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2-Bromo-6-Fluoroaniline

    • Product Name 2-Bromo-6-Fluoroaniline
    • Alias 2-Bromo-6-fluorobenzenamine
    • Einecs 629-055-8
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    535198

    Productname 2-Bromo-6-Fluoroaniline
    Casnumber 183238-49-5
    Molecularformula C6H5BrFN
    Molecularweight 190.02 g/mol
    Appearance Light brown to beige solid
    Meltingpoint 47-53 °C
    Density 1.7 g/cm3 (approximate)
    Purity Typically ≥97%
    Solubility Slightly soluble in water; soluble in organic solvents
    Smiles Nc1c(Br)cccc1F
    Inchikey HBEFVFQNOKTNJN-UHFFFAOYSA-N

    As an accredited 2-Bromo-6-Fluoroaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle labeled "2-Bromo-6-Fluoroaniline, 25g." Tamper-evident seal, hazard symbols, manufacturer details, and lot number displayed.
    Shipping 2-Bromo-6-Fluoroaniline is shipped in tightly sealed containers under ambient conditions, following all relevant hazardous material regulations. Packaging ensures protection from moisture and physical damage. Appropriate labeling and documentation are included for safe handling and compliance with international transport guidelines for chemicals. Shipment is handled by certified couriers experienced in hazardous materials.
    Storage 2-Bromo-6-Fluoroaniline should be stored in a tightly sealed container, in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers and acids. Keep it away from heat, moisture, and direct sunlight. Use in a chemical fume hood and handle with appropriate personal protective equipment. Ensure proper labeling and restrict access to trained personnel only.
    Application of 2-Bromo-6-Fluoroaniline

    Applications of 2-Bromo-6-Fluoroaniline in Industrial Manufacturing

    2-Bromo-6-Fluoroaniline serves as a key building block in various advanced chemical synthesis sectors. Our production-grade material enables high control over purity and traceability, meeting the precise standards required by major industrial segments. Below we detail specific downstream application routes, highlighting compliance, formulation ratios, process steps, and end-product types as used by global manufacturers.

    1. Pharmaceutical Intermediate Synthesis

    Manufacturers rely on 2-Bromo-6-Fluoroaniline as an essential intermediate during the synthesis of several active pharmaceutical ingredients (APIs), particularly for the preparation of heterocyclic compounds in oncology and anti-inflammatory research. The compound enters the production chain after the halogenation and amination stages, acting as a substrate for further cyclization or acylation. Downstream users often select this molecule for its reactivity and the ability to introduce both bromine and fluorine moieties within a single aromatic system, enabling diverse functionalizations and maintaining strict impurity profiles as laid out by international regulatory authorities.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • EU Regulation (EC) No 1907/2006 (REACH)
    • United States Pharmacopeia (USP) compliance for API intermediates
    • Chinese Pharmacopoeia GB 5009.257

    Typical usage ratio

    • Generally 0.2–1.5 molar equivalents relative to the target API, adjusted per synthetic route and reaction scale

    Downstream process integration

    • Added post-chlorination and pre-cyclization step; typically follows halide exchange or nucleophilic aromatic substitution in API intermediate production

    Final product types

    • Antitumor agent intermediates (e.g., kinase inhibitor scaffolds)
    • Non-steroidal anti-inflammatory drug (NSAID) cores
    • Final APIs for custom research chemicals

    2. Agrochemical Active Ingredient Production

    In the crop protection industry, 2-Bromo-6-Fluoroaniline functions as a core intermediate for the synthesis of several herbicide and fungicide actives, including pyridine or triazole derivatives. Agrochemical OEMs directly use it in closed-reactor halogen exchange or amidation reactions, where maintaining minimal metal residue levels and compliance with environmental limits on aromatic amines is mandatory. The compound’s dual halogen substituents allow agrochemical R&D teams to engineer targeted biological activity while facilitating downstream modification and blend formulations for field use.

    Industry compliance standards

    • FAO/WHO Guidelines for Pesticide Specifications
    • EPA 40 CFR Part 158 Pesticide Registration and Data Requirements
    • ISO 9001:2015 Quality Management Systems
    • Chinese National Standard GB 2763-2021 (Maximum Residue Limits for Pesticides)

    Typical usage ratio

    • Ranges from 0.8–1.2 equivalents per downstream target compound, optimized per active ingredient yield and purity specification

    Downstream process integration

    • Reacted post-condensation in sequential amidation and coupling steps, often within semi-batch reactors

    Final product types

    • Pyridine-based herbicide actives
    • Fungicidal aromatic amine derivatives
    • Seed treatment blend intermediates

    3. Dye and Pigment Intermediate Manufacturing

    Manufacturers in the specialty dye sector use 2-Bromo-6-Fluoroaniline as a selective diazotization substrate for synthesizing advanced azo and heterocyclic pigments. Its in-ring halogen atoms enable synthesis of colorants with improved thermal and light fastness, especially in fiber-reactive systems for synthetic textiles. Process operators use this intermediate to control electronic effects during electrophilic substitution, while enabling high batch-to-batch color uniformity and regulatory compliance for textile and ink applications.

    Industry compliance standards

    • OEKO-TEX Standard 100 for textile chemicals
    • EU REACH Annex XVII restrictions (aromatic amines in dyes)
    • ZDHC (Zero Discharge of Hazardous Chemicals) MRSL
    • ISO 9001:2015 for manufacturing quality

    Typical usage ratio

    • Used at 0.5–1.0 mole per dye unit, ratio set according to targeted chromophore substitution patterns and waste minimization protocols

    Downstream process integration

    • Introduced before diazotization step in pigment or dye intermediate synthesis, then directly funneled to coupling reactions for final chromophore assembly

    Final product types

    • Fluorinated azo disperse dyes
    • Textile and polyester pigments with enhanced lightfast properties
    • Specialty inkjet and toner colorants

    4. Specialty Electronic Chemical Synthesis

    The electronics manufacturing sector incorporates 2-Bromo-6-Fluoroaniline into the synthesis of specialty monomers and oligomers for use in semiconducting materials. Its robust halogenation pattern supports the creation of advanced functional materials, including fluorinated aromatic monomers essential for high-performance organic light-emitting diode (OLED) and organic photovoltaic (OPV) device fabrication. Manufacturers value precise charge transfer and polarity control contributed by this intermediate, as well as trace impurity reduction and batch lot traceability for sensitive electronic applications.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • JEDEC JESD625B Handling and Control of Electrostatic Discharge Sensitive Devices
    • ISO/TS 16949 (automotive quality management for electronics)
    • IPC-A-610 Acceptability of Electronic Assemblies

    Typical usage ratio

    • Typically 1.0–1.3 moles per monomer precursor unit, based on desired substitution level and subsequent cross-linking efficiency

    Downstream process integration

    • Charged into monomer assembly reactors pre-polycondensation, followed by controlled halide coupling or Suzuki-Miyaura cross-coupling for electronic grade specification

    Final product types

    • OLED emitter layer precursors
    • Fluorinated OPV semiconducting monomers
    • Photolithographic photoresist additives
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    Certification & Compliance
    More Introduction

    2-Bromo-6-Fluoroaniline: A Closer Look from Our Manufacturing Floor

    Understanding the Backbone of 2-Bromo-6-Fluoroaniline Production

    In the specialty chemical industry, the push for precision and reliability never eases up, especially with advanced intermediates like 2-Bromo-6-Fluoroaniline. Consistent, reproducible quality means the difference between success and setbacks in downstream syntheses. We manufacture 2-Bromo-6-Fluoroaniline from high-purity raw materials sourced through well-established supply chains. Every batch reflects years refining our bromination and fluorination steps. In practice, even a minor deviation in temperature control or reagent purity leads to unwanted by-products or lower yields. Our team monitors each phase carefully—right down to the post-reaction workup—to support high-conversion and low residual impurities.

    When it comes to pharmaceutical or agrochemical innovation, dependability in raw material quality is no luxury—it’s the baseline. Our on-site chemists run each finished lot through HPLC, GC-MS, and NMR to confirm a single, sharp product profile. Trace levels of related anilines or halogenated byproducts can trip up complex API or crop protection synthesis downstream. Custom solutions don’t happen in a vacuum; the fact that we manufacture at scale using our own reactors allows us to shift batch sizes as new projects arise, layer in customer feedback, and validate each adjustment before new material goes out the door.

    Key Properties and Product Model

    2-Bromo-6-Fluoroaniline, with the CAS number 391924-31-7, brings a clear profile: a pale to light tan solid, with a melting range typically around 40–44°C and molecular formula C6H5BrFN. Our product usually falls within a purity range above 99% by HPLC, off-white and low-odor, and stays stable in original packaging under dry storage. Water content is monitored in every lot, since free moisture increases risks of hydrolysis or clumping during shipment. Handling ease improves productivity at the bench—powdered, fine-granular consistency achieves quick dissolution in standard organic solvents, whether for reaction screening or scale-up operations.

    Our product model has been tuned through years of incremental feedback. Customers value lots that pour easily from wide-neck containers, resist sticking, and dissolve without undetectable residue in DMF, DMSO, or THF. Color and volatile organics are routinely checked since faint off-tones signal either degradation or subtle contamination during manufacturing. Aniline derivatives are notorious for darkening with improper exposure—the manufacturing environment keeps light, oxidants, and atmospheric moisture at strict minimums to protect each lot’s stability.

    Unique Features that Set 2-Bromo-6-Fluoroaniline Apart

    Every aniline derivative tells a story about selectivity. 2-Bromo-6-Fluoroaniline earns its spot in custom synthesis due to the direct introduction of both bromine and fluorine atoms at defined ortho positions on the aromatic ring. In practice, the fluoro group tunes electron density and reactivity of the amino function, offering a foothold for nucleophilic substitution or palladium-catalyzed cross-coupling. The bromine handles well in further halogen exchange or functionalization steps, but it’s the interplay of both substituents that enables advanced diversification.

    At the bench, we see this product shine in C–N and C–C coupling schemes. Medicinal chemistry groups routinely use it for the rapid assembly of heterocyclic scaffolds. The ortho-fluoro group serves double duty: it slows down unwanted side reactions and shapes the 3D orientation of the resulting molecules, improving potency in lead candidates. Agrochemical clients look for that same electronic twist to build crop protection agents targeting pests that have grown resistant to simple aromatic structures. 2-Bromo-6-Fluoroaniline handles well in Buchwald-Hartwig or Suzuki reactions, where both reactivity and selectivity hinge on fine-tuned electronic effects.

    Few intermediates offer the controlled performance profile of this compound. Manufacturing experience tells us that ortho-disubstituted anilines need strictly controlled processes. A careless approach risks dimerization or tar formation, both of which eat into yields and create real hazards for large batch operations. Our reactors precisely meter reactants and maintain tight agitation regimes for even product formation. These ground-level decisions matter just as much as top-line analytical confirmation—there is no shortcut when working with sensitive, high-value aromatic intermediates.

    Real-World Applications from Our Experience

    On the pharmaceutical front, the biggest advantage of this aniline derivative sits in its role as a building block for drug targets requiring both metabolic stability and selectivity. We’ve seen customers apply 2-Bromo-6-Fluoroaniline in the preparation of kinase inhibitors, anti-inflammatory agents, and CNS-active scaffolds. Its profile helps fine-tune the balance of hydrophobicity and hydrogen bonding in molecules where “one ring out of place” means years lost to failed screening. Our technical team frequently supports method development, troubleshooting chromatographic issues, or scaling up purification for medicinal chemistry campaigns running on compressed timelines.

    Agrochemical development calls for creative handling of resistant pest chemotypes. Introducing both bromine and fluorine at adjacent positions broadens the chemical space for new active substances. We have worked with crop protection teams using 2-Bromo-6-Fluoroaniline as a precursor for potent herbicides and insecticides. As environmental regulations tighten, the demand for clean, well-characterized inputs only increases. Off-grade material means complex waste issues and complicated EH&S audits, costs that far outweigh short-term savings.

    On the materials chemistry side, researchers reach for this compound when building specialty polymers and dyes requiring sharp absorption features or enhanced photo-stability. The unique substitution pattern delivers properties that simple mono-halogenated anilines can’t match—tighter bandgaps, sharper switching in sensor systems, or improved persistence under UV exposure. Every application makes a different demand on lot quality, and our team welcomes challenges ranging from new solvent compatibility tests to pilot-scale test runs for advanced materials projects.

    What Makes Our Manufacturing Approach Different

    As direct manufacturers, we oversee each gram of 2-Bromo-6-Fluoroaniline from initial synthesis through final QC. Production does not end with a finished batch—it expands to in-house stability testing, handling logistics, and application-specific support. Traders and resellers seldom control this level of detail. Common issues often come from product that’s been repacked, suffered temperature swings in transit, or exposed to high humidity. Our controlled workflow keeps all steps within our own facilities, with rigorous documentation accompanying each shipment.

    Training our operators and technical staff takes center stage. We emphasize not just “how” to execute each manufacturing protocol, but “why” specific parameters convert to higher purity, better yield, and lower downstream risk. Human judgement remains irreplaceable when identifying subtle color changes or small handling anomalies during large-scale crystallization. We invest in ongoing process improvement, testing the effects of incremental pH adjustments or agitation speeds. Years of experience filter into each tweak; a pilot-scale insight often translates into plant-wide improvement in future batches.

    Anilines as a class can be tricky—each bringing its own handling needs and reactivity quirks. Successful scale-up requires batch reproducibility, which in turn starts by listening closely to feedback from end users. Every time a customer flags an unusual analytic result or unexpected behavior, we bring this information back to our synthesis and QC teams for root-cause analysis. Early identification of trends, such as particular lots picking up more moisture over time or darkening more rapidly, allows us to adjust packaging, modify batch drying times, and communicate with users to prevent inventory loss.

    The in-house advantage does not just rest on process control or consistency. For restricted or highly regulated applications, compliance begins with batch traceability, chain-of-custody documentation, and the ability to offer Certificate of Analysis and impurity profiling on request. Many users face strict internal guidelines for impurity thresholds or supplier track records. Complete in-house documentation reassures end users at each step—a claim that trading intermediaries cannot always make.

    How 2-Bromo-6-Fluoroaniline Compares to Related Products

    Compared to simple anilines or monosubstituted halogenated products, 2-Bromo-6-Fluoroaniline opens up a wider synthetic utility. We also produce analogous compounds—2-Fluoroaniline, 2-Bromoaniline, or 2-Chloro-6-Fluoroaniline—but substitution at both the ortho positions brings kinetic and electronic profiles that are made for more demanding applications. Each additional halogen changes both solubility and biological activity potential. Our data show that adding a fluorine atom next to the amino group alters the basicity and hydrogen bonding, differentiating API libraries in ways that single-halogen analogs cannot.

    Process-wise, manufacturing this ortho-bromo-fluoro aniline involves more stringent control on reaction temperature, stoichiometry, and by-product removal. The increased complexity creates both a challenge and an opportunity for value. Users who work with less specialized intermediates often discover additional waste streams, purification headaches, or limits in final product yield. Scaling from gram to kilo levels introduces a new set of variables—solvent management, heat buildup, and consistent agitation. By making 2-Bromo-6-Fluoroaniline in-house, we adapt to these challenges, feed experience back into process improvements, and bring users higher confidence for both small and commercial batch needs.

    Customers in regulated industries have highlighted the difference in risk profile between direct-manufactured material and product passed through third parties. Fully documented, analytically characterized lots reduce regulatory uncertainty. Projects progress faster and fewer resources go into re-qualification or troubleshooting, which increases overall project throughput. For those working with high-throughput screening or time-sensitive discovery pipelines, this level of reliability proves decisive.

    Experiences and Challenges in Meeting Market Needs

    The move to more complex, specifically halogenated intermediates has not been driven by supply-side convenience but by growing demand for better selectivity and metabolic performance in new molecules. Today’s medicinal chemists and materials scientists favor unique substitution patterns for structure–activity relationship exploration. As a manufacturer, we watch this evolution closely. What was once a specialty compound requested only by custom order now sees regular demand and rapid turnover.

    Market demand has highlighted issues not only of synthetic accessibility but also operational safety. Aniline derivatives deserve respect: improper handling during large-scale bromination introduces real hazards, both for operators and the environment. Safe manufacturing requires modern PPE, rigorous exhaust and neutralization systems, and ongoing risk assessment for both stored raw materials and finished goods. Our facility has adopted closed reactor systems, continuous air monitoring, and comprehensive waste treatment protocols to keep safety central to every batch.

    Every scale-up brings challenges. Crystallizing 2-Bromo-6-Fluoroaniline at hundred-kilogram scale amplifies any variables identified at bench scale—agitation uniformity, solvent choice, cooling rate, and product isolation parameters all play a part. We have invested in high-shear mixing equipment and modern centrifugation tools to streamline isolation, reduce batch times, and boost overall recovery. Over years, these physical upgrades show up as lower process cost and narrower batch-to-batch variability.

    Supply chain reliability speaks volumes in specialty manufacturing. We have learned the value of redundant sourcing for both starting materials and consumables. Unexpected supply interruptions push prices up, complicate planning, and can delay critical research for our customers. By establishing relationships across multiple countries and qualifying alternative vendors, we build in resilience that benefits end-users who cannot afford late-stage project slowdowns.

    Storage and logistics play a decisive role in product stability. Small mistakes during transport—temperature excursions, rough handling, poor packaging—correlate with higher rejection rates, clumping, or color changes. We use airtight, moisture-proof containers tested under both humid climate simulation and extended shelf-life assessment. Regular feedback from customers and third-party shippers has led to improvements in container design, labeling, and shipment tracking. These actions build confidence for customers who draw down lots slowly across several months.

    Looking Forward: Solutions Grounded in Experience

    The next phase in specialty chemical manufacturing will focus on deeper partnership between producer and customer. More challenging targets, shorter project timelines, and narrower impurity thresholds define the future of both pharmaceutical and agrochemical innovation. As direct manufacturers, our solutions will rely on real-time data sharing, transparent lot performance tracking, and co-developed analytical protocols to address unique project needs.

    Collaborative process optimization stands front and center. Joint method development, shared stability studies, and open feedback loops let us address previously unseen bottle-necks. Our technical service team works alongside end users to troubleshoot and optimize handling, from bench preparation to scale-driven reaction development. By exchanging data and experiences, we drive both sides toward higher performance and lower risk.

    To keep pace with regulatory and market evolution, ongoing investment in environmental stewardship will remain non-negotiable. Our facility operates solvent recovery and waste minimization programs that do more than simply meet minimum requirements. Proactive measures—such as local air monitoring, safer raw material substitution, and lifecycle analysis—shape every decision. Customers gain assurance that not only are we delivering a high-purity product, but also handling it with respect for both communities and ecosystems.

    Manufacturing 2-Bromo-6-Fluoroaniline at scale blends technical rigor and flexibility. The ongoing dialogue between our production technicians, quality staff, and customer R&D teams raises the standard for what sophisticated intermediates can accomplish. As the field evolves, we expect new synthetic routes, smarter energy use, and targeted impurity control to drive continuous improvement. Each batch that ships out carries more than a chemical—it carries the cumulative insight of a manufacturer committed to user success, process safety, and the relentless pursuit of quality.