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3-Chlorosalicylic Acid

    • Product Name 3-Chlorosalicylic Acid
    • Alias 3-Chloro-2-hydroxybenzoic acid
    • Einecs 202-219-2
    • 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

    954012

    Chemical Name 3-Chlorosalicylic Acid
    Cas Number 320-73-6
    Molecular Formula C7H5ClO3
    Molecular Weight 172.57 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 155-158°C
    Boiling Point 344.2°C at 760 mmHg
    Solubility In Water Slightly soluble
    Density 1.551 g/cm3
    Flash Point 161.7°C
    Pka 2.94
    Smiles C1=CC(=CC(=C1Cl)C(=O)O)O
    Pubchem Cid 12070
    Inchi Key ZFVDLHCUMMAJHF-UHFFFAOYSA-N

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

    Packing & Storage
    Packing Amber glass bottle, screw cap, labeled with chemical name and hazard symbols, containing 100 grams of 3-Chlorosalicylic Acid.
    Shipping 3-Chlorosalicylic Acid is shipped in tightly sealed containers to prevent moisture and contamination. It should be handled with appropriate protective equipment. The product is transported according to regulations for non-hazardous chemicals, avoiding direct sunlight and extreme temperatures. Shipping documentation includes safety data and handling instructions to ensure safe delivery.
    Storage 3-Chlorosalicylic acid should be stored in a tightly sealed container, away from moisture, direct sunlight, and incompatible substances such as strong oxidizers. Keep in a cool, dry, well-ventilated area. Store at room temperature and avoid exposing the chemical to extreme heat. Proper labeling and access restriction are essential to ensure safe handling and prevent accidental exposure or contamination.
    Application of 3-Chlorosalicylic Acid

    Applications of 3-Chlorosalicylic Acid in Industrial Manufacturing

    As a direct manufacturer, we supply 3-Chlorosalicylic Acid for industrial formulations where this intermediate delivers critical functional benefits for specialized downstream sectors. The following sections detail major real-world applications, each featuring distinct compliance requirements, technically specified usage levels, integration methods into production lines, and final product classes manufactured by our customers.

    1. Pharmaceutical Intermediate for Non-Steroidal Anti-Inflammatory Drugs (NSAIDs)

    Major API manufacturers use this material as a building block for synthesizing advanced NSAID intermediates, particularly in the elaboration of chloro-substituted salicylate derivatives. Inclusion at the coupling or acylation step allows downstream producers to streamline the synthesis of anti-inflammatory agents in compliance with regulated good manufacturing practices.

    Industry compliance standards

    • ICH Q7 GMP Guidelines for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs relevant to active intermediates
    • US FDA 21 CFR Part 211 (Finished Pharmaceuticals)
    • EDQM CEP for controlled intermediates

    Typical usage ratio

    • 0.2—0.5 molar equivalents relative to parent aromatic acid, adjusted based on yield optimization and impurity profile during multi-step synthesis

    Downstream process integration

    • Added during early condensation or replacement step in multi-stage batch reactors, followed by crystallization or purification to isolate target pharmaceutical intermediates

    Final product types

    • Active pharmaceutical ingredients for NSAID classes (e.g. diflunisal derivatives)
    • Registered pharmaceutical grade intermediates
    • Custom chloroaromatic bulk APIs

    2. Dye and Pigment Intermediate Manufacturing

    Large-scale pigment and dye producers select this raw material for the introduction of chloro-functional groups in azo and anthraquinone chemistry, which imparts enhanced color fastness and improves dye uptake on textiles and plastics. Its unique substitution allows controlled chromophore modification at critical synthesis stages.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for chemical intermediates
    • OEKO-TEX Standard 100 (restricted substance content)
    • DIN EN ISO 105 (Color Fastness Testing)
    • Textile Industry Restricted Substances List (ZDHC MRSL)

    Typical usage ratio

    • 2—6% w/w relative to total organic input in dye coupling or diazotization, with level tailored to shade, solubility, and regulatory residue limits

    Downstream process integration

    • Dosed during the chlorination or diazo coupling steps within glass-lined reactors, followed by filtration and drying into bulk colorant intermediates

    Final product types

    • Reactive, direct and vat dyes for textile processing
    • Pigments for plastics coloration
    • Specialty colorant intermediates for ink blends

    3. Agrochemical Synthesis: Herbicide and Pesticide Intermediate

    Downstream agrochemical plants utilize this compound as a core functional intermediate in synthesizing chloroaromatic agents targeting weed and pest control. Its placement in the molecular backbone delivers specific herbicidal or pesticidal activity for end products requiring strict residue management and selectivity.

    Industry compliance standards

    • FAO/WHO Technical Guidelines for Pesticide Specifications
    • ISO 9001:2015 certified agrochemical manufacturing
    • EU Regulation (EC) No 1107/2009 for plant protection products
    • US EPA Registration for pesticide technical grade intermediates

    Typical usage ratio

    • 0.1—0.3 molar ratio per target active ingredient batch; dosage adjusted by structure-activity relationship and residue analysis

    Downstream process integration

    • Introduced at the targeted halogenation or condensation step, often under controlled pH and temperature to minimize byproducts in pilot- and production-scale reactors

    Final product types

    • Technical grade herbicide actives (e.g. chlorinated benzoic derivatives)
    • Pesticide intermediates for broadleaf weed control
    • Formulated crop protection agents

    4. Specialty Polymer Modification for Advanced Resins

    Within advanced materials production, processors integrate this compound during chain modification or crosslinking, exploiting its chloro and carboxyl functionalities to tune resin reactivity, enhance thermal stability, and introduce niche chemical resistance for electronics, coatings, and specialty engineering plastics.

    Industry compliance standards

    • ISO 9001 Quality Management for plastics and polymers
    • RoHS 2011/65/EU for electronics-grade resins
    • UL 94 (Flammability for Plastics)
    • REACH SVHC compliance for raw material input

    Typical usage ratio

    • 0.5—2% w/w based on total resin formulation; concentration depends on targeted glass transition temperature and crosslink density

    Downstream process integration

    • Fed into the melt or solution polycondensation stage prior to extrusion or casting; adjustment of feed sequence ensures uniform incorporation with minimal side-reactions

    Final product types

    • Modified epoxy and polyester resins for circuit boards
    • Functional coatings for electronic encapsulation
    • Structural thermoset compounds with enhanced chemical resistance

    5. Corrosion Inhibitor Additive for Industrial Fluids

    Manufacturers serving the industrial fluids market add this compound as an active inhibitor component within water-based and oil-based formulations to control oxidative degradation and metal surface passivation, especially in high-chloride or cyclic process environments where other aromatic acids underperform.

    Industry compliance standards

    • ASTM D1384 (Corrosion Testing of Engine Coolants)
    • ISO 8044 (Corrosion of Metals and Alloys)
    • REACH Annex XVII (Industrial Chemical Use)
    • OEM-specific in-house corrosion control protocols

    Typical usage ratio

    • 150–600 ppm by weight in finished concentrates; dosage fine-tuned per application, fluid chemistry, and system metallurgy

    Downstream process integration

    • Dosed at final blending stage before packaging to ensure homogeneity and stability, typically followed by filtration and final QC on corrosion metrics

    Final product types

    • Industrial cooling water treatments
    • Hydraulic and metalworking fluids
    • Anti-corrosion additive packages for automotive fluids
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    Certification & Compliance
    More Introduction

    Understanding 3-Chlorosalicylic Acid as a Core Intermediate

    Why 3-Chlorosalicylic Acid Stands Out in Technical Production

    As a chemical manufacturer, we encounter a range of benzoic acid derivatives, each with distinct structural tweaks that influence their chemical behavior and industrial performance. Among these, 3-chlorosalicylic acid (3-CSA) consistently delivers versatility and reliability on commercial scales. Producing 3-CSA in our reactors involves the careful chlorination of salicylic acid under controlled conditions, a process that we have refined for consistent purity. The end result is a colorless to slightly off-white crystalline powder with outstanding handling properties.

    Chemically, the molecule features a carboxyl group and a hydroxyl group ortho to a chlorine substituent on the aromatic ring. This placement fundamentally affects how 3-chlorosalicylic acid interacts with reagents and substrates. These structure-property relationships play out in our own synthesis lines where different salicylic acid derivatives often behave unpredictably during scale-up. Compared to para- or ortho-chloro compounds, the meta isomer (3-chloro) brings a carefully moderated level of reactivity for certain electrophilic processes and ring-substitution techniques. 3-CSA resists over-chlorination better than more reactive isomers, which can limit byproduct formation and improve reproducibility.

    We consistently produce 3-chlorosalicylic acid with a purity exceeding 99%, confirmed by HPLC and NMR. Our specifications cover moisture content below 0.5%, minimal chloride impurities, and a melting range of 157–161°C. Every lot is verified for trace residual solvents because our customers in pharma and fine chemicals need minimal interference in downstream reactions. Typical packing uses lined drums or fiber containers to protect material integrity until it enters the synthesis pathway. Over the past decade, our site has handled metric tons every year for domestic and export markets, so long-term reliability and consistent crystallinity matter greatly.

    Applications: Bridging Intermediates for Pharmaceuticals and Agrochemicals

    The main utility for 3-chlorosalicylic acid arises from its adaptability in synthetic chemistry. In our own experience, the compound serves as a robust building block for exploring new pharmaceutical analogues, especially those requiring orthogonal modification on the benzene ring without unwanted side reactions. Medicinal chemistry groups use 3-CSA in the development of non-steroidal anti-inflammatory drugs and as an intermediate in manufacturing kinase inhibitors. The presence of both a carboxylic acid and a phenolic hydroxyl offers two clear entry points for selective functionalization by acylation or alkylation.

    Agrochemical developers also request regular shipments of 3-CSA for new herbicide and fungicide targets. The compound’s structure interacts favorably with ring-closure reactions and amide linkages, which are pivotal in developing selective crop protection agents. Our technical team supports direct scale-up for these processes because 3-chlorosalicylic acid’s solubility profile allows for simple transfers from lab to pilot plant. Our product dissolves easily in hot ethanol, acetone, and dimethylformamide—a practical benefit for synthesis planning.

    In recent years, new market segments have emerged for 3-CSA in specialty pigment preparation and as a starting point for advanced dyes. Laboratory tests show the compound offers reliable chlorination patterns much more controllably than 4-chloro- or 5-chloro analogs. This is significant because uncontrolled halogenation creates costly purification headaches in complex dye synthesis. Our clients working on organic electronics and material science projects have noted improved yields and cleaner conversion profiles when using the purified meta-chloro isomer.

    Working with 3-Chlorosalicylic Acid: Practical Insights from Manufacturing

    Producing high-quality 3-chlorosalicylic acid at scale takes hands-on experience and a close watch on process controls. The chlorination of salicylic acid requires attention to temperature, solvent choice, and agitation rates. We target reaction temperatures below 70°C to minimize polychlorinated byproducts; small deviations can quickly decrease purity. Once chlorination reaches completion, we use vacuum filtration and sequential washing to remove inorganics. We train our operators to recognize the correct crystalline endpoints by color and morphology, which lets us pull precise samples for GC and titration spot-checks.

    Handling of the finished product reflects both our in-house needs and those of end users. 3-CSA’s low volatility keeps loss rates and operator exposures down, but static generation during drum filling poses a dust control challenge in dry winter months. We manage this by adjusting airflow and grounding all packaging stations. Maintaining granular integrity during transfer helps avoid dissolve-and-recrystallize steps for customers who need consistent sizing for batch reactors.

    We have found that the shelf life of 3-chlorosalicylic acid remains stable over three years when sealed with silica gel desiccants. Each shipment receives a unique batch identifier and test results, which go into our digital manufacturing record system for full traceability. Product recalls are rare in our experience—and we attribute this to lot integrity and robust QA procedures rather than just statistical luck.

    Technical Differentiation: Comparisons with Related Compounds

    The salicylic acid family covers a wide range of derivatives—some with alkyl, chloro, or nitro substitutions at various ring positions. Our process lines have manufactured these analogs side by side, so small differences between products in real-world settings become evident. Unlike 4-chlorosalicylic acid, the 3-position chloro group on 3-CSA typically slows down nucleophilic substitution on the ring, leading to fewer unplanned side products and a more stable intermediate under acidic or basic conditions. This moderation in reactivity becomes critical during lengthy multistep syntheses, especially for pharmaceutical targets where purity and reproducibility carry regulatory weight.

    Compared to 5-chlorosalicylic acid, the 3-chloro variant exhibits improved solubility in polar aprotic solvents, which supports higher reaction efficiency in acylation and etherification chemistries. In analytical labs, the meta isomer tracks more sharply by TLC and shows cleaner separation by column chromatography because its ring electronics differ from other isomers. These features have led to fewer purification steps for our processing partners, reducing their workload and material losses.

    Another distinction stands out in safety and handling. While all salicylic acid derivatives share general chemical family handling requirements, 3-CSA dust formation rates tend to be lower under routine plant conditions. This simplifies containment strategies and lessens the frequency of inhalation exposure risk in our packing areas. Toxicological profiles remain consistent across chloro isomers—none of them classified as acutely toxic under standard exposure scenarios—but we still recommend routine PPE and well-ventilated work environments.

    In terms of impurity profiles, our plant’s history with multiple isomers informs us that 3-chlorosalicylic acid permits tighter control over trace metal and halide contamination, especially compared to more reactive para- or ortho-isomers. Rigorous monitoring of raw material lots and strict adherence to clean-in-place protocols reduces the possibility of cross-contamination in our chlorination vessels. Experienced plant chemists recognize that these margins can define product acceptance or rejection at quality control gates.

    Supporting Modern Synthesis Scale-Up

    Our repeat customers prioritize robust quality and secure supply. We shift production schedules seasonally to meet bulk shipment timelines for pharmaceutical and agri-tech partners who are scaling up their own product launches. 3-chlorosalicylic acid continues to support these needs because it performs with fewer surprises during scale-up and kilogram-to-ton conversions. We share best practices with application engineers at customer sites, advising on solvent selection and optimal charging sequences to avoid unnecessary heat build-up or foaming during batch reactions.

    Feedback loops from our downstream partners shape our process improvements. Several formulation chemists have pointed to improved product shelf life when starting with 3-CSA instead of mixed isomer materials. We responded by refining our crystallization steps, which narrowed particle size distributions and further reduced water content per kilogram. Consistency from drum to drum matters most for high-throughput settings; no one wants a reactive intermediate that changes subtly from lot to lot.

    Maintaining open channels with our raw material suppliers lets us avoid price and availability shocks. Our procurement team establishes multi-year contracts for incoming salicylic acid and chlorine, tracking each supplier’s quality statistics and logistical reliability. This keeps production interruptions to a minimum—a lesson we have learned from years of global supply chain variability in specialty chemistry.

    Quality Assurance, Traceability, and Documentation

    Continuous improvement underpins our approach to quality. All production is backed by thorough documentation, electronic lot tracking, and archived analytical records. Randomly selected lots undergo confirmatory GC-MS screens and comprehensive Karl Fischer moisture assays. Routine XRPD (x-ray powder diffraction) tests verify polymorph consistency as this influences downstream reactivity for critical pharma APIs. For high-value customers, we support custom batch documentation, TSE/BSE-free declarations, and additional third-party lab verification as needed for international registrations.

    On rare occasions, clients have raised questions about trace impurities following extended storage. By working closely with formulation teams, we have identified critical storage points for product that spends months in interim warehousing. Air-tight packing and the inclusion of desiccant packets address most stability issues, reducing hydrolysis risk. These real-world lessons—rather than textbook theories—shape our standard operating methods today.

    Regulatory compliance forms an essential part of our business model. We have successfully registered 3-chlorosalicylic acid in major jurisdictions under REACH and other region-specific protocols. Our technical documents include detailed impurity profiling and Toxicological Safety Assessments, supporting both worker safety and downstream consumer product safety. Auditors from client companies and regulatory authorities perform scheduled and unscheduled inspections; their feedback consistently points to our site’s order and the documentation trail for each product lot.

    Looking Ahead: Market Trends and Development

    The demand landscape for 3-chlorosalicylic acid is evolving. Pharmaceutical innovation cycles now move quickly, with synthetic chemists favoring compounds they can tune efficiently for biological activity. Our 3-CSA production line has responded by pushing batch sizes upward and tightening purification procedures. Digitalization has made it easier for us to monitor and analyze trends in customer usage that forecast demand spikes, so we are prepared to allocate reactor capacity with minimal lead time.

    In the agrochemical sector, new herbicide and fungicide regulations drive requests for purer and more consistently sourced intermediates. On top of purity, end users now expect traceability for sustainability and compliance reasons. Our plant invests in tracking each critical raw material from supplier origin to final product drum, mirroring the transparency that modern clients require. These tools would have seemed excessive decades ago, but today they underpin long-term supplier-customer partnerships.

    Technological innovations open further application doors for 3-chlorosalicylic acid. R&D collaborations in the organic electronics field report successful adoption of this compound into charge-transfer dyes and donor–acceptor frameworks for flexible displays and sensors. Colorant and pigment chemists share similar success stories; controlled halogenation permits fine-tuning of hue and fastness properties not easily achieved with other starting materials. Even in niche fields like corrosion inhibitor research or optical brightener synthesis, our clients value reliability and the ability to predict how each lot will fit their process.

    Challenges and Solutions from the Manufacturer’s Perspective

    Production at scale is never painless. Unexpected events, from raw material quality swings to unplanned reactor shutdowns, impact both upstream and downstream partners. Over years of managing 3-chlorosalicylic acid synthesis, we have adapted by both doubling down on preventative maintenance and investing in operator technical training. Experienced employees can spot off-normal reaction profiles and troubleshoot process drift long before it threatens batch rejection. We cross-train staff on related product lines, which keeps production nimble and supports surge demand without compromising on product consistency.

    Waste minimization remains a focus—especially given tightening global environmental standards. Our ongoing projects examine efficient chlorine recovery and practical solvent recycling for reaction workups. These improvements directly cut operational costs and reduce environmental impact. On the effluent side, our biological treatment system eliminates residual aromatic and halogen compounds before discharge, verified by periodic third-party environmental audits.

    Supply chain stability plays a greater role every year. Geopolitical events, weather disruptions, and logistical bottlenecks have, at times, delayed shipments of crucial raw materials. Our approach combines maintaining diversified supplier relationships with rigorous incoming inspection against our specifications. Close communication with logistics teams limits downtime caused by customs or regulatory paperwork. These are not abstract plans—each improvement responds to challenges we confront every month.

    Supporting End Users: Technical Partnerships That Deliver

    Our goal as a manufacturer extends beyond filling drums. Many of our customer relationships begin with tailored technical support—guidance on reaction optimization, troubleshooting crystallization, or achieving precise purity for regulatory submissions. We often participate in joint piloting or scale-up exercises, both on-site and at customers’ locations, with our development chemists wearing protective gear alongside client staff. This boots-on-the-ground approach fosters the real-world insights that theory or remote consultancy can’t match.

    Feedback loops matter. We routinely survey customers on key performance metrics for each batch: appearance, solubility, reaction conversion, and impurities. Negative feedback gets logged, analyzed, and acted upon at monthly improvement meetings. Positive feedback is shared across operator teams as a reminder that incremental process improvements translate directly to customer success.

    Our documentation support doesn’t stop at the certificate of analysis. Increasing numbers of clients now require application notes, comparative studies with other isomers, and process safety overviews for laboratory management teams. Our internal application chemistry group generates case studies and “lessons learned” articles that share successes as well as failed experiments. The knowledge transfer helps chemists try new approaches—whether it means tweaking reaction conditions or choosing a less common solvent—and saves time by learning from real-world manufacturing setbacks.

    Conclusion

    Industry experience confirms that 3-chlorosalicylic acid continues to earn its place in the chemist’s toolkit, due not only to inherent molecular characteristics but from years of manufacturing and application refinement. From setting specifications to refining operational controls and solving day-to-day production challenges, we strive to meet the evolving demands of modern synthetic chemistry. We welcome collaboration, input, and innovation from formulation partners and research teams who see new potential in this versatile intermediate.