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4-Amino-2,6-Dichlorophenol

    • Product Name 4-Amino-2,6-Dichlorophenol
    • Alias 2,6-Dichloro-4-aminophenol
    • Einecs 225-078-4
    • 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

    996253

    Chemical Name 4-Amino-2,6-Dichlorophenol
    Molecular Formula C6H5Cl2NO
    Molecular Weight 178.02 g/mol
    Cas Number 17694-42-9
    Appearance Off-white to light brown crystalline powder
    Melting Point 143-147°C
    Solubility In Water Slightly soluble
    Pka Approx. 7.1 (phenolic OH)
    Density 1.56 g/cm³
    Synonyms 2,6-Dichloro-4-aminophenol
    Pubchem Cid 18013
    Hazard Statements Irritant to skin and eyes
    Inchi Key INUVJZZZEGZOSU-UHFFFAOYSA-N
    Storage Conditions Store in a cool, dry place, tightly closed

    As an accredited 4-Amino-2,6-Dichlorophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Sealed amber glass bottle, 25 grams, with tamper-evident cap, labeled with chemical name, CAS number, hazard symbols, and handling instructions.
    Shipping 4-Amino-2,6-Dichlorophenol should be shipped in tightly sealed, clearly labeled containers, protected from light, moisture, and physical damage. Transport under cool, dry conditions in compliance with local regulations. Use appropriate hazard labeling, and provide relevant safety data sheets. Handle with personal protective equipment to prevent exposure during transit.
    Storage 4-Amino-2,6-dichlorophenol should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and acids. Protect it from moisture and direct sunlight. Label storage containers clearly and use secondary containment to avoid spills or accidental contact. Always follow local safety regulations and chemical hygiene protocols.
    Application of 4-Amino-2,6-Dichlorophenol

    Applications of 4-Amino-2,6-Dichlorophenol in Industrial Manufacturing

    4-Amino-2,6-Dichlorophenol is a specialty chemical intermediate with key roles in downstream synthesis for industrial pharmaceutical, agrochemical, dye manufacturing, and polymer additive processes. As a direct manufacturer, we enable controlled, traceable supply for formulation operations demanding consistency and regulatory compliance. The following sections detail its specific applications in current industrial sectors, each supported by applicable international standards and processing requirements.

    1. Pharmaceutical Intermediate for Antibacterial API Synthesis

    In the pharmaceutical sector, 4-Amino-2,6-Dichlorophenol serves as a core building block during the synthesis of specific antibacterial active pharmaceutical ingredients (APIs), including those in the chlorinated phenol derivatives class. Production facilities typically utilize this compound in multi-stage synthesis processes, subject to GMP and quality control protocols. The downstream synthesis chain includes amide formation and further functional group modifications prior to final API isolation and purification.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • 21 CFR Parts 210/211 (US FDA)
    • European Pharmacopoeia monographs for intermediate use
    • China Pharmacopoeia processing requirements

    Typical usage ratio

    • 10–28% w/w relative to reaction batch mass, adjusted based on expected yield and subsequent protection/deprotection steps
    • Optimization guided by target impurity profile and regulatory submission data

    Downstream process integration

    • Input material in nucleophilic substitution and amide coupling reactions
    • Dosed after solvent charge under nitrogen blanket to prevent oxidative degradation

    Final product types

    • Antibacterial API intermediates (e.g., chloroaminophenol derivatives)
    • Finished APIs for oral and topical drug formulations
    • Hospital-grade disinfectant precursors

    2. Synthesis of Crop-Protective Herbicide Intermediates

    This raw material is widely employed in the synthesis of selective herbicide molecules, especially those utilizing dichlorophenolic scaffolds. Agrochemical formulators use it during early intermediate stages to introduce chloro and amino functionalities in active molecules. These processes require controlled addition protocols and trace impurity management to comply with global crop protection regulations.

    Industry compliance standards

    • FAO/WHO Specifications for Agricultural Pesticides
    • ISO 9001:2015 Quality Management Systems
    • REACH Regulation (EC 1907/2006) for raw material registration
    • China National Standard GB 2763 for pesticide product control

    Typical usage ratio

    • 5–20% by weight, tailored to target reaction conversion and specific crop-selectivity factors
    • Process engineers refine charges during scale-up to minimize secondary chlorination

    Downstream process integration

    • Charged during etherification or condensation reactions for synthesis of pre-herbicidal intermediates
    • Incorporated during continuous-flow or batch reactor operation, with in-line analytical checks for unreacted phenolics

    Final product types

    • Herbicide intermediates for cereal and legume crop protection
    • Active herbicidal compounds formulated into granules and emulsifiable concentrates
    • Pre-mix concentrates supplied for commercial farming operations

    3. Raw Material for Reactive Dye Synthesis

    4-Amino-2,6-Dichlorophenol acts as a core substrate in the synthesis of reactive dyes for textile applications, allowing precise introduction of amino and chloro moieties into chromophore structures. Dye manufacturers utilize it in controlled diazotization and azo coupling steps to produce colorants with tailored lightfastness and washfastness properties. Compliance with international dye safety and environmental emission norms is paramount throughout the production lifecycle.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textile chemicals
    • ZDHC MRSL (Manufacturing Restricted Substances List)
    • EU REACH Annex XVII conformity for azo dyes
    • Japan Law for Control of Household Products Containing Harmful Substances

    Typical usage ratio

    • 12–25% by mass of chromophore precursor batch
    • Final percentage set by target shade and chromatic depth, validated in pilot runs

    Downstream process integration

    • Dosed during primary amination and subsequent diazo coupling with phenol derivatives
    • Integrated into closed, automated reaction loops to minimize worker exposure

    Final product types

    • Reactive dyes for cotton, viscose, and blended textiles
    • Colorant dispersions for printing and dyeing houses
    • Custom dye preparations for fastness-critical applications (workwear, uniforms)

    4. Component in Antioxidant Additive Synthesis for Polymers

    Polymer additive producers incorporate this dichlorinated aminophenol to synthesize specialty antioxidant molecules for plastics and rubbers, targeting stabilization of end-use materials under high-heat and UV exposure. The compound typically reacts with aliphatic or aromatic intermediates, producing hindered phenol antioxidants. Downstream process flows prioritize impurity rejection and ash content control to meet automotive and food contact material standards.

    Industry compliance standards

    • FDA 21 CFR 177.1520 for polymers in food contact
    • ISO 9001:2015 QMS for polymer additives manufacturing
    • EU Regulation (EU) No 10/2011 for plastic food packaging
    • UL 94 Flammability Standard for Plastic Materials

    Typical usage ratio

    • 2–7% weight of total antioxidant formulation, depending on polymer matrix type
    • Adjusted down for transparent or medical-grade plastics where clarity and extractables are critical

    Downstream process integration

    • Added during condensation with alkylating agents to create hindered phenol antioxidants
    • Blended directly into masterbatch or resin compounding lines with direct QC sampling

    Final product types

    • Antioxidant masterbatches for polyethylene, polypropylene, and ABS
    • Stabilizer blends for synthetic rubbers and elastomers
    • Food-safe antioxidant additives for packaging

    5. Intermediate for Specialty Disinfectant Formulation

    Producers of industrial and institutional disinfectants utilize this phenol derivative as an intermediate in the synthesis of strong oxidizing biocidal agents. The material enters as a reactant during the preparation of chlorinated aromatic disinfectants effective against fungi, bacteria, and viruses. Manufacturing integrates stringent in-process monitoring to meet approvals for use in healthcare, food processing, and sanitation.

    Industry compliance standards

    • US EPA FIFRA regulations for antimicrobial pesticide chemicals
    • European Biocidal Products Regulation (BPR, Regulation (EU) 528/2012)
    • GB 38598-2020 Hygienic Standards for Disinfectants (China)
    • EN 1276 Testing for Bactericidal Activity of Chemical Disinfectants

    Typical usage ratio

    • 15–30% of biocidal intermediate batch, depending on target spectrum and application method
    • Ratio tuned to maximize active moiety yield and manage residual phenolic content

    Downstream process integration

    • Dosed after primary solvent mixing and neutralization
    • Incorporated into closed reactor systems with in-line HPLC verification of purity

    Final product types

    • Hospital-grade hard surface disinfectants
    • Food processing plant sanitizers
    • Public facility rapid-action cleaning solutions

    6. Precursor in Fine Chemical Manufacture of Analytical Reagents

    Laboratory and analytical reagent manufacturers use this dichlorinated aminophenol as a precursor to synthesize high-purity reference standards and colorimetric indicators for industrial and research analysis. Batch manufacturing maintains rigorous traceability and impurity profiling to enable effective downstream calibration and sample testing, complying with laboratory reagent norms.

    Industry compliance standards

    • ISO 17034 for Reference Material Producers
    • Analytical Reagent Grade specification standards (ACS, ISO)
    • Good Laboratory Practice (GLP) requirements
    • GMP for laboratory chemical synthesis

    Typical usage ratio

    • 18–32% by mass of indicator batch; refined to ensure complete reaction and prevent by-product formation
    • Purity target generally above 99.5% for analytical use

    Downstream process integration

    • Initiates reaction with azo or sulfonic acid containing species
    • Processed in glass-lined reactors to avoid ionic contamination

    Final product types

    • Analytical colorimetric reagents for titration and water analysis
    • Certified reference materials used in QA/QC labs
    • Industrial process monitoring indicators
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    Certification & Compliance
    More Introduction

    4-Amino-2,6-Dichlorophenol: Hands-On Experience From The Lab Floor

    Introducing Our Product

    Clean white powder, high stability, and reliable performance: these are the traits we look for in every batch of 4-Amino-2,6-Dichlorophenol we send out. Over the years, we have refined our production so each shipment of 4-Amino-2,6-Dichlorophenol arrives with consistent melting point, color, and purity value above 99%. Our technicians don’t settle for good enough. Day-to-day, their focus goes into tightening filtration and crystallization, reducing trace byproducts, and maintaining the crystalline texture so dissolving and handling the phenol becomes easier for formulators and researchers alike.

    What Sets 4-Amino-2,6-Dichlorophenol Apart?

    Our experience manufacturing this compound goes back to an era when purity above 98% for specialty intermediates seemed challenging. Since then, incremental tweaks have helped us reach industry-beating reproducibility and stability, especially for those running process scaleups or seeking repeatable results in dye synthesis and intermediate production. The dichlorinated aminophenol structure packs reactivity in the para-amino group and significant electron withdrawal at the 2 and 6 ring positions, opening access to downstream heterocycles, advanced dyes, and unique pharmaceutical scaffolds.

    Some of our peers stick to older reaction systems—stronger acids, metal catalysts, or untamed reaction profiles—leading to more variability, byproducts, or excess waste. By contrast, our dedicated phenolic production suits, paired with modern glass-lined vessels, ensure contamination-free output. Analytical chemists on the floor keep a close eye using GC, HPLC, and TLC throughout each run, so material meets both purity and trace metal specs expected in modern synthesis.

    Applications: Why It Matters In Real Synthesis

    Research teams in colorant industries, agrochemical labs, and pharma intermediates frequently ask about reliability batch to batch. No one likes finding a subtle impurity just before a scale-up or watching final product hues shift on account of a minor contaminant. Through hard-won experience, we've learned even small lapses in process control can cause changes in reactivity or interfere in later functionalization steps. 4-Amino-2,6-Dichlorophenol’s strong electron-withdrawing groups dramatically shift its reactivity, lending selectivity for nucleophilic substitution reactions that benefit developers building advanced molecular frameworks.

    For dye and pigment chemists, the dual chloro and amino functionality simplifies downstream steps—condensation, cyclization, and coupling happen cleanly, making the workflow straightforward. Years before, our lab would watch as off-spec batches led to fading or dull colors downstream. Through trial, error, and cleaner reaction matrices, we learned to prevent these frustrations at the source. Today, pigment and dye creators rely on the stability and clarity of our 4-Amino-2,6-Dichlorophenol to anchor their hues and shades.

    In pharmaceutical research, the core scaffold provides an entry point for many anti-infective and enzyme modulator investigations. The exact position of the substituents creates a unique environment for receptor binding or later functionalization. Here, trace contaminants or even minor regioisomeric impurities can change everything—from in vitro activity to scale-up yields. Our experience has taught us to over-deliver on material data and documentation, since every anomaly in these fields often leads to delayed timelines or ambiguous results.

    The Model We Supply

    4-Amino-2,6-Dichlorophenol production here centers on two standard models: one suited for dye-house applications demanding larger lots with stable melting range and color, and another custom-purified line for pharmaceutical and research applications that expect tight specifications for elemental impurities and infrared fingerprinting. Customers involved in pilot-scale pharmaceutical work often ask for additional spectral documentation and trace solvent/moisture reporting—so we submit every batch through FTIR and moisture-specific titration.

    Every container leaves the plant in HDPE drums with air- and moisture-tight liners. We use this setup after several rounds of trial packaging; it keeps the product bright white, reduces caking, and prevents the typical yellowing some customers have experienced with less-protected storage. The standard granular particle size also eases weighing, minimizes dusting, and supports efficient dissolution in many typical organic solvents.

    Where a process demands ultrapure grades, we can push beyond the routine specs through recrystallization, tighter distillation, and additional filtration, always confirming each customized run matches the customer's specific usage plan. Having supplied both kilo-scale and multi-ton orders, we know the pinch points—how a minor packaging error or shipping delay can upend a production schedule. That’s why our logistics team coordinates with labs and distribution to guarantee fast, traceable delivery.

    Differences Compared To Other Products

    Mixing up 4-Amino-2,6-Dichlorophenol with its close cousins like unsubstituted aminophenols, mono-chloro derivatives, or meta-configured analogues invites process failures. Each variant on the phenolic or amino group—when swapped in a reaction aiming for a specific fused ring system or color shade—changes overall reactivity, selectivity, and stability. Through thousands of real-world runs, we’ve witnessed unexpected shifts in downstream functionalization, solubility, and color quality when users opt for non-identical intermediates.

    Mono-chloroaminophenols, for example, can bring about faster couplings but lack the substrate selectivity crucial in pharmaceutical intermediate synthesis or advanced pigment molecules. On the other hand, the fully di-chlorinated, para-amino arrangement of our 4-Amino-2,6-Dichlorophenol confers a unique reactivity profile not attained with other aminophenols. Researchers running comparative studies have told us time and again about higher yields, more robust process window, and cleaner isolation when sticking with our compound as opposed to more commonly available meta- or non-chloro-substituted types.

    In terms of color, the dichloro structure resists oxidative darkening better than its mono- or unsubstituted siblings. This translates directly to brighter finished dyes and longer shelf life for pigments. Small-scale dye houses especially appreciate how our product avoids the brownish cast, which can creep in with lesser grades, and instead maintains stable chroma in the final application.

    Backstory: How Experience Shapes Quality

    Every batch run brings fresh lessons, but some insights stay with us across decades. At the start, operators noticed how humidity swings in certain seasons affected both powder texture and melting consistency. Lab investigations revealed trace water would alter downstream reactivity and sometimes even promote mild auto-oxidation over months in storage. New protocols ensured dehumidification and vacuum-packing directly at the filling station, which solved a slew of customer complaints downstream in final application development.

    On a handful of projects with dye and pharma clients in regions facing tighter environmental scrutiny, trace metal and halide contamination posed serious challenges. Only by shifting to advanced, acid-free chlorination steps and installing in-line detection for residual metals did we get below the strictest thresholds. The switch to cleaner, closed-loop processes made our 4-Amino-2,6-Dichlorophenol a clear favorite for advanced molecular platforms where sensitive downstream biology or optical purity really mattered.

    Close partnerships with our research customers have led to practical improvements, too. Some years back, a frequent pigment user flagged inconsistencies in their crystallization and color stability. Two weeks of collaborative troubleshooting, including dual-lab spectral analysis and shared process notes, revealed a subtle, seasonally-driven impurity from a prior step. Refining our solvent workup cut variability near zero and removed guesswork for everyone involved. In a field where one off-batch can disrupt operations for weeks, these open feedback channels mean a robust product every time.

    Supporting Sustainability And Safety

    Environmental protection and worker safety have become indispensable values, not just buzzwords. Chlorinated aromatics demand extra stewardship in waste and emissions handling. Our production supervisors track effluent streams and invest in onsite purification to bring discharge below regulatory targets. On the shop floor, every operator wears filtered masks and is trained to handle phenolic compounds safely, minimizing exposure and keeping cross-contamination at bay.

    Much of our waste reduction comes from continuous process improvements. For example, solvent recovery systems, originally installed just for cost-saving, now play a leading role in reducing hazardous waste. On the energy side, switching to high-efficiency reactors and managing water consumption at every step lets us shrink our footprint—small steps that, when multiplied across multiple product runs, make a real difference. Feedback from customers confirmed that these changes not only help the environment but offer peace of mind regarding compliance in their own operations.

    Transport and storage logistics reflect this commitment. Early on, many facilities struggled with unexpected degradation or spills during shipping. After a handful of tough lessons, our packaging line engineered robust, double-sealed containers and incorporated tamper-proof closures. This protects both the end product and those who handle it.

    Maintaining High Standards: Adapting To Industry Changes

    Throughout regulatory shifts—especially in regions following stricter REACH and EPA criteria—our approach hasn’t been to sit back. We reevaluate raw material sourcing, analytical screening, and documentation every time those rules change. That means regular investment in new lab equipment, staff training, and, at times, restructuring documentation processes so any user down the line, from bench chemist to regulatory auditor, can trace the entire lifecycle of each 4-Amino-2,6-Dichlorophenol lot we release.

    More customers now ask for tailored analysis—trace impurity data, extended moisture profiles, batch-to-batch comparability, and real-time tracking. Our in-house teams support these requests not as add-ons, but as integral parts of the production routine. We encourage partners to question our specs, request additional tests, or demand tighter tolerances, confident each run can withstand scrutiny. For international buyers, we keep documentation transparent and up to date, minimizing the bureaucratic hurdles that can otherwise stifle new projects.

    Digitalization also supports quality. With real-time production tracking, batch histories stay linked to QC data from start to finish. On more than one occasion, we’ve nipped a potential spec deviation before shipping, thanks to automated flagging and thorough human review. These checks help us and our clients avoid costly downstream disruptions or hidden incompatibilities.

    Stronger Partner Relationships Through Product Consistency

    Building long-term trust with laboratories, research teams, and manufacturers means delivering the same product with the same expected performance every time. Our open material records, willingness to jointly analyze any issue, and deep technical expertise make it possible for researchers to scale their projects with fewer unknowns. Mistakes never help anyone, and we have experienced our share of production and logistical hurdles. Rather than brush problems under the rug, we treat each as an opportunity to better our process, retrain staff where needed, and offer customers transparency until every challenge is solved.

    Strong technical support doesn’t stop at shipment. We routinely field calls about modifying handling conditions, optimizing storage, or finding best-fit solvents based on very particular downstream reactions. Sharing real process data helps users avoid common pitfalls we faced years ago. In-house R&D keeps scouting for new purification methods, green chemistry updates, and safer process adaptations. What starts out as an incremental upgrade for one project often ends up raising standards for every user.

    Challenges In Modern Production, And Tackling Them Head-On

    Continuous supply chain uncertainty, fluctuating raw material cost, mounting compliance criteria, and the push toward sustainability all shape how we make—and improve—our 4-Amino-2,6-Dichlorophenol. The trick isn’t to chase every trend, but to anchor improvements in real lab and customer feedback.

    Global logistics issues have repeatedly reminded us not to rest easy on longstanding sources for chlorinated solvents or amine feedstocks. Our sourcing team maintains backup suppliers and evaluates quality independently for every lot in. Fast communication lines let us flag inconsistencies before they cascade into finished product hiccups. In times of sudden market shifts, these safeguards have shielded both us and our partners from common material shortages or quality surprises.

    On occasion, customers have flagged regulatory changes affecting ingredient acceptability in their own markets. Our compliance staff keeps active watch and responds rapidly to documentation or reformulation requests. Equally, pressure for ultra-low environmental impact in both waste and solvent handling has spurred us to phase out more hazardous auxiliary chemicals where possible, keeping one step ahead of likely future restrictions.

    Looking Forward

    The need for reliable, high-purity specialty chemicals only increases each year, as both scientific ambition and environmental accountability climb higher. Teams counting on our experience—whether in colorants, advanced polymers, or pharmaceutical intermediates—require a supplier who sees around the next corner. By always seeking technical gains, keeping open lines with users, and reinforcing every batch with modern QA and sustainability checks, we continue to raise the bar for ourselves and all who rely on our 4-Amino-2,6-Dichlorophenol.