|
HS Code |
215908 |
| Chemicalname | 3,5-Dibromobenzaldehyde |
| Casnumber | 3132-99-8 |
| Molecularformula | C7H4Br2O |
| Molecularweight | 279.92 g/mol |
| Appearance | White to off-white solid |
| Meltingpoint | 120-123 °C |
| Boilingpoint | 338.8 °C at 760 mmHg |
| Density | 2.118 g/cm3 |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Smiles | C1=C(C=C(C=C1Br)Br)C=O |
| Inchi | InChI=1S/C7H4Br2O/c8-6-1-5(4-10)2-7(9)3-6/h1-4H |
| Refractiveindex | 1.658 |
As an accredited 3,5-Dibromobenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 3,5-Dibromobenzaldehyde, labeled with chemical name, hazard warnings, and supplier information. |
| Shipping | 3,5-Dibromobenzaldehyde is shipped in tightly sealed containers to prevent moisture and air exposure. The packaging complies with international regulations for hazardous chemicals, ensuring safety during transport. Proper labeling with hazard identification is provided, and shipments are handled by certified carriers to ensure safe and secure delivery to the destination. |
| Storage | 3,5-Dibromobenzaldehyde should be stored in a tightly closed container, in a cool, dry, well-ventilated area, away from direct sunlight and sources of ignition. Keep it separate from strong oxidizers and bases. Store at room temperature. Use appropriate chemical storage cabinets, ensuring that the chemical is clearly labeled and inaccessible to incompatible substances, children, and unauthorized personnel. |
Applications of 3,5-Dibromobenzaldehyde in Industrial Manufacturing3,5-Dibromobenzaldehyde is an essential aromatic building block in chemical synthesis for advanced material production. Its unique bromine substitution pattern allows precise functionalization, facilitating downstream transformations in multiple specialized sectors. As a direct manufacturer, we address strict industry specifications, support process integration, and provide consistent quality for demanding industrial applications. 1. Agrochemical Synthesis – Herbicide and Fungicide IntermediateAgrochemical producers utilize 3,5-Dibromobenzaldehyde as a key intermediate in synthesizing selective herbicides and fungicides. The regulated introduction of brominated aromatic units enhances the biological performance of active compounds. Manufacturers carry out condensation or nucleophilic substitution with the aldehyde group to achieve precise molecular structuring needed in modern crop protection agents. Industry compliance standards
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2. Active Pharmaceutical Ingredient (API) Intermediate ManufacturingIn pharmaceutical synthesis, 3,5-Dibromobenzaldehyde acts as a controlled intermediate for small-molecule APIs. It serves in carbon-carbon coupling and heterocyclization, helping construct core scaffolds in advanced medicinal chemistry programs. Downstream partners require strict traceability and purity for regulatory filings and clinical batch production. Industry compliance standards
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3. Organic Electronic Materials (OLED, Hole-Transport Layer Precursors)3,5-Dibromobenzaldehyde finds application in developing specialty monomers for organic electronics, particularly OLED and display technologies. Its doubly brominated structure supports selective cross-coupling and condensation steps, allowing precise tailoring of charge-transport and emission properties. Material scientists rely on high-purity input to achieve consistent film performance at scale. Industry compliance standards
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4. Specialty Polymer and Resin ManufacturingPolymer manufacturers incorporate 3,5-Dibromobenzaldehyde as a functional comonomer or backbone modifier to deliver controlled bromine incorporation. Its use enhances flame-retardant properties and enables advanced crosslinking in specialty thermosets and engineering plastics. Resin formulators require controlled input quality and consistent reactivity to meet demanding end-use requirements in electrical and automotive sectors. Industry compliance standards
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5. Fine Chemical R&D and Diagnostic Reagent SynthesisR&D laboratories and diagnostic reagent manufacturers exploit the formyl and dibromo functionality of 3,5-Dibromobenzaldehyde for preparing complex ligands, colorimetric probes, and crosslinking agents. Accurate input composition supports reproducibility in small-batch and pilot scale synthesis, critical for validating analytical kits and specialty diagnostic products. Industry compliance standards
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Every batch of 3,5-dibromobenzaldehyde that comes off our reactor tells its own story. This compound, with the molecular formula C7H4Br2O, stands out for its unique twin bromine atoms on the aromatic ring. Over the years, refining the oxidation of 3,5-dibromotoluene has taught us the real difference between technical statements and the subtle hands-on details that influence a product’s quality. The laboratory aroma that rises, that distinctive sharp aldehyde aligned with the heavy bromine note, clues us immediately into purity and precision—a sensory checkpoint every operator in production learns to recognize.
We control our process tightly. The melting point, which sits reliably between 86–89°C in well-made material, doesn’t wander outside spec if oxygen and temperature tuning are kept in check during oxidation. Each production run tells us how raw material quality, especially the toluene source, shifts our downstream purification. Many companies claim high purity, yet uncontrolled side reactions introduce colored byproducts requiring repeated column work or costly recrystallization cycles. We tackle this early, selecting oxidants, solvents, and timings not just by the book, but from years leaning over the bench, watching color and crystallization in real time.
Below the surface of white crystalline powder, the difference between a clean sample and the kind that raises questions in an audit comes from the level of precision imposed at each step. From past experience, small amounts of residual dibromotoluene or over-oxidized material manifest as persistent off-white color and unexpected signals on NMR. The smell even shifts, something every production chemist grows to detect. Stored correctly, protected from light and moisture, 3,5-dibromobenzaldehyde remains stable and easy to transfer, but any carelessness in drying or exposure to humid air invites partial hydrolysis and dulls product presentation.
Every order receives certification with HPLC confirming purity above 99%, and GC traces that customers trust. QA inspection involves visual and chemical checks at multiple moments through each batch—sampling isn’t just one point at the end but several across production and final packaging. Our consistency attracts long-term partnerships with researchers, scale-up labs, and pharmaceutical process teams who care about both purity and predictability.
In our facility, 3,5-dibromobenzaldehyde often heads into cross-coupling projects, where selective reactivity at the bromine positions gives access to richer aromatic scaffolds. Suzuki and Stille couplings rely heavily on the ortho/para positioning, so maintaining high site-specific substitution avoids formation of isomeric impurities later. This precision matters most during multi-step synthetic routes in pharma intermediates—one misstep with side products generates headaches and uncovers inefficiencies.
We work closely with R&D chemists building heterocycles and biaryl linkers. The aldehyde group lends itself to condensation with amines or active methylene compounds, opening pathways to imines, hydrazones, or more complex heteroaromatics. As a manufacturer, it becomes clear that the downstream requirements often shift batch needs: some customers want smaller, highly pure crystalline fractions for analytical uses, while process teams in larger plants ask for multi-kilogram dry, free-flowing lots to match batching scale. Our job is to deliver standard lots with both fine chemical and industrial applications, leaning on flexible drying, screening, and packing options so users focus on research, not troubleshooting material inconsistencies.
It’s tempting for buyers to imagine swapping in a benzaldehyde or selecting a cheaper dibromo isomer. Years of feedback reveal that substituent position means everything. The 3,5-dibromo arrangement gives a predictable balance of electron withdrawal and steric hindrance. Selectivity in derivatization, especially where organometallic chemistry comes into play, relies on this symmetry and reactivity. For advanced electronics, pharmaceuticals, or even specialty polymers, substitution pattern and purity rule out alternatives.
Some labs found lesser-quality 3,5-dibromobenzaldehyde triggers colored runs, unexpected byproducts, or unmanageable purification headaches. High-performance applications can’t tolerate impurity drift, especially if material must pass through several more steps. In one notable case, an end client tracing irregular HPLC peaks tracked the culprit back to off-brand 3,5-dibromobenzaldehyde contaminated with trace dibromobenzoic acid. Our manufacturing process, which invests in a precise semi-continuous route and multiple HPLC clearance steps, proved its worth as our product ran cleanly through their route, avoiding wasted material and delayed timelines.
Small-scale batches invite attention to detail, but real challenges appear as volumes rise. Thermal distribution across larger vessels requires careful agitation; bromination stages, never fully trivial, run cleanest with high-purity starting aromatics and careful dosing of oxidant. Demo-scale manufacturing uncovered a few tough lessons: unchecked exotherms threaten yield, and large drying trays create cold spots that harbor residual solvent or moisture, undermining stability. Learning to adjust not just by protocol but by the rhythm of the process—color, odor, and crystallization kinetics—helped us achieve reproducible lots from kilo to ton scale.
Many customers, especially those moving from gram discovery lots to multi-kg pilot work, crave transparent communication about scale-related impurity drift. We share analytical packages for every scale, not just a “representative COA,” to demonstrate process control. By over-communicating side impurities and minor shifts between batches, customers feel assured that scaling up with us means chemistry they can trust with little loss in project momentum.
No piece of equipment ever replaces the eye—and nose—of seasoned technicians. We take training seriously. New operators spend weeks shadowing line supervisors, learning the cues that guide each stage: the right appearance to judge endpoint, faint shifts in hue indicating over-oxidation, or adjustments needed in filtration to prevent wet cake sticking. Many of our staff move from basic bench roles to responsibility for shift overseeing once they’ve absorbed not only the standard operating manual but the unwritten practices handed down.
Every plant has its rhythm: how quickly raw material charges, preferred agitation styles, and quirks of local environmental controls. Training here focuses less on blind adherence to written procedure and more on empowering team members to notice and respond. This engrained experience shows up in consistently good product, minimal waste, and high morale—turnover remains low, and our product reliability stays high.
Some of our most valuable process improvements came from partnership with laboratories and production teams who shared how our product performed in real-world conditions. “The last batch crystallized a bit slower in our application,” one partner noted, prompting adjustments in our drying and screening to improve consistency. Another identified that a switch in lot yielded a higher melting fraction, leading us to fine-tune our solvent swapout for better uniformity.
Our support team includes chemists who walk customers through questions, not just sales reps with canned responses. We recognize that every lab faces unique bottlenecks. For clients working toward regulatory approval, detailed traceability of every lot matters much more than generic marketing claims. Building trust means responding to queries with full data, open dialogue about limitations, and readiness to tailor final lots within reasonable technical limits.
Not all brominated benzaldehydes behave the same way under reaction conditions. Substitution patterns alter reactivity and, more critically, shape downstream impurity profiles. We heard from one startup that expected to use a 2,4-dibromo analog in place of 3,5-dibromobenzaldehyde to save on lead time. Yields plummeted, work-up lengthened, and final intermediates failed quality review. Lessons like this, shared across the network, drive home why discipline in raw material selection means smoother research results and lower production costs.
Some assume that aldehyde functionality is fragile, or that bromine atoms increase stability risks. Our storage results tell a different story: under clean, sealed conditions, 3,5-dibromobenzaldehyde resists oxidative drift and hydrolysis far better than common wisdom suggests. We recommend users store away from light and moisture, but do so not because the compound proves unreliable—instead, we’ve seen careless laboratory habits introduce issues that careful handling avoids entirely.
Traditionally, customers turned to 3,5-dibromobenzaldehyde for specialty intermediates in pharma or advanced chemistry. Project by project, its spectrum of utility keeps expanding. Some groups now use it as a synthon for molecular frameworks in OLED precursors or high-value materials. Industrial partners revisit our material for new polymer backbones that take advantage of the selective bromination pattern and robust aldehyde reactivity, skipping several inefficient steps compared to legacy synthetic routes.
We see its popularity rising as academics, specialty chemical producers, and large-scale pharma companies uncover new synthetic pathways. Its consistent purity and site specificity allow direct scale-up—projects move from exploratory runs to production lots without shifting analytical methods or troubleshooting variable reactivity. Whether in micromole library synthesis or multi-ton campaigns, our customers speak of the same things: reproducibility, clean reaction profiles, and confidence in their route planning.
Brominated aromatics demand serious attention to waste handling and process air quality. Our manufacturing incorporates modern containment, solvent recovery options, and strict protocols for managing halogenated byproducts. We track both regulatory standards and local environmental codes—we don’t just seek compliance for paperwork’s sake, but because the people in our facility and community matter. All plant floors feature real-time monitoring for airborne hazards and specialized scrubbers for off-gassing steps, with regular reviews to tighten performance.
Training includes proper PPE use, protocols for minor spills, and real exercises in containment response. Over time, implementing “green” choices for solvents and investing in closed-loop cyclers reduced both waste disposal load and utility costs. We partner with hazardous waste handlers who share our standards, because a strong reputation comes from practical action, not self-congratulation.
A manufacturing business doesn’t stand still. Market trends, regulatory shifts, and scientific advances push us to refine both core process and analytical assessment. As detection limits tighten and downstream applications grow more sensitive, our QC lab invests in upgraded HPLC, GC-MS, and NMR systems. These tools let us catch even the traceest impurities—often ones our users haven’t anticipated yet—delivering confidence batch after batch.
Each year, we revisit process steps to drive out inefficiency, up purity, and reduce cycle time. We solicit feedback not only from our direct buyers but from the R&D teams working with our material at the frontline of discovery. This two-way feedback means real problems get fixed, not glossed over. The result: fewer surprise delays, lower waste, and better support for every end-user’s research or production needs.
Every researcher and process manager faces the scramble for reliable sourcing. We step beyond just batch-to-batch consistency: our network of logistics and documentation support means orders ship with real-time traceability, up-to-date spectral data, and full manufacturing transparency. We understand that for regulated industries, especially those pushing new drugs or electronics, any question of provenance or analytical backup introduces delays, headaches, and risk. That makes us proactive in sharing everything about manufacturing—from raw material credentials to process flows and final package inspection.
Out-of-specification events rarely escape our attention; contingency plans and backup lots exist in case a target batch faces an unexpected issue. Whether the challenge involves granulation size, drying level, or specialty packaging, we hand off experience and real solutions that arrive tested, not theoretical. Our value emerges not just from chemistry done right, but from the respect we pay to every link in the supply chain.
Customers keep pushing the boundaries of what 3,5-dibromobenzaldehyde can do, so our commitment to quality follows. We allocate resources for process innovation, new reaction pathways, and advanced analytical validation. More groups dedicate R&D lines to rare brominated aromatics, exploring structurally diverse building blocks for tomorrow’s therapies and next-generation materials.
For us, each shipment of 3,5-dibromobenzaldehyde reflects not just supply and demand, but years of honed practice—shaped by technical challenge, creative solutions, and relentless drive to serve real-world science with everyday dependability. From lab bench to pilot plant to industrial scale, the lessons we learn guide every improvement. Our product has grown with the industries and innovators it supports, and we remain dedicated to manufacturing in a way that stands up to scrutiny and delivers real, measurable value in every application.