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HS Code |
562613 |
| Chemical Name | 1-Bromo-2-(1-methylethyl)benzene |
| Molecular Formula | C9H11Br |
| Molecular Weight | 199.09 g/mol |
| Cas Number | 574-98-1 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 213-215 °C |
| Melting Point | -30 °C |
| Density | 1.32 g/cm3 |
| Refractive Index | 1.543 |
| Flash Point | 95 °C |
| Solubility In Water | Insoluble |
| Structure | Bromine substituted isopropyl benzene |
| Smiles | CC(C)C1=CC=CC=C1Br |
As an accredited 1-Bromo-2-(1-Methylethyl)Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 mL of 1-Bromo-2-(1-Methylethyl)Benzene, tightly sealed, labeled with hazard and handling information. |
| Shipping | 1-Bromo-2-(1-Methylethyl)Benzene is shipped in tightly sealed containers to prevent leaks and contamination. It should be handled as a hazardous material, kept away from heat, sparks, and incompatible substances. Transportation must comply with local, national, and international regulations for hazardous chemicals, ensuring safety for handlers and the environment. |
| Storage | 1-Bromo-2-(1-methylethyl)benzene should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizing agents. Protect from light and moisture. Ensure appropriate labeling and safety measures to prevent accidental exposure, and store in accordance with all applicable regulations and guidelines. |
Applications of 1-Bromo-2-(1-Methylethyl)Benzene in Industrial Manufacturing1-Bromo-2-(1-Methylethyl)Benzene serves as a critical intermediate in several industrial chemical syntheses, especially for the fine chemical, agrochemical, and specialty materials sectors. Our facility produces this compound with high consistency to match the strict demands of each downstream user segment, integrating seamlessly into advanced manufacturing processes. 1. Pharmaceutical Intermediate SynthesisMany active pharmaceutical ingredient (API) manufacturers utilize this compound as an aryl bromide precursor in cross-coupling and substitution reactions. It enables introduction of isopropylphenyl groups into complex molecules—key for certain non-steroidal anti-inflammatory drugs (NSAIDs) and antihistamines. Controlled halogenation and purity levels are vital for ensuring compliance with health authority standards, as the conversion proceeds under mild to moderately basic conditions in batch or continuous reactors. Industry compliance standards
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2. Agrochemical Active Ingredient ProductionKey crop protection manufacturers use this molecule to introduce isopropylphenyl motifs or as a halogen source during synthesis of herbicides and fungicides. The compound fits chlorination/Buchwald-type amination blocks, allowing flexibility in tailoring substitutions on aromatic rings. All procedures remain under Agrochemical industry-specific environmental and worker safety standards, using both batch and continuous-flow synthesis lines. Industry compliance standards
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3. Liquid Crystal Material SynthesisManufacturers of specialty liquid crystals for display technologies employ this compound to construct mesogenic intermediates. The isopropyl and bromine substitutions facilitate precise tuning of physical and optical properties, critical for display panel quality. Stringent control of bromide purity and positional selectivity ensures compatibility during subsequent multi-step etherification, alkylation, or esterification reactions. Consistency supports high-yield integration into advanced LC panel materials. Industry compliance standards
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4. Fragrance and Aroma Intermediate ManufacturingIndustrial fragrance and aroma compound manufacturers leverage this material as a building block in the creation of specialty alkyl-aromatic molecules. Its structure introduces unique olfactory notes and enhances thermal stability in finished compositions. Precise bromination allows for downstream Friedel–Crafts or Grignard transformations, all under IFRA and general chemical safety protocols to ensure product traceability and formulation reliability. Industry compliance standards
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We’ve worked with halogenated aromatic compounds for decades and have seen 1-Bromo-2-(1-Methylethyl)Benzene establish its place in many advanced organic synthesis workflows. This compound, known to chemists for its structural reliability, offers a practical route to more complex molecular architectures. In a world where intermediates rarely stay the same for long, this compound reliably meets the demands in both scale-up and bench work. It’s found utility in pharmaceutical research, agrochemical development, and electronic materials—areas where consistency and reactivity make the difference between a headache and a finished product.
Looking at 1-Bromo-2-(1-Methylethyl)Benzene, its structure gives chemists the edge in designing new molecules. The bromine on the aromatic ring, ortho to an isopropyl group, brings unique reactivity to cross-coupling reactions such as Suzuki or Buchwald–Hartwig aminations. This layout sets it apart from more symmetrical bromotoluene or bromoxylene compounds. The isopropyl group steers both steric and electronic effects, opening up more pathways in catalyzed processes. Seasoned process chemists favor this kind of selectivity when planning routes to target molecules.
In our hands, batches of this compound come colorless with a faint aromatic odor distinct to halogenated benzenes. We’ve grown accustomed to its profile: density and boiling range land right where they should, and our in-house analytical checks keep off-spec product out of sight.
Over years of direct supply to contract manufacturers and innovators, the core uses have gravitated around C–C and C–N coupling. Medicinal chemistry teams have built on this backbone for lead compound exploration, especially in programs involving stepwise functionalization through halide displacement, lithiation, or Grignard chemistry. This isn’t hearsay—from kilo-lab requests to pilot plant technical queries, our technical team sees scientists rely on this molecule’s predictable performance.
1-Bromo-2-(1-Methylethyl)Benzene shows steady reactivity under transition metal catalysis, even when other ortho-substituted benzenes slow things down. Each batch we confirm by GC and NMR for the absence of residual solvents or regioisomeric impurities, ensuring the reactivity profiles don’t drop off between shipments.
Experience teaches us that choosing the right bromoarene can affect overall synthesis cost, waste, and time-to-delivery. While structurally similar compounds like 4-bromoisopropylbenzene or 1-bromotoluene have their places, they don’t always match the regioselectivity or the balance of steric and electronic influence that the ortho-isopropyl position provides. Some chemists using less hindered bromoarenes hit sidereactions or run into trouble with purification at scale. Others try isomers, see yields take a dive, or gadgets clog up downstream purification with by-products.
We’ve supported projects where using 1-Bromo-2-(1-Methylethyl)Benzene means less time debugging reaction conditions and more time steering new scaffolds toward biological screening. Isomeric distinctions that may look subtle on paper shift whole synthetic plans in practice, whether downstream chemistry involves strong bases, acid chlorides, or selective hydrogenations.
Since process conditions demand reliability, we tailor shipments for compatibility with common manufacturing solvents—toluene, THF, and dichloromethane. Our production line avoids introducing unwanted minor contaminants that could complicate workup or scale-up. Chemists can charge this compound directly into reactors with minimal pre-processing, often skipping labor-intensive pre-purification steps that other supplies might require. Over time, this workflow difference stacks up in lower labor costs, tighter cycle times, and more predictable downstream analytics.
Tight manufacturing controls and vigilant analytical follow-through have shaped our strategy toward this compound. While producers sometimes regard small halogenated aromatics as “commodity,” our operators watch for even slight shifts in color or odor that could signal reactions running off target. We cut down risk by running periodic reference standard checks and maintaining traceable batch records, so clients see lot-to-lot consistency. Last year alone, we collaborated with several partners who switched to our supply after inconsistent purchases elsewhere led to on-hold or out-of-spec batches.
The molecule’s physical stability shines at typical storage temperatures, and we review label guidance every production cycle to retain this record. Since some users look for microbially clean shipments for pharmaceutical intermediates, our internal q.c. ensures nothing accidental slips through. We don’t ship unless GC traces match our in-house purity targets (usually north of 99%) and no secondary isomers can be found by NMR and LC–MS.
Manufacturing halogenated aromatics always brings environmental considerations. The regulations keep tightening each year, and our facility prioritizes waste minimization throughout every lot. We run internal solvent recovery from isolation steps, reducing both cost and our firm’s output of halogenated waste. This makes our process less resource-intensive and offers our customers a cleaner conscience for their own environmental compliance checks.
Some resin-bound production routes and in situ scavenging techniques we’ve implemented have pushed by-product generation well below the threshold typical of legacy synthesis. In customer audits, this commitment to greener production often helps us win projects where the final product enters sensitive end-uses or faces scrutiny under environmental certifications.
Anyone familiar with handling aromatic bromides knows local regulations often shift with little notice. We keep our safety data current, revisiting every year as authorities issue updates around brominated solvents and intermediates. Our shipping and handling procedures are shaped by decades of close calls and lessons learned—full PPE in the loading bay, redundant venting, and spill containment—backed by incident logs and operator retraining.
A key aspect of safety isn’t just paperwork: operators at our site spot-check shipments before anything leaves for customer sites, especially after any process tweaks. Having experienced a handful of close calls in the early 2000s, we now maintain double-barrier storage and real-time temperature monitors in the warehouse. These practices have paid off, keeping regulatory fines and workplace incidents low.
Chemists at both small startups and established giants expect more than just off-the-shelf chemicals. They require responsiveness as batch requirements evolve, sometimes mid-project. Our technical support team has re-tooled production to accommodate larger orders, tighter impurity thresholds, or even adjusted physical parameters to better match new automation tools. Requests for different container types or extra analytical reports don’t get pushed to a “requests” inbox—they move straight to our plant supervisors, who’ve heard every unique processing challenge under the sun.
Recently, developers working on high-throughput screening requested adjusted concentration standards for their robots. We coordinated with their team to pack product in customized vessel sizes, cutting down on their prep time. Other cases called for nontraditional isolation to preserve specific reactivities. Flexible manufacturing isn’t just a promise—it’s something built into our daily workload.
Supply chain issues became the sore point for many R&D programs worldwide through the last few years. Sourcing reliability sets apart suppliers who run manufacturing in-house from those who rely on unpredictable third parties. Our own direct production gives us real visibility into inventory, helping us inform partners and redirect production with little lag. If a process chemist anywhere on the line comes back with questions or unexpected analytics, our plant staff answer directly instead of relaying queries through layers of salespeople.
Working with multinationals and nimble startups, we’ve seen that short, clear feedback loops sharply reduce downtime when technical clarifications arise. Having our own QC and analytical staff, trained not by podcasts but by walking the line and fixing real-world issues, makes problem-solving faster and supports steady progress in customer projects.
Over time, comparisons with other bromoarenes have put 1-Bromo-2-(1-Methylethyl)Benzene in sharper perspective. For certain coupling-based campaigns, process teams have reported cleaner transitions between steps than with meta- or para-isopropyl analogues. This can mean fewer awkward peaks on HPLC, less downstream purification, and improved yields on the bench and mid-scale plant alike. Chemists don’t need to lose sleep over unwanted side products sneaking in at the late stages of API production.
We’ve also compared this compound to bromotoluenes—another common choice in cross-coupling work—but found the ortho-isopropyl group improves selectivity and bulk characteristics, especially for hydrophobic building blocks. Some projects pivot from para- to ortho-isomers halfway through a multistep project after encountering stubborn process inefficiencies. Years of supporting chemists through those mid-course corrections has taught us to keep more of the ortho compound in close reach.
Whether it’s a kilo for a first-time route scouting run or multi-ton lots for industrial preparations, we scale output with full traceability. Our assignments have included everything from bulk supply for generics to tailored lots for specialty research projects. Our ongoing investment in automated handling, full-spectrum monitoring, and integrated logistics pays back in reliability throughout the order cycle. We ship by drum, pail, or bottle—staggered or expedited, according to project needs.
Project teams benefit most from clear, accurate batch records and open access to the chemists who oversee daily production. Our operators can walk through every step of their day, describe any tweaks applied, and recognize deviations with sharp instincts honed by years on the job. That institutional memory helps avoid repeat mistakes and supports concurrent troubleshooting with customer chemists.
1-Bromo-2-(1-Methylethyl)Benzene remains a vital node in the fast-moving world of science-driven manufacturing. As advances in drug discovery, crop protection, and specialty polymers continue, our production lines stay responsive to the creative uses our partners dream up. We spend ongoing time learning about new catalytic cycles, greener alternatives to halogenated intermediates, and innovative separation techniques. That background lets us suggest process improvements, anticipate possible pitfalls, and ensure that our shipments align with the realities of modern synthetic chemistry.
From our long view operating on the ground, success in this market depends on more than simply filling barrels. It’s service, technical insight, willingness to adapt, and hard-won lessons from real production lines that move laboratory plans beyond theory and deliver practical, trustworthy ingredients for tomorrow’s discoveries.