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HS Code |
997485 |
| Iupac Name | 4-bromo-2-methoxyaniline |
| Molecular Formula | C7H8BrNO |
| Molecular Weight | 202.05 g/mol |
| Cas Number | 22990-77-8 |
| Appearance | Light yellow to brown solid |
| Melting Point | 86-88 °C |
| Solubility In Water | Slightly soluble |
| Density | 1.6 g/cm³ (approximate) |
| Smiles | COC1=C(C=C(C=C1)Br)N |
As an accredited 4-Bromo-2-Methoxy-Phenylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White powder sealed in a labeled amber glass bottle, 25 grams, with hazard symbols and product details for laboratory use only. |
| Shipping | 4-Bromo-2-Methoxy-Phenylamine is shipped in secure, airtight containers, clearly labeled with appropriate hazard warnings. It is packed according to international chemical transport regulations, ensuring protection from moisture, light, and physical damage, and includes safety documentation. Shipping is typically conducted via certified carriers specializing in hazardous materials. |
| Storage | 4-Bromo-2-Methoxy-Phenylamine should be stored in a tightly sealed container, away from moisture and light, in a cool, dry, and well-ventilated area. Keep it separate from oxidizing agents, acids, and incompatible materials. Properly label the container, and store it in a designated chemical storage cabinet to prevent unauthorized access and accidental exposure. Use secondary containment if possible. |
Applications of 4-Bromo-2-Methoxy-Phenylamine in Industrial ManufacturingAs an original manufacturer, we supply 4-Bromo-2-Methoxy-Phenylamine to downstream industries operating under regulated production frameworks. This intermediate sees consistent demand across selected specialty chemical sectors, where formulation precision, regulatory compliance, and process reliability define the route from our raw material to the customer’s finished product. 1. Pharmaceutical Intermediates for Active Pharmaceutical Ingredients (APIs)Pharmaceutical manufacturers integrate this compound as a key intermediate in the synthesis of certain small-molecule drugs, particularly within the segment of CNS (central nervous system) active compounds and emerging oncology agents. The compound is introduced during advanced synthetic steps that build up the functional core of target APIs, where its methoxy-bromo pattern is essential for further functionalization through amination or Suzuki coupling. Stringent in-process controls govern both raw material quality and batch traceability, and the precise usage ratio is calculated according to molecular stoichiometry for target molecule assembly. Industry compliance standards
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2. Agrochemical Intermediate for Herbicide and Fungicide SynthesisProducers of specialty agrochemicals use this phenylamine derivative as a building block in the development of certain heterocyclic herbicide and fungicide molecules, especially those requiring selective biaryl patterns for mode-of-action specificity. It is installed at the advanced cyclization or ring closure phase, following initial aromatic substitution protocols. Batch and continuous processes both require formulation optimization and waste minimization controls to ensure regulatory discharge limits are satisfied along with finished product purity. Industry compliance standards
Typical usage ratio
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3. Dyes and Organic Pigment IntermediateSpecialty dye and pigment manufacturers utilize 4-Bromo-2-Methoxy-Phenylamine in the design and scale-up of high-performance azo and anthraquinone colorants, where the methoxy and bromo-substituted core yields unique lightfastness and hue properties. The material is introduced during diazotization or directed aromatic substitution steps that are critical for achieving target chromophore alignment. Consistency in the purity grade and impurity profile directly affects shade reproducibility and batch quality assurance. Industry compliance standards
Typical usage ratio
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4. Specialty Chemical Research and Material ScienceAdvanced material companies and specialty chemical R&D centers source this compound for the synthesis of custom monomers, specialty ligands, and advanced aromatic linkers in polymer and supramolecular chemistry. The entry point typically involves targeted cross-coupling steps where the bromo and methoxy groups offer orthogonal reactivity for modular material synthesis. Strict purity requirements ensure reliable downstream functionalization and reproducible polymer properties. Industry compliance standards
Typical usage ratio
Downstream process integration
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Every chemical we put out into the world reflects our commitment to both precision and responsibility. With 4-Bromo-2-Methoxy-Phenylamine, the story is no different. This compound, known to specialists as a versatile aromatic amine, finds its place as a key intermediate across industries, mostly in pharma and specialty chemistry. Among aromatic amines, subtle shifts in structure radically change downstream performance. The bromo and methoxy substitutions on the phenyl ring shape reactivity, while the amine group, free from cumbersome protecting groups, makes this molecule easy to incorporate in more complex targets. Where manufacturing steps are concerned, quality is both art and discipline.
Some years ago, we noticed inconsistencies between lots made via older batch routes and what our strict controls demanded. Our team introduced additional in-process controls — not as a matter of compliance alone, but because even a 0.1% impurity in an intermediate can ripple out through many downstream reactions. Faulty chlorinated byproducts or trace isomeric impurities can disrupt both scale-up and analytical profiles of the final compounds. The 4-bromo positioning prevents unwanted side chain reactions, and any variance in substitution shows up starkly in yields or spectral fingerprints later down the line. So, if you have ever been frustrated by synthetic “mystery failures,” the source of the trouble often lies in unnoticed shifts in the upstream suppliers’ reliability.
By handling both the bromination and methoxylation steps under one roof, we eliminate questions over starting material integrity. Our staff includes long-serving operators whose experience on the shop floor brings a deep understanding of how small process drifts—slightly higher agitation during bromination, subtleties in the methoxylation temperature program—can affect purity. Outsourcing these steps usually bumps up all analytical and regulatory challenges; however, controlling them ourselves ensures the core amine meets the specifications required for reproducibility in R&D or manufacturing.
4-Bromo-2-Methoxy-Phenylamine sits as a true workhorse among intermediates for targeted synthesis. The substitution pattern has practical consequences for both reactivity and physical nature. Its solid state at room temperature, together with moderate solubility in both polar and nonpolar solvents, makes it manageable during handling—an aspect any process chemist respects.
Comparing it with 2-methoxyaniline or the para-bromo analog shows clear differences in chemical pathways. For example, bromination at the 4-position versus the 2-position directs downstream coupling steps differently; ortho effects subtly impact yields in nucleophilic aromatic substitutions, which many pharmaceutical chemists learn early in their careers, typically the hard way. The methoxy group on the 2-position activates the ring via resonance, but the presence of the bromine at the 4-position brings in a true difference in later synthetic decisions: it serves as a convenient anchor for palladium-catalyzed cross coupling, and cleans up well post-reaction.
Clients often ask about melting points, solubility, and stability under long-term storage. On our shop floor and in the packaging line, exposure to ambient air and light remains minimal. Fielding calls about shelf life from customers taught us that many research labs mistakenly leave similar amines open for days at a time, never realizing that tiny bits of color change hint at underlying degradation. We watched this over years and designed our packaging protocols accordingly: limiting headspace oxygen and using opaque containers. Having witnessed the headaches this compound can cause in the hands of the careless, we advise quick transfer to reaction vessels and tightly sealed storage—a lesson learned not from academic theory but the realities of real-world shipping and warehousing.
The mainstay use for 4-Bromo-2-Methoxy-Phenylamine remains in the synthesis of more elaborate heterocycles and functional materials. It forms an essential backbone in diverse active pharmaceutical ingredients, often as a precursor to tryptamine or indole-based drugs. Academics and industrial chemists alike gravitate towards this molecule because its synthetic flexibility saves both time and raw material during multi-step reactions.
This amine’s balanced structure helps in both microwave-assisted couplings and scale-up in jacketed reactors. The bromine atom confers specific reactivity—palladium-catalyzed Suzuki or Buchwald-Hartwig couplings can proceed smoothly, delivering high yields and cleaner workups. In one instance, a client’s drug program stalled for two quarters because erratic quality from another supplier produced extra byproducts. We stepped in, reviewed the analytics, refined their process, and their product registrations advanced without further delays.
Beyond pharma, the core scaffold fits neatly into the synthesis of specialty pigments and advanced materials, where electronic properties hinge on subtle ring modifications. The presence of both an electron-donating methoxy and an electron-withdrawing bromine changes the electron density of the ring—vital for fine-tuning fluorescence, color, and even conductivity. Over the years, we have partnered with material science teams across Asia and North America, observing firsthand how minute impurities from careless upstream manufacture cause major reproducibility problems in pilot-coating trials or device assembly. We built robust lines of communication with downstream QC labs to help them quickly troubleshoot using NMR, HPLC, or MS data—all so they can keep timelines on track and projects funded.
Differences from close analogs quickly become clear when placed in head-to-head reactivity tests. For example, 4-bromoaniline reacts differently under oxidative protocols compared to our compound. The methoxy group introduces selectivity that proves critical in multistep organic synthesis. Often researchers ask us to provide comparative samples of similar analogs; after decades of feedback, we find that the unique pattern in 4-Bromo-2-Methoxy-Phenylamine gives a consistently better yield profile in both direct coupling and amidation settings.
Bringing reliable chemicals to the bench or plant floor isn’t a matter of abstract standards. Points of variance in every batch—trace metal residues, differences in particle size, or lingering solvents—can spell the difference between a successful synthesis and wasted time. Laboratory teams pursuing targets under grant or compliance-driven timelines depend on knowing that each bottle contains what it should, free from unexpected byproducts. For our operations crew, every run undergoes hands-on scrutiny: visual inspection, IR, GC-MS, and spot checks on solubility before material moves forward. These steps cut off surprises before they ever reach a customer.
Seasoned process chemists in our facility know the story all too well of new technicians underestimating solvent-switching steps during isolation. Mishandling at this stage, such as using slightly wetter solvents or not respecting temperature profiles during crystallization, leads to batch splits or sticky product—factors that complicate delivery or cause downstream blockages in reactors. Having produced thousands of kilograms per year, we recognize how these “minor” variances build up troubleshooting costs and can even derail an entire quarter’s worth of R&D investment.
The analytical side pulls equal weight. Quality starts as a mindset—every bottle’s certificate of analysis must not just match specs but also align with real-world batch-to-batch performance. We have run long-term retention samples to monitor for unexpected degradants across transport and storage conditions. Our analytical teams have honed their understanding not only by routine QC, but also from chasing field complaints—sometimes spending days unpicking chain reactions set off by impurities introduced several months or even years earlier.
All these routines mean that over time, customers know they can expect dependable product. When changeovers arise—perhaps customers ask for a solvent-wet material or a modified particle size—our staff draws on decades of familiarity with the synthetic, purification, and packaging challenges. We’re not outsiders selling anonymous powder; we know the feel of the material in a glovebox, the color of a pure crystalline fraction, and the importance of on-time delivery when projects are riding on tight deadlines.
It’s easy to look at a catalog and see a list of “similar” aromatic amines. But the substitution pattern in 4-Bromo-2-Methoxy-Phenylamine creates a performance gap rarely apparent on first glance. Neighboring products like pure 4-bromoaniline, 2-methoxyaniline, or even ortho- and para-methoxy-bromo combinations all behave differently in real-world synthesis. In couplings or nucleophilic substitutions, rates may vary by orders of magnitude due to the electronic push-pull effect between the ortho-methoxy and para-bromo.
During one R&D project, a customer tried substituting 2-bromo-4-methoxy-aniline without flagging the change in documentation. Their entire process developed heavy tarry byproducts, yields crashed, and a two-month delay followed before the root cause became clear. The lesson stuck with both us and the client—structural details set downstream chemistry. Documentation and label clarity, including correct CAS and molecular structure, save huge costs over the product life cycle.
Our technical support rarely stops at shipping boxes. We help labs running pilot lots assess if a switch in material means downstream processing glitches—something that can cost tens of thousands in wasted work. A few years back, another manufacturer’s batch—technically correct by paper specs but differing slightly in odor and color—sparked a recall of finished goods. Our own experience has taught us that relying on outside suppliers, particularly those indifferent to feedback, risks both a manufacturer’s and a user’s reputation. We prioritize feedback loops with process teams at our customers’ sites, welcoming returns of vials with “unknowns” they have spotted, so we work the troubleshooting together. This embodies the difference between a true manufacturer and traders whose only expertise is moving boxes.
Modern chemical manufacturing includes more than flasks and columns. Traceability across production means an auditable footprint—something academic labs push for, but regulatory environments increasingly require as well. Our facility logs every step, from raw material lot numbers and reagent origins through to the final containers. In recent audits, our records showed trace brominating agents and solvents right back to the source, assuring downstream partners that their compliance forms rest on firm ground.
Sourcing the 4-Bromo-2-Methoxy-Phenylamine’s precursor requires partnerships that honor both cost discipline and social responsibility. Several years ago, forced labor reports out of certain chemical export zones forced a rethink in sourcing strategy. We revamped suplier review processes, cutting off any questionable partners—risking higher costs in the short term, but stronger foundations for customers reliant on clean, globally auditable supply chains.
Waste disposal and environmental controls feature prominently in our process design. Bromination steps generate acidic byproducts, which our staff neutralizes and sends through in-house effluent handling units. Regular upgrades and third-party audits keep this side of operations responsible—no discharge, no shortcuts, and a focus on running cleaner even as output grows. By inviting both customer and agency inspections as part of regular operations, we maintain transparency across every batch shipped.
Every year, we answer hundreds of technical service calls—not handled by a generic “support team,” but by the chemical engineers and synthetic chemists who helped set up our lines. Customers, from university labs to global pharma giants, sometimes ask about how 4-Bromo-2-Methoxy-Phenylamine reacts to various conditions, or why a given batch appears slightly off-color compared to a previous delivery. These field reports form the basis of our internal process reviews.
In more than one case, researchers realized after months of trial and error that the actual problem lay not with their synthetic protocol but in incorrect storage or minor cross-contamination with another aromatic amine. Sharing these stories in technical literature, as well as during on-site visits, helped tighten handling protocols industry-wide. Over time, our reputation has been forged on direct, honest communication—if a supply issue crops up, we flag it immediately, suggest interim workarounds, and ensure replacement. Customers appreciate not scripted answers, but partners willing to step into the lab or plant and tackle the issue shoulder-to-shoulder.
Our technical notes draw directly on years of running both glassware- and kilo-scale reactors. Handling 4-Bromo-2-Methoxy-Phenylamine means respecting both its potential and its challenges: moderate toxicity, moderate vapor pressure, and reactivity in both acidic and basic conditions. Routine stability studies under simulated transport conditions—jostling, moderate heating, humidity swings—build a database of what real-world shipping throws at this compound. Sharing these findings with customers downstream saves costly and avoidable setbacks.
The dialogue with users goes both ways. A research group in Scandinavia recently documented a way to process lower-grade amine by fractional crystallization, a technique we picked up, refined, and integrated on our own lines to boost recovery yields. This flow of ideas builds both stronger products and stronger partnerships.
Open catalogs make the chemical business look interchangeable. In reality, deep understanding at the manufacturing level shapes everything from specification to shelf life. Unlike brokers or generic distributors, we invest in the people who understand more than CAS numbers. Our long-serving operators can spot subtle off-odors or color shifts before any analytical instrument raises an alert. The site-based engineers who develop new routes remain on staff, bringing institutional memory to every improvement or remediation.
Our on-the-ground approach gives customers certainty not only in product performance but in how new requirements will be met. Changing a crystal polymorph, particle size, or wetness frequently involves pilot lots, custom runs, and industry-specific documentation. As trends in the market shift—tighter environmental regulations, more stringent pharmacopoeial standards, or new frontline chemistry around green synthesis—our close control of the source intermediates means we can adapt and evolve, not just resell.
Over decades, we learned to value clear batch labeling, open feedback with QC labs, and continuous retraining of operators as much as state-of-art reaction monitoring or high-throughput analytics. The bigger picture: delivering not just a commodity, but a relationship grounded in chemical expertise and transparency. That is 4-Bromo-2-Methoxy-Phenylamine as seen and crafted by a real manufacturer.