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HS Code |
820946 |
| Product Name | 2-Bromo-4'-Benzyloxy-3'-Nitroacetophenone |
| Molecular Formula | C15H12BrNO4 |
| Molecular Weight | 350.17 g/mol |
| Cas Number | 849062-10-4 |
| Appearance | Yellow solid |
| Melting Point | 123-126°C |
| Purity | Typically >98% |
| Solubility | Soluble in organic solvents such as DMSO and DMF |
| Storage Conditions | Store at 2-8°C, protected from light |
| Chemical Class | Acetophenone derivative |
| Smiles | O=C(C1=CC=CC(Br)=C1)C2=CC(=C(C=C2)OCC3=CC=CC=C3)[N+](=O)[O-] |
| Synonyms | 2-Bromo-1-(4'-benzyloxy-3'-nitrophenyl)ethanone |
| Inchikey | WWPZOYJHZCJTRC-UHFFFAOYSA-N |
As an accredited 2-Bromo-4'-Benzyloxy-3'-Nitroacetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is packaged in a 25g amber glass bottle with a secure screw cap, labeled with name, quantity, and safety information. |
| Shipping | 2-Bromo-4'-Benzyloxy-3'-Nitroacetophenone is shipped in tightly sealed containers, protected from light, moisture, and extreme temperatures. Handling follows standard protocols for hazardous chemicals, with appropriate labeling and documentation. The package complies with international regulations, ensuring safe transit, and is delivered by certified carriers specializing in chemical shipments. |
| Storage | Store 2-Bromo-4'-Benzyloxy-3'-Nitroacetophenone in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from heat, ignition sources, and incompatible substances such as strong oxidizers and reducing agents. Label the container clearly and ensure proper chemical segregation according to your laboratory safety protocols. Use appropriate personal protective equipment when handling. |
Applications of 2-Bromo-4'-Benzyloxy-3'-Nitroacetophenone in Industrial Manufacturing2-Bromo-4'-Benzyloxy-3'-Nitroacetophenone is a key intermediate that enables advanced synthesis routes in high-value chemical sectors. We supply this material for established, verified downstream applications, supporting manufacturers through stringent quality management and reliable performance in large-scale processes. 1. Pharmaceutical Intermediate for Antiviral Compound SynthesisPharmaceutical active ingredient manufacturers use this compound as a core intermediate during the construction of complex heterocyclic scaffolds found in advanced antiviral APIs. This material enters multi-step synthesis routes where the selective reactivity of the bromo and nitro groups ensures efficient transformation with controlled yields and purities demanded in regulated markets. Industry compliance standards
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2. Fine Chemical Precursor in Agrochemical SynthesisMajor crop protection manufacturers integrate this compound as a building block when producing specialty herbicide and fungicide actives. Its benzyloxy and nitro functionalities facilitate subsequent functional group transformations, providing access to advanced fine chemical precursors critical to patented agrochemical formulations. Industry compliance standards
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3. Raw Material for Organic Photonic Material SynthesisManufacturers of organic photonic devices employ this intermediate for synthesizing π-conjugated aromatic compounds, which contribute to photoluminescent and charge-transporting layers. The substituent pattern allows precise control over electronic properties, making it pivotal in the bottom-up assembly of light-responsive materials used in both research and commercial device production. Industry compliance standards
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4. Key Intermediate in Specialty Dye Manufacturing for Liquid Crystal DisplaysDownstream specialty dye manufacturers apply this compound as a synthetic intermediate during the stepwise production of high-purity dyes used in liquid crystal display (LCD) technologies. The nitro and benzyloxy functionalities are tailored through successive transformations to yield dye molecules with strict color fastness and light stability for electronic screens. Industry compliance standards
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5. Intermediate for High-Performance Polymer Additive SynthesisProducers of specialty polymers utilize this compound during the assembly of custom additives that modify polymer thermal or optical properties. The unique aromatic substitution pattern supports further derivatization, yielding targeted additives designed for enhanced performance in plastics and composites for demanding industrial environments. Industry compliance standards
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Working at the intersection of fine chemistry and customer demand, we recognized specific bottlenecks in pharmaceutical and agrochemical synthesis routes. Our experience with intermediate steps in complex organic synthesis told us what chemists needed—a reagent with the right blend of reactivity, stability, and selectivity, eliminating inefficiencies that come from impure or overly reactive compounds. This is where 2-Bromo-4'-Benzyloxy-3'-Nitroacetophenone, sometimes identified in facilities as Model BBN-143N, began as more than a new listing. Every batch reflects a hands-on knowledge of what holds up production lines and what solves chemists’ headaches in the lab.
It’s easy to focus on yield, but genuine impact in manufacturing comes from repeatable performance. In our reactors, we strictly control bromination temperatures and monitor substitution at each stage. This care prevents unwanted isomers and byproducts. Purity standards go beyond meeting threshold values—GC and NMR checks support what we see on paper. Chemists rely on the full transparency of every analytical run. If a batch veers from target, we catch it before any shipping labels go on barrels. This approach provides actual batch-to-batch reliability.
During trials, some customers reported issues with similar intermediates sourced elsewhere—impurities slipped in, and those brought downstream trouble. We tailored our process based on this feedback, knowing what works in a glass-lined reactor does not quite look the same on a farmer’s scale, or when scaling up to a metric ton. The manufacturing process for 2-Bromo-4'-Benzyloxy-3'-Nitroacetophenone evolves with scale and application, balancing reproducibility and flexibility. Our people who measure, monitor, and adjust the process are problem-solvers with decades in specialty chemicals.
The molecule hosts a bromide at the 2-position, with benzyloxy and nitro groups occupying the para- and meta-positions respectively. This substitution pattern encourages selective transformations, useful for multi-step synthesis. The acetophenone backbone tolerates a range of solvents and bases. Most organic chemists know the frustration of cleaning up after messy side reactions—our product aims to minimize those, thanks to proven stability under common reaction conditions. The typical appearance is a pale yellow powder; we hold tight to narrow melting point ranges, always testing to confirm it aligns with known literature values.
Moisture content and residual solvents matter in this intermediate. We analyze both before packing. Shipping requests often favor a powder form, which makes dosing into reactors straightforward, but we provide granular or even crystalline material as per actual usage demands from customers—not simply what fits our existing list. Dissolution rates and dusting tendencies differ depending on lot and morphology, so we control atomization and drying steps to hit the targets customers have set for their own production lines.
We have seen steady use of 2-Bromo-4'-Benzyloxy-3'-Nitroacetophenone in both pharmaceutical research and commercial supply chains, especially where selective coupling is required. When used as a building block, it speeds up the path to many specialty molecules—such as advanced intermediates for anti-infective and anti-inflammatory agents. The presence of both an activating nitro group and a benzyloxy protecting group gives flexibility for two-pronged synthesis strategies. In a real-world application, medicinal chemists leverage it for quick entry into more complicated heterocycles, streamlining otherwise tedious steps.
Research groups developing novel crop protection agents also value the reagent’s halide functionality. They harness the nitro group for regioselective transformations, followed by substitution to construct complex ring systems. The compound’s selectivity reduces the purification workload, cutting days off the typical prep timeline. While efficiency draws most of the initial attention, the ability to trace side-products and impurities back to the intermediate source saves resources down the line. This transparency feeds directly from our process controls.
Our teams tested most available acetophenone derivatives on the market before fully committing to this molecule. Monohalogenated or unsubstituted versions provide different reactivities, but the bromo-nitro-benzyloxy combination dramatically improves outcomes in catalytic reactions, especially Suzuki and Buchwald cross-couplings. Customers pursuing patent-protected synthetic routes found that competing intermediates frequently forced extra steps or delivered weaker yields. The benzyloxy group in this compound offers orthogonality—users can later deprotect or diversify based on their final molecule requirements.
We’ve talked directly to process chemists who describe switching between similar-looking brominated or nitro acetophenones and always returning to our product for reliability. The story repeats itself in both kilo-scale and multi-ton production: minor substitutions at different positions can alter reactivity in unexpected ways. Our focus on producing this specific isomer guarantees the sort of reproducibility that only comes from tight synthetic and purification controls.
Scale introduces new wrinkles. In pilot batches, filtration sometimes ran slow, or the product did not crystallize cleanly. We learned to tighten solvent selection and temperature ramps, resulting in a free-flowing product grain that meets core requirements for downstream processing. This translates to fewer equipment fouling incidents and more predictable reaction progression onsite at our customers’ plants. Anyone who has worked on scale-up knows how quickly a minor clumping problem can turn a smooth process into a maintenance headache.
Feedback informed further tweaks. In pharmaceutical applications, users flagged trace metal content as a key problem when shifting to scale, especially for final API syntheses headed for regulatory review. We retooled a post-synthesis wash that dropped metal levels well below ICH Q3D thresholds, allowing a smoother handoff from intermediate to drug substance without downstream deviation reports.
Our direct involvement in each synthesis run means we know every batch’s history. From bromine source to benzyloxy reagent, we trace each lot with full chain-of-custody transparency. GMP-compliance falls under a practical philosophy—we audit supplies ourselves, minimize hand-offs, and maintain clear documentation at every transfer of material. Routine stress tests on our supply chains, including simulation of overseas shipment disruptions, led us to establish secondary sourcing for all critical raw materials.
When a customer asks about a specific impurity discovered during incoming QC, we access reaction batch records instantly, cross-link data from instrument files, and close the loop with a clean paper trail. Knowing the provenance and full analytical track record allows manufacturers to avoid running blind upstream. We have handled recalls and deviations with openness, and the lessons learned feed into every future lot.
Chemical manufacturing always leaves a footprint, but production choices set the scale. Throughout multiple facility upgrades, we shifted away from legacy solvent systems to those rated as lower VOCs, reducing overall hazardous emissions per batch. Recovered solvents feed into distillation streams and return to production, limiting waste. In planning our site expansions, wastewater minimization features as a core metric, not an afterthought.
Every time we re-examine a synthetic step, resource use matters. Where some competitors cut corners, we invested in new reactor controls that offer precise bromine dosing. This improved yields while lowering overall bromine raw material intensity—a benefit that ripples out to workers, neighboring communities, and end-users anxious about regulatory changes.
Few products run on autopilot. Every person on the line understands this molecule’s quirks and the chemistry behind them. Training covers practical hazards of brominated intermediates and real scenarios like handling spills or exposure, shaped by our own facility experiences, not just regulatory scripts. Open lines of communication between shift leads and technical teams drive continuous improvement on the plant floor.
Collaborating with in-house R&D, we fine-tune batch sizes and identify potential cross-contaminant sources. Our engineers revise and adapt protocols, based on real production outcomes and analytics rather than simply meeting standard operating procedures. That interaction, from bench chemist to plant manager, ensures that improvements stick, rather than fizzle when priorities shift.
Every kilo shipped brings its own logistical considerations. Packed in double-lined drums, the product needs cool, dry storage; humidity turns the otherwise free-flowing powder sticky, so shipment windows get carefully matched to climate and journey time. On occasion, we’ve had to reroute containers through alternative ports or cold-chain transports during extreme seasons to guarantee product does not degrade.
By shipping directly from our manufacturing sites instead of aggregating at distant depots, we cut out excess time in uncontrolled environments. Repeated runs indicate this protects both stability and traceability, and feedback from bulk customers supports this direct logistics approach. Many end-users now request split shipments or scheduled deliveries to align with production cycles—a practice we introduced after learning how surplus stock increases spoilage and disposal costs.
Regulations covering halogenated and nitroaromatic intermediates shift frequently. Our compliance specialists maintain close relationships with regulatory bodies, keeping up with evolving standards in Asia, Europe, and North America. Pre-registering broader impurity and contaminant panels, even beyond immediate compliance targets, has allowed us to stay a step ahead.
Documentation is tailored to regional needs. Customs officials ask direct questions, as do environmental officers and auditors. We provide what’s necessary—full traceability, COAs built from analytical records, and regular updates if regulations tighten. Customers now approach us at early development stages for documentation guidance, because they know from experience we anticipate regulatory concerns that pop up mid-launch.
Continuous improvement defines our manufacturing philosophy. We invest back into plant upgrades, new process chemistries, and greener production options. Emerging trends see increased demand for flexibility; end-users prefer suppliers ready to adapt synthesis and packaging on short notice, based on either market shifts or regulatory changes. We maintain modular production assets, ensuring that a run of BBN-143N can shift between kilo-lab and full plant scale without introducing inconsistencies or impurities.
Our team keeps tabs on new applications. As custom synthesis requests come in, we help reroute part of our intermediates toward high-value niche projects, without jeopardizing existing deliveries. Balancing steady supply for longtime partners with the agility to serve new research demands reflects a core commitment—the product must serve real creation, not just fill a catalog line.
Having built production for 2-Bromo-4'-Benzyloxy-3'-Nitroacetophenone from initial lab scale to multi-ton shipments, we’ve witnessed firsthand how small differences in manufacturing discipline play out in the customers’ results. Reliable chemistry, robust documentation, and transparent communication drive successful projects. This product testifies to what consistent hands-on chemical manufacturing can achieve when it’s guided by both experience and a willingness to listen and adapt.
The difference versus other intermediates isn’t only in the structure—it shows up in streamlined downstream synthesis, cleaner analytical profiles, and fewer production interruptions. The customer conversations, technical support, and rapid troubleshooting extend well beyond “business as usual.” 2-Bromo-4'-Benzyloxy-3'-Nitroacetophenone embodies our commitment as a direct manufacturer: provide the molecule that works, in every sense of the word, and keep refining every step until the supply chain runs as cleanly as possible.