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4-Bromo-2,6-Di-Tert-Butylphenol

    • Product Name 4-Bromo-2,6-Di-Tert-Butylphenol
    • Alias 2,6-Di-tert-butyl-4-bromophenol
    • Einecs 624-249-3
    • 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

    628323

    Product Name 4-Bromo-2,6-Di-Tert-Butylphenol
    Cas Number 18617-11-1
    Molecular Formula C14H21BrO
    Molecular Weight 285.22 g/mol
    Appearance White to off-white solid
    Melting Point 99-103 °C
    Boiling Point None (decomposes)
    Solubility Slightly soluble in water; soluble in organic solvents
    Density 1.27 g/cm³ (approximate)
    Purity Typically ≥98%
    Storage Store at room temperature; keep container tightly closed
    Smiles CC(C)(C)c1cc(Br)c(O)c(C(C)(C)C)c1
    Synonyms 2,6-Di-Tert-Butyl-4-Bromophenol
    Hazard Statements May cause skin and eye irritation

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

    Packing & Storage
    Packing The 25g package is a sealed amber glass bottle with a white screw cap, labeled "4-Bromo-2,6-Di-Tert-Butylphenol, 25g, For Laboratory Use."
    Shipping 4-Bromo-2,6-Di-Tert-Butylphenol is shipped in tightly sealed containers under dry, cool conditions. The packaging meets regulatory requirements for hazardous materials. Proper labeling, including hazard symbols, is ensured, and the material safety data sheet (MSDS) accompanies each shipment. Transport follows national and international chemical shipping guidelines for safe handling and delivery.
    Storage **4-Bromo-2,6-Di-Tert-Butylphenol** should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from sources of ignition, heat, and incompatible materials such as strong oxidizers. Store under inert atmosphere if possible to prevent oxidation and degradation. Clearly label the container and follow all safety guidelines for handling hazardous chemicals.
    Application of 4-Bromo-2,6-Di-Tert-Butylphenol

    Applications of 4-Bromo-2,6-Di-Tert-Butylphenol in Industrial Manufacturing

    As an original manufacturer of 4-Bromo-2,6-Di-Tert-Butylphenol, we supply this specialty phenolic compound to a range of advanced industrial sectors. Our material plays a key role in the downstream synthesis and formulation of high-value products. Below are the primary application areas directly supported by global industrial demand.

    1. Antioxidant Intermediate for Synthetic Lubricants

    4-Bromo-2,6-Di-Tert-Butylphenol functions as an essential intermediate in synthesizing high-performance antioxidants for synthetic lubricating oils. These antioxidants enhance oxidative stability in automotive, aerospace, and industrial lubricants. The phenolic unit forms the core structure during antioxidant production, directly affecting long-term lubricant stability under high-temperature operation. Manufacturers incorporate this intermediate in the initial stages of custom antioxidant synthesis, relying on precise stoichiometric addition to control final antioxidant properties and compatibility with oil bases.

    Industry compliance standards

    • ASTM D4950: Engine Oil Classification
    • API LC: Lubricant Additive Chemical Requirements
    • REACH (EC) No 1907/2006: Substance Registration
    • OECD Series on Testing and Assessment No. 23

    Typical usage ratio

    • Implemented at 2–5% by weight during antioxidant synthesis.
    • Exact ratio adjusted per finished oil formulation and required oxidative stability index.

    Downstream process integration

    • Added in batch reactor during phenolic antioxidant core formation.
    • Post-reaction, further functionalization occurs before integration into lubricant additive packages.
    • Material undergoes quality control for purity and is filtered prior to blending.
    • Final antioxidant is metered into synthetic base oil blends in blending vessels.

    Final product types

    • Fully-formulated synthetic engine oils
    • High-temperature compressor lubricants
    • Hydraulic system fluids
    • Industrial gear oils

    2. Stabilizer Manufacturing for Polymer Resins

    Our 4-Bromo-2,6-Di-Tert-Butylphenol serves as a key phenolic precursor in the production of non-staining stabilizers used in polymer resin systems. This application targets sectors where color retention and resistance to degradation during processing and service are critical, including specialty polyolefins and PVC compounds. Chemical formulators depend on the bulky, hindered phenol structure to inhibit oxidative and thermal degradation, thereby extending polymer performance during extrusion, injection molding, and end-use exposure to demanding environments.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for Polymer Additives
    • FDA 21 CFR 177.1520: Polyolefin Resin Additives (for food-contact eligibility)
    • REACH Annex XVII: Polymer Additive Substance Limits
    • EN 71-3: Chemical Safety for Toys (for relevant polymer grades)

    Typical usage ratio

    • Applied at 0.1–0.5 wt% in the stabilizer synthesis step.
    • Final stabilizer is dosed at 0.05–0.2 wt% in compounding, depending on resin type and exposure level.

    Downstream process integration

    • Introduced during the initial stage of hindered phenolic stabilizer production by condensation or coupling reaction.
    • Stabilizer masterbatch formed for ease of dosing during polymer compounding.
    • Quality control via HPLC to ensure phenol consumption and product uniformity.
    • Directly dosed into compounding extruders or injection molding feed zones.

    Final product types

    • Clear polypropylene films
    • Low-color PVC profiles
    • Polyethylene packaging materials
    • Polymer-based technical molded goods

    3. Synthesis of Electronic Chemical Intermediates

    4-Bromo-2,6-Di-Tert-Butylphenol is integral in the synthesis of aryl bromide intermediates used in electronics and semiconductor applications. Specialty chemical manufacturers utilize this material for constructing complex molecules via cross-coupling reactions, especially Suzuki-Miyaura coupling, leading to advanced ligands, organic electronic substrates, and display materials. The unique steric hindrance and electronic characteristics provided by the tert-butyl groups allow for fine control over reactivity and purity in microelectronics supply chains.

    Industry compliance standards

    • IEC 62474: Material Declaration for Electrical/Electronic Products
    • IPC-1752A: Materials Declaration Management
    • RoHS III (EU 2015/863): Restriction of Hazardous Substances
    • IATF 16949: Automotive Electronics Production

    Typical usage ratio

    • Applied at 1.0–3.0 equivalents relative to coupling partners in cross-coupling synthesis.
    • Loading tailored to yield and downstream device layer thickness targets.

    Downstream process integration

    • Dosed into reaction vessels in the preparative phase for aryl halide cross-coupling.
    • Purified by column chromatography or crystallization as required for semiconductor-grade use.
    • Final intermediate transferred to device coating, display precursor, or circuit board solution baths.
    • Close monitoring to limit trace impurities for high-reliability electronics.

    Final product types

    • Organic light-emitting diode (OLED) materials
    • Semiconductor photoresists
    • Specialty printed circuit board coatings
    • Electronic-grade polymer dielectrics

    4. Building Block for Agrochemical Synthesis

    Chemical synthesis firms routinely employ 4-Bromo-2,6-Di-Tert-Butylphenol as a brominated phenol intermediate for fine-tuning the structure of selective agrochemical active ingredients. These active molecules serve in the formulation of advanced crop protection agents, where selectivity, environmental breakdown profile, and resistance management are essential. Bromination on the phenol ring confers specific electronic characteristics required for efficient subsequent reactions with heterocyclic and aryl chlorides, making this intermediate vital in modern agricultural chemistry workflows.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • ISO 17025: Testing Laboratory Accreditation
    • Sustainable Chemistry ISO 14001: Environmental Management
    • EU Regulation (EC) No 1107/2009: Plant Protection Products

    Typical usage ratio

    • Used at 1.0 equivalent per target active intermediate in the synthesis step.
    • Adjustments based on desired substitution pattern and yield optimization.

    Downstream process integration

    • Fed into the first-stage reactor for active pharmaceutical ingredient (API) synthesis.
    • Unreacted phenol checked and recovered in downstream crystallization if possible.
    • Coupling and derivatization finalize the molecule for formulated crop protection blends.
    • QC sampling ensures bromine content and residual solvent targets meet regulatory limits.

    Final product types

    • Selective herbicide actives
    • Novel fungicide intermediates
    • Chemical seed treatment actives
    • Plant growth regulator APIs

    5. Precursor in Custom Fragrance Ingredient Development

    Specialty fragrance and aroma chemical producers utilize 4-Bromo-2,6-Di-Tert-Butylphenol as a phenolic core in synthesizing advanced musk and woody scent molecules. Through controlled substitutive reactions, this compound enables the construction of intermediates that form the backbone of high-stability, long-lasting fragrance oils. Producers focus on compliance with global fragrance regulatory panels and demands for non-allergenic, stable compounds for long-wear applications in both fine fragrance and home care sectors.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards
    • Cosmetic Ingredient Review (CIR) Panel Guidelines
    • EU Regulation (EC) No 1223/2009: Cosmetic Products
    • ISO 22716: Cosmetic GMP

    Typical usage ratio

    • Dosed at 0.2–1.2 equivalents in aroma intermediate synthesis, depending on final note intensity and complexity.
    • Ratio influenced by reaction pathway and purity specification for fragrance-grade use.

    Downstream process integration

    • Introduced into batch reactors for aryl alkylation and subsequent cyclization reactions.
    • Purification follows via distillation and flash chromatography to meet fragrance purity criteria.
    • Intermediate compounds undergo further transformation before compounding in blending houses.
    • QC release includes odor profile evaluation and allergen content analysis.

    Final product types

    • Musk-fragrance oils for fine perfumery
    • Long-lasting woody fragrance components
    • High-purity aroma chemicals for detergents
    • Encapsulated scent delivery systems
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    Competitive 4-Bromo-2,6-Di-Tert-Butylphenol prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Introducing 4-Bromo-2,6-Di-Tert-Butylphenol: A Trusted Choice from the Manufacturer’s Experience

    At the manufacturing core, real understanding starts not in the meeting room but at the reactor, up close with the chemistry. 4-Bromo-2,6-Di-Tert-Butylphenol (CAS 19839-20-6) has become a familiar compound in our production cycles, valued among specialty phenols for its stability and reactivity. We produce this compound consistently to meet the demands of research labs, process engineers, and industrial clients who appreciate quality backed by process know-how.

    Model and Specifications Based on Process Reliability

    Years of hands-on batching and continuous optimization have taught us that consistency matters more than any sales pitch. Our 4-Bromo-2,6-Di-Tert-Butylphenol is manufactured with strict attention to purity, color, and moisture levels. The model we produce commonly reflects a purity of at least 98% by GC, supported by low bromide and phenol-related impurities. Solid, crystalline, and manageable in the drum or jar, it offers easy handling under standard laboratory and manufacturing conditions. Each lot is analyzed in-house using validated methods and checked for attributes such as melting point, color (APHA or Gardner), water content (by Karl Fischer titration), and elemental analysis.

    We collect product samples from actual output, not pilot projections, and time after time witness batch uniformity in response to the needs of both small and large order clients. If you request a specification sheet, what you find matches what leaves our plant floor—not a theoretical range, but the result of practiced procedure and quality checks.

    Practical Uses with a Track Record

    For over a decade, this brominated phenol has been entering more than just the storage cupboards of R&D teams—it drives value in processes from fine chemical intermediates to stabilizer additives in polymers. We’ve seen it act as a dependable building block in the synthesis of more complex aromatic compounds and a useful reagent in oxidative coupling. Real feedback comes from those synthesizing pharmaceuticals and agrochemical intermediates, noticing its selectivity and reactivity in halogenation and coupling reactions.

    On the industrial scale, manufacturers count on its antioxidant properties. Polymers and resins, especially those sensitive to thermal or photochemical oxidation, last longer with this compound as a stabilizer. From our angle, this comes down to its steric bulk and the electron-donating capability imparted by the tert-butyl groups, paired with the activating bromine atom. Chemists reporting from their own research bench tell stories about improved product shelf life and color retention when this additive finds its way into the formulation.

    What Makes 4-Bromo-2,6-Di-Tert-Butylphenol Stand Apart?

    Manufacturing is about knowing not only what your material can do, but also how it behaves compared to similar products. We've worked through the headaches of material inconsistencies from other sources before refining our process. For example, phenolic antioxidants appear similar on paper, but bromination adds distinct chemical properties. The 4-bromo position confers heightened selectivity in coupling reactions, while the tert-butyl groups support oxidative resistance not seen in unsubstituted phenol or mono-tert-butyl derivatives.

    Unlike simple phenol, which oxidizes quickly and emits a strong odor, our 4-Bromo-2,6-Di-Tert-Butylphenol holds up under heat and storage. The melting point remains consistently in the narrow range observed batch-to-batch, supporting precise dosing whether hand-weighed or through automated processes. Compared with 2,6-di-tert-butylphenol, the bromo substitution opens new synthetic pathways. For chemists who need a handle for further functionalization, the bromine becomes more than a trace additive—it’s a key that opens routes in cross-coupling, Suzuki, and Buchwald-Hartwig reactions.

    Supplier’s Perspective: Process Control and End-User Confidence

    Manufacturing excellence does not grow from pure theory—it's built batch by batch. We've witnessed how inadequate process monitoring leads to off-specification by-products, sometimes undetectable until costly downstream failures. That's why our process incorporates on-line reaction monitoring and thorough post-reaction workups to ensure tight control of bromine residuals and minimize phenolic subproducts.

    Quality for us means not just meeting a minimum, but aiming for the performance our end users need in tough real-world applications. For one, stabilization roles require that phenolic compounds have minimal non-volatile residues and trace metal contamination. We address this directly, sourcing reagents and solvents with certification and installing additional purification columns where needed. In the past, client feedback—sometimes from a single missed batch—has highlighted the value of these steps, especially in high-performance plastic production lines.

    Experience from the Shop Floor: Handling and Storage Realities

    Shipping and storage of this compound rarely bring surprises. It’s stable under typical warehouse conditions, resisting clumping or caking that plagues more hygroscopic phenols. Our production team documents low tendency toward dust formation, meaning safer handling and less product loss. This has practical importance: clients avoid the risk of inconsistent reactivity in small-scale or automated dosing, and workers in the plant environment appreciate lower airborne exposure. We package our product in sealed, inert-lined containers—practices tested by years of export and domestic transit.

    Batch-to-batch tracking remains strict on our end, not just for regulatory compliance but for customer trust. All containers feature production codes tied to our quality reports, so when a customer calls about a specific lot, our plant team can reference the exact details—no guesswork or generic replies. In rare events of shipping mishaps, immediate tracking leads to rapid resolution.

    Feedback from Industrial Users and Academic Labs

    Our connection with users does not end with a packing list. Open lines with purchasing groups, process engineers, and research scientists have influenced production changes over time. For example, requests for higher purity and lower moisture content in pharmaceutical synthesis drove improvements in vacuum drying and final filtration. Our production volumes have scaled up, but we still handle occasional requests for smaller bespoke orders, accommodating academic research or specialized industrial trials.

    Over the years, conversations with users have raised valuable perspectives. One found that using our 4-Bromo-2,6-Di-Tert-Butylphenol enabled a higher yield in their Arylation reaction, while another cited less coloration in molded polymers—a clear sign of successful stabilization. Some customers from academic circles comment that switching from a less pure supplier decreased the noise in their NMR spectrum, saving hours of troubleshooting. Every feedback loop, whether a call, email, or in-person visit, teaches which product qualities matter most in application, and these lessons find their way into our manufacturing SOPs.

    Comparisons that Matter: 4-Bromo-2,6-Di-Tert-Butylphenol and Its Alternatives

    The phenols landscape is broad. While phenol itself offers wide reactivity, it often introduces stability problems. Mono-substituted tert-butyl phenols give a modest boost in oxidation stability, but our customers in high-performance polymer applications tell us the di-tert-butyl backbone of this compound outpaces them all. Switching from non-brominated options to 4-Bromo-2,6-Di-Tert-Butylphenol adds a selective “activation” site, well-matched for those building advanced aromatic frameworks or catalytically driven coupling processes.

    Brominated phenols without tert-butyl groups lack the steric hindrance needed for robust antioxidant performance. In our own comparative tests, 4-Bromo-2,6-Di-Tert-Butylphenol resists degradation in accelerated aging conditions. Practical examples include polymer compounding lines, where it retains structural color and integrity longer than less hindered alternatives. Down the chain, this translates to end products—technical plastics, resins, coatings—lasting longer, with lower chances of property loss or discoloration.

    Challenges: Safety and Environmental Considerations in Manufacture and Use

    Handling brominated phenols means more than just hitting a purity number. Precautious attention to worker safety, emissions, and waste matters every day. Our production protocols mandate airtight systems where possible, and absorbent stations are positioned at likely points of minor release. Throughout production, environmental compliance never fades into the background. Waste streams are monitored for brominated organics according to local and international standards, preventing inadvertent release outside our plant.

    On the customer side, storage and usage guidelines are shaped by years spent in close contact with the end market. We offer genuine input on minimizing exposure risks and waste, based on hard-earned process experience, not just printed MSDS guidelines. Requests for detailed contaminant analysis are answered promptly; our in-house analytics cut waiting and help downstream users make faster, informed decisions. This collaborative approach keeps our process transparent and our clients’ operations running smoothly.

    Regulatory Insights from Decades in the Business

    Chemical regulation never stands still, and compliance builds trust in modern supply chains. Our long-haul experience in updating technical files, communicating with authorities, and staying prepared for audits leaves no room for last-minute document scrambles. Customers, especially those shipping internationally or developing regulated end products, have saved time and avoided roadblocks because our material arrives with the compliance trail intact.

    We navigate changing national and global lists for restricted substances, track emerging guidance on brominated compounds, and share updated safety data transparently. This way, customers get both technical substance and regulatory peace of mind.

    Role in Innovation and How Clients Advance with Confidence

    Innovation does not happen without reliable raw materials. Many downstream breakthroughs—a novel electronic material, a more durable UV-resistant coating—start with a bottle or drum of precisely prepared 4-Bromo-2,6-Di-Tert-Butylphenol. Over the years, clients have shared early technical papers and patent filings where our product stands out. Some report how switching to our compound resolved previous batch variability, enabling work under tighter analytical standards. Our input occasionally extends beyond supply—we advise on scale-up tips or recommend storage tweaks based on failures or successes observed across years of shipments.

    The relationship with advanced users brings insights back to our R&D, leading to process tweaks or packaging experiments. For instance, one high-throughput client in electronics requested antistatic packaging to avoid contamination, while a research group requested UV-opaque bottles. Direct conversation drives improvements, not corporate distance.

    Looking Forward: Supporting Growth in Crucial Industries

    Demand for robust phenolic compounds continues from diverse sectors—electronics, specialty polymers, advanced synthetic intermediates, and more. Each brings its own operational quirks and regulatory standards, which our manufacturing teams have learned to anticipate. Our high-purity 4-Bromo-2,6-Di-Tert-Butylphenol has supported expansions in many of these industries over the last decade.

    As we see technology grow more complex, relying on trusted suppliers saves our clients both time and cost. Years of direct feedback, root-cause investigation of failures, and continuous technical dialogue ensure our product fits real-life needs. This approach enables successful process scale-up and high reproducibility from trial stage to full commercial production.

    Summary on 4-Bromo-2,6-Di-Tert-Butylphenol as a Manufacturer’s Perspective

    Quality raw materials never begin and end with just molecules—they represent service, knowledge, and adaptability. Our story with 4-Bromo-2,6-Di-Tert-Butylphenol reflects years of hands-on manufacturing, practical feedback, and industry-driven evolution. Users who choose it know they are getting more than a fine chemical—they secure reliable performance with each lot, supported by a supplier who listens, improves, and documents every batch that leaves the facility.

    For ongoing and new projects, we continue to refine both product and partnership, committed to supplying not just what is needed, but what advances your research, production, or application on every shipment. Experience from a manufacturer who understands the journey from raw material to finished product lays a foundation that no catalogue or third-party distributor can match.