen how off-grade material can soften or cake, causing devastating downtime in automated synthesis lines. Fine crystalline stability isn’t a side feature; it’s a direct factor in bench-to-plant reproducibility.
Superior batch-to-batch consistency means researchers gain confidence when moving from grams to multi-kilo lots. One research group uses our 1,3-Dibromo-5-Chlorobenzene to generate polyfunctional biphenyl scaffolds for new OLED emitters. Substitution precision matters here, since misplaced halogens cripple device efficiency and scale-up. Downstream, polymer scientists prefer the three-halogen pattern for stepwise coupling strategies. Catalysts such as palladium complexes display predictable activity when the substrate profile matches the literature—something only achieved with scrupulous control upstream.
Pharmaceutical manufacturers aiming to introduce complexity or alter molecular geometry at late stages use this compound’s bromo and chloro positions for convergent assembly. Recently, an agrochemical developer approached us with solubility issues in a late-stage process flow. They’d been sourcing cheaper dichlorobenzenes but found cross-coupling selectivity and product yield lacking. Our technical service group provided samples and analytical data, and after pilot runs, the client’s full-scale process switched to our batch. Frequent conversations like these reveal the trust built on real process experience—a streak of good QC data and few customer complaints grows only from meticulous production.
Commercial routes remain old-school, but small tweaks mean a lot. By carefully charging N-bromosuccinimide under calibrated agitation and monitoring endpoint by TLC and HPLC, we now catch the reaction at optimal conversion. This reduces the persistent trace of tribromo side products and gives a crisp color and melting range in the final product. Old procedures suffered from static buildup, sticky fines, and frustrating handling by end-users; our modifications—a finer control of particle size, denser packing, and dedicated storage protocols—came straight from field feedback and staff input.
Reactor hygiene often goes overlooked by those who never run thousands of liters each month. In one winter, we noticed trace color drift in output. Inspection revealed a forgotten gasket, swollen from reactive intermediates. Replacement and extra post-reaction charcoal treatment cleared the problem—a simple fix, discovered only by working through full-scale production ourselves. This is the kind of supply chain diligence we practice daily, with the batch signature of every staff member tied, without exceptions, to each output drum.
Suppliers tout “purity,” but many shy away from discussing residual solvents or process waste. Our internal lab pushes both metrics—our standard requires benzene traces under 30 ppm and residual acetic acid below 20 ppm. We share reports from each lot because, having dealt with frustrated complaints on competitor batches that spike unexpectedly in HPLC, we know customer trust hinges on what ships out of our doors. Chipping away at even tiny side products takes sweat and incremental improvement. Meticulous operator logs and daily recalibrations—these routines keep impurity drift to a minimum.
For export, our focus on batch containment and regulatory documentation stems from witnessing half-checked shipments denied at ports, affecting production timelines abroad. On several occasions, strong documentation and verified material content convinced customs inspectors and avoided unnecessary delays. Large pharmaceutical clients have told us directly that a supplier’s ability to transparently document batch origin and analytical records often outweighs a cents-per-kilo price difference.
We listen closely to customer complaints and service requests. A few years back, one polymer manufacturer flagged flow issues with their dosing gear. Our response led to a tighter spec on powder size distribution and a revamped drying system. Such improvements don’t appear in glossy marketing, but they define long-term supplier relationships. Regular exchange of samples for application trials built a feedback loop—one that shortens production headaches and saves time for both sides.
Another key improvement—preventing airborne loss during handling—came from running our own upstream benchtop trials, simulating customer blending environments. Adding finer mesh sieving and denser anti-static linings actually lowered atmospheric dust. With high-output facilities, these tweaks mean less loss, safer conditions, and less regulatory headache on the customer end.
Halogenated aromatics, including 1,3-Dibromo-5-Chlorobenzene, demand responsible handling. We have moved from batch storage in loose bags to tightly sealed, vented drums designed to resist moisture. Each batch receives an environmental load calculation to help minimize waste and emissions. Over time, fugitive emissions fell by more than 70%, while workplace complaints over odor or skin contact dropped to near zero.
Operator safety matters most in bulk production—case after case, we have seen even tiny leaks or spills in line with competitors cause trace contamination or slip-and-fall risks. Our training emphasizes not just compliance, but proactive detection of leaks and container wear. Such diligence prevents incidents and builds a culture of responsibility, which hinges on the experience and buy-in of every technician on the floor.
Real trust only comes after months or years of stable supply and honest communication. No shortcut or brochure can replace the accumulated good will of hundreds of lots shipped, customer complaints resolved, and process tweaks made. Each parameter tweaked, every equipment upgrade, grows from the pressure of customer demand and the feedback from real operators on the ground. By focusing on narrow, practical improvements batch after batch, our 1,3-Dibromo-5-Chlorobenzene finds ready acceptance by technical scientists moving toward difficult syntheses.
End users care most about outcome certainty. We provide supply contracts that back up our delivery record, anchored by tracked, repeatable quality. Any deviation large enough to throw off a downstream reaction triggers a process review—not to assign blame, but to fix root causes before the next shipment.
From startup labs synthesizing new ligands to bulk manufacturers running week-long campaigns, the practical advantages of tightly controlled 1,3-Dibromo-5-Chlorobenzene show up in reduced downtime, fewer purification troubles, and less regulatory churn. In our own trials, cleaner product lines let us cut several hours from purification cycles, speeding time to product and reducing solvent burden.
The direct differences between well-made, traceable dibromo-chloro aromatics and less carefully sourced material grow larger as scale increases. A run that looks simple at 100 grams reveals new risks and subtle faults at several tons. Based on years in chemical manufacturing, we know which tiny faults will scale up and which pass through without impact. Our teams spend daily effort improving those edges—no change too small if it spares headache for a downstream process chemist or bench scientist.
We advocate direct dialogue between our technical group and end users—this has brought in a range of useful new product characteristics based on real application feedback, not just marketing wish lists. As new cross-coupling catalysts appear, and as regulatory demands tighten on trace contaminants, we stay ready to refine every thread of the production process. Lessons learned from past errors feed into everyday routines and keep quality high, because at the end of each run, product that works well for the customer makes everything worth the effort.
Our goal is simple: help clients focus on synthesis and development, not batch inconsistencies or supply troubleshooting. Making 1,3-Dibromo-5-Chlorobenzene well means more than hitting a number—each success strengthens the manufacturer’s bond with its research partners. The product leaves the plant ready for real work in real processes, building value quietly, drum after drum, for every group that counts on reliable, traceable materials.