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2-Amino-3,6-Dichlorobenzoic Acid

    • Product Name 2-Amino-3,6-Dichlorobenzoic Acid
    • Alias 2-Amino-3,6-dichlorobenzoic acid
    • Einecs 223-024-9
    • 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
    VTB
    Specifications

    HS Code

    974180

    Name 2-Amino-3,6-Dichlorobenzoic Acid
    Cas Number 7577-77-1
    Molecular Formula C7H5Cl2NO2
    Molecular Weight 206.03 g/mol
    Appearance Off-white to light yellow solid
    Melting Point 206-210 °C
    Solubility Slightly soluble in water
    Purity Typically >98%
    Synonyms 2-Amino-3,6-dichlorobenzoic acid; 3,6-Dichloroanthranilic acid
    Smiles C1=C(C=C(C=C1Cl)Cl)C(=O)O
    Inchikey SDQBHHRNZSRIFS-UHFFFAOYSA-N
    Storage Temperature Room temperature
    Hazard Class Irritant

    As an accredited 2-Amino-3,6-Dichlorobenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 100g package is a sealed amber glass bottle with a white screw cap, featuring hazard labels and a clear product identification label.
    Shipping 2-Amino-3,6-Dichlorobenzoic Acid is shipped in tightly sealed containers, protected from moisture and incompatible substances. It should be handled with appropriate safety measures, and transported according to local, national, and international chemical regulations. Ensure upright transport, avoid extreme temperatures, and follow all hazard labeling and documentation requirements during shipping.
    Storage 2-Amino-3,6-Dichlorobenzoic Acid should be stored in a tightly closed container in a cool, dry, well-ventilated area, away from incompatible substances such as strong oxidizers. Protect it from moisture and direct sunlight. Ensure the storage area is equipped with adequate ventilation and comply with all chemical safety regulations to prevent contamination and degradation of the chemical.
    Application of 2-Amino-3,6-Dichlorobenzoic Acid

    Applications of 2-Amino-3,6-Dichlorobenzoic Acid in Industrial Manufacturing

    As a direct manufacturer engaged in fine chemical synthesis, we supply 2-Amino-3,6-Dichlorobenzoic Acid to established downstream sectors, supporting consistent formulation processes and adherence to regulatory and customer-specific requirements. Our technical team focuses on quality control, batch traceability, and collaborative process adjustments with end-users in diverse industrial production lines.

    1. Active Pharmaceutical Ingredient Intermediates for Antibacterial Drugs

    Pharmaceutical formulators use this acid as a core intermediate in the multi-step synthesis of select quinolone and benzoic acid-based antibacterial agents, especially for the production of specialty APIs indicated for resistant bacterial infections. The material must comply with strict impurity limits, and precise coupling reactions ensure correct electronic effects on target intermediates within regulated pharmaceutical cGMP environments. Each synthesis step receives careful in-process control, as even minor variations in this precursor sequence directly impact assay and impurity profiles of the final API.

    Industry compliance standards

    • Current Good Manufacturing Practices (cGMP, ICH Q7)
    • US Pharmacopeia (USP) relevant API monographs
    • European Pharmacopoeia (Ph. Eur.) for APIs
    • FDA and EMA impurity and trace contaminant guidance

    Typical usage ratio

    • 0.3–0.7 molar equivalents per final API batch, adjusted based on process yield and stage-specific stoichiometric requirements

    Downstream process integration

    • Nitration-reduction and amide coupling step before ring closure in API synthesis trains
    • Input into pharmaceutical reactors with continuous monitoring for acid and amine purity
    • User calibrates amount per targeted API batch size and impurity management plan
    • On-site batch verification through in-house HPLC and GC analysis

    Final product types

    • Generic and patent-specific quinolone antibiotic APIs
    • Broad-spectrum antibacterial drug substances for oral and injectable forms
    • Pharmaceutical intermediates for licensed drug supply chains
    • Regulated antibiotic primary building blocks

    2. Dye and Pigment Synthesis for Textile and Leather Processing

    Users in the colorant industry employ this raw material in the diazotization and coupling stages of producing high-performance azo and anthraquinone dyes. Its dichloro and amino substitution allows synthesis of colorfast, shade-stable pigments frequently specified for technical textiles, synthetic fabrics, and specialty garment applications under heavy washing and sunlight exposure. In pigment operations, operators balance dosage to achieve consistent batch-to-batch tinting strength and compliance with textile and leather chemistry standards.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textile chemicals
    • REACH Regulation (EC) No. 1907/2006
    • ZDHC Manufacturing Restricted Substances List (MRSL)
    • Local Textile and Leather Environmental Regulations (GB/T 17592-2011 in China, EU Ecolabel)

    Typical usage ratio

    • 5–15% of target dye molecule weight, adjusted to match shade depth, substrate compatibility, and lightfastness requirements

    Downstream process integration

    • Diazotization and coupling reactions in dye and pigment reactors
    • Inclusion in colorant precursor feed tanks with controlled temperature and pH
    • Used before drying, grinding, and dispersing steps
    • Batch verification for purity, residual chlorine, and water solubility prior to textile application

    Final product types

    • Reactive and acid dyes for cotton and wool textiles
    • Anthraquinone pigments for automotive textiles and fashion fabrics
    • Colorfast powder dyes for synthetic leathers and upholstery
    • Technical colorants for workwear and industrial textiles

    3. Agrochemical Synthesis for Selective Herbicides

    Leading crop protection chemical manufacturers utilize this compound as a building block in multi-stage syntheses of specialty benzoic acid-based herbicides. The dichloroamino substitution facilitates selectivity and metabolic stability needed for weed control agents compatible with modern rotational crop systems. End users require clear documentation on content uniformity, residual solvents, and channel-specific right-to-operate certifications, as incorrect feed ratios or contamination may impact downstream herbicide efficacy and regulatory status.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • EPA (40 CFR Part 174) Pesticide Manufacturing Standards for the US
    • European Regulation (EC) No 1107/2009 for Plant Protection Products
    • ISO 9001:2015 quality management for agrochemical suppliers

    Typical usage ratio

    • 0.2–0.5 molar ratio per target herbicide batch, customized for desired efficacy and crop selectivity profiles

    Downstream process integration

    • Amidation and further derivatization during preformulation of active herbicide substances
    • Direct input to closed synthesis systems post-initial filtration and drying steps
    • Continuous monitoring for degradation and residual starting material
    • Trace-level QC evaluation to comply with pre-marketing authorization

    Final product types

    • Selective post-emergent herbicide actives
    • Formulated wettable powder and granular herbicides for commercial agriculture
    • Technical-grade herbicide concentrates for bulk supply
    • Custom pre-mixes for integrated weed management programs

    4. Specialty Chemical Feedstock for Halogenated Resin Modifiers

    Polymer and composite manufacturers use our material to introduce controlled amino and dichloro groups onto aromatic monomers and resins, enhancing flame retardancy, thermal stability, and chemical resistance in engineering plastics. Feedstock purity and controlled substitution impact crosslinking capability and ensure resin performance in finished automotive, aerospace, or electronic components. Production managers select this raw material during the initial formulation blend and fine-tune its input based on the desired mechanical and safety properties of end-use polymers.

    Industry compliance standards

    • UL 94 Flammability Standard for Plastic Materials
    • RoHS Directive 2011/65/EU regarding halogen content
    • REACH (EC) No 1907/2006 for polymer additives
    • ISO 9001/ISO 14001 for resin and composite production

    Typical usage ratio

    • 1.5–6% by weight in base polymer blend, with range tailored to target thickness, processing temperature, and ignition resistance

    Downstream process integration

    • Addition at monomer pre-polymerization or melt-compounding stage
    • Mixing in closed system blenders before extrusion or molding
    • Quality inspection for homogeneity and halogen distribution
    • Post-processing physical property assessment on pilot resin lots

    Final product types

    • Halogenated modified polyamides and polyesters
    • Flame-retardant composite panels for transportation sector
    • High-performance cable insulation resins
    • Specialty electronic encapsulation compounds
    Free Quote

    Competitive 2-Amino-3,6-Dichlorobenzoic Acid prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    2-Amino-3,6-Dichlorobenzoic Acid: Insights from the Manufacturer

    A Closer Look at Our 2-Amino-3,6-Dichlorobenzoic Acid

    Every batch of 2-Amino-3,6-Dichlorobenzoic Acid leaving our facility shares the same goal: uncompromising quality and consistency for chemical producers who count on reliable intermediates. Producing this compound for years has meant running into real-world challenges and iterating processes that work not only on paper, but at scale and in genuine operational contexts. The chemical—sometimes referred to as our Model: ADCA-02—offers a specific set of features that regular dichlorobenzoic acids or aminobenzoic acids miss, and over time those differences have shown up in everything from downstream yield to ease of handling.

    What Sets 2-Amino-3,6-Dichlorobenzoic Acid Apart?

    The substitution pattern on the aromatic ring matters a great deal when it comes to process chemistry. As we have refined our synthesis route for 2-Amino-3,6-Dichlorobenzoic Acid, the positional selectivity—chlorine atoms sitting at the 3 and 6 positions and an amino group at 2—has opened doors for our partners in dye, pharmaceutical, and agrochemical work. With each chlorination and amidation step, complexities emerge that only steady practice reveals: solvent choices, temperature profiles, distillation rates, and purification techniques all must hit their mark to avoid isomeric byproducts and color impurities. Unlike 3,5 or 4,6 dichloro isomers, this molecule helps clients avoid competitive side reactions in the presence of certain catalysts or coupling agents.

    In practical terms, we see fewer complaints about product stability and downstream discoloration from our 2-amino-3,6 variant than from broader-spectrum dichlorobenzoic acids. The molecule’s unique substitution gives it a solubility profile essential for specific amide couplings or Suzuki reactions, especially when used at elevated temperatures or in water-sensitive catalyst systems. Partnering with project chemists, we’ve witnessed firsthand how an extra impurity from a tangled synthesis chain can trip up final assays and batch acceptances.

    Key Characteristics Shaped by Manufacturing

    We make this product in our main bench to pilot-scale plant, where traceability and batch documentation stay open for customer review. Our highest-selling specification is designed with purity exceeding 99% by HPLC, with related chlorinated aromatic impurities kept below 0.2%. Moisture content never drifts above 0.5%—a detail we target specifically for users running high-throughput, trace-moisture sensitive coupling work. Free-flowing powder is never just about aesthetics; it saves hours in loading, transfer, and reaction cycling, especially for automated or semi-automated production lines.

    Granule size in this product often surprises first-time customers. Over-milled, dust-laden batches have caused headaches for both chemists and production supervisors in the past, notably leading to filter blockages and irregular slurry formation. We’ve optimized our sieving and drying to deliver a material that doesn’t clump or segregate during handling, even in high-humidity regions or in batch reactors running several shifts back to back.

    Our main clients see physical appearance and pack integrity as non-trivial. Lumpy, off-color acid signals something unacceptable either in purity, moisture, or trace contaminants. We run colorimetric checks alongside chromatographic quantification, so our powder appears as an off-white to pale yellow solid. Even a hint of brown or green inflection leads to full root-cause analysis before shipping.

    Usage and Application: Ground-Level Realities

    End-users tap this acid for its power as a building block, not as a commodity. As such, it finds its way most directly into amide-formation processes in pharmaceutical intermediate synthesis, as well as into pigment and dye precursor routes where the pattern of amino and chloro substitution tunes optical and solubility properties. In sodium salt form, we’ve observed it flowing efficiently through multi-stage reactors, minimizing clogging and rate-limiting transfer steps.

    For one major customer scaling a generic drug intermediate, a switch to our 2-Amino-3,6-Dichlorobenzoic Acid—and away from previous stocks blended with isomeric content—trimmed rejected lots by 8% across the fiscal year. We worked with their analytical team to debug process inconsistencies, and our tighter spec on isomeric purity proved to be the lever. Other producers using our acid in azo dye production have cited sharper batch coloration and improved stability in textile applications, particularly in regions where water quality and standardization for coloring agents fluctuate.

    In agri-chemicals, ring-functionalized benzoic acids sometimes struggle with shelf-life or reactivity problems if not processed correctly upstream. Careful control over the acid’s purity and granule form helps blenders and co-formulators avoid both loss of activity and caking during storage. Over our years in manufacture, we’ve collaborated with several formulators to modify our drying and packaging regimes, bringing in anti-static liners and robust layered protection for overseas shipments. Feedback from these partners—fielding material under varied warehouse climates—shows a marked decrease in hardening, clumping, and performance failures at the blending stage.

    Comparison with Other Products: What Matters in Practice

    Direct competitors typically offer broader spectrum dichlorobenzoic acids or related nitro derivatives, but the selectivity and reactivity of the 2-Amino-3,6 isomer brings notable advantages. Pharma-grade applications count on lowest possible isomer impurity to minimize both side product formation and downstream purification headaches. It’s not uncommon for customers to try out-of-the-box replacements bearing similar aromatic profiles—3-amino-2,5-dichlorobenzoic or 2,6-dichloroisonicotinic acids—yet they often circle back due to reactivity mismatches and uneven yields in later coupling or reduction steps.

    The specific arrangement of substituents can make or break a multi-step synthetic campaign. Some partners in the dye sector have attempted to cut costs by trialing more available or superficially similar benzoic acids, only to encounter color fastness or solubility setbacks at pilot scale. Feedback has consistently indicated that the performance and purity of our 2-Amino-3,6-Dichlorobenzoic Acid, with its tightly controlled process and impurity monitoring, reduces such unpleasant surprises. In crop protection product synthesis, where consistency of intermediates directly influences final efficacy and regulatory clearance, that consistency translates to fewer failed batches and more reliable final outcomes. Aromatic acids with loosely defined amino or chlorine positions, or with slightly different solubility characteristics, sometimes slip past initial screening but disappoint in scale-up trials with unexpected fouling or byproduct formation.

    While some see the differences between dichloro and mono-chloro amino acids as relatively minor, in real process terms this can mean a doubling of purification workload at each downstream step. That’s a lesson we’ve learned by not just producing but troubleshooting along with our customers. When customers reached out with issues related to incomplete reactions or variable yields, a careful analysis revealed mismatched identities or grades in the competing feedstocks, reinforcing the value of sticking with a specifically manufactured—and verified—product.

    Continuous Improvement: Insights from the Factory Floor

    Our production teams and process engineers treat optimization as a daily necessity, not a set-and-forget routine. Over several campaigns, after feedback from formulation chemists and operators, we have adjusted not just reaction conditions but the entire handling pathway for 2-Amino-3,6-Dichlorobenzoic Acid. By moving from an older dry milling technique to a modern fluid-bed granulation approach, dust and oversize particles dropped out of customer reports. Such changes did not come as directives from market surveys—they grew from interplay between real production data and client results.

    By minimizing in-process hold times and switching to inert-gas protected packaging, we observed a drop in unwanted hydrolysis or oxidation markers. These findings link directly to downstream pain points—formulators dealing with unexpected color changes or performance drops found the new batch conforms more closely to target specifications. Shifting to higher grade purification media for final filtration offered another bump in performance, measured in real savings for our larger-volume customers who demanded predictable, low-impurity intermediates.

    In-process sampling and early feedback loops make more difference than late-stage quality control. Early in our ramp-up years, we learned that a batch doesn’t care about the calendar—if a spectral marker starts drifting outside norms, we trace back all the way to raw material intake and reclaim or blend out the deviation. Customers remembered the time lost dealing with rejected shipments from generic suppliers or traders sharing no root-cause transparency. Our staff worked directly with partners to reconstruct entire synthesis trees, identify pinch points, and tune production lots until the output turned dependable.

    Environmental and Safety Considerations: Manufacturing Responsibility

    Making specialty chlorobenzoic acids carries environmental and occupational safety commitments. Chlorinated intermediates sometimes attract stricter local regulation and require more advanced effluent handling systems—and this is not just a regulatory checkbox for us, it’s a reflection of experience surviving audits and continuously improving the zero-discharge and reclamation setups. Staff handling 2-Amino-3,6-Dichlorobenzoic Acid manage both routine and non-routine releases as part of their usual workflow, using metered dosing and closed-system transfers to keep exposure low.

    We maintain rigorous documentation for all precursor and byproduct stream analyses, so downstream users know what is—and isn’t—present as a trace or residual in their own batches. Waste minimization gets attention at each step in the sequence; spent filtrates and washings wind into reclamation loops with recovery rates reported monthly and process changes triggered by loss trends instead of rigid calendar timelines.

    Over the years, evolving guidance around dichloroaromatic compounds prompted us to recalibrate our storage and disposal. We partner with outside auditors and local inspectors, opening our balances and system logs to review. The facility investing in local community support and workforce protection practices demonstrates a willingness to meet expectations not just from law, but from our own standards of long-term operation. Clients querying for REACH or other regional documentations can request supporting files at any stage. For us, this transparency isn’t marketing—it’s part of attracting users who actually care what happens after the acid leaves our loading bay.

    Partnering for Better Outcomes: Client Collaboration Drives Progress

    Synthetic chemists, formulators, and process managers become part of our feedback loop by necessity. We encourage process visits and send technical leads directly onto client sites when issues or improvements appear on the horizon. Many downstream users grew tired of canned responses from bulk suppliers; by engaging early and troubleshooting shoulder-to-shoulder, we’ve prevented more late-stage failures than any standard product literature can promise.

    Recently, a client in the pigment field faced unexpected filter fouling in their semi-solid dye reactor process. Instead of long-distance troubleshooting or guesswork based on standard specs, our lead chemist joined their production run, traced the fouling to insoluble trace salts unique to their water source, and recommended minor in-plant process tweaks. The issue resolved within two batches, saving a week of downtime and thousands in lost production hours.

    Active partnerships foster valuable product improvements. We treat every downstream process report—favorable or critical—as a tool for improvement, not a liability report. This ongoing real-world input, not just in-bound quality complaints, shapes our further chemical development. Case in point: after one pharmaceutical client shared extraction profiles over a multi-month period, we retooled our recrystallization solvent regime, offering tighter particle size control that boosted their blend rates and reduced impurity pickup.

    Looking Forward: Serving Next Generation Chemical Manufacturing

    We see the future of 2-Amino-3,6-Dichlorobenzoic Acid not in bulk production for commodity markets, but as a specialty intermediate carried by flexibility and tight process tailoring. Our team scrapes through feedback from every major production scale-up, ties data back to production metrics, and seeks out both internal and third-party analyses for validation. This loop, built from years on the factory floor and stubborn root cause analysis, keeps product batches moving forward with actual client requirements—not theoretical specifications—in mind.

    In daily practice, every drum or container tells a story of iterative improvement, adjusting to what our customers see on line—whether smoother dissolving rates, cleaner extractions, or faster cycling without caking. As manufacturing partners, we drive toward ever-better quality through chemical insight, practical flexibility, and open communication. The line between producer and user blurs—instead of one-sided handoffs, our product history exists as a mutually shaped narrative.

    Progress in chemical manufacturing depends on learning, adaptation, and the willingness to discard old assumptions in favor of real, observed outcomes. The path that brought us here—operational tweaks, direct user engagement, zero-excuse handling of failures—continues to define our commitment to anyone relying on our 2-Amino-3,6-Dichlorobenzoic Acid. Each year, new challenges from partners push us to refine, expand, and deliver with greater assurance. That’s not a tagline, it’s the ongoing experience we take back onto the plant floor every single day.