|
HS Code |
815826 |
| Chemical Name | 3,5-Dibromo-2-Methoxybenzoic Acid |
| Cas Number | 64697-40-1 |
| Molecular Formula | C8H6Br2O3 |
| Molecular Weight | 325.94 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 178-182 °C |
| Solubility | Slightly soluble in water |
| Boiling Point | Decomposes |
| Density | 2.13 g/cm³ (estimated) |
| Synonyms | 2-Methoxy-3,5-dibromobenzoic acid |
| Smiles | COC1=C(C=C(C=C1Br)Br)C(=O)O |
| Inchi | InChI=1S/C8H6Br2O3/c1-13-8-6(7(11)12)2-4(9)3-5(8)10/h2-3H,1H3,(H,11,12) |
| Pubchem Cid | 187684 |
| Storage Conditions | Store at room temperature, tightly closed, in a dry place |
As an accredited 3,5-Dibromo-2-Methoxybenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g chemical is packaged in an amber glass bottle with a secure screw cap, labeled with hazard warnings and product details. |
| Shipping | **Shipping Description:** 3,5-Dibromo-2-Methoxybenzoic Acid is shipped in tightly sealed containers to prevent moisture or contamination. It should be transported in compliance with local and international chemical regulations, typically labeled as a non-hazardous solid. Store and ship at ambient temperature. Protect from physical damage and keep away from incompatible substances. |
| Storage | 3,5-Dibromo-2-Methoxybenzoic Acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizers. Keep the container clearly labeled and protected from moisture. Always follow laboratory safety protocols and store at room temperature unless otherwise specified by the manufacturer’s recommendations. |
Applications of 3,5-Dibromo-2-Methoxybenzoic Acid in Industrial Manufacturing3,5-Dibromo-2-Methoxybenzoic Acid serves as a critical intermediate for synthesis workflows in multiple specialized segments of fine chemicals and high-value manufacturing. As original producers, we focus consistently on quality control from the earliest production stages to address the stringent QA/QC and regulatory needs of our downstream industrial customers. 1. Pharmaceutical Intermediate for Antibacterial Drug SynthesisThis material acts as a halogenated benzoic acid derivative required in the synthesis of select antibacterial pharmaceutical agents. Its precise bromine substitution pattern offers functionality prized in the formation of specialty intermediates. Customers deploy this compound in the multi-step construction of active pharmaceutical ingredient (API) side chains and ring systems. During production, manufacturers maintain close control of impurity profiles, bromide residues, and esterification conversion rates to conform with GMP expectations for human drug actives. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Intermediate in Herbicide and Fungicide Additive SynthesisLeading agrochemical producers use 3,5-Dibromo-2-Methoxybenzoic Acid as a functionalized aromatic precursor in the production of new-generation herbicide safeners and select fungicide molecules. The methoxy and bromine groups deliver targeted biological performance after transformation through amidation or esterification. Organizations involved in crop protection chemical formulation require consistent purity and stable supply from GMP-aligned sourcing to guarantee crop safety status and regulatory dossier support. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Electronic Chemicals: Photoresist Advanced Material SynthesisThe compound enters the electronic chemicals sector, specifically in the development of advanced intermediates for photoresist resin and etching aid ingredients. Its unique aromatic backbone and halogen substitution allow precision reactions necessary for high-purity electronic chemical production. Manufacturers choose this material due to its reliability in downstream polymerization or integration into specialty block copolymer matrices used by semiconductor lithography suppliers. Stringent EHS controls and metal-ion specification limits are enforced to match semiconductor industry needs. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Specialty Dye and Pigment Intermediate for High-Performance MaterialsDye and pigment producers leverage this benzoic acid derivative in the synthesis of bromine-containing colorants used for technical plastics, inks, and specialty coatings. By introducing methoxy and dibromo functionalities into the chromophore backbone, formulators create heat- and light-resistant pigments with controlled solubility profiles. Producers operate in accordance with end-market tox assessment and application-specific statutory norms, focusing on batch traceability, non-volatile impurity removal, and color strength optimization in mass production. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 3,5-Dibromo-2-Methoxybenzoic Acid prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
Every manufacturer talks about precision, but for those who make 3,5-Dibromo-2-Methoxybenzoic Acid, attention to detail is how reliability gets built into every batch. In our business, those details start long before the final product leaves the reactor. “3,5-Dibromo-2-Methoxybenzoic Acid” serves a well-defined need in organic synthesis, but its true value comes from what a consistent, high-quality supply chain can do for downstream chemists and process engineers pressed for yield, reproducibility, and manageable impurities.
Our focus sits squarely on offering a product with tight lot-to-lot consistency. This compound appears as an off-white to tan crystalline powder, setting it apart from many other benzoic acid derivatives, which often exhibit broader color variation due to byproducts or residual solvents. By optimizing the brominating reagents and the methoxylation step, we avoid speckling and discoloration. Moisture content, melting point, and purity metrics form the foundation of our internal release standards. Most chemists see product listed at assay levels above 98%, but we watch trace halogenation and residual solvents with even greater scrutiny, thanks to routine GC and HPLC runs.
3,5-Dibromo-2-Methoxybenzoic Acid finds its way into multiple settings, but we see it most with process development groups at pharmaceutical or agrochemical companies. In the world of small-scale screening, a reliable benzoic acid derivative gives synthetic chemists a predictable backbone for Suzuki couplings or amide-bond formations. The dibromo substitution pattern not only serves as a handle for further functionalization, but also lends more control to regioselective transformations. During scale-up, that extra halogen provides a useful springboard in the construction of new aromatics. We have witnessed biochemists request lots cleaned of trace organics to meet preclinical requirements—especially when compounds approach in vivo testing, where unknowns turn into regulatory headaches.
For chemists doing heavy lifting on new molecule development, the main difference between 3,5-Dibromo-2-Methoxybenzoic Acid supplied by a manufacturer and material sourced through traders or brokers revolves around impurity profiles. It takes less effort to reach a raw material at 97-98% purity than to make sure trace isomeric byproducts stay below quantifiable limits. By keeping every reaction and post-processing step in-house, a manufacturer can regularly monitor for known process impurities, chlorinated side-products, and residual catalysts. Our vacuum drying equipment and solvent systems cut down on moisture pickup, which remains critical for labs running sensitive transformations.
Producing specialty benzoic acid derivatives cannot rely solely on standard melting point and chemical purity measurements. Each batch we release passes through rigorous QC that tracks not only HPLC and GC profiles, but also includes NMR checks for minor substitution errors. It’s not uncommon for downstream transformations to fail or generate impurities if the parent acid contains positional isomers—traders and distributors have less leverage to spot these issues in real time. Within our facility, a chromatograph never collects dust. Staff rotate between prep and analytical instruments, and no batch ships out before every peak’s been accounted for, from starting materials to solvent residues to any possible low-level halogenated analogs.
Process traceability gets overlooked outside of manufacturing, but in practice, it’s fundamental for repeatable results. Over the years, feedback from our long-term customers has shown that direct communication between the end-user and manufacturer can mean quicker troubleshooting when oddities turn up in reaction runs. Any time a customer reaches out with data on an unidentified peak or unexpected side-product, we dig back into our batch records and, if needed, run re-analysis on retention samples held onsite. Raw materials get logged from vendor to weigh-up, and all process water and solvents go through quality checkpoints. We keep our line open to those working under the pressure of tight project windows, because finding the cause of a few unexpected parts-per-million can make or break a submission for further development.
3,5-Dibromo-2-Methoxybenzoic Acid stands out among benzoic acid derivatives largely due to its dual bromine atoms and methoxy group on the ring. Some labs switch between mono-brominated and di-brominated benzoic acids, but those doing directed cross-coupling or attempting to build denser substitution patterns see how the 3,5-positions change the reactivity landscape. The methoxy substituent at the ortho- position offers unique electron-donating effects, modulating the acid’s reactivity compared to its plain or methylated counterparts. Process teams who rely on predictable reactivity avoid uncertainty by specifying this model, even if the cost per gram runs higher. Unlike the more abundant 4-bromo-2-methoxy acid, the 3,5-isomer introduces branching points for new library designs, which impacts not just lab-scale synthesis but also upscaling decisions.
Years making this compound have taught us the importance of listening to the labs we supply. We’ve had requests for more rigorous residual solvent checks, as certain pharmaceutical clients battle interference in downstream HPLC assays. Some teams ask for microbially-tested material when moving into cell-based testing or high-sensitivity screens. We have invested in line upgrades and dust-free packaging due to customer complaints about caking, and even overhauled our standard drum sizes to fit in automated powder dispensers. The best improvements tend to come from open conversations, not standard operating procedures, so we’ve built flexibility into lot sizes, container choices, and labeling to fit the work style of each client.
Handling large-scale halogenations and methoxylations creates tricky waste streams that traders rarely see. The regulatory scrutiny on brominated organics tightens each year, so our teams track process yields and waste reduction closely. We reclaimed solvents and worked with approved incinerators to deal safely with spent mother liquors. Many companies talk about “responsible sourcing” as a buzzword, but a real difference gets made when staff on site check drum labeling, log solvent returns, and recycle drums through certified suppliers. Going direct not only protects intellectual property, but also means less packaging waste from added handling steps.
Our experience has shown that direct supply chains perform best for customers deeply invested in synthesis reliability, especially those running dozens or hundreds of screens or multi-gram scale-ups. The longer the chain between maker and user, the more hidden risks creep in—ranging from delays caused by ambiguous lot IDs to confusion over which sample represents which shipment. Direct conversations with process development teams upstream produce the best results, as we can pivot purification or packaging approaches to fit actual support needs. When a customer shares a chromatogram and flags an issue with a side-product, we can jump straight to root cause.
As regulations shift around import, hazard labeling, and waste tracking for halogenated aromatics, we’ve seen demand shift toward full documentation. Export into EU or North America brings additional requirements for REACH, TSCA, or other region-specific lists. In-house regulatory specialists manage Safety Data Sheets, certificates—like irradiation-free or animal-free status—and transport documentation tied back to specific batch histories. By keeping all production under one roof, traceability remains airtight and new documentation requests don’t involve a round-robin of resellers or warehousing firms. Approved production lots keep meeting threshold requirements for major market audits, simplifying customer compliance burdens.
Our research partners have shown us the value of early joint planning. At pilot and scale-up stages, subtle impurities—such as trace dibromoanisoles or unwanted methoxy isomers—can trigger cascading issues. Rather than respond after problems appear, we keep an open line with process engineers and analytical chemists. Small modifications, like holding back trace hydrolysis or switching out filter aids, can boost downstream yields. We’ve also shared historical retention samples for comparative studies when clients spot something unusual. Labs working on innovative coupling or cyclization sequences deserve more than generic grade materials; they benefit from a supplier who treats requests for tighter or tailored specs as normal project work.
Competing in this space means facing two main issues: maintaining analytical rigor and keeping flexible while scaling up. Analytical lag—even of a few hours—can derail timelines in high-throughput programs. Our QC team runs dual-shift schedules to prevent analysis slowdowns and logs all test results in centralized, queryable formats. Unexpected issues, such as an out-of-tolerance impurity spike or a packaging flaw, move straight from the lab to production meetings. For customers, this means faster resolution and fewer lost days chasing answers. No batch goes out the door without a clear record of its synthetic history and test results accessible to end-users.
From the chemist running a few grams to the process team handling dozens of kilograms, scaling up 3,5-Dibromo-2-Methoxybenzoic Acid demands more than a copy-paste approach. Heat transfer, solvent changeovers, and minimization of side-reactions all get recalibrated on larger equipment. Our engineers keep granular records of each scale transition, learning from issues such as temperature control gaps or slurry handling inefficiencies. By sharing feedback loops with end-users, we capture not just theoretical yields, but practical “work-up” losses, informing future batches. Chemists scaling up appreciate direct access to technical teams who know the quirks of each reactor and drying oven.
Front-line experience with hundreds of batches draws a sharp distinction between direct manufacturing and third-party intermediaries. Consistent purity and low-level impurity tracking stand as the main value adds. When customers trust that their 3,5-Dibromo-2-Methoxybenzoic Acid comes straight from a process-validated, single-site producer, project unpredictability drops. For those chasing regulatory approvals or working under compressed timelines, supplier transparency and the ability to discuss data directly with the people making the batch streamlines development. Quality isn’t an ad campaign—it’s a day-to-day job in temperature control, solvent checks, NMR runs, and packaging audits. Direct links between manufacturer and end-user pay off in fewer headaches and more reproducible chemistry.
We see new demands each year from the researchers pushing the boundaries of benzoic acid chemistry. Lower residual metal specs, halogen-free labeling, and trace solvent reductions have all become standard client requests. While we offer a familiar product today, we keep open channels with scientists doing method development or trialing next-gen synthesis schemes. Sharing batch samples, supporting trial runs, and fielding hard questions about trace contaminants all shape how we invest next. Tomorrow’s 3,5-Dibromo-2-Methoxybenzoic Acid will differ from today’s, if only because our best clients push us to keep improving every chemist’s experience, one batch at a time.