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HS Code |
736505 |
| Cas Number | 1731-85-3 |
| Molecular Formula | C9H9BrO2 |
| Molecular Weight | 229.07 |
| Iupac Name | 2-bromo-1-(3-methoxyphenyl)ethanone |
| Appearance | White to off-white crystalline solid |
| Melting Point | 54-56°C |
| Density | 1.53 g/cm3 |
| Solubility In Water | Slightly soluble |
| Smiles | COC1=CC=CC(=C1)C(=O)CBr |
| Synonyms | 3'-Methoxyphenacyl bromide; 2-Bromo-1-(3-methoxyphenyl)ethanone |
As an accredited 3'-Methoxyphenacyl Bromide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25-gram amber glass bottle securely sealed, labeled with hazard warnings and product details for 3'-Methoxyphenacyl Bromide storage and transport. |
| Shipping | 3'-Methoxyphenacyl Bromide should be shipped in tightly sealed containers, protected from light and moisture, and kept at controlled room temperature. It must be packed according to hazardous materials regulations due to its potential health and environmental risks. Ensure clear labeling and include appropriate safety documentation with the shipment. |
| Storage | 3'-Methoxyphenacyl Bromide should be stored in a cool, dry, and well-ventilated area, away from moisture and incompatible substances such as strong oxidizers and bases. Keep the container tightly closed and protected from light. Store in a tightly sealed, labeled container to prevent contamination and avoid exposure to heat and direct sunlight to ensure chemical stability and safety. |
Applications of 3'-Methoxyphenacyl Bromide in Industrial Manufacturing3'-Methoxyphenacyl Bromide plays a specialized role in a limited set of demanding downstream sectors, mainly as a reactive intermediate for synthesis in small-molecule manufacturing. Its utility is defined by strict adherence to regulatory standards, precise formulation ratios, clear integration points in production lines, and direct influence on high-value end products. 1. Pharmaceutical Intermediate SynthesisPharmaceutical manufacturers use this compound as a key alkylating agent in active pharmaceutical ingredient (API) synthesis, particularly in the construction of complex heterocyclic scaffolds and photo-cleavable protecting groups. The material enters workflows concerned with high-purity batch operations, requiring stringent impurity control, traceability, and documentation due to its influence on final product quality and regulatory certification demands. Industry compliance standards
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2. Agrochemical Active Ingredient ProductionCompanies producing selective herbicides and fungicides apply this raw material as a building block for synthesizing arylalkanone moieties within bioactive compounds. Its precise introduction supports consistent batch-to-batch performance, and documentation of compliance guides downstream certification for environmental compatibility and residue control. Industry compliance standards
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3. Photoinitiator and Photoresist ManufactureWithin the photochemistry sector, this material enables production of advanced photoinitiators and photoresist additives for microelectronics fabrication. Fabricators and formulators demand narrow impurity profiles and batch consistency for reproducible downstream lithography performance. Regulatory and EHS documentation is critical for export and in-fab regulatory declarations. Industry compliance standards
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4. Fine Chemical Intermediates for Fragrance IndustryIn specialty fragrance and aroma chemical synthesis, downstream producers utilize this compound to access protected ketone intermediates, which serve as key building blocks in musky and woody note molecules. Strict adherence to IFRA and regional chemical quality standards underpins all formulation, as well as tracking for final consumer safety certification. Industry compliance standards
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Years of hands-on process development have shown that 3'-Methoxyphenacyl Bromide (CAS No. 2631-55-0) remains a reliable choice for any chemist looking to introduce methoxy and bromide reactivity in a single step. In our own batch units, we produce this compound under controlled temperatures using verified raw material supplies, ensuring dust-free, sharp-melting crystals for downstream needs. The white-to-off-white solid is easily handled in standard lab or plant conditions. Custom lot sizing can be arranged for kilo-scale or modest R&D projects, and every batch receives structure confirmation using HPLC, GC-MS, and proton NMR, not just dry certificate paperwork.
You don’t always need glossy spec sheets. What matters: our 3'-Methoxyphenacyl Bromide targets a purity level over 99%. Moisture and impurity controls keep the risk of side-products down in scale-up routines. We consistently deliver a melting range of 49–51°C, limiting the chance of sticky residues during work-up, an issue we’ve seen with lower-cost imports. Every drum or bottle ships under nitrogen with the lot history traceable to raw receipt and process log. Monthly reevaluation checks flag any drift in physical or chemical properties, and shipments only leave our floor if they pass these tests.
Over the years, we’ve sent this compound to research operations, pharmaceutical process teams, and specialty polymer plants. 3'-Methoxyphenacyl Bromide functions most often as a photolabile protecting group for carbonyl groups, particularly when you need clean removal by UV or visible light irradiation. In-house, we have deployed it to temporarily mask functional groups during multi-step organics, especially in conditions where acid-sensitive substrates would decompose using harsher alternatives. The methoxy group at the meta position can dampen electron withdrawal, giving a bit more selectivity or stability compared to simple phenacyl bromide. When you’re running condensation or alkylation steps, this property shaves time off purification and cuts down on unwanted byproducts.
Staff chemists who have spent a decade handling various bromides can pick out differences in substrate compatibility and downstream reaction handling. 3'-Methoxyphenacyl Bromide offers finer control due to the resonance effects from its methoxy group. With methyl, ethyl, or chloro analogs, we see much less stability in some photoprotected intermediates, particularly in liquid-phase synthesis. Competitor products often include higher levels of unreacted starting material or colored impurities; the yellow tinge or odor may not matter in bench-scale tests but causes problems in plant reactors, especially during photolysis, where small color changes signal side reactions. Our process improvement crew optimizes the work-up flow to consistently reduce colored residues, using multi-cycle solvent washes that are hard to replicate in makeshift or contract facilities. This care pays off in cleaner NMRs and less downtime during purification.
Years of plant experience have taught us the practicalities: 3'-Methoxyphenacyl Bromide requires dry, dark storage, and the bottles come sealed under nitrogen. On the floor, exposure to direct sunlight or damp air can degrade potency, so staff limit time outside the container before charging reactors. Unlike more common bromoacetophenones, which sometimes produce excessive dust or static during jar filling, our optimized crystallization protocol yields a coarser particle that scoops easily but doesn’t clump or aerosolize. This detail matters on foggy mornings, and we always recommend a glove box for sub-dividing, not just fume hoods. For scale-up operators, the absence of sticky caking during addition allows faster charging and smoother agitation. Safety training draws from our own mishap logs—always double-bag inside secondary containers, and purge storage boxes with dry nitrogen after each access.
The methoxy placement isn’t cosmetic. We have run many test reactions to verify that 3'-Methoxyphenacyl Bromide’s electronic profile improves selectivity in certain UV-triggered cleavage steps, preventing overphotolysis or loss of sensitive moieties. Direct feedback from peptide and oligonucleotide researchers confirms less byproduct contamination compared to unsubstituted analogs. In our trials, yields consistently trend higher, and purification times shorten when the methoxy group sits at the three-position. This isn’t always obvious to chemists who haven’t run both side by side, but for those who scale reactions, such tweaks can be the difference between a manageable column and hours lost to troubleshooting.
While working with a major drug candidate, one contract customer ran into low yield from unsubstituted phenacyl bromide, especially on the penultimate photolytic deprotection. Our technical services team proposed a switch to 3'-Methoxyphenacyl Bromide, sent out a rapid sample on spec, and walked their chemists through the solvent compatibility checks. Yields improved by 14% after adjusting lamp exposure times, supported by tighter impurity control and a faster work-up. This real-world fix, not just a lab curiosity, directly cut production costs and reduced operator stress. Lab notebooks and scale-up logs tell this story better than any blog post—asked technicians still reference that case for future process scale selections. We’ve compiled several such case study summaries at regular technical roundtables for staff and long-term customers alike.
Suppliers sometimes cut corners by shortening purification steps or using contaminated starting stocks. In our plant, we emphasize extended crystallization and dual-solvent recrystallization, backed by close HPLC monitoring. We’ve seen batches from other firms test out at under 95% pure, showing residual bases or trace chlorides, which can poison catalysts or cause ghost peaks on HPLC. Our storage and shipping practices eliminate these headaches before they reach your bench or your plant vessel. We pick up plenty of urgent orders for replacement lots after other sources fail to meet audit checks, and plant logs keep a tight record trail. Long-term customers report having fewer failed reactions after switching supply to us, a point we hear about in their quarterly feedback.
We make ongoing investments in environmental safeguards, focusing on minimizing brominated waste and capturing vented solvents using closed-loop systems. Older production lines sometimes allowed vented HBr or brominated byproducts into scrubbers inefficiently; our upgrades redirect overheads through adsorbent traps, cutting emissions and keeping the production staff safer. Staff rotate through cross-training so every batch records environmental checks alongside QA/QC, and we review waste minimization steps with monthly process audits. These hands-on improvements stem from years on the floor, not just regulatory pressure. It’s not a canned answer: production techs and maintenance staff submit suggestions that directly feed into next season’s upgrade plans.
We’ve worked through multiple raw material shortages and shipping bottlenecks, particularly in harder-to-source anisole derivatives. Being a direct manufacturer means we control the process dock-to-delivery, so we can offer steady lead times and quickly ramp up output if needed. Whenever pricing jumps because of bromine market volatility, we insulate our regular contracts by long-term sourcing or building stock in anticipation of storm seasons. In the rare event of a supply interruption, customers get direct updates, not excuses or run-arounds. Years spent in logistics, not just procurement offices, lets us anticipate customs, packaging, and carrier holidays so advance supply plans keep your own schedule steady. This approach works for kilo-labs as well as bulk production, and our track record on on-time delivery speaks for itself in plant downtime logs.
New protecting groups surface constantly in synthetic literature, and some promise easier removal or greater stability. In practice, our experience with 3'-Methoxyphenacyl Bromide shows you get a balance of reactivity and handling ease without the expense or risk of yet-unproven photolabile scaffolds. Plenty of process chemists return to this product after trying alternatives that bring cleanup or side-product headaches. In multi-kilo operations, a minor but repeatable yield advantage compounds quickly when you factor in work-up simplification or fewer recycles. Reviewing our own technical support records, more customers stick with meta-methoxy protection when batch records prove out its predictable deprotection and low impurity carryover.
Nothing beats the feedback from staff who weigh, pour, and QC this material every week. Operators have refined filling lines so that packed bottles resist static and powder loss, and shift supervisors actively monitor color and texture to flag any out-of-spec phenomena before release. Customer complaints on solubility or side-reactions drop off after months of regular shipments, pointing to a learning curve that’s now built into our liner training. Vendors, logistics, packaging, batch release—each stage links back to direct report forms, not distant web forms or outsourced customer service. Our people know if a lot shifts in smell, hue, or melt point, it halts for investigation, not just passed along. This practical QC focus translates into the reliable product that process chemists and bench scientists have come to expect.
Customers approach us with special requests: extended shelf-life, custom packing sizes for glovebox transfer, even tailored blends for combinatorial libraries. Our technical group integrates application feedback into future product refinement—one project now evaluates alternative solvents for final washing, looking to cut extractable residues for biologics intermediates. Direct talks between production, logistics, and customer QA always drive these advances, skipping corporate lag. As flow chemistry and automated platforms become more common in synthesis labs, we’re fine-tuning product specs to reduce downtime and streamline integration, taking direct cues from R&D partners’ pilot runs.
Access to real factory process data, not just catalog numbers, gives customers the transparency and reliability they need. Manufacturers carve efficiency and QHSE improvements each quarter through batch reviews and operator feedback, protecting end users from recall headaches and sudden purity shifts. Our documentation comes from firsthand plant logs, not repackaged sales scripts—years of routine process improvement go into each order. This approach brings a steady supply chain, robust technical troubleshooting, and honest communication that lets chemists plan confidently. Amid shifting raw material markets or new regulatory demands, direct manufacturer partnership delivers consistency and flexibility that brokers or resellers can’t match. In the end, it’s the floor workers, technical staff, and production engineers that build the kind of reliability that shapes new possibilities for 3'-Methoxyphenacyl Bromide in chemical synthesis.