|
HS Code |
746763 |
| Productname | 3-Chloro-2,6-Dibromo-4-Fluoroaniline |
| Casnumber | 951893-32-2 |
| Molecularformula | C6H2Br2ClFN |
| Molecularweight | 317.35 |
| Appearance | Solid |
| Purity | Typically >98% |
| Solubility | Slightly soluble in organic solvents |
| Smiles | Nc1c(Br)cc(F)c(Cl)c1Br |
| Inchi | InChI=1S/C6H2Br2ClFN/c7-2-1-3(10)4(8)6(11)5(2)9/h1H,9H2 |
| Synonyms | 2,6-Dibromo-3-chloro-4-fluoroaniline |
| Storagetemperature | Store at 2-8°C |
As an accredited 3-Chloro-2,6-Dibromo-4-Fluoroaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25g net weight, screw cap, chemical label includes structure, hazard symbols, batch number, and handling instructions. |
| Shipping | **Shipping Description:** 3-Chloro-2,6-Dibromo-4-Fluoroaniline is shipped in tightly sealed containers, protected from light and moisture. Handle with care, using appropriate personal protective equipment. Ensure compliance with local, national, and international regulations for hazardous chemicals. Store at room temperature in a well-ventilated area, away from incompatible substances. Transport under authorization by trained personnel. |
| Storage | Store **3-Chloro-2,6-Dibromo-4-Fluoroaniline** in a tightly sealed container, away from light, moisture, and incompatible substances such as strong oxidizers and acids. Keep it in a cool, dry, well-ventilated area designated for hazardous chemicals. Label the container clearly, and ensure access is restricted to trained personnel. Wear appropriate personal protective equipment when handling or transferring the substance. |
Applications of 3-Chloro-2,6-Dibromo-4-Fluoroaniline in Industrial Manufacturing3-Chloro-2,6-Dibromo-4-Fluoroaniline supports multiple advanced industrial synthesis routes. Our manufacturing clients deploy this intermediate to achieve controlled halogenation profiles in regulated settings. Below, we detail real-world downstream sectors, clarified by specific requirements in compliance, precise formulation, integration methodology, and finished product output. 1. Agrochemical Active Ingredient SynthesisMajor crop protection formulators select this halogenated aniline when optimizing the aromatic core of new-generation herbicides. Its electron-withdrawing profile advances substitution reactions at the intermediate stage, resulting in stable active ingredients with environmental persistence control. Precise molecular design offers enhanced selectivity for target weeds. Production follows jurisdiction-specific guidelines from pilot to final technical material. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Pharmaceutical Intermediate for Heterocyclic SynthesisSpecialty fine chemical producers utilize this compound as a functionalized aromatic aniline in synthesizing new heterocyclic scaffolds for drug discovery. Its halogen pattern drives regioselective cyclization in medicinal chemistry, enabling the production of targeted kinase inhibitors and CNS-active molecules. Regulatory audits require full traceability from raw material entry to API output stage, in line with current cGMP requirements. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Electronic Chemical for OLED & Organic Semiconductor SynthesisElectronic device material companies require aromatic compounds that introduce defined halogen and amine functionalities in conjugated organic molecules. This chemical advances synthesis of light-emitting and electron-transport layers. Exact halogenation patterns control energy levels and color purity in OLED and thin-film transistor production. All manufacturing stages follow sector-specific EHS controls with rigorous impurity profiling. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Specialty Chemical for Dye and Pigment ManufacturingDye producers integrate this aniline during controlled halogen substitution, expanding accessible shade ranges and boosting photostability of specialty pigments. Direct use in high-performance dyes for plastics, fibers, and coatings depends on batch analytics verifying halide uniformity and amine reactivity. Colorant manufacturing must document all raw batch data for harmonized market supply. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Intermediate for High-Performance Polymer ModificationPolymer manufacturers deploy this aryl amine to modulate backbone properties in advanced engineering plastics. Its halogen and amine groups assist in synthesizing copolymers with increased dimensional stability, flame retardancy, and chemical resistance. Integrating this intermediate requires closed-system feeding with in-line monitoring to align with final property specifications and safety standards for polymer additives. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 3-Chloro-2,6-Dibromo-4-Fluoroaniline 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!
Our journey with 3-Chloro-2,6-Dibromo-4-Fluoroaniline has been shaped by decades of hands-on production, customer feedback, and applied use across many industries. Handling halogenated anilines is never simple, but this specific molecule reflects a balance between reactivity and selective substitution that stands out from others in its class. The aromatic ring, outfitted with chlorine, bromine, and fluorine, drives targeted reactions in downstream manufacturing, especially in agrochemical and pharmaceutical synthesis.
We have observed unique benefits in introducing both bromo and fluoro groups onto the aniline core. The bromines at the 2 and 6 positions shield the ring from many side reactions that tend to plague less substituted analogs. Fluorine at the 4 position increases molecular stability for customers designing products for harsh environments. Chlorine at the 3 position, which may appear subtle on a structure diagram, ends up crucial; its electronic influence contributes to selective reactivity in cross-coupling stages and nucleophilic aromatic substitutions.
Our team first scaled up 3-Chloro-2,6-Dibromo-4-Fluoroaniline more than a decade ago in response to research needs demanding precise halogen placement. Others might offer generic halogenated anilines, but only a handful combine multiple heavy halogens and a fluoro group like this one. We have found that end users require predictability—batch-to-batch variation causes real problems downstream. In our setup, we stick to high-purity synthesis routes using rigorously selected raw materials and stepwise control, because any shortcut leads to detectable impurities or unpredictable reaction profiles later.
Our staff in the quality control lab routinely measures not just assay and identity, but a strict profile on trace contaminants. The reason is simple: many applications, including formation of advanced pharmaceutical intermediates, react badly to trace organics or inorganic salts. Impurities left from corner-cutting synthetic steps can alter final compound activity, crop tolerance, or shelf stability. By handling all core processes in-house, we keep a tight chain of custody and can guarantee repeat specifications. Others buy intermediates externally; in our experience, that always increases the risk of hidden trace contaminants slipping through.
We assign model 3CDFA to our in-house product line, reflecting rigorous process controls set at each stage. Physical attributes such as appearance and melting range are checked for every lot shipped, though most customers care most about molecular integrity and the precise halogen arrangement. For pharmaceutical or agrochemical innovators, sidechain modifications on this scaffold can introduce new biological activities. Analytical teams cite that our material resists unwanted redox transformations during further synthesis, a fact we have verified with multiple partners in both small and large-scale projects.
A recurring application involves cross-coupling of this aniline with complex aryl groups to access building blocks for active pharmaceutical ingredient (API) synthesis. The combined electronic effects of bromine, chlorine, and fluorine make the molecule both reactive enough for palladium-catalyzed steps, and selective enough to avoid polysubstitution or ring breakdown that plague simpler haloanilines. Our customers often report that small changes in our synthesis approach—changes that may go unnoticed if only purity specs are considered—can influence yield by several percent, which at industrial scale means significant cost and waste reduction.
We've seen many companies default to single-substituted or dihalogenated anilines for simpler reasons—lower costs, easier sourcing, or a belief that “close enough” chemistry will suffice. Over the years, feedback from end users keeps correcting this assumption. Adding the fluorine increases resistance to acid hydrolysis and oxidation, which means real shelf life and process robustness for products exposed to environmental stress. The extra bromine shields positions that often undergo extemporaneous substitution, leading to cleaner API isolations. Chlorine moderates electron density, allowing more controlled downstream functionalization. Such effects cannot be duplicated by mere isomers or by switching out for monochlorinated or monobrominated analogs.
Other manufacturers tend to blend batches or rely on external toll processors to produce a wide array of similar anilines. From our practical perspective, this approach brings unacceptably wide variability in reproducibility. Several times, we have been approached to “rescue” product lines facing unknown impurities, after customers discovered that switching to our directly produced batches fixed previously unexplained variability in bioassays and process outcomes.
In many process industries, sustainable sourcing and continuity of supply are major concerns. It's easy for remote suppliers to offer irregular quality with limited documentation. By keeping all stages—halogenation, purification, final polishing—in-house, we safeguard traceability. Our own chemists document and review every lot, and this direct oversight enables honest troubleshooting if any anomaly crops up in your production. One batch may look like another on paper, but the real test is in long-term partner feedback and the shelf stability of complex products synthesized downstream.
Our logistics crew coordinates shipment directly, so both temperature and moisture risks are minimized. We have seen products from brokers arrive caked or discolored, which nearly always means at least part of the cargo experienced uncontrolled conditions. Because 3-Chloro-2,6-Dibromo-4-Fluoroaniline undergoes changes if exposed to sustained high humidity or trace acids, we custom-package each shipment to maintain original quality from departure to final customer receipt. This hands-on approach costs a bit more, but feedback from R&D teams confirms the savings in time and troubleshooting justify the effort.
Researchers and formulation chemists often value collaboration with manufacturers who have deep process knowledge and can offer material with consistent impurity profiles and complete trace data. This molecule started life in lab-scale exploratory pharmaceutical synthesis, but its robustness expanded its use into more demanding fields including advanced agricultural formulations and specialty polymers. Regulatory teams have come to us for transparent supply records and technical disclosure—elements often unavailable from generic “bulk” chemical sources. For regulated markets, that transparency is a must.
Our R&D lab works alongside major innovators who continually push for more active molecular scaffolds. They’ve shown that small changes in synthetic approach—what solvent we select for the bromo introduction, the temperature range for final amination, even the quenching time—have measurable effects on downstream activity and shelf stability. These are not theoretical concerns; bioassay results confirm the reality. The customers who succeed are the ones who work with a supply partner attentive to these “invisible” process controls. Having been in the trenches, we recognize there is no shortcut to building this track record.
Leading pesticide producers incorporated our 3CDFA into their pipeline after encountering persistent issues with competing products: inconsistent melting point, visible impurity haze, and mysterious batch fouling under storage. After switching, their teams reported reductions in waste, smoother purification steps, and fewer anonymized impurity peaks during HPLC profiling. Similar examples surfaced in the pharmaceuticals sector, where final API yields rose after controlling for just two trace contaminants we routinely screen out. Our QC methods stem directly from customer project feedback, not simply generic industry guidelines.
Downstream performance drives our ongoing synthesis revisions. We have never seen a batch of this material manufactured outside a fully controlled environment maintain both the desired physical characteristics and a reproducible reaction profile in complex multi-step syntheses. Full halogen profile and aromatic integrity matter more than stated purity alone. Our internal validation runs test the product in typical transformations—some batch-to-batch nuances become apparent only under genuine process conditions, and our chemists adjust parameters to keep these within functional limits.
Producing 3-Chloro-2,6-Dibromo-4-Fluoroaniline is no trivial pursuit. Many producers hesitate to handle multiple halogens due to equipment corrosion and waste stream concerns. We have invested in lined reactors and bespoke scrubbing systems to handle both the formation and purification of this and related molecules. This not only preserves operator safety, but also creates a controlled environment minimizing byproduct generation. Over the years we have reduced halogen emissions through better waste capture, and ongoing process upgrades keep our plant ahead of regulatory requirements.
There’s a constant temptation in the chemicals business to minimize costs by outsourcing challenging steps. Yet for this compound, retaining all halogen introduction under our own roofs protects quality and allows us to intervene swiftly if any anomaly appears. Quick responses can make or break a time-sensitive production schedule. Spanning the gap between basic research and multi-ton scale production demanded serious engineering investments. We learned early that off-the-shelf catalytic columns and standard purification approaches do not deliver the purity or consistency needed here. Customized synthesis lines, trained operators, and thorough, record-driven batch oversight keep our product line robust even as order volumes fluctuate.
Whether chemists are targeting new active molecules, crop protection solutions, or intermediates for specialty polymers, our experience with 3-Chloro-2,6-Dibromo-4-Fluoroaniline supports projects from pilot stage through to commercial scale. Our technical team responds to process queries, sharing practical guidance on optimizing reaction times, solvent choices, and compatible catalysts. Where projects benefit from a structural or process tweak, we work side-by-side with formulation experts, helping select the best downstream transformation pathway for their application. Many long-term clients began with simple sample requests but moved quickly to contracted supply after seeing measurable process benefits.
Supporting partners through both regulatory clearance and process optimization means keeping meticulous batch records, providing transparent analysis data, and updating technical documents as methods evolve. We consider it part of our mission to share these updates proactively, avoiding any surprises. In our experience, collaborators value responsiveness—from small-scale R&D to full-scale processing—over mere document compliance. Our supply team prioritizes adaptable logistics, with shipment planning designed around customer handling needs and critical project timelines.
Our direct end-to-end control matters for sensitive compounds such as 3-Chloro-2,6-Dibromo-4-Fluoroaniline. Working directly with the raw halogens each day gives our staff unmatched familiarity with hazard mitigation, waste management, and all kinetics affecting the core process. This internal expertise does more than safeguard product—it shields downstream innovation from the headaches of undiagnosed process variation. Comparing material made under strict controls with mass-market analogs reveals the difference: consistency, batch security, and reliable reactivity in every order.
Others often cut corners in their supply chain, contracting core intermediates out to less specialized shops or batch consolidators. We have learned which process variables influence yield, impurity, and safety. Retaining our own synthesis, purification, and packaging lines pays off for customers when complex transformations call for maximum reliability. With stringent internal standards in place, our teams can identify and resolve any deviations before they reach the loading dock. Our in-house analytical techs document product history, not just a final purity result, providing deeper context for any troubleshooting downstream.
We bring more to 3-Chloro-2,6-Dibromo-4-Fluoroaniline than metric tons and purity ratings. Drawing on direct feedback from fields as diverse as pharmaceutical R&D and agricultural innovation, our manufacturing know-how keeps projects on track. Consistency, transparency, and direct, hands-on synthesis control continue to separate our product from those of less specialized producers. In the end, it’s about creating reliable value backed by real chemical expertise—helping partners overcome both inevitable process challenges and emerging opportunities for new molecular discovery.