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4-Chloro-3-Hydroxybenzoic Acid

    • Product Name 4-Chloro-3-Hydroxybenzoic Acid
    • Alias 4-Chloro-m-hydroxybenzoic acid
    • Einecs 253-993-4
    • 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
    VTB
    Specifications

    HS Code

    852125

    Chemical Name 4-Chloro-3-Hydroxybenzoic Acid
    Cas Number 18984-00-4
    Molecular Formula C7H5ClO3
    Molecular Weight 172.57 g/mol
    Appearance White to off-white powder
    Melting Point 210-214°C
    Solubility In Water Slightly soluble
    Density 1.54 g/cm3 (approximate)
    Pka 4.2 (carboxylic acid group, approximate)
    Smiles C1=CC(=C(C=C1Cl)O)C(=O)O
    Inchi InChI=1S/C7H5ClO3/c8-5-2-1-4(7(10)11)3-6(5)9/h1-3,9H,(H,10,11)

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

    Packing & Storage
    Packing White, opaque plastic bottle containing 100 grams of 4-Chloro-3-Hydroxybenzoic Acid; screw cap, tamper-evident seal, hazard labeling.
    Shipping 4-Chloro-3-Hydroxybenzoic Acid is shipped in tightly sealed containers, protected from moisture and light. Transport complies with relevant chemical safety regulations, including labeling and documentation. The chemical should be handled by trained personnel, ensuring proper ventilation and personal protective equipment during transfer and storage. Store in a cool, dry, well-ventilated area.
    Storage 4-Chloro-3-hydroxybenzoic acid should be stored in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers. Keep the container tightly closed and protected from moisture and direct sunlight. Use appropriate, chemical-resistant containers to prevent contamination or leakage, and ensure that the storage area is clearly labeled and secured from unauthorized access.
    Application of 4-Chloro-3-Hydroxybenzoic Acid

    Applications of 4-Chloro-3-Hydroxybenzoic Acid in Industrial Manufacturing

    As the direct manufacturer of 4-Chloro-3-Hydroxybenzoic Acid, we support advanced industrial customers worldwide with consistent, high-purity supply. This material finds real, technically relevant use in a range of targeted downstream sectors, predominantly within organic synthesis and specialty chemical applications. The following application scenarios demonstrate established industrial integration, including specific compliance, formulation, and process details essential for international buyers and formulators.

    1. Intermediate for Pharmaceutical Active Ingredient Synthesis

    Pharmaceutical companies utilize 4-Chloro-3-Hydroxybenzoic Acid as a core intermediate in the synthesis of various active pharmaceutical ingredients (APIs), particularly within anti-inflammatory and antimicrobial projects. This intermediate supports key ring modification steps during multi-stage API building. Formulation chemists adjust its dosage according to yield targets and subsequent reaction compatibility, emphasizing analytic traceability under cGMP requirements. The stage of integration and stringent process controls directly influence batch consistency and final API performance.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Part II (APIs)
    • US FDA 21 CFR Part 211 for finished pharmaceuticals
    • USP/NF, Ph. Eur. monographs for relevant APIs

    Typical usage ratio

    • Ranges from 0.2 to 0.6 molar equivalents versus coupling agents within stepwise synthesis; the exact amount depends on API structure and targeted conversion rates.

    Downstream process integration

    • Introduced in the early to mid-stage steps of multi-component condensations, particularly for constructing substituted benzoic acid motifs within API molecules. Quality assurance requires complete consumption monitoring and product purity validation prior to downstream hydrogenation or esterification.

    Final product types

    • NSAID intermediates
    • Quinolone-based antimicrobial precursors
    • Pharmaceutical fine chemicals
    • Finished oral or injectable drugs containing synthetic derivatives

    2. Raw Material for Specialty Dye Manufacturing

    Producers of specialty dyes and pigments employ 4-Chloro-3-Hydroxybenzoic Acid as a stable aromatic building block in the synthesis of metal-complex and azo dye dispersions used in textile and inkjet printing. Formulators value its functional groups for enhancing dye solubility and fixation stability on fibers, requiring precise ratio adjustments according to target colorfastness and compatibility with other chromophoric agents. Environmental and workplace safety protocols mandate strict attention to waste handling after sulfonation or diazotization processes.

    Industry compliance standards

    • Oeko-Tex Standard 100 for textile chemicals
    • REACH registration for industrial dye precursors (EC No. 1907/2006)
    • ZDHC Manufacturing Restricted Substances List (MRSL)
    • ISO 9001:2015 for pigment batch quality management

    Typical usage ratio

    • Used at 5–15% w/w relative to total aromatic starting materials; ratio determined by dye hue intensity and dispersibility requirements for specific fiber or ink systems.

    Downstream process integration

    • Charged in the azo-coupling or metal complexing stages of dye synthesis, sometimes through in situ acylation before chromophore extension. Introduced prior to purification and milling, with spectral verification for batch reproducibility.

    Final product types

    • Textile disperse dyes
    • Inkjet printing pigment concentrates
    • Industrial color pastes for plastics
    • Specialty chromophores for electronic display applications

    3. Monomer Precursor for Advanced Polymer Additives

    Chemical manufacturers incorporate this raw material in the preparation of aromatic monomers and oligomers, which serve as essential co-monomers in synthesizing high-performance resins and coating additives. The hydroxyl and chlorine substituents facilitate easy functionalization in phenol-formaldehyde or polyester resin chains, controlling polymer branching and rigidity. Additive formulators tune dosing based on polymerization kinetics and required mechanical or thermal properties while satisfying all chemical registration standards in regional markets.

    Industry compliance standards

    • US EPA TSCA Inventory listing for polymer intermediates
    • EU CLP Regulation (EC 1272/2008)
    • ISO 14001 Environmental Management Systems in resin production
    • UL 94 plastics flammability standards for end-use applications

    Typical usage ratio

    • Generally between 2–8% by weight relative to base monomers. Precise ratio depends on molecular weight targets, copolymer composition, and performance specifications for the finished resin or additive.

    Downstream process integration

    • Fed during initial polymerization charging or as a late-stage chain modifier, typically in solvent or melt-form, allowing custom distribution throughout the polymer matrix. Post-addition QA ensures desired incorporation via NMR or FTIR.

    Final product types

    • Engineering plastics with flame resistance enhancements
    • High-durability coating additives
    • Specialty adhesives
    • Modified resin dispersions for composite layup

    4. Synthesis Intermediate for Agrochemical Actives

    Agrochemical companies select this material for use as an aromatic intermediate in the multistep synthesis of certain herbicide, fungicide, and plant growth regulator active ingredients. The presence of both chloro and hydroxy functional groups enables precise reactivity in electrophilic substitution reactions, allowing for tailored assembly of key aromatic fragments required in modern crop protection molecules. Downstream processors adjust input quantity based on target molecule complexity and required batch scale.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • OECD Good Laboratory Practice Principles (GLP) for active ingredient development
    • ISO 17025 accredited analytical methods for impurity profiling
    • REACH and country-specific pesticide registration (e.g., EPA in USA, EC directive 1107/2009 in EU)

    Typical usage ratio

    • Typically at 0.05–0.3 molar equivalents versus primary synthon; precise value derived from reaction stoichiometry, yield optimization, and impurity controls at pilot or commercial scale.

    Downstream process integration

    • Charged during the key coupling phase in aromatic alkylation, esterification, or condensation reactions as part of stepwise API assembly; rigorous in-process controls assure residue minimization before formulation into technical concentrates.

    Final product types

    • Selective herbicide actives
    • Systemic fungicide precursors
    • Growth regulation compounds
    • Technical active ingredients for crop protection formulations

    5. Raw Material for High-Purity Electronics Chemicals

    Manufacturers of specialty chemicals for the electronics sector rely on this compound as a precursor in the synthesis of microelectronic cleaning agents, photoresist intermediates, and dielectric modifiers. Trace impurities and metal content must meet ultra-pure specifications demanded by semiconductor and display panel producers. Material addition follows controlled, small-batch protocols with process integration at the oligomerization or surface-modification step, and process adjustments ensure compliance with electronics-industry qualification tests.

    Industry compliance standards

    • SEMI E49.6 purity guidelines for photoresist raw materials
    • IPC-5704 certification for chemical purity in PCB manufacturing
    • ISO 9001:2015 and ISO 14001 for production traceability and environmental control
    • IEC 62474 declarative standards for hazardous substances in electronic products

    Typical usage ratio

    • 1–5% w/w in chemical blends for surface treatment; dosing tailored based on targeted resist thickness, compatibility, and absence of ionic contaminants.

    Downstream process integration

    • Fed into reactor either as a solution or melt early in the formulation of wet-processing chemicals or during functionalization of photoresist polymers. Strict sub-10 ppb contaminant checks precede batch release.

    Final product types

    • Microelectronic cleaning solutions
    • Photoresists and crosslinker intermediates for semiconductor lithography
    • Functional coatings for display glass
    • Specialty additive packages for integrated circuit fabrication chemicals
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    Certification & Compliance
    More Introduction

    4-Chloro-3-Hydroxybenzoic Acid: Product Overview from a Manufacturer’s Perspective

    Introduction to 4-Chloro-3-Hydroxybenzoic Acid

    Working daily with aromatic acids, we find that each subtle change in substitution can reshape a molecule’s characteristics and its practical impact in the downstream process. 4-Chloro-3-Hydroxybenzoic Acid (also known as 4-chlorosalicylic acid) proves this with its unique balance of reactivity and selectivity. As a chemical manufacturer with decades spent optimizing benzoic acid derivatives, we have watched the demand for this compound evolve across pharmaceuticals, agrochemicals, and specialty chemistry sectors. The structure—benzoic acid ring functionalized with a chloro group at the para and a hydroxy at the meta position—creates opportunities for both direct applications and further syntheses.

    Quality Starts at Raw Materials and Processing

    Our experience teaches us that consistent results begin with raw materials. For 4-chloro-3-hydroxybenzoic acid, impurity management starts at chlorinating agents and monitoring phenolic intermediates. In our own facility, we apply a continuous monitoring system, blending high-purity chlorinating agents with strict temperature control to manage isomer distribution. We sample throughout critical reaction steps to target minimal levels of 3,4-dichloro and 3,5-dichloro byproducts. Tightly controlled crystallization yields a fine, white to off-white powder—a physical characteristic we have found to reflect high product purity along with robust analytical data. Every batch passes targeted HPLC retention time and area normalization against certified standards.

    Specifically, our model meets a purity of at least 99%, with chloride content checked by both ion chromatography and titration. Appearance, melting point (around 214–217°C), and solubility in polar organic solvents provide quick assessment before further quantification. Routine elemental and NMR analysis ensures the chloro and hydroxy positions remain correctly oriented, an important check our customers trust before engaging in downstream synthesis or registration activities.

    Applications and Real-World Usage

    Manufacturing teams like ours keep track of both the regulatory scene and practical user challenges. 4-Chloro-3-hydroxybenzoic acid stands out as a preferred intermediate for various active pharmaceutical ingredients and advanced agrochemical molecules. For instance, in pain and inflammation drug research, this compound often features as a specific-building block in selective cyclooxygenase inhibitors. Medicinal chemists look for this compound when a meta-oriented hydroxy group is required for hydrogen bonding or targeted substitutions—sometimes enabling easier glycosylation or esterification compared to its ortho- counterparts.

    Beyond pharmaceuticals, our agriculture partners press for high-purity acidic intermediates to avoid plant toxicity or off-target biological effects. Some herbicides and fungicides incorporate this structure to modulate water solubility and control reactivity. Over years of supporting pilot and commercial-scale syntheses, we see consistent feedback from clients: low-level contaminants—even at parts per thousand—can create regulatory headaches or unexpected side reactions. That’s why we stress continuous batch analytics and transparent lot documentation.

    Distinctive Features and Comparison with Closely Related Products

    On paper, it’s easy to mix up 4-chloro-3-hydroxybenzoic acid with related compounds. Experience has shown us that the hydroxy position determines both chemical reactivity and biological interaction. Move the hydroxy to the ortho position as in 4-chlorosalicylic acid, and its acidity, metal-chelating potential, and UV reactivity shift. A para-hydroxy (coupled with other ring substitutions) often changes both melting point and solvent compatibility—not to mention differences in downstream reaction pathways.

    Users sometimes ask about direct substitution with 4-chlorobenzoic acid or 3-hydroxybenzoic acid: unfortunately, these shifts in substitution pattern alter the electron density and sterics, making them poor one-to-one substitutes for most synthetic applications. Consistent analytical monitoring during process optimization has shown that certain catalysts or coupling partners respond very differently to meta-hydroxy versus ortho- or para-hydroxy benzene rings. Even small changes in polarity or resonance can influence the selectivity in Suzuki couplings and other C–C bond-forming reactions.

    As a manufacturer, we handle both 4-chloro-3-hydroxybenzoic acid and structurally similar benzoic acids. This lets us offer informed advice on which product variant best fits the end-use chemistry. Sometimes, customers ask about the cost savings in “close enough” alternatives, only to realize later that reaction yields or purification costs quickly offset small differences in raw material prices. Drawing on bench-level and pilot-scale data, we guide on selection rather than simply filling orders.

    Production Methodology and Traceability

    Producing 4-chloro-3-hydroxybenzoic acid at scale requires balancing batch efficiency with safety and regulatory traceability. Our reactors run under inert gas with automated temperature feedback during both chlorination and hydrolysis steps. Water and solvent effluent are collected for neutralization, with analytics run on both organic layer and aqueous wash streams. This is not just regulatory best practice; it directly impacts both crude yield and environmental compliance.

    We store lot-level data extending from raw material certificate of analysis to finished product HPLC chromatograms and NMR spectra. This end-to-end traceability is born from real-world experience—customers facing surprise audits, product recalls, or regulatory submissions count on being able to trace every kilo back to source documentation. Our quality assurance protocols don’t just “tick the box”—they reflect lessons gathered from actual plant-floor challenges and industry partnerships.

    Packing, Handling, and Shipping

    Anyone dealing with fine chemicals understands that packaging matters just as much as what comes off the reactor. 4-chloro-3-hydroxybenzoic acid is a stable solid at room temperature, but prolonged exposure to light or moisture can lead to discoloration or slow hydrolysis. We've shifted to using multi-layer lined drums and high-density polyethylene bags, which keep the product stable during long-distance shipping and warehouse storage—a direct response to customer feedback about caking and contamination.

    We monitor temperature and humidity during transit for large shipments, and small lab quantities are packed under nitrogen for critical research use. All containers feature tamper-evident seals and batch number labeling. Customers regularly request documentation certifying compliance with REACH, TSCA, and other regulations—so our staff keeps all relevant registration and status papers ready alongside each shipment.

    Challenges and Industry Concerns

    Supplying high-purity aromatic acids is not free of challenges. Over the years, we’ve dealt with shifting global supply chains for chlorinating agents, tighter environmental rules around effluent disposal, and evolving customer requirements for trace-level impurity data. Customers sometimes send samples from other sources for reanalysis—and discrepancies in purity or isomer content almost always trace back to upstream process shortcuts.

    As regulations have tightened, both in the European Union and Asia-Pacific, we have expanded in-house analytical capability to include LC-MS and GC-MS impurity profiling. What began as an internal improvement soon became a requirement for many international customers. For instance, a pharmaceutical client’s audit of our plant prompted us to overhaul certain solvent recovery and residue-handling practices. Because we adapted early, we didn’t need to return or recall material, and the client maintained their regulatory timeline.

    Handling of hazardous waste also stands as a major focus. Having invested in a closed-system neutralization and off-gas scrubbing setup, our team captures and treats all process-side halogenated effluent. These environmental safeguards helped us avoid production stoppages during sudden regulatory inspections. Investments in analytics and environmental control don’t always show a quick return, but our team has learned their real value surfaces in both credibility and customer retention.

    Continuous Improvement and Customer Feedback

    Open feedback channels with users help us identify bottlenecks in both application and supply. A few years ago, several buyers in pharmaceutical R&D informed us of a trend: some competitors’ supplies failed to dissolve cleanly in standard reagents, leading to fouling of downstream columns. We undertook a root-cause investigation, tracing the problem to subtle differences in drying technique and crystal form. By moving to freeze-drying and fine-mesh sieving, we now supply a product that dissolves rapidly without clumping—a direct result of user-driven improvements.

    We also hear from clients scaling up to semi-bulk or bulk applications. Here, attention to reproducibility becomes critical. One kilo produced under ideal lab conditions may behave very differently when manufactured at the multi-ton scale. Our technical staff supports process validation and troubleshooting. Once, an agrochemical customer found unexpected precipitation during scale-up—drawing on historical process records, we pinpointed a trace-level impurity missed in early pilot runs and modified the wash sequence to remove it at source.

    Many of our customer relationships have persisted for over a decade, in part because our sales and technical teams have real hands-on experience. Communicating complications—rather than hiding or downplaying them—lets partners avoid costly surprises. Our willingness to release selected in-process data, in confidence, has led several customers to engage us in joint development programs.

    Sustainability Initiatives and Future Directions

    Chemical sourcing is under the lens for both customers and authorities. As market pressures for sustainable chemicals intensify, we’ve invested in process analytics to reduce solvent and water usage per kilo produced. By repurposing waste streams and adapting modern crystallization techniques, our team has managed to increase yield while shrinking the overall waste footprint. These efficiencies have translated into smaller carbon footprints for ourselves and our downstream partners.

    We also participate in chemical recycling pilot programs with university partners—seeking out ways to recover and reprocess halogen-bearing streams. These programs sometimes uncover new market insights; for example, a process previously seen as inefficient may find use for another industry’s effluent as a feedstock. Working with these networks has provided creative alternatives to waste disposal and highlighted opportunities for green chemistry practices throughout our operations.

    As advanced material topics gain importance, inquiries keep coming about 4-chloro-3-hydroxybenzoic acid’s use in specialty polymer and coating chemistry. While pharmaceuticals and agrochemicals still account for most sales, customers increasingly experiment with this compound to modulate adhesion and tuning cross-linking rates in resins and new plastics. These emerging uses keep challenging our technical staff and often lead to collaborative product development.

    Conclusion: Trust Built on Consistency, Expertise, and Openness

    Our day-to-day work refining production and documentation practices puts us in a strong position to support users who demand clear product identification, robust analytical traceability, and technical partnership. 4-chloro-3-hydroxybenzoic acid is more than a catalog item—it’s the result of careful optimization at every step, from reagent selection through to secure shipment. The compound’s unique balance of reactivity and functional group orientation supports a wide range of end-uses, but also requires real-world know-how and open communication to ensure that each batch meets the pace and rigors of modern industry.

    Whether the end-use is a tightly regulated pharmaceutical ingredient, a new crop protection molecule, or a specialty polymer modifier, our team combines technical knowledge with a commitment to solving real user problems. Facing evolving global standards, supply chain complexities, and ever-tightening regulatory expectations, we stay focused on data-backed improvements and responsive service. For those looking to build stable, long-term supply partnerships, transparency and hands-on expertise continue to be the values that set our product—and our approach—apart from the rest.