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4-Bromo-3-Nitrotoluene

    • Product Name 4-Bromo-3-Nitrotoluene
    • Alias 4-Bromo-1-methyl-3-nitrobenzene
    • Einecs EINECS 214-729-4
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    645508

    Chemical Name 4-Bromo-3-nitrotoluene
    Molecular Formula C7H6BrNO2
    Molecular Weight 216.03 g/mol
    Cas Number 5085-67-4
    Appearance Yellow to orange crystalline solid
    Melting Point 60-63°C
    Density 1.71 g/cm3 (approximate)
    Solubility In Water Slightly soluble
    Ec Number 225-797-7
    Pubchem Cid 122896
    Smiles CC1=C(C=C(C=C1Br)[N+](=O)[O-])
    Storage Conditions Store in a cool, dry place away from light

    As an accredited 4-Bromo-3-Nitrotoluene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 500g of 4-Bromo-3-Nitrotoluene is supplied in a sealed amber glass bottle with a secure screw cap and hazard labeling.
    Shipping 4-Bromo-3-Nitrotoluene is shipped in tightly sealed containers to prevent leakage and contamination. It should be handled as a hazardous material, following all relevant shipping regulations. The chemical is packed with appropriate hazard labels and documentation, and transported by trained personnel to ensure safety and compliance with international transport guidelines.
    Storage 4-Bromo-3-nitrotoluene should be stored in a tightly sealed container in a cool, dry, and well-ventilated area away from direct sunlight, heat sources, and incompatible materials such as strong oxidizers and acids. Ensure proper labeling and avoid sources of ignition. Store in accordance with local regulations and use secondary containment to prevent accidental spillage.
    Application of 4-Bromo-3-Nitrotoluene

    Applications of 4-Bromo-3-Nitrotoluene in Industrial Manufacturing

    4-Bromo-3-Nitrotoluene serves as a specialty intermediate in several chemical synthesis pipelines, supporting the production of advanced materials, pharmaceuticals, and colorants. The following sections outline actual industry practices, compliance standards, application ratios, downstream processing details, and end-use product types for core application fields.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) Synthesis

    As a well-established building block in the synthesis of select APIs, 4-Bromo-3-Nitrotoluene enters manufacturing workflows for heterocyclic drug molecules, especially in the modification and construction of complex aromatic frameworks. Its bromine and nitro functionalities facilitate further transformations such as Buchwald–Hartwig amination, Suzuki coupling, and reduction steps crucial to producing key intermediates for anti-infective and central nervous system medications. Careful quality control at intake and throughout synthesis is essential to comply with international pharmaceutical manufacturing norms.

    Industry compliance standards

    • ICH Q7 GMP (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • U.S. FDA 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals)
    • European Pharmacopoeia (Ph. Eur.) monograph requirements for intermediates
    • USP General Chapter <823>

    Typical usage ratio

    • Between 0.8-6% w/w of the total reaction mixture, subject to exact stoichiometric calculation based on target molecule and scale.
    • Ratios adjusted according to downstream molar requirements and impurity control during multi-stage reactions.

    Downstream process integration

    • Input as a key substrate in condensation and coupling reactions after initial solvent conditioning and micronization, often under nitrogen atmosphere.
    • Follows strict QC release—HPLC and GCMS purity assessment—before batch charging for intermediate or final API step.

    Final product types

    • Pyridazine- and triazole-based pharmaceutical APIs
    • Antibacterial agent intermediates
    • CNS-active compound scaffolds
    • Generic drug intermediates for regulated and export markets

    2. Agrochemical Intermediate for Herbicide Manufacture

    This compound remains integral in manufacturing certain nitroaromatic herbicides, acting as a key halogenated intermediate for achieving target selectivity in weed control agents. Downstream processors value its reactivity in nitration and amination steps for synthesizing active herbicidal substances where precise positioning of functional groups is essential for activity and regulatory approval. Producers must adhere to crop residue and environmental exposure limitations, as well as batch-wise traceability for field application safety.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management System
    • REACH EC No. 1907/2006 registration for intermediates (EU)
    • EPA 40 CFR Part 180 – Tolerances and Exemptions for Pesticide Chemical Residues

    Typical usage ratio

    • Employs a 1.5–7% molar ratio depending on active ingredient synthesis path and desired conversion rate, fine-tuned via process optimization trials.
    • Batch integration balanced with solvent selection and reaction temperature for process safety and yield.

    Downstream process integration

    • Added in halogenation reactors under controlled temperature to influence regioselectivity for subsequent amide or ether formation.
    • Fed continuously or batchwise with co-catalysts and staged work-ups to ensure low impurity profiles.

    Final product types

    • Halo-nitrotoluene based pre-emergent herbicides
    • Nitroaromatic herbicide technical concentrates
    • Wettable powder and emulsifiable concentrate formulations
    • Bulk intermediates for multinational agrochemical brands

    3. Dye and Pigment Synthesis

    The aromatic bromonitro structure of this intermediate finds key roles in the colorants sector, particularly in the manufacturing of specific monoazo and disperse dyes. Its electron-withdrawing nitro group and reactive bromine optimize chromophore construction and fastness properties, critical for high-performance textiles and plastics. Producers must maintain analytical traceability and comply with global standards limiting contaminant residues and banned amine precursors.

    Industry compliance standards

    • OEKO-TEX® Standard 100 – Chemical Compliance for Textile Dyes
    • EU Regulation (EC) No. 1907/2006 (REACH)—Annex XVII restrictions on azo dyes
    • ISO 9001:2015 for quality process validation
    • ZDHC Manufacturing Restricted Substances List (MRSL)

    Typical usage ratio

    • Incorporated at 2–10 mol% relative to primary amines in diazotization-coupling reactions, with actual concentration set by shade strength requirements and coupling efficiency.
    • Usually optimized by pilot-scale lab trials linked to target color index.

    Downstream process integration

    • Charged post-diazotization step, actively participating in azo coupling or reduction-alkylation pathways within agitated reactor systems.
    • Product isolated through filtration, washing, and spray drying with downstream fineness adjustment.

    Final product types

    • Monoazo textile disperse dyes
    • Specialty pigments for polyester and acetate fibers
    • Color concentrates for plastics
    • Technical grade intermediates for pigment lakes

    4. Synthesis of Specialty Chemical Intermediates for Photographic and Imaging Chemicals

    Specialty formulators utilize this compound for its precision in introducing halogenated and nitrated motifs required for highly sensitive imaging agents. Its inclusion supports downstream transformations used in silver halide emulsion chemistry and fine-tuned developer/inhibitor production. All process streams are designed for trace-level contaminant monitoring to prevent image fog or instability, and full compliance with hazardous material handling standards is nonnegotiable.

    Industry compliance standards

    • ISO 9001:2015 and ISO 14001:2015 for quality/environmental management
    • ANSI IT9.2-1998 for imaging chemical permanence
    • Globally Harmonized System (GHS) for chemical safe use and labeling
    • Controlled hazardous materials storage as per NFPA 400

    Typical usage ratio

    • Integrated at between 0.5–3% w/w in developer or sensitizer intermediate formulations, adjusted based on target analytical grade and batch yield review.
    • Stringent rationing follows internal QC protocol to avoid byproduct formation impacting emulsion sensitivity.

    Downstream process integration

    • Undergoes active halogenation or nucleophilic displacement as an electronic modifier, typically introduced at pre-filtration stage before crystallization or solvent stripping.
    • Downstream isolation completed in cleanroom conditions to minimize background contamination.

    Final product types

    • Photographic film emulsions
    • Fine chemical developer intermediates
    • Contrast and toner agents for industrial imaging
    • Specialty laboratory calibration targets
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    Certification & Compliance
    More Introduction

    The Role and Value of 4-Bromo-3-Nitrotoluene in Modern Industry

    Introduction to 4-Bromo-3-Nitrotoluene

    4-Bromo-3-Nitrotoluene, with the molecular formula C7H6BrNO2, stands out as an aromatic compound carrying promise for multiple chemical industries. Featuring both a bromine atom and a nitro group attached to a toluene backbone, this molecule often finds itself at the heart of specialized chemical transformations. The bromine sits on position 4 of the toluene ring, the nitro group finds its place on position 3, while a methyl group decorates the ring, all providing this compound with highly sought-after reactivity.

    In my years around the world of fine chemicals and specialty intermediates, few building blocks offer the blend of selectivity and function that 4-Bromo-3-Nitrotoluene does. Whether you’re working in agrochemicals, pharmaceuticals, or dye manufacturing, its unique structure anchors many syntheses and introduces features that are hard to replicate by other reagents.

    The Essential Qualities: Model, Physical Form, and Chemical Behavior

    The crystalline yellow color signals its purity and identity. 4-Bromo-3-Nitrotoluene melts between 61–63°C and generally maintains stability under normal laboratory storage. Humidity or prolonged UV exposure won't trigger unexpected degradation. That physical stability matters for storage and consistent yields, whether a bench chemist scales up or a commercial operator manages inventory over weeks or months.

    Aromatic halogenation gives the molecule ample flexibility. The bromine atom functions as an excellent leaving group for further couplings or substitutions, while the nitro group withdraws electron density, tuning the ring’s overall reactivity. The methyl tail slightly increases hydrophobicity, nudging solubility in organic solvents but holding back in water. These qualities make it accessible in both research and manufacturing environments. Even with all the chemical jargon stripped away, people handling the stuff rely on these baseline facts so as not to run into costly delays or lab mishaps.

    Practical Applications: Bringing More Than Just a Label

    One thing folks quickly realize is that 4-Bromo-3-Nitrotoluene serves best as a chemical intermediate. It bridges the gap between basic toluenes and more complex frameworks needed for life sciences or materials science. Many organic chemists, including myself, saw this molecule open up new synthesis pathways in aromatic amine production, because the nitro group makes reduction both targeted and reliable. In the past, you'd spend days wrestling with poor conversions or messy mixtures. Now, strategic use of this bromonitrotoluene lets you dial in selectivity and streamline the route.

    This compound comes up a lot in the development of specialty dyes and pigments. Brominated aromatic units lend vibrant color and chemical durability to synthetic pigments. I've seen workshops where technicians solve performance gaps in electronic display dyes by switching to precisely brominated intermediates like this one. That methyl group adds a structural tweak you don't get from unsubstituted nitrobenzenes, ushering in better stability against photobleaching or thermal breakdown.

    In the pharmaceutical sector, the blend of nitro and bromine handles lets synthetic designers build scaffolds for active pharmaceutical ingredients (APIs). Medicinal chemists, seeking complexity and specificity, trust these double-activated rings for Suzuki, Heck, or Buchwald-Hartwig couplings. The result: streamlined access to biaryl structures central to new drugs and research tools. In my work, I’ve seen young chemists struggle with less versatile starting points, only to switch to 4-Bromo-3-Nitrotoluene and watch their hit rates improve.

    Comparing 4-Bromo-3-Nitrotoluene to Related Chemicals

    Chemists always weigh options. 4-Bromo-3-Nitrotoluene manages to carve out a space between simpler molecules like 4-nitrotoluene or mono-bromo toluenes. Those alternatives often fail to provide the same range of cross-coupling or directed functionalization. It offers more than the sum of its parts because the nitro and bromine steer reactivity into sweet spots.

    Let’s take 3-Nitrotoluene or 4-Bromotoluene alone. Each serves as a stepping stone, but they lack the simultaneous power this compound brings. The absence of one group means fewer reaction handles, slower routes, or less control over downstream products. From the broader lens of process chemistry, efficiency gains translate to real dollars saved, less waste generated, and faster timelines in R&D cycles. We’ve all heard the pain of reworking protocols because a key intermediate left too much to chance; compounds with this sort of fine-tuned substitution pattern helped push projects from pilot to production while competitors stayed stuck in neutral.

    Where cost becomes an issue, some teams may reach for less substituted nitrobenzenes or chlorinated analogs. The cost per gram might drop, but yield reliability and final product quality often slide. The bromine in 4-Bromo-3-Nitrotoluene, heavier and more reactive than chlorine, allows coupling under milder conditions. This usually means milder temperatures, lower catalyst loads, and fewer by-products clogging up a process.

    The Roadblocks and Questions Still Facing Its Use

    Nothing about synthetic chemistry is one-size-fits-all, and that includes 4-Bromo-3-Nitrotoluene. Its best features sometimes create challenges elsewhere. For one, handling requirements can escalate—bromoaromatics have known risks for skin or respiratory systems if proper ventilation slips or spill response lags. I’ve watched lab rookies forget gloves and learn safety lessons the hard way. The nitro group, while wonderful for downstream transformations, brings concerns if waste management or environmental controls aren’t robust.

    Commercial and laboratory supply chains face price fluctuations. Bromine itself, sourced from limited global bases, fluctuates in cost depending on mining output and import regulations. The resulting market can swing unexpectedly for those who rely on just-in-time procurement—painful for companies estimating margins by the penny.

    Ethical, Environmental, and Compliance Considerations

    Responsibility matters at every level, especially around aromatic nitro compounds. Waste control, effluent treatment, and air quality standards govern how facilities must operate. In my experience, teams embracing green chemistry approaches gain long-term resilience. Options include optimized reaction conditions that cut reagent use or swap greener solvents for common ones like dichloromethane. I've seen pilot lines retrofit scrubbers specifically because of aromatic nitrogen compounds, learning the hard way that local authorities pay close attention to this type of chemistry.

    The path forward includes better recycling of solvents and even catalytic systems designed to minimize by-product streams. As companies and labs grabble with increasing environmental expectations, 4-Bromo-3-Nitrotoluene remains in use, but only where teams commit to strong compliance and education. The industry keeps moving in this direction not just out of legal necessity, but because skilled chemists and operators demand safer workplaces and cleaner operations. In my circles, early-career chemists expect clearer environmental reporting than their predecessors ever did.

    What Matters for Procurement and Usage

    Buyers and lab managers who stock this product keep an eye on several critical markers. Purity, trace metal content, moisture, and packaging integrity come at the top of any checklist. From startups to established pharmaceutical giants, mishaps trace back when chemical quality slips below expectation. Powders caking up, samples arriving off-color, or detection of excessive heavy metal traces trigger costly returns, waste, and schedule disruptions.

    Shipment and storage mark another pain point worth planning for. Tightly sealed containers, desiccant inclusion, cool and dry warehouse spaces all help maintain shelf life and reliability. In my years on the procurement side, supplier reliability and transparent quality documentation make as much difference as headline price per kilo. Responding to regulatory or market audits means keeping paperwork organized and knowing each batch's provenance.

    Collaboration between chemists and supply teams builds resilience. Open feedback loops about purity or packaging issues let suppliers up their game and keep customers running smoothly. I’ve seen mutual trust produce not just better service but also new application notes and shared troubleshooting guides, all perks that never show up in a basic product listing.

    Improving Safety and Handling in Practice

    Safety doesn’t happen by accident. Many newcomers gravitate toward trusted chemical intermediates and may overlook laboratory risks. Clear standard operating procedures—good ventilation, tested gloves, regular hazard reviews, and timely spill response training—all keep small errors from becoming disasters. I've led safety workshops where simple reminders about wearing goggles or dispensing in the fume hood cut near-miss incidents in half.

    Across small business and academic labs, easy access to up-to-date safety data sheets and visible labeling in English and local languages makes all the difference. Even if everyone on a team handles dozens of compounds each week, safety culture sharpens around those with acute toxicity or flammable vapors. Teams that treat each new order of 4-Bromo-3-Nitrotoluene with fresh eyes and not routine complacency handle surprises better.

    On a larger scale, investment in local exhaust systems or safer bottle designs pays back over time. Fewer accidents mean better morale and less regulatory hassle. In my experience, nothing brings a lab together like the day someone’s quick thinking stops a spill from turning into a news item, sparking a real sense of pride in the group.

    Building Better Chemistry with Informed Choices

    4-Bromo-3-Nitrotoluene keeps showing up in scientific publications and new process breakthroughs. Specialists across material science, medicinal chemistry, and product engineering cite it for reliable functionalization and value as a strategic intermediate. The learning curve isn’t especially steep; academic literature, accessible training videos, and peer discussion forums break down key synthesis strategies and troubleshooting tips. Working chemists tend to share both failed and successful use cases freely, building an ecosystem of open data sharing that benefits everyone from graduate students to commercial process operators.

    As industry moves toward continuous chemistry, digital automation, and data-driven design, this compound’s features may grow even more prized. Real-time process monitoring and automated sampling reduce errors and make scale-up safer and more consistent. Smart labs already set up sensors to flag trace impurity spikes or packaging breaches before trouble starts. Building these digital and real-world feedback loops speeds up learning and strengthens both safety and efficiency.

    Balancing Competing Priorities in Product Choice

    No reagent exists in a vacuum. Labs and companies weigh tradeoffs—cost, function, safety, and environmental footprint—each time they restock. For 4-Bromo-3-Nitrotoluene, its unique combination of substitution pattern, reactivity, and ease of downstream modification often tip the scale, especially where performance or timeline beats small differences in raw material price.

    A pragmatic approach acknowledges the pluses—a familiar, well-characterized intermediate with published use cases—against known challenges like supply chain risk or hazardous waste considerations. Experienced teams, in my experience, build contingency plans, vet suppliers carefully, and prepare backup reaction routes just in case. The result: fewer rushed decisions, less downtime, and more reproducible science.

    Potential Solutions for Current Industry Pain Points

    Where pain points exist, the industry moves to solve them. High-quality supplier networks, tighter quality controls, and pre-shipment testing help ensure product arrives as advertised. Waste and environmental issues find answers in better solvent management, smarter catalyst choices, and batch process optimization. Teams deploying 4-Bromo-3-Nitrotoluene in large volumes benefit from investing in dedicated storage solutions, in-house waste neutralization systems, and robust incident reporting routines.

    Further, partnerships between manufacturers, universities, and regulatory bodies keep the entire supply chain more transparent and responsive. Sharing anonymized data on product integrity hiccups or near-miss incidents helps build safer playbooks for everyone involved.

    At the level of research and bench science, improvements in digital inventory tracking, internal peer-review of synthesis plans, and even shared reagent libraries streamline procurement and reduce unnecessary stockpiling. These steps, small on their own, add up to smoother, more efficient operations over time.

    The Future of 4-Bromo-3-Nitrotoluene in Evolving Industries

    Specialty chemicals never remain static. Advances in computational chemistry let development teams model reaction pathways, find greener alternatives, and predict impurity profiles before committing resources. For example, machine learning applications can pinpoint scenarios where 4-Bromo-3-Nitrotoluene offers a genuine performance jump, helping labs allocate budgets more strategically.

    As regulations tighten on aromatic nitro compounds and brominated chemicals, ongoing innovation becomes crucial. New synthetic methods promise less toxic by-products or improved atom economy. Teams investing in sustainable manufacturing practices—recycling solvents, closing material loops, and minimizing emissions—model the kind of long-term thinking that will shape which intermediates stay in favor.

    Based on years in the field, I’ve noticed research funding and commercial incentives increasingly reward process upgrades that push both environmental stewardship and technical performance. 4-Bromo-3-Nitrotoluene’s future will likely rely on its ability to integrate into this changing landscape while keeping its practical strengths front and center.

    Conclusion

    Across decades, 4-Bromo-3-Nitrotoluene established itself as an anchor point for countless synthetic schemes. Its value rests in more than basic chemical properties—real-world use reflects reliability, consistent quality, and a balance of safety, performance, and environmental care. The lesson I keep seeing is that success with specialty intermediates comes less from chasing novelty and more from planning, collaboration, and practical know-how. Whether building new medicines, functional dyes, or advanced materials, teams thrive when they draw on shared experience, rigorous processes, and a commitment to both human and environmental health.