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HS Code |
453343 |
| Cas Number | 586-99-2 |
| Molecular Formula | C7H4BrNO |
| Molecular Weight | 198.02 g/mol |
| Appearance | White to pale yellow crystalline powder |
| Melting Point | 53-56°C |
| Boiling Point | 270°C |
| Density | 1.66 g/cm3 |
| Solubility | Insoluble in water; soluble in organic solvents |
| Purity | Typically ≥98% |
| Flash Point | 123°C |
| Storage Temperature | Store at 2-8°C |
| Synonyms | 4-Bromophenyl isocyanate |
| Smiles | C1=CC(=CC=C1N=C=O)Br |
| Refractive Index | 1.648 |
As an accredited P-Bromophenyl Isocyanate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | P-Bromophenyl Isocyanate is supplied in a 25g amber glass bottle, tightly sealed with a PTFE-lined cap and hazard labeling. |
| Shipping | P-Bromophenyl Isocyanate should be shipped in tightly sealed containers, protected from moisture and incompatible substances. It must be labeled as a hazardous material, complying with DOT and IATA regulations. Package in containers resistant to isocyanates and brominated compounds, and include appropriate hazard communication labels. Store and transport in a cool, dry place. |
| Storage | **P-Bromophenyl Isocyanate** should be stored in a tightly closed container in a cool, dry, well-ventilated area, away from moisture, heat, and incompatible substances such as acids, bases, and alcohols. It should be kept out of direct sunlight and separated from oxidizing agents. Proper chemical storage cabinets and personal protective equipment are recommended to prevent accidental exposure or reactions. |
Applications of P-Bromophenyl Isocyanate in Industrial ManufacturingP-Bromophenyl Isocyanate serves as a critical intermediate in specialty chemical production, supporting several precise industrial processes. As a manufacturer, we supply this compound for value-added transformation in key downstream sectors where strict standards and process controls apply. 1. Active Pharmaceutical Ingredient (API) SynthesisMature pharmaceutical manufacturers use P-Bromophenyl Isocyanate for building complex molecular structures in non-steroidal anti-inflammatory drugs, anti-cancer agents, and targeted therapies. Its isocyanate group reacts with amines to form essential urea and carbamate functional groups. Typical applications require precise control of impurities and full documentation for regulatory submissions. Our material supports consistent batch reproducibility, purity levels, and robust process validation in GMP environments. Industry compliance standards
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2. Agrochemical Intermediate ProductionAgrochemical formulating companies apply P-Bromophenyl Isocyanate during synthesis of urea or carbamate-based herbicides and fungicides. It is valued for specific brominated aromatic structures, enabling targeted bioactivity and environmental stability. Process engineers use dedicated closed systems due to the reactive isocyanate group, with detailed risk management for personnel and environmental exposure. Industry compliance standards
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3. Specialty Polymer and Polyurethane SynthesisEngineered polymer producers incorporate P-Bromophenyl Isocyanate in high-performance thermoset resin systems, including isocyanate-cured polyurethanes and polyureas. The bromine substituent imparts specific flame retardancy or enhances thermal stability for advanced electronics or insulation products. Formulators utilize moisture control systems and sealed reactors to ensure controlled exothermic reactions and chain extension. Industry compliance standards
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4. Performance Dye and Pigment ManufacturingColorant and pigment manufacturers use P-Bromophenyl Isocyanate for synthesis of brominated organic dyes, particularly as coupling agents in the preparation of azo and phthalocyanine derivatives. The isocyanate group offers high selectivity during diazo coupling, ensuring color fastness and purity for specialty inks and plastics. Proper handling is essential to control residual isocyanates and guarantee end-product safety. Industry compliance standards
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5. Fine Chemical Synthesis for Research and DiagnosticsProducers in the life science and analytical sector select P-Bromophenyl Isocyanate to synthesize reference standards, analytical reagents, and custom intermediates for diagnostic kits and sensors. Its high reactivity allows for functional group incorporation in complex marker molecules, while precise batch traceability and impurity documentation support use in regulated laboratory protocols. Industry compliance standards
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Working in chemical manufacturing gives a person a clear understanding of how certain raw materials shape the progress of specialty synthesis. In the plant, P-Bromophenyl Isocyanate often stands out as one of those compounds that chemists remember—not because it draws attention through color or scent, but because it reliably delivers results where many others fall short. P-Bromophenyl Isocyanate serves as a solid, practical tool for researchers and process engineers who need to execute transformations that demand selectivity, high yield, and consistent purity. What separates this compound from the dozens of similar-sounding isocyanates lining our storeroom shelves boils down to both its chemical structure and its repeatable performance in bench and plant-scale reactions.
For many years, our team worked hand in hand with researchers running pharmaceutical intermediates, agrochemical building blocks, and polymer modification projects. As a pure organic intermediate, P-Bromophenyl Isocyanate fits roles that require a phenyl ring equipped with a bromine atom at the para position and a reactive isocyanate group. The product’s appearance as an off-white to light brown crystalline powder or sometimes a viscous liquid demonstrates the variability natural to a batch process, but the specification consistently meets strict purity standards set by regulated markets. During quality control, attention always centers on the melting point, specific bromine content, and absence of side products that could complicate downstream synthesis.
The difference between one batch and the next comes down to how closely we monitor temperature gradients, agitation speeds, and feed rates during chlorination, bromination, and phosgenation steps. At this level, our experience matters more than a technical data sheet. Operators learn not only how to avoid over-bromination but also how to steer crystal formation toward easy filtration. In the rare cases where a batch falls out of spec, we catch the deviation early enough that there’s no risk of it reaching a customer’s plant. By working directly with end-users, we receive feedback quickly and watch how researchers apply the material in divergent routes, which keeps us on our toes.
Over time, the use cases we've seen with P-Bromophenyl Isocyanate have expanded beyond what textbooks predict. Medicinal chemistry groups use this intermediate to introduce both aryl isocyanate and para-bromine units into candidate molecules in a single synthetic step, impacting everything from kinase inhibitors to diagnostic agents. The para-bromo group grants a powerful synthetic handle—enabling easy further substitution, Suzuki or Buchwald coupling, or bridging to heterocycles—without the risk of meta or ortho contamination that plagues mixed isomers.
In the world of functional polymers, R&D departments take advantage of the isocyanate group’s versatility. P-Bromophenyl Isocyanate reacts efficiently with active hydrogens in alcohols and amines, building custom-tailored polymer backbones or creating reactive cross-linking points. In coatings and adhesives, the brominated aromatic ring brings added fire resistance and alters solubility profiles in ways plain phenyl isocyanate cannot. These material changes translate to more robust, predictable end-products, which any manufacturer values when balancing quality with commercial viability.
Agrochemical synthesis also benefits from what the combination of para-bromo and isocyanate offers. The straightforward reactivity pattern leads to fewer side products and a cleaner working mixture. For producers seeking to minimize purification steps or handle manufacturing scale-up with fewer headaches, the time and resource savings are substantial.
P-Bromophenyl Isocyanate draws fair comparison to both unsubstituted phenyl isocyanates and their ortho or meta-bromo counterparts. Experience in our labs shows that the para-bromo arrangement leads to a more predictable physical form and easier handling. The crystalline or solidified product is less volatile than phenyl isocyanate and much less prone to problematic dimerization or isocyanurate formation during storage. The single, sharp melting point and low moisture uptake also grant a shelf-life that consistently exceeds basic requirements, eliminating most end-user concerns about quality drift over time.
Compared to ortho- and meta-brominated isomers, the para product minimizes byproduct formation because reactive centers sit farther from one another. This structural distinction narrows the impurity profile, which simplifies compliance testing under pharmacopeia or REACH standards. Those who have tried to substitute non-para versions often tell us they face stickier filtration and trickier isolations, especially when scaling up from bench to pilot plant. The difference is not only academic but practical, as our partners realize efficiency gains through reductions in rework and less downstream cleanup.
Historically, we see losses under 1% in post-process isolation, even when batches approach multi-kilogram scales. Analytical controls such as HPLC and NMR confirm purity tightness batch after batch, with impurity spectra falling well within global regulatory limits. A consistent feedback loop developed; pharmaceutical clients confirmed that process impurity carryover remained below 0.1% w/w, eliminating costly extra steps. Polymer producers noted that moisture-vapor transmission rates fell when using the brominated aromatic isocyanate versus the unsubstituted product, a bonus for packaging and protective coatings. Agrochemical users pointed to higher conversion rates and lower run times.
These field results tell us that the premium paid for para-bromo substitution is not lost revenue—it gets recouped through easier process control and fewer regulatory headaches. In the competitive world of custom synthesis, where reproducibility and traceability matter most, these practical benefits mean a lot more to the buyer than any theoretical lab demonstration.
Behind every story of successful use lies a background of careful handling and risk management. P-Bromophenyl Isocyanate carries reactivity you want—selective enough to target functional groups of choice, but not so jumpy that you battle runaway oligomerization. The para-bromo ring directs the molecule’s stability, lowering its volatility compared to phenyl isocyanates without halogenation. This contributes to better shelf handling and less inhalation risk on the packaging line.
From a production manager’s perspective, working with this compound means less time spent managing hazardous off-gassing or moisture-triggered polymerization in storage tanks. Over years of experience, we find safe operation hinges on the usual basics: dry, nitrogen-blanketed lines, sealed transfer, and effective PPE protocols rather than constant firefighting. That stability has enabled us to ship to customers across three continents with confidence, knowing spoilage and handling incidents remain very rare.
The advantages start in upstream processes, where the raw bromobenzene’s quality dictates not only final yield but also impurity type and residual solvent levels. Sourcing real para-bromobenzene, not contaminated with meta or ortho cuts, becomes critical. Any hiccup here leads to downstream difficulties—from high melting point by-products to product retained in filters and crystallizers. Years of relentless attention to input quality have taught us these shortcuts only bring delays.
Downstream, users designing their synthetic routes appreciate the shortcut the para-substitution brings. In peptide chemistry, the isocyanate reacts swiftly with amines under mild conditions to give ureas, carbamates, or differently substituted diamides. Chemists gravitate toward P-Bromophenyl Isocyanate as a dependable choice for introducing the bromo-phenyl unit late in a sequence, reducing protection-deprotection steps and avoiding repeated halogen exchange reactions. Simple workups, cleaner extracts, and improved throughput arise from design decisions made by both molecule architects and the manufacturing team bringing them the raw material.
Feedback from industrial partners always focuses on stability, traceability, and honest communication about batch changes or raw material source shifts. We keep open records showing manufacturing dates, detailed impurity profiles, and any deviations to empower users to validate their incoming material, even when regulatory scrutiny increases. The trust we build translates into long-term relationships, with some clients returning year after year, often with new project requests based on the performance of previous lots. In complex supply chains, transparency becomes more valuable than any price discount.
Quality is never static in this business. Every year, regulatory benchmarks tighten, trace impurity thresholds fall, and pure labeling requirements raise. We meet enhanced NMR assay needs and respond swiftly to requests for full elemental analysis, because the partners who depend on us value consistency as much as innovation. Rather than passively waiting for audits, we operate with open labs and invite direct visits; more than once, a quick on-site review has solved a customer’s process puzzle or given us insight into what matters most: practical, reliable supply.
Access to specialty isocyanates like P-Bromophenyl Isocyanate often gets restricted not by demand, but by sporadic supply interruptions, regulatory swings, and international shipping delays. Responding to these realities means carrying larger precursor stocks and building redundancy into our own vendor relationships. Since many custom synthesis partners rely on short lead times, we invest in modular production capacity, enabling batch upscaling within weeks instead of months. This agility lowers total project risk, especially for drug development pipelines or crop protection launches requiring sudden volume increases.
Pricing volatility, driven by upstream bromine and phosgene markets, challenges both buyers and producers. Long-term contracts and transparent raw material sourcing practices shield our customers from most market shocks. Our experience shows that strong supplier partnerships—constantly sharing forecasts, order flows, and technical advances—smooth price cycles and minimize the frequency of abrupt changes that can throw a fine chemical project off schedule.
Continuous improvement in process safety and resource efficiency remains top of mind in our plant. The need to use phosgene and handle brominated intermediates drives us to adopt best-in-class containment systems, effluent treatment, and waste minimization programs. We invest in thermal recovery and scrubber units that recycle or neutralize hazardous vapors, not only to meet regulations but also to protect our local environment and team. These measures prove their worth each year, translating to lower operational risks and earning the trust of safety auditors who tour our site.
Mature process analytics—integrated PAT loops, inline FTIR, and constant temperature/humidity monitoring—enable us to shave reaction times and improve yield per batch beyond historic norms. Leaning on years of collective operator experience helps in preventing the smallest deviations from growing into quality headaches. Our track record with single-digit ppm impurity batches did not emerge from automation alone; hands-on know-how makes sure every inflection point is handled with care and attention.
Our closest work happens with researchers facing ambitious synthesis targets. From the first inquiry, we dig for specifics—how sensitive is the route to trace water? Is batch super-saturation a concern? Can the route tolerate minor colored byproducts, or is an extra recrystallization inevitable? Engaging in these technical discussions early often avoids downstream coordination costs, and leads us down unexpected avenues. Sometimes a customer’s new analytical tool highlights an impurity we never noticed; sometimes we catch a missing handling best practice and share proven solutions that can save thousands in remediation expense.
The stories that stay with us involve problems solved under tight time lines—salvaging a peptide synthesis by rapidly swapping to a cleaner P-Bromophenyl Isocyanate batch, or supporting a startup’s polymer launch after a competitor’s lot failed spectral testing. We never view these results as the product of luck, but as the outcome of a working culture that values information sharing and flexible process troubleshooting. Close technical engagement strengthens both our teams and the customers’ ability to take on more challenging molecular targets.
As new drug classes and specialty materials push the demands on fine chemical building blocks, P-Bromophenyl Isocyanate will keep playing a key part in advanced organic synthesis and cross-linked material design. The foundational lessons—building product reliability stepwise from input screening to final packing, engaging closely with users, innovating for process safety and sustainability—will anchor how we operate. Expectations for tighter analytical confirmation, regulatory harmonization, and documented supply chain traceability will only increase in the years ahead. We already invest in digital batch records, RFID tags for error-proof tracking, and cloud-linked process control to meet these needs before they become tomorrow’s requirement.
Whenever a partner chooses P-Bromophenyl Isocyanate for their synthesis route, it signals trust in our raw material stewardship as well as belief in the compound’s unique reactivity. The cumulative knowledge built across hundreds of batches, cross-referenced with direct feedback from R&D chemists, regulatory teams, and production managers, forms the basis of every strategic improvement. Delivering an intermediate that moves project timelines forward and simplifies both compliance and handling is a responsibility we carry seriously. Success comes from putting practical experience above advertising, and crafting every batch as if our own research depended on it.
P-Bromophenyl Isocyanate remains an essential intermediate for pharmaceutical, polymer, and agrochemical applications. Its value stems not only from its molecular structure but from the know-how, quality systems, and commitment to transparency behind every lot shipped. By focusing on user collaboration and adapting production processes to changing market needs, we help researchers and manufacturers turn their concepts into commercial reality. The lessons learned in delivering this chemical translate to better products, stronger partnerships, and a manufacturing culture built on reliability, safety, and innovation.