2-Bromotoluene

    • Product Name: 2-Bromotoluene
    • Alias: o-Bromotoluene
    • Einecs: 203-393-9
    • Mininmum Order: 1 g
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
    • CONTACT NOW
    Specifications

    HS Code

    712410

    Name 2-Bromotoluene
    Cas Number 95-46-5
    Molecular Formula C7H7Br
    Molar Mass 171.04 g/mol
    Appearance Colorless to pale yellow liquid
    Melting Point -24 °C
    Boiling Point 183-185 °C
    Density 1.395 g/cm3 at 25 °C
    Flash Point 70 °C
    Solubility In Water Insoluble
    Refractive Index 1.5700 at 20 °C

    As an accredited 2-Bromotoluene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 500 mL of 2-Bromotoluene, sealed with a screw cap and labeled with safety and hazard information.
    Shipping 2-Bromotoluene should be shipped in tightly sealed containers, protected from light, heat, and moisture. It is classified as a hazardous material and must comply with local, national, and international regulations for the transport of flammable liquids. Proper labeling and documentation, including safety data sheets, are required during shipping.
    Storage 2-Bromotoluene should be stored in a cool, dry, well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed and protected from light. Store in a flammable liquids cabinet if possible. Ensure proper labeling and keep away from heat, sparks, and open flames to prevent fire hazards.
    Application of 2-Bromotoluene

    Applications of 2-Bromotoluene in Industrial Manufacturing

    2-Bromotoluene, an essential aromatic bromine compound, supports several advanced industrial sectors through its reactivity and purity profile. As a direct manufacturer, we supply large-scale users who require consistent quality and regulatory transparency for their end applications. Below we outline the primary downstream segments and provide detailed, production-focused information for each use case.

    1. Synthesis of Agrochemical Intermediates

    Advanced crop protection molecules require halogenated aromatic building blocks, and 2-Bromotoluene functions as a critical intermediate in the manufacture of selective herbicides and fungicides. Agrochemical formulators implement this compound in the construction of key molecular frameworks via Suzuki and Ullmann coupling reactions. Purity and controlled isomer content influence catalytic activity and regulatory acceptance. Industrial customers optimize feed ratios to control selectivity, minimize byproducts, and meet seasonal production cycles for major agricultural active ingredients.

    Industry compliance standards

    • EU Regulation (EC) No 1107/2009 for crop protection active substances
    • US EPA 40 CFR Part 174 for pesticide ingredients
    • Japanese Agricultural Chemicals Regulation Law
    • ISO 9001:2015-certified manufacturing traceability systems

    Typical usage ratio

    • Batch feed: 0.8–1.05 molar equivalents per target intermediate
    • Adjustment based on specific bonding site yields and impurity profiles
    • Process chemists modulate dosing per catalyst loading and raw material recovery strategies
    • Higher ratios for sequential one-pot transformations with alkyl or aryl amination

    Downstream process integration

    • Direct addition into palladium- or copper-catalyzed coupling reactors
    • Isomeric purity validated before blending with auxiliary reactants
    • Monitored via inline HPLC to guide transfer to downstream derivatization stages
    • Residual management protocols for spent brominated solvents

    Final product types

    • Herbicide actives (e.g., for rice and maize systems)
    • Benzylated fungicides for cereal crops
    • Intermediate compounds for insecticidal formulations
    • Active ingredient precursors for global agrochemical majors

    2. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers use 2-Bromotoluene as a ring-functional precursor during early stage synthesis of active pharmaceutical ingredients, especially in the anti-inflammatory and CNS drug pipelines. The material’s bromine substituent assists in selective halogen–metal exchange, facilitating downstream Grignard or lithium derivatizations. Purity and trace metal levels must comply with regulatory monographs and impurity Q3A/B guidelines. In multi-step active ingredient production, material traceability supports API identification and impurity trending for filings in regulated markets.

    Industry compliance standards

    • ICH Q7 and ICH Q11 for API starting material quality management
    • USP and EP monographs for intermediate impurities
    • GMP part II guidelines for non-sterile intermediates
    • Pharmacopoeial heavy metal specifications (e.g., ≤20 ppm Br)

    Typical usage ratio

    • Stoichiometry: 1.00–1.10 molar equivalents in halogen–metal exchange
    • Adjustments to control excess unreacted halide
    • Optimization based on subsequent ring-closing reaction kinetics
    • Minimized overfeed to reduce downstream purification costs

    Downstream process integration

    • Charge into anhydrous reactor systems for controlled metalation steps
    • Monitored for water and trace acid content before use
    • Employed prior to coupling or cyclization for pharmacore assembly
    • Sequence confirmed by LC-MS for lot release to final API synthesis

    Final product types

    • Non-steroidal anti-inflammatory API intermediates
    • Benzylamine-based CNS molecules
    • Quinoline or indole building blocks for generic APIs
    • Pre-final intermediates used in US/JP/EU regulated markets

    3. Dye and Pigment Manufacturing

    2-Bromotoluene acts as an aryl halide donor in the synthesis of specialized azo and anthraquinone dyes for plastics, textiles, and inkjet formulations. Pigment producers incorporate this material via controlled halogenation and coupling steps, where the reactivity of the ortho-brominated ring ensures targeted chromophore substitution. The downstream color strength and purity in batch processes depend on the reagent’s isomeric accuracy. Precise material flows facilitate color-fastness and regulatory requirements for direct and disperse dye series.

    Industry compliance standards

    • OEKO-TEX STANDARD 100 (Class II/III for textiles)
    • EN 71-3:2019 Toy Safety (heavy metal migration)
    • REACH Annex XVII (aromatic amines restriction)
    • ISO 14001 environmental management in pigment manufacturing

    Typical usage ratio

    • 0.9–1.2 molar equivalents per chromophore scaffold
    • Batch-to-batch adjustments for color intensity calibration
    • High-purity grades for premium pigment dispersion lines
    • Fine-tuned ratios during azo coupling for chromatic reproducibility

    Downstream process integration

    • Halogen source in initial color body synthesis
    • Introduced in diazotization and coupling reactors
    • Integrated quality checks for off-odour and residual bromide
    • Filtration and solvent purification steps post-reaction

    Final product types

    • Disperse and direct textile dyes
    • Anthraquinone pigments for automotive plastics
    • Inkjet and digital ink colorants
    • Color masterbatches for technical compounding

    4. Chemical Synthesis of Fragrance Intermediates

    Fragrance ingredient manufacturers use 2-Bromotoluene to construct methylbenzyl moieties in musk and woody note compounds. Its reactivity profile supports Friedel–Crafts and ring functionalization pathways for aroma material development. Purity directly impacts finished odour profile and shelf stability. Experienced process teams manage feedstock ratios and processing times to achieve the required substitution on the aromatic ring, with traceability for IFRA and regulatory submission.

    Industry compliance standards

    • IFRA (International Fragrance Association) Code of Practice
    • EU Cosmetics Regulation 1223/2009 on aromatic intermediates
    • FEMA (Flavor and Extract Manufacturers Association) GRAS assessment where relevant
    • ISO 9001:2015 lot tracking for raw and intermediate materials

    Typical usage ratio

    • Batch inclusion: 1.00–1.25 molecular equivalents per aroma scaffold
    • Adjusted per fragrance note intensity and target compound isomer
    • Lower ratios in high-value specialty musk syntheses
    • Reaction time calibrated to limit unreacted feed residuals

    Downstream process integration

    • Charged into alkylation and cyclization units
    • Purified by short-path or fractional distillation before blending
    • Pre-dosed based on pilot-scale odour panel evaluation
    • Residue verified by GC/FID for compliance prior to batch release

    Final product types

    • Musk ketone intermediates
    • Woody note synthetic aroma compounds
    • Methylated aromatic aldehyde bases
    • Precursor intermediates for perfumer’s alcohols
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    Certification & Compliance
    More Introduction

    2-Bromotoluene: Practical Insights from Our Manufacturing Floor

    Introduction and Real-World Overview

    In our years of producing fine chemicals, no two intermediates have attracted quite as much steady, day-in-day-out use as 2-Bromotoluene. Known among chemists for its reliability in industrial synthesis, this compound fits easily into a long line of key aromatic building blocks. Workers in our plant see it frequently rolling through batch reactors destined for pharmaceuticals, agricultural actives, and varied organic materials. The molecular formula—C7H7Br—gives an idea of its structure: a toluene ring with a bromine attached at the ortho position. The position of the bromine on the ring gives it completely different behavior compared to its isomers, and over hundreds of projects, we’ve seen firsthand why this matters to chemists producing advanced molecules.

    Specification and Purity: Our Practical Experience

    Every drum that leaves our facility undergoes more than a quick batch check. Customers demand material that won’t slow batch reactors or introduce trace impurities into catalyst-based processes. That means chemical purity matters a great deal. For jobs needing 2-Bromotoluene, we often manufacture to purities of 99.5% or higher, with moisture content below 0.05%. In our plant, routine use of gas chromatography confirms each lot stays within the requested specifications. Our experience shows skilled filtration, precise distillation, and careful material handling make a big difference in keeping color clear and chlorinated or iodinated byproducts out of the product.

    We package most volumes in steel drums lined to resist corrosion from aromatic halides. Some customers, mainly in pharma, call for smaller glass or HDPE bottles—these requests don’t faze us, since we’ve adapted our lines over time for flexible packing. Each lot receives a specific batch code linked to certificates of analysis, which our QC staff generate after comparing results to reputable external standards.

    Why Ortho-Bromo? Use-Cases and Feedback from the Industry

    After producing and shipping metric tons, we get regular feedback from medicinal chemists, process developers, and production staff. The placement of the bromine atom on the benzene ring, in the ortho position relative to the methyl group, is not a detail that a laboratory ignores. It has real consequences for reactivity in carbon–carbon and carbon–heteroatom bond-forming reactions. Many synthetic plans that aim at complexity—especially those heading for APIs, novel agrochemical actives, or industrial photoinitiators—call for highly predictable substitution patterns.

    Aryl halides stand as mainstays in cross-coupling chemistry: Suzuki, Heck, and Buchwald-Hartwig reactions. Out of all the toluene-derived isomers, it’s 2-Bromotoluene that proves valuable in building ortho-substituted aromatic scaffolds, thanks to its unique electronic and steric properties. For researchers scaling up bench chemistry, finding a reliable source for this material reduces variation, making the downstream separation of target products more practical.

    In agricultural chemistry, experienced formulators have requested our 2-Bromotoluene for the synthesis of certain herbicide and fungicide precursors, where ortho-brominated aromatic intermediates enable easier divergence into multi-step synthetic paths.

    Handling, Storage, and Practical Concerns from the Factory Floor

    Years spent moving bulk lots of this compound have taught us the importance of proper storage and equipment selection. 2-Bromotoluene remains a clear, colorless to pale yellow liquid under ambient temperatures, but direct sunlight and open drums can spark degradation or lead to color impurities. We advise all receiving sites to store drums in a cool, shaded area with solid ventilation. Our operators transfer the liquid using stainless steel or PTFE-lined pumps, avoiding contact with strong oxidizers or acids. During distillation, unnecessary agitation or overheating can raise the risk of byproduct formation, so we favor gentle heating profiles and nitrogen blanketing.

    From filling lines to shipping, our staff work with flameproof lighting and use flame-arresters on vent lines, since aromatic bromides are combustible. Protective gloves and goggles are standard, since skin exposure brings irritation risks. Air monitoring for brominated volatiles keeps the workspace safe, and regular health and safety workshops keep handling procedures fresh in the minds of all operators.

    Comparison to Other Bromo and Toluene Derivatives

    Among aromatic halides, not every isomer shares the same properties. 2-Bromotoluene differs from 3- and 4-Bromotoluene not as a technicality but in how they participate in organic synthesis. For example, electrophilic aromatic substitution reactions will target different ring positions, offering route flexibility to downstream chemists. Isomer mixing can compromise product performance in fine chemical or API production; even small traces of 3- or 4-isomers in a 2-Bromotoluene batch can reduce catalytic yield or complicate chromatographic purification.

    Comparing 2-Bromotoluene to other halides like 2-Chlorotoluene or 2-Iodotoluene, our production data and customer needs often show that bromine achieves a sweet spot of reactivity and safety. Chlorides resist certain cross-coupling reactions, requiring harsher conditions. Iodides excel in coupling but come with price and stability drawbacks.

    In industrial settings, procurement teams regularly balance cost, reactivity, and downstream waste. From repeated requests, 2-Bromotoluene has established itself as a mid-range option that doesn't overwhelm catalyst stability and won't choke a process with excessive side product formation. That’s not mere marketing—it’s feedback shared from hands-on chemists, both in-house and on the customer side.

    Sustainability, Waste Management, and Regulatory Aspects

    As chemical manufacturers, we face mounting demands for responsible production. Brominated organics require careful monitoring from synthesis through waste disposal. During synthesis, brominating agents present their own handling challenges, producing hydrogen bromide and wastewater. Over the past decade, newer process controls, phase separation units, and solvent recovery systems have changed the narrative around environmental control. Adopting closed-loop solvent recirculation, we find opportunities to cut waste and deliver cleaner product every year.

    Bromide-containing byproducts, including inorganic slags and traces in wash waters, face careful effluent treatment in our facility. We track and document waste outputs, for both regulatory filings and customer audits. Our ESG auditors, skeptical at first, have seen improvements as in-line waste neutralization curbs risk not just to our own staff but also to neighboring communities. The aim is not just regulatory compliance, but a step towards more responsible chemical practice—the kind we want to be known for.

    On the finished product side, we work with regulatory filings for major markets. 2-Bromotoluene must meet strict impurity profiles, with limits on residual halides and other volatile organic compounds. Finished drums are labeled per GHS standards, and our compliance staff monitor evolving global transport and safety data requirements. We lean on real-world shipment experience to keep documentation efficient—packing paperwork with clarity, not excessive jargon.

    Application Case Studies: Feedback from the Industry

    Working in chemical manufacturing brings us in contact with an array of end users, from small-scale university research labs to major industrial sites. For example, in the pharmaceutical sector, two leading drug companies have relied on our 2-Bromotoluene across multi-year development programs. The ortho-bromo motif provides a foundational platform for C–C and C–N bond formation, with downstream metabolites maintaining their integrity under human clinical trial conditions. Synthesis routes involving Suzuki coupling show clear improvements—higher yield, lower catalyst loading, and improved workup—when 2-Bromotoluene is the selected substrate.

    In one agricultural chemical application, farm chemical producers require ortho-substituted benzylic amines for fungicide construction. Classic nucleophilic substitutions proceed with high selectivity using our product, leading to robust field performance of the end chemical. Agricultural buyers report consistent reactivity and minimal byproduct drag, which aligns closely with our in-plant tracking of batch consistency.

    Advanced materials companies, particularly those producing photoresists and OLED intermediates, also regularly specify 2-Bromotoluene over alternatives. The ortho position allows for controlled synthesis of target monomers, impacting film formation and longevity in display applications. Here, electronic performance metrics can depend heavily on trace impurities, and our ability to keep such contaminants out of our lots helps reinforce the case for batch-specific documentation and regular feedback cycles.

    Product Evolution and Lessons Learned

    Successful producers in our industry do not stand still. Over the years, feedback loops between operations, customers, and QC have shifted our formulations. An early lesson came from a batch intended for a large pharmaceutical project, where traces of 4-Bromotoluene caused a stall in downstream hydrogenation. From that point, we tightened distillation parameters and invested in more sensitive analytical instruments. Today, our staff can track isomeric purity down to fractions of a percent, and those controls directly benefit customers who stake whole research programs or manufacturing campaigns on reliable upstream intermediates.

    We’ve also switched supply chains on key raw materials. Early suppliers of bromine sometimes delivered product with variable impurity profiles, impacting our own conversion rates and color formation during bromination. Working with specialty suppliers offering traceability and purity improvements has reduced our reprocessing rates and helped drive reliability. Customers, in turn, see shorter lead times and reduced annualized costs. The investment in upstream quality has paid for itself in customer retention and downstream process yield.

    Quality Control Philosophy: Doing the Job Right, Every Batch

    We know paperwork and external audits only go so far. Quality happens in the details: trained batch operators who spot changes in reflux temperature or product color, cleaning staff that verify residual solvent-free packing, and experienced chemists watching for subtle spectroscopic shifts. Our spectroscopists compare clean NMR and GC-MS peaks against commercial and in-house standards. They don’t rubber-stamp batches—a spike in minor peaks or a new impurity means repeat analysis or lot reprocessing.

    Our facility’s batch logs span decades and cover the full history of process tweaks, purification details, and customer complaints. Each improvement gets recorded and, where effective, implemented plant-wide. We’ve come to see consistency as much a function of people as equipment. Operators with decades at the same facility spot patterns and root causes quicker than any software.

    Bridging R&D and Production: Supporting Innovation

    A significant number of laboratory successes fail when scaled to manufacturing. Our process engineers work with R&D staff at customer sites to help adapt bench-scale literature chemistry to industrial reactors. Transferring a Suzuki coupling that works on 100 mg to 100 kg brings up issues with mixing, heat control, and unwanted side reactions. 2-Bromotoluene’s predictable behavior in scale-up reactions has made it a popular first choice, especially for groups bringing new active species out of the pilot plant and into full-production campaigns. Our process engineers often receive real-time questions and provide technical guidance on how to manage stirring rates, solvent choices, and heat gradients that influence brominated aromatic stability on large scales.

    We welcome feedback from pilot plants and process development labs, using learnings to tighten protocols, and the cycle continues at every production run. We’re proud of the open exchange, since many of the improvements in our purification or isolation approaches came from such collaborations. True technical progress happens where operations, QA, and research meet, and the customer’s challenge becomes our shared project.

    Market Trends and the Changing Role of 2-Bromotoluene

    In past decades, brominated aromatics were sometimes more plentiful and cheaper to source. Modern regulatory frameworks, coupled with increased demand in specialized markets like electronics and advanced polymers, have influenced both supply and pricing. We noticed that buyers now look past basic price-per-kilogram data. They want reliable supply, detailed batch tracking, and sustainability information with every shipment.

    Regions with heavy pharmaceutical and materials chemistry activity—North America, Western Europe, and parts of East Asia—rely on predictable logistics chains and rapid order fulfillment. Global supply chain pressures, whether from environmental events or geopolitical tension, have led us to reinforce our raw material stocks, qualify additional vendors, and open lines of communication with end users to anticipate needs. Those steps build resilience on both sides.

    We’ve been prompted by buyers to share not just specifications, but also real-world storage and handling guidelines. Where possible, we include technical documents to support downstream process safety and troubleshooting.

    Technical Solutions to Common and Uncommon Challenges

    Not every batch runs trouble-free. In production, high-boiling heavy ends can sometimes linger, threatening color quality and purity. Our operators designed column modifications to dial up selectivity during distillation, pulling tighter fractions that produce product meeting stainless steel reactor requirements. Rapid cooling and in-line nitrogen sparging have reduced trace oxidation—borne out by cleaner product and fewer customer complaints of color drift or residue formation.

    For international customers, paperwork and customs often present more hassle than technical product handling. We assign specific staff to track shipment progress, flag up any potential delays, and maintain open communication with buyers dealing with local authorities or freight carriers. These often-underappreciated actions ensure a product like 2-Bromotoluene, critical to a dozen processes at a receiving site, reaches its destination ready for immediate deployment.

    Future Outlook: Meeting the Needs of Next-Generation Chemistry

    Market trends in pharmaceuticals, agrochemicals, and advanced electronics show continuing demand for aromatic bromides, but the bar for quality, sustainability, and traceability has never been higher. Our production, QC, and compliance teams keep pace by investing in real-time analytics, waste minimization, and technical support training. We see customers leaning into collaborative process development, treating the chemical manufacturer almost as an extension of their own R&D and production teams.

    For projects targeting regulatory approval, reproducibility and data transparency have become non-negotiable. We audit our recordkeeping and batch release protocols to ensure every shipment has a documented history traceable down to raw material lots and purification systems. These steps support the demands faced by our customers in heavily regulated industries.

    Looking forward, we continue to challenge old assumptions and work towards cleaner, safer, and smarter manufacturing. Feedback from longtime users shapes our thinking, and as needs shift towards greener synthesis and digital tracking, the knowledge built up on the factory floor positions us to stay ahead.

    In the end, 2-Bromotoluene is more than just a catalog entry. It represents a web of customer relationships, technical challenges, and collective learning. Every batch carries not just chemical value, but experience from all who handle, analyze, and deliver it. Our commitment to reliability, technical support, and sustainable practice ensures that each lot supports a chain of creation stretching from pilot plant to finished product. This perspective, grown over years on the ground and in the lab, guides us as we move forward in the world of advanced fine chemicals.

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