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3,5-Dichloro-4-Hydroxybenzoic Acid

    • Product Name 3,5-Dichloro-4-Hydroxybenzoic Acid
    • Alias 3,5-Dichloro-4-hydroxybenzoate
    • Einecs 207-718-6
    • 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

    140103

    Chemical Name 3,5-Dichloro-4-hydroxybenzoic acid
    Cas Number 36071-21-1
    Molecular Formula C7H4Cl2O3
    Molecular Weight 207.01 g/mol
    Appearance White to off-white powder
    Melting Point 241-243 °C
    Solubility Slightly soluble in water
    Boiling Point Decomposes before boiling
    Pubchem Cid 98779
    Smiles C1=C(C(=CC(=C1Cl)O)Cl)C(=O)O
    Inchi InChI=1S/C7H4Cl2O3/c8-3-1-4(7(11)12)2-5(9)6(3)10/h1-2,10H,(H,11,12)
    Synonyms 3,5-Dichloro-4-hydroxybenzoic acid; 2,6-Dichloro-4-carboxyphenol

    As an accredited 3,5-Dichloro-4-Hydroxybenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White, sealed HDPE bottle containing 100 grams of 3,5-Dichloro-4-Hydroxybenzoic Acid, labeled with hazard warnings and chemical details.
    Shipping 3,5-Dichloro-4-Hydroxybenzoic Acid is shipped in tightly sealed containers to prevent moisture or contamination. Packages comply with regulations for chemical transport, properly labeled with hazard information. Standard shipping includes cushioning to avoid breakage, and transport is carried out by certified carriers, ensuring safe and timely delivery to the destination.
    Storage 3,5-Dichloro-4-hydroxybenzoic acid should be stored in a tightly sealed container, away from direct sunlight and moisture, in a cool, dry, and well-ventilated area. Keep it away from incompatible substances such as strong oxidizing agents and bases. Proper labeling and secure storage are essential to prevent accidental exposure or contamination. Always follow relevant safety and handling guidelines.
    Application of 3,5-Dichloro-4-Hydroxybenzoic Acid

    Applications of 3,5-Dichloro-4-Hydroxybenzoic Acid in Industrial Manufacturing

    3,5-Dichloro-4-Hydroxybenzoic Acid serves as a key intermediate in specialized downstream chemical sectors. The following sections detail its real industrial applications, highlighting compliance, dosage guidelines, manufacturing process steps, and the final commercial products in each area.

    1. Pharmaceutical API Intermediate Synthesis

    This compound functions as a precursor in the multi-step synthesis of pharmaceuticals, particularly certain bacteriostatic agents and anti-inflammatory drugs. Process chemists introduce it in the amidation or esterification stage under controlled batch or flow conditions. Its substitution pattern influences the final activity and impurity profile, making specification control essential for GMP manufacturing. End uses focus on high-purity APIs, with strict traceability from raw material sourcing through to finished tablets or injectables.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP/NF and EP monograph requirements for residual solvents and impurities
    • REACH and CLP regulations for hazardous chemical handling
    • FDA cGMP 21 CFR Part 211 for pharmaceutical manufacturing

    Typical usage ratio

    • 0.8 to 1.2 molar equivalents relative to target API intermediate
    • Adjusted according to yield optimization and impurity control needs

    Downstream process integration

    • Added in step 2 or 3 of multi-step organic synthesis for non-steroidal compounds
    • Introduced after initial aromatic substitution or halogenation stages, prior to final condensation

    Final product types

    • Oral and injectable anti-infective pharmaceuticals
    • Pain management and anti-inflammatory tablets
    • Specialty generic drug intermediates

    2. Agrochemical Formulation Intermediate

    Downstream manufacturers incorporate this hydroxybenzoic acid derivative in the production of selective herbicide or fungicide actives. The chlorinated structure assists in building heterocyclic scaffolds with improved degradation resistance. Integration typically takes place during early condensation or coupling reactions under controlled temperature and pH. Product quality teams enforce strict isomer and residue controls to ensure field safety compliance.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticides (JMPS)
    • ISO 9001 certified manufacturing standards
    • EU Regulation (EC) No 1107/2009 for plant protection products
    • EPA PRIA and Clean Air Act regulations for process emissions

    Typical usage ratio

    • 8% to 16% by weight in active ingredient synthesis batches
    • Formulation ratio depends on target molecule and crop registration requirement

    Downstream process integration

    • Dosed directly in heteroaromatic ring formation step
    • Blended before inert material incorporation for wettable powder or suspension concentrate preparation

    Final product types

    • Triazole-based fungicides
    • Selective herbicides for cereal crops
    • Agrochemical technical concentrates

    3. Polymer Additives and Specialty Resins

    Producers of specialty resins and advanced polymer additives use this material to introduce halogenated benzoic units into epoxy or polyester resin chains. The compound’s reactivity profile aids in crosslink density control and enhances flame retardancy without heavy metal catalysts. Its addition occurs at the prepolymer stage, with close monitoring of molecular weight distribution and end-group analysis for QC release.

    Industry compliance standards

    • UL 94 flammability standards for plastics and resins
    • RoHS Directive 2011/65/EU for halogenated substances
    • ISO 14001 environment management for chemical processing
    • REACH Annex XVII restricted substances

    Typical usage ratio

    • 0.5% to 3.0% by weight in prepolymer blends
    • Ratio selected based on targeted flame resistance level and viscosity control

    Downstream process integration

    • Introduced at initial resin monomer blending phase
    • Polymerized under inert atmosphere before molding or extrusion

    Final product types

    • Flame retardant epoxy resins
    • High-performance PCB laminates
    • Polyester casting compounds for electrical insulation

    4. Analytical Reference Material Production

    Specialty chemical reference providers use this compound as a calibration and matrix spike standard in the development of analytical solutions. Its defined purity and stability enable precise quantification in residual pesticide and pharmaceutical analysis by LC-MS/MS and GC-MS. Manufacturers synthesize, purify, and package under ISO 17034 requirements, ensuring traceability and batch homogeneity for global laboratory customers.

    Industry compliance standards

    • ISO 17034 for certified reference material producers
    • ISO/IEC 17025 for analytical testing and traceability
    • REACH registration for laboratory chemicals
    • GHS labelling for packaging and transport

    Typical usage ratio

    • Supplied as neat standard or in 1–1000 μg/mL calibration solutions
    • Exact concentration determined by analytical method and detection limit

    Downstream process integration

    • Dissolved in certified solvents for high-accuracy weighing and dilution
    • Packed into amber ampoules or vials under controlled environment

    Final product types

    • Certified calibration standards for chromatography
    • Reference materials for laboratory accreditation
    • Matrix spike solutions for environmental residue analysis
    Free Quote

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    Certification & Compliance
    More Introduction

    3,5-Dichloro-4-Hydroxybenzoic Acid: Crafting Purity and Reliability in Chemical Production

    Commitment to Trusted Manufacturing

    For those of us who handle chemistry at the source, there’s no secret shortcut to building credibility. Our business runs on trust earned over decades, backed up with careful process design and stubborn insistence on clean, consistent batches. 3,5-Dichloro-4-Hydroxybenzoic Acid, often drawn up as 3,5-DCHBA, reflects this philosophy as keenly as any compound in our catalog. Over the years, not only did we see widespread demand from research labs and specialty synthesis operations, but we witnessed end users growing wary of inconsistency. Any hint of impurity or batch variability can derail sensitive reactions—rework carries a real cost, both in time and reputation.

    We manufacture this compound from scratch, employing rigorous raw material selection and multi-stage purification steps. Our technicians stick to strict protocols, watching for color deviations and tracking every QC datapoint from titration results to melting point. If someone calls up with a concern or a traceability question, we're ready with the answer, not because regulations tell us to, but because that's how reliable supply gets built.

    Model, Specifications, and Batch Verification in Real-World Practice

    3,5-Dichloro-4-Hydroxybenzoic Acid sits within a narrow family of benzoic acid derivatives. Our current production model aims for solid form purity exceeding 99%, typically achieved through multi-solvent crystallization and careful drying cycles. That purity doesn’t just appear on a spec sheet; it must withstand the crucible of practical use. Our onsite QC lab verifies composition using HPLC and GC-MS. Melting point range stays between 227-230°C, confirmed for every batch. We keep sulfated ash content below 0.2%. Water content is monitored and held beneath 0.5% through Karl Fischer titration, as moisture plays havoc in downstream applications. Each shipment includes a full breakdown of analytical results, tied directly to the run and operator responsible.

    We choose glass-lined reactors and stainless steel contact surfaces to avoid corrosion and product contamination. Finished compound is packed in inert polyethylene containers designed for easy access in standard laboratory environments. Technical staff seal and label each drum themselves, crosschecking against our records to prevent mix-ups during busy shipping seasons.

    Bringing Raw Chemistry to Real Applications

    Years spent supporting customers in pharmaceuticals, agrochemical formulation, and material science have shown us just how particular the needs can be for this compound. In one sector, it gets deployed as a synthetic intermediate during the creation of specialty herbicides. Downstream, it appears in dye chemistry, taking its role as a core scaffold for more complex molecules. We’ve worked side-by-side with various R&D teams to refine production so each batch offers predictable reactivity, supporting consistent yields and bench-to-scale translation.

    Not every derivative of benzoic acid offers the same blend of functional groups. Here, the dichloro substitution patterns on the aromatic ring play a defining role, not just in physical properties but in reactivity under common coupling and substitution reactions. Labs grappling with multi-step synthesis know they can’t afford a wild card; a missing or misplaced halide throws off yields, spoils product, or generates side products that take hours to chase down by chromatography.

    Beyond chemical structure, team familiarity with process challenges matters. For instance, during scale-up, some chemistries risk violent exotherms or trace formation of undesired byproducts. We've faced these pitfalls before. Designing reaction profiles at the plant means we test runs on multiple scales, using everything from pilot kettles to full-scale reactors, watching for subtle process hiccups. Where variance appears, we adjust solvent choices, agitation patterns, and purification steps until every kilogram matches our exacting standard.

    Contrast with Similar Benzoic Acid Compounds

    Comparison to closely related benzoic acid derivatives—like 2,4-dichlorobenzoic acid or 3-chloro-4-hydroxybenzoic acid—often comes up in conversations with newcomers. While these analogs share base structures, even small differences in substitution pattern shift boiling points, solubility profiles, and downstream reactivity. The double chloro group in the 3,5 positions sets unique electron density on the ring, impacting both stability and activating the molecule differently for acylation, alkylation, or condensation chemistry. Ignoring these differences jeopardizes whole research programs, something our partners in pharmaceuticals learned the hard way from lesser-documented sources.

    Many chemical suppliers repackage material purchased in bulk or rely on intermediaries. We cut out these steps, seeing how this direct approach pays dividends. Trace metals content comes back lower. Color and consistency stay uniform, reducing the chance of batch variation. When buyers compare spectral fingerprints or test reactivity, the difference becomes clear: direct manufacturing avoids the degradation, unwanted isomers, or contamination that can creep in with repackaged lots.

    Supporting Innovation and Collaboration

    In the manufacturing world, supply is only part of the challenge. Research moves quickly. Customers often want to modify order quantities, run custom specs, or push technical limits. Our team—drawn from both legacy bench chemists and younger process engineers—listens carefully. A few years ago, we worked with a specialty materials producer requiring extra low residual solvent content, far beyond standard regulatory limits. Our crew trialed new drying regimens, then ran joint pilot lots at both sites to tighten the profile. They hit their targets, opening new doors for the customer’s thin-film project. On another occasion, supporting a pharmaceutical API program, we staggered production windows to match rapid development timelines, aided by cross-checking with their QC teams to ensure analytical-match boarding.

    Rapid feedback flows between the plant and our lab partners. Someone might report an unusual crystal habit or assay deviation: our operators adjust process temperature or switch solvent ratios, keeping responsiveness sharp. This mindset stands in stark contrast to arms-length procurement, which leaves producers several steps removed from the real-world needs of scientists at the bench or on the factory floor.

    Handling Challenges in Production Scale-Up

    Transitioning from lab scale to industrial manufacturing often brings out unexpected hurdles. We’ve seen how process parameters that look solid on paper can shift under the brute force of larger reaction volumes. Most chemistry plant managers know that agitation intensity, temperature uniformity, and solvent recovery make or break a synthesis at scale. With 3,5-Dichloro-4-Hydroxybenzoic Acid, our plant teams track these variables closely—down to how reactor feed lines or even stirring speed impact endpoint purity.

    Intensive analytical backup bridges the laboratory bench and the warehouse. We’ve invested in both in-line process analytics and post-batch sample stations, speeding up deviation detection and correction. A run with off-spec color or water content triggers full investigation with digital record-keeping to guide retraining or process revision. In total, our yield metrics reflect production consistency: batch yields above 95% across six months, with rework rates held below industry averages.

    Environmental and Safety Considerations

    Producing chlorinated aromatics places specific demands on safety and waste management. Our staff trains extensively, emphasizing containment and safe handling. Every stage employs closed-loop systems for solvents, minimizing worker exposure and environmental release. Spent process streams are collected separately and sent for certified treatment. Regular upgrades to our scrubbers, filters, and emissions monitoring gear lower the environmental risk and keep us compliant with the latest standards.

    Safer chemistry often means robust documentation. All operators are equipped with standard operating procedures that reflect both international norms and plant-specific controls. Periodic reviews lead to improvements that keep both the team and our neighbors safe. Sharing lessons from incidents through open reporting reduces repeat issues and fosters a culture of caution and improvement.

    Our Outlook: Emerging Markets and Technical Growth

    Demand for 3,5-Dichloro-4-Hydroxybenzoic Acid reflects the growth in fine chemical applications around the world. New materials research and the rise of personalized medicine continue to broaden its relevance. We work hand-in-hand with R&D labs in Europe and Asia, who are innovating uses we couldn't predict a few years ago. Just last year, customers in specialty pigment synthesis reported higher reactivity and color stability using our material compared to generic stocks.

    Industry doesn’t stand still. We commit resources to both laboratory method development and advanced process analytics to support tighter controls and faster batch release. Upgrades to reactor design and control systems bring down both manufacturing risk and environmental impact. In the coming years, we see automation and machine learning making further inroads in quality control, enabling smarter, faster feedback and pushing our standard even higher.

    Our Relationship with the Science Community

    The strength of any manufacturer lies in feedback from those who actually use the chemical. We value relationships with academic labs testing new applications, as much as major producers ordering in bulk. Feedback loops—through performance reports, direct samples, or even the occasional troubleshooting conversation—fuel ongoing improvement. A partnership built this way beats one built on faceless transactions every time.

    We regularly share insights at industry conferences, without shying away from technical pitfalls or production stories. A discussion with a materials chemist might spark a process tweak; a detailed failure report could inform a plant-wide retraining session. These two-way roads are essential for moving chemistry forward, one real batch at a time.

    Conclusion: Precision in Practice, Responsibility in Delivery

    Making 3,5-Dichloro-4-Hydroxybenzoic Acid isn’t just about running a validated process. It’s about supporting our partners and upholding commitments, even when the technical job throws up challenges. We keep records open, processes transparent, and lines of communication flexible. For us, purity and reliability aren’t buzzwords—they’re production targets, measured daily at the plant floor and proven across thousands of kilograms shipped worldwide. As new technologies, markets, and scientific questions emerge, we stay where we’ve always been: at the intersection of chemistry, accountability, and progress.