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HS Code |
660231 |
| Cas Number | 444807-66-9 |
| Iupac Name | 2-bromo-4-fluorotoluene |
| Molecular Formula | C7H6BrF |
| Molecular Weight | 189.03 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 182-184°C |
| Melting Point | -7°C |
| Density | 1.486 g/cm³ at 25°C |
| Purity | Typically ≥98% |
| Smiles | CC1=CC(=C(C=C1)F)Br |
| Synonyms | 2-Bromo-p-fluorotoluene |
| Refractive Index | 1.5400 at 20°C |
As an accredited 2-Bromo-4-Fluorotoluene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 100 grams, sealed with a screw cap, printed hazard symbols, product and chemical name, manufacturer, and lot number. |
| Shipping | 2-Bromo-4-Fluorotoluene is shipped in tightly sealed containers made of compatible materials, typically amber glass bottles, to prevent exposure to light and moisture. Packages are labeled according to relevant hazardous material regulations. This chemical is generally shipped as a hazardous material and must comply with all local, national, and international transport guidelines. |
| Storage | **2-Bromo-4-Fluorotoluene** should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition, heat, and incompatible substances such as strong oxidizers. Keep the chemical protected from moisture and direct sunlight. Use appropriate safety labeling and ensure it is stored according to local regulations for hazardous chemicals. |
Applications of 2-Bromo-4-Fluorotoluene in Industrial Manufacturing2-Bromo-4-Fluorotoluene serves as a valuable halogenated aromatic intermediate across several tightly regulated chemical manufacturing processes. Selected below are major application fields based on direct downstream industry practices, including pharmaceuticals, agrochemicals, advanced materials, electronic chemicals, and pigment synthesis. 1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredients (APIs)Manufacturers use this raw material in constructing complex heterocyclic scaffolds during active ingredient synthesis, particularly in anti-cancer, anti-viral, and CNS drug development. Its ortho-bromo and para-fluoro substituents enable efficient cross-coupling reactions under Suzuki or Buchwald-Hartwig conditions, facilitating the creation of final API backbones. Tight compliance with Good Manufacturing Practices (GMP) is key at this stage; production lines continuously monitor impurity profiles and residual solvent limits to satisfy ICH Q7 and USP monograph requirements. Quality control chemists routinely analyze reaction yields, optimize catalyst selection, and adjust reagent ratios to limit undesired side products. Industry compliance standards
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2. Agrochemical Intermediate for Herbicide SynthesisProducers of modern florinated phenylurea and triazine herbicides rely on this specialized raw material to create target-specific active ingredients. Aromatic halogenation patterns are preserved during downstream amination, cyanation, or nucleophilic aromatic substitution. Batch reactors operate within regulated thresholds for heavy metals and pesticide precursor residuals, referencing key standards such as FAO/WHO Joint Meeting on Pesticide Specifications (JMPS). Production teams calibrate molar charge based on the specific reactive site, with ongoing analytical support ensuring controlled residual bromide and fluorine retention in the intermediates. This approach maximizes bioactivity specificity in the field while maintaining supply chain compliance. Industry compliance standards
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3. Functional Additive for OLED and Electronic Chemical SynthesisProcess engineers utilize the halogenated aromatic unit as a structural motif in the synthesis of key intermediates for organic light-emitting diode (OLED) emitters and related optoelectronic materials. Precision in molar charge and reaction duration is critical when coupling onto larger polyaromatic systems. Finished intermediate purity is monitored via HPLC and GC-MS to meet IPC (In-Process Control) technical cleanliness and EHS (Environment, Health & Safety) procedures, in accordance with industry protocols such as IEC 62474 and RoHS directives. Integration at the Suzuki or palladium-catalyzed cross-coupling stage helps ensure robust emission spectra and electron mobility in the downstream electroluminescent layers. Industry compliance standards
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4. Dye Intermediate for Pigment and Colorant ManufacturingSpecialty pigment and dye companies incorporate this aromatic chemical as a key intermediate for developing high-performance colorants, particularly where chromophore modification by halogenation increases stability and lightfastness. The material reacts in controlled aromatic substitution, diazotization, and azo coupling processes typically monitored under ISO 9001 quality management principles. Usage ratios depend on target pigment tonality, shade stability, and solvent solubility characteristics. Batch production teams perform real-time spectral analysis and adjust substitution patterns to yield superior color intensity and environmental performance for end-user coatings and plastics. Industry compliance standards
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Here at our facility, 2-Bromo-4-Fluorotoluene isn’t just another name on a catalog sheet. We oversee production at every stage, working right where the chemistry happens. We start with carefully sourced raw materials—aromatic rings, toluene foundations, then build up using controlled bromination and selective fluorination. The result? Each batch shapes into a crystalline liquid with clear, recognizable characteristics, holding its own under GC analysis. The compound, known among chemists by its CAS as 87892-84-6, carries a well-defined profile: a para-positioned methyl group, bromine and fluorine carefully arrayed for consistent reactivity. Purity typically lands in the high nineties on our chromatograms, which is the standard expected by process chemists and pharma innovators alike.
Instead of producing for a generic market, we think from the user’s bench. Research teams and formulation scientists tell us what matters—a reliable starting material for complex molecule assembly. For 2-Bromo-4-Fluorotoluene, the ortho-bromine triggers cross-coupling with high selectivity. The fluorine at the para-position introduces valuable electronic modulation, especially for targets in advanced medicinal chemistry or fine chemicals development. Chemists often reach for it in Suzuki, Stille, or Heck couplings, because the bond strengths and steric layout lower risk of side reactions. The methyl group sitting on the ring picks up new substituents with clean transitions, leading straight into aromatics with tailored pharmacological profiles or high-value agrochemicals.
Other isomers—like 3-Bromo-4-Fluorotoluene or 2-Bromo-5-Fluorotoluene—show different behaviors in the lab. Our product’s para-fluorine activates unique sites on the benzene ring, shifting the reactivity that seasoned synthetic chemists watch out for in multistep processes. We control key specs not because regulators ask for it, but because we’ve seen how small impurities ripple through a synthesis campaign. During scale-up, even minor byproducts or trace halogenated leftovers can scramble a high-value intermediate. This understanding shapes our in-process tests—each drum, tote, or flask receives a detailed analysis long before it leaves our doors.
As a group running reactors and columns, we work closely with users facing pressures on time, yield, and regulatory compliance. We’ve tuned our workflow for scale-up runs and gram-to-multikilogram orders. The product dissolves easily in polar aprotic solvents and withstands both inert and open-atmosphere bench chemistry. Batch-to-batch consistency defines our operation. Customers who run demanding reactions such as lithiation, metal-catalyzed couplings, or directed ortho-metalation give us feedback that guides tweaks to our purification stages. We pursue levels where aromatic purity and halogen content pass muster in applications as different as fragment-based drug discovery and new specialty polymers.
Researchers—especially in academic labs—sometimes underestimate the need for dedicated storage conditions. 2-Bromo-4-Fluorotoluene handles oxygen and moderate changes in humidity with little fuss, but benefits from sealed containers and stable room temperatures. In high-throughput facilities, we’ve invested in inert gas purging capabilities for bulk drums, making long-term stability less of a guessing game. Our own warehouse stores finished product under strict inventory rotation: we label, check, and move quickly, never letting a drum sit until it's lost its spec. Transport partners comply with our requirements, using lined drums or fluorinated polymer liners to prevent unexpected reactions. These aren’t just checkboxes—each step avoids surges in peroxide content or degraded material that could turn up later in syntheses or QA blips.
It’s easy to list halogenated aromatics from bulk traders, but these alternatives often fall short in process chemistry. Our direct approach improves outcomes for pharma clients who can’t risk unknown impurities or shifts in analytical profiles. Several multi-nationals have found that switching from off-the-shelf material to ours squeezed more yield out of Suzuki couplings, or dropped their filtration times by half. The difference appears in the details—by fine-tuning the distillation range and close monitoring of byproduct elimination, we prevent build-up of side-products common in mass-market material. Feedback loops—internal QC reports, external validation, and real-world synthesis data—drive iterative improvement that large distributors can’t replicate at arm’s length.
Today’s chemistry rarely follows a straight line from starting material to finished product. Contract development and manufacturing organizations (CDMOs), life sciences start-ups, and academic inventors push deeper into complex scaffolds and multi-functionalized aromatic rings. Our in-house experts often provide guidance on how to adapt their plans around 2-Bromo-4-Fluorotoluene’s properties. The compound’s versatility gives it a place in diverging pathways: some use it as a coupling partner for kinome inhibitors, others as a launchpad for photoactive dyes or as a reactive handle in OLED research. We field questions every month about solvent compatibility, recycling of mother liquors, or separating regioisomeric byproducts, and we draw on hands-on experience—answering with practical advice, not theory.
Documentation matters, but we know QC reports mean nothing if the next batch doesn’t align with the last. Spectral data—NMR, MS, FT-IR—underpin each release, run by chemists who calibrate their own equipment and check against secondary in-house standards, not just publicly available spectra. We don’t just issue certificates; we build QA into each corner of production, from raw halogen sources through to final filtration.
Contamination and polymorphic variation trigger immediate action. We conduct in-process controls that spot trouble before a batch gets beyond the reactor wall. Any anomaly—be it a fluctuating GC peak at 14.2 minutes or a color change on standing—prompts a halt and hands-on troubleshooting. We’ve invested over ten years of accumulated know-how in resolving issues—from minimizing trace iron from reactor fittings to recognizing early signs of ring-halogen exchange. Each step reinforced our view: quality isn’t a checkbox for compliance; it’s the difference between a library compound that works and one that sits unused in inventory.
In halogenated toluenes, subtle changes in substitution mean big changes in use. 2-Bromo-4-Fluorotoluene stands out over its siblings. The balance of electronic effects (mesomeric versus inductive) enables distinct reactivity in electrophilic aromatic substitution, protecting chemists from downstream surprises. Some clients have switched from 3-bromo analogs, only to discover higher rates of undesired ortho-lithiation. Our isomer’s unique configuration protects against this, favoring cleaner transformations in both research and production. Analysts working in chromatography or preparative separations note sharper retention times, reflecting predictable physicochemical behavior, not a mixed bag of isomeric contaminants.
Direct users experiment—sometimes pushing our product into uncharted territory. Every year, we encounter novel applications, from building up modified ligands for asymmetric catalysis to constructing halide-rich materials for electronics. We see the best results when users bring us into the loop before scale-up, allowing us to guide tweaks for optimal dissolution rates or handling protocols. One case stands out: a pharma team struggled with poor solubility using a less pure alternative; after switching to material from our reactors, their process not only streamlined workup, but improved overall conversion by a measurable margin. Such gains come from the hands-on, adaptable mindset we keep at our core.
Regulatory landscapes in both EU and North America keep evolving—new standards, traceability demands, and stricter impurity controls. 2-Bromo-4-Fluorotoluene, as a non-scheduled intermediate, currently sits outside the most intense regulatory glare, yet we anticipate new requirements yearly. Instead of scrambling to keep pace, we designed batch tracking systems years back that link every drum to a full process history. Clients in regulated industries value this transparency; their auditors appreciate our real-time digital logs and archival capacity. We tie each step to a documented SOP—signed, timestamped, archived—because shortcuts only make headaches downstream.
Many innovations tested on a 100-gram scale fall apart when production scales up. The difference? Small-batch intermediates from traders often hide process residues, water content, or variable halide sources that poison palladium catalysts or disrupt crystallization steps. Our experience bridges this gap. We’ve watched our own product flow from R&D benches to commercial reactors running in the hundreds of liters, supporting both low-volume specialty APIs and intermediates required by the drum. In each scenario, we address changing parameters—heating, agitation, workup chemistry—by collaborating directly with users, not referring back to distant customer support lines. This approach catches issues before they snowball, keeping process economics and production reliability predictable.
We draw insight from every production cycle, drawing on direct feedback from the researchers and engineers using our material daily. Analytical chemists flag traces spotted by LC-MS; process teams report flow anomalies; regulatory staff share evolving requirements. Instead of siloing these lessons, we hold monthly reviews, updating protocols, training new staff, and shopping for new instrumentation where necessary. Our team knows the meaning of missed specs—not just a failed number on a sheet, but lost hours and trashed product on a busy pilot line. So our standards keep evolving, pulling us to ever-higher reproducibility in reactivity and handling.
Every drum moving from our warehouse carries more than contents: years of running reactors, scaling up purification, and solving chemistry puzzles hands-on. When users hit stumbling blocks—solubility quirks, reaction side-channels, unexpected batch effects—our chemists get on calls, review data sets, and recommend actionable steps. This collaboration builds confidence on both sides. For teams running continuous improvement campaigns or developing processes for new regulatory hurdles, open sharing makes for smarter, safer, and more economically sound chemistry—whether at gram scale or metric tons.
Selling 2-Bromo-4-Fluorotoluene goes beyond shifting commodities. Our approach as hands-on manufacturers depends on depth of experience, direct accountability, and continual adaptation. We view every batch as a partnership between our production floor and those running synthesis projects, not a faceless transaction. The small differences—tight quality control, process design rooted in practice, open engagement with users—shape the real-world value of the product from flask to drumroom. By maintaining high standards and responsive support, we help move innovative chemistry forward, batch by batch.