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2-Chloro-4-Fluoroaniline

    • Product Name 2-Chloro-4-Fluoroaniline
    • Alias 2-Chloro-4-fluorobenzenamine
    • Einecs 217-731-7
    • 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

    186841

    Chemical Name 2-Chloro-4-Fluoroaniline
    Cas Number 578-43-2
    Molecular Formula C6H5ClFN
    Molecular Weight 145.56
    Appearance Light yellow to brown solid
    Melting Point 52-56°C
    Boiling Point 207-209°C
    Density 1.39 g/cm3
    Solubility In Water Slightly soluble
    Flash Point 97°C
    Purity Typically ≥98%
    Synonyms 2-chloro-4-fluoroanilin, 4-Fluoro-2-chloroaniline
    Smiles C1=CC(=C(C=C1Cl)F)N
    Refractive Index 1.607 (at 20°C)
    Storage Conditions Store in a cool, dry place

    As an accredited 2-Chloro-4-Fluoroaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 100-gram amber glass bottle labeled "2-Chloro-4-Fluoroaniline," features hazard symbols, lot number, concentration, and manufacturer information.
    Shipping 2-Chloro-4-Fluoroaniline is shipped in tightly sealed, chemically-resistant containers to prevent leaks and contamination. It is classified as hazardous, requiring proper labeling and documentation. Transport must comply with relevant regulations (such as DOT, IATA, or IMDG), ensuring segregation from incompatible substances and minimizing exposure to heat, sparks, or open flames.
    Storage 2-Chloro-4-fluoroaniline should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and acids. Keep it away from heat, sparks, and open flames. Store in a chemical storage cabinet designed for hazardous chemicals, with proper labeling and access restricted to trained personnel. Use secondary containment to prevent leaks.
    Application of 2-Chloro-4-Fluoroaniline

    Applications of 2-Chloro-4-Fluoroaniline in Industrial Manufacturing

    As a direct manufacturer of 2-Chloro-4-Fluoroaniline, we supply this compound to specialized B2B clients who integrate it within targeted industrial manufacturing workflows. Our experience covers its established uses in pharmaceutical intermediates, agrochemical synthesis, specialty dye production, and advanced material modification. For each segment below, we outline compliance standards, precise dosage ranges, process entry points, and real finished products to support downstream quality and regulatory requirements.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) Synthesis

    API manufacturers and contract development organizations routinely select 2-Chloro-4-Fluoroaniline as a key building block to create aniline-based core structures during the multi-step synthesis of certain antineoplastic and anti-infective compounds. Its specific halogen pattern enables selective coupling and further derivatization, affording high-value intermediates under strict cGMP environments.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211
    • European Pharmacopoeia (Ph. Eur.) monographs (as relevant to end API)
    • Chinese Pharmacopoeia (ChP) for specific intermediates

    Typical usage ratio

    • 0.12–0.25 molar equivalents relative to the primary condensation partner, with exact ratio determined by the synthetic route and scale; adjustment based on reactivity of subsequent nucleophilic aromatic substitution step

    Downstream process integration

    • Introduced during the early-to-intermediate stage of heterocyclic API synthesis via Buchwald-Hartwig, Ullmann-type, or acylation reactions; monitored for residual aniline content by HPLC in process QC

    Final product types

    • Anticancer drug intermediates featuring substituted benzene motifs
    • Anti-tuberculosis intermediates, specifically for multi-halogenated phenazines
    • Custom fluorinated aniline derivatives for clinical trials
    • Non-commercialized active material prototypes in early research

    2. Herbicide and Fungicide Intermediate Manufacturing

    Major crop protection manufacturers utilize this compound to introduce robust chlorine and fluorine substitution patterns into herbicidal and fungicidal actives, conferring increased metabolic stability and target specificity. Downstream synthesis requires careful control of halogen content and adherence to environmental and agrochemical standards.

    Industry compliance standards

    • FAO/WHO Guidelines on the Quality Control of Pesticides
    • ISO 9001:2015 Quality Management Systems in agrochemical production
    • REACH (EC 1907/2006) for substance registration
    • China ICAMA pesticide registration for raw material sourcing

    Typical usage ratio

    • Used at 8–17% of the core batch composition by mass for triazine, pyridine, or pyrimidine herbicide backbones; dosage refined by desired halogenation degree and targeted field activity range

    Downstream process integration

    • Undergoes direct amination or condensation as the primary nucleophilic aromatic partner in final-step active ingredient formation, followed by purification through crystallization or distillation; trace analysis by GC-MS during process validation

    Final product types

    • Pre-emergent herbicides for rice, wheat, and corn
    • Systemic fungicide actives for high-value vegetable crops
    • Crop protection formulations requiring slow-release active compounds
    • Registered technical-grade actives for bulk pesticide formulations

    3. Specialty Dyestuff and Pigment Intermediate Synthesis

    Dye and pigment manufacturers leverage this raw material for its halogen functionalities, facilitating the creation of azo, anthraquinone, and metal-complex dyestuffs with precision color performance. Its integration supports rigorous purity demands and compliance with international textile and materials standards, especially for non-migratory, weather-resistant colors in advanced applications.

    Industry compliance standards

    • OEKO-TEX Standard 100 for textile dye residues
    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) risk assessment guidelines
    • ZDHC (Zero Discharge of Hazardous Chemicals) MRSL v3.1
    • REACH Annex XVII (Dyes and Pigments restriction/substance authorization)

    Typical usage ratio

    • Added at 15–22% by mass in batch synthesis of functionalized dye intermediates, with precise percentage set by the chromophore structure and desired depth of shade or fastness properties

    Downstream process integration

    • Feeds into diazotization and subsequent coupling stages in multi-component dye synthesis; monitored for unreacted amine residue and halogen release in effluent treatment systems

    Final product types

    • Reactive dyes for polyamide and polyester textiles
    • Color pigments for high-performance industrial coatings
    • Specialty inks used in security and packaging applications
    • Non-leachable colorants for plastic and elastomer coloration

    4. Advanced Polymer Modification and Performance Additive Production

    Chemical companies in polymer modification use this compound as a monomer precursor to introduce fluorinated and chlorinated functionalities into specialty engineering plastics and resins. Such modifications improve flame resistance, chemical inertness, and dielectric properties, particularly in electronic and automotive material applications. Material formulators rely on tightly controlled feeding and consistent quality to meet stringent performance and environmental criteria.

    Industry compliance standards

    • UL 94 Flammability Standards for plastics
    • RoHS 3 (EU 2015/863) Hazardous Substances Directive
    • ISO 17855 for polyamide and related polymer testing
    • TSCA (Toxic Substances Control Act, US EPA) notification for chemical substances

    Typical usage ratio

    • Incorporated at 2.5–6% by weight relative to polymer backbone or blend, adjusted for targeted end-property spectrum such as limiting oxygen index (LOI) or electrical insulation capacity

    Downstream process integration

    • Fed into polycondensation or chain-extension reactions during melt processing of fluorinated or chlorinated polyamides, polyethers, or polyesters; QC includes FTIR and elemental analysis for halogen incorporation

    Final product types

    • Flame-retardant engineering plastics for electronics enclosures and automotive underhood parts
    • High-durability cable sheathing resins
    • Dielectric insulation layers for printed circuit boards
    • Advanced composite prepregs for aerospace panels
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    Certification & Compliance
    More Introduction

    2-Chloro-4-Fluoroaniline: Purpose-Built for Advanced Synthesis

    Our Experience with 2-Chloro-4-Fluoroaniline

    In all our years developing specialized intermediates for fine chemical and pharmaceutical enterprises, certain compounds stand out for their utility and performance. 2-Chloro-4-Fluoroaniline has become one of those building blocks. We began producing this compound at scale in response to requests from pharmaceutical and agrochemical manufacturers who sought consistent quality and purity for demanding downstream syntheses. Our hands-on involvement, beginning with the sourcing and purification of the starting chlorinated nitrobenzene, has given us a close-up understanding of the practical strengths and production intricacies of this molecule.

    Model, Appearance, and Essential Details

    The 2-Chloro-4-Fluoroaniline we supply comes in crystalline form. Having run countless batches, we have refined the process to yield a product with minimal residual solvents and main assay consistently above 99 percent. The compound usually presents as a pale beige to off-white crystalline material, flowing freely and easy to weigh, pack, or dissolve.

    We ship as standard lots of 25 kg fiber drums, each lined with polyethylene and tested to maintain dryness. For clients with smaller scale needs—pilot projects, research labs, custom synthesis campaigns—we prepare as little as 1 kg in robust HDPE bottles. Maintaining batch homogeneity and traceability has always been central to our operation, so each lot comes with supporting documentation, including NMR, GC, HPLC, and moisture analysis reports.

    Chemically, the product bears CAS number 367-25-9 and features both a chloro and a fluoro substituent on the aniline ring: the chlorine at position 2 and the fluorine at position 4. These specifically oriented substituents have a profound impact on its utility as a precursor—an insight that explains the tight tolerances we enforce for impurity levels such as ortho- and para-isomers, and for residual aniline.

    Application in the Industry

    Our team interacts directly with R&D chemists and process engineers from the pharmaceutical and crop protection sectors. Most customers use 2-Chloro-4-Fluoroaniline to access more complex, highly functionalized heterocycles or actives based on an aniline core. For example, the fluorine and chlorine substituents, arranged as present here, have proven strongly activating for nucleophilic aromatic substitution. This allows for the selective installation of sidechains or further halogenation steps in a tightly controlled manner. The compound has gained widespread adoption as a coupling partner for urea or amide synthesis, as well as for Suzuki and Buchwald-Hartwig cross-couplings.

    In practical workflow, many clients highlight the favorable behavior of our product during scale-up reactions. Consistent melting point and color profile translate to higher recovery of crystalline intermediates. In particular, pharmaceutical process chemists have reported high yields and minimal side products in key amide bond-formations derived from 2-Chloro-4-Fluoroaniline. We attribute this to our close monitoring of hydrolysable impurities, and our ongoing investment in automated recrystallization and drying equipment.

    Distinctiveness Compared to Other Halogenated Anilines

    Over the decades, we’ve handled a wide spectrum of halogenated anilines, from standard 4-chloroaniline to more niche trifluoromethylated variants. Feedback from synthetic chemists has clarified how the simultaneous presence of both chloro and fluoro groups, precisely at the 2 and 4 positions, yields a unique reactivity and solubility profile. Unlike simple mono-halogenated anilines, 2-Chloro-4-Fluoroaniline offers a delicate balance: the electron-withdrawing nature of fluorine at position 4 tends to increase chemical stability, while the chloro group at position 2 routes nucleophilic aromatic substitution specifically at remaining ortho and para sites.

    This product distinguishes itself from 4-fluoroaniline or 2-chloroaniline, which often display greater susceptibility to over-reduction or unintended byproducts. In our own tests and in clients’ published literature, 2-Chloro-4-Fluoroaniline has enabled cleaner transformations with reduced formation of colored tars or problematic side streams. The positional pattern of the halogen atoms also influences downstream pharmacology, as certain target molecules require exactly this spatial arrangement for desired biological activity.

    Some chemists looking for aniline intermediates ask about comparing our product with 2-fluoro-4-chloroaniline (the isomer with swapped substituents). In our experience, reaction rates and selectivity can shift significantly depending on which atom occupies each position—so much so that running control experiments with both isomers can alter an entire developmental campaign. While closely related structurally, each exhibits different reactivity toward typical acylation or alkylation. Supply reliability and reproducibility remain crucial in both cases, but we've consistently seen higher uptake for the 2-chloro-4-fluoro variant, from those working on patented or high-performance molecules.

    Quality and Traceability

    At our facility, we manage the entire production chain for 2-Chloro-4-Fluoroaniline. Starting from high-quality nitrobenzene derivatives, we control each stage: catalytic reduction, halogenation, and purification. Trace contaminants—such as mixed isomer anilines, trace metals, or residual acidity—can derail batch processing in pharmaceutical plants or cause cGMP compliance headaches. Experience has taught us to push analytical techniques as far as necessary: every batch receives full-profile testing for iron and copper levels, GC separation of minor isomeric forms, and, where required, tests for potential nitrosamine precursors.

    We share our COA and spectral data freely, and we maintain multi-year retention samples for every production lot. Occasionally, a partner requests extended impurity mapping or needs to meet new regulatory thresholds. We collaborate with them, sharing historical data and in-house analytical findings to enable a smooth qualification phase. In cases where especially tight phthalate, silica, or solvent residues are required, we have developed multi-step wash and filtration approaches, grown out of practical experience from previous custom projects.

    Safety, Handling, and Environmental Responsibility

    Direct experience with handling aniline derivatives reinforces the need for robust procedures and transparent communication. Employees throughout our production lines receive annual training in handling, storage, and cleanup. Our storage areas use climate-controlled, fume-monitored rooms, sharply reducing the risk of environmental loss and keeping product integrity stable for extended periods.

    Disposal and effluent management remain high on our priority list. The chemical pathways for 2-Chloro-4-Fluoroaniline lend themselves to both controlled incineration and advanced biological treatment, thanks to low vapor pressure and predictable breakdown products. We invest in on-site regeneration of spent solvents and in continuous improvement of our aqueous wastewater treatment plant. Ensuring minimal exposure risks and limiting our environmental footprint gives peace of mind to both our team and the regulatory oversight bodies who audit us. We see repeat business not only because of product quality, but because buyers expect—and receive—evidence of best practices in site management and safety compliance.

    From Lab-Scale to Process-Scale

    A good intermediate adapts well, whether for gram-scale medicinal chemistry or for synthesizing commercial API lots. Our technical staff collaborates closely with process engineers—adjusting particle size, refining filtration protocols, and troubleshooting unusual crystallization or color pickup. For many clients, the transition from lab to kilo lab reveals critical process bottlenecks, as subtle differences in the intermediate’s particle structure or solvent carryover can affect the downstream yield and purity. Our long experience lets us offer practical advice on solvent compatibility and expected impurities.

    Some partners request advice on custom derivatives—intending to attach unique leaving groups or to modify solubility for proprietary projects. We host annual roundtable sessions with our partners’ chemists, sharing both our real-world performance data and industry anecdotes. One project, for instance, involved adapting the process to favor a specific polymorph, meeting tighter dissolution criteria for a new drug filing. These collaborative partnerships drive our ongoing improvements and often spark innovation in purification strategies or even new routes for functionalization. Our supply track record shows that forward planning, combined with responsive technical support, lets buyers avoid delays, minimize plant downtime, and meet increasingly complex regulatory demands.

    Addressing Industry Challenges

    Sourcing reliable, high-purity aniline derivatives strains many supply chains. Our customers often mention batch-to-batch variation, inconsistent documentation, and ambiguity about the origins of critical intermediates when dealing with less experienced suppliers. Commitment to in-house manufacturing has allowed us to own the process from start to finish, identify and correct problems swiftly, and engage directly with those who rely on our chemistries. Strict protocols—spanning automated filtration, closed charging of all hazardous materials, and regular analytical audits—stem from decades refining our methods in a high-compliance sector.

    Regulatory shifts pose their own challenges, as newly emerging guidance requires tighter reporting and lower impurity thresholds. We engage with international agencies and participate in consortia tasked with establishing industry standards. Ongoing process validation, frequent method updates, and keeping open communication with site inspectors form a core part of our commitments.

    Perspectives from the Production Floor

    Walking the production line, we see in real-time how tiny variations in upstream reactant purity, temperature, or mixing rates lead to measurable shifts in acid number, color, or melting point. Engineers in our plant share a sense of direct responsibility—the habit of routinely testing for hydrolysis-prone impurities, for instance, grew from past lessons, where a batch destined for a long-standing customer almost failed to meet their kinetic color threshold. Such experiences have driven home the point: close monitoring and immediate corrective action always outperform “fix-it-later” approaches.

    We also see clear regional trends. Markets with stricter environmental mandates push for more thorough documentation and lower impurity baselines. Labs operating under FDA or EMA oversight require not just chemical compliance, but transparent lot histories and risk assessment statements. These expectations keep us sharpening our protocols, from adopting lower-detection-limit methods in analytical chemistry to investing in predictive stability testing. On the other hand, fast-moving custom manufacturing jobs sometimes challenge our batch scheduling and testing capacity—so we have honed a flexible production system, pairing high-throughput standard lots with “quick-response” pilots for urgent small-scale needs.

    Evolution of the End-Use Landscape

    Over the years, we’ve watched 2-Chloro-4-Fluoroaniline’s application portfolio expand. Drug discovery teams now use this molecule in high-throughput screening libraries. Crop protection companies incorporate it as a key precursor, seeking to fine-tune the selectivity and efficacy of new active ingredients for resistant weeds or pests. The automotive coatings segment has shown interest in leveraging the unique substituent effects for crafting corrosion inhibitors or color-stable specialty pigments.

    Adapting to these uses means sometimes adjusting specifications: one group may need micronized material for superior slurry handling, another may request tailored packaging for high-throughput robotic reactors. We value these collaborations for how they highlight practical new requirements—color point testing, dust minimization strategies, or anti-static packaging. Fielding these questions and improving delivery standards keeps us attuned to the evolving needs of advanced users.

    Continuous Improvement, Grounded in Reality

    Continuous improvement doesn’t just mean chasing marginal analytical gains or adding incremental automation. Listening to the chemists, engineers, and logistics staff who use (or ship) our products exposes unforeseen challenges. For example, we discovered through a customer’s pilot project that trace silica levels affected catalytic hydrogenation downstream; iterating our purification delivered the needed fix. Ongoing dialogue and transparency have taught us that product stewardship covers every phase—procurement, handling, shipping, and aftersales support.

    We don’t believe in resting on past performance. Each request for deeper impurity analysis, every question on trace residual content, and all feedback about delivery timeliness feed back into our system. Demand for regulatory clarity and trace contaminant data rises each year, especially among API manufacturers seeking seamless submissions to regulatory bodies. Our specialized analytics group retains samples, archives spectra, and provides historical data access upon request; this allows manufacturers to assemble detailed impurity maps and robust validation packages for new product filings or ongoing site inspections.

    Supporting Growth in an Uncertain World

    Recent years have brought disruptions in raw materials markets, supply chain uncertainties, and evolving regulatory expectations. Our direct, on-site manufacturing with closely guarded synthesis intellectual property assures customers that their supply of 2-Chloro-4-Fluoroaniline stays shielded from most market shocks or third-party distribution risks. We maintain multi-month safety stock, dual-reactor redundancy for key production steps, and a dedicated in-house safety and compliance team who review every change that could impact end-user workflow.

    A close focus on process reliability and personal accountability—combined with a commitment to regularly investing in both people and plant—underpins every lot we ship. Internally, we share stories where preparation and agility let us quickly pivot to meet critical requests, or where an overlooked detail in packaging led to days shaved off a delivery. These practical lessons animate our team-wide meetings and steer our improvement priorities.

    Looking Forward

    The chemical landscape never stays still. As new uses for 2-Chloro-4-Fluoroaniline keep emerging, so do new challenges—whether in ultra-trace impurity detection, specialized custom batches, or evolving environmental rules. We see every project as an opportunity to refine, adapt, and deliver long-term value. Close ties to research teams, an open-door approach for feedback, and a realistic sense of the demands faced by downstream manufacturers remain central to our ongoing development of this product.

    By drawing on technical know-how, real production expertise, and feedback loops with actual users, we strive to keep 2-Chloro-4-Fluoroaniline precisely tuned for what matters most—dependable synthesis, reliable supply, and outcomes that support our partners’ goals over the long term.