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1-Bromo-4-Tert-Butylbenzene

    • Product Name 1-Bromo-4-Tert-Butylbenzene
    • Alias 4-tert-Butylbromobenzene
    • Einecs 211-249-0
    • 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

    659838

    Chemical Name 1-Bromo-4-tert-butylbenzene
    Cas Number 19694-11-0
    Molecular Formula C10H13Br
    Molecular Weight 213.12
    Appearance Colorless to pale yellow liquid
    Boiling Point 232-234°C
    Melting Point -18°C
    Density 1.223 g/cm3
    Refractive Index 1.524
    Smiles CC(C)(C)C1=CC=C(C=C1)Br
    Pubchem Cid 66828
    Solubility Insoluble in water
    Flash Point 97°C
    Ec Number 243-222-3

    As an accredited 1-Bromo-4-Tert-Butylbenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle with secure screw cap, labeled "1-Bromo-4-Tert-Butylbenzene, 25g," includes hazard warnings and safety information.
    Shipping 1-Bromo-4-tert-butylbenzene is shipped as a hazardous material, typically in sealed glass or HDPE containers to prevent leaks. It must be labeled according to regulations (such as UN 1993, Flammable Liquids) and transported with appropriate documentation, ensuring secure packaging to avoid exposure during transit. Handle with care and follow safety guidelines.
    Storage 1-Bromo-4-tert-butylbenzene should be stored in a cool, dry, and well-ventilated area away from sources of ignition and incompatible materials such as strong oxidizers. Keep the container tightly closed, protected from light, and clearly labeled. Store in a flameproof cabinet if possible, and avoid exposure to heat, moisture, and direct sunlight to maintain chemical stability.
    Application of 1-Bromo-4-Tert-Butylbenzene

    Applications of 1-Bromo-4-Tert-Butylbenzene in Industrial Manufacturing

    As an established manufacturer of 1-Bromo-4-Tert-Butylbenzene, we enable reliable supply for specialized downstream sectors. The following industrial scenarios detail how formulators and processors incorporate this compound at scale for targeted transformation across advanced chemical syntheses. Our continuous oversight and participation in industry forums and customer audits reinforce the material’s role in compliant manufacturing environments worldwide.

    1. Pharmaceutical Intermediate Synthesis

    Leading active pharmaceutical ingredient (API) producers order this aromatic bromo compound to introduce tert-butylphenyl motifs in custom small-molecule APIs. Nucleophilic substitution, Suzuki, or Buchwald-Hartwig reactions leverage the aryl bromide functionality to achieve site-specific arylation in complex drug scaffolds, as required by late-stage development projects. The compound enters pilot and production routes where its purity facilitates efficient downstream coupling and reduces process by-products.

    Industry compliance standards

    • ICH Q7A (Good Manufacturing Practice for APIs)
    • EU GMP Part II (Active Substances)
    • USP–NF Monographs (as referenced in specific API registration dossiers)
    • 21 CFR Part 210/211 (United States cGMP Regulations)

    Typical usage ratio

    • 0.5–3.5 molar equivalents per reaction step; varies by the target molecule’s arylation requirements.

    Downstream process integration

    • Added in batch or semi-batch reactors during the initial halide-substituted arylation step.
    • Subject to post-reaction extraction and purification prior to subsequent transformation.

    Final product types

    • Key intermediates for anti-inflammatory, anti-neoplastic, and CNS drug APIs.
    • Regioselectively functionalized aromatic APIs for clinical candidate supply.

    2. Agrochemical Active Ingredient Manufacture

    Manufacturers of herbicide and fungicide actives utilize this compound for the synthesis of tert-butylphenyl-substituted agrochemicals. The controlled introduction of bulky aromatic groups directly impacts the efficacy and environmental stability of crop protection agents. Bromination reactivity ensures precise placement in multi-step organic syntheses, enabling reliable scale-up from pilot to commercial fermentation escorts.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products (FAO/WHO/UNEP)
    • ISO 9001:2015 Quality Management for Chemical Manufacturing
    • REACH Registration (European Union Regulation)
    • EPA FIFRA Compliance (United States—active ingredient registration)

    Typical usage ratio

    • 0.2–1.8 equivalents per key coupling or alkylation reaction, depending on molecular target and plant process conditions.

    Downstream process integration

    • Charged in the synthesis train during Grignard or cross-coupling reactions.
    • Used post-fermentation as a halogenation/coupling intermediate in the final synthetic stage.

    Final product types

    • Active ingredients for pre- and post-emergence herbicide formulations (e.g., tert-butylphenyl derivatives).
    • Custom fungicide actives for cereal and vegetable protection.

    3. Electronic Chemical Raw Material for Liquid Crystal Intermediates

    Advanced materials developers in the electronics sector apply this compound as a key precursor in the production of high-purity liquid crystal intermediates. Selective bromine and tert-butyl substitution confer rigidity and thermal stability essential for high-voltage (HV) and extended-temperature display technologies. Stringent inert-atmosphere handling and distillation protocols conserve the substrate’s structure throughout scale-up syntheses.

    Industry compliance standards

    • ISO 9001:2015 (Quality for Electronic Chemicals)
    • JIS (Japanese Industrial Standards for Display Materials)
    • RoHS Directive 2011/65/EU Annex II (Restriction of Hazardous Substances)
    • China GB/T Electronic Grade Chemical Standards

    Typical usage ratio

    • 0.6–2.2 molar equivalents per condensation reaction with biphenyl or cyclohexane derivatives, adjusted by rigid-core structure design.

    Downstream process integration

    • Introduced in sealed, nitrogen-purged reactors at the arylation stage of liquid crystal intermediate synthesis.
    • Final purification by vacuum distillation and crystallization.

    Final product types

    • Liquid crystal monomers and oligomers for LCD televisions, monitors, and instrument panel displays.
    • Alignment and dielectric materials for specialty electronics.

    4. Custom Polymer Additive Preparation

    Specialty polymer producers employ this chemical as a reactive additive for preparing advanced polymer architectures. The bromide group enables targeted grafting onto polystyrene or polyolefin chains, facilitating further functionalization with bulky side groups without impairing matrix integrity. Such modifications enhance impact resistance, optical clarity, or solvent resistance in engineered resins for demanding applications.

    Industry compliance standards

    • ISO 14001:2015 (Environmental Management for Polymer Production)
    • EN 71-3 (Safety of Toys—Migration of Certain Elements, for specialized resins)
    • SGS Polymer Compliance Testing
    • REACH Annex XVII (Restrictions on certain dangerous substances in consumer products)

    Typical usage ratio

    • 0.1–1.0% by polymer weight during prepolymer stage; specific ratio set by target functionalization level and polymer system.

    Downstream process integration

    • Blended with monomers or prepolymers in reactive extrusion or solution polymerization steps.
    • Followed by post-polymerization purification and melt-compounding with base resins.

    Final product types

    • High-performance optical grade plastics for lighting, display housings, or automotive interiors.
    • Polymer blends with flame-retardant and antistatic properties.

    5. Fine Chemical Building Block for Fragrance and Aroma Intermediates

    Aroma chemical manufacturers integrate this compound during the synthesis of specialty benzene derivatives for fragrance creation. Its tert-butyl structure and reactive bromine allow precision substitution, building aromatic scaffolds essential for musky, woody, and high-durability base notes in premium fragrance bases. Robust analytical QC tracks trace impurities critical to olfactory quality benchmarks.

    Industry compliance standards

    • IFRA (International Fragrance Association) Code of Practice
    • ISO 9235:2013 (Natural and Synthetic Aroma Chemicals)
    • GHS/CLP Regulation EC No. 1272/2008 (Classification, Labelling, and Packaging for chemicals in consumer products)
    • FEMA registration process for new aroma ingredients

    Typical usage ratio

    • 0.2–2.5 molar equivalents per proprietary synthesis step, modulated by target molecular complexity and downstream functionalization.

    Downstream process integration

    • Dosed in catalytic aromatic substitution or alkylation reactions early in fragrance intermediate development cycles.
    • Processed through GC/MS-verified distillation and isolation protocols for quality assurance.

    Final product types

    • Key intermediates for luxury perfume bases and specialty aroma compositions.
    • Fragrance components for personal care product formulations.
    Free Quote

    Competitive 1-Bromo-4-Tert-Butylbenzene prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    1-Bromo-4-Tert-Butylbenzene: Thoughtful Manufacturing for Advanced Synthesis

    Delivering Consistent Quality in Aromatic Bromides

    Walking through our facility, every batch of 1-Bromo-4-Tert-Butylbenzene stands as proof of what focused chemical work can achieve. We've produced aromatic bromides for years, and this compound challenges chemists and plant workers with its demands. Its structure, a benzene ring bearing a tert-butyl group at the para position and a bromine, makes it practical for use as a reliable intermediate in a range of syntheses. End-users count on precise bromination, distinctly pure product, and reliable sourcing. Each time we address customers looking beyond standard halobenzenes, we find they don't want to compromise on reactivity or handling. That’s why every phase—raw material sourcing, distillation, and the washing steps—calls for attention most people wouldn’t notice until something goes wrong.

    Our product—CAS number 4981-24-6—has found a place in advanced chemical synthesis. You’ll often see it discussed by research teams who need specific substitution patterns. The tert-butyl group at the para position doesn't just change reactivity: it gives the molecule steric bulk that blocks sites on the benzene ring. If you work in pharmaceuticals, agrochemicals, or polymer additives, you see how this feature opens new routes that plain bromobenzene just can’t reach. From years on the floor, I see that purity standards for 1-Bromo-4-Tert-Butylbenzene make all the difference. Residual solvents or isomeric impurities affect downstream yields, especially with modern methods like Suzuki coupling and lithiation.

    Each production run starts by ensuring the quality of tert-butylbenzene. We use gas-phase bromination methods that take temperature control and precise feed rates to minimize unwanted side products. The process swings sharply if humidity or trace ions sneak in—anyone who's run the distillation knows this. Chlorinated or dibrominated impurities decrease product value. By regular analytical checks, from GC to NMR, we catch problems before scale-up. Purification steps, from aqueous workups to fractional distillation, have developed over decades. We've listened to end-users who need their 1-Bromo-4-Tert-Butylbenzene not just white but snow-bright, with odorless, dry crystals that handle without clumping or static.

    Working Applications That Call for Authentic Tert-Butyl Substitution

    We talk to chemists every week who want a clean entry point for Grignard reagents, Suzuki couplings, or nucleophilic aromatic substitution. The para-tert-butyl group’s bulk means you can target transformations that would quickly go awry with unsubstituted bromobenzene. It's less susceptible to side reactions on the ring and lets you drive selectivity with confidence. This pattern matters for building blocks in dye chemistry, pharmaceutical actives, and material science. Imagine attaching functional groups specifically to the meta or ortho position: the tert-butyl directs traffic with a bigger presence than methyl, and it also boosts solubility in nonpolar solvents.

    Many new users wonder why not just use 1-bromobenzene? After years on the manufacturing side, I’ve seen that the tert-butyl group’s shielding makes a world of difference for those catalytic couplings and directed ortho-metalations, especially at scale. Customers working on polymers or liquid crystals explain how bulky para-substituents affect thermotropic behavior and molecular packing. The molecule’s size and weight, compared to plain bromobenzene and alkyl-substituted analogues, brings advantages—and sometimes unexpected handling quirks. A little extra mass means the product settles quicker in crystallizers, but it can challenge filtration and packing procedures, especially when moving from lab scale to multi-hundred-kilo batches.

    Our development teams know this product sees action as a precursor for tailored ligands and specialty additives. Others use it as a regulated marker in research or develop new medicinal scaffolds. The bromine atom remains a superb leaving group for C–C and C–N bond formation under palladium or copper catalysis. Adjusting reactor setups for this substrate streamlines workflows, but takes a careful hand and a few process tweaks—a lesson we’ve picked up over repeat campaigns.

    Specification as Experienced in Practice

    Most researchers call for a purity above 99 percent, often confirmed with HPLC and proton NMR. Our batches hit this mark reliably, taking advantage of fractional distillation under reduced pressure. That way, we avoid the thermal decomposition seen with marginal cooling, which can lead to sticky residues or darkening. Physical form matters—a lot. Users prefer a low-melting solid (melting range around 46-50°C) or sometimes a heavy, colorless liquid if slightly above ambient. Even a small amount of oxidation or exposure to moisture can affect both handling and downstream processes. We process with anhydrous conditions and package product fresh to avoid any doubts in appearance or performance. Inventory controls cut down shelf aging, which is especially important for those who move straight from delivery to reaction setup.

    On the analytical side, 1-Bromo-4-Tert-Butylbenzene’s characterization means more than just ticking a box on a COA. GC-MS gives a sharp parent peak. NMR integration reflects the distinctive tert-butyl methyl and aromatic patterns. Trace metals from earlier steps, if present, can compromise coupling yields. Our experience shows regular, detailed impurity checks save headaches. Even customers with challenging applications—those demanding the lowest ppm levels of metallic or halogen contaminants—see the benefit of deep process control. We embrace this scrutiny, inviting plant audits and sharing process documentation, because open conversation with end-users has always led to improvements in both product quality and application confidence.

    We take packaging seriously. Standard glass bottles work for smaller volumes, but at scale, high-density polyethylene drums guarantee integrity over longer hauls. At the end of the filling line, technicians run paperwork and sample checks to make sure every container holds only fresh product, nothing leftover from previous runs. Hearing back from seasoned warehouse staff, it's clear that tightly sealed containers cut product loss and reduce headaches during large transfers. Our long-term partners in logistics keep us honest on this front—when something’s lacking in the packaging, we hear about it and fix it on the next run.

    Specific Differences from Other Halogenated and Alkyl-Substituted Benzenes

    People often lump all brominated benzenes together, but 1-Bromo-4-Tert-Butylbenzene stands apart once you look closely at reaction results and real-world performance. The tert-butyl group’s size dwarfs smaller alkyls like methyl and ethyl. This effect pushes every aspect of physical behavior: melting point, solubility, and volatility. 4-Bromo-toluene runs as an easier melt, more volatile, and less demanding in storage, but it can't offer the same orthogonal reactivity for dense molecular scaffolds. On the other side, polybromobenzenes or ortho-substituted analogues might boost reactivity for some processes, yet introduce costly separation problems with their own impurity profiles.

    Anyone who’s used raw bromobenzene in coupling chemistry finds selectivity drops off sharply in multi-step reactions, especially when ortho or meta substitution is needed downstream. The tert-butyl unit on our compound blocks para and a big swath of the ring, reducing side reactions during metalation, halogen exchange, or nucleophilic attack. This delivers purer cuts in batch chemistry, with less need for painstaking column chromatography at the analytical lab bench. Our product’s heavier molecular weight also sees less evaporation loss—colleagues in environmental labs mention tighter control on emissions data.

    Compared to other commonly used alkyl-substituted bromobenzenes, such as 1-bromo-3,5-dimethylbenzene or 1-bromo-2-ethylbenzene, customers find the tert-butyl group holds its own under higher temperature reactions, resisting breakdown and outgassing. Pharmaceutical process chemists prefer this robustness for active ingredient synthesis, especially where moieties must survive repeated heating, catalysis, and pH stress. Our real-world experience with bench-to-pilot scaleups taught us early to never underestimate the subtle differences such molecular tweaks can produce in both yield and final product consistency.

    Supporting Customers and Ensuring Regulatory Compliance

    With every lot of 1-Bromo-4-Tert-Butylbenzene, we stand by full traceability and support. Regulations in major regions—Europe, North America, Asia—call for strict handling, labeling, and transport protocols, including compliance with REACH, TSCA, and relevant inventory listings. Our plant certifications reflect years spent adapting to shifting regulatory needs, from keeping records of water discharges to audits on employee training and material tracking. Customers in highly regulated industries—pharma, electronic materials—rely on our compliance to smooth out their own internal processes.

    Sometimes small procedural details make the greatest difference—accurate labeling on every drum, batch certificates with clear analysis, shipment tracking that keeps users up to date whether they’re importing or storing for local use. We keep close communication with freight and hazard-goods carriers, tracking product down to the last kilometer, so delays or temperature excursions are flagged early. All documentation accompanying the product includes careful instructions for storage and shelf life, based on what our partners in chemical logistics have shown us in practice.

    We understand that chemicals like this introduce hazards, from skin and eye irritation to potential environmental impacts in case of leaks. Our years of process development have taught us the value of engineering controls—closed handling, high-efficiency ventilation, and full PPE for our workers. Downstream users receive up-to-date SDS, along with advice and process notes based on our own plant lessons. Regular internal training and drills prepare our team not just for routine handling, but for emergency procedures and accident prevention. Our aim isn’t just to ship product, but to make sure anyone using our chemicals has a partner looking out for safety at every step.

    Issues in Global Supply and Collaborative Solutions

    The last few years have shown how tightly chemical supply links are woven together. Market instability, supply chain disruptions, and energy price shocks all hit producers of specialty aromatics like 1-Bromo-4-Tert-Butylbenzene. Sourcing bromine, maintaining uninterrupted raw material flows, and weathering regulatory delays all draw on practical experience and committed supplier partnerships built over decades. There’s no shortcut here: disruptions down the line always feed back into availability and lead times for this compound.

    Facing material shortages and logistics problems, we’ve responded not by cutting standards, but by deepening our raw material supplier network and building inventory where possible. This pays off for customers who value regularity and planning. We field requests for short lead-time deliveries or sudden scale-up batches, and our production planners maintain flexible scheduling so that emergencies or late-stage project adjustments can be met. To do this, we run regular risk assessments with supply partners and transportation teams, checking everything from forecasting for bromine delivery, to packaging stock, to specialized transport permits for dangerous goods.

    Our strategy for the future includes digital order tracking, regular open communications with customer procurement teams, and plant investments in energy-saving processes. Experience with equipment upgrades—swapping out legacy chlorination lines for catalytic bromination, honing solvent recycling—helps us keep production viable and costs controlled, even as raw material fluctuations chew at margins. By talking directly with end-users about what features matter—particle size, dryness, purity—we avoid wasting time on specs that offer no benefit and focus on the ones that drive real application value.

    Collaborating directly with users in pharma, materials science, and specialty chemistry has changed how we define our targets. Early feedback from development teams pointed us to tweak purification—extra washes, tighter cuts in distillation—and it’s made a difference batch over batch. We keep samples on hand, ready for customer re-testing, and always take feedback through plant visits and lab exchanges seriously. Instead of waiting for a complaint, our teams invite dialogue, gather real performance data, and push right back into process improvements for future runs.

    Building Trust Between Manufacturer and Customer

    Delivering 1-Bromo-4-Tert-Butylbenzene means more than moving a reagent down the supply chain. It’s about trust. End-users in demanding industries choose suppliers who demonstrate transparency, technical depth, and reliability. Decades of plant experience tell us the users who reach out, ask tough questions, and demand documentation are the partners who push us to maintain our edge. We welcome audits, technical exchanges, and continuous feedback, whether it’s about a stray impurity, a shipping glitch, or even minor packaging issues. Big outcomes rest on these small details.

    Looking across our years in this field, we see that each successful batch reflects not just technical skill, but ongoing learning from handling problems, customer input, and evolving market or regulatory trends. Better technology, from analytical tools to process reactors, only works well when people behind them care about outcomes, not just yield or throughput. We recruit plant personnel who want to become experts, not just operators, and provide them with the training and support to grow that expertise over the years.

    Through all this, the team behind our 1-Bromo-4-Tert-Butylbenzene continues to focus on why it matters: delivering a product that lets researchers, process engineers, and formulators rely on each kilo for the next breakthrough or smooth scale-up. By keeping our processes open, investing in robust systems, and learning from every run, we step up to the challenges that come with producing fine chemicals at scale. The commitment to real-world application and customer partnership moves us forward—batch by batch, year after year.