4-Chloroaniline

    • Product Name: 4-Chloroaniline
    • Alias: p-Chloroaniline
    • Einecs: 202-302-7
    • Mininmum Order: 1 g
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
    • CONTACT NOW
    Specifications

    HS Code

    896696

    Cas Number 106-47-8
    Molecular Formula C6H6ClN
    Molecular Weight 127.57 g/mol
    Appearance White to light brown crystalline solid
    Melting Point 69-73 °C
    Boiling Point 232 °C
    Density 1.223 g/cm³
    Solubility In Water 1.1 g/L at 20 °C
    Vapor Pressure 0.01 mmHg at 25 °C
    Flash Point 118 °C
    Odor Aromatic, amine-like
    Pka 4.15

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

    Packing & Storage
    Packing **4-Chloroaniline** is supplied in a 500g amber glass bottle with a screw cap, labeled with hazard warnings and handling instructions.
    Shipping 4-Chloroaniline is shipped as a hazardous material, typically in tightly sealed containers compliant with regulatory standards. It should be protected from physical damage, moisture, and incompatible substances. Proper labeling, documentation, and handling in accordance with DOT, IATA, and IMDG regulations are required to ensure safety during transportation.
    Storage 4-Chloroaniline should be stored in a tightly closed container, in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers and acids. Protect from moisture and direct sunlight. Keep away from sources of ignition and heat. Store in a chemical safety cabinet specifically designed for toxic or hazardous materials, and ensure easy access to safety equipment in case of spills or exposure.
    Application of 4-Chloroaniline

    Applications of 4-Chloroaniline in Industrial Manufacturing

    4-Chloroaniline serves as a critical intermediate in various chemical syntheses. The following sections demonstrate established industrial uses with details on compliance, typical loading levels, process integration, and final product categories.

    1. Production of Agricultural Herbicides

    Many herbicide manufacturers use 4-chloroaniline as a core precursor in the synthesis of phenylurea-based herbicides, particularly for the preparation of compounds like diuron and linuron. Production lines require specific handling and compliance, as the substance enters the early amination steps before transformation into the functional molecule. Accurate metering ensures high yield and strict residue control in field applications, so producers must tailor ratio based on downstream formulation demands and plant scale-up specifications.

    Industry compliance standards

    • REACH registration (EU)
    • EPA TSCA (US Toxic Substances Control Act)
    • ISO 9001:2015 (Quality Management System)
    • FAO/WHO pesticide specification guidelines

    Typical usage ratio

    • 0.75–1.2 mol equivalent per mole of isocyanate or other co-reactant
    • Adjusted by reactivity of raw materials and desired batch scale

    Downstream process integration

    • Charged in first-stage amination or condensation reactor
    • Requires controlled addition due to exothermic nature
    • Integrated QC sampling for purity >99.0% prior to next process
    • Direct transfer to urea condensation step

    Final product types

    • Diuron (3-(3,4-dichlorophenyl)-1,1-dimethylurea)
    • Linuron (3-(3,4-dichlorophenyl)-1-methoxy-1-methylurea)
    • Other substituted urea herbicides for broadleaf weed control
    • Pre-mixed technical-grade herbicide formulations

    2. Manufacture of Dyes and Pigments

    Dye factories utilize 4-chloroaniline in azo and anthraquinone dye synthesis, especially for polyamide, polyester, and acetate fiber dyeing applications. The compound participates in diazotization and coupling reactions, forming colorant intermediates with stable shade reproducibility. Its controlled dosing and purity directly impact batch-to-batch repeatability and compliance with textile regulations.

    Industry compliance standards

    • ZDHC Manufacturing Restricted Substances List (MRSL)
    • Oeko-Tex Standard 100 chemical requirements
    • ISO 14001 (Environmental Management for Dye Manufacturing)
    • ETAD Code of Ethics (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers)

    Typical usage ratio

    • 0.8–1.0 mol equivalent as amine base per mole of diazotizing agent
    • Adjusted according to target chromophore and fiber application

    Downstream process integration

    • Initiated in diazotization reaction with acid and nitrite
    • Followed by azo coupling or condensation with other aromatic substrates
    • Enters microfiltration and purification before blending
    • Color strength standardized by spectrophotometric QC

    Final product types

    • Acid dyes for nylon and wool textiles
    • Disperse dyes for polyester applications
    • Pigment dispersions for plastics and inks
    • Azo dye intermediates for export and in-house processes

    3. Active Pharmaceutical Ingredient (API) Synthesis

    API manufacturers employ 4-chloroaniline as a building block in synthesizing molecules with antibacterial or antidiabetic properties. It participates in N-acylation, nucleophilic aromatic substitution, and cyclization steps for sulfonamide or phenylhydrazine derivatives. Strict controls on residual levels, trace impurities, and pharmaceutical GMP compliance are standard throughout the operation, with quality heavily dependent on input consistency.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice Guide for APIs)
    • USP/NF or EP (Pharmacopoeia) identity and purity tests
    • 21 CFR Part 211 (FDA cGMP for Finished Pharmaceuticals)
    • Pharmaceuticals Export Promotion Council of India (PHARMEXCIL) guidelines

    Typical usage ratio

    • 1.0–1.05 mol equivalent per acyl chloride, sulfonyl chloride, or ketone used
    • Adjusted for stoichiometry and impurity profile

    Downstream process integration

    • Reacted via amination or acylation during main intermediate synthesis
    • Isolated intermediates proceed to heterocyclization or further purification
    • Required to meet pharma-grade analytical spec (>99.5%)
    • Multiple points for in-process and final batch testing

    Final product types

    • Sulfonamide-based antimicrobials (e.g., sulfamethoxazole intermediates)
    • Antidiabetic agents (e.g., glibenclamide precursors)
    • Bulk volume intermediates for contract API synthesis
    • Regulated pharmaceutical intermediates for global export

    4. Rubber Chemicals Manufacturing

    Producers of rubber accelerators and antidegradants use 4-chloroaniline in the synthesis of phenylthioureas and diarylamines. The compound reacts under nitrogen atmosphere in closed reactors, providing high selectivity for targeted accelerator grades, with every production step tracking batch purity and color index for downstream tire or industrial rubber applications.

    Industry compliance standards

    • ASTM D4670/D4670M (Standard Specification for Rubber Compounding Materials)
    • ISO 9001 (Rubber Chemical Quality System)
    • EU Regulation 1907/2006 (REACH Annex XVII)
    • Certifications for tire-safe secondary amines (customer specifications)

    Typical usage ratio

    • 0.95–1.1 mol equivalent per thiocarbamoyl chloride or diaryl reactant
    • Usage optimized based on yield and molar efficiency audit

    Downstream process integration

    • Introduced during synthesis of accelerator precursor under inert conditions
    • Employed in condensation and cyclization for ultimate rubber-active compound
    • Output subject to secondary purification
    • Intermediate analysis for free amine content and batch traceability

    Final product types

    • Rubber accelerators (e.g., N-phenylthiourea derivatives)
    • Industrial antioxidant systems for tires
    • Compounded masterbatch chemicals
    • Custom-formulated rubber compounding additives

    5. Synthesis of Corrosion Inhibitors

    Manufacturers of industrial water treatment chemicals apply 4-chloroaniline during the formation of aromatic amine-based corrosion inhibitors. The compound enters post-alkylation and neutralization steps to afford amine salts that adsorb onto metal surfaces, enabling specific inhibition of acidic or neutral industrial fluids. Strict handling, residual testing, and effluent monitoring ensure compliance with industrial safety and environmental standards.

    Industry compliance standards

    • ANSI/AWWA B202 (Water Treatment Chemical Specifications)
    • ISO 14001 (Environmental Impact for Chemical Production)
    • OSHA 29 CFR 1910 (Safe Handling of Amines)
    • REACH SVHC compliance for downstream applications

    Typical usage ratio

    • 0.6–0.95 mol per alkylating or acidifying agent depending on inhibition strength needed
    • Dosing based on fluid volume and metal type

    Downstream process integration

    • Charged after pre-neutralization during amine functionalization
    • Undergoes controlled reaction with alkylating agents
    • Formulates as soluble amine salt for blending
    • QC checks for stability, purity, adsorption capacity before packaging

    Final product types

    • Corrosion inhibitor concentrates for circulating water systems
    • Ready-to-use formulations for boiler and heat exchanger fluids
    • Blended anti-corrosive agents for cooling towers
    • Oilfield corrosion protection chemicals

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    Certification & Compliance
    More Introduction

    4-Chloroaniline: A Reliable Intermediate Crafted with Experience

    Understanding 4-Chloroaniline as a Core Chemical Building Block

    In our modern industry, sourcing reliable intermediates matters as much as refining finished goods. Within the labs and reactors of chemical manufacturing, 4-chloroaniline—also known by its CAS Number 106-47-8—often serves as an early-stage workhorse. Over the years, we have tracked countless technical inquiries rooted in this core chemical’s needs. Any chemist working on dye precursors, pharmaceuticals, or agrochemicals has probably worked with it or weighed out its crystalline needles at some stage.

    This compound carries a molecular formula of C6H6ClN, and forms pale, needle-shaped crystals at room temperature. Its melting point, typically around 70°C, signals a clear physical characteristic that buyers and lab techs observe closely for quick quality checks. Density hovers near 1.2 g/cm³, which makes pouring, weighing, and metering pretty straightforward in either batch or continuous operations.

    Our experience has shown that product consistency and low impurity content rescue customers from unexpected disruptions down the synthesis line. 4-Chloroaniline sourced directly from our workshops stands out for its robust purity—purity over 99% w/w assured through careful synthesis and final-stage UNO-grade filtration. In our day-to-day QC, we check for 2-chloroaniline and polychlorinated impurities, since even minor traces of these byproducts can tangle up downstream conversions.

    Nuances of Production and Handling in Practice

    Our production lines execute aniline chlorination under strictly controlled temperature, venting, and flow rate parameters. It took several iterations to dial in process conditions that balance conversion with selectivity. During production peaks, we monitor for non-chlorinated aniline, water content, and residual acidity, which all play into product stability and safety when packing large tonnage drums or 25-kilogram bags.

    Workers here recognize the eggy, faintly smoky odor of 4-chloroaniline—an unmistakable sign around transfer lines and storage tanks. Because of its toxicity, all equipment, from small batch kettles to intermediate bulk containers, must pass strict maintenance. This isn’t about regulatory boxes. Even a slightly dirty valve or an old gasket may lead to complaints or, worse, force a customer shutdown.

    Dust control, while filling or transferring, sits high on our safety checklist. Packing crews wear full protection, not just gloves but also positive-pressure masks. Since skin contact leads to readily absorbed exposure, we’ve learned that every extra step pays off. Over time, these routines have reduced accidents, and they also cut back on batch-to-batch variability by keeping moisture and reactive agents at bay.

    Proper labelling, hazardous shipping documents, and careful drum-lining score just as highly here as batch yields. The “downtime” this attention prevents easily pays for itself compared to the disruptions one poorly handled consignment can cause—agrochemical users, especially, rely on tight margins and timelines.

    How 4-Chloroaniline Drives Synthesis in End-User Industries

    In dyes and pigments manufacturing, 4-chloroaniline forms a backbone for azo and triarylmethane structures. Our long-term clients often describe it as indispensable for colorfast red or violet pigments, especially where cost or reactivity calls for chlorine-substituted rings. For each ton of dye exported, this single intermediate sets the reliability baseline.

    Agrochemical synthesis uses 4-chloroaniline to produce herbicides, insecticides, and growth regulators that have shaped modern agriculture. It finds its way into established APIs such as butachlor or other acylanilide herbicides. These molecules, designed for stability in paddy fields or open-air soil contact, show optimal selectivity when produced using high-purity intermediates, with trace contaminants held to tight limits.

    Our pharmaceutical partners often highlight its value as an intermediate—not for direct ingestion, of course, but as a key precursor. 4-Chloroaniline enables numerous substitutions, coupling reactions, and cross-couplings that underpin active pharmaceutical ingredient (API) synthesis. We often get detailed feedback after trial batches, and any impurity or isomer deviation can stall FDA filings or trigger requalification rounds costing weeks.

    Comparing across industries, dye makers tolerate slightly wider impurity bands than their pharma or agrochemical peers. Some small molecule drugs or next-generation pesticides call for 4-chloroaniline with residual solvent levels measured in the parts-per-million range. Large colorant producers, on the other hand, may work with 98% grades when running robust synthesis and final purification in-house. We adjust QC thresholds, packaging, and documentation standards according to the project’s end use.

    How We Distinguish Ourselves Beyond Standard Specifications

    Talking to customers over the years, we’ve learned that every gram of 4-chloroaniline can mean the difference between a smooth campaign and a week of troubleshooting. Storing and transporting a reactive aromatic amine, we’ve discovered, works best in lined, sealed drums kept out of direct sunlight. We rotate inventory quickly, so clients never face handling an old, degraded lot—this way, there’s one less concern on the customer’s quality checklist.

    Clients in rapidly growing markets, particularly those pushing new research, often ask about batch-specific impurity profiles, reactivity, and solvent compatibility. Analysts in our labs regularly perform HPLC and GC quantification, providing more than just standard COAs; we dig deeper into the impurity fingerprint, including uncommon isomer or halide contaminants sometimes missed by standard methods. This attention helps prevent failed scale-ups after years of development work.

    Over time, patterns emerged in customer feedback. Some competitors supply bulk 4-chloroaniline that’s technically within published specs but displays faint yellow tints or insoluble residues by the time it reaches the reactor. Internal investigations at fine chemical users traced certain batch failures back to improper stabilization or container type during transit. This firsthand feedback led us to switch to polymer-lined barrels and nitrogen-blanketing methods, reducing the risk of air or moisture ingress.

    End-users operating continuous processing benefit from delivery in flexible intermediate bulk containers, pre-weighed and sealed to avoid lengthy titration or dilution steps. For pharma-grade applications, we offer lots certified free of nitro-aniline byproducts, since nitro intermediates—even in sub-ppm amounts—pose unacceptable downstream risk. Achieving this level of quality demands careful attention to precursor sourcing and strict audit trails—not just lab-scale purification.

    Our commitment to repeatable, scalable batches means we record every detail, from daily reactor temp logs to shipping batch codes. Most downstream users appreciate this level of traceability, which speeds up troubleshooting should questions arise months after receipt.

    4-Chloroaniline vs. Other Building Blocks: Nuanced Selection Process

    Many first approached our company while comparing 4-chloroaniline to alternatives such as 2-chloroaniline, monochloroanilines, or unchlorinated aniline. Over weeks to years, project chemists find that the small difference in the chlorine’s ring position leads to wide differences in reactivity, byproduct risk, and cost. Syntheses aiming for para-substituted end groups, like certain advanced dyes or next-gen pesticides, show markedly superior yields when using 4-chloroaniline as a starting point.

    In our technical evaluations, switching from 2-chloroaniline to 4-chloroaniline alters not only yields but also the downstream processability of the final molecule. For some aryl-amine-based targets, 4-chloroaniline offers a better base for selective coupling, making it favored in carbamide or amide bond formation steps. Its less electron-rich para position slows unwanted side reactions, keeping downstream purification cleaner and lowering energy consumption in subsequent steps.

    Traditional aniline, unchlorinated, finds roles where the additional reactivity of halide atoms poses a risk. For chlorinated intermediates, 4-chloro versions fit best where selective reactivity or increased solubility in certain solvents holds value. Pharmaceutical GMP lines especially require not only a clean parent structure but reliably low halide content or a known halogen profile—this level of detailed traceability comes from extended experience, not from off-the-shelf products.

    In comparing 4-chloroaniline to bulk monochloroanilines or cheaper synthetic grades sourced overseas, experienced buyers spot subtle but crucial differences. Off-odors, color changes over time, and polymerization risk signal storage or stabilizer issues, often invisible until downstream quality assurance flags a problem. Such seemingly minor deviations can threaten production runs worth millions, especially in API or regulated pesticide markets. We work closely with users to ensure that our product arrives stable, pure, and documented from drum to final dose or application.

    Continuous Improvement through Real-World Partnership

    Years of direct feedback from chemical engineers and production managers have shaped our continuous-improvement efforts. We run trial collaborations with clients scaling up their synthesis, providing pilot lots for new plants or expansions—sometimes even sending technical staff onsite to ensure safe handling and smooth integration into their system.

    As emerging markets grow and regulations tighten, traceability through QR codes, digital logbooks, and full product lineage have become part of our toolkit. We invite questions, host technical seminars, and regularly publish detailed impurity or stability findings accessible to our customers. These efforts foster trust—more than any certificate or audit alone ever could.

    Handling 4-chloroaniline every day, from raw material receipt to final loading, gives us a grounded understanding of both its strengths and potential hazards. We believe every improvement in purification, packaging, or service ultimately empowers downstream innovation—whether a pigment creator, crop science chemist, or pharmaceutical innovator stands at the other end.

    By focusing on consistent purity, user safety, and total traceability, we've built reliable partnerships across continents and industries. Our experience, attention to detail, and willingness to adapt under real-world feedback help set our 4-chloroaniline above commoditized alternatives. For chemical manufacturers, purchasing departments, and R&D labs seeking a dependable, well-understood intermediate, our 4-chloroaniline remains a foundation—not because of a specification sheet but thanks to generations of practical experience, constant learning, and shared goals within the chemical trade.

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