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HS Code |
539099 |
| Product Name | 2-Bromo-5-Methoxybenzoyl Chloride |
| Cas Number | 351003-97-7 |
| Molecular Formula | C8H6BrClO2 |
| Molecular Weight | 249.49 g/mol |
| Appearance | White to off-white powder |
| Purity | Typically ≥ 97% |
| Solubility | Reacts with water; soluble in organic solvents like dichloromethane |
| Storage Temperature | Store under inert atmosphere, at 2-8°C |
| Reactivity | Reacts with nucleophiles (e.g., amines, alcohols) |
| Synonyms | 2-Bromo-5-methoxybenzoyl chloride; 5-Methoxy-2-bromobenzoyl chloride |
| Safety Hazards | Corrosive, causes burns to skin and eyes |
| Inchikey | QZZJVAAKDDPAGV-UHFFFAOYSA-N |
As an accredited 2-Bromo-5-Methoxybenzoyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 2-Bromo-5-Methoxybenzoyl Chloride is supplied in a 25g amber glass bottle, sealed, labeled with hazard warnings and product details. |
| Shipping | 2-Bromo-5-Methoxybenzoyl Chloride is shipped in sealed, chemical-resistant containers to prevent moisture and contamination. It should be transported as a hazardous material, with appropriate labeling and documentation in compliance with local regulations, ensuring temperature and light protection. Shipping must follow all guidelines for corrosive and environmentally hazardous substances. |
| Storage | 2-Bromo-5-Methoxybenzoyl Chloride should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from moisture and incompatible substances such as strong bases and oxidizers. Keep it under inert atmosphere, such as nitrogen, to prevent hydrolysis. Store at recommended temperatures, typically below 25°C, and protect from light to maintain chemical stability. |
Applications of 2-Bromo-5-Methoxybenzoyl Chloride in Industrial Manufacturing2-Bromo-5-Methoxybenzoyl Chloride is a specialized acyl chloride used primarily as an intermediate in complex molecule synthesis. Our direct production process ensures fine purity and consistent reactivity, meeting stringent industry demands for downstream applications that require precision in organic transformations. 1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredients (APIs)This material serves as a key acylating agent in the synthesis of advanced intermediates for various APIs, including benzamide-structure drugs and kinase inhibitors. Pharmaceutical manufacturers prefer this compound for constructing specific aromatic frameworks under controlled conditions. Production often involves a two-step process: first, integrating the acyl chloride into the target moiety via nucleophilic substitution or Friedel–Crafts acylation, and second, further functionalization to the required drug intermediate. In this context, our product supports consistent yield, stringent impurity control, and traceability as required for regulated API synthesis. Industry compliance standards
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2. Agrochemical Synthesis for Herbicide IntermediatesManufacturers of selective herbicides and plant growth modulators use this acyl chloride to prepare key aromatic intermediates. Its substitution pattern aids in high selectivity during downstream alkylation or nitration steps, contributing to the synthesis of substituted benzoyl derivatives with agrochemical application. The process demands reliable reactivity and compatibility with large-scale continuous flow reactors, supporting batch-to-batch consistency in agrochemical ingredient preparation. Industry compliance standards
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3. Custom Synthesis for Liquid Crystal MonomersLeading LCM manufacturers select this compound for tailored functionalization, especially in the development of mesogenic cores for high-performance liquid crystals. As a site-specific acylating agent, it enters synthesis routes that build up the rigid aromatic structure required for thermal and optical stability. This material allows precise introduction of brominated and methoxy functionalities, enhancing the anisotropic properties essential for modern display technology. Industry compliance standards
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4. Research-Grade Synthesis for Organic Electronic MaterialsSpecialty chemical laboratories and electronic material manufacturers use this acyl chloride for creating precursors to conductive and semiconductive polymers. Its defined bromine and methoxy substitutions facilitate cross-coupling reactions (such as Suzuki or Stille syntheses), where precise electronic and steric effects are critical for optimizing the final materials’ performance in devices. Our controlled synthesis supports downstream requirements for batch documentation and reproducible reactivity in pilot scale and commercial runs. Industry compliance standards
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Producing 2-Bromo-5-Methoxybenzoyl Chloride in our facility doesn’t come down to simply pushing “go” on a reactor. It demands a solid grasp of halogenated aromatic synthesis, tenacity to control purification steps, and consistency that satisfies even the most stringent research chemists and formulators. The chemical formula—C8H6BrClO2—only tells part of the story. In the plant, this compound moves from a carefully sourced 2-bromo-5-methoxybenzoic acid through exacting chlorination. Our technicians monitor color, purity, and moisture tightly, since even a measure of water can hydrolyze chloride and ruin the batch. Every kilogram out of the reactor has already passed dozens of hands-on checks fitting actual lab needs, not just certificate checkboxes.
Every year, demand for aryl halide reagents climbs, with good reason. In practice, this benzoyl chloride variant stands out in the synthesis of pharmaceuticals, agricultural intermediates, and advanced organic materials. Labs working on new heterocyclic scaffolds or biotech firms modifying enzymes for kit conjugation—these teams trust this material for its predictable behavior and functional compatibility. Our own experience shows that the methoxy group at the 5-position gives a useful electronic modulation, increasing selectivity in Friedel-Crafts acylations or facilitating regioselective transformations. The bromine leaves a handle for subsequent cross-coupling; this often comes up in Suzuki and Buchwald-Hartwig amination projects, where efficiency and selectivity dictate commercial viability.
Fielding questions from both global catalog buyers and boutique research houses has taught us what truly matters in a batch of 2-Bromo-5-Methoxybenzoyl Chloride. Color should remain off-white or pale yellow—anything darker usually points to side-reactions or storage issues. Moisture must be extremely low; trace water triggers hydrolysis and loses potency for sensitive reactions. Our process delivers purity above 98% minimum as validated by HPLC and NMR, because researchers want product ready for immediate use, not further purification. Pack sizes range from grams to multi-kilo quantities, sealed against air and moisture. We test every lot not only by certificate, but by using it ourselves in test syntheses, which weeds out subtle problems that paper specs can miss.
On paper, 2-Bromo-5-Methoxybenzoyl Chloride seems like another catalog compound—until the work starts. Sourcing from a pure trading company, you may see variability in particle size, color, and even byproduct contamination. Our approach differs: we control each stage, from choice of chlorinating agent to reaction quench and final washings. This in-plant control protects against persistent issues like residual acids or byproducts that complicate downstream use. We have compared batches from various producers—side-by-side evaluations in real synthetic runs reveal differences in solubility profiles and impurity profiles that directly impact reaction yields.
Practical chemists see these differences immediately in nucleophilic substitutions or coupling reactions. Even minor impurities can shift catalyst activity, slow conversion, or introduce unwanted byproducts in demanding syntheses. Since we also supply related acid chlorides and bromo-substituted benzoic acid derivatives, we’ve learned that the combination of a bromo at position 2 and a methoxy at 5 gives an edge for selectivity and reactivity over alternatives like 4-methoxy or 2,4-dibromo analogs.
No one wants to retool an entire synthesis just to accommodate unreliable raw materials. Our partners cite this frequently: an unstable or impure acid chloride brings downtime, failed scale-ups, and unnecessary purification steps. By choosing 2-Bromo-5-Methoxybenzoyl Chloride made with control from start to finish, downstream chemists avoid headaches. Organic synthesis thrives on reliable reactivity. Having run dozens of gram-to-kilo scale routes ourselves, we know firsthand how overlooked trace impurities—like residual dichloromethane or unreacted acid—can sabotage overall project timelines.
Customers working in medicinal chemistry or advanced polymer research find unique advantages. The methoxy substituent increases electron density, usually leading to better acylating agent activity compared to unsubstituted benzoyl chlorides. The bromo atom unlocks further functionalization through halogen-metal exchange or palladium-catalyzed transformations. Over the years, novel anti-cancer drug analogs and performance polymers have been traced back to use of this specific intermediate.
Even seasoned chemists have stories about hydrolyzed, degraded, or underperforming aryl chlorides because production cut corners. Moisture is not just a storage inconvenience—chlorides like this one hydrolyze to carboxylic acid and HCl, often ruining reactions before they start. We minimize this with in-house drying protocols and with specialty packaging that resists atmospheric ingress. For every batch, our quality group takes freshly prepared samples and checks them against typical reaction protocols. If a batch doesn't stand up to rigorous testing, it never leaves the site. This level of vigilance takes time, but avoids customer setbacks.
We maintain a tested shelf-life under standard storage for sealed, unopened containers. By keeping all materials in nitrogen-filled drums with tamper-proof seals, we protect your starting line for critical reactions.
The transition from milligram-scale work in a university lab to kilogram or tonne-scale in manufacturing is rarely smooth. Scale-up exposes weaknesses in material quality and supply reliability. We own and operate our synthetic lines, so we design process changes to deliver the same product profile at all volumes. On-site chemists tweak reaction parameters, monitor impurities, and adjust workups to hold consistency that third-party blenders struggle to match. This becomes especially important as regulatory and safety requirements tighten for pharmaceutical or agrochemical intermediates.
Project-based clients often ask for traceable production routes, batch-specific impurity records, and open access to stability data. We can trace every kilo back to production logs, since each lot is tracked through digital and physical records. With the increase in regulatory scrutiny, such data makes qualifying a new starting material faster and easier.
Our product catalog includes a variety of substituted benzoyl chlorides, from the basic to the highly functionalized. Compared to unsubstituted benzoyl chloride, 2-Bromo-5-Methoxybenzoyl Chloride proves less corrosive and more amenable to selective transformations. The methoxy group tempers reactivity of the acid chloride, affording greater control. Those working with simply bromo-substituted variants often report lower yields in coupling chemistry without the push from a supportive methoxy group.
Alternatives lacking the ortho bromo or para methoxy cannot match the versatility of this molecule. We have supplied both academic groups and commercial partners experimenting with 3-bromo, 4-bromo, or di-methoxy versions, but the combination of 2-bromo with 5-methoxy consistently unlocks downstream chemistry not accessible by the others. Real-world casework includes selective arylation, site-specific drug intermediate synthesis, and custom flavor/fragrance chemistry where subtle ring electronics are make-or-break.
Over decades in production, we’ve seen shipping delays, compliance surprises, and customs disruptions. Sourcing controlled chemicals and hazardous organics adds complexity. Supplying hazardous compounds like 2-Bromo-5-Methoxybenzoyl Chloride means strict adherence to transport regs and global compliance. Our shipping team keeps every package labeled, documented, and routed for timely delivery. Bottling, filling, and sample dispatch all occur on-site, so there’s no lag from third-party warehouses or repacking.
New users sometimes point to high costs or limited source options as barriers. We counteract this by managing raw material contracts long-term and forecasting client demand, preventing the supply shocks that derail actual project timelines. Our technical sales team draws not only from paperwork but from involvement in the plant’s day-to-day, offering advice on storage, use, and safety—right from the source.
We track hundreds of applications across pharmaceutical, fine chemical, and specialty material projects. Many chemists share success stories of improving yield or cutting purification steps after adopting our batches. One particularly memorable example involved a university team developing new kinase inhibitors who reported a triple-digit percentage increase in overall yield, simply by switching to our high-purity batches. In another case, a custom synthesis partner cited less time spent clearing trace acid residues, which meant faster time to project milestones.
Our team regularly solicits and acts on customer feedback. Several improvements in our drying process, as well as re-tooling our chlorination step, resulted directly from collaborative problem-solving with our buyers. This “back and forth” proves particularly valuable in research and scale-up scenarios where every detail counts. No batch ships without alignment between lab data and customer needs.
Fields like pharmaceutical research and smart materials engineering keep evolving, demanding purer, more consistent, and more versatile reagent streams. We pour ongoing R&D resources into refining production—reducing byproducts, improving energy efficiency, and strengthening our analytical checks. This means every container that leaves our site offers a reproducible starting point for creative science.
We closely monitor trends in regulatory change, green chemistry requirements, and demand shifts created by biotech and electronics markets. When new compliance requirements roll in—like halogen management, trace metal limits, or carbon-neutral mandates—we implement changes plant-wide so clients downstream stay ahead, not behind. Updating technology, training technicians, and maintaining “open-door” technical support helps us keep product quality high as industry standards move forward.
Years of experience in direct chemical production have made us acutely aware of the pitfalls and payoffs of offering specialty building blocks like 2-Bromo-5-Methoxybenzoyl Chloride. Beyond the molecular structure and technical literature, the product’s true value emerges in practical lab and manufacturing environments. Real purity, traceability, control over the full production process, and readiness to solve challenges with customers set meaningful products apart from the generic crowd.
We remain committed to driving ongoing improvement and responsive support, so each batch empowers chemists and engineers to innovate with confidence, precision, and peace of mind.