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2,4-Dichloro-5-Hydroxyaniline

    • Product Name 2,4-Dichloro-5-Hydroxyaniline
    • Alias 4-Amino-3,5-dichlorophenol
    • Einecs 221-076-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    652379

    Chemical Name 2,4-Dichloro-5-Hydroxyaniline
    Molecular Formula C6H5Cl2NO
    Molecular Weight 178.02 g/mol
    Cas Number 28492-34-0
    Appearance Solid (usually crystalline powder)
    Color Light beige to brown
    Melting Point 180-185°C
    Solubility In Water Slightly soluble
    Boiling Point Decomposes before boiling
    Density 1.55 g/cm3 (approximate)
    Purity Typically ≥98% (varies by supplier)
    Synonyms 2,4-Dichloro-5-aminophenol
    Chemical Structure Benzene ring with two chlorine atoms at positions 2 and 4, hydroxy at position 5, and amino group at position 1
    Storage Conditions Store in a tightly closed container, cool, dry place
    Pubchem Cid 3464577

    As an accredited 2,4-Dichloro-5-Hydroxyaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250g of 2,4-Dichloro-5-Hydroxyaniline is supplied in a sealed amber glass bottle with a tamper-evident cap and hazard labeling.
    Shipping **Shipping Description for 2,4-Dichloro-5-Hydroxyaniline:** This chemical should be shipped in tightly sealed, labeled containers, protected from moisture and incompatible substances. Handle as a potentially hazardous solid. Comply with relevant regulations for transport of chemicals, including proper documentation and, if required, UN classification. Store in a cool, dry, well-ventilated area during transit.
    Storage Store 2,4-Dichloro-5-Hydroxyaniline in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and acids. Protect from direct sunlight and moisture. Clearly label the container and restrict access to trained personnel. Use appropriate personal protective equipment when handling and ensure spill containment procedures are in place.
    Application of 2,4-Dichloro-5-Hydroxyaniline

    Applications of 2,4-Dichloro-5-Hydroxyaniline in Industrial Manufacturing

    2,4-Dichloro-5-Hydroxyaniline serves as a key intermediate for various specialty chemicals, playing a critical role in synthesis chains where controlled reactivity and reliable compatibility are required. Our production expertise ensures that each batch meets demanding industrial requirements for downstream processes in select sectors.

    1. Azo Pigment Intermediate in Organic Colorant Manufacturing

    As a coupling component, this aniline derivative enters the diazo coupling stage to produce high-performance yellow and orange azo pigments. Its consistent reactivity supports precise shade targeting in pigment synthesis, particularly for applications requiring durability in plastics and inks. Formulators adjust loading based on target shade depth and lightfastness, integrating the intermediate at regulated process points for high batch reproducibility.

    Industry compliance standards

    • EN 71-3:2019 (Toy Safety - Migration of Certain Elements)
    • ISO 9001:2015 (Quality Management Systems)
    • REACH Regulation (EC) No 1907/2006 registration
    • GMP for Colorants in Food Packaging (where applicable)

    Typical usage ratio

    • 0.7–1.2 molar equivalents per aryl diazonium compound; adjustment by pigment loading and desired color strength

    Downstream process integration

    • Introduced in the pigment synthesis by coupling with diazotized aromatic amines under controlled pH and temperature

    Final product types

    • High-fastness azo yellow pigments
    • Organic orange pigments for plastics
    • Decorative and packaging inks
    • Industrial coating pigments

    2. Intermediate for Agrochemical Synthesis (Herbicide and Fungicide Building Block)

    This compound acts as a specific precursor for synthesizing certain chloro-substituted phenylurea and triazole herbicides. The hydroxy and chloro groups enable refined nucleophilic substitution steps, ensuring selectivity for active ingredient synthesis. Downstream tasks involve amidation or cyclization, where the purity profile directly impacts final formulation stability and bioactivity.

    Industry compliance standards

    • FAO/WHO Pesticide Specifications (JMPS)
    • ISO 17025:2017 (Testing and Calibration Laboratories)
    • China GB 2763 Maximum Residue Limits if exported to China
    • ECHA REACH Annex II for chemical intermediates

    Typical usage ratio

    • Used at 1.0–1.5 stoichiometric ratio according to target actives' synthetic pathways; adjustments depend on yield optimization trials

    Downstream process integration

    • Enters synthesis at nucleophilic substitution or condensation stage, reacting with isocyanates or hydrazines

    Final product types

    • Chlorophenylurea herbicide technical concentrates
    • Triazole fungicide intermediates
    • Finished crop protection active ingredients

    3. Dye Intermediate for Acid and Reactive Dye Production

    The aniline ring structure equipped with chloro and hydroxy functionality provides unique chemoselectivity in dye-molecule formation. It is integral in crafting acid dyes used for wool, silk, and polyamide fibers, as well as reactive dyes for cellulose, where color stability and water solubility are critical. Its inclusion impacts dye exhaustion and wash fastness, so proportioning is tightly controlled through formulation trials as per specific color indexes.

    Industry compliance standards

    • OEKO-TEX® Standard 100 Annex 4 (restricted substance list for textile dyes)
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals, Manufacturing Restricted Substances List)
    • ISO 14001:2015 (Environmental Management Systems) for dyehouse supply chains

    Typical usage ratio

    • Add at 0.9–1.1 equivalent relative to diazotized intermediate; tailored per dye structure and required color depth

    Downstream process integration

    • Coupling agent in the condensation or functionalization stage for sulfonated acid dyes or monochloro triazine reactive dyes

    Final product types

    • Acid dyes for wool yarns
    • Reactive dyes for cotton fabrics
    • Dye stuffs for leather finishing

    4. Intermediate in Pharmaceutical API Synthesis (Antifungal and Antimicrobial Agents)

    In the pharmaceutical sector, this material is used as a building block in multi-step organic syntheses aimed at producing key scaffolds for antifungal and certain antibacterial APIs. The specific substitution pattern confers controlled reactivity in stepwise coupling and ring formation, minimizing side-product formation and enabling cleaner purification in GMP environments. Input quantities depend on target batch size and reaction efficiency.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • USP/NF, Ph.Eur. monographs as applicable for intermediates
    • FDA 21 CFR Part 210/211 (cGMP for drugs)
    • EDQM Certificate of Suitability if used for European supply

    Typical usage ratio

    • 1.0–1.10 molar equivalent per coupling partner in key intermediate formation; loading varies with process yields and impurity profile management

    Downstream process integration

    • Introduced at aromatic substitution, etherification, or condensation stage in API multi-step synthesis under GMP process controls

    Final product types

    • Triazole antifungal API intermediates
    • Chloro-substituted phenol antimicrobial precursors
    • Final drug substance after further synthesis and purification
    Free Quote

    Competitive 2,4-Dichloro-5-Hydroxyaniline prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    2,4-Dichloro-5-Hydroxyaniline: Practical Insights from the Factory Floor

    Getting to Know 2,4-Dichloro-5-Hydroxyaniline in Our Manufacturing Process

    Stepping into our plant, you notice the rhythmic pulse of machines and tanks—an orchestra tuned to create specialty chemicals that don’t often get headlines but serve as crucial building blocks across many industries. Among this roster, 2,4-Dichloro-5-Hydroxyaniline stands out, not for a catchy name, but for versatility and the special niche it fills in downstream synthesis and applied chemistry.

    Practical Experience: Appearance, Model, and Handling

    Every batch of our 2,4-Dichloro-5-Hydroxyaniline presents as a fine powder with a pale beige to light brown hue, reflecting its unique aromatic structure. We produce it under controlled conditions to maintain a consistent particle size, ensuring it neither clumps excessively nor produces dust that floats into the air during transfer. Maintaining low moisture helps prevent degradation and clumping, which can bog down customer processes, so our team frequently checks water content with reliable Karl Fischer titration. Each lot undergoes purity tests using HPLC and gas chromatography, revealing levels that meet the standards required for further synthesis—especially where minute impurities can either stall a reaction or introduce unwanted byproducts downstream.

    Model designation for internal tracking may read as “2,4DCA-5HY-N” for standard production runs, though customers rarely ask for models by code. Instead, they ask about reproducibility and scale. We offer packaging in drums lined with inert materials, which keeps the product stable during transportation and storage. In the rare instance a batch strays from specification, the cause usually traces back to a shift in reaction temperature or unexpected contamination. Years of troubleshooting have refined our process further, minimizing such setbacks.

    Places Where 2,4-Dichloro-5-Hydroxyaniline Makes a Difference

    This compound rarely stands alone—it’s a workhorse serving as a critical intermediate in the synthesis of specialty dyes, pharmaceuticals, and advanced agrochemicals. Its aromatic ring and amine function combine lending reactivity that supports stepwise growth of more complex molecules. For dye manufacturers, the hydroxyl group at the 5-position opens pathways to vivid, fastness-boosted colorants used in textile and leather finishing. Chemists building molecular scaffolds for veterinary or crop treatment formulas value how the dichloro substitution modulates reactivity: it can drive selectivity for nucleophilic aromatic substitution or support regioselective coupling where stereo control matters.

    We often field requests for technical support when a customer pushes the product into a new reaction mechanism—some reactions proceed sluggishly due to the electronic profile of the dichloro substitutions, while others move efficiently thanks to solubility or reactivity. The feedback loop between our production staff and customers sharpens both our understanding and our ability to tweak process parameters when scale-up snags appear. Sometimes a simple change in solvent during recrystallization improves throughput, or it prevents caking in storage. These details matter not merely for output, but for the viability of the customer’s end-product in a market where consistency and reliability command loyalty.

    Where 2,4-Dichloro-5-Hydroxyaniline Sets Itself Apart

    In chemical manufacturing, it’s easy to get lost in catalog numbers and commodity mindset. Yet, direct comparison with more familiar aniline derivatives explains why customers return to this specific compound despite slight premium costs. For example, 3,5-dichloroaniline, though useful in many similar reactions, lacks the ortho hydroxyl group, which changes both reactivity and downstream options—especially for azo dye synthesis where unique shades and fastness properties matter. Simple chloroaniline or hydroxyaniline can’t provide the same platform for further halogenation without stepping through several extra synthetic operations, driving up both cost and potential waste.

    A less tangible but important distinction arises from purity and control of trace contaminants. Downstream formulators sensitive to unreacted aniline or high chloride can see marked differences in final product yields or even color shades. Customers feedback to us about subtle off-odors or color drifts that competitors’ lots produced. These observations pushed us to install deeper in-process checks and to adjust our upstream purification steps. By curbing trace starting materials and leftovers, we’ve carved a reputation for providing a more reliable feedstock, saving customers frustration and reworking expenses.

    Day-to-Day Manufacturing Lessons

    Every run teaches something new, whether it’s a downstream problem manifesting as a slight color shift or a grad student emailing about an unexpected byproduct. From the operator’s point of view, reproducibility hinges on small details—a sudden humidity spike in the factory, for instance, might subtly alter a batch’s drying profile, leading to longer downstream filtration or increased solvent usage. Close attention to vessel cleaning helps avoid ghost traces of the previous batch, which can play havoc in sensitive dye-forming reactions or high-spec analytical samples.

    We’ve learned not to cut corners with raw material sourcing, as minor contaminants (like ortho isomers from recycled chlorobenzene) can carry through to finished product, influencing both bulk physical properties and downstream reactivity. The process route we use favors catalytic processes over outdated batchwise chlorination, reducing formation of potentially persistent byproducts. Waste minimization matters—both for the environment and for economic survival—as local regulators watch discharge streams closely. By striving for clean conversions and efficient extraction, we reduce overhead and environmental burden.

    Why Manufacturers Are Moving Toward 2,4-Dichloro-5-Hydroxyaniline

    Environmental concerns and regulatory scrutiny have sharpened the focus on process efficiency and product traceability. Suppliers face mounting pressure to offer products with defined impurity profiles and low environmental impact. 2,4-Dichloro-5-Hydroxyaniline, when produced under tightly controlled conditions, supports these aims: lower waste per unit output and fewer hazardous byproducts to treat. Several large dye houses report measurable improvements in effluent treatment loads when switching to our grade compared to less purified alternatives.

    Pharmaceutical intermediates users particularly value documented batch histories and backward traceability. With digital batch records and committed QA reporting, we enable routine, transparent audits by multinational firms, which increasingly insist on more than just an assurance of minimum purity. The traceability and openly shared analytical data build partnerships, shorten troubleshooting loops, and cut costs by minimizing rework. We see this trend only intensifying, as green chemistry and compliance pressures rise.

    Field Reports: How Our Customers Put It to Work

    Lab managers at dye plants regularly describe smoother synthesis steps, faster filtration, and reduced rework rates compared to more variable sources. A customer in southeast Asia once told us they could run lighter color shades using our 2,4-Dichloro-5-Hydroxyaniline without the “shadow” tones appearing. Another group scaling up an agrochemical intermediate reported more robust yields, especially in step-growth polymerizations, because impurities that might act as chain stoppers didn’t interfere. Pharmaceutical chemists have commented on easier downstream purification thanks to limited byproduct formation—a detail that only emerges with repeated, real-world use.

    Some stepwise optimizations came directly from end-user feedback. For example, heat-up profiles during final recrystallization required smoothing out so the product stayed within a solid, non-hygroscopic zone—a practical fix arising from a customer trialing a new continuous reactor design. Sharing this kind of hands-on experience helps everyone along the supply chain and turns what started as a small specialty product into a quietly vital ingredient behind the scenes.

    Comparing with Other Specialty Anilines: Beyond the Formula

    Chemistry rarely offers free lunches. The 2,4-dichloro configuration, with the added hydroxyl group at position 5, tips the balance between cost and reactivity in ways simple technical data often overlook. Consider a parallel with 4-chloro-2-hydroxyaniline, which lacks the synthetic flexibility needed for many dye intermediates. Chemists searching for specific reactivity windows—those dependent on both electron density and steric effects—learn that structural nuances decide whether a synthesis runs clean or throws a wrench midstream.

    Some newcomers to the market try to insert generic hydroxyaniline grades in an effort to save cost. Years of experience say that this usually results in longer purification tails and extra spending down the line, not least because shifted reaction profiles create more waste. Our own clients originally selected the compound to cut back on after-the-fact purification—and to eliminate the need to spike in scavengers that neutralize side reactions.

    A less visible benefit comes to light in environmental compliance. Our customers operating in strict regulatory climates in Europe and North America see faster clearance for finished downstream products because our manufacturing process avoids contaminants highlighted on regional blacklists. This is not only about hitting a number on a data sheet; fewer problematic side-products means easier toxicology filings, swifter pilot-trial signoff, and smoother moves toward market.

    Our Take on Supply Risks and Opportunities

    Reliable chemical manufacturing faces increasing volatility, from raw material cost spikes to unforeseen shutdowns. Close-knit links to upstream chlorobenzene and phenol markets have taught us to hedge wisely and maintain sufficient inventory buffers. Our established position as an actual manufacturer, not a trader, allows us to offer clarity on batch scheduling, real-time troubleshooting, and sudden surge supply. Many buyers only realize the value of this relationship after late deliveries from middlemen sabotage their production schedules.

    In our own experience, demand bunches seasonally—textile dye manufacturers ramp up in the spring, while crop protection makers accelerate pre-planting. Agile scheduling, trusted logistics partners, and nimble in-house warehousing keep us aligned with fluctuating needs. We learned the hard way that a missed shipment can undo months of goodwill, so we focus on practical reliability—batch transparency, quick corrections, honest lead time estimates.

    Challenges: From Waste Minimization to Final Mile Issues

    With upgraded reactor trains and better solvent recycling, our process now leaves much less waste than older industry standards. Even so, there’s always more to shave off. Some waste streams still require specialized handling, and byproduct sales into secondary markets (for example, as reducing agents or specialty solvent additives) help lower the overall environmental footprint. Factory neighbors appreciate improvements to emissions and water discharge—and so do downstream partners, who prefer not to answer awkward regulatory questions years after purchase.

    Another layer of challenge comes with final-mile logistics. Proper packaging, robust labeling, and adaptive shipment tracking help keep material intact from loading dock to end user. Customers report that drum integrity, proper sealing, and clear lot labeling matter as much as purity for their GMP processes and safe internal handling. As a producer, this means rigorous in-plant checks but also responsive after-sales service if any shipment comes in less than perfect.

    What Drives Us Forward: Partnership, Integrity, and Problem Solving

    Our commitment starts with the raw materials and ends with supporting customer applications—whether that’s a new patentable dye, a generic agro intermediate, or a high-purity feedstock for pharma synthesis. Every improvement, from raw material sourcing to final customer support, results from keeping channels open and responding to real-world issues, not just reference standards in a binder. Direct conversations with users give depth to quality claims and show us what makes a genuine impact in the field.

    We don’t aim to be the lowest-cost option at every turn; we aim to be the supplier whose 2,4-Dichloro-5-Hydroxyaniline brings peace of mind, straightforward integration into batch or continuous operations, and consistent results year over year. For teams invested in developing new colorants, medicines, or crop protectants, this partnership wipes out avoidable headaches—saving time and money that’s better spent on innovation than on sorting through process fallout.

    Across every ton delivered, from small lab lots to truckloads, we carry forward the trust built through careful manufacturing, humble attention to detail, and a willingness to learn from every process hiccup. In a chemical market thick with options, most of them generic or faceless, our direct involvement and day-to-day plant experience shape a product that quietly, but reliably, enables the chemistry of the future.