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3-Chloro-4-Hydroxyaniline

    • Product Name 3-Chloro-4-Hydroxyaniline
    • Alias 4-Amino-2-chlorophenol
    • Einecs 236-628-5
    • 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

    535886

    Product Name 3-Chloro-4-Hydroxyaniline
    Cas Number 17609-80-2
    Molecular Formula C6H6ClNO
    Molecular Weight 143.57
    Appearance Off-white to light brown solid
    Melting Point 111-114°C
    Solubility In Water Slightly soluble
    Purity Typically ≥98%
    Smiles Nc1ccc(O)c(Cl)c1
    Inchi InChI=1S/C6H6ClNO/c7-4-1-2-6(9)5(8)3-4/h1-3,9H,8H2
    Storage Conditions Store in a cool, dry, well-ventilated place, away from incompatible substances.

    As an accredited 3-Chloro-4-Hydroxyaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging for 3-Chloro-4-Hydroxyaniline (25g) is a sealed amber glass bottle, labeled with hazard warnings and product details.
    Shipping 3-Chloro-4-Hydroxyaniline should be shipped in tightly sealed containers, protected from light and moisture. It must be clearly labeled and packed according to local, national, and international regulations for hazardous chemicals. During transit, it requires handling by trained personnel and transportation in compliance with UN and DOT guidelines for potentially harmful substances.
    Storage 3-Chloro-4-Hydroxyaniline 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. Protect from light and moisture. Store at room temperature, clearly labeled, and limit access to trained personnel only. Follow all applicable safety and chemical hygiene protocols during storage and handling.
    Application of 3-Chloro-4-Hydroxyaniline

    Applications of 3-Chloro-4-Hydroxyaniline in Industrial Manufacturing

    As the direct producer of 3-Chloro-4-Hydroxyaniline, we supply to critical industrial sectors where targeted molecular performance is required. Below are concrete application scenarios spanning key industries with dedicated standards, specified usage ratios, process integration details, and finished product references.

    1. Synthesis of Azo Dyes for Polyester and Cellulosic Fibers

    Textile dye manufacturers use 3-Chloro-4-Hydroxyaniline as a diazo component or coupling precursor during the production of specific yellow, orange, and brown azo dyes suitable for polyester and cotton fiber applications. Our material provides high-purity intermediacy for oxidative or acidic dyeing methods, ensuring compliance with color fastness norms and restricted amine release. Downstream processors incorporate this intermediate post-nitration or chlorination, facilitating sulfonation, diazotization, or coupling with specific phenols. Dye formulators adjust input ratios based on fiber type, target chromophore intensity, and environmental regulatory thresholds.

    Industry compliance standards

    • OEKO-TEX® Standard 100
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals Manufacturing Restricted Substances List)
    • EU REACH Annex XVII (Aromatic amines restrictions)
    • ISO 105 family (Textile color fastness testing)

    Typical usage ratio

    • Diazo or coupling component at 0.5–1.5 molar equivalents per final dye molecule depending on reactive structure
    • 0.2–3.0% by mass in formulated dye pastes targeting fiber load and shade depth
    • Adjust ratio for batch dyeing versus pad-dyeing processes

    Downstream process integration

    • Charged to diazotization step in batch reactors after dissolution and filtration
    • Used as intermediate for direct coupling with naphthol or H-acid partners
    • Undergoes purification post-synthesis via crystallization or solvent extraction pre-blend
    • Final blended dye standardized prior to shipment to textile finishing units

    Final product types

    • Reactive and disperse azo dyes for polyester fabrics
    • Direct dyes for cellulosic material
    • Color concentrates for yarn and knits
    • High-performance inks for textile digital printing

    2. Pharmaceutical API Intermediate – Sulfa Drug Precursors

    Pharmaceutical synthesis plants utilize 3-Chloro-4-Hydroxyaniline during multi-step routes to construct key intermediates for sulfonamide antibiotic APIs. This raw material undergoes controlled diazotization and subsequent coupling as a regio-selective step prior to sulfonation or amidation. Strict validation of residual chlorine and byproduct content aligns with pharmacopeial and cGMP documentation. Process chemists determine charge ratios based on downstream yield and impurity pathway management, driven by API regulatory filings.

    Industry compliance standards

    • United States Pharmacopeia (USP)
    • European Pharmacopoeia (Ph. Eur.)
    • China GMP (Good Manufacturing Practices for pharmaceuticals)
    • ICH Q7 Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients

    Typical usage ratio

    • 0.85–1.1 molar equivalents as ring-substituted precursor depending on target API
    • Batch-wise adjustments based on multistep conversion efficiency (80–98%)
    • Material input calculated per synthetic scheme validation

    Downstream process integration

    • Introduced at defined step prior to diazotization and sulfonamide formation
    • Purity and water content controlled via in-process HPLC/GC
    • Residue filtration post-reactor followed by transfer to sulfonation tanks
    • Integrated documentation for full batch traceability

    Final product types

    • Sulfanilamide derivatives and related antibiotic APIs
    • Pharmaceutical grade intermediates for Heterocyclic compounds
    • Fine chemicals supporting generics and contract manufacturing
    • Validated intermediates for regulatory submissions

    3. Agrochemical Formulation – Herbicide Intermediate

    Major crop protection active ingredient producers employ 3-Chloro-4-Hydroxyaniline as a precursor in the preparation of pre-emergence herbicide intermediates, particularly for amide and triazine class products. The chemical enters the synthesis via nucleophilic or electrophilic substitution steps, helping to build core scaffolds with specific selectivity toward target weed species. Compliance with agrochemical registration and residue protocols requires rigorous control of process impurities and stability. Usage ratios fluctuate according to nominated herbicide chemistry and global formulation regulations.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • Regulation (EC) No 1107/2009 (EU pesticide registration)
    • US EPA 40 CFR Part 180 (Tolerance for Residues in Food)
    • ISO 9001:2015 for agrochemical manufacturing

    Typical usage ratio

    • 0.95–1.2 equivalents per mole of active core, depending on final herbicide pathway
    • Batch charge typically 5–15% by weight in multi-component intermediate reactions
    • Adjustment based on targeted selectivity and environmental fate data

    Downstream process integration

    • Added as primary aromatic amine in early-stage synthesis reactors
    • Feeds directly into formation of carbamate, triazine, or amide herbicide scaffolds
    • Analytical QC on input material prior to each batch
    • Integration with solvent recovery and effluent treatment units

    Final product types

    • Pre-emergent herbicide active intermediates
    • Formulated technical grade pesticide
    • Herbicide blends for cereals, soy, and cotton crops
    • Micro-encapsulated weed control formulations

    4. Development of Specialty Pigments for Colorant Industries

    Pigment producers incorporate 3-Chloro-4-Hydroxyaniline as a tailored intermediate for manufacturing complex heterocyclic and benzimidazolone pigment molecules. This enables preparation of high-stability yellow and orange organic pigments especially for automotive paints, plastics, and high-end printing inks. The chemical is introduced during selective coupling or cyclization steps within closed reactor systems, directly impacting pigment crystal lattice formation and dispersibility enhancements. Ratio settings depend on pigment grade and end-use exposure requirements.

    Industry compliance standards

    • ASTM D3723 (Organic pigment blend testing for plastics)
    • EN 71-3 (Safety of toys: migration of certain elements)
    • ISO 18451-1 (Pigments and extenders terminology)
    • RoHS Directive 2011/65/EU (for electronic colorant safety)

    Typical usage ratio

    • 1.0 molar equivalent per pigment core molecule during cyclization or coupling
    • Typically 2–8% by mass in pigment batches targeting final shade and opacity
    • Formulation optimized for particle size and application substrate

    Downstream process integration

    • Material loaded into high-temperature kettles for pigment base reaction
    • In-process monitoring for particle morphology and purity
    • Post-reaction washing and milling to control aggregate formation
    • Final pigment concentrate standardized for dispersibility and tinting strength

    Final product types

    • Automotive-grade organic pigments (yellow, orange)
    • Masterbatch concentrates for plastics
    • Offset and inkjet colorants
    • Exterior architectural coating dispersions
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    Certification & Compliance
    More Introduction

    Understanding 3-Chloro-4-Hydroxyaniline in Modern Chemical Manufacturing

    Our Unique Perspective as a Primary Producer

    Over decades at the core of the chemical industry, our team has constantly seen changes in technical demands and end-user requirements. Genuine chemical manufacturing experience teaches us a few things that often get missed in clipped, catalog-style listings. 3-Chloro-4-Hydroxyaniline, or 4-Amino-3-chlorophenol, plays a bigger role than most immediately recognize. It’s taken for granted in the early development of active pharmaceutical ingredients, performance dyes, pigments, and specialty polymer additives. While industry trends ebb and flow, requests for this compound steadily grow alongside new synthetic routes in R&D centers and large-scale production facilities alike.

    Looking at our facilities, we see 3-Chloro-4-Hydroxyaniline move from kilo-scale reactors up to multi-ton batches. Consistency in as-synthesized purity, moisture content, and particle morphology becomes a measure of a manufacturer's technical depth. Our own batches run over 99% certified assay by HPLC and meet an array of physical specifications because these details cascade through to our clients’ final products. A small deviation in the hydroxy or amino substitution brings unexpected consequences downstream—whether that’s inconsistent color in pigment dispersions or lower yields in fine chemical synthesis. True to our ethos, we push for exacting in-process controls at every stage, right through drying, milling, and packaging.

    From Synthesis to Specification — Our Daily Challenges

    Years of direct process improvement shape the way we work with aromatic amine intermediates like 3-Chloro-4-Hydroxyaniline. Drawing on real cycles, each lot must pass material balance on chloride content, residual by-product profile, and trace metal analysis via ICP-MS. Many end-users set tight limits for iron, copper, and even manganese traces that, at first glance, seem overcautious. Experience shows contamination at even ppm levels can generate off-campaign results, including failed catalytic hydrogenations and unwanted tinting in color-sensitive batches. The source is often equipment wear or minor upstream reagent shifts—risks flagged only by those who live the manufacturing detail day in, day out.

    We’ve worked long enough in this sector to see that simple purity percentages do not tell the whole story. Manufacturers who repackage or broker material frequently lack information about trace profile reproducibility. Direct producers spend much time with real-life sampling and trend analysis, investigating any unexpected result, and running parallel comparative studies on different drying techniques. One recent example—switching from vacuum oven drying to fluidized bed drying—eliminated thermal decomposition artefacts and noticeably improved final product color. We also examine bulk particle size distributions because end-users’ dissolution rates in solvents respond sharply to these invisible metrics. Distribution uniformity does not sound glamorous, but anyone scaling up for toner dyes or pharmaceutical synthesis soon asks for supporting sieve or laser diffraction data.

    Use Cases Shaped by Industry Demands

    The most consistent application for 3-Chloro-4-Hydroxyaniline remains as a building block in one-step and multi-step synthesis chains. In dye manufacturing, it acts as a key intermediate for developing colorants that resist degradation under invisible and visible light exposure. Having worked directly with pigment makers, we’ve come to appreciate how slight impurities alter chromatic strength and fading profiles. Performance coatings relay the same demands, as batch consistency in aromatic amine inputs often differentiates a formula that performs in sunlight and pollution from one that fails.

    Pharmaceutical manufacturers rely on the compound’s reactivity to introduce both chloro and hydroxy legs into designer molecules—integral for newer APIs looking for metabolic stability and targeted activity. One advantage of working as a direct producer lies in building custom grades for specific routes. We’ve developed processes where trace by-products are suppressed, catering to customers dealing with sensitive condensing agents and catalysts. In some of these customizations, water content deviation as small as half a percent can affect salt formation or crystallization steps. Due to the high-throughput environments these clients operate in, we’ve opened regular technical dialogue for feedback, usually ending up with written assurances of both lot-to-lot and year-on-year uniformity.

    Polymer additive manufacturers form a steadily growing segment, using 3-Chloro-4-Hydroxyaniline to insert functional moieties into engineering plastics. Substitution controls here lay the foundation for targeted chemical and thermal stability. We field frequent requests for reduced dusting and specific flow properties to integrate more seamlessly into their automated metering and extrusion lines. Often, our direct feedback loop highlights that controlling the hydration state, and not just the nominal assay, removes bottlenecks from material handling steps.

    Comparison with Similar Aromatic Amines

    Conversations with end-user chemists often get candid about the decision to go with 3-Chloro-4-Hydroxyaniline versus other substituted anilines or phenols. Non-chlorinated para-aminophenols, for instance, display different reactivity and oxidative stability. Chloro and hydroxy group positioning on the aromatic ring impacts solubility and impacts downstream coupling reactions—insights obvious only once batch-use results come back from running real reactions. Our familiarity with customers switching between isomers, including 2-chloro-4-hydroxyaniline and 3-chloro-2-hydroxyaniline, makes it clear that unintended substitutions throw off product consistency and can create regulatory headaches.

    Regulatory compliance also interlinks with specificity. Some markets prohibit certain positions or analogues owing to legacy toxicity data. As manufacturers, we routinely supply individual batch COAs (Certificates of Analysis) and have retooled QA/QC reports to detail both position-specific testing and impurity profiling. There’s an operational difference here: direct manufacturers generate these data sets in-house, as opposed to resellers who simply relay past numbers. Several projects have required us to develop specialized detection runs to distinguish between closely related impurities that could affect regulatory status. This effort rarely shows up in glossy sales brochures but matters deeply for anyone subject to regular audits.

    Handling, Storage, and Environmental Responsibility

    Practical handling of 3-Chloro-4-Hydroxyaniline presents unique challenges that seldom reach the surface in datasheets. Over time, we’ve learned that the compound’s affinity for atmospheric moisture, and sensitivity to extended air exposure, warrants not just sealed packaging, but often nitrogen blanketing. Transport during high humidity months affects both flow and caking characteristics. Anyone with years in bulk chemical production knows the headaches that come from repulping or handling agglomerated drums. We developed incremental packaging upgrades to minimize wasted material and time. Feedback from plant operators has shaped a switch towards double-liner packaging, including desiccant integration where warranted by shipping conditions.

    On a broader scale, environmental responsibility comes with being an originator. Waste minimization and effective by-product management get more attention from customers and regulatory agencies alike. Our synthesis routes have transitioned from classic chlorination methods to greener, lower-effluent options. This shift reduces both worker exposure risks and downstream water treatment burdens. Having invested in in-house waste oxidation units, we also convert spent mother liquors into less hazardous discharge before any offsite disposal. Byproduct purification workflows, integrated into standard operating procedures, capture and neutralize minor aromatics not just for compliance but to ensure long-term site safety.

    We share best practices with global manufacturing partners, recognizing that sustainable operation forms the foundation of continued customer trust. From monitoring stack emissions to routine soil and water testing at and around our main plant, environmental stewardship shapes decision-making at every step. Buyers increasingly consider supplier practices before placing orders, particularly in pharmaceuticals and food-related intermediates. To maintain those relationships, we assemble regular technical updates on synthetic route improvements, emissions captured, and material stewardship progress for review by both auditors and clients.

    Quality Assurance That Comes from Years on the Plant Floor

    Sourcing managers speak openly to us about the reliability gaps between direct manufacturers and traders. There’s no replacement for traceability that begins with raw materials procurement and doesn't end until the drums ship. Each batch of 3-Chloro-4-Hydroxyaniline leaving our plant tracks back to supplier-certified monochloro precursors, and field technicians maintain batch logs—handwritten, not just digital—for cross-checking anomalies. Our QC laboratory runs a rotating double-blind analysis of both reactor output and packaged product; if one analyst detects an outlier, we trace the deviation all the way back, which can sometimes mean pausing the line to replace filter media or swap out an upstream solvent batch.

    Clients have walked our facilities and observed real-time QC sample prep, sometimes even bringing their own analytical standards. Transparency breeds trust, so every deviation triggers a full incident timeline followed by corrective action. There’s pride in catching a rare out-of-spec run before the product ever ships. In several cases, customer R&D partners bring us feedback on subtle changes in odor or color, and we work around the clock to troubleshoot both root causes and optimal fixes. True quality assurance, for us, grows out of patience, scrutiny, and a willingness to learn from both successes and mistakes.

    Between classic melting point measurements and modern analytical runs, we’ve found that cross-validating older techniques with current equipment pays dividends. HPLC, GC-MS, and NMR analytics only deliver their full value when undergirded with hands-on chemical intuition piqued by decades of comparative sampling. Analytical chemists with years in the sector provide early warning for impurity drifts that newer software can miss. In practice, this vigilance saves both us and our clients potentially costly recalls or campaign slowdowns.

    Keeping Up with Customer Collaboration and New Demands

    Many technical advances originate not in R&D labs, but in collaborative feedback between direct producers and their key accounts. We’ve responded to requests for custom lot sizes—from modest 5-kilo R&D runs to multi-ton scale-outs exactly tailored to campaign starts—and built dedicated lines that ship according to just-in-time tankers or containerized packaging. End-user issues surface rapidly, and our technical support team stays available well beyond standard office hours. Staff chemists field questions about raw material changes, provide second-opinion analyses, or suggest modifications to improve downstream robustness. As the shape of global chemical markets evolves, flexibility and dependability keep material flowing where it’s needed most.

    Chemical procurement teams care deeply about onboarding transparent, responsive suppliers who’ll stand behind every lot sent. Long-term partnerships grow when technical staff on both sides build open channels not frozen by commercial arrangements. Our practice involves on-site technical visits to observe how our 3-Chloro-4-Hydroxyaniline integrates into downstream plants, often uncovering subtle opportunities to tweak manufacture or act as a direct consultant for clients’ own troubleshooting.

    Facing Regulation and Shifting Market Dynamics

    Markets for 3-Chloro-4-Hydroxyaniline face periodic regulatory review, especially as toxicological datasets change or analytic techniques grow sharper. From our vantage, regulatory compliance is not a ceiling but a baseline. Our product documentation packs not just batch analytics, but all documentation that ever reached the environmental, health, and safety departments of our clients. This full-documentation approach reduces response times for customer audits, letting downstream users clear their own regulatory hurdles quicker. Our in-house regulatory experts maintain tabs on shifting national laws affecting aromatics, ensuring our own process adaptations sync with the most restrictive jurisdictions our customers may face.

    With other manufacturing countries tightening controls on aromatic amines, the global supply landscape has seen sudden spot shortages and unplanned quality dips. Our plant benefits from redundancy—multiple reactor lines, on-site analytics, and trained staff sized to flex for unexpected demand. Over years, clients have changed source countries, sometimes because a single out-of-spec delivery elsewhere shut down a critical colorant or pharmaceutical production batch. The market increasingly rewards manufacturers who understand not just radical chemistry, but also logistics, technical support, and regulatory navigation.

    Looking Ahead—Building the Next Generation of Technical Partnerships

    Direct manufacturers of 3-Chloro-4-Hydroxyaniline, especially those who continually reinvest in people and process, provide the essential backbone chemical industries rely on. Our own journey began decades ago with modest bench-scale reactors and progressed through stages of process intensification, waste minimization, and end-user partnership. Modern 3-Chloro-4-Hydroxyaniline production no longer means churning out anonymous drums—each campaign is tightly managed, tailored to both regulatory and technical realities.

    Technical buyers now expect continuous improvements, not just price competition. Market feedback flows both ways: customers push for greener, safer material, while producers like us deliver by testing new reagents, automating diversion detection, and deploying advanced purification methods. The outcome is safer materials, more reliable performance, and fewer environmental headaches—outcomes that spring from living and breathing chemical manufacture every day.

    Reflecting on Experience—What Truly Matters

    Looking back, the lesson holds that real value in 3-Chloro-4-Hydroxyaniline does not rest in nominal assay values or flowery catalog descriptions. It rests in the hard-won understanding of what makes a batch good, the willingness to investigate anomalies, and a respect for the end application—whether that means a pharmaceutical’s efficacy or a pigment’s fade resistance. The market will always feature a diversity of sellers, but few can claim the practical insight that comes from watching material move from raw feedstock through every tough, technical checkpoint and onward into hundreds of high-stakes products.

    The next generation of manufacturing brings new challenges—greater scrutiny on green chemistry, evolving user requirements, and competition sharper than ever. Those stakes motivate direct manufacturers to keep refining, keep collaborating, and above all, keep learning from every shipment that leaves the line. At the factory floor, that means one thing: every batch of 3-Chloro-4-Hydroxyaniline is not just a product, but the end result of deep experience, attention, and a commitment to getting the detail right, every time.