|
HS Code |
567994 |
| Product Name | 2'-Bromo-4'-Fluoroacetanilide |
| Molecular Formula | C8H7BrFNO |
| Molecular Weight | 232.05 g/mol |
| Cas Number | 218301-93-6 |
| Appearance | White to off-white solid |
| Melting Point | 110-114°C |
| Boiling Point | No data available |
| Solubility | Slightly soluble in organic solvents |
| Purity | Typically >98% |
| Smiles | CC(=O)NC1=CC(=C(C=C1)Br)F |
| Inchi | InChI=1S/C8H7BrFNO/c1-5(12)11-8-3-2-6(9)7(10)4-8/h2-4H,1H3,(H,11,12) |
| Density | No data available |
| Refractive Index | No data available |
As an accredited 2'-Bromo-4'-Fluoroacetanilide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging for 2'-Bromo-4'-Fluoroacetanilide (25 grams) is a sealed amber glass bottle with a tamper-evident screw cap. |
| Shipping | 2'-Bromo-4'-Fluoroacetanilide is shipped in tightly sealed, chemical-resistant containers, clearly labeled according to regulatory standards. It is packaged to prevent leaks and contamination, and typically transported as a non-regulated solid at ambient temperature. All handling and shipping comply with local and international chemical safety and transportation guidelines. |
| Storage | Store 2'-Bromo-4'-Fluoroacetanilide in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep the chemical protected from direct sunlight and moisture. Always follow standard laboratory safety protocols, including the use of appropriate chemical storage cabinets for hazardous materials. |
Applications of 2'-Bromo-4'-Fluoroacetanilide in Industrial ManufacturingAs a direct manufacturer integrating R&D, process optimization, and quality assurance, we support industrial partners with high-purity 2'-Bromo-4'-Fluoroacetanilide for well-defined synthesis steps across specialty chemical sectors. Our material is formally supported by analytical validation and aligns with downstream user QA systems, ensuring reliable performance from kilo-lab evaluation to plant-scale adoption. 1. Pharmaceutical Intermediate for Fluorinated Aniline-based API SynthesisThis compound serves as a sequenced intermediate in the multi-step synthesis of select active pharmaceutical ingredients, especially involving fluorinated aniline functional groups. Process chemists incorporate it after halogen-exchange steps to introduce orthogonal bromine and fluorine positions, which enables subsequent nucleophilic substitutions and acylations during the construction of advanced intermediates for prescribed APIs targeting respiratory and anti-inflammatory indications. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Intermediate for Selective Herbicide SynthesisFormulators in crop protection utilize this compound as a core scaffold in the synthesis pathway for modern selective herbicides. The dual halogen-substituted acetanilide backbone is leveraged in post-coupling steps to fine-tune the reactivity and metabolic stability essential for efficient residue control. It enters the process sequence after the initial condensation of fluorinated aromatic precursors and regulates the subsequent substitution rate under controlled base and temperature conditions. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Intermediate for Fluorinated Dyestuffs ManufacturingIn specialty pigments and dye manufacturing, producers employ this compound to construct key intermediates with optimized halogen patterns, supporting solvent- or heat-stable colorants for industrial and textile applications. The precise bromo-fluorinated substitution confers wash fastness and enhanced light stability when processed through azo coupling or condensation with heterocyclic donors. Manufacturers adapt process conditions to maximize the selectivity of color shade development and ensure batch consistency under stringent QC frameworks. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Custom Synthesis Building Block in Fine Chemicals R&DSpecialty material and contract research organizations incorporate this compound as a highly specific building block for structure-activity relationship (SAR) libraries and exploratory synthesis in life science and electronic material research. The unique ortho-bromo, para-fluoro configuration offers functional selectivity in constructing molecular frameworks, supporting applications where substitution pattern control is critical to exploring new chemical entities with proprietary utility. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Intermediate for Veterinary Pharmaceutical SynthesisAnimal health manufacturers apply this compound in the semi-synthesis of fluorinated benzanilide pharmaceutical actives designed for companion animal use. Its defined dual halogenation is critical for structure specificity during advanced intermediate assembly for antiparasitic or anti-inflammatory agents. The feedstock supports downstream cyclization or coupling reactions under defined process windows validated for both potency and safety endpoints in veterinary formulations. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 2'-Bromo-4'-Fluoroacetanilide prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
Over the years, demand for tailored organic intermediates has driven our technical team deep into the nuances of halogenated acetanilide derivatives. Among them, 2'-Bromo-4'-Fluoroacetanilide stands apart for its steady performance and value in downstream syntheses. Every batch draws on a disciplined routine, shaped by hard-won lessons and feedback from pharma, specialty chemicals, and R&D labs.
The market expects more than purity on a certificate. Chemists told us what counts: reliable melting point, batch-to-batch reactivity, stable shelf life under ambient storage, and minimal trace contaminants. Our standard output for 2'-Bromo-4'-Fluoroacetanilide delivers a purity above 98% by HPLC, which holds up in coupling reactions and amidation routes. Moisture content remains tightly controlled—each drum packs dry, free-flowing material that doesn’t clump or degrade after a week in the lab fridge. Through trial and iteration, we learned that too fine a grind causes dusting losses, while granules outside a narrow mesh take longer to dissolve. Today’s lot comes with a balanced particle size, straight from customer requests for faster charging and less handling loss.
Some customers run kilo to ton-scale syntheses, where trace byproducts gum up reactors or cause color shifts in sensitive intermediates. To tackle this, we pushed filtration and crystallization cuts sharper during work-up. Our technical team strips out unreacted starting material until mass spectra flatline at all flagged impurity peaks. This practical discipline rewards process developers on the receiving end, who can now skip extra wash steps or protracted quality investigations. We know efficiency matters as much as the molecule itself.
2'-Bromo-4'-Fluoroacetanilide attracts interest because the ortho-positioned bromine and para-fluorine handle several functional transformations. Medicinal chemists use it as a scaffold to access libraries based on acetanilide cores. The product opens up Buchwald-Hartwig or Suzuki couplings, where selectivity between the two halogen sites plays a significant role. The bromo behaves as a convenient leaving group for C–N or C–C bond forming; the para-fluoro group survives tough conditions and steers electronic properties in finished molecules.
On the factory line, some teams order this compound for fine-tuning photoactive molecules. For these groups, trace iron or transition metal residues ruin advanced experiments. To address this, our last campaign integrated a new filtration cartridge system and an acid-wash protocol, which shrank headspace iron readings below 1 ppm. Such changes only happened after real users shared process bottlenecks—there’s no substitute for learning from downstream pain points.
A few years ago, we worked side-by-side with researchers comparing 2'-Bromo-4'-Fluoroacetanilide against mono-halogen acetanilides, and even some chloro-derivatives. The difference becomes clear in reaction success rates and product cleanup. Monohalo substrates tend to suffer from incomplete conversion in palladium-catalyzed couplings, making recovery tougher and affecting yields. When both bromo and fluoro populate the molecule, the reactivity window broadens: customers have options for site-selective transformations, opening a pathway into complex molecular scaffolds, especially pharmaceuticals prepping for biological screening. It also brings down cycle time in scale-up—several teams noted they could side-step additional protection/deprotection steps that usually drag out multi-gram programs.
During process optimization runs, we tracked powder stability under real warehouse conditions. Chlorinated analogues showed higher propensity to evolve odor or yellowing over months, especially under high humidity. Our 2'-Bromo-4'-Fluoroacetanilide batches shrugged off both, giving users fewer headaches with inventory aging. It simplifies planning and reduces supply interruptions—a practical gain often overlooked on spec sheets.
Building a robust manufacturing train for this product needed careful control over exotherms and byproduct filtration. Early on, we used standard halogenation and acetylation conditions, but that approach ran into yield plateaus and sticky cake layers that slowed throughput. On the next campaign, we began metering in reagents at fixed intervals, controlling jacket temperature with a tighter PID loop and using a specialized phase separator. This adjustment reduced side-product formation and flushed out color bodies that later complicated purification. Every process tweak grew from hands-on scale-up, not just theoretical design.
Some customers asked for lots with ultra-low metals or certain specified solubility profiles. Achieving these relied on hands-on cleaning protocols, double rinsing, and extra settling time. Our technical documentation grew out of these conversations. Each Certificate of Analysis and supporting chromatograms tells a story of in-house troubleshooting and direct feedback. These aren’t generic claims but reflect day-to-day handling and adaptation to real-world process needs.
Many fine chemical distributors focus on shelf-ready packs shipped in winterized containers and tracked in barcode systems. As the actual manufacturer, we learned that avoiding excess handling between isolation and packing made a real difference to product homogeneity. By tuning the production plan to customer consumption habits, we now offer both bulk charges and specialty fills, cutting down on repackaging steps that introduce contamination risks. Last summer, heavy rains and logistics delays tested this approach: direct loading from drying room into climate-controlled outbound storage meant clean product left our factory, regardless of external weather swings.
Some end-users flagged temperature spikes in their warehouses. From these alerts, we now supply the product stabilized under nitrogen. We charge each container only after in-line moisture testing, which avoids shifts in melting or reactivity even during transport through hot zones. These direct lessons, earned through seasons of distribution, feed back into every batch.
Over half our regular buyers work in pharmaceutical research and custom synthesis. Several lead projects use this molecule as a starting point for amide coupling, introducing new substituents on the aromatic ring. In high-throughput screening labs, clear product bands and low background in TLC remain priorities. Our experience trimming color impurities and polar tars has cut down on ghost bands—customers tell us they save hours per week across dozens of assays. The compound also streams into material science, especially for tuning mesogenic properties in advanced liquid crystals. Each application rewards the same qualities: purity, consistent solubility, and tight control on byproducts.
If a downstream group has a sudden need for higher reactivity, our process allows for “fresh grind” options, offering faster dissolution by request. We once collaborated with a photonics lab that hit yield drops from source material packed for over nine months. Their report pinpointed moisture uptake. Switching to micro-lot packaging with desiccant inserts raised recovery rates—since then, we carry this as a standard offering. These in-the-trenches adaptations add real-world value.
On pure technical grounds, 2'-Bromo-4'-Fluoroacetanilide gives users a unique window into site-selective chemistry. Unlike 2-bromoacetanilide or 4-fluoroacetanilide, the combination of ortho-bromine and para-fluorine pushes reactivity in distinct directions on the aromatic ring. Couplings, nucleophilic substitutions, or further halogenations can be tuned for high selectivity. For example, pulling off the bromine delivers new amides not accessible from mono-halogenated feedstocks. The para-fluorine remains robust under harsh basic or acidic work-up, letting researchers set up sequential transformations without worrying about group loss.
Handling feedback proves another key difference. Mono-halogenated products, especially in technical grades, often show more tailing in chromatograms and leave more colored tarlike leftovers in reaction flasks. We traced this to less stringent controls on quench and filtration steps, especially after batch upsets. For 2'-Bromo-4'-Fluoroacetanilide, our protocol runs purer, even for scale-ups, resulting in less rework and fewer line shutdowns on the user side.
In storage trials comparing similar acetanilides, our product stood out for physical stability, holding its free-flowing texture. As a manufacturer responsible for the last 150 tons released, we see users report fewer clotting or polymerizing problems during shipping surges or off-season holds. This saves time at both receiving and production steps—a small detail, but it matters where downtime costs accumulate quickly.
No direct commentary on halogenated intermediates can ignore waste management and safe handling. Our synthesis operates with tight solvent recycle protocols to reduce halogenated organic output. The in-house environmental management system tracks every liter of spent acid and waste extract. Most downstream users appreciate that our Certificate of Analysis includes measured levels of residual solvents, especially chlorinated byproducts, supporting their compliance filings for regulated environments.
Every drum comes labeled with clear handling precautions, drawn from actual incident learning—not just safety data sheets copied from literature. Years back, an operator flagged a skin splash risk during tub emptying. Simple but vital—now, we ship all charges with attached dispensing guidelines and PPE reminders, minimizing operator risk on customer lines. As legislation narrows around persistent halogens, we engage in industry roundtables to further green our manufacturing and supply chain. These steps don’t just box-check compliance—they reduce exposure and show respect for users operating under rising regulatory pressure.
Over decades in the business, we learned that success for 2'-Bromo-4'-Fluoroacetanilide depends not just on chemistry skill but on the willingness to adapt routines according to real user feedback. In one instance, a multinational client requested traceability back to original process batches—a need for audit readiness matched by seldom any distributor stock. We answer such asks with full production records, linked lot numbers, and stability testing logs. It didn’t happen overnight—building these records meant changing staff routines, digitalizing older archives, and putting process controls in the right hands.
Production improvements rarely roll out by memo. Each advance comes from root-cause work after outlier feedback: an unexpected cloudiness in a dissolved sample, a slow filtration in a downstream hydrogenation, or line fouling from missed purification. Each complaint closes a loop—it tells us where the processes sit, and how to recalibrate for better outcomes. As a chemical manufacturer, we hold this daily conversation with every kilo, every drum, and every returned sample.
Demand keeps shifting–sometimes towards even more complex halogenation patterns, sometimes toward eco-friendly alternatives as regulatory bars climb. Our technical roadmap now explores catalytic methods with less waste and simpler downstream neutralization. Higher yields from greener conditions matter to us, but so does feedback from users running high-throughput platforms or kilogram reactors. We invite new technical challenges: be it specialty customizations, scale-up support, or advice on clearing regulatory hurdles.
Every lot of 2'-Bromo-4'-Fluoroacetanilide traces its origin to accountable, hands-on manufacturing. Every production tweak, from mesh sizing to advanced filtration, stems from conversations with real users—chemists, engineers, and procurement teams looking for stable, high-purity building blocks in increasingly selective chemistries. What works in our plants translates directly to time saved on the customer bench and in the pilot bay. Reliability, traceability, and product stability remain our commitment, built on feedback you can track down to the factory ledger. The molecule delivers value because the people behind it stand by their work, grounded in hands-on experience and backed by a record of continuous, practical improvements.