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HS Code |
740190 |
| Cas Number | 3964-84-1 |
| Molecular Formula | C11H15Br |
| Molecular Weight | 227.14 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Melting Point | -6 °C |
| Boiling Point | 252-254 °C |
| Density | 1.188 g/cm³ at 25 °C |
| Refractive Index | 1.541 |
| Purity | Typically ≥98% |
| Solubility | Insoluble in water, soluble in organic solvents |
| Synonyms | 1-Bromo-4-(tert-butylmethyl)benzene |
| Flash Point | 109 °C (closed cup) |
| Storage Conditions | Store at room temperature, tightly closed, in a dry and well-ventilated place |
As an accredited 4-Tert-Butylbenzyl Bromide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of 4-Tert-Butylbenzyl Bromide is supplied in a sealed amber glass bottle with a tamper-evident cap and hazard labeling. |
| Shipping | 4-Tert-Butylbenzyl bromide is shipped in tightly sealed containers to prevent moisture and light exposure. It is packaged in accordance with hazardous material regulations, typically in chemical-resistant bottles within rigid outer packaging. Appropriate labeling, documentation, and handling precautions are ensured for safe transportation, complying with international and local shipping standards. |
| Storage | 4-Tert-Butylbenzyl Bromide should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and moisture. Protect it from light and avoid exposure to heat sources. Store under inert gas if possible, and label the container clearly. Use secondary containment to prevent spills or leaks. |
Applications of 4-Tert-Butylbenzyl Bromide in Industrial Manufacturing4-Tert-Butylbenzyl Bromide serves as a key intermediate in multiple specialized industrial verticals, supporting downstream synthesis in fine chemicals, advanced polymers, agrochemical actives, and pharmaceutical intermediates. Below, we detail major application avenues with specific compliance, formulation, process integration, and end-market product information. 1. Synthesis of Active Pharmaceutical Ingredient IntermediatesThis compound enables targeted benzylation steps in the synthesis of selective API intermediates, particularly for antihypertensive and CNS pharmaceutical classes. Process chemists employ controlled alkylation to introduce the tert-butylbenzyl group into aromatic scaffolds, essential for building functionalized molecules with increased bioavailability and specific pharmacological profiles. Production must observe material track-and-trace and impurity control to remain within regulated pharmaceutical parameters. Industry compliance standards
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2. Manufacture of Functional Polymers and Specialty ResinsThe tertiary-butylbenzyl group acts as an advanced building block in the polymerization of specialty resins and thermoset systems where specific aromatic substituents improve thermal stability and chemical inertness. Producers use the raw material in alkylation or as an initiator within bulk or solution polymerization systems, driving performance improvements in engineered plastics and coatings used in electronics and automotive assemblies. Industry compliance standards
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3. Synthesis of Agrochemical Active Ingredients and IntermediatesProduction lines employ 4-Tert-Butylbenzyl Bromide as a benzylation reagent in the synthesis of pre-emergent and post-emergent herbicides, certain fungicidal intermediates, and plant growth regulator precursors. High reaction selectivity is critical to maintaining downstream actives profile and meeting residue control measures for safe crop application. Industry compliance standards
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4. Chemical Synthesis of Fragrance and Specialty Aroma CompoundsFragrance compound manufacturers utilize the raw material for introducing tert-butylbenzyl motifs into aldehydes and nitriles in aroma molecule synthesis. Controlled bromination and subsequent coupling steps ensure that aroma profile consistency remains within tight sensory specifications, critical for fine fragrance formulation and high-volume household products. Industry compliance standards
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5. Raw Material for Quaternary Ammonium Compound SynthesisChemical production facilities employ this bromide to synthesize specialty quaternary ammonium compounds, essential as antistatic additives, phase transfer catalysts, and biocidal agents. Reactivity and selectivity at elevated temperatures require sophisticated feedstock handling and close titration monitoring, ensuring the resulting quaternaries meet purity profiles demanded in electronics and water treatment sectors. Industry compliance standards
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Within the world of specialty chemicals, 4-Tert-Butylbenzyl Bromide plays a vital role in organic synthesis, pharmaceutical intermediates, and specialty polymer applications. Its appeal isn’t just in what the molecule can do—it’s found in the details of its structure, the reliability of its performance, and the added value that direct manufacturing brings to every stage of its life cycle.
The backbone of consistent quality starts in our synthesis process. 4-Tert-Butylbenzyl Bromide, with the chemical formula C11H15Br, emerges from carefully controlled alkylation and bromination steps. Each batch reflects the expertise gained from years of hands-on production. We have focused fanatically on purity. At every stage, we draw samples and run analyses—NMR, GC-MS, HPLC—to guarantee levels above 99% where possible. Impurities, such as dibromo- or isomeric compounds, can complicate downstream synthesis, especially for pharmaceutical or electronic industry use. By tightening production controls and rejecting off-spec materials, we deliver both predictability and value to chemical engineers counting on our reagents.
The fine white crystalline form or occasionally faintly beige crystals never appear by accident. Raw material quality, temperature control, and exact reagent addition determine crystal habit and ease of handling. Those “small” variations are meaningful in the plant, lab, or formulation room. Product that packs well, dissolves cleanly, and stores without agglomeration is the result of repeated small improvements in filtration, drying, and size reduction.
Across the spectrum of benzyl bromides, the tert-butyl-substituted derivative carves out a unique spot. Compared to unsubstituted benzyl bromide, the bulky tert-butyl group shields the aromatic ring and enhances selectivity in alkylation reactions. In research and pilot plants, this makes a difference. Highly pure 4-Tert-Butylbenzyl Bromide can alkylate nucleophiles like amines, alcohols, or thiols with greater control, leading to fewer by-products. For customers scaling up to commercial syntheses, these savings in purification costs justify the extra attention—and justify working with manufacturers who know these subtleties.
Consider the needs of pharmaceutical process chemists. The choice of alkylating agent often comes down to reactivity, residue profile, stability, and regulatory status. While benzyl chloride might initiate reactions faster under some conditions, benzyl bromides like our 4-Tert-Butylbenzyl Bromide introduce less risk of over-chlorination or residual chloride interfering with sensitive APIs. The difference becomes pronounced in scale-up, where even tenths of a percent in impurity profile or residue add up to regulatory headaches and batch failures.
Our facility produces 4-Tert-Butylbenzyl Bromide to specifications honed through extensive in-house and customer testing. Typical analysis yields minimum purity of 99%. Moisture control is stringent—the compound’s stability against hydrolysis matters for both storage and use—so we validate every batch’s water content via Karl Fischer titration. We select only low-odor lots; even trace by-product presence can signal unwanted side reactions or plant process drift.
We found that customers working in advanced polymers request narrow particle size distributions or particular crystalline forms to improve dissolution in certain solvents. By re-tooling crystallization tanks, optimizing cooling rates, and designing custom sieving operations, we answer these needs directly. This is not simply a compliance exercise. Each specification revision results from close dialogue between our technical team, process control chemists, and end users tackling unexpected snags on the shop floor.
Beyond regular 4-Tert-Butylbenzyl Bromide (CAS 770-69-6), we occasionally develop tailored variants in cooperation with academic groups or innovators in the electronics sector. Those projects teach us new handling, packaging, and analytical insights, feeding back into the standard product. By keeping both mainline and specialty variants under one roof, we hold ourselves to a higher level of accountability—every tweak aims for measurable benefits in yield, safety, or shelf life.
Consistent bromination reactions take vigilance. We’ve witnessed how an otherwise steady process can shift quickly, responding to slight changes in temperature, mixing, or the purity of starting materials, such as tert-butylbenzyl alcohol or bromine. To keep color and bromide content precisely on target, we set up in-line monitoring. Sampling automation and real-time spectrometric feedback help us spot deviations early—and fix them before they scale into costly waste or difficult rework batches.
Reactivity profiles distinguish our benzyl bromides from bulk, off-the-shelf grades. Customers switching from standard benzyl bromide sometimes report delayed reaction times or inconsistent conversions. These insights led us to invest in process improvements for tighter control over unreacted starting materials and organic impurities. A small fraction of a single brominated by-product can spell repeated headaches in process optimization for researchers and production engineers. Meeting their demands required more than changes to the reactor jacket or the raw material filters. It meant committing to regular method reviews—auditing not just compliance but hands-on work practices—so that the end result holds up even after months in storage or long international shipments.
The use cases for 4-Tert-Butylbenzyl Bromide have expanded well beyond early research days. Its alkylating power tailored for selective functionalization underpins the synthesis of several specialty intermediates. In pharmaceutical research, it supports the introduction of the tert-butylbenzyl group in drug candidates, giving rise to better controlled metabolic pathways, increased lipophilicity, or improved target binding.
In polymer chemistry, this compound finds use in the controlled preparation of functional resins, especially those requiring chemical resistance or specific surface characteristics. Silane-modified or functionalized polymers often rely on benzyl-type alkylation for crosslinking or side-chain modification. By using a tert-butyl-substituted structure, chemists tune polymer performance for adhesives, coatings, or elastomers exposed to harsh processing environments.
Between fine chemicals, crop science intermediates, and pilot-scale novel material production, our regular customers span a large range of industries. We’ve fielded requests from laboratories seeking efficient means to introduce tert-butylbenzyl groups as protecting agents, as well as from electronics firms using the material for advanced molecular assemblies. Each segment challenges us to raise the bar—on purity, analytical depth, batch documentation, and responsiveness to questions about the synthesis route.
Having handled a portfolio of alkyl halides for many years, we can speak candidly about distinctions that become clear only through practical use. While simple benzyl bromide offers indispensable functionality in many reactions, substituting the tert-butyl group fundamentally shifts both physical properties and chemical reactivity. The increased molecular volume changes both handling properties and the types of selectivity achieved in synthesis. Thermal stability improves; volatility is reduced compared to unsubstituted benzyl bromide, which matters in large-scale processing.
Practitioners report less odor and reduced side reactions when scaling up with 4-Tert-Butylbenzyl Bromide compared to lighter analogues—contributing to a safer operator environment and fewer post-reaction purification cycles. Outgassing and exotherm control on alkylation reactions show marked improvement, simply because the extra bulk at the para-position of the benzene ring tunes the kinetics and energy profile.
Among benzyl halides, the bromide atom serves as a sweet spot—activating the benzyl group for nucleophilic substitution while balancing shelf-life stability and safe handling. The variations in solubility and melting point tune formulation ease for customer-specific protocols. Where crude or technically pure alternatives may fail to meet these process or application goals, our high-purity, physically consistent batches allow scalable, reproducible chemistry.
We support a broad range of projects, so we hear stories every week. A research chemist scaling up from a few grams to kilogram-quantities of a specialized material discovers small but critical handling differences compared to bulk benzyl halides. Moisture control and crystal size become more than lab curiosities—they can define success. Polymers processing teams want “just enough flow” without dusting and demand consistent reactivity with minimal waste. Electronics firms need rigorous guarantees that each batch avoids problematic ions or reaction residues. These conversations drive the technical tweaking behind each batch.
Some customers struggle with curveballs: a pilot synthesis that ran well on one supplier’s batch suddenly fails after a switch, or an impurity profile unexplained by published data gums up HPLC traces in a new intermediate. We’ve learned to keep communications clear and analytical data flowing—never hiding behind vague performance claims or unexplained formulation changes. The lessons we take shape the continuous improvements in our facility, from double-sealed drum closures to improved spectral fingerprinting and support for post-shipment inquiries.
Anyone in the chemical industry knows supply chain hiccups arise from far more than shipping schedules. Reliable 4-Tert-Butylbenzyl Bromide supply starts from certainty in raw materials sourcing, tight alliances with logistics partners, and living up to the highest standards for batch reproducibility. In reality, deviations must be anticipated before they reach production lines. We proactively share technical bulletins, update quality agreements, and maintain dual-validated equipment streams to ensure uninterrupted deliveries, regardless of external disruption.
Having a direct manufacturing and technical support channel eliminates much of the uncertainty customers dread. If a freight delay threatens an urgent lot, or a new application requests unique drying conditions, direct line dialogue with our engineering and compliance staff brings fast, practical responses. Over time, this relationship-driven supply chain benefits everyone: fewer lost batches, reduced inventory risk, and nimble adaptation to regulatory or market-driven changes.
We recognize customers must comply with ever-tightening documentation and analytical requirements. Each batch ships with a full suite of analytical results—purity profiles, chromatograms, spectra—satisfying all common reporting standards without room for guesswork. If downstream process teams need additional insight—say, trace residual solvents content or analysis of potential by-products on specialized columns—our laboratory opens its data and methods for scrutiny.
This culture of openness flows naturally from manufacturing the product ourselves. There’s no ambiguity in records or origins: raw materials batches, production date, process steps, and QA records remain documented from initial charge to final packaging. This builds deep confidence in both technical and regulatory discussions, improving collaborations for those customers commercializing new molecules or running validation batches in GMP environments.
The hazards associated with alkyl halides are well known; 4-Tert-Butylbenzyl Bromide is no exception. Longevity in this business requires relentless attention to packaging quality and end-user safety. Sealed, chemical-resistant containers, clear hazard warning labels, and lot-specific documentation are the norm. The subtle differences between technical and high-purity grades sometimes surface here: the “clean” packaging assures users there’s been attention beyond just product synthesis.
Supporting safe usage means every drum, bottle, or bulk package offers controlled opening, detailed handling guidance, and access to our technical team for any application-specific concerns. As overwhelmed storage teams or hurried operators sometimes miss a critical label or SDS update, we take it as our job to bring clear, plain-language instructions alongside every shipment.
Efforts to reduce environmental impacts ripple through our facility. Our bromine usage protocol prioritizes maximum recovery and reuse, while our spent solvent handling prevents unnecessary emissions or hazardous buildup. Critical waste streams undergo continuous monitoring, and off-gassing from bromination stages is tightly controlled. Each improvement trickles down—not just as a line on a sustainability report, but as a more predictable supply of product without environmental compliance surprises for our customers.
We also track packaging lifecycle and shipping safety—directly responding to customer requests for reusable containers and returnable bulk drums. More than public relations, these changes emerge from realizing that cleaner processes, less waste, and steady product quality ultimately benefit downstream operations just as much as our own margins.
Manufacturing 4-Tert-Butylbenzyl Bromide is more than a chemical reaction—it's a sum of thousands of process decisions, risk controls, and direct customer connections. Companies building new molecules, refining polymer systems, or optimizing specialty syntheses keep returning to us because they value how direct conversation clarifies technical barriers and delivers real solutions for the challenges at hand.
Over time, the difference between direct manufacturer and anonymous supplier becomes clear. Customers get answers—even on arcane technical points or regulatory gray areas—that only those running the reactors and managing the QA labs can provide. This isn’t theoretical; we often assist in de-bugging processes gone awry, rapidly customize drum sizes, or develop new analytical methods that match up with a client’s workflow or approval cycle.
Almost every week brings new projects—novel applications in life sciences, electronics, or high-performance polymer sectors that weren’t imaginable just a few years ago. The understanding acquired from manufacturing, controlling, and analyzing each batch positions us to support these emerging needs—often before a customer can clearly articulate the scope of their next synthesis challenge.
No two days are quite the same at our production site. Sometimes, the work means scaling up a new intermediate at a moment’s notice; sometimes, it’s documenting subtle tweaks to our analytical standards. What remains unchanged is the satisfaction of knowing our 4-Tert-Butylbenzyl Bromide stands up in the world’s most demanding environments—reliable, pure, and backed by real expertise at every step. For those building the next generation of chemistry, that difference becomes tangible where it matters most: on the shop floor, in the test reactor, or at the bench, turning scientific ideas into commercial reality.