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HS Code |
596097 |
| Product Name | 2-Bromo-4'-Methylacetophenone |
| Cas Number | 26137-42-2 |
| Molecular Formula | C9H9BrO |
| Molecular Weight | 213.08 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 42-45°C |
| Purity | Typically ≥98% |
| Smiles | CC(=O)C1=CC=CC(Br)=C1C |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Storage Temperature | Store at 2-8°C |
| Synonyms | 1-(2-Bromo-4-methylphenyl)ethanone |
As an accredited 2-Bromo-4'-Methylacetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g quantity of 2-Bromo-4'-Methylacetophenone is packaged in a sealed amber glass bottle with a tamper-evident screw cap. |
| Shipping | 2-Bromo-4'-Methylacetophenone is shipped in tightly sealed, chemical-resistant containers to prevent leakage. It is packed according to hazardous material regulations, including appropriate labeling and cushioning. Transportation occurs via certified carriers, ensuring compliance with safety and environmental guidelines. Shipping documentation includes safety data sheets and hazard identification, supporting secure and responsible handling during transit. |
| Storage | 2-Bromo-4'-Methylacetophenone should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizers. Keep it away from moisture and sources of ignition. Properly label the container, and follow all safety guidelines for handling hazardous organic compounds. Store at room temperature if no specific conditions are stated. |
Applications of 2-Bromo-4'-Methylacetophenone in Industrial Manufacturing2-Bromo-4'-Methylacetophenone supports several specialized downstream sectors as a key functional building block for targeted chemical synthesis. Our production specifications meet sustained quality benchmarks required by leading industrial customers. Find below detailed application scenarios, process integration notes, and typical industry usage metrics for this material. 1. Pharmaceutical Intermediate SynthesisThis compound serves as an advanced intermediate in active pharmaceutical ingredient (API) synthesis, especially within antihypertensive and neuroactive agent development. Chemical teams utilize its bromoacetyl moiety for selective coupling in complex molecules requiring high regioselectivity and purity. We recommend controlled addition based on stoichiometry and reaction stage to ensure yield consistency and final batch traceability. Industry compliance standards
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2. Agrochemical Active Ingredient ManufacturingResearchers and technical production teams in crop protection use this raw material for targeted bromination in the synthesis of herbicide and fungicide backbones. The compound’s reactivity allows controlled introduction of functional groups, supporting derivatives that meet regulatory limits for minimal residuals and maximum bioactivity. Environmental and worker exposure protocols determine permissible handling procedures at this stage. Industry compliance standards
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3. Advanced Dye and Pigment IntermediateOur material is widely adopted in colorant intermediate manufacturing, where its precise functional group arrangement enables selective further reactions such as azo-coupling and Friedel-Crafts acylation. Quality control focuses on minimizing contamination from unreacted halides and consistent chromophore build-up. Specialty dye producers rely on validated processes to ensure compatibility with environmental and product safety standards. Industry compliance standards
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4. Fragrance and Aroma Intermediate ProductionFragrance compound manufacturers utilize this ketone derivative for the synthesis of specific musk and aromatic bases used in perfumery and cosmetic formulations. The compound enables high-yield acylation reactions, securing product purity that aligns with IFRA safety guidelines. Specialized blending tanks and dedicated pipelines prevent cross-contamination with unrelated fragrance notes. Industry compliance standards
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5. Fine Chemical Building Block in Specialty Chemical SynthesisThis specialty molecule supports custom synthesis of advanced fine chemicals, especially for research and pilot-scale specialty applications. Chemists employ the compound for precision alkylation, halogen exchange, and subsequent structural modifications, delivering tailored end-molecules required by the electronics, analytical, and polymer modification sectors. All production campaigns include rigorous batch release analysis. Industry compliance standards
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In chemical manufacturing, consistency means everything. 2-Bromo-4'-Methylacetophenone is no exception. The way we produce this compound isn’t just about ticking boxes for compliance—the integrity of every batch lives under the microscope, literally and figuratively. With every order, the demand for reliability grows, especially for intermediates used in pharmaceuticals and advanced organic synthesis. We're well-familiar with the special care this molecule requires during production, storage, and transport.
Seeing the attention customers give to purity levels, we've committed to offering 2-Bromo-4'-Methylacetophenone with specifications that reflect real-world lab needs. Each batch runs through high-performance liquid chromatography, confirming impurities down to trace levels. This intermediary is not an off-the-shelf commodity, but a product refined by careful process design. We keep the melting point controlled, avoid moisture ingress, and package under an inert atmosphere. Such practices aren’t optional extras; they’re safeguards built from decades of close calls and successes alike in bulk and specialty chemical synthesis.
Looking at the molecular structure—C9H9BrO—brings a set of physical requirements. 2-Bromo-4'-Methylacetophenone presents as a white to off-white solid at room temperature, with a characteristic acetophenone odor. Analytically, we've narrowed the melting range down to a reliable window around 52-56°C, with each lot checked upon packing. Our spectroscopic data check for minor tautomers, since many end-users, particularly pharmaceutical researchers, do not flex around unexpected peaks in their analyses. By keeping water content below 0.5% and purities at or above 99%, we've seen a drastic drop in downstream process interruptions.
We synthesize 2-Bromo-4'-Methylacetophenone using a bromination pathway supported by stoichiometric tuning, rather than brute-force excess reagent methods. This cuts waste and ensures that the final product can integrate into medicinal chemistry research, custom peptide synthesis, and agrochemical routes. Since the compound’s role often lies as a building block in more complex syntheses—like the production of substituted benzylamines or aryl ketones—each contaminant, moisture trace, or color impurity risks throwing off multi-step research programs. An intermediate like this sees heavy use in both pilot plants and small-scale optimization runs, so reliability is measured by the number of times customers tell us they ran a reaction without purification mid-stream.
One point routinely asked about is why not just use 2-Bromoacetophenone, or any other similar bromo ketone? The answer, from years of hands-on synthesis, comes down to selectivity and outcome in key reactions. The methyl group at the para position does more than shift melting points; it has real impact on reactivity for Friedel–Crafts acylations or coupling reactions. In pharmaceutical or crop protection research, differences might seem minor on paper, but they show up as dramatic shifts in yield and byproduct profiles.
We see that 2-Bromo-4'-Methylacetophenone provides greater regioselectivity in most ortho-directed transformations. The methyl group can block undesired substitutions, raising the probability of successful downstream conversion. Our long-term users—ranging from university research groups to multinational pharma—have repeatedly cited the compound’s role in improving reproducibility over simpler bromoacetophenone analogs. When comparing stability, the para-methyl substitution reduces sensitivity to oxygen or light somewhat, extending shelf life under ordinary storage. Sometimes that margin makes or breaks a month-long synthetic route.
Real feedback comes from the bench. Organic chemists in R&D value this intermediate for its ability to serve as a masked nucleophile or electrophile depending on conditions, often appearing as a key branching point in synthetic maps. Peptide engineers look to acylate amine-functionalized scaffolds with it, aiming for selective mono-alkylation without scrambling their product slate. Others leverage 2-Bromo-4'-Methylacetophenone as a precursor to biologically active heterocycles, adding value that flows into antimicrobial, antiviral, and anti-inflammatory candidates.
One frequent usage scenario: Suzuki-Miyaura and Buchwald-Hartwig couplings. We have seen several process groups adopt our material to construct biaryl or aryl-amine frameworks, skipping over issues tied to less selective brominated sources. Downstream, this impacts process economy—less need for post-reaction purification, more predictable scale-up to the pilot plant, and fewer failed batches.
Other industries, including flavors, fragrances, and specialty polymer research, take advantage of the molecule’s dual reactivity at both the keto and bromide positions. This enables stepwise grafting or modification without premature side reactions. The methylated variant of bromoacetophenone outperforms the unsubstituted variant in stability assays, allowing more comfortable handling in facilities less accustomed to volatile, unstable intermediates.
Experience has taught us that acetophenone derivatives can pose shipping headaches. Moisture wicks in—even through micro-cracks—and ruins months of warehouse stability. Strict controls on water content and air exposure prevent caking or slow decomposition. By nitrogen-purging bags, using double-lined containers, and storing away from direct light, we've consistently preserved both purity and color. End-users repeatedly voice relief when opening packages weeks after shipment, finding a free-flowing, uncontaminated product.
Logistics teams lean on tried-and-true inner packs that eliminate the brittle packaging issues of years past. Temperature doesn’t swing the way it does with more volatile analogs, meaning both global and cross-region deliveries reach clients without unexpected product degradation. We follow these measures out of necessity; early failures taught us that compromised batches lead to lost business and erode trust faster than any supply chain mishap.
Supplying 2-Bromo-4'-Methylacetophenone draws us into active and ongoing relationships with research staff and process development engineers. FAQ lists rarely solve real issues—they want assurance from people who actually make the material, not just repack it. Over the years, we've been drawn into discussions about tweaking synthetic steps, adjusting lot sizes for semester projects, and supporting troubleshooting by sharing spectral data and historical batch notes.
Quality assurance doesn’t rest on batch certificates alone. We supply detailed NMR and HPLC runs with every order, and stand behind the spectra our customers trust. Post-sale feedback loops—especially following process failures or unexplained results—let us refine both analytical processes and production methodology. Everyone learns from root-cause analyses; each batch history writes the next chapter in what repeat clients expect from us.
Participants in large-scale programs sometimes run 2-Bromo-4'-Methylacetophenone through automated synthesis robots or continuous flow reactors. Through their feedback, we've helped develop best practices for rapid dissolution, minimizing line blockage, and ensuring cross-compatibility with polymeric catalyst systems. These lessons translate into fewer stoppages, smoother tech transfers, and regular acknowledgment of lot-to-lot consistency.
Raw bromine chemistry poses significant worker safety and environmental risks. Early iterations of our manufacturing workflow used excess bromine, causing headaches for both plant crews and local air quality monitors. Process changes toward more selective reagents and enclosed reactor systems have reduced risk. By capturing bromine off-gasses and recycling solvents, we maintain compliance with increasingly stringent local guidelines and cut down both direct and hidden operating costs.
Persistent demand for greener chemistry keeps our process engineers iterating. We continue to evaluate new catalysts and alternative feedstocks to further curb hazardous waste. Wastewater coming off 2-Bromo-4'-Methylacetophenone runs today leaves our factory with lower halogen content than a decade ago. These steps aren’t simply motivated by law, but by downstream customer inquiries and our own desire to leave a better legacy than we found.
Experienced line operators push every batch through controlled temperature ramps, mindful that overheating risks undesired rearrangements or byproduct spikes. Our analytics crew works with small, daily samples, checking color and purity before consolidating production lots. Reduced use of energy-intensive steps has paid off in lower per-kilo emissions. Each technical improvement in production lives under shared scrutiny—managers, chemists, and supply chain staff—because no one shoulder carries the burden of modern chemical stewardship.
No product survives solely on technical specs. In our early years, customers called with issues: poor solubility, color changes under storage, unexpected boil-off. Each complaint became a prompt for process upgrades. In one discovery, we realized that certain stabilizers added to counteract bromine volatility reacted badly in peptide coupling reactions; we pivoted toward inert gas blanketing as a result. Instead of patches, we redesigned.
Inconsistent lots posed repeated issues for academic labs, where a one-off experiment relies on tight deadlines and even tighter grant budgets. Our solution lay in QA sheets stapled right onto each container—date, run number, full spectroscopic profile. This way, no one stands in the dark about the batch they're using. Customers returned, crediting us for product traceability when replicating literature protocols.
As markets change, we stay close to the front lines. More clients treat specialty intermediates like core R&D reagents, not just commodity trade goods. This raises the bar for all of us. Expectations for documentation, environmental compliance, and customer support keep rising. Rather than lower standards, we’ve deepened investment in analytical capabilities, staff education, and quality control system upgrades.
We envision 2-Bromo-4'-Methylacetophenone fitting within a broader push for specialty molecules that serve tomorrow’s biopharma, advanced materials, and green chemistry goals. The shift toward continuous processing and automation on the customer side makes consistency and transparency not just desirable, but essential. More users ask for real-time lot data before purchase. This transparency helps everyone in the supply chain spot mismatches before they block months of research or drive up rework.
We acknowledge that no molecule, not even a niche intermediate, stays frozen in its use case. End-users continually explore new synthetic transformations—one year, it’s leveraged in traditional cross-coupling; the next, it’s the gateway substrate for a photo-redox catalyzed sequence. Our role as a manufacturer grows with these evolutions, as does our responsibility for providing materials that don’t confound research or pilot-scale trials.
What sets a manufacturer apart isn’t just technical proficiency, but willingness to engage in candor and problem-solving with those downstream. Every batch heading out our loading bays carries with it not only the result of synthetic mastery, but the real-world lessons of troubleshooting, iterative process change, and dialogue with practicing chemists. This exchange of information, often informal and project-driven, seeds improvements—crystal morphology, packaging resistance, or new detection limits—guided less by paperwork, more by practical know-how.
Manufacturing 2-Bromo-4'-Methylacetophenone underscores how specialty chemicals production thrives on teamwork. We know the routes, pitfalls, and workarounds because we've run the reactors, pulled the samples, and heard the feedback. From specification tweaks to shipping solutions, product improvement emerges directly from honest collaboration.
Looking past buzzwords, production of 2-Bromo-4'-Methylacetophenone lives at the intersection of chemistry, logistics, and trust built on lived experience. We translate feedback from process engineers and bench chemists into tangible changes—deeper QA, steadier supply, and avoidance of shortcuts that compromise end goals. We focus on the practical differences that methyl substitution makes for reactivity, on the challenges of scaling shipments safely, and on the days spent revisiting our own SOPs after each unexpected incident.
Each kilogram is a joint result: trained hands, decades of trial and error, and respect for a field where details often decide outcomes. The future for intermediates like 2-Bromo-4'-Methylacetophenone will reward not only process innovation, but also close partnerships between those who make and those who create with it. As demand for specialized intermediates grows, so does our commitment to listening, learning, and supplying exactly what research and production demand. Nobody at the plant has time for empty guarantees—we’re too busy living the reality our customers face every day in their work.