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4-Bromo-2,6-Dimethylanisole

    • Product Name 4-Bromo-2,6-Dimethylanisole
    • Alias 4-Bromo-2,6-dimethyl-1-methoxybenzene
    • Einecs 614-056-4
    • 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
    VTB
    Specifications

    HS Code

    569386

    Cas Number 60481-07-4
    Molecular Formula C9H11BrO
    Molecular Weight 215.09 g/mol
    Iupac Name 4-bromo-2,6-dimethoxy-1-methoxybenzene
    Appearance White to off-white crystalline solid
    Melting Point 37-39°C
    Boiling Point 256-258°C
    Density 1.43 g/cm3
    Purity Usually ≥98%
    Solubility Slightly soluble in water; soluble in organic solvents such as ethanol and ether

    As an accredited 4-Bromo-2,6-Dimethylanisole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g package of 4-Bromo-2,6-Dimethylanisole comes in a sealed amber glass bottle with a printed chemical label.
    Shipping 4-Bromo-2,6-Dimethylanisole is shipped in tightly sealed containers, protected from moisture and light, and labeled according to relevant regulations. Handle with care, avoiding physical damage. Store in a cool, dry, and well-ventilated location. Ensure compliance with all local, national, and international chemical transport requirements for safe delivery.
    Storage **4-Bromo-2,6-dimethylanisole** should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and direct sunlight. Keep it separate from incompatible substances such as strong oxidizers and acids. Ensure effective labeling and access control, with proper protective measures to avoid inhalation or skin contact during handling.
    Application of 4-Bromo-2,6-Dimethylanisole

    Applications of 4-Bromo-2,6-Dimethylanisole in Industrial Manufacturing

    4-Bromo-2,6-Dimethylanisole serves as a functional intermediate in several advanced chemical syntheses. Below, our manufacturing expertise details its focused industrial applications, compliance control, usage ratios, engineered process integration, and realized product categories.

    1. Pharmaceutical Active Intermediate Synthesis

    Leading pharmaceutical companies incorporate this molecule during the syntheses of advanced heterocyclic compounds. It directly participates as a key arylating agent in multi-step reactions for targeted APIs, especially in selective hormone modulation or oncological drug projects. High-purity lots are critical here, as impurities can propagate through complex synthesis chains, affecting regulatory filings and batch releases.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • USP-NF Monographs concerning intermediates
    • Local authority substance registration (FDA DMF, EMA Article 54)
    • ISO 9001:2015 for quality management systems

    Typical usage ratio

    • 10–25 mol% relative to main starting amines or ketones depending on route complexity; fine-tuned per stoichiometric models and impurity profile monitoring

    Downstream process integration

    • Charged during mid-stage step (commonly Stage 2 or 3) following initial scaffold assembly
    • Employed under inert atmosphere, in polar aprotic solvents at controlled temperatures
    • Residuals strictly quantified before next transformations

    Final product types

    • Aromatase inhibitor precursors
    • Pyridine or benzoxazole derivative API intermediates
    • Specialty pharmaceutical candidate scaffolds

    2. Agrochemical Intermediate for Fungicide Production

    Agrochemical formulators utilize the compound to build triazole and strobilurin fungicides. It functions as a late-stage arylation building block for increasing lipophilicity and field stability. Rigorous traceability and feedstock control ensure consistent performance under shifting regulatory regimes focused on environmental residuals and worker safety.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • EU Regulation (EC) No 1107/2009 for Plant Protection Products
    • ISO 9001:2015 in agrochemical manufacturing
    • REACH registration and downstream user notifications

    Typical usage ratio

    • 2–12% by weight of total key intermediates, depending on targeted efficacy and synthesis complexity

    Downstream process integration

    • Charged after triazole or pyridine ring formation to complete aromatic substitution
    • Compact batch reactor or continuous stirred-tank reactor (CSTR) operation, solvent selection based on downstream purification
    • Stringent in-process purity testing for halogenated byproducts

    Final product types

    • Triazole-based fungicide active compounds
    • Strobilurin precursors
    • Benzimidazole derivative crop protectants

    3. Electronic Chemical Synthesis for OLED Materials

    Downstream producers of organic light-emitting diode (OLED) devices deploy this raw material as a controlled aryl halide input for intelligent design of emissive and conductive layers. Its methyl and bromo substituents enable regioselective cross-coupling reactions that define the emission wavelength and carrier mobility in next-generation display and lighting technologies.

    Industry compliance standards

    • IEC 61249-2-21 for halogen-free electronic materials
    • RoHS Directive 2011/65/EU for hazardous substances
    • QC per IPC-A-610 standards for electronic assemblies
    • Internal SOPs for ESD-safe chemical handling

    Typical usage ratio

    • 0.1–3 mol% relative to base fluorenes or carbazole derivatives; precise dosage custom-calibrated in R&D then scaled up for reproducible device performance

    Downstream process integration

    • Introduced during last coupling step in Suzuki–Miyaura or Buchwald–Hartwig reactions under anhydrous conditions
    • Reaction vessel selection prioritizes minimized metal contamination
    • QC includes HPLC/GC-MS tracking of trace residual aryl bromides

    Final product types

    • Blue and green emissive layers for OLED panels
    • Charge-transporting matrix materials
    • Display and smart lighting device substrates

    4. Fragrance and Flavor Intermediate for Fine Chemicals

    Manufacturers in the flavors and fragrance sector use the bromoanisole as an advanced intermediate for assembling complex aroma molecules, especially specialty anisole and musk derivatives. The material’s methyl and methoxy profile supports syntheses that require controlled electron density for select functionalizations, optimizing the final product's scent profile and regulatory acceptability.

    Industry compliance standards

    • IFRA Standards (International Fragrance Association)
    • Food Chemicals Codex (FCC) referencing for food-contact safe intermediates
    • EU Regulation (EC) No 1334/2008 for flavorings
    • ISO 9001:2015 for manufacturing traceability

    Typical usage ratio

    • 1–8% by total batch mass, commonly optimized during pilot scaleups on the basis of chromatographic purity and olfactive test panels

    Downstream process integration

    • Charged into aromatic etherification or oxidative coupling steps
    • Controlled heating and pressure parameters preserve ester and aldehyde notes
    • Lot-release tested for absence of banned nitro and polycyclic impurities

    Final product types

    • Specialty musk bases for perfume
    • Methylated anisole fragrances
    • Complex aroma compositions for luxury consumer goods

    5. Veterinary Drug Intermediate Manufacturing

    This material enters targeted animal health supply chains where it constructs key precursors for selective veterinary pharmaceuticals. Stakeholders prioritize validated impurity profiles and batch-to-batch consistency to meet country-level veterinary drug registrations and global stewardship programs. The molecule’s unique substitution enhances selectivity in enzyme inhibitor synthesis for companion and food animal drugs.

    Industry compliance standards

    • VICH GL10 Good Manufacturing Practice for APIs used in Veterinary Medicinal Products
    • Ph. Eur. regulations for veterinary intermediates
    • USP Veterinary Drug Monographs (where applicable)
    • ISO 9001:2015 and animal-specific quality systems

    Typical usage ratio

    • 8–16 mol% relative to lead amine or heterocycle precursor; ratio optimized for target therapeutic index and toxicological evaluation

    Downstream process integration

    • Added at the functionalization stage of core scaffold assembly
    • Pilot validation includes residue and carryover tests to guarantee withdrawal period safety
    • Subsequent purification aligns with QA release for veterinary APIs

    Final product types

    • Companion animal anti-parasitic agents
    • Livestock enzyme inhibitors
    • Avian infection control drugs
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    Certification & Compliance
    More Introduction

    4-Bromo-2,6-Dimethylanisole: A Manufacturer’s Introduction

    Understanding 4-Bromo-2,6-Dimethylanisole from the Source

    Anyone who manages production lines knows the character of a specialty compound the first time they crack open a fresh barrel. Seeing the off-white powder of 4-Bromo-2,6-Dimethylanisole (BMDA) pour clean—without clumps, without trace odors—is the kind of assurance that only people close to the process can guarantee. There’s something reliable in rigid batch controls, starting with 2,6-dimethylanisole itself. The quality of raw input shapes the conversation before the syntheses even begin.

    At our plant, every drum of BMDA begins as a batch of hand-verified dimethylanisole, and each run through the reactor gets logged, sampled, and compared against a decades-built archive of reference samples. The end result doesn’t come by accident. Our material has a melting point within the 66–69°C bracket, and the purity levels—consistently >99% by GC—matter more than numbers on a spec sheet; they mean users don’t deal with secondary peaks, distracting background signals, or inconsistent reactivity.

    Features that Matter on the Shop Floor

    Whether folks in the industry are scaling custom molecules, maintaining a constant product output, or tweaking a formulation for a new application, certain qualities matter more than others. Uniform color and consistency might sound cosmetic, but anyone who has run a process that relies on legacy data knows how slight changes in form can ripple downstream. Pure, crystalline BMDA simplifies every step, from weighing and charging to final filtration and drying.

    The methyl and bromo substitution on the ring brings its distinctive reactivity profile. While many anisole derivatives exist, and some have bromo groups at other positions, very few combine the 2,6-dimethyl geometry and para-methoxy group. This combination tends to offer balanced solubility in most organic solvents, and the material dissolves cleanly in ether, chloroform, and dichloromethane. That quality reduces process hold-ups: the product comes out smoothly, both in pilot projects and full-scale production.

    What Sets Our BMDA Apart From Other Options

    Some buyers ask why not settle for a lower-grade bromoanisole or use a structurally different methyl-substituted alternative. From the experience of running chromatograms late into a shift, what stands out with our BMDA is predictability in yield and purity. Cheaper grades often hit the market with trace iodides or residual starting material—problems that prove stubborn during purification or catalytic coupling steps. These traces don’t always show up in early stages but haunt users during scale-up, fouling catalysts or complicating final purification.

    Choosing a 4-bromo substitution, specifically with methyl groups at the 2 and 6 positions, delivers a more locked-in structure. The crowding around the aromatic ring makes it less prone to side reactions than 3,5- or mono-methyl variants. For synthetic chemists and engineers, that means more consistent results in halogen exchange, palladium-catalyzed cross-couplings, and other transformations critical for pharmaceutical intermediates or specialty flavors.

    True Differences Born in Manufacturing Practice

    People in our field see real differences not in paperwork, but right in the vessel. With 4-Bromo-2,6-Dimethylanisole, anyone who has watched the exotherm of the bromination stage knows that containment and quenching technique—not just theoretical yield—dictate how cleanly product comes out. Every batch gets cooled and worked up manually by seasoned technicians. We register every deviation immediately and adjust washing or recrystallization steps, never leaving the decision to a formula or set-and-forget automation.

    In routine use, technicians appreciate being able to scoop out manageable, dust-free crystals. Some suppliers deliver a sticky cake or fine powder prone to caking, which slows down charging powder into reactors or synthesizers. Our process control—dialed in over years—delivers a consistently free-flowing crystalline material. That consistency won’t show up in a sales pitch, but it keeps lines running and reduces off-spec scrap.

    Applications Enabling Real Progress

    4-Bromo-2,6-Dimethylanisole often heads into research labs, but its impact resonates far wider. Each year formulators explore tweaks to agricultural chemicals, and BMDA’s reactivity gives them new levers. The bromo group lends itself to a host of metal-catalyzed couplings. Adding a couple methyls on the ring influences the steric landscape—critical for tuning interaction strength in target molecules. When real-world deadlines close in, reliability of the input chemical reduces headaches in pilot-plant or large-scale runs.

    Process chemists who move BMDA into active pharmaceutical ingredient intermediates often share feedback that no two sources perform alike. Some batches from spot-market traders arrive with inconsistent crystal morphology or with entrained solvent, slowing downstream processing. Long-term relationships with direct manufacturers matter here, because it means both sides troubleshoot collectively. Whether it’s minimizing step losses, or dialing in particle size for filtration, these tweaks keep production both rapid and predictable.

    Concrete Examples from the Field

    Years of supporting customers in pharmaceutical and fine chemical synthesis have illustrated how BMDA helps push projects forward. In cross-coupling reactions—Suzuki or Buchwald-Hartwig couplings, for example—some other bromoanisoles lag due to competing side reactions or require tedious purification. The 2,6-dimethyl configuration reduces these issues, leaving cleaner product mixtures, fewer repeats, and lower overall solvent use. These process improvements reflect in higher overall yields, less waste, and tighter timelines.

    One recurring story comes from makers of specialty flavors. A batch of 4-Bromo-2,6-Dimethylanisole, brought in to introduce an ether-linked sidechain, produced a subtly different aroma profile. Comparing samples, the team traced it to micro-impurities present in non-manufacturer lots purchased in bulk from resellers. After years of troubleshooting, switching to our direct-sourced product resolved the inconsistencies, eliminating the haze that plagued organoleptic testing.

    We have also received feedback from agrochemical developers about the role of BMDA in producing targeted herbicide precursors. Maintaining the methylated structure prevents unexpected ring-activation, granting better control during later substitution. Unexpected side-products from lower-quality grades can set back commercial launches by months—challenges many manufacturers underestimate until they hit production scale.

    Quality Control: Not Just a Checkbox

    Hands-on involvement begins with raw material tracking. All routes use high-purity 2,6-dimethylanisole and N-bromosuccinimide or equivalent sources, and reaction temperatures are held precisely. The most sensitive phase, the ring halogenation, gets tight time and temperature surveillance. Technicians don’t simply log numbers; they sample real-time and check for off-spec color or odd odor shifts. Batches out of line get held for deeper rework rather than forced into the supply chain.

    Our lab team maintains extensive reference archives. Instead of relying only on third-party assays, we run in-house gas chromatography on every lot—looking not just for total purity, but for pattern-matching to past “best case” batches. Subtle shifts in retention time, traces of over-brominated byproducts, or presence of unconverted starting material mean another round of refinement. This approach keeps shipments consistent from batch to batch.

    Logistics staff package BMDA in high-integrity polyethylene liners, double-sealed to keep atmospheric moisture and contaminants out. During transit, shipping teams protect every drum from exposure and prevent accidental compaction—the details operators notice after years dealing with damaged goods. It’s never just an entry in the manifest; it’s a chain of trust built from the manufacturing floor to the customer’s bench.

    Environmental and Regulatory Considerations on Factory Grounds

    Production of organobromo compounds involves the responsible handling of halogenating agents and safe waste management. Our site design includes on-site containment and scrubbing systems. Brominated waste streams are collected and treated to reduce emissions, and solid byproducts are stabilized before disposal. Only by controlling every aspect, from reagent delivery to final packaging, does the product arrive as expected, with minimum downstream complications.

    Inspections from local environmental health officers occur regularly, and auditors track every stage of solvent management. We report disposal, emissions, and batch traceability to authorities, and any improvements gleaned from feedback lead to updated SOPs. Being the manufacturer carries both commercial incentive and public responsibility; controlling every step of the process makes a difference, not just to customers, but to the surrounding community.

    Direct Supply: Why the Source Matters

    Some customers in need of BMDA find offers across trading platforms, with a plethora of grades at varying prices. Experience has shown that manufacturers controlling their own synthesis secure greater accountability than those working through traders or distant brokers. We notice increased requests for documentation, traceability, and consistency. Relying on a third-party introduces variables—unknown transit history, environmental exposure, and potential adulteration—that only manufacturers can directly mitigate.

    Directly engaging with end users keeps lines of communication open for technical questions, special packing needs, or support with method development. Synthetic teams come across challenges unique to their lines—variations in mixing, reactor volume, drying, or desired particle size distribution. Working as the origin point, we adapt QA-QC or production parameters to help partners keep their own lines running smoothly.

    Supporting Ongoing Innovation

    The applications for 4-Bromo-2,6-Dimethylanisole evolve every year as researchers optimize catalysts, invent new linker chemistries, or look for cleaner downstream transformations. Each time new methods catch on, users want to know their starting material won’t be the unknowable factor in their risk matrix. No two production runs are exactly alike, but manufacturing with decades of institutional memory lets us support burgeoning fields—biosimilar production, aroma development, new pharmaceutically relevant heterocycles—without forcing customers to recalibrate their entire process due to shifting input quality.

    Inquiries about process optimizations arise regularly. Maybe a team wants lower dust levels for an automated feed system, or a collection of smaller-particle grades for improved surface reactivity. Flexibility in production only comes with direct access to reactors, crystallizers, and the freedom to tweak cleaning and drying procedures on the factory line itself.

    Comparisons to Related Chemicals from a Practical Perspective

    On paper, BMDA may appear similar to many other bromoanisoles. In synthesis, the differences come through quickly. Size and position of methyl groups exert a powerful influence on reaction rate and side-product profile. For example, a simpler 4-bromoanisole lacks the steric bulk on the ring, which can permit more reactive—but also more uncontrollable—substitutions. The double methyls in BMDA act like gatekeepers, slowing unwanted additions and improving selectivity in catalytic steps.

    Some formulators have considered 3,5-dimethylanisole variants for cross-coupling, only to find yields drop or purification steps multiply. With BMDA, experience shows side-stream formation drops, filtration steps run faster, and post-reaction clean-up requires less solvent. These advantages don’t always surface until real production lines—where every kilogram of lost product or hour spent reworking means measurable impact.

    Anyone sourcing chemicals at scale understands the value of drawing clear boundaries between similar molecules. The cost of reclaiming product from a poorly-behaved batch offsets apparent savings secured by simply picking the lowest price listing. For teams running multi-step synthesis, recurrent problems with inconsistent bromoanisole shorts production schedules, wastes solvent, and risks entire lots at QA. These aren’t issues that pop up in abstract product literature but emerge through years at the bench and in the plant.

    Feedback Loops from Downstream Users

    Direct customer feedback often sparks internal improvements. Early on, a partner in the fragrance sector requested a special filtration for ultra-low particulate grades. Iterative logbook adjustments to the recrystallization process, informed by actual application feedback, now feed into standard output—benefitting everyone who requires low-dust input for sensitive analytical or blending work. Working from the manufacturing side means every customer conversation can influence the product seen by the next recipient.

    Pharma developers routinely send assay reports highlighting new peaks or impurities. Not all issues center around product purity; sometimes a shift in storage conditions at a distribution partner affects performance. As direct manufacturer, open feedback channels let us react, occasionally dispatching technical teams or running side-by-side tests to isolate root causes. That level of interaction benefits both sides—users get improved product, and we absorb knowledge that would otherwise slip beyond reach.

    Carrying Forward: Why Direct Manufacturing Makes a Difference

    Over the years, watching the market shift to new entrants and resellers, it’s clear that only manufacturers in direct control of input, synthesis, and QC routines can offer reliability built over time. Every shift runs through the same core protocol because new hands learn alongside staff holding decades of aggregate experience. Each problem solved locally—whether plugging a vessel leak or tuning a drying oven—improves overall output, not just on paper but on the bench where it matters most.

    With a compound like 4-Bromo-2,6-Dimethylanisole, supporting years of R&D and production across sectors, every granular adjustment adds up. Our focus never falls on glossy marketing, but on building actual knowledge into each step—from starting material selection, reaction control, and work-up, through lab testing and packing. Working directly as the manufacturer means the conversation never ends with a single order, but continues, evolving with every new application and every new user insight that comes in.