|
HS Code |
344285 |
| Cas Number | 1711-49-3 |
| Molecular Formula | C7H4BrNO |
| Molecular Weight | 198.02 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Density | 1.6 g/cm³ |
| Boiling Point | 119-121 °C at 10 mmHg |
| Flash Point | 112 °C |
| Purity | Typically ≥98% |
| Solubility | Reacts with water, soluble in organic solvents like ether and chloroform |
As an accredited 3-Bromophenyl Isocyanate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25g amber glass bottle securely sealed, featuring a yellow hazard label marked “3-Bromophenyl Isocyanate” with cautionary handling instructions. |
| Shipping | 3-Bromophenyl Isocyanate should be shipped in tightly sealed containers under dry, cool conditions and protected from light. Classified as a hazardous material, it must comply with all relevant safety regulations for toxic and moisture-sensitive chemicals. Appropriate hazard labels and shipping documentation are required to ensure safe handling and transport. |
| Storage | 3-Bromophenyl Isocyanate should be stored in a cool, dry, well-ventilated area, away from moisture, heat, and incompatible substances such as acids, bases, and strong oxidizers. Keep the container tightly closed and protected from light. Use only with proper personal protective equipment and ensure that emergency spill cleanup materials are readily accessible. Store under an inert atmosphere if possible. |
Applications of 3-Bromophenyl Isocyanate in Industrial Manufacturing3-Bromophenyl Isocyanate serves as a key intermediate in several advanced chemical manufacturing sectors. The following sections present real-world downstream industry applications, showing how process integrators use this material within regulatory, formulation, and operational frameworks. 1. Synthesis of Agrochemical IntermediatesManufacturers produce complex herbicide and fungicide actives using 3-Bromophenyl Isocyanate as an essential isocyanate source for urea and carbamate linkage formation. The compound enables selective introduction of brominated aromatic units in multi-step syntheses. Process operators must manage isocyanate handling, reaction temperature, and controlled coupling with amines and alcohols to achieve consistent intermediate quality. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. API Intermediate for Pharmaceutical SynthesisPharmaceutical companies rely on 3-Bromophenyl Isocyanate for constructing advanced building blocks in the synthesis of active pharmaceutical ingredients, especially in targeted cancer therapeutics and CNS drugs. The isocyanate group enables selective coupling with protected amines, facilitating efficient step-growth assembly under validated batch protocols, with full genealogical traceability at each transformation stage. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Performance Coatings: Polyurethane Curing AgentSpecialty coatings manufacturers use 3-Bromophenyl Isocyanate as an aromatic isocyanate in high-performance polyurethane system formulations. The material is dosed directly for tailored crosslink density and enables improved chemical and thermal resistance through the presence of the bromine substituent. Production teams control moisture, catalyst levels, and dosing conditions to avoid gelling and ensure uniform film properties in final coatings. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Fine Chemical Synthesis: Specialty Urea and Carbamate ManufactureProducers in the fine chemical sector incorporate 3-Bromophenyl Isocyanate to synthesize advanced aromatic ureas and carbamates, crucial for specialty monomers, dyes, and chemical research reagents. The reagent acts as a controlled reactant in solution or solid-phase condensations, allowing precise introduction of functionalized aryl isocyanate moieties to expand compound diversity and reactivity for further downstream transformations. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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Every chemist knows the stakes change the moment you leave the textbook and step into a working plant. Behind every ton we deliver, countless choices about raw material sourcing, reaction conditions, waste minimization, and purity controls line up. Our facility started offering 3-Bromophenyl Isocyanate after seeing a spike in demand for precision intermediates in high-value organic synthesis, particularly for customers fabricating custom pharmaceuticals and advanced polymers. Many buyers used to trust only larger brands, but word grew once we consistently supplied isocyanates with fewer side reacts, clean documentation, and a transparent process chain right through to logistics.
3-Bromophenyl Isocyanate’s value lies in its ability to introduce an isocyanate group to aromatic structures with a bromine handle, making it uniquely reactive for subsequent coupling. Each batch runs to tight targets for purity—residual amine and unreacted starting material need more than a quick check by HPLC. We rely on in-house reaction profiling; we’ve learned over years of batch records when trace impurities cause issues downstream. That comes from processing real orders and talking to formulators who don’t have time for surprises.
Isocyanates look simple on paper but can be unforgiving during scale-up. The 3-bromo position gives extra flexibility in directed ortho-metalation and cross-coupling chemistry, especially in pharmaceutical development. Customers who previously used phenyl isocyanate or para-substituted versions described issues with regioselectivity or unwanted by-products during heterocycle synthesis. Our 3-bromo variant often sidesteps those problems, helping scientists build specific scaffolds without as much purification hassle.
We don’t just dump powders in bags and wave goodbye. In earlier years, we lost business to traders offering low prices on material full of polymeric by-products. Repeated reports of unpredictable reactivity, storage instability, and lost yield forced us to redesign the last purification and packaging steps. Today, humidity control and nitrogen-purged drums come standard for this product. Many of our customers discovered that careful attention to packaging meant longer shelf life and batch-to-batch reproducibility.
Each production lot of 3-Bromophenyl Isocyanate starts from controlled bromobenzene input. A lot of care goes into keeping the aromatic bromine intact throughout the conversion. Side reactions lurk on the production floor—hydrolysis from trace water can turn isocyanates into low-yield ureas or diphenylureas, which cause trouble in follow-up reactions. Drying steps and quick, sealed transfer between reactors cut that risk. Real plant experience means equipment gets assigned for single shifts, limiting cross-contamination.
We monitor the color and melting range starting the minute material leaves the reactor. Faint yellowing often betrays overreaction or polymerization, tipping us off before formal analysis. Over time, we’ve optimized distillation cuts, flash chromatography profiles, and temperature settings. Routine GC and NMR checks confirm both purity and correct substitution patterns, but minor tweaks add up when customers judge us on performance, not spec sheets.
We offer 3-Bromophenyl Isocyanate as a free-flowing crystalline solid. Typical batches stay within 97-99 percent purity range, though we can push higher if clients need. Moisture content stays below 0.5 percent, with regular Karl Fischer water tests run in tandem with every dispatch. The model number system used internally might not mean much to outsiders, but each code logs reactor history, full lot traceability, and the precise time window for quality checks.
Our experience finds most researchers want manageable container sizes for lab-scale synthesis—often 100-gram to 5-kilogram drums. Larger process runs usually get 25-kilogram drums shipped on nitrogen with tamper seals. We deliberately avoid glass since earlier incidents with brittle glassware during transport taught us metal-lined composite packaging holds up better and keeps the isocyanate dry and stable, even if the freight sits on a dock for days.
We’ve studied substitution effects and downstream reactivity for several years. For example, tert-butyl phenyl isocyanates and plain phenyl isocyanates work for broad applications, but don’t have the same ability to serve as dual-use functional handles. Our 3-bromo variant draws specifically from medicinal chemistry—a chemist trying to build a library of kinase inhibitors or an agrochemical firm developing pre-planting agents finds more pathways open with this brominated ring.
Sometimes lower-cost alternatives push buyers toward straight phenyl isocyanate, which lacks a handle for selective modification. In screening rounds, customers report our 3-bromophenyl isocyanate gives more consistent yields in stepwise couplings and can take on both nucleophilic addition and palladium-catalyzed cross coupling without fighting through side products. Mid-size drug developers who prefer direct contact with chemists rather than buying generic supply from traders tell us the difference shows up in saved synthesis time and less post-purification effort.
Sourcing through distributors dilutes the feedback loop from bench to factory. As the actual producers, we hear quickly if something shifts in reactivity, color, or handling. Last summer, when one round of high humidity slipped into packaging, three clients flagged minor losses in performance. We shut that line, re-checked dryers, and installed redundant sensors. This type of rapid adaptation doesn’t show up in paperwork but keeps calls coming from regular buyers who value reliability over bulk price concession.
We invest in both kilo-scale and several-tonne monthly capacities. Fine chemical synthesis depends on steady back-end supply. Reagent starvation during key project windows frustrates everyone; our stock buffer absorbs short-term surges without stretching lead times. Our size lets us remain agile—short supply chains, no third-party reliance, and direct conversation with chemists working at the bench.
One medicinal chemistry group approached us, struggling to get targeted ureas from ordinary isocyanates. Conventional routes involved first coupling, then adding bromine, but those steps added time and introduced more by-products. Our 3-bromophenyl derivative allowed them to run just two clean, sequential steps—forming the urea, then coupling at the bromine site using a Suzuki-Miyaura catalyst. Yields jumped by double-digits, and they skipped at least one laborious chromatography round.
Another example comes from the pigment industry. Isocyanates often play a small but strategic role in linking chromophores to other aromatic groups. For one client, access to a bromo handle enabled direct functionalization onto custom quinoline backbones, skipping complex protection-deprotection sequences and letting them launch small colorant runs with lower pilot costs.
And among our agrochemical clients, precise control over isocyanate substitution matters for developing pre-formulated libraries of pesticide candidates. The bromine substitution lets R&D quickly test how electronic or steric changes shift biological activity, instead of re-building from scratch each development cycle.
Working with isocyanates, especially aromatic types with direct halogenation, forces tighter safety margins than other reagents. Years of direct site management have shown us the importance of air-tight storage, dry transfer lines, and operator training. We fit every outgoing drum with both desiccant pouches and moisture indicators. Clients remark how a simple color-change tag saves them from guessing about material stability after a shipment delay or warehouse mishap.
Several customers have tried trading house material and reported mismatched documentation or inconsistent safety data. By controlling the full process, we ensure consistency not only in purity, but also in trace element content and max allowable residual monomers. All shipments include updated safety profiles and full COA datasets, sourced from real QC records—not just printer-pressed PDFs.
Modern buyers demand transparency to minimize risk and meet regulatory requirements. We’ve opened up our plant to client audits for those working with restricted chemicals or scaling for GMP production. Traceability here isn’t about marketing but about showing every lot’s origin, raw input, in-process checks and operator signatures.
This approach means chemists avoid the usual delays: no waiting for overseas shipping, no surprise customs hang-ups, and no time wasted tracking down missing batch information. A steady focus on supply visibility lowered stockouts for several contract manufacturing partners and allowed us to deliver emergency runs for urgent drug development projects.
Our production team meets weekly to review feedback from active customers. Complaints about trace odors or minor color changes have sent us back to the drawing board to improve filtration and finishing protocols. Conversations with users at conferences have sparked tweaks in drying techniques or batch sizes, helping labs cut waste and move faster between screening rounds.
A few years back, we switched from glass ampoules to lined steel drums due to routine breakage. Even small improvements help customers avoid headaches and ultimately deliver better results in their own work. Open communication with real chemists shapes our batches far more than anonymous “market analyses.”
Managing isocyanate chemistry generates unique waste challenges. Our plant operates a closed-loop recovery process for solvents, distilling and reusing material where possible to cut emissions and disposal needs. Where waste is unavoidable, we work with certified handling partners rather than shuttling responsibility downstream. For clients with strict environmental targets, detailed breakdowns of process outputs and waste streams can be provided, supporting downstream audits and lifecycle assessments.
Several customers selecting between multiple intermediates have opted for our process, not only for material purity but also because our operation offers lower overall cradle-to-gate impact. Being transparent about reagents and waste management draws investment from partners working on green chemistry goals.
As regulations tighten and synthetic chemists push boundaries of structure-activity relationships, demand will grow for high-purity, precisely functionalized isocyanates like 3-bromophenyl isocyanate. We continue to monitor trends in drug discovery, crop protection, and custom monomer research, updating our processes with each new challenge from the field.
Our greatest asset stems from the direct flow of information and feedback from end users. This knowledge cycles into our process improvements, packaging choices, and technical support. Each batch we ship reflects years of accumulated know-how, not just a formula run through reactors. By keeping production decisions anchored in real chemical work and end-user outcomes, we build reliability that traders can’t easily copy.
True progress in the chemical industry depends on mutual trust and shared problem-solving. By participating at every production step—from sourcing and synthesis through purification, packaging, and shipping—we help chemists gain an edge in R&D and commercial-scale projects. Our years of direct experience enable us to see beyond specs and provide working solutions, built through hands-on manufacturing and customer collaboration.
Whether supporting a biotech startup or a multinational formulation house, our experience producing 3-bromophenyl isocyanate means partners depend on not just a reagent, but a source of consistent reliability, innovation, and technical depth. The field grows by sharing real-world stories, listening to those closest to the chemistry, and acting quickly on what works. That spirit of collaboration and precision shapes every order, large or small, that leaves our facilities.